11.4% Efficiency non-fullerene polymer solar cells with trialkylsilyl substituted 2D-conjugated polymer as donor.

Simutaneously high open circuit voltage and high short circuit current density is a big challenge for achieving high efficiency polymer solar cells due to the excitonic nature of organic semdonductors. Herein, we developed a trialkylsilyl substituted 2D-conjugated polymer with the highest occupied molecular orbital level down-shifted by Si-C bond interaction. The polymer solar cells obtained by pairing this polymer with a non-fullerene acceptor demonstrated a high power conversion efficiency of 11.41% with both high open circuit voltage of 0.94 V and high short circuit current density of 17.32 mA cm-2 benefitted from the complementary absorption of the donor and acceptor, and the high hole transfer efficiency from acceptor to donor although the highest occupied molecular orbital level difference between the donor and acceptor is only 0.11 eV. The results indicate that the alkylsilyl substitution is an effective way in designing high performance conjugated polymer photovoltaic materials.

Bulk-heterojunction <span class="Chemicn class="Chemical">al">polymer solar cells (PSCs) are composed of a blend active layer of a p-type conjugated <ne">span>n class="Chemical">polymer as donor and an n-type semiconductor as acceptor sandwiched between an anode and a cathode where at least one of the two electrodes should be transparent123. The n-type semiconductors used as acceptor in the PSCs include fullerene derivatives4, n-type conjugated polymers56789101112 and n-type organic semiconductors (n-OS)1314151617181920212223. Among the acceptors, n-OS acceptors show distinguished advantages of easy tuning of absorption and electronic energy levels, strong absorbance, good morphology stability and more suitable for flexible devices. Therefore, the non-fullerene PSCs with n-OS as acceptor have attracted great attention recently, and their power conversion efficiency (PCE) has rapidly increased to 9–11% (refs 24, 25, 26).

In PSCs, due to the low dielectric permittivity and relatively large exc<span class="Chemicn class="Chemical">al">itons binding energy of organic semdonductor, <ne">span>n class="Chemical">polymer donor and acceptor with cascading enegy levels (the lowest unoccupied molecular orbital (LUMO) and highest occupied molecular orbital (HOMO) levels of the conjugated polymer donor should be higher than the correponding LUMO and HOMO levels of the acceptor) are specially required to provide a driving force for excitons dissociation at the heterojunction interface27282930. In this cascade model, it is generally accepted that the LUMO/HOMO energy levels differences between the donor and acceptor (ΔELUMO and ΔEHOMO) should be larger than 0.3 eV for efficient excitons dissociation to overcome binding energy (usually 0.3–0.5 eV) of the excitons produced in the donor and acceptor phases by absorbing photons27303132. One crucial issue of the PSCs is their relatively large photon energy loss (Eloss) at 1 sun illuminaiton which is defined as Eloss=Eg–eVoc, where Eg is the lowest optical bandgap of the donor and acceptor components27333435. The reported Eloss in the most efficient fullerene-based PSCs is typically 0.7–1.0 eV. The larger Eloss is associated with the larger driving force for excitons dissociation and the relative large non-radiative recombinations27283637, thus creating a great challenge to simultaneously obtain a large open circuit voltage (Voc) and a high short circuit current density (Jsc) in the PSCs.

In the non-<span class="Chemicn class="Chemical">al">fullerene PSCs, medium bandgap <span>n class="Chemical">polymer donor–low bandgap n-OS acceptor pairs are particular interesting due to their complementary absorption in the visible-near infrared region, providing an effective approch for getting a high Jsc. In these systems, another interesting feature is the easy energy level matching to get higher Voc with lower Eloss of 0.6–0.7 eV (refs 21, 25, 26, 38). For example, the non-fullerene PSCs based on a medium bandgap D-A copolymer PffT2-FTAZ-2DT as donor and a low bandgap n-OS IEIC (ref. 19) (Eg of 1.59 eV) as acceptor with a ΔEHOMO of 0.17 eV showed a PCE of 7.3% with a Voc of 0.998 V and a Eloss of ca. 0.60 eV (ref. 38). The device based on a 2D-conjugated D-A copolymer PBDB-T as donor and a low bandgap n-OS ITIC (ref. 20) (Eg of 1.59 eV) as acceptor with a ΔEHOMO of 0.18 eV demonstrated a PCE of 11.21% with a Voc of 0.899 V and a Eloss of 0.64 eV (ref. 26). Notably, the lower Eloss was attained with a relatively low ΔEHOMO, suggesting a low driving force needed for excitons dissociation in this system. These encouraging results provide a plausible approach to well remove the trade-off between the Voc and Jsc. Recently, we developed a series medium bandgap 2D-conjugated D-A copolymers based on bithienyl-benzodithiophene (BDTT) donor unit and fluorine-substituted benzotriazole (FBTA) acceptor unit2539, which showed good photovoltaic performance in the PSCs with the polymers as donor and n-OS as acceptors1125. Among the polymers, J61 as donor blending with the n-OS ITIC as acceptor with a ΔEHOMO of 0.16 eV in the non-fullerene PSCs displayed a high PCE of 9.53% with a Voc of 0.89 V and a Eloss of 0.68 eV (ref. 25). The high photovoltaic performance of the non-fullerene PSCs with the small ΔEHOMO between donor and acceptor is a very important phenomenon for the development of high performance PSCs by increasing Voc and decreasing Eloss.

To probe the posn class="Chemical">siblity of further increasing the Voc and PCE of the non-<span class="Chemical">fullerene PSCs with smaller ΔEHOMO value, herein we try to further decrease HOMO energy level of the <span class="Chemical">BDTT-FBTA-based 2D-conjugated D-A copolymers by introducing trialkylsilyl substituents on BDTT unit. The trialkylsilyl substituents instead of alkyl side chains make HOMO energy level of the synthesized polymer J71 down-shifted to −5.40 eV and its absorbance enhanced in comparison with its analogue polymer J52 with alkyl side chains25. Very interestingly, the non-fullerene PSC based on J71 as donor and ITIC as acceptor with a smal ΔEHOMO of 0.11 eV demonstrates a high PCE of 11.41% with high Voc of 0.94 V, high Jsc of 17.32 mA cm−2 and a low Eloss of 0.63–0.65 eV. The PCE of 11.41% is one of the highest efficiency of the single junction PSCs reported in literatures till now. The results indicate that the alkylsilyl substitution is an effective way in designing high performance conjugated polymer photovoltaic materials.

Results

Design and synthesis of J71

In the molecular design of conjugated <n class="Gene">span class="Chemical">polymer <span class="Species">donor materials for PSCs, the main chain engineering (such as alternative donor (D)-acceptor (A) copolymerization)4041 and side chain engineering (such as conjugated side chains and electron-withdrawing substituents)3042 are widely used strategy to tune absorption spectra and electronic energy levels of the conjugated polymers. Silicon (Si)-containing fused rings, such as dibenzosilole and dithienosilole, are representative donor units in the high performance D-A copolymer donor materials. Silicon bridging atom in the Si-containing fused rings plays an important role in improving the planarity of the backbone and modifying the electronic properties of the polymers43444546. The effect of the Si-atom on the electronic properties are mostly related to the bond interaction of the low-lying σ* orbital of the Si atom with the π* orbital of the aromatic units, which results in stabilization of the LUMO energy level and lowering of HOMO energy level47. For example, Si-bridged bithiophene (dithienosilole, DTS) has lower HOMO and LUMO energy levels compared with those of its C-bridged counterpart (CDT)47. In addition, the Si-bridging atom also showed a significant effect on the crystallinity of the polymer due to the longer C–Si bond length compared with the C–C bond, leading to stronger π–π stacking. Inspired by the special-function of the Si-atom connecting with conjugated system, herein we designed another BDTT-FBTA-based D-A copolymer J71 by introducing alkylsilyl substituents on thiophene conjugated side chains of BDTT unit for down-shifting HOMO energy level and strengthening interchain interaction of the polymers by the σ* (Si)–π*(C) bond interaction.

The <span class="Chemicn class="Chemical">al">polymer J71 was synthesized by Stille-coupling polycondensation between M1 (<ne">span>n class="Chemical">BDTT-Si) and M2 (FTAZ-based mononmer)48, as shown in Fig. 1a. The structure of BDTT-Si obtained by X-ray crystallography was also shown in Fig. 1a, and the crystallographic data of BDTT-Si (CCDC number: 1478875) are listed in Supplementary Table 1 and Supplementary Table 2.

Figure 1

Synthetic route of J71 and the effect of the alkylsilyl substitution on the physicochemical properties of the monomers.

(a) Synthetic route of J71 with the structure of BDTT-Si obtained by X-ray crystallography. (b) Absorption spectra of the monomers BDTT-Si and BDTT-C chloroform solutions with concentration of 1 × 10−5 mol l−1. (c) Cyclic voltammograms of BDTT-Si and BDTT-C in 0.1 mol l−1 Bu4NPF6 acetonitrile solution at a scan rate of 20 mV s−1, the ferrocene/ferrocenium (Fc/Fc+) couple was also provided for an internal reference. (d) Energy level diagrams of BDTT-Si and BDTT-C.

To better understand the effect of alkyln class="Chemical">silyl substitution on the electronic properties of the monomer and <span class="Chemical">polymer, we compared the absorption spectra and electronic energy levels of <span class="Chemical">BDTT-Si with the alkylsilyl substituents and BDTT-C with alkyl substituents on the thiophene conjugated side chains of the BDTT units, as shown in Fig. 1b. It can be seen that the absorption maximum (λmax) of BDTT-Si is at 380 nm which is 5 nm red-shifted than that (375 nm) of BDTT-C. And the absorption coefficient of BDTT-Si is higher than that of BDTT-C, indicating that alkylsilyl substitution affords not only broader but also stronger absorption. HOMO energy levels of the two monomers were measured by cyclic voltammetry. The onset oxidation potentials (ϕox) of BDTT-Si and BDTT-C are 0.99 and 0.90 V versus Ag/AgCl (Fig. 1c), and the HOMO energy levels (EHOMO) were calculated to be −5.35 eV for BDTT-Si and −5.26 eV for BDTT-C (the calculation equation will be discussed below in the section on the electronic energy level measurements of J71). The LUMO levels of BDTT-Si and BDTT-C, estimated from their absorption edges and HOMO levels, are −3.40 and −3.27 eV respectively. Clearly, alkylsilyl substituted BDTT-Si has lower HOMO and LUMO enrgy levels compared with those of its alkyl substituted counterpart BDTT-C (Fig. 1d). The results suggest that the alkylsilyl side chain engineering can afford the similar effect of the Si–C bond interaction as that in Si-bridged aromatic compounds47, while the alkylsilyl side chain approach developed in this work is more simple and convenient in down-shifting the HOMO energy level and strengthening the absorption. To further understand the effect of the alkylsilyl side chains on the electronic energy levels of the monomers, we performed the theoretical calculation by the DFT method on the molecules at the DFT B3LYP/6-31G(d) level with the Gaussian 03 program package. The calculated HOMO and LUMO energy levels of BDTT-Si are lower than those of BDTT-C (Supplementary Fig. 1), which is consistent with the experimental results mentioned above.

The synthesis details of J71 were described in the Method section. J71 exhibits good solubility in many chlorin class="Gene">nated solvents, such as <span class="Chemical">chloroform, <span class="Chemical">chlorobenzene and dichlorobenzene. The number average molecular weight (Mn) of J71 is 23.5 kDa with a polydispersity index of 2.0, which was measured by high temperature Gel permeation chromatography (GPC). Thermogravimetric analysis (TGA) demonstrated a good thermal stability of the polymer with a 5% weight-loss temperature at 354 °C, as shown in Supplementary Fig. 2.

Absorption spectra and electronic energy levels

Figure 2a shows the molecular structures of the <span class="Chemicn class="Chemical">al">polymer J71 and the <ne">span>n class="Chemical">n-OS ITIC acceptor, and Fig. 2b displays the absorption spectra of J71 solution and film together with the film absorpiton of ITIC for comparison. In solution, J71 shows defined absorption profile with two peaks at about 528 and 573 nm, which can be ascribed to the vibronic bands associated with the (0-1) and (0-0) transitions respectively. The emergence of these features is believed to be associated with the partial aggregation of the fluorinated polymer chains. The absorption of J71 film is red-shifted by about 14 nm along with a stronger (0-0) transition peak in the long wavelength range. The red-shift of its absorption in the solid film indicates more ordered structure and stronger π–π stacking interaction, which should benefit higher hole mobility and better photovoltaic performance of the polymer. The absorption edge of J71 film is at 632 nm, which correponds to an optical bandgap of 1.96 eV. The film maximum extinction coefficient of J71 is 0.96 × 105 cm−1, which is higher than its polymer analogue J52 with alkyl chain (0.73 × 105 cm−1)25. In addition, as one of the series of BDTT-FBTA-based copolymers112539, J71 also demonstrates well complementary absorption with that of ITIC n-OS acceptor in the wavelength range of 400–800 nm, which is beneficial for light harvesting in the non-fullerene PSCs.

Figure 2

Chemical structure and physicochemical properties of J71.

(a) Chemical structures of J71 polymer donor and ITIC n-OS acceptor. (b) Absorption spectra of J71 and ITIC. (c) Cyclic voltammogram of J71 polymer film on a platinum electrode measured in 0.1 mol l−1 Bu4NPF6 acetonitrile solutions at a scan rate of 20 mV s−1, the inser figure (blue line) shows the Cyclic voltammogram of ferrocene/ferrocenium (Fc/Fc+) couple used as an internal reference. (d) Energy level diagram of J71 and ITIC.

The HOMO and LUMO energy levels of J71 were measured by electrochemical cyclic voltammetry4950, for investigating the effect of the tripropyln class="Chemical">silyl substitution on the electronic energy levels of the 2D-conjugated <span class="Chemical">polymers. The HOMO/LUMO energy levels (EHOMO/ELUMO) can be calculated from onset oxidation/reduction potentials (ϕox/ϕred) in the cyclic voltammograms according to the equations of EHOMO/ELUMO=−e (ϕox/ϕred+4.8−ϕFc/Fc) (eV)4950 where ϕFc/Fc is the redox potential of ferrocene/ferrocenium (Fc/Fc+) couple in the electrochemical measurement system, and the evergy level of Fc/Fc+ was taken as 4.8 eV below vacuum. The electrochemical measurement was performed in a 0.1 M acetonitrile solution of tetrabutylammonium hexafluorophosphate (n-Bu4NPF6) with the sample (J71 or ITIC) film deposited on Pt disc electrode as working electrode, Ag/AgCl as reference electrode. ϕFc/Fc+ was measured to be 0.44 V versus Ag/AgCl in this measurement system, and then the calculation equations are EHOMO/ELUMO=−e (ϕox/ϕred+4.36) (eV).

Figure 2c shows the cyclic voltammegram of J71 film, from which the onset oxidation potential (ϕox) and onset reduction potentin class="Chemical">al (ϕred) of J71 were measured to be 1.04 and −1.10 V versus Ag/<span class="Chemical">AgCl respectively (Supplementary Fig. 3). The HOMO energy level (EHOMO) and LUMO energy level (ELUMO) of J71 were calculated to be −5.40 and −3.24 eV respectively (see Fig. 2d), according to the Equations mentioned above. Under the same experimental conditions, the EHOMO and ELUMO of ITIC were measured to be −5.51 and −3.84 eV respectively (see Fig. 2d and Supplementary Fig. 3b).

It should be noted that the EHOMO of J71 is 0.19 and 0.08 eV deeper than that of its <span class="Chemicn class="Chemical">al">polymer analogue J52 with alkyl substituent (EHOMO=−5.21 eV, see Supplementary Fig. 4) and J61 with alkylthio substituent (EHOMO=−5.32 eV) respectively25. The results indicate that the alkylsilyl substitution (with σ* (Si)–π*(C) bond interaction) is effective in lowering the HOMO energy level of the 2D-conjugated <ne">span>n class="Chemical">polymers. It should be mentioned that the electrochemical bandgap (ELUMO -EHOMO) of J71 is 2.16 eV, which is 0.2 eV larger than that (1.96 eV) of its optical bandgap. The larger electrochemical bandgap is a common phenomenon for the conjugated polymers and is reasonable in considering the energy barriers needed for the charge transfer in electrochemical oxidation and reduction reactions on the electrode.

Photovoltaic properties

PSCs were fabricated with a traditional device structure of <n class="Gene">span class="Chemical">ITO (<span class="Chemical">indium tin oxide) /PEDOT: PSS (poly (3, 4-ethylenedioxythiophene): poly (styrene-sulfonate)) /J71: ITIC (1:1, w/w) /PDINO51 (perylene diimide functionalized with amino N-oxide)/Al, where PDINO was chosen as the cathode interlayer for lowering the work funciton of Al51. The weight ratio of J71 donor: ITIC acceptor is 1: 1 according to our recent work in the studies of non-fullerene PSCs based on J61:ITIC25, considering the similar chemical structure of J71 with J61. The active layers with a thickness of about 100 nm were prepared by spin-coating the J71: ITIC blend solution with a total blend concentration of 12 mg ml−1 in chloroform at 3000, r.p.m. Figure 3a shows the current density–voltage (J–V) curves, and the corresponding incident photon to converted current efficiency (IPCE) spectra are shown in Fig. 3b. For a clear comparison, the detailed photovoltaic performance data are listed in Table 1. The as-prepared PSCs based on J71: ITIC showed a PCE of 9.03% with a high Voc of 0.96 V, a Jsc of 14.81 mA cm−2 and a FF of 63.63%. After thermal annealing at 150 °C for 10 min, the PCE of the PSC was further improved to 11.41% with a high Voc of 0.94 V, a high Jsc of 17.32 mA cm−2 and a FF of 69.77%. The PCE of 11.41% is one of the highest efficiency for the single junction PSCs reported in literatures so far. And very importantly, both high Voc and high Jsc were achieved in the J71:ITIC-based PSCs, which is a big challenge for the high performance PSCs.

Figure 3

Photovoltaic performance of the PSCs based on J71:ITIC without (open circles) and with (filled circles) thermal annealing at 150 °C for 10 min.

(a) J–V curves of the champion PSCs, under the illumination of AM 1.5 G, 100 mW cm−2, (b) IPCE spectra of the corresponding PSCs; (c) Light intensity dependence of Jsc of the PSCs; (d) dark currents of the PSCs, the inset shows the equivalent circuit of the PSCs.

Table 1

Photovoltaic performance parameters of the PSCs based on J71:ITIC under the illumination of AM1.5 G, 100 mW cm−2.

Devices	Voc (V)	Jsc (mA cm−2)	FF (%)	PCE (%)	RsΩ cm2	Rsh kΩ cm2	μh 10−4 cm2 V−1 s−1	μe 10−4 cm2 V−1 s−1	μh/μe
As-	0.96	14.81	63.63	9.03	10.38	0.57	2.08	0.96	2.17
prepared	0.96±0.004*	14.55±0.56	63.85±0.51	8.94±0.24
Thermal-	0.94	17.32	69.77	11.41	1.13	1.9	3.78	3.07	1.23
annealed†	0.94±0.003	17.40±0.37	68.09±1.12	11.2±0.29

*Average values with standard deviation were obtained from 30 devices.

†Thermal annealing at 150 °C for 10 min.

It can be seen that the PSCs based on J71: ITIC exhibited high Voc in the range of 0.94–0.96 V, which is certainly benefitted from the low-lying HOMO energy level of the alkyln class="Chemical">silyl substituted J71. As mentioned in the Introduction part, a crucial issue in the studies of PSCs is to minimize the device photon energy loss (Eloss) which is defined as Eloss=Eg–<span class="Chemical">eVoc, where Eg is the lowest optical band gap among the donor and acceptor components333435. In the present PSCs based on J71: ITIC, the lowest Eg is 1.59 eV for the ITIC acceptor with onset absorption at 782 nm (see Supplementary Fig. 5b). Therefore the Voc of 0.94–0.96 V results in a low Eloss of 0.63–0.65 eV, which is smaller than that of most PSCs and approaching the empirically low threshold of 0.6 eV. It should be mentioned that using the onset absorption to determine Eg is the commonly accepted and wide used method by different groups3334355253. And this method can provide a straight forward comparison of our results with those results previously reported (see Supplementary Table 3). Recently, Scharber et al. proposed a more accurate method to measure the Eg value of the active layer (blend of donor and acceptor) of the PSCs from IPCE spectrum36. With this method, we obtained a Eg of 1.58 eV from the onset of IPCE spectrum of the PSC based on J71:ITIC (as shown in Supplementary Fig. 6) which is consistent with the Eg value of 1.59 eV from the absorption edge of ITIC mentioned above.

The plot of <span class="Chemicn class="Chemical">al">eVOC against Eg, and the plots of PCE and <ne">span>n class="Chemical">IPCEmax against Eloss for the PSCs reported in literatures are provided in Supplementary Fig. 7, and the detailed data of the corresponding devices are listed in Supplementary Table 3 for a clear comparison. It should be noted that the PCE and the IPCEmax (76.5%) of the PSC based on J71/ITIC are in fact the highest values among the fullerene and non-fullerene PSCs reported in literatures with Eloss less than 0.65 eV. Such small Eloss is benefitted from the small ΔEHOMO of 0.11 eV in the PSCs based on J71/ITIC.

The IPCE spectra of the PSCs based on J71: ITIC (Fig. 3b) demonstrate broad and high photo-response from 300 to 790 nm, which indicates high photo-conversion efficiency for the absorptions of both <n class="Gene">span class="Chemical">J71 polymer donor and ITIC acceptor. The IPCE spectra in the wavelength range of 650–790 nm are corresponding to the excitons dissociation of the ITIC acceptor with the hole transfer from the HOMO of ITIC to that of J71. The high IPCE values in this range confirm that efficient hole transfer process did occour even though the ΔEHOMO between J71 donor and ITIC acceptor is only 0.11 eV. The Jsc values integrated from the IPCE spectra are 16.564 mA cm−2 for the thermal annealed device and 14.688 mA cm−2 for the as-prepared device, which agrees well with those values obtained from the J–V curves within 5% mismatch (Table 1). It should be noted that the low ΔEHOMO request can provide big chance in the molecular design of photovoltaic materials, such as for the polymer donor to further downshift its EHOMO toward a larger Voc, thus it will be promising to address the big challenge of PSCs for maximizing Voc and Jsc at the same time and ultimately getting a high-efficiency.

We also tried to fabricate the inverted PSCs with a device structure of <n class="Gene">span class="Chemical">ITO/ZnO /J71: ITIC (1:1, w/w) /MoO3/Al. The inverted PSC with thermal annealing at 150 °C for 10 min showed a PCE of 10.7% with a Voc of 0.93 V, a Jsc of 17.36 mA cm−2 and a FF of 66.05%, as shown in Supplementary Fig. 8. The slightly lower PCE of the inverted device could be due to the electrode buffer layer materials used in the inverted PSCs, and the optimization of the inverted PSCs is underway.

The charge carrier mobilities of the PSCs were measured by space-charge-limited current (<n class="Gene">span class="Disease">SCLC) method to investigate the effect of thermal annealing. The plots of the current density versus voltage of the devices for the mobility measurements are shown in Supplementary Fig. 9. For the as-cast blend film, their hole mobility μh and electron mobility μe are estimated to be 2.08 × 10−4 cm2 V−1 s−1 and 0.96 × 10–4 cm2 V−1 s−1 respectively with μh/μe of 2.17, while after thermal annealing the μh and μe values were increased to 3.78 × 10–4 cm2 V−1 s−1 and 3.07 × 10–4 cm2 V−1 s−1 respectively with the improved μh/μe ratio of 1.23. The improved photovoltaic performance of the PSCs with thermal annealing could be ascribed to the higher and more-balanced charge carrier mobilities of the thermal-treated J71: ITIC film. Figure 3c shows the dependance of Jsc values on the light-intensity (Plight) which reflects the charge recombination behaviour of the devices. In general, the relationship between Jsc and Plight can be described as Jsc∝Plight. If the bimolecular recombination of the charge carriers is negligible, the power-law exponent α should be unity. The values of α for the as-prepared and thermal treated devices are 0.922 and 0.986, respectively (Fig. 3c). The higher α value of the thermal-treated device suggests the reduced charge recombination in its device, which correlates well with the balanced charge carrier mobilities of the devices mentioned above.

The effect of thermal annen class="Chemical">aling on the device performance was further studied by analysing the series resistance (Rs) and shunt resistance (<span class="Chemical">Rsh) of the devices from their dark J–V curves (Fig. 3d), and the Rs and Rsh values are also listed in Table 1. The Rs and Rsh values of the as-prepared device are 10.38 Ω cm2 and 0.57 kΩ cm2 respectively, while after thermal annealing, Rs was decreased to 1.13 Ω cm2 and Rsh was increased to 1.9 kΩ cm2, suggesting the better overall diode characteristics after the thermal annealing, which is also reflected in the lower ideality factor n (1.51 for the thermal-annealed device in comparison with 1.92 for the as-prepared device) and lowest dark saturation current density Jo (1.89 × 10−10 mA cm−2 for the thermal-annealed device while it is 1.44 × 10–8 mA cm−2 for the as-prepared device).

Morphological characterization

For non-<span class="Chemicn class="Chemical">al">fullerene PSCs, morphology can be a determining factor governing the devcie performance5455. Here, the microstructural features and surface morphologies of the neat J71 and ITIC films as well as their blend films with or wihtout thermal annealing were investigated by grazing incident wide-angle X-ray diffraction (GIWAXS) plots56 and tapping-mode atomic force microscopy (AFM). Figure 4 shows the plots and images of the GIWAXS measurements. Strong diffraction peaks of the neat J71 film, as shown in Fig. 4b, reveal the semicrystalline structure and strong preference for face-on orientation in the <span>n class="Chemical">polymer film. In addition, characteristic of the long range order and crystallinity in the film was observed in the in-plane direction. The high crystallinity is largely benefitted from its proper side chain42 and fluorination effect48. For neat ITIC film, its lamellar (100) peak is located at 0.360 Å−1 and π–π stacking (010) peak is at 1.75 Å−1 (Fig. 4a,e), corresponding to lamellar distance of 17.44 Å and a π–π stacking distance of 3.58 Å. Its large azimuthal distribution of the diffraction peaks suggests randomly oriented crystallites, which is related to the steric effect of its tetrahexylphenyl substituents.

Figure 4

Plots and images of the GIWAXS measurements.

Line cuts of the GIWAXS images of (a) neat ITIC film and (b) neat J71 film, (c) as cast J71: ITIC blend films and (d) thermal annealed J71: ITIC blend films. GIWAXS images of (e) the neat ITIC film, (f) neat J71 film, (g) as acst J71: ITIC film and (h) thermal annealed J71: ITIC film.

For the blend films, the GIWAXS plots demonstrated microstructurn class="Chemical">al features with the diffraction patterns contributed from individual components (Fig. 4c,g). After thermal annealing, the J71: ITIC blend film is more prone to adopt a prominent face-on orientation (Fig. 4d,h) as evidenced by the small azimuthal distribution of the (010) π-π stacking in the out-of-plane direction. Further looking into diffraction patterns, it can be found that, the peak intensities become significantly stronger accompanied by their narrower peak widths (Fig. 4d,h). Furthermore, a 3.85 Å π-π-stacking distance (q=1.63 Å−1) is seen in the thermal treated blend films, which is slighltly smaller than that of the as-cast J71: ITIC film (3.88 Å, q=1.62 Å−1). All the behaviour is related to the higher crystalline characteristics of the thermal treated blend film, and the combination of the preferred face-on orientation and the tight π-π-stacking of the <span class="Chemical">polymer backbone is known to assist intermolecular charge transport and suppress the charge carrier recombination, which eventually improves the photovoltaic performance.

The AFM images, as shown in Supplementary Fig. 10, reveal that the blend films have relatively smooth surface with a root-mean-square (RMS) roughness of 0.722 nm for the as-cast J71: ITIC blend film and 0.741 nm for the thermn class="Chemical">al annealed blend film, indicating the good miscibility between the alkylsilyl substituted <span class="Chemical">J71 polymer donor and ITIC acceptor. From the AFM phase images in Supplementary Fig. 10d, it can be seen that with the thermal annealing, enhanced crystalline domains with nano-networks around 20 nm are visualized. This highly intercrystalline morphology asross the active layer enhances the polymer donor domain connectivity and thereby improves the hole transport, which correlates well with its superior device performance.

Hole transfer and charge separation dynamics

As mentioned above, it is likely that hole transfer from ITIC to J71 is highly efficient, despite the energy difference between HOMO levels (ΔEHOMO) of ITIC and J71 is only 0.11 eV which is much smaller than the empiricn class="Chemical">al threshold of 0.3 eV for effective exc<span class="Chemical">iton dissociation. To confirm the assessment, we performed transient absorption spectroscopy measurement to investigate the charge transfer dynamics of photo-induced carriers in the blend film of J71: ITIC. The primary absorption peaks for J71 and ITIC are well separated in spectral domain (Fig. 2b), so we can extract the spectral and temporal characteristics of hole transfer dynamics with selected excitation. The pump wavelengths of 540 and 710 nm were selected to excite J71 and ITIC, respectively. The excitation density is kept in a weak regime below 1 μJ cm−2 to avoid the effect of exciton-exciton annihilation. The pump-probe experiments measure the pump-induced differential change of the probe transmission, ΔT/T=(Tpump-on−Tpump-off)/Tpump-off.

Figure 5 shows the results of transient absorption spectrn class="Chemical">oscopy with excitation wavelength at 710 nm. At this pump wavelength, only ITIC is excited as confirmed by the absence of transient absorption signal from the neat sample of J71 (Supplementary Fig. 11). A bleaching signal peaked at 710 nm appears in both neat ITIC and the blend (Fig. 5a,b). This signal at the absorption peak of ITIC can be naturally ascribed to the ground state bleaching (<span class="Chemical">GSB) of the transition in ITIC. In addition, clear bleaching peaks at 540 and 590 nm appear in the transient absorption spectrum of blend (Fig. 5b). These wavelengths are exactly the absorption peaks of J71 (Fig. 2b). The spectral feature is also consistent with the GSB signal from J71 observed with resonant excitation at 540 nm (Supplementary Fig. 11). Figure 5c compares the transient absorption spectra from the blend sample at different time delays with the initial GSB spectra observed in J71 and ITIC under resonant excitations. Basically, the bleaching signals at 540 and 590 nm are built up with the decays of bleaching signal at 710 nm, suggesting the transfer of excitations from ITIC to J71. The excitation photon energy (at 710 nm) is much smaller than that required for exciton absorption of the polymer, therefore, the bleaching signals (540 and 590 nm) cannot be ascribed to energy transfer process. Notably, the bleaching signals at about 540 nm and about 590 nm appear simultaneously with the decay of the GSB signals of ITIC at about 710 nm (Fig. 5c), such excitation transfer can be naturally assigned to the hole transfer since the LUMO level of ITIC is much lower than that of J71.

Figure 5

Transient absorption measurements for the study of hole transfer dynamics.

transient absorption signal recorded from the films of (a) neat ITIC and (b) J71: ITIC (1:1, w/w) blend excited by 710 nm. (c) Transient absorption spectra from the blend film exicted by 710 nm (orange line) at different time delays. The lower panel shows the transient absorption spectra recorded at 1 ps from ITIC excited by 710 nm and J71 excited by 540 nm (blue line), respectively. (d) Dynamics probed at 710 nm recorded from the films of neat ITIC and blend J71: ITIC (1:1, w/w). (e) Dynamic curves probed at 540 and 590 nm recorded from the film of blend. (f) A schematic digram of the hole transfer in the film of J71: ITIC (1:1, w/w) blend.

Figure 5d compares the dynamics probed at 710 nm for the films of neat ITIC and blend J71:ITIC in a normalized scn class="Chemical">ale. For the early stage at less than 20 ps, the relaxation rate becomes dramatically faster in the blend film with respect to the neat ITIC, indicating the presence of additional relaxation channel of hole transfer in the blend film. We quantify the early-stage kinetics with a bi-exponetial decay function (Supplementary Fig. 12). The lifetime parameters for the two components are about 0.72 ps and about 15.0 ps respectively for the neat ITIC which decreases to about 0.29 ps and about 4.5 ps in the blends. Correspondingly, the buildup of signals probed at 540 and 590 nm in blend film is different from the abrupt rises observed in J71 excited at 570 nm (Supplementary Fig. 11). The onset shows two exponential growth components with lifetime parameters of about 0.3 ps and about 4.8 ps, respectively (Fig. 5e), confirming the hole transfer is the primary origin of the <span class="Chemical">GSB signal at the absorption band of J71. With these results, we briefly summarize the dynamics in Fig. 5f where the hole transfer from ITIC is quite efficient with rate up to 3 ps−1. Moreover, it is worthy noting that the <span class="Chemical">GSB signals at 540, 590 and 710 nm in the blend film persist to nanosecond scale which is much longer than those in neat samples of J71 and ITIC. The results suggest the existence of the long-lived dissociated excitons in the blend which is beneficial for electricity generation.

Discussion

In conclusion, another <n class="Gene">span class="Chemical">BDTT-FBTA-based 2D-conjugated <span class="Chemical">D-A copolymer J71 with tripropylsilyl substituents on thiophene conjugated side-chain of BDTT unit, was synthesized. J71 possesses a low-lying HOMO energy level at −5.40 eV and high film absorption extinction coefficients which is benefitted from the σ* (Si)–π*(C) bond interaction with the trialkylsilyl substitution. Non-fullerene PSCs were fabricated with J71 as donor and a narrow bandgap n-OS ITIC as acceptor, and the PCE of the PSCs based on J71/ITIC (1:1, w/w) with thermal annealing at 150 °C for 10 min reached 11.41% with simultaneously high Voc of 0.94 V and a high Jsc of 17.32 mA cm−2. The PCE of 11.41% is one of the highest efficiencies of the single-junction PSCs reported in literatures till now. The high Voc, which results in a low Eloss of 0.63–0.65 eV for the PSC, is benefitted from the low-lying HOMO level of the J71 donor. The high Jsc should be ascribed to the extraordinarily high exciton charge separation efficiency even though the HOMO energy difference between the donor and acceptor is quite small (only 0.11 eV). And the high hole transfer efficiency from ITIC to J71 was confirmed by transient absorption spectra. The results indicate that the alkylsilyl substitution is an effective way in designing high performance conjugated polymer photovoltaic materials and the driving force for the hole transfer from the acceptor to donor could be quite small in the non-fullerene PSCs with the n-OS as acceptor.

Methods

Materials and synthesis

ITIC was purchased from Solarmer Materials Inc. The other chemicn class="Chemical">als and solvents were purchased from J&K, Alfa Aesar or <span class="Gene">TCI Chemical Co. The monomers and polymer J71 were synthesized according to Scheme 1. The Benzo[1,2-b:4,5-b′]dithiophene-4,8-dione and M2 was synthesized according to the procedure reported in the literatures39.

Monomer 1 was synthesized as follows: Under protection of <n class="Gene">span class="Chemical">argon, to a solution of <span class="Chemical">thiophene (8.4 g, 100 mmol) in THF (100 ml) at −78 °C was added n-BuLi (40 ml, 2.5 M in hexane) slowly, the mixture was kept at −78 °C for 1 h and warmed slowly to room temperature. Then, chlorotripropylsilane (19.2 g, 100 mmol) was added, and the mixture stirred overnight. The mixture was extracted by diethyl ether twice, washed by water and brine. Further purification was carried out by column chromatography using hexane as eluent to obtain pure tripropyl(thiophen-2-yl)silane (1). as a colourless liquid. (22.3 g, 93% yield). 1H NMR(400 MHz, CDCl3), δ (p.p.m.): 7.57-7.56 (d, 1H), 7.22 (d, 1H), 7.16-7.15(t, 1H), 1.40-1.32 (m, 6H), 0.96-0.92(m, 9H), 0.80-0.75(m, 6H).

Monomer <span class="Chemicn class="Chemical">al">BDTT-Si was synthesized as follows: Under protection of <span class="Chemical">argon, to a solution of compound 1 (7.2 g, 30 mmol) in THF (30 ml) at 0 °C was added n-BuLi (12 ml, 2.5 M in hexane), the mixture was kept at 0 °C for 15 min and heated to 50 °C and strirred for 2 h. Then, Benzo[1,2-b:4,5-b′]dithiophene-4,8-dione (2.2 g, 10 mmol) was added quickly, and the mixture stirred for 2 h. After cooling down to the room temperature, SnCl2·2H2O (18 g, 80 mmol) in 10% HCl (35 ml) was added, and the mixture was stirred for 3 h. The mixture was extracted by diethyl ether twice, washed by water and brine. The crude product purified with column chromatography using petroleum ether as eluent to obtain pure 4,8-bis(5-(tripropylsilyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophene (BDTT-Si) as a light yellow solid. (2.8 g, 42% yield). 1H NMR (400 MHz, CDCl3), δ (p.p.m.): 7.65-7.64(d, 2H), 7.57-7.56 (d, 2H), 7.47-7.45 (d, 2H), 7.36-7.35(d, 2H), 1.53-1.42(m, 12H), 1.05-1.00(m, 18H), 0.92-0.86 (m, 12H). 13C NMR (100 MHz, CDCl3), δ (p.p.m.):145.0, 139.3, 139.1, 136.6, 134.9, 129.3, 127.7, 124.2, 123.6, 18.6, 17.6, 16.5.

Monomer M1 was synthesized as follows: To a solution of <n class="Gene">span class="Chemical">BDTT-Si (1.332 g, 2 mmol) in <span class="Chemical">THF (20 ml) at −78 °C was added n-BuLi (2 ml, 2.5 M in hexane). After the addition, the mixture was kept at −78 °C for 40 min; trimethyltin chloride (6 ml, 1 M in THF) was added dropwise. The resulting mixture was stirred for 2 h at room temperature. Then, it was poured into water and extracted with diethyl ether, washed by water and brine and after drying over MgSO4, the solvent was removed and the residue was recrystallized with methanol to afford a yellow crystal (5,5′-(2,6-bis(trimethylstannyl)benzo(1,2-b:4,5-b′)dithiophene-4,8-diyl)bis(thiophene-5,2-diyl))bis(tripropylsilane) (M1) (1.56 g, 78.8% yield). 1H NMR (400 MHz, CDCl3), δ (p.p.m.): 7.74-7.67(t, 2H), 7.60–7.59(d, 2H), 7.36(d, 2H), 1.53–1.45(m, 12H), 1.04–0.97(m, 18H), 0.91–0.87(m, 12H), 0.46-0.32(t, 18H). 13C NMR (100 MHz, CDCl3), δ (p.p.m.):205.9, 144.9, 142.3, 141.4, 137.8, 136.5, 133.9, 130.4, 128.0, 121.5, 30.0, 17.6, 16.6, 15.3, −7.4, −7.5, −9.3, −11.0, −11.1.

<span class="Chemicn class="Chemical">al">Polymer J71 was synthesized as follows: M1 (248 mg, 0.25 mmol) and M2 (175 mg, 0.25 mmol) and dry <ne">span>n class="Chemical">toluene (10 ml) were added to a 25 ml double-neck round-bottom flask. The reaction container was purged with argon for 20 min, and then Pd(PPh3)4 (10 mg) was added. After another flushing with argon for 20 min, the reactant was heated to reflux for 12 h. The reactant was cooled down to room temperature and poured into MeOH (200 ml), then filtered through a Soxhlet thimble, which was then subjected to Soxhlet extraction with methanol, hexane, and chloroform. The polymer J71 of 275 mg (Yield 91%) was recovered as solid from the chloroform fraction by precipitation from methanol, and was dried under vacuum. GPC: Mn=23.5 kDa; Mw/Mn=2.0. Anal. Calcd for C66H85F2N3S6Si2 (%): C, 65.68; H, 7.10; N, 3.48. Found (%):C, 64.79; H, 7.06; N, 3.55. 1H NMR (CDCl3, 400 MHz): δ (p.p.m.) 8.15–8.12 (br, 2H), 8.01–7.45 (br, 6H), 7.20–6.90 (br, 2H), 4.69 (br, 2H), 2.24–0.83 (br, 73H).

General characterization

1H n class="Chemical">NMR spectra were measured on a Bruker DMX–400 spectrometer with d–<span class="Chemical">chloroform as the solvent and <span class="Chemical">trimethylsilane as the internal reference. Ultraviolet–visible absorption spectra were measured on a Hitachi U–3010 Ultraviolet–vis spectrophotometer. Mass spectra were recorded on a Shimadzu spectrometer. Elemental analyses were carried out on a flash EA 1112 elemental analyser. Thermogravimetric analysis (TGA) was conducted on a Perkin–Elmer TGA–7 thermogravimetric analyser at a heating rate of 20 °C min−1 under a nitrogen flow rate of 100 ml min−1. Gel permeation chromatography (GPC) measurements was performed on Agilent PL-GPC 220 instrument with high temperature chromatograph, using 1,2,4-trichlorobenzene as the eluent at 160 °C. Photoluminescience (PL) spectra were measured with a Shimadzu RF-5301PC fluorescence spectrophotometer. Electrochemical cyclic voltammetry was performed on a Zahner IM6e Electrochemical Workstation under a nitrogen atmosphere. The cyclic voltammograms of J71 polymer film and ITIC film on a Pt disk electrode (working electrode) were measured with a potential scan rate of 20 mV s−1 in an acetonitrile solution of 0.1 M tetrabutylammonium hexafluorophosphate (n-Bu4NPF6) with a Ag/AgCl reference electrode and a platinum wire counter electrode. The ferrocene/ferrocenium (Fc/Fc+) couple was used as an internal reference. Thin films of J71 or ITIC were prepared by drop-casting 1.0 μl of their chloroform solutions (analytical reagent, 1 mg ml−1) onto the working electrode and then dried in the air. The J71 or ITIC film and J71:ITIC blend film for morphology measurements were prepared by spin-coating the corresponding solution in chloroform with a concentration of 10 mg ml−1 on indium tin oxide (ITO) glass at 3,000 rpm for 30 s. The film morphology was measured using an atomic force microscope (AFM, SPA-400) using the tapping mode.

Hole and electron mobilities were measured using the the n class="Gene">space charge limited current (<span class="Disease">SCLC) method, with the hole-only device of <span class="Chemical">ITO/PEDOT:PSS/J71: ITIC(1:1, w/w) /Au for hole mobility measurement and electron-only device of ITO/ZnO/J71: ITIC (1: 1, w/w) /PDINO/Al for electron mobility measurement. The SCLC mobilities were calculated by MOTT-Gurney equation:5758

Where J is the current density, ɛ is the relative dieletiric constant of active layer materin class="Chemical">al usually 2–4 for organic semiconductor, herein we use a relative dielectric constant of 4, ɛ is the permittivity of empty space, μ is the mobility of hole or electron and L is the thickness of the active layer, V is the internal voltage in the device, and V=Vapp–Vbi, where Vapp is the voltage applied to the device, and Vbi is the built-in voltage resulting from the relative work function difference between the two electrodes (in the hole-only and the electron-only devices, the Vbi values are 0.2 and 0 V respectively).

Grazing-incidence wide-angle X-ray scattering (GIWAXS) measurements were conducted at PLS-II 9A USAXS beam line of the Pohang Accelerator Laboratory in Korea. X-<span class="Species">raysn> coming from the in-vacuum undulator (IVU) were monochromated (wavelength λ=1.109 94 Å) using a double crystal monochromator and focused both horizontally and vertically (450 (H) × 60 (V) μm2 in fwhm at sample position) using K-B type mirrors. The GIWAXS sample stage was equipped with a 7-axis motorized stage for the fine alignment of sample, and the incidence angle of X-ray beam was set to be 0.13–0.135° for <span class="Chemical">polymer films, ITIC film and their bend films. GIWAXS patterns were recorded with a 2D CCD detector (Rayonix SX165), and X-ray irradiation time was 6–9 s, dependent on the saturation level of the detector. Diffraction angles were calibrated using a <span class="Chemical">sucrose standard (monoclinic, P21, a=10.8631 Å, b=8.7044 Å, c=7.7624 Å, β=102.938°), and the sample-to-detector distance was ∼231 mm.

For transient absorption spectrn class="Chemical">oscopy, pump pulses with tunable wavelength were from an optical parametric amplifier pumped by a regenerative amplifier (Libra, Coherent, 1 kHz, 90 fs). The carrier dynamics was probed by a broadband supercontinuum light source that was generated by focusing a small portion of the beam of the amplifier onto a sapphire plate. The chirp of the probe supercontinuum was corrected with error to be less than 100 fs over the whole spectral range. The transient absorption signal was then analysed by a high speed charge-coupled device (S11071-1104, Hamamatsu) with a monochromater (Acton 2358, Princeton Instrument) at 1 kHz enabled by a custom-built board from Entwicklun<span class="Chemical">gsbuero Stresing. The angle between the polarizations of pump and probe beam was set at the magic angle.

Device fabrication and characterization

The PSCs were fabricated with a structure of <span class="Chemicn class="Chemical">al">ITO/PEDOT: PSS (40 nm)/active layer/<ne">span>n class="Chemical">PDINO/Al. A thin layer of PEDOT: PSS was deposited through spin-coating on precleaned ITO-coated glass from a PEDOT: PSS aqueous solution (Baytron P VP AI 4083 from H. C. Starck) at 2,000 rpm and dried subsequently at 150 °C for 15 min in air. Then the device was transferred to a nitrogen glove box, where the active blend layer of J71 and ITIC was spin-coated from its chloroform solution onto the PEDOT: PSS layer under a spin-coating rate of 3,000 r.p.m. After spin-coating, the active layers were annealed at 150 °C for 10 min for the devices with thermal annealing treatment. The thickness of the active layers is about 100 nm. Then methanol solution of PDINO at a concentration of 1.0 mg ml−1 was deposited atop the active layer at 3,000 r.p.m. for 30 s to afford a PDINO cathode buffer layer with thickness of about 10 nm. Finally, top Al electrode was deposited in vacuum onto the cathode buffer layer at a pressure of about 5.0 × 10−5 Pa. The active area of the devices was 4.7 mm2. Optical microscope (Olympus BX51) was used to define the active area of the devices. The current density–voltage (J–V) characteristics of the PSCs were measured in a nitrogen glovebox (O2<0.1 p.p.m., H2O<0.1 p.p.m.) on a computer-controlled Keithley 2450 Source-Measure Unit. The voltage scan is from −1.5 to 1.5 V with voltage step of 10 mV and delay time of 1 ms. Oriel Sol3A Class AAA Solar Simulator (model, Newport 94023A) with a 450W xenon lamp and an air mass (AM) 1.5 filter was used as the light source. The light intensity was calibrated to 100 mW cm−2 by a Newport Oriel 91150V reference cell. Masks made by laser beam cutting technology with a well-defined area of 2.2 mm2 were used to define the effective area for accurate measurement of the photovoltaic performance. All the measurements with mask or without mask gave consistent results with relative errors within 0.5%. Actually, the measurement with mask give a slightly higher PCE mainly due to its slightly higher FF. The PCE results in the manuscript are from the measurement without mask. PCE statistics were obtained using 30 individual devices fabricated under the same conditions. The input photon to converted current efficiency (IPCE) was measured by Solar Cell Spectral Response Measurement System QE-R3-011 (Enli Technology Co., Ltd., Taiwan). The light intensity at each wavelength was calibrated with a standard single-crystal Si photovoltaic cell.

Data availability

The data that support the findings of this study are available from the corresponding author on request.

Additional information

How to cite this article: Bin, H. et al. 11.4% Efficiency non-<n class="Gene">span class="Chemical">fullerene polymer solar cells with <span class="Chemical">trialkylsilyl substituted 2D-conjugated polymer as donor. Nat. Commun. 7, 13651 doi: 10.1038/ncomms13651 (2016).