Enhancing Water-Splitting Efficiency Using a Zn/Sn-Doped PN Photoelectrode of Pseudocubic α-Fe2O3 Nanoparticles.

α-Phase hematite photoelectrodes can split water. This material is nontoxic, inexpensive, and chemically stable; its low energy gap of 2.3 eV absorbs light with wavelengths lower than 550 nm, accounting for approximately 30% of solar energy. Previously, we reported polyhedral pseudocubic α-Fe2O3 nanocrystals using a facile hydrothermal route to increase spatial charge separation, enhancing the photocurrent of photocatalytic activity in the water-splitting process. Here, we propose a p-n junction structure in the photoanode of pseudocubic α-Fe2O3 to improve short carrier diffusion length, which limits its photocatalytic efficiency. We dope Zn on top of an Fe2O3 photoanode to form a layer of p-type semiconductor material; Sn is doped from the FTO substrate to form a layer of n-type semiconductor material. The p-n junction, n-type Fe2O3:Sn and p-type Fe2O3:Zn, increase light absorption and charge separation caused by the internal electric field in the p-n junction.

Introduction

To build a sustainable, renewable, and clean energy economy, solar-driven photoelectrochemical (PEC) water-splitting offers a promising route for effective solar fuel production. Most semiconductor materials possess reasonable sunlight absorption and conversion efficiencies as well as active catalytic properties; thus, they are strong candidates for photoelectrodes. Notably, hematite has attracted much attention because of its nontoxicity, high chemical stability, environmental compatibility, low cost, and low energy gap of 2.3 eV, which can effectively absorb wavelengths of less than 550 nm of visible light [1-5]. However, the PEC performance for water oxidation on α-Fe2O3 photoanodes [6, 7] is limited by their poor charge conductivity [8, 9] and mobility [10, 11], low absorption coefficient [8, 12], and rapid electron-hole recombination [13-15], which depresses the oxygen evolution reaction. To address these limitations, numerous approaches have focused on enhancing light absorption, the kinetics of the water oxidation reaction, and the charge-carrier collection efficiency through modifying electronic structural elements. For example, some studies have reported that introducing several types of ions into hematite could significantly improve the hematite carrier concentration and charge transfer rate at the surface [16-18]. In our previous study, we proposed facilitating the preferential migration of electrons and holes in semiconductors using differences in work functions at various crystal facets, which improved the spontaneous charge spatial separation during the water-splitting process [1, 19, 20]. In the present study, we sought to go further to improve the performance of water splitting based on the results of our previous study, combining the advantages of the existence of heteroions in photoanodes. Two types of ions, Zn and Sn, were incorporated into a layer of shaped controlled hematite cubes from the top and bottom, respectively, which also created concentration gradience differences in the two types of ions within the active layer of hematite (Fig. 1). In our previous study, Sn doping occurred spontaneously from the FTO substrate during the post-annealing process, and Zn doping was performed by spin-coating precursors of zinc acetate solution on the top surface of photoanodes and thermally reduced during post-annealing; this modified the flat-band potential at the semiconductor-electrolyte interface.

Fig. 1

Concept of the p-n junction in a photoelectrode of polyhedral pseudocubic α-Fe2O3

Concen class="Chemical">pt of the p-n junctionpan> in a photoelectrode of polyhedral pseudocubic α-n class="Chemical">Fe2O3

Methods

Pseudocubic α-Fe2O3 nanocrystals were prepared through a hydrothermal route. In the synthesis of (012)-pseudocubic α-Fe2O3 nanocrystals, precursor Fe(acac)3 (2 mmol) and aqueous NaOH (0.6 M, 20 mL) were sequentially added to a solution of ethanol (20 mL) and DI-water (20 mL) with homogeneously vigorous stirring. Next, the mixed solution was placed in a Teflon-lined autoclave (100 mL) and maintained at 180 °C for 24 h. After being cooled to room temperature, the products were collected by centrifugation at 8000 rpm for 3 min and washed several times with n-hexane.

Subsequently, the products were ground into a powder and mixed with n-propyl ethanol (5 mL of n-propyl ethanol/0.1 g of powder) to obtain a suspension. In the doping process of Zn, we mixed zinc acetate and ethanol (0.1 g of zinc acetate + 2 mL of ethanol) to obtain zinc acetate solution. Finally, the pseudocubic α-Fe2O3 photoelectrodes were prepared using a spin-coating method and sintered at 450 °C for 10 h (heating rate = 2.5 °C/min) on the FTO substrate. In addition, Zn doping was prepared with a thermal diffusion method. We mixed zinc acetate and ethanol (0.1 g of zinc acetate + 2 ml of 99.5% ethanol) to obtain zinc acetate solution, which was then dropped 200 μL onto the pseudocubic α-Fe2O3 film. The active area of each sample was 1 × 1 cm2, and the mass loading of the Fe2O3 was approximately 0.2 mg. The prepared photoanode sintered at 450 °C for 10 h (heating rate = 2.5 °C/min) on the FTO substrate.

Characterizations of the pseudocubic Fe2O3 photoelectrode were performed using a field-emission scanning electron microscope (FE-SEM; S-4800, Hitachi) and high-resolution transmission electron microscope (HR-TEM; JEM-2100, JEOL). TEM samples were prepared by drop-casting an ethanol suspension of pseudocubic Fe2O3 NPs onto a copper grid. The composition and crystallinity of this Fe2O3 photoelectrode were determined using X-ray diffraction (XRD; D8 SSS Bruker). To study improvements to the separation of photoinduced charges, photoluminescence (PL) spectroscopy was performed to examine the recombination rate of photogenerated electron-hole pairs. The photon absorption properties of polyhedral α-Fe2O3 nanocrystals and their plasmon resonance were observed using ultraviolet-visible spectroscopy (UV-Vis; Lambda 650S, PerkinElmer). Photoelectrochemicals were measured using an electrochemical analyzer (CHI 6273E, CH Instruments) with a three-electrode electrochemical cell system in a darkroom (working electrode: hematite thin films, reference electrode: Ag/AgCl, counter electrode: carbon rod). The electrolyte was 1 M NaOH (pH = 14). In the photoelectrochemical measurement process, the light source was 532-nm laser irradiation (green solid laser, ALPHALAS) with a calibrated power density of 320 mW/mm2 with a spot size 1 mm in diameter. Hydrogen production was measured using gas chromatography (GC, China Chromatography GC1000TCD). Furthermore, the gas product was sampled every 20 min for 2 h.

Results and Discussion

Figure 2 presents TEM images of the α-Fe2O3, which indicate that the obtained particles possessed a pseudocubic shape and measured approximately 20 nm. The pseudocubic α-Fe2O3 consisted of (012) and (112) facets, and the crystallographic orientation was determined through the FFT pattern and high-resolution TEM images shown in Fig. 2b and c. These pseudocubic nanocrystals had an oblique parallelepiped morphology, where the dihedral angle between two adjacent facets was 86° or 94°. The FFT diffraction pattern shows that the (012) and (112) planes were nearest, and the interplanar distance was indicated as 3.7 Å along the [012] direction.

Fig. 2

a TEM image of pseudocubic-Fe2O3 NPs. b High-resolution TEM image of a pseudocubic-Fe2O3 NP. c The FFT pattern in b reveals an α-Fe2O3 NP along its projection

Figure 3 presents the XPS spectra of pseudocubic-Fe2O3:Zn/Sn for examining their chemical bonding state and electron bonding energy. In Fig. 3a, the presence of Zn in a-Fe2O3 was exhibited in the XPS spectrum, in which the peaks located at 1020.6 and 1044.1 eV were related to Zn 2p3/2 and Zn 2p1/2, respectively. In Fig. 3c, the high-resolution Zn 2p spectrum exhibits a pronounced peak centered at 1021.8 eV, corresponding to Zn 2p3/2, where the binding energy of Zn 2p3/2 is the typical value for ZnO; this suggested that the Zn dopant existed in the form of Zn2+. Zn was proved to be successfully doped within the Fe2O3. According to Fig. 3b, the XPS spectrum of Fe 2p3/2 and Fe2p1/2 in the Zn in a-Fe2O3 could be fitted as peaks at 710.7 and 724.3 eV, which was consistent with the binding energy of Fe3+ in the Fe2O3 origin.

Fig. 3

X-ray photoelectron spectroscopy (XPS) analysis of the Zn/Sn-doped p-n pseudocubic Fe2O3 photoelectrode: a survey XPS spectrum; b Fe 2p; and c Zn 2p

Figure 4a–f shows a scanning transmission electron microscope with high-angle annular dark field (STEM-HAADF) cross-section micrograph of a Zn/Sn-doped PN pseudocubic Fe2O3 photoelectrode on an FTO-coated glass substrate. For protection purposes, Pt was coated onto the surface of the hematite film during the preparation of the TEM sample. Energy-dispersive spectroscopy (EDS) elemental maps of the Zn, Fe, Sn, and Si elemental distributions are shown in Fig. 4b–f, respectively. The pseudocubic Fe2O3 NPs could be observed to cover the FTO-coated substrate conformably. To examine the doping concentration distribution in depth, we performed an XPS depth scan. Figure 4 g depicts the atomic percentage (at%) of the elemental distributions as a function of sputter time for the pseudocubic-Fe2O3:Zn/Sn photoelectrode, along with a schematic representation of each layer. In this concentration depth profile, we observed the Zn 2p to exhibit the highest concentration at the top surface (approx. 20%), which decreased with sputter time. In addition, Sn diffusion from the FTO substrate was observed in our photoelectrode, which intercrossed with the Zn signal line at a sputter time of 50 min. The perfect spatial distribution of both Zn and Sn demonstrated a successful doping atom arrangement in the Zn/Sn-doped PN pseudocubic Fe2O3 photoelectrode. This result contributed toward an enhancement of the reaction photocurrent.

Fig. 4

Cross-sectional imaging and chemical mapping of Zn/Sn-doped p-n pseudocubic Fe2O3 photoelectrode: a–f STEM images of the cross-section of an Zn/Sn-doped PN pseudocubic Fe2O3 photoelectrode. Note that the thin Pt layer seen in the image was deposited over the sample as a protection layer for the focused ion beam (FIB) milling step for cross-sectional sample preparation. g EDS mapping showing Zn, Fe, Sn, and Si elemental distributions respectively for the same sample as in a

Cross-sectionpan>al imaging and chemical mapping of Zn/Sn-doped p-n pseudocubic Fe2O3 photoelectrode: a–f STEM images of the cross-section of an Zn/Sn-doped PN pseudocubic Fe2O3 photoelectrode. Note that the thin Pt layer seen in the image was deposited over the sample as a protection layer for the focused ion beam (FIB) milling step for cross-sectional sample preparation. g EDS mapping showing Zn, Fe, Sn, and Si elemental distributions respectively for the same sample as in a

To identify the effect of pseudocubic Fe2O3:Sn with and without Zn doping, the absorption spectra of the Fe2O3:Sn and Fe2O3:Zn/Sn photoelectrodes were measured, as shown in Fig. 5a. The absorption spectrum of the Fe2O3:Zn/Sn (p-n junction) photoelectrode exhibited a stronger photon absorption crossover in the UV-to-visible light range. In addition, a small bump of an absorption peak appearing at 440 nm was observed; this was consistent with the absorption peak of the Zn NPs, which was because of the substitution between zinc and iron atoms [21-23]. Notably, a slight blue shift phenomenon was observed in the absorption spectrum after the Zn NPs were doped in the pseudocubic Fe2O3:Sn photoelectrode [24-26]. This phenomenon may be attributable to the Zn NP doping possibly raising the band gap of essential semiconductors [27-31]. Moreover, Mott-Schottky plot is performed for Zn/Sn -doped PN photoelectrode of pseudocubic α-Fe2O3 and have been characterized in Figure S1 in the supporting information. In the case of Zn/Sn-doped pseudocubic α-Fe2O3, it has been noted that both positive and negative slopes are observed, implying that the existence of the p and n type electronic behavior in our photoelectrode (shown in supporting information, Figure S2).

Fig. 5

a Absorption spectrum of the photoelectrodes of Fe2O3:Sn and Fe2O3:Zn/Sn; b PL analysis of the Fe2O3:Sn and Fe2O3:Zn/Sn photoelectrodes; and c J-V scans collected for different doped Fe2O3

a Absorptionpan> spectrum of the photoelectrodes of Fe2O3:Sn and Fe2O3:Zn/Sn; b PL analysis of the Fe2O3:Sn and Fe2O3:Zn/Sn photoelectrodes; and c J-V scans collected for different doped Fe2O3

To further investigate the charge transfer of the photogenpan>erated electron and hole pairs in pseudocubic Fe2O3:Zn/Sn, p-n junction system, this study used photoluminescence (PL) analysis, which could indicate the recombination of free charge carriers. Figure 5b shows the PL spectra of different samples with an excitation wavelength of 263 nm (4.71 eV). The pseudocubic Fe2O3:Zn/Sn displayed a lower PL intensity at approximately 580 nm, which was because of carrier diffusion between the p- and n-type semiconductor materials. This implied a decrease in electron and hole pair recombination, attributed to the p-n junction internal electric field.

Photocurrent responses were measured using a traditional three-electrode cell system. It was designed in a quartz cell, in which hematite thin films were used as the working electrode, Ag/AgCl as a reference, and a carbon rod as a counter electrode. The electrolyte was 1 M NaOH (pH = 14). In Fig. 5c, two different photoelectrodes with and without Zn doped, respectively, were tested under 532-nm laser irradiation. The pseudocubic Fe2O3:Sn and Fe2O3:Zn/Sn exhibited photocurrent densities of 4.1 × 10−3 and 5.3 × 10−3 A/cm2, respectively, at a bias voltage of 0.8 V. As expected, with superior performance in terms of the absorption spectrum and PL, the photocurrent-voltage (J-V) response of the pseudocubic Fe2O3:Zn/Sn (photocurrent density = 5.22 mA/cm2) was approximately 30% higher than that of the pseudocubic Fe2O3:Sn under 532-nm laser irradiation.

The long-term stability of the Fe2O3:Zn/Sn photoelectrodes was tested under 532-nm laser irradiation for 7 h in Fig. 6a. The p-n junction system achieved a high light current response in a previous measurement. After irradiation for 7 h, the current response of the Fe2O3:Zn/Sn photoelectrode had only decayed by 35%, which confirmed that the Zn/Sn-doped PN pseudocubic Fe2O3 photoelectrode possessed strong photocurrent response stability. Finally, we examined H2 and O2 production to demonstrate a possible application of this high-performance PN photoelectrode; a comparison of H2 and O2 production from water-splitting was conducted and is presented in Fig. 6b for both the Fe2O3:Sn and Fe2O3:Zn/Sn samples. The Fe2O3:Zn/Sn photoelectrode generated approximately 1200 μmol of H2 and 520 μmol of O2 in 120 min, which were two times greater than those of pseudocubic Fe2O3:Sn.

Fig. 6

a Stability study of pseudocubic Fe2O3:Zn/Sn photoelectrodes (inset photo: our test system). b Production of H2 and O2 from pseudocubic Fe2O3:Zn/Sn photoelectrodes

Conclusions

This study successfully demonstrated an enhanced charge spatial separation effect in pseudocubic Fe2O3:Zn/Sn photoelectrodes, which significantly improved performance in terms of photocurrent response and water-splitting gas products because of the built-in electric field. Furthermore, the Fe2O3:Zn/Sn photoelectrodes exhibited promising long-term stability, remaining at 70% magnitude of the initial photocurrent over 7 h of operation. This provides a significant water-splitting approach for sustainable energy conversion.

Additional file 1: Figure S1. Mott-Schottky plot of the Zn/Sn doped PN photoelectrode of pseudocubic α-Fe2O3. Figure S2. The comparison of XRD before/after operation.