Ferroelectric Polarization-Enhanced Photocatalysis in BaTiO3-TiO2 Core-Shell Heterostructures.

Suppressing charge recombination and improving carrier transport are key challenges for the enhancement of photocatalytic activity of heterostructured photocatalysts. Here, we report a ferroelectric polarization-enhanced photocatalysis on the basis of BaTiO3-TiO2 core-shell heterostructures synthesized via a hydrothermal process. With an optimal weight ratio of BaTiO3 to TiO2, the heterostructures exhibited the maximum photocatalytic performance of 1.8 times higher than pure TiO2 nanoparticles. The enhanced photocatalytic activity is attributed to the promotion of charge separation and transport based on the internal electric field originating from the spontaneous polarization of ferroelectric BaTiO3. High stability of polarization-enhanced photocatalysis is also confirmed from the BaTiO3-TiO2 core-shell heterostructures. This study provides evidence that ferroelectric polarization holds great promise for improving the performance of heterostructured photocatalysts.

1. Introduction

Organic synthetic dyes in wastewater has become a hard-to-solve source of pollution, causing serious environmental and health problems because of their high solubility and chemical stability in water. Several techniques, including physical adsorption and biological or chemical treatments, have been developed for dye degradation, but they are limited in terms of their practical applications due to their intrinsic disadvantages caused by harmful active byproducts [1,2]. Photocatalysis is a promising pathway for wastewater purification, in which photogenerated charges in catalysts are reacted with water to induce actives of hydroxyl radicals (OH•) and superoxide anions (•O2−) for dye degradation [3]. To achieve an effective degradation, catalysts need to possess the following characteristics: broad light absorption, efficient charge separation and transport, as well as good chemical stability. A large amount of photocatalysts including oxide semiconductors [4,5] and sulfide semiconductors [6,7] with a comparatively high degradation efficiency have been reported. Among them, TiO2 is one of the most widely used photocatalysts, benefiting from its excellent chemical stability, non-toxicity, and low cost. Mesoporous TiO2 nanoparticles have a large surface area, which is favorable for the creation of numerous active sites for photocatalytic reactions [8,9]. However, the mesoporous TiO2 cannot fully support space charge effects for the separation of photogenerated charges as a result of its nanoscale grain size [10]. Because the photogenerated charges and photocatalytic reaction products are produced in close proximity to each other, the relatively high rate of charge recombination in mesoporous TiO2 nanoparticles often results in a low quantum yield and poor efficiency of photocatalytsis [11]. Accordingly, it is necessary to develop functional photocatalysts with suppressed charge recombination.

One potential solution is to build an internal electric field in heterostructured photocatalysts. An internal electric field in heterostructured photocatalysts can arise from ferroelectric polarization, polar surfaces, p-n junctions, and polymorph junctions [12]. In ferroelectrics, spontaneous polarization due to displacements of atoms or ions in the crystal lattice creates high-density charges on the surfaces of both ends of the polarization vector [13,14]. When a ferroelectric material is involved in a heterostructure, polarization charges in ferroelectrics cannot be fully compensated by low-concentration free charges in the adjacent semiconductor, resulting in an internal electric field in the heterostructure. Several studies have demonstrated the effectiveness of implementing ferroelectric polarization to improve the performance of semiconductor devices through a polarization-induced internal field. For instance, ferroelectric LiNbO3 and BaTiO3 were employed to facilitate charge separation and transport in dye-sensitized solar cells to increase cell efficiency [15,16]. Recently, applications of ferroelectric polarization were also explored to enhance photocatalytic performance [17,18,19]. Although ferroelectric-enhanced photocatalysis has been verified by various experiments, the mechanism remains unclear. In addition, the wide band gap of typical ferroelectric materials exclude their single phases from the applications depending on light absorption efficiency. In this paper, we report an approach of ferroelectric polarization-enhanced photocatalysis on the basis of BaTiO3-TiO2 core-shell heterostructures synthesized via a hydrothermal process. Through an optimized hydrolysis reaction, mesoporous TiO2 nanoshells were coated on BaTiO3. In comparison with pure TiO2 nanoparticles, a higher photocatalytic performance was seen in the BaTiO3-TiO2 core-shell heterostructures of all weight ratios adopted in this work, which was due to the lower recombination rate of photogenerated electron-hole pairs as evident from photoluminescence (PL) spectroscopy [20,21,22,23]. The internal field arising from ferroelectric BaTiO3 core acts as a driving force for the separation of photogenerated electron-hole pairs and promotion of charge transport to the surface of TiO2, resulting in increased photocatalytic activity with excellent stability. This approach provides a successful demonstration of the ferroelectric polarization-induced internal field in heterostructured photocatalysts as an effective strategy for improving the photocatalytic performance.

2. Materials and Methods

2.1. Material Preparation

A hydrothermal process [24] was employed to synthesis the BaTiO3-TiO2 core-shell heterostructures, and the meroporous TiO2 nanoparticles as a reference sample. Commercial BaTiO3 crystallines (99%, KJ Group, Hefei, China) were ultrasonically dispersed in ethanol, followed by the addition of hexadecylamine (HDA, 90%, Sigma-Aldrich, St. Louis, MO, USA) and NH3·H2O, and the mixture was ultrasonicated continuously at room temperature for 10 min to create a homogeneous solution. Subsequently, titanium isopropoxide (TIP, 95%, Sigma-Aldrich, St. Louis, MO, USA) as the precursor of TiO2 was dropwise added into the above solution under stirring for a hydrolysis reaction of 12 min. NH3·H2O is used as a catalyst to promote the hydrolysis reaction of TIP. HDA is used as a surfactant segregated to the surface of BaTiO3 crystallines. Hydrogen-bonding interactions between HDA molecules and TIP oligomers occur to generate inorganic–organic composites that coat BaTiO3. The amount of TIP (0.12, 0.16, 0.2 mL) and NH3·H2O (0, 0.1, 0.2 mL), and the stirring rate during the hydrolysis reaction (160, 200, 240 rpm) were adjusted to build core-shell geometries.

The resultants of BaTiO3-TiO2/HDA nanocomposites were collected by centrifugation. After washing with ethanol and deionized (DI) water, the BaTiO3-TiO2/HDA nanocomposites were dispersed in a mixture of 20 mL ethanol and 10 mL DI water, and then sealed in a teflon-lined autoclave. The hydrothermal reaction was proceeded at 160 °C for 16 h. The HDA molecules could be removed with the solvothemal treatment at 160 °C to generate mesoporous in TiO2 that remained as the nanoshells. The obtained BaTiO3-TiO2 samples were washed with ethanol and DI water to remove residual organics, then dried at 80 °C for 12 h.

BaTiO3-TiO2 core-shell heterostructures with different weight ratios of BaTiO3 to TiO2 (1:1, 1.2:1, 1.4:1) were synthesized through the hydrolysis reaction followed by the hydrothermal treatment. The optimum synthesis condition was verified by checking photodegradation efficiency of the catalysts synthesized at the different amount of TIP and NH3·H2O, and the varied stirring rate during the hydrolysis reaction, as shown in Figure S3. Meanwhile, mesoporous TiO2 nanoparticles were synthesized at the absence of BaTiO3 while the other conditions remained unchanged.

2.2. Characterization

X-ray diffraction (XRD, DX-2700 diffractometer) with a Cu Kα radiation (35 kV, 25 mA) was used to record phase structures of the as-synthesized BaTiO3-TiO2 core-shell heterostructures and TiO2 nanoparticles, and the commercial BaTiO3 crystallines. The morphology and crystal structure of the samples were characterized by a high resolution transmission electron microscope (HRTEM, JEM-2100F, JEOL Ltd., Tokyo, Japan and a field-emission scanning electron microscopy (FESEM, JSM-7800F, JEOL Ltd., Tokyo, Japan). Brunauer–Emmett–Teller (BET) surface areas of the samples were analyzed by Quadrasorb 2MP using N2 as the adsorption gas. Ferroelectricity of the BaTiO3 crystallines following the hydrothermal process was validated using an atomic force microscopy (AFM, Cypher™, Oxford Instruments, Goleta, CA, USA) via recording phase-voltage hysteresis and amplitude-voltage butterfly loops with switching spectroscopy piezoresponse force microscopy (SSPFM) [25], which is an effective tool for demonstrating of local ferroelectric characteristics. The photoluminescence (PL) spectra were recorded using PL mapping system (iHR320, Horiba Ltd., Kyoto, Japan) at an excitation wavelength of 325 nm ranging 300–600 nm.

2.3. Photocatalytic Activity Measurements

The photocatalytic activity was evaluated by degradation of rhodamine-B dye (RhB) solution under UV light irradiation. Photocatalysts of 30 mg were mixed into 50 mL of 15 ppm RhB solution with pH value of 5.7 ± 0.5. A UV spotlight (L9566-02, Hamamatsu Photonics, Hamamatsu, Japan) equipped with a 200 W mercury-xenon lamp and a 280–400 nm filter was used as the UV light source. The total optical power impinging on the mixture solution was 10 mW/mL. Prior to UV light irradiation, the mixture was stirred in the dark for 30 min to reach desorption–absorption equilibrium. A suspension of 3 mL was drawn out at the given time and then centrifuged at 8000 rpm to remove the photocatalyst completely. The RhB degradation rates were calculated from the UV-vis absorption spectra of the supernatant measured by a UV-vis spectrophotometer (Persee T10, PERSEE Analytics, Auburn, CA, USA) over the range 300–700 nm. The calibration curve was run at the maximum peak of 554 nm, as seen in Figure S5.

3. Results and Discussion

BaTiO3 is a typical perovskite ferroelectric with a Curie temperature around 120 °C. Below the Curie temperature, phase transition from a cubic paraelectric to a tetragonal ferroelectric occurs accompanied with lattice distortion due to Ti ions shift along the [001] axis, as seen in Figure S1, producing a spontaneous polarization (Ps = 27 µC/cm2) [26]. In this work, commercial BaTiO3 crystallines were used as the core material. After being subjected to the hydrothermal process, the BaTiO3 crystallines with a size of 100–300 nm showed excellent ferroelectricity, as seen in Figure S2, which coincides with the size-dependent ferroelectric property in BaTiO3 [27].

As seen in Figure 1a, the XRD patterns confirm that all the BaTiO3-TiO2 composites consist of tetragonal BaTiO3 (JCPDS 05-0626) and anatase TiO2 (JCPDS 21-1272). All the diffraction peaks can be indexed as well-crystallized BaTiO3 and TiO2. No impurity peaks were found in the BaTiO3-TiO2 composites, implying no impurity phases formed in the composites. The representative structure of an individual BaTiO3-TiO2 composite (1.2:1) was characterized by a field emission TEM (FETEM). The low-resolution FETEM image shows a distinguishable core-shell structure that the outer shell consists of mesoporous TiO2 nanoparticles at a thickness less than 100 nm, as seen in Figure 1b, which is comparable to the depletion width [28]. A high-magnification FETEM image revealed a good lattice match of the core-shell structure. The lattice spaces of about 0.283 nm and 0.192 nm measured from the core and shell portions are in an agreement with the (110) and (200) planes of tetragonal BaTiO3 and anatase TiO2, respectively, as seen in Figure 1c. The BaTiO3-TiO2 core-shell configuration was further confirmed by the energy dispersive X-ray spectrometry (EDS) analysis, as seen in Figure 1d, and line-scan EDS profile crossing the core-shell structure, as seen in Figure S4b.

Figure 1

(a) X-ray diffraction (XRD) patterns of the as-synthesized BaTiO3-TiO2 composites and TiO2 nanoparticles, and commercial BaTiO3 crystallines after being subjected to the hydrothermal process. high resolution transmission electron microscope (HRFEM)images at low solution (b) and high solution (c) of the BaTiO3-TiO2 composite (1.2:1), (d) energy dispersive X-ray spectrometry (EDS) analysis of the BaTiO3-TiO2 composite.

Surface area of photocatalyst is an important factor influencing photocatalysis; a larger surface area can provide more active sites on the surface for photodegradation of organic dyes. BET surface areas of all the samples used in this work were examined and are listed in Table 1. The BaTiO3-TiO2 core-shell heterostructures with different weight ratios of BaTiO3 toTiO2 demonstrated smaller surface areas via a comparison with the pure TiO2 nanoparticles. Among the BaTiO3-TiO2 core-shell heterostructures, the surface area decreased slightly with the increase of the weight ratio.

Table 1

Surface areas of the samples.

Catalysts	Pure BaTiO3	Pure TiO2	BaTiO3-TiO2 Core-Shell Heterostructures
			1:1	1.2:1	1.4:1
Surface area (m2/g)	25.66	70.79	36.81	35.77	34.25

To demonstrate the effect of ferroelectric polarization on the photocatalytic activity of BaTiO3-TiO2 core-shell heterostructures, the degradation capability on RhB was evaluated under the UV light irradiation. For comparison, the photodegradation ability of the pure TiO2 nanoparticles and BaTiO3 crystallines was also evaluated at the same experimental conditions. As seen in Figure 2, the results show that slight photodegradation of RhB was detected using the pure BaTiO3 crystallines as the catalyst under UV light irradiation. However, all the BaTiO3-TiO2 core-shell heterostructures exhibited enhanced photocatalytic activity despite a decrease in their surface areas in comparison with the pure TiO2 nanoparticles. The BaTiO3-TiO2 core-shell heterostructures (1.2:1) had the best photodegradation activity, which was 1.8 times stronger than that of the pure TiO2 nanoparticles after a 120 min photocatalysis. The results illustrate that a BaTiO3-TiO2 heterostructure is necessary for inducing an efficient photocatalytic activity. Moreover, the weight ratio of BaTiO3 to TiO2 in the heterostructures also plays an important role in photocatalytic activity. The room temperature band gap of both BaTiO3 [28] and anatase TiO2 [29] can be taken to be 3.2 eV on the basis of the available data; therefore, difference in the light absorption of these two materials is negligible. In addition, the large decrement in C/C0 of the pure BaTiO3 crystallines at 120 min might have been caused by pyroelectric effect of BaTiO3 [30] because the temperature changed noticeably after 90 min irradiation of the UV light.

Figure 2

Degradation of RhB as a function of irradiation time in the presence of the as-synthesized BaTiO3-TiO2 core-shell heterostructures and TiO2 nanoparticles, and the commercial BaTiO3 crystallines under UV light irradiation. The ratios in Figure are a ratio of BaTiO3 to TiO2.

Suppressing charge recombination and improving carrier transport are key challenges for the enhancement of the photocatalytic activity of heterostructured photocatalysts. Mesoporous TiO2 nanoparticles with a large surface area can benefit from the creation of numerous active sites for photocatalytic reactions; however, this process can also cause charge recombination by decreasing electron diffusion length and impeding charge transport due to the highly random surfaces/boundaries and the absence of interfacial space charges. Our concept for this work was to use ferroelectric polarization-induced internal field from the BaTiO3 core to facilitate charge carrier separation and further promote charge transport to the surface of TiO2 nanoparticles for an efficient photocatalytic reaction. Figure 3 is the schematic illustration of photogenerated charge separation and transport facilitated by polarization-induced internal field and degradation of RhB based on the BaTiO3-TiO2 core-shell heterostructures. Polarization charges in the BaTiO3 core can attract charges with opposite signs in the TiO2, which move toward the core; meanwhile, the same sign charges are repelled to the outer shell. An internal electric field can be created in the heterostructure because the polarization charges with a high density in the BaTiO3 cannot be fully compensated by low-concentration free charges in the adjacent TiO2. The average internal electric field formed from the BaTiO3 crystallines can be estimated by adopting the classical dipole field model [31] where ε is the relative permittivity of TiO2, σ is the polarization charge density, n is the unit normal to the surface, and f is the volume fraction occupied by the BaTiO3 nanocrystallines. Taking ε = 100 and f = 1 yield an estimated electric field of ~40 V/µm. This polarization-induced internal field generated locally in the heterostructure can penetrate the mesoporous TiO2 with a thickness less than the depletion width; it can also act as a driving force for separating electron-hole pairs and promoting them to transport toward to degradation reaction on the TiO2 surfaces [32]. As a result, the BaTiO3-TiO2 core-shell heterostructures with smaller surface areas present enhanced photodegradation activities compared with the pure TiO2 nanoparticles used as the catalyst. The dependence of photocatalytic activities on weight ratio might be relevant to the configuration of the core-shell structures. Too few or too many of BaTiO3 can lead to inharmonious configurations with the formation of either thicker TiO2 shells (>100 nm) or BaTiO3 aggregates with multiple crystallines, thus weakening the effect of polarization-induced internal field from the BaTiO3 core.

Figure 3

The schematic illustration of charge separation and transport facilitated by polarization-induced internal field and photodegradation of RhB based on the BaTiO3-TiO2 core-shell heterostructures.

PL signals of semiconductor materials result from the recombination of photogenerated charge carriers. In general, the lower the PL intensity, the lower the recombination rate of photogenerated electron-hole pairs and the higher the photocatalytic activity of semiconductor photocatalysts. In this work, PL spectra are employed to monitor the influence of ferroelectric polarization-induced internal field on the dynamic behaviors of photogenerated charge carriers in the BaTiO3-TiO2 core-shell heterostructures. As shown in Figure 4, PL intensities of all the BaTiO3-TiO2 core-shell heterostructures decreased in comparison with those of the pure TiO2 nanoparticles, which confirms the decrease in recombination rate of photogenerated charge carriers in the presence of light illumination. Among the heterostructures, the weight ratio of 1.2:1 exhibits the lowest PL intensity due to the lower recombination rate of photogenerated electron-hole pairs than the others. This explains the improved photodegradation activity, which is in agreement with the photocatalysis characteristics, as shown in Figure 2.

Figure 4

Photoluminescence spectra of the pure TiO2 nanoparticles and the BaTiO3-TiO2 core-shell heterostructures excited at 325 nm. The ratios in Figure are the ratio of BaTiO3 to TiO2.

The BaTiO3-TiO2 core-shell heterostructures (1.2:1) that has the best photodegradation activity was used to evaluate the stability of photcatalysis by checking their cyclic degradation ability. As shown in Figure 5, a small reduction (~3%) in the photodegradation activity was detected after four consecutive cycles of photocatalysis. The results demonstrate that the BaTiO3-TiO2 core-shell heterostructures possess good stability of photogenerated charge separation and transport during long-term operation which can be attributed to the polarization-induced internal field.

Figure 5

The cyclic degradation curves of the BaTiO3-TiO2 core-shell heterostructures. The BaTiO3 to TiO2 ratio is 1.2:1.

4. Conclusions

In summary, we fabricated BaTiO3-TiO2 core-shell heterostructures with a varied weight ratio of BaTiO3 to TiO2 for photodegradation of RhB. The mesoporous TiO2 nanoshells were formed on the BaTiO3 core by optimizing the hydrolysis reaction followed by the hydrothermal process. The BaTiO3-TiO2 core-shell heterostructures exhibited considerably higher photocatalytic activity than the pure TiO2 nanoparticles, with a maximum 1.8 times enhancement obtained from the heterostructures with the optimal weight ratio of 1.2:1. Such an enhanced photocatalytic activity is attributed to the facilitation of charge separation and transport based on the internal electric field originated from the spontaneous polarization of ferroelectric BaTiO3. No remarkable reduction of photocatalytic activity was observed after four consecutive cycles, indicating good stability of polarization-enhanced photocatalysis for the BaTiO3-TiO2 core-shell heterostructures. This research demonstrated that the ferroelectric polarization could be an effective approach to enhance performance of heterostructured photocatalysts.