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TiO2光阳极
Energy Technology · 2019 ·Vol. 7 ·期 7 ·1801128 · IF 3.163

In Situ Decorating Coordinatively Unsaturated Fe Sites for Boosting Water Oxidation Performance of TiO2 Photoanode

Weicheng Cui,Hongye Bai,Konggang Qu,Fagen Wang,Peng Guan,Dongbo Xu,Weiqiang Fan,Weidong Shi

Kinetics play a critical role in the photoelectrochemical (PEC) system, whereas co-catalysis is mainly responsible for reducing the reaction barrier and facilitates water splitting. Here, the unsaturated Fe sites through the metal-organic framework (MOFs) structure promote the kinetics of water oxidation over TiO 2 are successfully in situ decorated. This heterostructure further helps us to better understand the PEC behaviors of organic–inorganic hybrid systems. MIL-100(Fe), as the typical MOFs model, is facilely achieved by an FeOOH sacrificial template method, a strategy which could anchor the compact and ultrathin MIL-100(Fe) films on the surface of TiO 2 to obtain abundant unsaturated Fe sites. The photocurrent density of MIL-100(Fe)/TiO 2 reaches about 2.4 times at 1.23 V vs reversible hydrogen electrode (RHE) compared with bare TiO 2 , and the incident photon to current conversion efficiency value increases up to 47% (at 390 nm). Furthermore, the photocurrent density of MIL-100(Fe)/TiO 2 is maintained at 84% after 3 h, showing that the organic component of MIL-100(Fe) takes a nature of favorable stability. The configuration of MIL-100(Fe)/TiO 2 will bring a new insight for learning the basic function of unsaturated metal sites in the PEC system.

CAS / MDL: 64-17-5 64-19-7 554-95-0
研究领域: 材料科学 · 能源化学
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APPLIED CATALYSIS A-GENERAL · 2024 · IF 4.7

Positive Potential Pretreatment of TiO2 Photoanode Towards Efficient Charge Separation

Li Zou,Jiale Xie,Shuxiang Wang,Yixing Yu,Jing Huang,Liuliu Wang,Pingping Yang,Wenyan Tao

Low charge separation efficiency ( η sep ) of TiO 2 impedes its applications of photoelectrochemical (PEC) water splitting. A positive potential pretreatment approach has been developed to construct a surface polarization with −OH groups at a potential of 1.48 V RHE . When the pretreatment time of 6   h is used, the η sep and photocurrent density ( J ph ) reach up to 54% (vs. 24%, TiO 2 ) and 0.92   mA   cm −2 (vs. 0.32   mA   cm −2 , TiO 2 ) under AM 1.5   G illumination, respectively. The photovoltage can be increased from 0.17   V to 0.52   V. When the pretreatment time is extended to 22   h, a higher J ph of 1.57   mA   cm −2 and η sep of 87% can be obtained. Furthermore, the positive potential pretreated TiO 2 possesses excellent PEC stability. The PEC improvements can be attributed to the surface polarization with the −OH groups and favorable surface states of Ti-OH, but not to the formation of Ti 3+ or oxygen vacancies.

研究领域: 材料科学 · 能源科学
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RESEARCH ON CHEMICAL INTERMEDIATES · 2025 · IF 3.5

The effect of small molecular linkers on the solar driven photoelectrochemical hydrogen production performance of CdS quantum dot-sensitized TiO2 photoanodes

Li Zhen,Guo Guizhang,Yu Zhou,Ma Zengyue,Yu Libo

In the pursuit of highly efficient hydrogen production through photoelectrochemical water splitting, expanding the utilization of the visible spectrum and extending the lifetime of photogenerated electrons are crucial challenges for improving the efficiency. To address these challenges, we prepared CdS sensitized TiO 2 photoanodes using a one-step hydrothermal method, employing thioglycolic acid (TGA) and mercaptopropionic acid (MPA) as linkers. The successful synthesis of CdS QDs and the CdS/TiO 2 photoanode was confirmed through various characterization techniques, including transmission electron microscopy (TEM), X-ray diffraction, and scanning electron microscopy. Performance evaluations revealed that the TGA-decorated CdS/TiO 2 photoanode exhibited superior photocurrent density and stability compared to the MPA-modified counterpart. Notably, its applied bias photo-to-current conversion efficiency was 1.7 times greater than that of the MPA-modified CdS/TiO 2 photoanode. Furthermore, UV–visible absorption spectrum analysis demonstrated that the incorporation of CdS QDs significantly broadened the spectral response of the TiO 2 photoanode, extending it from the ultraviolet to the visible range. This enhancement is crucial for improving light harvesting capabilities. Additionally, our analysis of electron lifetime indicated that the shorter molecular chains of TGA effectively minimize the transfer distance for photogenerated electrons from the CdS QDs to the TiO 2 , resulting in improved electron lifetimes and, consequently, enhanced photocurrent density.

研究领域: 材料科学 · 能源科学 · 光电化学
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2019 · IF 3.261

Constructing micro-flower modified porous TiO2 photoanode for efficient quantum dots sensitized solar cells

Yuxuan Li,Weixin Li,Lei Zhao,Jing Ge,Xuan He,Wei Fang,Hui Chen

TiO 2 photoanode as the light harvest skeleton and electron transport material plays a critical role in the photovoltaic performance of the quantum dots sensitized solar cells (QDSSCs). In this paper, a bilayer-structured film with micro-flower TiO 2 as an overlayer and hierarchical porous TiO 2 as an underlayer is fabricated. The hierarchical porous TiO 2 film is synthesized by the virtue of foam and the TiO 2 micro-flower is introduced by spin-coating method. This TiO 2 micro-flower supplies more adsorption sites for CdSe quantum dots, thus leading to the enhanced light harvesting efficiency. The staggered structure between the anatase nanoparticle and the rutile micro-flower will facilitate the separation of electron-hole pairs and promote the injection process of electron. Consequently, the photovoltaic performance of QDSSCs based on the TiO 2 micro-flower modified photoanode is about 43% higher than that of the bare porous TiO 2 photoanode.

研究领域: 材料科学 · 能源技术
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OPTIK · 2019 · IF 1.914

Online corrosion monitoring of photoelectrochemical cathodic protection of carbon steel using particle video microscope

Xianqiang Xiong,Liya Fan,Yiming Xu,Qiqiang Zhang,Jiangshan Li,Yong Wang,Guihua Chen,Chenglin Wu,Tianding Li,Shuai Fu,Guolin Zhang

The photo induced open circuit potential and Tafel curves have been widely used to evaluate the photoelectrochemical cathodic protection performance, but these conventional measurements cannot real-time monitor the images of the protected metal, and thus we are not able to judge whether the metal is protected or not during operation. To address these issues, in situ imaging technique based on particle video microscope (PVM) probe is developed to visually monitor the real-time images of the carbon steel. Anatase and rutile TiO 2 in different nanostructures were selected as the model photoelectrode materials, and their photogenerated cathodic protection performance was investigated by conventional electrochemical characterizations and in-situ PVM measurements, respectively. The in-situ imaging tool reveals that pitting corrosion can destroy the carbon steel in the chloride containing environment. However, once coupled with the TiO 2 photoanodes, the carbon steel can maintain a long-term stability without being corroded. Therefore, the in-situ imaging technique developed in this study provide us a direct route to detect and evaluate the long-term photocathodic protection performance, which will allow us to better clarify the corrosion mechanism, and finally for the better design of photoanode materials.

研究领域: 材料科学 · 电化学 · 腐蚀与防护
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International Journal of Electrochemical Science · 2023 · IF 1.5

A Photoelectrochemical Sensor for the Sensitive Detection of Rutin Based on a CdSe QDs Sensitized TiO2 Photoanode

Liying Wei,Xiaokun Li,Suxiang Feng

In this paper, a CdSe quantum dots (QDs) sensitized TiO 2 photoanode was synthesized by molten-salt-assisted self-assembly (MASA) on a fluorine-doped tin oxide (FTO)-coated glass (CdSe QDs-TiO 2 /FTO), and an efficient photoelectrochemical (PEC) sensor was constructed for the sensitive detection of rutin. CdSe can transfer photo-excited electrons to the conduction band of TiO 2 , thus enhancing the photoelectric activity of TiO 2 . The experimental results show that the PEC sensor has excellent selectivity, good stability, and a wide linear response range for rutin of 0.025–50.0 μM with a low detection limit of 0.007 μΜ. Moreover, the PEC sensor was successfully applied to the detection of rutin content in serum sample.

研究领域: 分析化学 · 生物医学工程 · 材料科学
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NEW JOURNAL OF CHEMISTRY · 2024 · IF 2.7

Improved efficiency of quantum dot-sensitized solar cells based on transparent black TiO2 modified photoanodes

Yin Peng,Jianyu Wang,Liying Wang,Xijia Yang,Yang Gao,Xuesong Li,Wei Lü

Transparent TiO2 photoanodes offer promise for new solar technology due to their high light transmittance, but the persistently inadequate solar conversion efficiency continues to pose obstacles for practical application. This research utilized n-butyl titanate and black P25 TiO2 (B-P25) to construct transparent TiO2 photoanodes for quantum dot sensitized solar cells (QDSSCs). The B-P25 presents rich oxygen vacancies after reduction, along with the generation of more pore structures in the TiO2 photoanode films, facilitating the transport of photogenerated charge carriers in the photoanode films. Therefore, the photoelectric conversion efficiency (PCE) is significantly enhanced from 1.77% to 5.04%, with an increase in the short-circuit current density in the J–V curve from 8.10 to 17.67 mA cm−2. This study demonstrates that B-P25 prepared using the reduction method can effectively fabricate photoanodes with high photovoltaic performance, which improves the optical properties and solar cell efficiency of QDSSCs.

研究领域: 材料科学 · 能源技术
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OPTICAL MATERIALS · 2024 · IF 3.8

Design and fabrication of layered TiO2/rGO composited photoanode and its photovoltaic performance regulation for dye-sensitized solar cells

Liguo Wei,Xiaohu Xu,Lishuang Zhao,Junyun Liu,Run Wang,Xindan Zhang

To improve the photovoltaic performance of the traditional TiO 2 photoanode for dye-sensitized solar cells (DSSCs), a series of layered TiO 2 /rGO composited DSSCs photoanode was assembled by changing the morphologies of the TiO 2 and introducing reduced graphene oxide (rGO) into different areas of the photoanode films. Firstly, TiO 2 nanoflowers (TiO 2 -NFs), TiO 2 nanorods (TiO 2 -NRs) were prepared employing the hydrothermal method and used as photoanode materials to explore the synergistic effect of TiO 2 with different morphologies in layered photoanode. Then, TiO 2 -NFs/rGO composited photoanode (TNF/rGO) were fabricated to research the mechanism of rGO on improving electron transmission in the layered photoanode. The effect of adding rGO at different parts of the layered photoanode on the performance of DSSCs was also investigated. Attributing to the enhancement of light absorption and charge transfer, a champion power conversion efficiency ( η ) of 9.21 % ( J sc  = 23.36 mA cm −2 , V oc  = 0.74 V, FF  = 0.53) was achieved with the layered TiO 2 /rGO composited photoanode containing two consecutive layers of TiO 2 -NFs/rGO and P25/rGO, which exhibited an 82.01 % increase than traditional TiO 2 (pure P25) photoanode ( η  = 5.06 %, J sc  = 12.09 mA cm −2 , V oc  = 0.73 V, FF  = 0.58). It is an effective way to design and fabrication of layered TiO 2 /rGO composited photoanode to regulate the photovoltaic performance of traditional TiO 2 photoanode for DSSCs based on the synergistic effect of its multi-layer structure, TiO 2 morphologies and introduction of rGO.

研究领域: 材料科学 · 能源科学
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CATALYSIS LETTERS · 2022 ·Vol. 152 ·期 12 ·3594-3606 · IF 2.936

PPy/WO3 Co-modified TiO2 Photoanode Based Photocatalytic Fuel Cell for Degradation of Rhodamine B and Electricity Generation Under Visible Light Illumination

Yao Haoyang,Xu Yunlan,Zhong Dengjie,Zeng Yundong,Zhong Nianbing

In order to inhibit rapid recombination of electron–hole pairs of photoanode and expand its light response wavelength, PPy-14%/WO 3 /TiO 2 /Ti photoanode was prepared. The maximum photocurrent density is 2.31 mA·cm −2 , which is 1.76 times higher than that of WO 3 /TiO 2 /Ti at 1.1 V (vs. SCE). The maximum power density, phontocurrent density and Rhodamine B degradation rate of photocatalytic fuel cell (PFC) with PPy-14%/WO 3 /TiO 2 /Ti photoanode and Cu cathode are 25.48 μW·cm −2 , 0.25 mA·cm −2 and 88.5%, respectively. The excellent performance is mainly due to the good carrier migration rate of PPy and the synergistic effect of PPy/WO 3 /TiO 2 /Ti ternary hybrid electrode, so that photogenerated electrons and holes can accumulate in the conduction band of WO 3 and HOMO of PPy, respectively. This not only expands the light absorption range and enhances the light absorption intensity, but also improves the separation of electron–hole pairs, and finally significantly enhances the Rhodamine B degradation and electricity generation performance of PFC. Graphical Abstract In order to inhibit rapid recombination of electron–hole pairs of photoanode and expand its light response wavelength, PPy-14%/WO 3 /TiO 2 /Ti photoanode was prepared. The excellent performance is mainly due to the good carrier migration rate of PPy and the synergistic effect of PPy/WO 3 /TiO 2 /Ti ternary hybrid electrode, so that photogenerated electrons and holes can accumulate in the conduction band of WO 3 and HOMO of PPy, respectively.

研究领域: 环境科学 · 材料科学
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JOURNAL OF HAZARDOUS MATERIALS · 2023 · IF 13.6

Gas diffusion TiO2 photoanode for photocatalytic fuel cell towards simultaneous VOCs degradation and electricity generation

Chongyi Wang,Yuxin Liu,Rong Chen,Xun Zhu,Dingding Ye,Yang Yang,Qiang Liao

In this work, a photocatalytic fuel cell (PFC) with a gas diffusion TiO 2 photoanode is proposed to directly convert chemical energy contained in volatile organic compounds into electricity by using solar energy. The gas diffusion TiO 2 photoanode is prepared by coating TiO 2 nanoparticles onto Ti mesh, whose intrinsic porous structure allows for gaseous pollutants to directly transfer inside the photoanode and thereby enhances mass transport. The feasibility of the developed gas diffusion photoanode is demonstrated by degrading toluene as a model gaseous pollutant. It is shown that the newly-developed PFC yields better electricity generation and toluene removal efficiency due to the enhanced mass transport of toluene and the eliminated interference of gas bubbles. The short-circuit current density and maximum power density of the PFC with a gas diffusion TiO 2 photoanode (0.1 mA/cm 2 and 0.02 mW/cm 2 ) are about 3.3 times and 4 times as those of the bubbling PFC (0.03 mA/cm 2 and 0.005 mW/cm 2 ), respectively. Both the discharging performance and toluene removal efficiency increase with increasing the light intensity and electrolyte concentration, while there exists an optimal gas flow rate leading to the best performance. The present work provides an innovative strategy for clean processing of volatile organic compounds while recycling the contained chemical energy.

CAS / MDL: 64-17-5 1310-73-2
研究领域: 环境科学 · 能源科学 · 材料科学
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JOURNAL OF SOLID STATE ELECTROCHEMISTRY · 2016 ·Vol. 21 ·期 3 ·715-724 · IF 2.327

Study of quasi-solid electrolyte in dye-sensitized solar cells using surfactant as pore-forming materials in TiO2 photoelectrodes

Zhang Kaiyue,Chen Si,Feng Yaqing,Shan Zhongqiang,Meng Shuxian

A novel polymer gel electrolyte was used to improve the performance and long-term stability in dye-sensitized solar cells (DSSCs). The polymer gel electrolyte (PGE) was prepared by mixing 5 wt% poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and 2 % TiO 2 nanoparticles. The conductivity of PGE with P25 reached 9.98 × 10 −3  S/cm, which increased by 34.9 % compared with 7.40 × 10 −3  S/cm of PGE without P25, and the diffusion coefficient was also increased by 19.0 %. Different photoelectrodes were obtained by using three kinds of surfactants (cetylamine, octadecylamine, and P123) as pore-forming materials, and their morphologies were contrasted through scanning electron microscopy (SEM). The results showed that gel electrolyte can increase the short-circuit current density ( J sc ) from 11.01 to 12.99 mA/cm 2 in DSSCs. Moreover, unlike the liquid electrolyte, the gel electrolyte is more conducive to the TiO 2 photoelectrodes with larger pores. In conclusion, the efficiency of DSSC with gel electrolyte and P123 as pore-forming material was 6.73 %, which was 12 % higher than the liquid electrolyte in the same test condition. In addition, the sealed gel electrolyte DSSCs showed better stability than did liquid electrolyte DSSCs during nearly 600 h.

研究领域: 材料科学 · 能源技术
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JOURNAL OF POWER SOURCES · 2019 · IF 7.467

A microfluidic all-vanadium photoelectrochemical cell with the N-doped TiO2 photoanode for enhancing the solar energy storage

Hao Feng,Xiaohong Jiao,Rong Chen,Xun Zhu,Qiang Liao,Dingding Ye,Biao Zhang,Wei Zhang

In this work, the nitrogen-doped TiO 2 photocatalyst is synthesized and applied in a microfluidic all-vanadium photoelectrochemical cell for enhancing the solar energy storage. The use of the nitrogen-doped TiO 2 photoanode and the minimization design can ensure the visible-light response, increased specific surface area, vigorous pore structure and enhanced photon and mass transport as well as more uniform light distribution. Various characterizations are performed to evaluate the developed photocatalyst and microfluidic all-vanadium photoelectrochemical cell. The results confirm that the developed nitrogen-doped TiO 2 photoanode can provide both the extended absorption spectrum and the small anatase crystal size as well as the obviously enlarged specific surface area with plentiful pore structure. Because of these merits, the microfluidic all-vanadium photoelectrochemical cell with the nitrogen-doped TiO 2 photoanode yield the average photocurrent density of 0.103 mA/cm 2 during the long-term operation, which is much higher than those with the un-doped TiO 2 photoanode (0.086 mA/cm 2 ) and commercial P25 TiO 2 photoanode (0.073 mA/cm 2 ), presenting 19.8% and 41% improvements, respectively. The results demonstrate not only the promotion of the vanadium reversible redox pairs conversion but also the inherently excellent stability by the nitrogen-doped TiO 2 photoanode.

研究领域: 材料科学 · 能源技术 · 光电化学
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