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Enhanced Photoelectrocatalytical Performance of Inorganic-Inorganic Hybrid Consisting BiVO 4 , V 2 O 5 , and Cobalt Hexacyanocobaltate as a Perspective Photoanode for Water Splitting
Electrocatalysis ( IF 3.1 ) Pub Date : 2019-12-10 , DOI: 10.1007/s12678-019-00566-x
K. Trzciński , M. Szkoda , M. Sawczak , A. Lisowska-Oleksiak

Thin layers of BiVO4/V2O5 were prepared on FTO substrates using pulsed laser deposition technique. The method of cobalt hexacyanocobaltate (Cohcc) synthesis on the BiVO4/V2O5 photoanodes consists of cobalt deposition followed by electrochemical oxidation of metallic Co in K3[Co(CN)6] aqueous electrolyte. The modified electrodes were tested as photoanodes for water oxidation under simulated sunlight irradiation. Deposited films were characterized using UV-Vis spectroscopy, Raman spectroscopy, and scanning electron microscopy. Since the V2O5 is characterized by a narrower energy bandgap than BiVO4, the presence of V2O5 shifts absorption edge (ΔE = ~0.25 eV) of modified films towards lower energies enabling the conversion of a wider range of solar radiation. The formation of heterojunction increases photocurrent of water oxidation measured at 1.2 V vs Ag/AgCl (3 M KCl) to over 1 mA cm-2, while bare BiVO4 and V2O5 exhibit 0.37 and 0.08 mA cm-2, respectively. On the other hand, the modification of obtained layers with Cohcc shifts onset potential of photocurrent generation into a cathodic direction. As a result, the photocurrent enhancement at a wide range of applied potential was achieved.

Graphical Abstract



中文翻译:

增强的BiVO 4,V 2 O 5和六氰基钴酸钴作为透视光阳极的无机-无机杂化材料的光电催化性能

使用脉冲激光沉积技术在FTO基板上制备BiVO 4 / V 2 O 5薄层。在BiVO 4 / V 2 O 5光电阳极上合成六氰基钴酸钴(Cohcc)的方法包括钴沉积,然后在K 3 [Co(CN)6 ]水溶液中对金属Co进行电化学氧化。在模拟的阳光照射下,将改性电极作为光阳极进行水氧化测试。使用UV-Vis光谱,拉曼光谱和扫描电子显微镜对沉积的膜进行表征。自V 2 O 5具有比BiVO 4窄的能带隙的特点,V 2 O 5的存在使改性膜的吸收边缘(ΔE=〜0.25 eV)向较低的能量移动,从而可以转换更宽的太阳辐射范围。异质结的形成将在1.2 V相对于Ag / AgCl(3 M KCl)的条件下测得的水氧化光电流增加至超过1 mA cm -2,而裸BiVO 4和V 2 O 5表现出0.37和0.08 mA cm -2, 分别。另一方面,用Cohcc对获得的层的改性将光电流产生的起始电势转移到阴极方向上。结果,实现了在广泛的施加电势下的光电流增强。

图形概要

更新日期:2020-04-21
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