期刊
CATALYSIS SCIENCE & TECHNOLOGY
卷 9, 期 23, 页码 6769-6781出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cy01692a
关键词
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资金
- Department of Science and Technology (DST) Inspire program [DST/INSPIRE/04/2015/000239]
- DST Science and Engineering Research Board (SERB) [YSS/2015/000100]
Photoelectrochemical (PEC) water splitting being a greener and ecofriendly pathway has become a renowned technique to generate hydrogen (H-2). To attain remarkable photoconversion efficiency, it is highly required to develop efficient photoelectrodes for PEC water splitting. For this, ternary metal chalcogenide ZnInxSy (x = 1.6, 2, 2.2, and 3) is synthesized as an efficient photoanode for PEC water splitting. Tuning of morphology helps to improve the PEC performance through enhanced light absorption and charge transportation. Similarly, elemental doping is a very fruitful strategy to modulate the band structure. Here, a facile hydrothermal approach is developed to synthesize thin sheets of ZnInxSy (x = 1.6, 2, 2.2, and 3) followed by calcination. Through controlling the calcination time and the indium content, the band structure and morphology of ZnInxSy are modulated. The observed results indicate that ZnIn2.2Sy has the optimum and appropriate amount of indium content and oxygen doping. ZnIn2.2Sy can generate a maximum photocurrent density of 4.83 mA cm(-2) at '0.7767' vs. RHE. Furthermore, with the help of Mott-Schottky analysis the carrier density is calculated. The calculated carrier density of ZnIn2.2Sy is 7.886 x 10(21) cm(-3), which is 2.37, 1.77, and 3.69-fold higher compared to ZnInxSy (x = 1.6, 2, and 3). Photoconversion efficiency (eta) is direct evidence to legitimize the superiority of ZnIn2.2Sy; it shows a maximum efficiency of 2.744% at potential 0.507 V vs. RHE. ZnIn2.2Sy shows high stability, i.e., it can generate nearly unaltered photocurrent density for 1000 seconds. The determined band alignment of ZnIn2.2Sy indicates the more negative shift of valence band energy compared to others, which promotes easy oxidation of H2O to O-2.
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