Runyu Chen, Linxing Meng, Changda Wang, Weiwei Xu, Yulong Huang, Li Song, Liang Li
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引用次数: 0
摘要
建造高效光阳极对于开发出色的光电化学(PEC)分水电池至关重要。此外,载流子传输能力不足和缓慢的表面水氧化动力学限制了其应用。我们采用溶热退火策略,在 In2S3 光阳极表面原位制备了非全度 In-S(NS)基团,意外地形成了载流子的 II 型传输路径,从而减少了界面重组,促进了体分离。第一性原理计算和综合特性分析表明,NS基团是一种出色的氧进化协同催化剂(OEC),能有效促进载流子传输,降低表面过电位,增加表面活性位点,并通过精确改变*到*OH和*O到*OOH的速率决定步骤,加速表面氧进化反应动力学。这些协同效应显著提高了 PEC 性能,在 1.23 V 电压下与可逆氢电极相比,光电流密度高达 5.02 mA cm-2,起始电位负移 310 mV。这项工作为原位制备高效 OEC 提供了一种新策略,并为构建优良的载流子传输和运输通道提供了思路。
Nonstoichiometric In–S group yielding efficient carrier transfer pathway in In2S3 photoanode for solar water oxidation
The construction of high‐efficiency photoanodes is essential for developing outstanding photoelectrochemical (PEC) water splitting cells. Furthermore, insufficient carrier transport capabilities and sluggish surface water oxidation kinetics limit its application. Using a solvothermal annealing strategy, we prepared a nonstoichiometric In–S (NS) group on the surface of an In2S3 photoanode in situ and unexpectedly formed a type II transfer path of carrier, thereby reducing the interfacial recombination and promoting the bulk separation. First‐principles calculations and comprehensive characterizations demonstrated NS group as an excellent oxygen evolution cocatalyst (OEC) that effectively facilitated carrier transport, lowered the surface overpotential, increased the surface active site, and accelerated the surface oxygen evolution reaction kinetics by precisely altering the rate‐determining steps of * to *OH and *O to *OOH. These synergistic effects remarkably enhanced the PEC performance, with a high photocurrent density of 5.02 mA cm−2 at 1.23 V versus reversible hydrogen electrode and a negative shift in the onset potential by 310 mV. This work provides a new strategy for the in situ preparation of high‐efficiency OECs and provides ideas for constructing excellent carrier transfer and transport channels.