Zheng Haihong, Lu Yizhen, Ye Kai-Hang, Hu Jinyuan, Liu Shuai, Yan Jiawei, Ye Yu, Guo Yuxi, Lin Zhan, Cheng Jun, Cao Yang
State Key Laboratory of Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China.
Guangzhou Key Laboratory of Clean Transportation Energy Chemistry, School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
Nat Commun. 2021 Jan 4;12(1):91. doi: 10.1038/s41467-020-20341-7.
Achieving high-efficiency photoelectrochemical water splitting requires a better understanding of ion kinetics, e.g., diffusion, adsorption and reactions, near the photoelectrode's surface. However, with macroscopic three-dimensional electrodes, it is often difficult to disentangle the contributions of surface effects to the total photocurrent from that of various factors in the bulk. Here, we report a photoanode made from a InSe crystal monolayer that is encapsulated with monolayer graphene to ensure high stability. We choose InSe among other photoresponsive two-dimensional (2D) materials because of its unique properties of high mobility and strongly suppressing electron-hole pair recombination. Using the atomically thin electrodes, we obtained a photocurrent with a density >10 mA cm at 1.23 V versus reversible hydrogen electrode, which is several orders of magnitude greater than other 2D photoelectrodes. In addition to the outstanding characteristics of InSe, we attribute the enhanced photocurrent to the strong coupling between the hydroxide ions and photo-generated holes near the anode surface. As a result, a persistent current even after illumination ceased was also observed due to the presence of ions trapped holes with suppressed electron-hole recombination. Our results provide atomically thin materials as a platform for investigating ion kinetics at the electrode surface and shed light on developing next-generation photoelectrodes with high efficiency.
实现高效的光电化学水分解需要更好地理解光电极表面附近的离子动力学,例如扩散、吸附和反应。然而,对于宏观三维电极,通常很难将表面效应和体相中各种因素对总光电流的贡献区分开来。在此,我们报道了一种由InSe晶体单层制成的光阳极,该单层被单层石墨烯包裹以确保高稳定性。在其他光响应二维(2D)材料中我们选择InSe,是因为它具有高迁移率和强烈抑制电子 - 空穴对复合的独特性质。使用原子级薄的电极,我们在相对于可逆氢电极1.23 V的电压下获得了密度大于10 mA cm的光电流,这比其他二维光电极大几个数量级。除了InSe的出色特性外,我们将光电流的增强归因于阳极表面附近氢氧根离子与光生空穴之间的强耦合。结果,由于存在捕获离子的空穴且电子 - 空穴复合受到抑制,即使在光照停止后也观察到了持续电流。我们的结果为研究电极表面的离子动力学提供了原子级薄的材料平台,并为开发高效的下一代光电极提供了启示。