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基于存储在非晶态二氧化钛上的电子/质子的析氢过程。

Hydrogen evolution based on the electrons/protons stored on amorphous TiO.

作者信息

Zeng Shuwen, Zhang Ling, Wang Wenzhong, Shao Dengkui, Hao Hongchang

机构信息

State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Dingxi Road, Shanghai 200050, P. R. China.

出版信息

Phys Chem Chem Phys. 2017 Nov 8;19(43):29053-29056. doi: 10.1039/c7cp06067j.

Abstract

The hydrogen evolution reaction (HER) using recyclable mediator is being actively pursued as a route for solar energy conversion. Herein, we introduce a catalyst mediator (MoS) that enables proton-coupled electron transfer (PCET) process on the recyclable TiO (H-TiO/e) to a separate, catalytic hydrogen production step without requiring post-light energy input. This approach supplies a new insight to hydrogen evolution with the recyclable proton-electron pairs, stored at the semiconductor after the light irradiation. It was found that 80% of the electrons stored on TiO could be devoted to the reduction of H into H on MoS nanosheets in the dark. The electron transfer to MoS occurs at a rate of 455 μmol h g and 947 μmol h g in the dark and excited state, respectively.

摘要

利用可循环介质的析氢反应(HER)作为太阳能转换的途径正受到积极探索。在此,我们引入一种催化剂介质(MoS),其能使可循环的TiO(H-TiO/e)上的质子耦合电子转移(PCET)过程进入一个单独的催化产氢步骤,而无需后续光能输入。这种方法为利用光照后存储在半导体中的可循环质子 - 电子对进行析氢提供了新的见解。研究发现,在黑暗中,存储在TiO上的80%的电子可用于在MoS纳米片上将H还原为H。电子向MoS的转移在黑暗和激发态下的速率分别为455 μmol h g和947 μmol h g。

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