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压电催化中的助催化剂工程:促进析氢的一种有前景的策略

Cocatalyst Engineering in Piezocatalysis: A Promising Strategy for Boosting Hydrogen Evolution.

作者信息

Yang Guodong, Chen Qin, Wang Weijun, Wu Shijie, Gao Binjia, Xu Yanbo, Chen Zheng, Zhong Shuxian, Chen Jianrong, Bai Song

机构信息

Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Life Sciences, Zhejiang Normal University, Jinhua, Zhejiang 321004, P. R. China.

College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua, Zhejiang 21004, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2021 Apr 7;13(13):15305-15314. doi: 10.1021/acsami.1c01550. Epub 2021 Mar 28.

DOI:10.1021/acsami.1c01550
PMID:33775098
Abstract

Piezoelectric semiconductor-based piezocatalysis has emerged as a promising approach for converting mechanical energy into chemical energy for renewable hydrogen generation and wastewater treatment under the action of mechanical vibration. Similar to photocatalysis, piezocatalysis is triggered by the separation, transfer, and consumption of piezo-generated electrons and holes. Inspired by this, herein, we report that the cocatalyst, which is widely used in photocatalysis, can also improve the semiconductor-based piezocatalytic properties. In the proof-of-concept design, well-defined Pd as a model cocatalyst has been deposited on the surface of piezoelectric BiFeO nanosheets, which not only facilitates the separation of charge carriers by accepting the piezoelectrons from BiFeO but also lowers the activation energy/overpotential through supplying highly active sites for the proton reduction reaction. Consequently, the as-obtained hybrid piezocatalyst delivers a high H evolution rate of 11.4 μmol h (10 mg of catalyst), 19.0 times as high as that of bare BiFeO. The band tilting induced by the piezoelectric potential is proposed to lower or eliminate the Schottky barrier and smooth the electron transfer from BiFeO to Pd, while the exposed facet, domain size, and loading amount of Pd cocatalyst are proved to be the key parameters determining the ultimate piezocatalytic activity. Our work provides some enlightenment on advancing the design and fabrication of more efficient piezocatalysts for H evolution based on rational engineering on the cocatalyst.

摘要

基于压电半导体的压电催化已成为一种很有前景的方法,可在机械振动作用下将机械能转化为化学能,用于可再生制氢和废水处理。与光催化类似,压电催化是由压电产生的电子和空穴的分离、转移和消耗引发的。受此启发,在此我们报道,在光催化中广泛使用的助催化剂也可以改善基于半导体的压电催化性能。在概念验证设计中,已将定义明确的 Pd 作为模型助催化剂沉积在压电 BiFeO 纳米片表面,这不仅通过接受来自 BiFeO 的压电电子促进了电荷载流子的分离,还通过为质子还原反应提供高活性位点降低了活化能/过电位。因此,所获得的混合压电催化剂实现了 11.4 μmol h(10 mg 催化剂)的高析氢速率,是裸 BiFeO 的 19.0 倍。提出由压电势引起的能带倾斜可降低或消除肖特基势垒,并使电子从 BiFeO 到 Pd 的转移更加顺畅,同时证明 Pd 助催化剂的暴露晶面、畴尺寸和负载量是决定最终压电催化活性的关键参数。我们的工作为基于助催化剂的合理工程设计和制造更高效的析氢压电催化剂提供了一些启示。

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