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

材料科学 光催化 压电 过电位 半导体 肖特基势垒 制氢 纳米技术 催化作用 化学工程 光电子学 复合材料 物理化学 电极 生物化学 化学 有机化学 电化学 二极管 工程类
作者
Guodong Yang,Qin Chen,Weijun Wang,Shijie Wu,Binjia Gao,Yanbo Xu,Zheng Chen,Shuxian Zhong,Jianrong Chen,Song Bai
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (13): 15305-15314 被引量:122
标识
DOI:10.1021/acsami.1c01550
摘要

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 BiFeO3 nanosheets, which not only facilitates the separation of charge carriers by accepting the piezoelectrons from BiFeO3 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 H2 evolution rate of 11.4 μmol h-1 (10 mg of catalyst), 19.0 times as high as that of bare BiFeO3. The band tilting induced by the piezoelectric potential is proposed to lower or eliminate the Schottky barrier and smooth the electron transfer from BiFeO3 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 H2 evolution based on rational engineering on the cocatalyst.
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