4.8 Article

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

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 13, 页码 15305-15314

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c01550

关键词

piezocatalysis; cocatalyst; Schottky barrier; exposed facet; domain size

资金

  1. National Natural Science Foundation of China [21603191, 21775138]
  2. Zhejiang Provincial Natural Science Foundation of China [LY20B030003, LQ16B010001]
  3. Key Research and Development Program of Zhejiang Province [2021C03163]
  4. Foundation of Science and Technology Bureau of Jinhua [20204185]
  5. Public Welfare Technology Application Research Plan Project of Zhejiang Province (Analysis Test Item) [2017C37024]
  6. SelfTopic Fund of Zhejiang Normal University [2020ZS04]

向作者/读者索取更多资源

Piezoelectric semiconductor-based piezocatalysis shows promise for hydrogen generation, and introducing cocatalysts typically used in photocatalysis can enhance performance. Key parameters influencing activity include band tilting, surface characteristics, and loading amount of cocatalyst.
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 H-2 evolution rate of 11.4 mu mol 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 H-2 evolution based on rational engineering on the cocatalyst.

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