氮化碳
氮化物
压电
极化(电化学)
结晶学
分解水
电场
材料科学
化学
电子转移
化学物理
纳米技术
光化学
物理化学
催化作用
物理
复合材料
光催化
量子力学
生物化学
图层(电子)
作者
Cheng Hu,Jingcong Hu,Zijian Zhu,Yue Lu,Shengqi Chu,Tianyi Ma,Yihe Zhang,Hongwei Huang
标识
DOI:10.1002/anie.202212397
摘要
Developing efficient piezocatalytic systems for two-electron water splitting (TEWS) with producing H2 and H2 O2 shows great promise to meet the industrial demand. Herein, Ag single atoms (SAs) and clusters are co-anchored on carbon nitride (AgSA+C -CN) to serve as the multifunctional sites for efficient TEWS. The Ag SAs enhance the in-plane piezoelectric polarization of CN that is intimately modulated by the atomic coordination induced charge redistribution, and Ag clusters afford strong interfacial electric field to remarkably promote the out-of-plane migration of piezoelectrons from CN. Moreover, AgSA+C -CN yields a larger piezoresistive effect that elevates carrier mobility under strain. Consequently, a superior H2 and H2 O2 evolution rate of 7.90 mmol g-1 h-1 and 5.84 mmol g-1 h-1 is delivered by AgSA+C -CN, respectively, far exceeding that of the previously reported piezocatalysts. This work not only presents the SAs decoration as an available polarization enhancement strategy, but also sheds light on the superiority of multi-sites engineering in piezocatalysis.
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