光催化
分解水
材料科学
光化学
酰亚胺
光催化分解水
量子效率
三嗪
催化作用
化学
有机化学
高分子化学
光电子学
作者
Minghui Liu,Guigang Zhang,Xiaocong Liang,Zhiming Pan,Dandan Zheng,Sibo Wang,Zhiyang Yu,Yidong Hou,Wei Wang
标识
DOI:10.1002/ange.202304694
摘要
Abstract In situ photo‐deposition of both Pt and CoO x cocatalysts on the facets of poly (triazine imide) (PTI) crystals has been developed for photocatalytic overall water splitting. However, the undesired backward reaction (i.e., water formation) on the noble Pt surface is a spontaneously down‐hill process, which restricts their efficiency to run the overall water splitting reaction. Herein, we demonstrate that the efficiency for photocatalytic overall water splitting could be largely promoted by the decoration of Rh/Cr 2 O 3 and CoO x as H 2 and O 2 evolution cocatalysts, respectively. Results reveal that the dual cocatalysts greatly extract charges from bulk to surface, while the Rh/Cr 2 O 3 cocatalyst dramatically restrains the backward reaction, achieving an apparent quantum efficiency (AQE) of 20.2 % for the photocatalytic overall water splitting reaction.
科研通智能强力驱动
Strongly Powered by AbleSci AI