异质结
三元运算
光催化
材料科学
氢
分解水
纳米技术
光电子学
化学工程
化学
催化作用
工程类
计算机科学
有机化学
生物化学
程序设计语言
作者
Vandung Dao,Luis A. Cipriano,Sang-Woo Ki,Sunny Yadav,Wenmeng Wang,Giovanni Di Liberto,Kai Chen,Hoki Son,Jin‐Kyu Yang,Gianfranco Pacchioni,In‐Hwan Lee
标识
DOI:10.1016/j.apcatb.2023.122586
摘要
Direct Z-scheme designs perform well in light-to-fuel conversion. Here, an active and stable ternary Z-scheme core-shell heterojunction for photocatalytic hydrogen evolution (PHE) is fabricated consisting of hexagonal 2D α-Fe2O3 (as photocatalyst II) and 2D nitrogen-doped graphene (NGr as photocatalyst I) functionalized with the Pt single-atoms (SAs) cocatalyst. Under visible light, the 2D/2D α-Fe2O3 @NGr3PtSAs (NGr shell thickness of 3 nm and Pt loading of 0.5 wt%) achieves a remarkable PHE of 6.4 µmol mgcat−1 h–1, which is 16.4- and 3.28-times higher than those of free NGr (0.39 µmol mgcat−1 h–1) and binary α-Fe2O3 @NGr3 (1.95 µmol mgcat−1 h–1), thus outperforming the currently-advanced PHE catalysts. The outstanding performance is due to the superiority of a direct 2D/2D Z-scheme core-shell fabrication, including a large surface area for light harvesting, facile charge separation and transfer, and the workability of Pt SAs sites. Theoretical investigations provide additional insight into the mechanistic process of the ternary system for PHE reactions.
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