异质结
光催化
热解炭
材料科学
氢
纳米技术
分解水
可见光谱
化学工程
化学
光电子学
催化作用
热解
有机化学
工程类
作者
Xiaoyu He,Yujia Ding,Zhennan Huang,Min Liu,Miaofang Chi,Zili Wu,Carlo U. Segre,Chunshan Song,Xiang Wang,Xinwen Guo
标识
DOI:10.1002/ange.202217439
摘要
Abstract A photocatalyst TiO 2 /Ti‐BPDC‐Pt is developed with a self‐grown TiO 2 /Ti‐metal–organic framework (MOF) heterojunction, i.e., TiO 2 /Ti‐BPDC, and selectively anchored high‐density Pt single‐atomic cocatalysts on Ti‐BPDC for photocatalytic hydrogen evolution. This intimate heterojunction, growing from the surface pyrolytic reconstruction of Ti‐BPDC, works in a direct Z‐scheme, efficiently separating electrons and holes. Pt is selectively anchored on Ti‐BPDC by ligands and is found in the form of single atoms with loading up to 1.8 wt %. The selective location of Pt is the electron‐enriched domain of the heterojunction, which further enhances the utilization of the separated electrons. This tailored TiO 2 /Ti‐BPDC‐Pt shows a significantly enhanced activity of 12.4 mmol g −1 h −1 compared to other TiO 2 ‐ or MOF‐based catalysts. The structure‐activity relationship further proves the balance of two simultaneously exposed domains of heterojunctions is critical to fulfilling this kind of catalyst.
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