异质结
光催化
材料科学
催化作用
热解炭
化学工程
氢
纳米技术
化学
光电子学
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/anie.202217439
摘要
A photocatalyst TiO2 /Ti-BPDC-Pt is developed with a self-grown TiO2 /Ti-metal-organic framework (MOF) heterojunction, i.e., TiO2 /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 TiO2 /Ti-BPDC-Pt shows a significantly enhanced activity of 12.4 mmol g-1 h-1 compared to other TiO2 - 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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