Engineering a Self‐Grown TiO2/Ti‐MOF Heterojunction with Selectively Anchored High‐Density Pt Single‐Atomic Cocatalysts for Efficient Visible‐Light‐Driven Hydrogen Evolution

Author:

He Xiaoyu1,Ding Yujia2,Huang Zhennan3,Liu Min1,Chi Miaofang3,Wu Zili34,Segre Carlo U.2,Song Chunshan15,Wang Xiang1,Guo Xinwen1ORCID

Affiliation:

1. State Key Laboratory of Fine Chemicals PSU-DUT Joint Center for Energy Research School of Chemical Engineering Dalian University of Technology Dalian 116024 China

2. Department of Physics and CSRRI Illinois Institute of Technology Chicago IL 60616 USA

3. Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA

4. Chemical Sciences Division Oak Ridge National Laboratory Oak Ridge TN 37831 USA

5. Department of Chemistry Faculty of Science the Chinese University of Hong Kong Shatin Hong Kong SAR China

Abstract

AbstractA 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.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

General Chemistry,Catalysis

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