A facile strategy to prepare single-atom catalysts anchored on TiO2 with multiple oxygen vacancies for photocatalytic hydrogen evolution

IF 6.5 1区 化学 Q2 CHEMISTRY, PHYSICAL
Cailing Wu , Mingming Sun , Xinyang Gao , Qifei Huang , Zhaojun Min , Yanxing Zhang , Jianji Wang
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Abstract

Single atom catalysts (SACs) supported on metal oxide are usually prepared at high temperature, high pressure, and complex process. Herein, a new strategy is developed to prepare SACs anchored on vacancy-rich TiO2 using Ti2O3 as the support precursor under mild conditions, where Ti3+ on Ti2O3 surface acts as “traps” to capture and then reduce metal ions through electron transfer without using reducing agents. This approach is universally applicable for different single metal atoms supported on diverse phases of TiO2 (anatase, rutile, metastable and mixed counterpart). The as-obtained Pt1/TiO2 with controllable Pt loading and multiple oxygen vacancies (Ov) exhibits excellent activity in photocatalytic H2 evolution. At optimal conditions, the H2 evolution rate is up to 95,180 μmol g−1 h−1, which is the highest for TiO2 supported SACs reported.

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来源期刊
Journal of Catalysis
Journal of Catalysis 工程技术-工程:化工
CiteScore
12.30
自引率
5.50%
发文量
447
审稿时长
31 days
期刊介绍: The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes. The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods. The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.
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