A strategy to construct a highly active Co x P/SrTiO 3 (Al) catalyst to boost the photocatalytic overall water splitting reactions
Source abstract
Abstract
Hydrogen production from overall water splitting using SrTiO3(Al)-based semiconductors is one of the most promising routes to address energy and environmental concerns. Noble metals are needed to accelerate water splitting by promoting the charge transfer and providing active sites. However, noble metal-based catalysts have high prices and rare resources. Herein, we demonstrate a strategy to construct highly active CoxP/SrTiO3(Al) for overall water splitting. Hydrothermal method followed by an ultrasonic process was applied to prepare CoxP dots, which were loaded on the whole surface of SrTiO3(Al) as bifunctional cocatalysts. Interestingly, the CoxP dots on the (110) planes of SrTiO3(Al) were partially oxidized for the OER reaction. However, CoxP dots on the (100) planes of SrTiO3(Al) for HER kept it as it was. The as-prepared CoxP/SrTiO3(Al) photocatalyst shows a stable HER rate of 1.36 mmol-1 h-1 and OER rate of 0.635 mmol-1 h-1. The strong interaction between CoxP and SrTiO3(Al) not only facilitates rapid charge separation but also provides a highly active site for overall water splitting. Our study provides a valuable method for constructing noble-metal-free SrTiO3(Al)-based photocatalysts.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Copper-based nanomaterials and applications · Electronic and Structural Properties of Oxides
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shenzhen International Graduate School, Tsinghua University, Shenzhen City, 518055, China
The Key Laboratory of Advanced Materials of Ministry of Education, School of Materials Science and Engineering, Tsinghua University, Beijing City, 100084, China
Funding
Special Foundation for the Development of Strategic Emerging Industries of Shenzhen
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