Related Experiment Video
Updated: Oct 5, 2025

Photochemical Oxidative Growth of Iridium Oxide Nanoparticles on CdSe@CdS Nanorods
Published on: February 11, 2016
A strategy to construct a highly active CoP/SrTiO3(Al) catalyst to boost the photocatalytic overall water splitting
Shangchun Lv1, Mengxi Pei1, Yuxiang Liu1,2
1Shenzhen International Graduate School, Tsinghua University, Shenzhen City, 518055, China. si.zhichun@sz.tsinghua.edu.cn.
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 CoP/SrTiO3(Al) for overall water splitting. Hydrothermal method followed by an ultrasonic process was applied to prepare CoP dots, which were loaded on the whole surface of SrTiO3(Al) as bifunctional cocatalysts. Interestingly, the CoP dots on the (110) planes of SrTiO3(Al) were partially oxidized for the OER reaction. However, CoP dots on the (100) planes of SrTiO3(Al) for HER kept it as it was. The as-prepared CoP/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 CoP 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.
More Related Videos
10:21Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
12:47Preparation and Use of Photocatalytically Active Segmented Ag|ZnO and Coaxial TiO2-Ag Nanowires Made by Templated Electrodeposition
Published on: May 2, 2014
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
The Z-Scheme of Electron Transport in Photosynthesis
Catalysis
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...