Two-dimensional metal–organic frameworks offer all-in-one cocatalysts for photocatalytic overall water splitting
Abstract
Photocatalytic overall water splitting holds great promise for sustainable hydrogen production. For overall water splitting performed by one-step excitation, both the hydrogen evolution and oxygen evolution reactions are hindered kinetically; hence, it is necessary to employ site-selective modification of photocatalysts with hydrogen-evolving and oxygen-evolving cocatalysts. However, critical challenges remain, including the need for cumbersome, multi-step photodeposition processes and durable blocking layers to inhibit the reverse reactions. Here we find a conductive, two-dimensional metal–organic framework to serve as a simple, multifunctional cocatalyst. We loaded this framework on SrTiO3:Al, an overall water-splitting photocatalyst, using a one-step self-assembly method. The framework cocatalyst promoted steady photocatalysis with an apparent quantum efficiency of 31.5% at 350 nm, free from the reverse reaction even without blocking layers. We proposed the operational principles for the cocatalyst activity using spectroscopic, electrochemical and theoretical analyses. This two-dimensional metal–organic framework offers an all-in-one approach for designing efficient and practical one-step excitation overall water-splitting systems. Overall water splitting using one-step excitation holds great promise as a green hydrogen production technology, but precisely loading multiple inorganic cocatalyst species on photocatalysts offers only mixed success. Now it has been shown that a single, conductive, two-dimensional metal–organic framework can serve as an all-in-one cocatalyst.
Fields of Study & Subjects
Advanced Photocatalysis Techniques
Electrocatalysts for Energy Conversion
Metal-Organic Frameworks: Synthesis and Applications
Publication details
- Journal / source
- Nature Chemistry
- Publisher
- Springer Science and Business Media LLC
- Volume
- 18
- Issue
- 6
- Pages
- 1053–1061
- Publication date
- 23 April 2026
- Language
- EN