High-Performance H Photosynthesis from Pure Water over Ru-S Charge Transfer Channels.

Precis Chem

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.

Published: September 2024

AI Article Synopsis

  • Hydrogen (H) is identified as a promising clean energy source to address energy crises and environmental issues, particularly via photocatalytic water splitting.
  • The study showcases that adding Ru single atoms into ZnInS (Ru-ZIS) significantly boosts light absorption and enhances hydrogen production to 735.2 μmol g h under visible light without any sacrificial agents.
  • With an apparent quantum efficiency of 7.5% and stable hydrogen output after 330 days, this research presents a novel approach to improve charge separation in photocatalytic processes, potentially influencing future catalyst designs.

Article Abstract

As a versatile energy carrier, H is considered as one of the most promising sources of clean energy to tackle the current energy crisis and environmental concerns, which can be produced from photocatalytic water splitting. However, solar-driven photocatalytic H production from pure water in the absence of sacrificial reagents remains a great challenge. Herein, we demonstrate that the incorporation of Ru single atoms (SAs) into ZnInS (Ru-ZIS) can enhance the light absorption, reduce the energy barriers for water dissociation, and construct a channel (Ru-S) for separating photogenerated electron-hole pairs, as a result of a significantly enhanced photocatalytic water splitting process. Impressively, the productivity of H reaches 735.2 μmol g h under visible light irradiation in the absence of sacrificial agents. The apparent quantum efficiency (AQE) for H evolution reaches 7.5% at 420 nm, with a solar-to-hydrogen (STH) efficiency of 0.58%, which is much higher than the value of natural synthetic plants (∼0.10%). Moreover, Ru-ZIS exhibits steady productivity of H even after exposure to ambient conditions for 330 days. This work provides a unique strategy for constructing charge transfer channels to promote the separation of photogenerated electron-hole pairs, which may motivate the fundamental researches on catalyst design for photocatalysis and beyond.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11504019PMC
http://dx.doi.org/10.1021/prechem.4c00035DOI Listing

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