Precise fabrication of single-atom alloy co-catalyst with optimal charge state for enhanced photocatalysis

Abstract

While the surface charge state of co-catalysts plays a critical role for boosting photocatalysis, studies on surface charge regulation via their precise structure control remain extremely rare. Herein, metal-organic framework (MOF) stabilized bimetallic Pd@Pt nanoparticles, which feature adjustable Pt coordination environment and a controlled structure from core-shell to single-atom alloy (SAA), have been fabricated. Significantly, apart from the formation of a Mott-Schottky junction in a conventional way, we elucidate that Pt surface charge regulation can be alternatively achieved by changing its coordination environment and the structure of the Pd@Pt co-catalyst, where the charge between Pd and Pt is redistributed. As a result, the optimized Pd ₁₀@Pt ₁/MOF composite, which involves an unprecedented SAA co-catalyst, exhibits exceptionally high photocatalytic hydrogen production activity, far surpassing its corresponding counterparts.

Abstract

The MOF-stabilized Pd ₁₀@Pt ₁ single-atom alloy was fabricated, featuring optimized Pt surface charge state and greatly boosted photocatalysis, thanks to the charge redistribution regulated by Pt coordination environment and Pd@Pt microstructure.