Boosting hydrogen and methane formation on a high-entropy photocatalyst by integrating atomic d0/d10 electronic junctions and microscopic P/N heterojunctions

TL;DR

This study develops a high-entropy photocatalyst with integrated atomic and microscopic heterojunctions, significantly boosting hydrogen and methane production efficiency for clean energy applications.

Contribution

It introduces a novel combination of atomic d0/d10 electronic junctions with P/N heterojunctions in a high-entropy oxide to enhance photocatalytic performance.

Findings

H2 production reaches 0.71 mmol/g.h

CH4 evolution reaches 2.40 umol/g.h

72% selectivity for methanation

Abstract

The formation of green energy carriers such as hydrogen (H2) and methane (CH4) via photocatalytic processes provides a clean method for addressing environmental and energy issues. To achieve highly efficient photocatalysts for H2 and CH4 generation, the present work introduces the P/N heterojunctions in a high-entropy oxide (HEO) with d0/d10 electronic junctions. The study uses CuO as a P-type semiconductor and the HEO containing d0 (Ti, Zr, Nb, Ta) and d10 (Zn) cations as an N-type semiconductor. The material exhibits improvements in optical properties, such as light absorption, charge mobility and reduced electron-hole recombination. The integration of two concepts, atomic-scale d0/d10 electronic junctions and micro-scale P/N heterojunctions, leads to enhanced H2 and CH4 production. Particularly after the partial removal of vacancies in the heterojunction, H2 production from photocatalytic water splitting reaches 0.71 mmol/g.h, and CH4 evolution from CO2 conversion reaches 2.40 umol/g.h with 72% selectivity for methanation. The integrated strategy of this study has a high potential in developing active heterostructured catalysts for clean fuel production.