Surface Electronic Modulation with Hetero-Single Atoms to Enhance Oxygen Evolution Catalysis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 34184891.
- Also identified by DOI 10.1021/acsnano.1c02989.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Oxygen evolution catalysis plays a crucial role in the solar-to-fuel conversion for green energy applications. However, developing efficient and stable catalysts for the oxygen evolution catalysis remains a great challenge. Here, we successfully activate an inefficient oxygen evolution catalyst using a simple single atom tailoring strategy. The Rh element with its unfilled 4d<sup>8</sup> electron configuration was selected to atomically implant into a Cu oxide matrix, which has a filled 3d<sup>10</sup> electron configuration. The hetero-Rh single atom (SA) migration was achieved by dispersing Cu<sub>2</sub>O nanocubes in a RhCl<sub>3</sub> aqueous solution, enabling an ion exchange process. The activated catalyst (Cu<sub>2</sub>O-RhSA) exhibited significantly enhanced catalytic activity toward oxygen evolution in alkaline media, surpassing the performance of pristine Cu<sub>2</sub>O nanocubes and commercial IrO<sub>2</sub>. A theoretical study further confirmed that the migrated hetero-Rh SAs can tailor the interaction between the Cu and O sites, modulating the electron density distribution on the surface of Cu<sub>2</sub>O, leading to a more favorable oxygen evolution process.