Heteroatom-Driven Coordination Fields Altering Single Cerium Atom Sites for Efficient Oxygen Reduction Reaction

Author:Date:2023-04-13Views:15

论文题目:Heteroatom-Driven Coordination Fields Altering Single Cerium Atom Sites for Efficient Oxygen Reduction Reaction

论文作者:Leilei Yin, Shuai Zhang, Mingzi Sun, Siyuan Wang, Bolong Huang*, Yaping Du*

发表期刊:Advanced Materials 202302485

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Abstract

For current single-atom catalysts (SACs), modulating the  coordination environments of rare earth (RE) single atoms with complex  electronic orbital and flexible chemical states is still limited.  Herein, we report cerium (Ce) SAs supported on the P, S, and N co-doped  hollow carbon substrate (Ce SAs/PSNC) for oxygen reduction reaction  (ORR). The as-prepared Ce SAs/PSNC possessed a half-wave potential of  0.90 V, a turnover frequency value of 52.2 s−1 at 0.85 V, and  excellent stability for ORR, which far exceeds the commercial Pt/C and  most recent SACs. The Ce SAs/PSNC-based liquid zinc-air batteries (ZABs)  exhibited a high and stable open circuit voltage of 1.49 V and a  maximum power density of 212 mW cm−2. As the catalyst of air  cathode, it also displayed remarkable performances in flexible  electronic devices. Theoretical calculations have revealed that the  introduction of S and P sites has induced significant electronic  modulations to the Ce SA active sites. The P and S dopings promote the  electroactivity of Ce SAs and improve the overall site-to-site electron  transfer within the Ce SAs/PSNC. This work can offer a unique  perspective for modulating RE-based SACs in a complex coordination  environment towards superior electrocatalysis and broad applications in  energy conversion and storage devices.