Abstract
Designing multifunctional catalysts with high activity, stability, and low-cost for energy storage and conversion is a significant challenge. Herein, a trifunctional electrocatalyst is synthesized by anchoring individually dispersed Co atoms on N and S codoped hollow carbon spheres (CoSA/N,S-HCS), which exhibits outstanding catalytic activity and stability for the oxygen reduction reaction, oxygen evolution reaction, and hydrogen evolution reaction. When equipped in liquid or flexible solid-state rechargeable Zn–air batteries, CoSA/N,S-HCS endows them with high power and energy density as well as excellent long-term cycling stability, outperforming benchmark batteries based on a commercial Pt/C + RuO2 dual catalyst system. Furthermore, a self-driven water splitting system powered by flexible Zn–air batteries is demonstrated using CoSA/N,S-HCS as the sole catalyst, giving a high H2 evolution rate of 184 mmol h−1. The state-of-art experimental characterizations and theoretical calculations reveal synergistic cooperation between atomically dispersed Co-N4 active sites, nearby electron-donating S dopants, and the unique carbon support to single-atom catalysts (SACs). This work demonstrates a general strategy to design various multifunctional SAC systems with a tailored coordination environment.
Original language | English |
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Article number | 2002896 |
Journal | Advanced Energy Materials |
Volume | 10 |
Issue number | 48 |
DOIs | |
Publication status | Published - Dec 22 2020 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2020 Wiley-VCH GmbH
ASJC Scopus Subject Areas
- Renewable Energy, Sustainability and the Environment
- General Materials Science
Keywords
- coordination environment
- self-driven water splitting
- single-atom catalysis
- trifunctional electrocatalysts
- Zn–air batteries