z-logo
Premium
Atomically Dispersed Cobalt Trifunctional Electrocatalysts with Tailored Coordination Environment for Flexible Rechargeable Zn–Air Battery and Self‐Driven Water Splitting
Author(s) -
Zhang Zheye,
Zhao Xiaoxu,
Xi Shibo,
Zhang Lili,
Chen Zhongxin,
Zeng Zhiping,
Huang Ming,
Yang Hongbin,
Liu Bin,
Pennycook Stephen J.,
Chen Peng
Publication year - 2020
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.202002896
Subject(s) - catalysis , materials science , electrocatalyst , battery (electricity) , oxygen evolution , chemical engineering , water splitting , cobalt , carbon fibers , oxygen reduction reaction , nanotechnology , dopant , electrode , electrochemistry , doping , chemistry , power (physics) , organic chemistry , optoelectronics , metallurgy , physics , quantum mechanics , photocatalysis , engineering , composite material , composite number
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 + RuO 2 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 H 2 evolution rate of 184 mmol h −1 . The state‐of‐art experimental characterizations and theoretical calculations reveal synergistic cooperation between atomically dispersed CoN 4 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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom