
Binary Atomically Dispersed Metal‐Site Catalysts with Core−Shell Nanostructures for O 2 and CO 2 Reduction Reactions
Author(s) -
Yang Xiaoxuan,
Wang Maoyu,
Zachman Michael J.,
Zhou Hua,
He Yanghua,
Liu Shengwen,
Zang Hong-Ying,
Feng Zhenxing,
Wu Gang
Publication year - 2021
Publication title -
small science
Language(s) - English
Resource type - Journals
ISSN - 2688-4046
DOI - 10.1002/smsc.202100046
Subject(s) - catalysis , materials science , chemical engineering , metal , electrocatalyst , carbon fibers , thermal stability , nanostructure , nanotechnology , chemistry , electrochemistry , composite material , organic chemistry , electrode , metallurgy , composite number , engineering
Engineering atomically dispersed metal site catalysts with controlled local coordination environments and 3D nanostructures effectively improves the catalytic performance for the oxygen reduction reaction (ORR) and the carbon dioxide reduction reaction (CO 2 RR), which are critical for clean energy conversion and chemical production. Herein, an innovative approach for preparing core−shell nanostructured catalysts with different single‐metal sites in the core and the shell, respectively, is developed. In particular, as the shell precursors, covalent organic polymers with a thin layered structure that is polymerized in situ and coated on a metal‐doped ZIF‐derived carbon core are used, followed by a controlled thermal activation. The selective combination and construction of different metal sites increase active site density in the surface layers, promote structural robustness, facilitate mass/charge transfer, and yield a possible synergy of active sites in the core and the shell. The p‐FeNC(shell)@CoNC(core), consisting of a polymerized FeTPPCl‐derived carbon layer (p‐FeNC) on a Co‐doped ZIF‐derived carbon (CoNC), exhibits remarkable ORR activity and stability in acidic media along with encouraging durability in H 2 –air fuel cells. Likewise, a p‐FeNC(shell)@NiNC(core) catalyst demonstrates outstanding CO 2 RR activity and stability. Hence, integrating two appropriate single‐metal sites in core and shell precursors, respectively, can modulate morphological and catalytic properties for a possible synergy toward different electrocatalysis processes.