4.7 Article

Trace amount of ceria incorporation by atomic layer deposition in Co/CoOx-embedded N-doped carbon for efficient bifunctional oxygen electrocatalysis: Demonstration and quasioperando observations

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 77, Pages 38258-38269

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.09.082

Keywords

Atomic layer deposition; Bifunctional oxygen electrocatalysis; Quasi-operando XPS; Metal-organic framework; Ceria

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This study utilizes atomic layer deposition to introduce trace amounts of ceria into a Co/CoOx-embedded N-doped carbon nanostructure, enhancing catalytic activity and durability. The optimally prepared catalyst exhibits excellent performance in oxygen reduction and oxygen evolution reactions, with quasi-operando observations revealing the multifaceted roles of the introduced ceria.
As a promising class of alternatives to noble metal-based oxygen electrocatalysts, hybrids of metal/metal oxide (M/MO) and N-doped carbon have been widely explored. To address the often-insufficient catalytic activity of single M/MO-embedded N-C systems, researchers have introduced a second M/MO, usually via wet processes. In this work, we leverage the unique capability of atomic layer deposition (ALD) to enable the introduction of a trace amount of ceria throughout a Co/CoOx-embedded N-doped carbon nanostructure in a highly uniform and dispersed manner to maximize heterogeneous interfacial areas and thus catalytically active sites. An optimally prepared catalyst achieves an ORR onset potential of 0.95 V (0.1 M KOH) and an OER potential of 1.53 V at 10 mA cm(-2) (1 M KOH) and exhibits excellent cyclic durability. Quasi-operando observations reveal the multifaceted roles of the tiny amount of introduced ceria in facilitating electrocatalytic activity and enhancing durability. The ceria activates reactant adsorbates and transfers the activated intermediates to neighboring CoOx and electronically couples with Co and N species for enhanced catalytic activity. A high concentration of trivalent Ce state is readily and continuously restored during ORR/OER for an uninterrupted activation of reactants, also contributing to a highly stable reaction. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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