%0 Journal Article
%T N-doped ZrO2 nanoparticles embedded in a N-doped carbon matrix as a highly active and durable electrocatalyst for oxygen reduction.
%A Cao X
%A Zheng S
%A Wang T
%A Lin F
%A Li J
%A Jiao L
%J Fundam Res
%V 2
%N 4
%D 2022 Jul
%M 38933999
暂无%R 10.1016/j.fmre.2021.08.014
%X Fabricating highly efficient and robust oxygen reduction reaction (ORR) electrocatalysts is challenging but desirable for practical Zn-air batteries. As an early transition-metal oxide, zirconium dioxide (ZrO2) has emerged as an interesting catalyst owing to its unique characteristics of high stability, anti-toxicity, good catalytic activity, and small oxygen adsorption enthalpies. However, its intrinsically poor electrical conductivity makes it difficult to serve as an ORR electrocatalyst. Herein, we report ultrafine N-doped ZrO2 nanoparticles embedded in an N-doped porous carbon matrix as an ORR electrocatalyst (N-ZrO2/NC). The N-ZrO2/NC catalyst displays excellent activity and long-term durability with a half-wave potential (E1/2) of 0.84 V and a selectivity for the four-electron reduction of oxygen in 0.1 M KOH. Upon employment in a Zn-air battery, N-ZrO2/NC presented an intriguing power density of 185.9 mW cm-2 and a high specific capacity of 797.9 mA h gZn -1, exceeding those of commercial Pt/C (122.1 mW cm-2 and 782.5 mA h gZn -1). This excellent performance is mainly attributed to the ultrafine ZrO2 nanoparticles, the conductive carbon substrate, and the modified electronic band structure of ZrO2 after N-doping. Density functional theory calculations demonstrated that N-doping can reduce the band-gap of ZrO2 from 3.96 eV to 3.33 eV through the hybridization of the p state of the N atom with the 2p state of the oxygen atom; this provides enhanced electrical conductivity and results in faster electron-transfer kinetics. This work provides a new approach for the design of other enhanced semiconductor and insulator materials.