Highly Defective Ultrafine Carbon Nanoreactors Enriched with Edge‐Type Zn‐N <sub>3</sub> P <sub>1</sub> Moiety Boosting Oxygen Electrocatalysis

Y Yangyang Tan (College of Materials Science and Engineering Fuzhou University Fuzhou 350108 P. R. China) Z Zeyi Zhang F Fei Guo S Suhao Chen (College of Materials Science and Engineering Fuzhou University Fuzhou 350108 P. R. China) H Haoran Jiang R Runzhe Chen (College of Materials and Chemical Engineering Minjiang University Fuzhou Fujian China) Z Zichen Wang (China-Australia Joint Research Center for Functional Molecular Materials, School of Chemical Science and Engineering) Q Qianwei Chen P Pei Yuan S Shu‐Juan Bao (Institute for Clean Energy &amp; Advanced Materials School of Materials and Energy Southwest University Chongqing 400715 China) M Maowen Xu (School of Materials and Energy Southwest University Chongqing 400715 P. R. China) N Niancai Cheng (College of Materials Science and Engineering Fuzhou University Fuzhou 350108 P. R. China)

Abstract

Abstract High‐active nonplatinum group metal oxygen reduction reaction (ORR) catalysts have great potential to improve fuel cell and metal–air battery performance due to their efficiency and cost‐effectiveness. However, a fundamental understanding of their size‐dependent structure–performance relationships remain elusive. Here a mesoporous‐dominant carbon nanoreactor with dimensions in the range of 15–43 nm with edge‐rich defective atomic Zn sites is designed. The crystal size and pore diameter of this carbon nanoreactors can be precisely adjusted to enable tunable mass diffusion pathways and porosities. Importantly, the hydrophobic nature of 25 nm nanoreactors maximizes the nonkinetic advantages of active site exposure and rapid O 2 mass transfer at the triple‐phase interface. The developed Zn‐N‐P/NPC catalysts delivers outstanding alkaline and acidic ORR performance with half‐wave potentials of 0.92 and 0.80 V, respectively, as well as excellent zinc–air battery performance with charge/discharge over 400 h under 20 mA cm −2 . X‐ray absorption spectroscopy and theoretical calculations indicate that the enhanced ORR catalytic activity of Zn‐N‐P/NPC stems from the introduction of P atoms and edge carbon defects effectively exciting the localized electronic asymmetric distribution of Zn species. The findings provide new perspectives on the size effect of porous carbon supports for the development of efficient cathodes catalysts with multifunctionality.

Article Details

Volume / Issue Vol. 37, Issue 26
Published July 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (12)

Y

Yangyang Tan

College of Materials Science and Engineering Fuzhou University Fuzhou 350108 P. R. China

Z

Zeyi Zhang

F

Fei Guo

S

Suhao Chen

College of Materials Science and Engineering Fuzhou University Fuzhou 350108 P. R. China

H

Haoran Jiang

R

Runzhe Chen

College of Materials and Chemical Engineering Minjiang University Fuzhou Fujian China

Z

Zichen Wang

China-Australia Joint Research Center for Functional Molecular Materials, School of Chemical Science and Engineering

Q

Qianwei Chen

P

Pei Yuan

S

Shu‐Juan Bao

Institute for Clean Energy &amp; Advanced Materials School of Materials and Energy Southwest University Chongqing 400715 China

M

Maowen Xu

School of Materials and Energy Southwest University Chongqing 400715 P. R. China

N

Niancai Cheng

College of Materials Science and Engineering Fuzhou University Fuzhou 350108 P. R. China