Synergy of Pyridinic-N and Co Single Atom Sites for Enhanced Oxygen Redox Reactions in High-Performance Zinc-Air Batteries.

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Tác giả: Masood S Alivand, Saeed Askari, Parisa Biniaz, Parama Chakraborty Banerjee, Swarit Dwivedi, Matthew R Hill, Sibudjing Kawi, Kang Hui Lim, Mainak Majumder, Akshat Tanksale, Adri C T van Duin, Ali Zavabeti

Ngôn ngữ: eng

Ký hiệu phân loại: 579.323 *Aerobic-microaerophilic, motile, helical-vibrioid gram-negative bacteria

Thông tin xuất bản: Germany : Small (Weinheim an der Bergstrasse, Germany) , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 690319

Cobalt single-atom catalysts (SACs) have the potential to act as bi-functional electrocatalysts for the oxygen-redox reactions in metal-air batteries. However, achieving both high performance and stability in these SACs has been challenging. Here, a novel and facile synthesis method is used to create cobalt-doped-nitrogen-carbon structures (Co-N-C) containing cobalt-SACs by carbonizing a modified ZIF-11. HAADF-STEM images and EXAFS spectra confirmed that the structure with the lowest cobalt concentration contains single cobalt atoms coordinated with four nitrogen atoms (Co-N₄). Electrochemical tests showed that this electrocatalyst performed exceptionally well in both oxygen reduction reaction (ORR) (E1/2 ≈ 0.859 V) and oxygen evolution reaction (OER) (Ej = 10: 1.544 V), with excellent stability. When used as a bi-functional electrocatalyst in the air cathode of a rechargeable zinc-air battery (ZAB), a peak power density of 178.6.1 mW cm
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