电催化剂
氧还原反应
电池(电)
碳纤维
多孔性
化学工程
氧气
材料科学
兴奋剂
氧还原
化学
无机化学
电极
电化学
有机化学
复合材料
复合数
物理化学
功率(物理)
工程类
物理
量子力学
光电子学
作者
Vaishna Priya K.,Geeta Pandurang Kharabe,Sidharth Barik,Alaa Mohamed,Sreekumar Kurungot,Unnikrishnan Nair Saraswathy Hareesh
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2024-04-09
卷期号:38 (8): 7196-7207
标识
DOI:10.1021/acs.energyfuels.4c00059
摘要
Metal–organic frameworks are considered ideal precursors for the preparation of transition-metal, heteroatom-doped carbon catalysts that are perceived to be efficient electrocatalysts for energy storage devices. Herein, we demonstrate the synthesis of ZIF-67-derived Co-incorporated N-doped porous carbon catalysts supported on high surface area microporous carbon prepared from a lotus seed shell. The combination of the two carbon catalysts in different weight ratios resulted in Co-incorporated N-doped carbon sheets with tuned surface area and porosity, enabling enhanced oxygen reduction reaction (ORR) activity in an alkaline medium. The optimized carbon catalyst ZL 600 (3:1) exhibited a half-wave potential of 0.79 V vs RHE and a limiting current density of −4.38 mA cm–2 in 0.1 M KOH solution with higher stability and methanol tolerance. The optimized sample ZL 600 (3:1) demonstrated as a cathode in a zinc–air battery exhibited an open circuit voltage of 1.29 V with a flat discharge profile at a current rate of 10 mA cm–2. The homemade system produced a specific capacity of 610 mAh g–1 and a peak power density of 111 mW cm–2, comparable to the cathode made with Pt/C. The high micro-mesoporosity, pyridinic and pyrrolic nitrogen contents, as well as enriched Co-active centers protected by carbon sheets favorably contributed to the efficient ORR mechanism.
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