催化作用
限制电流
介孔材料
热解
塔菲尔方程
化学工程
碳纤维
化学
甲醇
材料科学
无机化学
电化学
电极
有机化学
复合材料
复合数
物理化学
工程类
作者
Kanda Su,Jie Li,Xinxin Zhang,Xiangxiong Chen,Ziyu Luo,Junhua Li,Dong Qian,Jinlong Liu,Geoffrey I. N. Waterhouse
标识
DOI:10.1021/acs.iecr.3c01472
摘要
The commercialization of zinc–air batteries (ZABs) and many types of fuel cells hinges on the discovery of non-precious metal catalysts with high activity and durability for the oxygen reduction reaction (ORR). Herein, we describe a simple and scalable l -alanine-assisted thermal pyrolysis strategy [utilizing l -alanine, urea, Ketjenblack carbon (KB), and CoCl 2 as precursors] that yielded a Co@N–C/N–KB catalyst with outstanding ORR performance in alkaline media. The addition of l -alanine in the pyrolysis-step increased the proportion of pyridinic-N + graphitic-N in the Co@N–C/N–KB catalyst, with highly conductive KB-promoting electron transfer kinetics during ORR. These attributes, together with the hierarchical porosity of the catalyst [presence of micropores, mesopores (dominant), and macropores], gave Co@N–C/N–KB an onset potential of 0.91 V vs RHE, a half-wave potential of 0.84 V vs RHE, a limiting current density of −5.86 mA cm –2, a Tafel slope of 63.7 mV dec –1, and an excellent durability and methanol tolerance (superior to a commercial 20 wt % Pt/C catalyst in almost all these aspects). A ZAB constructed with Co@N–C/N–KB as the cathode catalyst delivered an impressive open-circuit voltage of 1.519 V, a high power density of 204.5 mW cm –2, an energy density up to 790 mA h g Zn –1, and very stable operation with charge–discharge cycling, thus offering great promise for practical devices.
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