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江汉大学 柔性光电材料与技术教育部重点实验室,武汉 430056
Received:10 April 2026,
Revised:2026-05-12,
Accepted:13 May 2026,
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HU Qing, YAO Zhenhua, HU Maocong. Carbon support regulation of Co-N-C catalysts and zinc-air battery performance[J/OL]. CIESC Journal, 2026.
HU Qing, YAO Zhenhua, HU Maocong. Carbon support regulation of Co-N-C catalysts and zinc-air battery performance[J/OL]. CIESC Journal, 2026. DOI: 10.11949/0438-1157.20260490.
以乙酸钴与1
10-菲罗啉为前驱体,分别选用鸟嘌呤、碳黑Vulcan XC-72及羧基化多壁碳纳米管为碳基底,通过可控热解制备了三种Co-N-C催化剂(CoNC-G、CoNC-CB及CoNC-CNT),系统探究了碳基底对催化剂结构及氧还原反应(ORR)性能的影响。结果表明,以碳黑Vulcan XC-72为基底的CoNC-CB性能最优:XPS图谱证实其Co-N键比例高达39.28%,N
2
吸附-脱附测试显示其总孔容达0.4627 cm
3
·g
-1
且介孔-大孔占比97.99%。电化学测试表明,CoNC-CB的半波电位为0.83 V(vs. RHE),塔菲尔斜率低至55.14 mV·dec
-1
,电子转移数接近4,且具备优异的稳定性及抗甲醇毒化性能。在锌-空气电池中,CoNC-CB基电池最大功率密度达163 mW·cm
-2
,比容量为795.94 mAh·g
-1
,循环寿命达877 h,性能显著优于商用Pt/C+IrO
2
。本研究阐明了碳基底在调控Co-N-C催化剂活性位点构筑与传质优化中的关键作用,为高性能非贵金属ORR催化剂的设计提供了重要参考。
Three Co-N-C catalysts (CoNC-G
CoNC-CB
and CoNC-CNT) were prepared by controlled pyrolysis using cobalt acetate and 1
10-phenanthroline as precursors and guanine
carbon black Vulcan XC-72
and carboxylated multi-walled carbon nanotubes as carbon supports
respectively. The effects of carbon supports on the structure and oxygen reduction reaction (ORR) performance of the catalysts were systematically investigated. The results showed that CoNC-CB
with carbon black Vulcan XC-72 as the support
exhibited the best performance: XPS spectra confirmed that the proportion of Co-N bonds was as high as 39.28%
and N
2
adsorption-desorption tests indicated that the total pore volume was 0.4627 cm
3
·g
-1
with mesopores and macropores accounting for 97.99%. Electrochemical tests revealed that the half-wave potential of CoNC-CB was 0.83 V (vs. RHE)
the Tafel slope was as low as 55.14 mV·dec
-1
the electron transfer number was close to 4
and it had excellen
t stability and methanol tolerance. In zinc-air batteries
the maximum power density of the CoNC-CB-based battery was 163 mW·cm
-2
the specific capacity was 795.94 mAh·g
-1
and the cycle life was 877 h
significantly outperforming commercial Pt/C + IrO
2
. This study clarified the crucial role of carbon supports in regulating the construction of active sites and optimizing mass transfer in Co-N-C catalysts
providing an important reference for the design of high-performance non-precious metal ORR catalysts.
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