Zhang Wei, Pei Supeng, Xu Kangwei, Han Zhiyue, Ma Jialu, Zhang Yingge, Liu Guipeng, Xu Xiaojun
School of Chemical and Environmental Engineering, Shanghai Institute of Technology Shanghai 201418 China
RSC Adv. 2022 Nov 28;12(52):33981-33987. doi: 10.1039/d2ra05877d. eCollection 2022 Nov 22.
Transition metal and nitrogen codoped carbon materials have emerged as one of the most promising candidates to replace noble metal-based oxygen reduction reaction (ORR) catalysts. However, the development of high-efficiency, stable and low-cost metal-nitrogen-carbon catalysts still remains a challenge. In this study, cobalt and nitrogen codoped carbon sheet catalysts were successfully prepared by a simple self-injected vapor phase growth and template method. The catalysts exhibited a multilevel pore structure with a large specific surface area and resulting physical characteristics. The catalysts have excellent onset and half-wave potentials during the ORR. Notably, the onset ( ) and half-wave potential ( ) in alkaline media for the Co-N-C-43.8 catalyst are 31 mV and 3 mV higher than those of a commercial Pt/C catalyst, respectively. Moreover, the durability of the Co-N-C-43.8 catalyst remains at a 93% current density after 10 000 s, while that of a commercial Pt/C catalyst only remains at 83%. Also, the Co-N-C-43.8 catalyst has little change in the current density after the addition of methanol. These results indicate that the Co,N-doped carbon sheet is a promising ORR catalyst.
过渡金属与氮共掺杂的碳材料已成为替代基于贵金属的氧还原反应(ORR)催化剂的最有前景的候选材料之一。然而,开发高效、稳定且低成本的金属 - 氮 - 碳催化剂仍然是一项挑战。在本研究中,通过简单的自注入气相生长和模板法成功制备了钴和氮共掺杂的碳片催化剂。这些催化剂展现出具有大比表面积和相应物理特性的多级孔结构。在ORR过程中,这些催化剂具有优异的起始电位和半波电位。值得注意的是,Co - N - C - 43.8催化剂在碱性介质中的起始电位( )和半波电位( )分别比商业Pt/C催化剂高31 mV和3 mV。此外,Co - N - C - 43.8催化剂在10000 s后电流密度保持在93%,而商业Pt/C催化剂仅保持在83%。而且,添加甲醇后,Co - N - C - 43.8催化剂的电流密度几乎没有变化。这些结果表明,Co,N掺杂的碳片是一种有前景的ORR催化剂。