Ma Fei-Xiang, Zhang Guobin, Wang Meiyu, Liang Xiongyi, Lyu Fucong, Xiao Xufen, Wang Peng, Zhen Liang, Lu Jian, Zheng Lirong, Yang Li Yang, Xu Cheng-Yan
Sauvage Laboratory for Smart Materials, School of Materials Science and Engineering, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China; Department of Mechanical Engineering, City University of Hong Kong, Kowloon, Hong Kong, China.
Department of Mechanical Engineering, City University of Hong Kong, Kowloon, Hong Kong, China.
J Colloid Interface Sci. 2022 Aug 15;620:67-76. doi: 10.1016/j.jcis.2022.04.002. Epub 2022 Apr 5.
Construction of single-atom catalysts (SACs) with maximally exposed active sites remains a challenging task mainly because of the lack of suitable host matrices. In this study, hierarchical N-doped carbon nanoboxes composed of ultrathin nanosheets with dispersed atomic Mo (denoted as hierarchical SA-Mo-C nanoboxes) were fabricated via a template-engaged multistep synthesis process. Comprehensive characterizations, including X-ray absorption fine structure analysis, reveal the formation of Mo-N atomic sites uniformly anchored on the hierarchical carbon nanoboxes. The prepared catalysts offer structural and morphological advantages, including ultrathin nanosheet units, unique hollow structures and abundant active Mo-N species, that result in excellent activity with a half-wave potential of 0.86 V vs. RHE and superb stability for the oxygen reduction reaction in 0.1 M KOH; thus, the catalysts are promising air-cathode catalysts for Zn-air batteries with a high peak power density of 157.6 mW cm.
构建具有最大暴露活性位点的单原子催化剂(SACs)仍然是一项具有挑战性的任务,主要原因是缺乏合适的主体基质。在本研究中,通过模板参与的多步合成过程制备了由具有分散原子Mo的超薄纳米片组成的分级N掺杂碳纳米盒(表示为分级SA-Mo-C纳米盒)。包括X射线吸收精细结构分析在内的综合表征揭示了均匀锚定在分级碳纳米盒上的Mo-N原子位点的形成。所制备的催化剂具有结构和形态优势,包括超薄纳米片单元、独特的中空结构和丰富的活性Mo-N物种,这导致其在相对于可逆氢电极(RHE)的半波电位为0.86 V时具有优异的活性,并在0.1 M KOH中对氧还原反应具有出色的稳定性;因此,这些催化剂有望成为锌空气电池的空气阴极催化剂,其峰值功率密度高达157.6 mW/cm²。