| Literature DB >> 29504227 |
Gang Wan1,2, Pengfei Yu3, Hangrong Chen1, Jianguo Wen4, Cheng-Jun Sun4, Hua Zhou5, Nian Zhang3, Qianru Li1,2, Wanpeng Zhao1,2, Bing Xie6, Tao Li5,7, Jianlin Shi1.
Abstract
The development of cost-effective catalysts to replace noble metal is attracting increasing interests in many fields of catalysis and energy, and intensive efforts are focused on the integration of transition-metal sites in carbon as noble-metal-free candidates. Recently, the discovery of single-atom dispersed catalyst (SAC) provides a new frontier in heterogeneous catalysis. However, the electrocatalytic application of SAC is still subject to several theoretical and experimental limitations. Further advances depend on a better design of SAC through optimizing its interaction with adsorbates during catalysis. Here, distinctive from previous studies, favorable 3d electronic occupation and enhanced metal-adsorbates interactions in single-atom centers via the construction of nonplanar coordination is achieved, which is confirmed by advanced X-ray spectroscopic and electrochemical studies. The as-designed atomically dispersed cobalt sites within nonplanar coordination show significantly improved catalytic activity and selectivity toward the oxygen reduction reaction, approaching the benchmark Pt-based catalysts. More importantly, the illustration of the active sites in SAC indicates metal-natured catalytic sites and a media-dependent catalytic pathway. Achieving structural and electronic engineering on SAC that promotes its catalytic performances provides a paradigm to bridge the gap between single-atom catalysts design and electrocatalytic applications.Entities:
Keywords: electrocatalysis; media dependence; metal-adsorbate interactions; selectivity; single-atom dispersed catalysts
Year: 2018 PMID: 29504227 DOI: 10.1002/smll.201704319
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281