| Literature DB >> 31120620 |
Meiling Xiao1,2, Jianbing Zhu2, Gaoran Li2, Na Li3, Shuang Li3, Zachary Paul Cano2, Lu Ma4, Peixin Cui5, Pan Xu2, Gaopeng Jiang2, Huile Jin1, Shun Wang1, Tianpin Wu4, Jun Lu6, Aiping Yu2, Dong Su3, Zhongwei Chen2.
Abstract
Combining the advantages of homogeneous and heterogeneous catalysts, single-atom catalysts (SACs) are bringing new opportunities to revolutionize ORR catalysis in terms of cost, activity and durability. However, the lack of high-performance SACs as well as the fundamental understanding of their unique catalytic mechanisms call for serious advances in this field. Herein, for the first time, we develop an Ir-N-C single-atom catalyst (Ir-SAC) which mimics homogeneous iridium porphyrins for high-efficiency ORR catalysis. In accordance with theoretical predictions, the as-developed Ir-SAC exhibits orders of magnitude higher ORR activity than iridium nanoparticles with a record-high turnover frequency (TOF) of 24.3 e- site-1 s-1 at 0.85 V vs. RHE) and an impressive mass activity of 12.2 A mg-1 Ir , which far outperforms the previously reported SACs and commercial Pt/C. Atomic structural characterizations and density functional theory calculations reveal that the high activity of Ir-SAC is attributed to the moderate adsorption energy of reaction intermediates on the mononuclear iridium ion coordinated with four nitrogen atom sites.Entities:
Keywords: adsorption energy; fuel cells; iridium; oxygen reduction reaction; single-atom catalyst
Year: 2019 PMID: 31120620 DOI: 10.1002/anie.201905241
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336