| Literature DB >> 30082882 |
Yasong Zhao1,2, Jiawei Wan1, Huiying Yao3, Lijuan Zhang1, Kaifeng Lin2, Lei Wang4, Nailiang Yang5, Daobin Liu6, Li Song6, Jia Zhu7, Lin Gu8, Lei Liu9, Huijun Zhao10, Yuliang Li11, Dan Wang12,13,14.
Abstract
The oxygen reduction reaction (ORR) is a fundamental reaction for energy storage and conversion. It has mainly relied on platinum-based electrocatalysts, but the chemical doping of carbon-based materials has proven to be a promising strategy for preparing metal-free alternatives. Nitrogen doping in particular provides a diverse range of nitrogen forms. Here, we introduce a new form of nitrogen doping moieties -sp-hybridized nitrogen (sp-N) atoms into chemically defined sites of ultrathin graphdiyne, through pericyclic replacement of the acetylene groups. The as-prepared sp-N-doped graphdiyne catalyst exhibits overall good ORR performance, in particular with regards to peak potential, half-wave potential and current density. Under alkaline conditions it was comparable to commercial Pt/C, and showed more rapid kinetics. And although its performances are a bit lower than those of Pt/C in acidic media they surpass those of other metal-free materials. Taken together, experimental data and density functional theory calculations suggest that the high catalytic activity originates from the sp-N dopant, which facilitates O2 adsorption and electron transfer on the surface of the catalyst. This incorporation of chemically defined sp-N atoms provides a new synthetic route to high-performance carbon-based and other metal-free catalysts.Entities:
Year: 2018 PMID: 30082882 DOI: 10.1038/s41557-018-0100-1
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427