| Literature DB >> 30259742 |
Yan Wang1, Yuesong Shen1, Yiwen Zhou1, Zhiwei Xue1, Zhenyuan Xi1, Shemin Zhu1.
Abstract
N, S, and B-doped graphene was fabricated by thermally treating graphene oxide with heteroatom-containing precursors and its catalytic behavior for NO decomposition reaction was evaluated. For the first time, the feasibility for heteroatom-doped graphene to be effectively used for decomposing NO was experimentally confirmed. The activity of different heteroatom-doped graphene follows the order: N-doped graphene > S-doped graphene > B-doped graphene. The electronegativity difference, specific area, and unique functional groups (pyridinic N and thiophene S) of the heteroatom-doped graphene play a crucial role in the catalytic performance. Furthermore, the effect of pyridinic N and thiophene S on the reaction mechanism was proposed. Pyridinic N and thiophene S can transfer extra electrons into π-antibonding orbit of NO, thus weakening N-O bond.Entities:
Keywords: direct decomposition; heteroatom-doped graphene; nitric oxide
Year: 2018 PMID: 30259742 DOI: 10.1021/acsami.8b09503
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229