| Literature DB >> 30203573 |
Jian Yang1, Zongyang Qiu2, Changming Zhao1, Weichen Wei1, Wenxing Chen3,4,5,6, Zhijun Li2, Yunteng Qu1, Juncai Dong3,4,5,6, Jun Luo3,4,5,6, Zhenyu Li1, Yuen Wu1.
Abstract
The arrangement of the active sites on the surface of a catalysts can reduce the problem of mass transfer and enhance the atom economy. Herein, supported Ni metal nanoparticles can be transformed to thermal stable Ni single atoms, mostly located on the surface of the support. Assisted by N-doped carbon with abundant defects, this synthetic process not only transform the nanoparticles to single atoms, but also creates numerous pores to facilitate the contact of dissolved CO2 and single Ni sites. The proposed mechanism is that the Ni nanoparticles could break surface C-C bonds drill into the carbon matrix, leaving pores on the surface. When Ni nanoparticles are exposed to N-doped carbon, the strong coordination splits Ni atoms from Ni NPs. The Ni atoms are stabilized within the surface of carbon substrate. The continuous loss of atomic Ni species from the NPs would finally result in atomization of Ni NPs. CO2 electroreduction testing shows that the surface enriched with Ni single atoms delivers better performance than supported Ni NPs and other similar catalysts.Entities:
Keywords: CO2 electroreduction; nickel; porous carbons; single-atom catalysts; thermal atomization
Year: 2018 PMID: 30203573 DOI: 10.1002/anie.201808049
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336