| Literature DB >> 28691392 |
Yanfang Song1, Wei Chen1, Chengcheng Zhao1, Shenggang Li1,2, Wei Wei1,2, Yuhan Sun1,2.
Abstract
CO2 electroreduction is a promising technique for satisfying both renewable energy storage and a negative carbon cycle. However, it remains a challenge to convert CO2 into C2 products with high efficiency and selectivity. Herein, we report a nitrogen-doped ordered cylindrical mesoporous carbon as a robust metal-free catalyst for CO2 electroreduction, enabling the efficient production of ethanol with nearly 100 % selectivity and high faradaic efficiency of 77 % at -0.56 V versus the reversible hydrogen electrode. Experiments and density functional theory calculations demonstrate that the synergetic effect of the nitrogen heteroatoms and the cylindrical channel configurations facilitate the dimerization of key CO* intermediates and the subsequent proton-electron transfers, resulting in superior electrocatalytic performance for synthesizing ethanol from CO2 .Entities:
Keywords: CO2 electroreduction; C−C coupling; N-doped carbon; cylindrical channels; ethanol
Year: 2017 PMID: 28691392 DOI: 10.1002/anie.201706777
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336