| Literature DB >> 31338908 |
Shiyong Mou1, Tongwei Wu2, Junfeng Xie3, Ya Zhang2, Lei Ji2, Hong Huang2, Ting Wang4, Yonglan Luo4, Xiaoli Xiong1, Bo Tang3, Xuping Sun2.
Abstract
Electrocatalysis has emerged as an attractive way for artificial CO2 fixation to CH3 OH, but the design and development of metal-free electrocatalyst for highly selective CH3 OH formation still remains a key challenge. Here, it is demonstrated that boron phosphide nanoparticles perform highly efficiently as a nonmetal electrocatalyst toward electrochemical reduction of CO2 to CH3 OH with high selectivity. In 0.1 m KHCO3 , this catalyst achieves a high Faradaic efficiency of 92.0% for CH3 OH at -0.5 V versus reversible hydrogen electrode. Density functional theory calculations reveal that B and P synergistically promote the binding and activation of CO2 , and the rate-determining step for the CO2 reduction reaction is dominated by *CO + *OH to *CO + *H2 O process with free energy change of 1.36 eV. In addition, CO and CH2 O products are difficultly generated on BP (111) surface, which is responsible for the high activity and selectivity of the CO2 -to-CH3 OH conversion process.Entities:
Keywords: CH3OH; CO2 reduction reaction; boron phosphide; density functional theory; metal free
Year: 2019 PMID: 31338908 DOI: 10.1002/adma.201903499
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849