TY - JOUR
T1 - Silica-nickel catalyst interfaces promote highly efficient CO2 electroreduction to CO with a wide potential range
AU - Xie, Yijun
AU - Xia, Wei
AU - Jia, Shuaiqiang
AU - Han, Shitao
AU - Yao, Ting
AU - Fang, Minghui
AU - Zhou, Dawei
AU - Xing, Xueqing
AU - Wu, Haihong
AU - He, Mingyuan
AU - Han, Buxing
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/4/1
Y1 - 2023/4/1
N2 - CO2 electroreduction reaction (CO2RR) offers a promising route to scale up CO2-to-CO using renewable electricity and close the anthropogenic carbon cycle. To date, the undesirable hydrogen evolution reaction (HER) still occurs at the catalyst surface in CO2RR, diminishing CO2-to-CO production. In this work, we introduced silica on Ni to create active Ni-SiOx interface sites and prepared silica-modified nickel nanoparticles on carbon nanotubes (Si-Ni-CNTs-800) as a highly effective electrocatalyst for CO2-to-CO over a wide potential range. The catalyst achieved high CO Faradaic efficiency (FECO) of > 90 % in a wide potential range from −0.6 to −1.1 V vs RHE with a maximum FECO of 98 % at −0.9 V vs RHE with a CO partial current density of 21.5 mA cm−2 by using standard H-type cell, and the catalyst could be used stably at least 12 h. With the support of X-ray absorption fine structure (EXAFS) and spectroscopic analysis, we demonstrated that the chemical bonds of Si-C and O-Si-C in the catalysts favor CO2 activation to form the CO* intermediate and inhibition of HER, finally enhanced CO2-to-CO conversion.
AB - CO2 electroreduction reaction (CO2RR) offers a promising route to scale up CO2-to-CO using renewable electricity and close the anthropogenic carbon cycle. To date, the undesirable hydrogen evolution reaction (HER) still occurs at the catalyst surface in CO2RR, diminishing CO2-to-CO production. In this work, we introduced silica on Ni to create active Ni-SiOx interface sites and prepared silica-modified nickel nanoparticles on carbon nanotubes (Si-Ni-CNTs-800) as a highly effective electrocatalyst for CO2-to-CO over a wide potential range. The catalyst achieved high CO Faradaic efficiency (FECO) of > 90 % in a wide potential range from −0.6 to −1.1 V vs RHE with a maximum FECO of 98 % at −0.9 V vs RHE with a CO partial current density of 21.5 mA cm−2 by using standard H-type cell, and the catalyst could be used stably at least 12 h. With the support of X-ray absorption fine structure (EXAFS) and spectroscopic analysis, we demonstrated that the chemical bonds of Si-C and O-Si-C in the catalysts favor CO2 activation to form the CO* intermediate and inhibition of HER, finally enhanced CO2-to-CO conversion.
UR - https://www.scopus.com/pages/publications/85148667981
U2 - 10.1016/j.cej.2023.141938
DO - 10.1016/j.cej.2023.141938
M3 - 文章
AN - SCOPUS:85148667981
SN - 1385-8947
VL - 461
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 141938
ER -