Enhancing the CO2-to-CO Conversion from 2D Silver Nanoprisms via Superstructure Assembly
Author(s) -
Kun Qi,
Yang Zhang,
Ji Li,
Christophe Charmette,
Michel Ramonda,
Xiaoqiang Cui,
Ying Wang,
Yupeng Zhang,
Huali Wu,
Wensen Wang,
Xiaolin Zhang,
Damien Voiry
Publication year - 2021
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/acsnano.1c01281
Subject(s) - overpotential , materials science , selectivity , electrochemistry , superstructure , catalysis , chemical engineering , electrocatalyst , nanotechnology , electrode , reversible hydrogen electrode , chemistry , working electrode , organic chemistry , oceanography , engineering , geology
The electrochemical reduction of CO 2 in a highly selective and efficient manner is a crucial step toward its reuse for the production of chemicals and fuels. Nanostructured Ag catalysts have been found to be effective candidates for the conversion of CO 2 -to-CO. However, the ambiguous determination of the intrinsic CO 2 activity and the maximization of the density of exposed active sites have greatly limited the use of Ag toward the realization of practical electrocatalytic devices. Here, we report a superstructure design strategy prepared by the self-assembly of two-dimensional Ag nanoprisms for maximizing the exposure of active edge ribs. The vertically stacked Ag nanoprisms allow the exposure of >95% of the edge sites, resulting in an enhanced selectivity and activity toward the production of CO from CO 2 with an overpotential of 152 mV. The Ag superstructures also demonstrate a selectivity of over 90% for 100 h together with a current retention of ≈94% at -600 mV versus the reversible hydrogen electrode and a partial energy efficiency for CO production of 70.5%. Our electrochemical measurements on individual Ag nanoprisms with various edge-to-basal plane ratios and the Ag superstructures led to the identification of the edge ribs as the active sites thanks to the ≈400 mV decrease in the onset potential compared to that of the Ag (111) basal planes and a turnover frequency of 9.2 × 10 -3 ± 1.9 × 10 -3 s -1 at 0 V overpotential.
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