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Enhanced electrocatalytic CO2 reduction via field-induced reagent concentration
by
De Luna, Phil
, de Arquer, F. Pelayo García
, Pang, Yuanjie
, Xu, Jixian
, Kelley, Shana O.
, Dinh, Cao Thang
, Liu, Min
, Filleter, Tobin
, Sinton, David
, Voznyy, Oleksandr
, Zheng, Xueli
, Safaei, Tina Saberi
, Cao, Changhong
, Klinkova, Anna
, Zhang, Bo
, Mepham, Adam
, Sargent, Edward H.
, Kumacheva, Eugenia
, Fan, Fengjia
in
639/301/299/886
/ 639/638/161/886
/ Alkali metals
/ Carbon dioxide
/ Carbon monoxide
/ Catalysts
/ Cations
/ Chemical properties
/ Chemical reduction
/ Chemical research
/ Electric fields
/ Electrochemical reactions
/ Electrochemistry
/ Electrodes
/ Gold
/ Humanities and Social Sciences
/ letter
/ multidisciplinary
/ Palladium
/ Reagents
/ Science
/ Spectrum analysis
2016
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Enhanced electrocatalytic CO2 reduction via field-induced reagent concentration
by
De Luna, Phil
, de Arquer, F. Pelayo García
, Pang, Yuanjie
, Xu, Jixian
, Kelley, Shana O.
, Dinh, Cao Thang
, Liu, Min
, Filleter, Tobin
, Sinton, David
, Voznyy, Oleksandr
, Zheng, Xueli
, Safaei, Tina Saberi
, Cao, Changhong
, Klinkova, Anna
, Zhang, Bo
, Mepham, Adam
, Sargent, Edward H.
, Kumacheva, Eugenia
, Fan, Fengjia
in
639/301/299/886
/ 639/638/161/886
/ Alkali metals
/ Carbon dioxide
/ Carbon monoxide
/ Catalysts
/ Cations
/ Chemical properties
/ Chemical reduction
/ Chemical research
/ Electric fields
/ Electrochemical reactions
/ Electrochemistry
/ Electrodes
/ Gold
/ Humanities and Social Sciences
/ letter
/ multidisciplinary
/ Palladium
/ Reagents
/ Science
/ Spectrum analysis
2016
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Enhanced electrocatalytic CO2 reduction via field-induced reagent concentration
by
De Luna, Phil
, de Arquer, F. Pelayo García
, Pang, Yuanjie
, Xu, Jixian
, Kelley, Shana O.
, Dinh, Cao Thang
, Liu, Min
, Filleter, Tobin
, Sinton, David
, Voznyy, Oleksandr
, Zheng, Xueli
, Safaei, Tina Saberi
, Cao, Changhong
, Klinkova, Anna
, Zhang, Bo
, Mepham, Adam
, Sargent, Edward H.
, Kumacheva, Eugenia
, Fan, Fengjia
in
639/301/299/886
/ 639/638/161/886
/ Alkali metals
/ Carbon dioxide
/ Carbon monoxide
/ Catalysts
/ Cations
/ Chemical properties
/ Chemical reduction
/ Chemical research
/ Electric fields
/ Electrochemical reactions
/ Electrochemistry
/ Electrodes
/ Gold
/ Humanities and Social Sciences
/ letter
/ multidisciplinary
/ Palladium
/ Reagents
/ Science
/ Spectrum analysis
2016
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Enhanced electrocatalytic CO2 reduction via field-induced reagent concentration
Journal Article
Enhanced electrocatalytic CO2 reduction via field-induced reagent concentration
2016
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Overview
Gold and palladium nanoneedle electrocatalysts benefit from field-induced reagent concentration to improve the efficiency of carbon dioxide reduction in the synthesis of carbon-based fuels using renewable electricity.
Boosting CO
2
reduction with nanostructured electrodes
Electrochemical reduction of carbon dioxide (CO
2
) to carbon monoxide is the first step in the manufacture of fuels and feedstocks using renewable electricity, but it is a slow process owing to low CO
2
concentration near the CO
2
reduction sites on the electrocatalysts. Min Liu
et al
. show that electrodes with sharp nanometre-sized tips produce local high electric fields that increase local CO
2
concentrations near the active electrocatalyst surface. Gold nanoneedles exploiting this field-induced reagent concentration (FIRC) effect outperform the best gold nanoparticles and oxide-derived noble metal catalysts. Similarly, palladium nanoneedle electrocatalsts produce formate from CO
2
with high selectivity and efficiency, proving the wider applicability of the FIRC concept and its value for the design of superior electrocatalysts.
Electrochemical reduction of carbon dioxide (CO
2
) to carbon monoxide (CO) is the first step in the synthesis of more complex carbon-based fuels and feedstocks using renewable electricity
1
,
2
,
3
,
4
,
5
,
6
,
7
. Unfortunately, the reaction suffers from slow kinetics
7
,
8
owing to the low local concentration of CO
2
surrounding typical CO
2
reduction reaction catalysts. Alkali metal cations are known to overcome this limitation through non-covalent interactions with adsorbed reagent species
9
,
10
, but the effect is restricted by the solubility of relevant salts. Large applied electrode potentials can also enhance CO
2
adsorption
11
, but this comes at the cost of increased hydrogen (H
2
) evolution. Here we report that nanostructured electrodes produce, at low applied overpotentials, local high electric fields that concentrate electrolyte cations, which in turn leads to a high local concentration of CO
2
close to the active CO
2
reduction reaction surface. Simulations reveal tenfold higher electric fields associated with metallic nanometre-sized tips compared to quasi-planar electrode regions, and measurements using gold nanoneedles confirm a field-induced reagent concentration that enables the CO
2
reduction reaction to proceed with a geometric current density for CO of 22 milliamperes per square centimetre at −0.35 volts (overpotential of 0.24 volts). This performance surpasses by an order of magnitude the performance of the best gold nanorods, nanoparticles and oxide-derived noble metal catalysts. Similarly designed palladium nanoneedle electrocatalysts produce formate with a Faradaic efficiency of more than 90 per cent and an unprecedented geometric current density for formate of 10 milliamperes per square centimetre at −0.2 volts, demonstrating the wider applicability of the field-induced reagent concentration concept.
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