TY - JOUR
T1 - Tuning selectivity of electrochemical reduction reaction of CO2 by atomically dispersed Pt into SnO2 nanoparticles
AU - Zhou, Xiaoxia
AU - Song, Erhong
AU - Kuang, Zhaoyu
AU - Gao, Zhe
AU - Zhao, Han
AU - Liu, Jianjun
AU - Sun, Shuhui
AU - Mou, Chung Yuan
AU - Chen, Hangrong
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China (51961165107, 21973107), the Shanghai International Cooperation Project (19520761000), the Shanghai Natural Science Foundation (19ZR1464500, 21ZR1472900). CYM thanks the support by a MOST grant (108-2218-E-002-039-MY3).
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2022/2/15
Y1 - 2022/2/15
N2 - Electrochemical reduction of CO2 into fuels offers an attractive approach to environmental and energy sustainability. Herein, we designed atomically dispersed Pt into SnO2 catalyst (Pt atom/SnO2). Such catalyst dramatically improves the adsorption performance of CO2 and lowers the activation energy of CO2. DFT calculations indicate that the doping of Pt in SnO2 could induce charge redistribution and tune active electronic state, showing higher adsorption energy for intermediates CO2*, HCOO* and HCOOH*, which is different from the Pt NPs loaded SnO2 mainly for H2 generation. As a result, a higher Faradaic efficiency (82.1 ± 1.4%) and the production rate (5105 μmol h−1 cm−2) of HCOO– are achieved at −1.2 V vs. RHE. Moreover, the current density and Faradaic efficiency of HCOO– nearly remain unchanged in 8 h on the Pt atom/SnO2, indicating its high stability. This work opens up a new avenue to tune product selectivity by atomically dispersed catalysts.
AB - Electrochemical reduction of CO2 into fuels offers an attractive approach to environmental and energy sustainability. Herein, we designed atomically dispersed Pt into SnO2 catalyst (Pt atom/SnO2). Such catalyst dramatically improves the adsorption performance of CO2 and lowers the activation energy of CO2. DFT calculations indicate that the doping of Pt in SnO2 could induce charge redistribution and tune active electronic state, showing higher adsorption energy for intermediates CO2*, HCOO* and HCOOH*, which is different from the Pt NPs loaded SnO2 mainly for H2 generation. As a result, a higher Faradaic efficiency (82.1 ± 1.4%) and the production rate (5105 μmol h−1 cm−2) of HCOO– are achieved at −1.2 V vs. RHE. Moreover, the current density and Faradaic efficiency of HCOO– nearly remain unchanged in 8 h on the Pt atom/SnO2, indicating its high stability. This work opens up a new avenue to tune product selectivity by atomically dispersed catalysts.
KW - atomically dispersed Pt
KW - CO reduction
KW - DFT
KW - HCOO
KW - SnO
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U2 - 10.1016/j.cej.2021.133035
DO - 10.1016/j.cej.2021.133035
M3 - Article
AN - SCOPUS:85117683717
SN - 1385-8947
VL - 430
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 133035
ER -