Synthesis of Cu2O@Cu-Fe-K Prussian Blue analogue core–shell nanocube for enhanced electroreduction of CO2 to multi-carbon products

[Display omitted] •Cu2O@Cu-Fe-K PBA was prepared by a template-engaged redox deposition approach.•Cu2O@Cu-Fe-K PBA serves as an efficient CO2ER catalyst to promote the C2+ products.•Fe and K elements can modulate the interface engineering of Cu2O surface. Cu2O@Cu-Fe-K Prussian Blue analogue (K-PBA)...

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Veröffentlicht in:Materials letters 2020-02, Vol.260, p.126868, Article 126868
Hauptverfasser: Cheng, Yuan-Sheng, Li, Hong, Ling, Min, Li, Na, Jiang, Binbin, Wu, Fang-Hui, Yuan, Guozan, Wei, Xian-Wen
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container_start_page 126868
container_title Materials letters
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creator Cheng, Yuan-Sheng
Li, Hong
Ling, Min
Li, Na
Jiang, Binbin
Wu, Fang-Hui
Yuan, Guozan
Wei, Xian-Wen
description [Display omitted] •Cu2O@Cu-Fe-K PBA was prepared by a template-engaged redox deposition approach.•Cu2O@Cu-Fe-K PBA serves as an efficient CO2ER catalyst to promote the C2+ products.•Fe and K elements can modulate the interface engineering of Cu2O surface. Cu2O@Cu-Fe-K Prussian Blue analogue (K-PBA) core–shell nanocube was synthesized by a facile template-engaged redox deposition approach, and could be used as an efficient catalyst for CO2 electrochemical reduction (CO2ER). The presence of K-PBA shell not only can protect the Cu2O active core, but also promote the ratios of multi-carbon products to competing methane in CO2ER, achieving a total C2+ Faradaic efficiency (FE) of 23.9% (ethylene 10.8%, ethanol 3.6% and n-propanol 9.5%) at −1.11 V (vs. reversible hydrogen electrode (RHE), while jtotal = 6.2 mA cm−2. It is suggested that K-PBA shell coating alter inherent adsorption energetics of Cu2O, which contributes to the C–C coupling step in CO2ER.
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Cu2O@Cu-Fe-K Prussian Blue analogue (K-PBA) core–shell nanocube was synthesized by a facile template-engaged redox deposition approach, and could be used as an efficient catalyst for CO2 electrochemical reduction (CO2ER). The presence of K-PBA shell not only can protect the Cu2O active core, but also promote the ratios of multi-carbon products to competing methane in CO2ER, achieving a total C2+ Faradaic efficiency (FE) of 23.9% (ethylene 10.8%, ethanol 3.6% and n-propanol 9.5%) at −1.11 V (vs. reversible hydrogen electrode (RHE), while jtotal = 6.2 mA cm−2. 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Cu2O@Cu-Fe-K Prussian Blue analogue (K-PBA) core–shell nanocube was synthesized by a facile template-engaged redox deposition approach, and could be used as an efficient catalyst for CO2 electrochemical reduction (CO2ER). The presence of K-PBA shell not only can protect the Cu2O active core, but also promote the ratios of multi-carbon products to competing methane in CO2ER, achieving a total C2+ Faradaic efficiency (FE) of 23.9% (ethylene 10.8%, ethanol 3.6% and n-propanol 9.5%) at −1.11 V (vs. reversible hydrogen electrode (RHE), while jtotal = 6.2 mA cm−2. 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Cu2O@Cu-Fe-K Prussian Blue analogue (K-PBA) core–shell nanocube was synthesized by a facile template-engaged redox deposition approach, and could be used as an efficient catalyst for CO2 electrochemical reduction (CO2ER). The presence of K-PBA shell not only can protect the Cu2O active core, but also promote the ratios of multi-carbon products to competing methane in CO2ER, achieving a total C2+ Faradaic efficiency (FE) of 23.9% (ethylene 10.8%, ethanol 3.6% and n-propanol 9.5%) at −1.11 V (vs. reversible hydrogen electrode (RHE), while jtotal = 6.2 mA cm−2. It is suggested that K-PBA shell coating alter inherent adsorption energetics of Cu2O, which contributes to the C–C coupling step in CO2ER.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.matlet.2019.126868</doi><orcidid>https://orcid.org/0000-0003-0707-8882</orcidid></addata></record>
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subjects Carbon dioxide
Catalyst
Chemical reduction
Composite materials
Copper oxides
Electrochemical reduction
Ethanol
Materials science
Pigments
Protective coatings
Structural
title Synthesis of Cu2O@Cu-Fe-K Prussian Blue analogue core–shell nanocube for enhanced electroreduction of CO2 to multi-carbon products
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