Photoelectrocatalytic Reduction of CO2 to Paraffin Using p-n Heterojunctions
Nowadays, photoelectrocatalytic (PEC) reduction of CO2 represents a very promising solution for storing solar energy in value-added chemicals, but so far it has been hampered by the lack of highly efficient catalyst of photocathode. Enlightened by the Calvin cycle of plants, here we show that a seri...
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Published in | iScience Vol. 23; no. 1; p. 100768 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
24.01.2020
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Nowadays, photoelectrocatalytic (PEC) reduction of CO2 represents a very promising solution for storing solar energy in value-added chemicals, but so far it has been hampered by the lack of highly efficient catalyst of photocathode. Enlightened by the Calvin cycle of plants, here we show that a series of three-dimensional C/N-doped heterojunctions of Znx:Coy@Cu are successfully fabricated and applied as photocathodes in the PEC reduction of CO2 to generate paraffin product. These materials integrate semiconductors of p-type Co3O4 and n-type ZnO on Cu foam to construct fine heterojunctions with multiple active sites, which result in excellent C-C coupling control in reduction of CO2. The best catalyst of Zn0.2:Co1@Cu yields paraffin at a rate of 325 μg·h−1 under −0.4 V versus saturated calomel electrode without H2 release. The apparent quantum efficiency of PEC cell is up to 1.95%.
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•Heterojunctions of Znx:Coy@Cu are applied in photoelectrocatalytic reduction of CO2•Multiple active sites result in excellent C-C coupling like natural photosynthesis•Photoelectrocatalytic system can tolerate the higher voltage without H2 emission•Paraffin product is reported for the first time in CO2 reduction
Catalysis; Electrochemical Materials Science; Materials Design |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Lead Contact |
ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2019.100768 |