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Selective electrochemical reduction of CO(2) on compositionally variant bimetallic Cu–Zn electrocatalysts derived from scrap brass alloys

The electrocatalytic reduction of carbon dioxide (CO(2)RR) into value-added fuels is a promising initiative to overcome the adverse effects of CO(2) on climate change. Most electrocatalysts studied, however, overlook the harmful mining practices used to extract these catalysts in pursuit of achievin...

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Detalles Bibliográficos
Autores principales: Badawy, Ibrahim M., Ismail, Ahmed Mohsen, Khedr, Ghada E., Taha, Manar M., Allam, Nageh K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9355942/
https://www.ncbi.nlm.nih.gov/pubmed/35931804
http://dx.doi.org/10.1038/s41598-022-17317-6
Descripción
Sumario:The electrocatalytic reduction of carbon dioxide (CO(2)RR) into value-added fuels is a promising initiative to overcome the adverse effects of CO(2) on climate change. Most electrocatalysts studied, however, overlook the harmful mining practices used to extract these catalysts in pursuit of achieving high-performance. Repurposing scrap metals to use as alternative electrocatalysts would thus hold high privilege even at the compromise of high performance. In this work, we demonstrated the repurposing of scrap brass alloys with different Zn content for the conversion of CO(2) into carbon monoxide and formate. The scrap alloys were activated towards CO(2)RR via simple annealing in air and made more selective towards CO production through galvanic replacement with Ag. Upon galvanic replacement with Ag, the scrap brass-based electrocatalysts showed enhanced current density for CO production with better selectivity towards the formation of CO. The density functional theory (DFT) calculations were used to elucidate the potential mechanism and selectivity of the scrap brass catalysts towards CO(2)RR. The d-band center in the different brass samples with different Zn content was elucidated.