Selective electrochemical reduction of carbon dioxide to formic acid using indium-zinc bimetallic nanocrystals

For the electrochemical reduction of CO 2 (CRR) with high selectivity for HCOOH, In-Zn bimetallic nanocrystals (NCs) were synthesized as catalysts by in situ reduction of In 2 O 3 -ZnO NCs with various compositions. All In-containing bimetallic catalysts exhibited excellent selectivity to produce HC...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019, Vol.7 (4), p.22879-22883
Hauptverfasser: Kwon, Ik Seon, Debela, Tekalign Terfa, Kwak, In Hye, Seo, Hee Won, Park, Kidong, Kim, Doyeon, Yoo, Seung Jo, Kim, Jin-Gyu, Park, Jeunghee, Kang, Hong Seok
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:For the electrochemical reduction of CO 2 (CRR) with high selectivity for HCOOH, In-Zn bimetallic nanocrystals (NCs) were synthesized as catalysts by in situ reduction of In 2 O 3 -ZnO NCs with various compositions. All In-containing bimetallic catalysts exhibited excellent selectivity to produce HCOOH, while Zn NCs favor CO production. A composition with In : Zn = 0.05 has higher catalytic activity than In NCs, with a faradaic efficiency of 95% and a HCOOH production rate of 0.40 mmol h −1 cm −2 at −1.2 V vs. RHE. The enhanced catalytic performance is in part ascribed to the fewer surface oxide layers, which increase the conductivity and facilitate the charge transfer. Density functional theory calculations revealed that the In-Zn interfacial sites make the HCOOH pathway significantly energy-favorable, which supports the higher production rate of Zn 0.95 In 0.05 than that of In. Zn-In bimetallic nanocrystals exhibit excellent selectivity for electrochemical CO 2 reduction to HCOOH, whose efficiency is greatly enhanced with 5% In composition.
ISSN:2050-7488
2050-7496
DOI:10.1039/c9ta06285h