Stabilized High‐Valent Indium for Promoted Formate Production from Electrochemical CO 2 Reduction

Electrocatalysts based on high‐valent indium are promising for formate production via CO 2 electroreduction. However, reconstruction often occurs during the reaction progress, resulting in a decline in catalytic performance. Here, a composite of In 2 O 3 /In 2 S 3 is developed, and its catalytic per...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Advanced functional materials 2024-12, Vol.34 (49)
Hauptverfasser: Ma, Tengfei, Wang, Feng, Jing, Wenhao, Qiu, Haoran, Liu, Ya, Guo, Liejin
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Electrocatalysts based on high‐valent indium are promising for formate production via CO 2 electroreduction. However, reconstruction often occurs during the reaction progress, resulting in a decline in catalytic performance. Here, a composite of In 2 O 3 /In 2 S 3 is developed, and its catalytic performance exceeds that of either individual phase, particularly in stability. Analysis of morphology, valence state, and in situ Raman spectroscopy reveals that In 2 O 3 is well preserved during the reaction. Theoretical calculations suggest that the desorption energy of lattice oxygen on In 2 O 3 can be strengthened due to In 2 O 3 ‐In 2 S 3 bonding within the composite. This reinforcement facilitates the formation of more active sites and promotes CO 2 adsorption, further decreasing the energy barrier of formate production to only 0.12 eV. As a result, the composite exhibits a formate selectivity over 95.05% at –1.13 V vs reversible hydrogen electrode accompanied by a partial current density of 434.4 mA cm –2 . Notably, the selectivity of formate maintains over 95% even after 50 h at an industrial‐level current density of 200 mA cm –2 , 17 times longer than the individual phase. Furthermore, 18.33% solar‐to‐formate and 19.49% solar‐to‐fuel are obtained when coupled with III‐V solar cells, demonstrating its feasibility.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202408977