Indium Arsenide Quantum Dot Derived Catalyst for Selective CO2 Electrochemical Reduction to Formate
Source abstract
Abstract
Despite a currently limited market size, formate is finding innovative applications as a hydrogen carrier and carbon source for upgrading processes to hydrocarbons and oxygenates. In this study, we combine the unique key features of In-based electrodes in the electrocatalytic CO 2 reduction reaction (e.g., limited hydrogen evolution reaction activity, near-to-unity carbon selectivity toward formate) with the remarkable results obtained using nanostructured and highly defective quantum dot derived catalysts. After developing a scalable, safe and cheap InAs quantum dots synthesis based on a mild and nonpyrophoric reducing agent (i.e., NaCNBH 3 ), a thorough voltammetric study allowed us to retrieve kinetic and thermodynamic data on their transformation into the actual catalytically active species (i.e., In 0 ). In a flow electrolyzer operating under alkaline conditions at industrially relevant current densities, the catalyst achieved near-to-unity faradaic efficiency toward formate, with a remarkable production rate of ca . 1276 g Formate h –1 m –2 at ca . −0.73 V vs RHE (η Formate = 0.61 V).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Advanced Thermoelectric Materials and Devices · Ionic liquids properties and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Istituto Italiano di Tecnologia (IIT), Via Morego 30, Genova, 16163, Italy
Università degli Studi di Genova (UniGe), Via Dodecaneso 31, Genova, 16146, Italy
Quantum Solutions, 1 Venture Road, Southampton, SO16 7NP, United Kingdom
Dipartimento di Scienza Applicata e Tecnologie (DISAT), Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, Italy
Funding
Agenzia Nazionale per le Nuove Tecnologie, l'Energia e lo Sviluppo Economico Sostenibile · H2020 European Research Council
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