Manganese(I) Diamine Electrocatalysts: Electrochemical Carbon Dioxide Reduction to Carbon Monoxide

Author:

Dhakal Badrinath1ORCID,Corbin Brooke A.1,Sosa Parada Alberto2,Sakai Jonathan G.2,Felton Emily A.3,McDonald Lauren T.2,Gross Anthony J.2ORCID,Nichol Gary S.4ORCID,Felton Greg A. N.2ORCID

Affiliation:

1. Department of Chemistry, Oakland University, Rochester, MI 48309, USA

2. Department of Chemistry, Eckerd College, St. Petersburg, FL 33711, USA

3. Department of Biology, University of Tampa, Tampa, FL 33606, USA

4. School of Chemistry, University of Edinburgh, Edinburgh EH9 3FJ, UK

Abstract

Novel organometallic complexes Mn(benzene-1,2-diamine)(CO)3Br, Mn-1, Mn(3-methylbenzene-1,2-diamine)(CO)3Br, Mn-2, and Re(benzene-1,2-diamine)(CO)3Cl, Re-1, have been synthesized and characterized by IR, UV/Vis, 1H-NMR, EA and HRMS. The structures of Mn-2 and Re-1 were confirmed by X-ray crystallography. The three novel compounds were studied for their electrocatalytic reduction of carbon dioxide to carbon monoxide using cyclic voltammetry in acetonitrile solutions. Controlled potential electrolysis was used to obtain information on faradaic yield, with product formation being confirmed by GC. Using earth-abundant manganese, compounds Mn-1 and Mn-2 display turnover frequencies of 108 s−1 and 82 s−1, respectively, amid selective production of carbon monoxide (faradaic yields ~85%), with minimal co-production of dihydrogen (<2%), and low overpotential of 0.18 V. The rhenium congener, Re-1, displays no activity as an electrocatalyst for carbon dioxide reduction under identical conditions.

Funder

Florida Space Grant Consortium

Publisher

MDPI AG

Subject

Inorganic Chemistry

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