Buffer p K a Impacts the Mechanism of Hydrogen Evolution Catalyzed by a Cobalt Porphyrin-Peptide

• Published in: Inorganic chemistry 2020-05, Vol.59 (12), p.8061-8069
• Main Authors: Alvarez-Hernandez, Jose L, Sopchak, Andrew E, Bren, Kara L
• Format: Article
• Language: English
• Subjects: Chemistry
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.0c00362

The effect of buffer p on the mechanism of electrochemical hydrogen evolution catalyzed by a cobalt porphyrin peptide (CoMP11-Ac) at constant pH is presented. The addition of buffer to CoMP11-Ac in water and KCl leads to an enhancement of the catalytic current of up to 200-fold relative to its value in the absence of a buffer. Two distinct catalytic regimes are identified as a function of the buffer p . In the presence of buffers with p ≤ 7.4, a fast catalysis regime limited by diffusion of buffer is reached. The catalytic half-wave potential ( ) shifts anodically (from -1.42 to -1.26 V vs Ag/AgCl/KCl ) as the buffer p decreases from 7.4 to 5.6, proposed to result from fast Co(III)-H formation following the catalysis-initiating Co(II/I) reduction. With higher-p buffers (p > 7.7), an = -1.42 V, proposed to reflect the Co(II/I) couple, is maintained independent of the buffer p , consistent with rate-limiting Co(III)-H formation under these conditions. We conclude that the buffer species p impacts catalytic current and potential and the rate-determining step of the reaction.