Proton-donating and chemistry-dependent buffering capability of amino acids for the hydrogen evolution reaction

John Brown; Alexis Grimaud

doi:10.1039/d3cp00552f

Proton-donating and chemistry-dependent buffering capability of amino acids for the hydrogen evolution reaction

Phys Chem Chem Phys. 2023 Mar 15;25(11):8005-8012. doi: 10.1039/d3cp00552f.

Authors

John Brown^{1

2}, Alexis Grimaud^{1

2

3}

Affiliations

¹ Chimie du Solide et de l'Energie (CSE), Collège de France, UMR 8260, 75231, Paris Cedex 05, France.
² Réseau sur le Stockage Electrochimique de l'Energie (RS2E), CNRS FR 3459, 80039, Amiens Cedex 1, France.
³ Department of Chemistry, Boston College, Chestnut Hill, Massachusetts, 02467, USA. grimauda@bc.edu.

PMID: 36876498
DOI: 10.1039/d3cp00552f

Abstract

The hydrogen evolution reaction (HER) has been widely demonstrated to have a strong dependence on pH and on the source of protons, where a clear kinetic advantage arises in acidic conditions over near-neutral and alkaline conditions due to the switch in reactant from H₃O⁺ to H₂O. Playing on the acid/base chemistry of aqueous systems can avoid the kinetic frailties. For example, buffer systems can be used to maintain proton concentration at intermediate pH, driving H₃O⁺ reduction over H₂O. In light of this, we examine the influence of amino acids on HER kinetics at platinum surfaces using rotating disk electrodes. We demonstrate that aspartic acid (Asp) and glutamic acid (Glu) can act not only as proton donors, but also have sufficient buffering action to sustain H₃O⁺ reduction even at large current density. Comparing with histidine (His) and serine (Ser), we reveal that the buffering capacity of amino acids occurs due to the proximity of their isoelectric point (pI) and their buffering pK_a. This study further exemplifies HER's dependence on pH and pK_a and that amino acids can be used to probe this relationship.