Why halides enhance heterogeneous metal ion charge transfer reactions

The reaction kinetics of many metal redox couples on electrode surfaces are enhanced in the presence of halides (i.e., Cl(−), Br(−), I(−)). Using first-principles metadynamics simulations, we show a correlation between calculated desorption barriers of V(3+)–anion complexes bound to graphite via an inner-sphere anion bridge and experimental V(2+)/V(3+) kinetic measurements on edge plane pyrolytic graphite in H(2)SO(4), HCl, and HI. We extend this analysis to V(2+)/V(3+), Cr(2+)/Cr(3+), and Cd(0)/Cd(2+) reactions on a mercury electrode and demonstrate that reported kinetics in acidic electrolytes for these redox couples also correlate with the predicted desorption barriers of metal–anion complexes. Therefore, the desorption barrier of the metal–anion surface intermediate is a descriptor of kinetics for many metal redox couple/electrode combinations in the presence of halides. Knowledge of the metal–anion surface intermediates can guide the design of electrolytes and electrocatalysts with faster kinetics for redox reactions of relevance to energy and environmental applications.