, Volume 7, Issue 1, pp 87–96

Evaluating Activity for Hydrogen-Evolving Cobalt and Nickel Complexes at Elevated Pressures of Hydrogen and Carbon Monoxide

Original Research

DOI: 10.1007/s12678-015-0281-y

Cite this article as:
McCrory, C.C.L., Szymczak, N.K. & Peters, J.C. Electrocatalysis (2016) 7: 87. doi:10.1007/s12678-015-0281-y


Molecular cobalt and nickel complexes are among the most promising homogeneous systems for electrocatalytic hydrogen evolution. However, there has been little exploration into the effect of gaseous co-additives such as CO and H2, which may be present in operating hydrogen-evolving or carbon-dioxide reduction systems, on the performance of these molecular electrocatalysts. In this report, we investigate the electrocatalytic activity of six cobalt and nickel complexes supported by tetraazamacrocyclic or diazadiphosphacyclooctane ligands for the reduction of p-toluenesulfonic acid to hydrogen in acetonitrile under inert atmosphere and in the presence of CO and H2. We present an elevated-pressure electrochemical apparatus capable of reaching CO and H2 pressures of ca. 15–520 pounds per square inch (psia) (∼1–35 atm), and we use this apparatus to determine binding constants for CO addition for each catalyst and study the inhibition of the electrocatalysis as a function of CO and H2 pressure. In the case of CO, the extent of catalytic inhibition is correlated to the binding constant, with the cobalt complexes showing a greater degree of catalyst inhibition compared to the nickel complexes. In the case of H2, no complex showed appreciable electrocatalytic inhibition even at H2 pressures of ca. 500 psia.


Electrocatalysis Hydrogen evolution Water splitting Solar fuels 

Supplementary material

12678_2015_281_MOESM1_ESM.pdf (260 kb)
ESM 1(PDF 260 kb)

Copyright information

© Springer Science+Business Media New York 2015

Authors and Affiliations

  1. 1.Division of Chemistry and Chemical EngineeringCalifornia Institute of TechnologyPasadenaUSA

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