TY  - JOUR
AU  - Geer, Ana M.
AU  - Musgrave III, Charles
AU  - Webber, Christopher
AU  - Nielsen, Robert J.
AU  - McKeown, Bradley A.
AU  - Liu, Chang
AU  - Schleker, P. Philipp M.
AU  - Jakes, Peter
AU  - Jia, Xiaofan
AU  - Dickie, Diane A.
AU  - Granwehr, Josef
AU  - Zhang, Sen
AU  - Machan, Charles W.
AU  - Goddard, William A.
AU  - Gunnoe, T. Brent
TI  - Electrocatalytic Water Oxidation by a Trinuclear Copper(II) Complex
JO  - ACS catalysis
VL  - 11
IS  - 12
SN  - 2155-5435
CY  - Washington, DC
PB  - ACS
M1  - FZJ-2021-05736
SP  - 7223 - 7240
PY  - 2021
AB  - We report a trinuclear copper(II) complex, [(DAM)Cu3(μ3-O)][Cl]4 (1, DAM = dodecaaza macrotetracycle), as a homogeneous electrocatalyst for water oxidation to dioxygen in phosphate-buffered solutions at pH 7.0, 8.1, and 11.5. Electrocatalytic water oxidation at pH 7 occurs at an overpotential of 550 mV with a turnover frequency of ∼19 s–1 at 1.5 V vs NHE. Controlled potential electrolysis (CPE) experiments at pH 11.5 over 3 h at 1.2 V and at pH 8.1 for 40 min at 1.37 V vs NHE confirm the evolution of dioxygen with Faradaic efficiencies of 81% and 45%, respectively. Rinse tests conducted after CPE studies provide evidence for the homogeneous nature of the catalysis. The linear dependence of the current density on the catalyst concentration indicates a likely first-order dependence on the Cu precatalyst 1, while kinetic isotope studies (H2O versus D2O) point to involvement of a proton in or preceding the rate-determining step. Rotating ring-disk electrode measurements at pH 8.1 and 11.2 show no evidence of H2O2 formation and support selectivity to form dioxygen. Freeze-quench electron paramagnetic resonance studies during electrolysis provide evidence for the formation of a molecular copper intermediate. Experimental and computational studies support a key role of the phosphate as an acceptor base. Moreover, density functional theory calculations highlight the importance of second-sphere interactions and the role of the nitrogen-based ligands to facilitate proton transfer processes.
LB  - PUB:(DE-HGF)16
UR  - <Go to ISI:>//WOS:000664333800044
DO  - DOI:10.1021/acscatal.1c01395
UR  - https://juser.fz-juelich.de/record/904166
ER  -