RSC Adv. 2023 Apr 18;13(18):12065-12071. doi: 10.1039/d3ra01186k. eCollection 2023 Apr 17.
The use of metal-organic compounds as electrocatalysts for water splitting reactions has gained increased attention; however, a fundamental understanding of the structural requirement for effective catalytic activity is still limited. Herein, we synthesized water-coordinated mono and bimetallic copper complexes (CuPz-H2O·H2O, CuPz-H2O, CuBipy-H2O·H2O, and CuMorph-H2O) with varied intermetallic spacing (pyrazine/4,4′-bipyridine) and explored the structure-dependent oxygen evolution reaction (OER) activity in alkaline medium. Single crystal structural studies revealed water-coordinated monometallic complexes (CuMorph-H2O) and bimetallic complexes (CuPz-H2O·H2O, CuPz-H2O, CuBipy-H2O·H2O). Further, CuPz-H2O·H2O and CuBipy-H2O·H2O contained lattice water along with coordinated water. Interestingly, the bimetallic copper complex with lattice water and shorter interspacing between the metal centres (CuPz-H2O·H2O) showed strong OER activity and required an overpotential of 228 mV to produce a benchmark current density of 10 mA cm-2. Bimetallic copper complex (CuPz-H2O) without lattice water but the same intermetallic spacing and bimetallic complex with increased interspacing but with lattice water (CuBipy-H2O·H2O) exhibited relatively lower OER activity. CuPz-H2O and CuBipy-H2O·H2O required an overpotential of 236 and 256 mA cm-2, respectively. Monometallic CuMorph-H2O showed the lowest OER activity (overpotential 271 mV) compared to bimetallic complexes. The low Tafel slope and charge transfer resistance of CuPz-H2O·H2O facilitated faster charge transfer kinetics at the electrode surface and supported the enhanced OER activity. The chronoamperometric studies indicated good stability of the catalyst. Overall, the present structure-electrocatalytic activity studies of copper complexes might provide structural insight for designing new efficient electrocatalysts based on metal coordination compounds.
PMID:37082374 | PMC:PMC10111156 | DOI:10.1039/d3ra01186k