Decrypting the hydrogen evolution in alkaline water with novel magnetoactive cobalt(II) complex-driven cobalt oxide electrocatalysts

Under the gravity of future socio-economic development, the viability of water electrolysis still hinges on the accessibility of stable earth-abundant electrocatalysts and net energy efficiency. This work emphasizes the design and synthesis of two newly developed cobalt(II) complexes, [Co(HL) (NCS) ] (Comono) and [Co (L) (CH OH)]ClO (Codi), with a (N,O)-donor ligand, HL (2-methoxy-6-(((2-methoxyphenyl)imino)methyl)phenol). The study delves into understanding their structural, morphological, magnetic, and charge transport characteristics. Moreover, the study explores the potential of these complexes in catalyzing hydrogen production through heterogeneous electrocatalysis. The X-ray crystal structure of Comono reveals the octahedral geometry of the Co(II) ion, adopting two HL units and two NCS units. The Codi complex exhibits a doubly-phenoxo-O-bridged (μ ) dinuclear complex, forming a typical octahedral geometry for both the Co(II) centres in coupling with three units of L-. Temperature-dependent magnetic susceptibility measurements showed that all of the Co(II) ion in Comono shows a typical paramagnetic behaviour for high spin octahedral Co(II) ions while the Co(II) centres in Codi are coupled with doubly-phenoxo-bridges bearing weak ferromagnetic characteristics at low temperature. Electron transport properties of the Co(II) complex-mediated Schottky device address the superior carrier mobility ( ) for Codi (9.21 × 10 ) over Comono (2.02 × 10 m v s ) with respective transit times of 1.70 × 10 and 7.77 × 10 s. Additionally, electron impedance spectral analysis supports the lower electrical transport resistance of Codi relative to Comono. The heterogeneous electrocatalytic HER activity of Codi and Comono in 0.1 M KOH shows excellent electrocatalytic efficiency in terms of the various electrochemical parameters. Constant potential electrolysis, multi-cycle CVs, and post-HER analysis reveal the pre-catalytic nature of the complexes, which in turn delivers Co O nanoparticles as the active catalysts for efficient hydrogen evolution.