Heterogenous HER activity of Ni(II)N2S2 molecular catalysts

Abstract

Green hydrogen, generated through the electrolysis of water using renewable energy sources, is recognized as a highly promising alternative to fossil fuels in the pursuit of net-zero carbon emissions. Electrocatalysts are crucial for reducing overpotentials and enhancing the efficiency of the hydrogen evolution reaction (HER) for the production of green hydrogen. Homogeneous HER serves as a primary method to assess the activity and mechanisms of novel non-precious molecular electrocatalysts in pursuit of replacing precious platinum standards. However, these catalysts can sometimes exhibit instability under reductive and acidic conditions during homogeneous HER. Thus, it is also essential to evaluate catalysts through heterogeneous HER for initial assessment and practical application. In this study, we examine a series of structurally related N₂S₂ chelated Ni(II) complexes, which are tailored to optimize the basicity of the catalyst for heterogeneous HER activity. These complexes are insoluble in 0.5 M H₂SO₄, and the films formed after catalyst deposition on glassy carbon electrodes (GCEs) exhibit catalytic currents during HER, demonstrating moderate to good overpotentials, Tafel slopes, and charge transfer resistance. Furthermore, we observe the anticipated structure–activity relationship that arises from tuning the catalyst structure. The complexes maintain stability over extended reductive cycling, as confirmed by various surface characterization techniques, including SEM, EDX, XPS, and XRD. This study highlights the potential of utilizing catalyst basicity to develop efficient and robust heterogeneous HER catalysts.