Synthesizing transition metal catalysts to replace precious metal ones such as IrO 2 and RuO 2, achieving efficient acidic oxygen evolution reaction while balancing intrinsic activity, stability, and cost-effectiveness always been a dream pursued by scientists and industrialists, but still remains a challenge. Here, we present an efficient catalytic system formed by graphdiyne-induced high-spin state cobalt-based oxide (HSS-CoO x /GDY) for enhancing the activity and stability of the acidic oxygen evolution reaction. Experimental and theoretical results demonstrate that the bonding of electron-rich sp -hybridized carbon and Co atoms initiates the Jahn-Teller effect of CoO 6 octahedra, which regulates the occupied d -orbital of Co atoms and generates the high-spin Co 3+ . Such spin occupancy breaks the spin-forbidden effect and optimizes the adsorption/desorption ability of HSS-CoO x /GDY toward key reaction intermediates, thereby promoting the coupling of O-O bonds and the evolution of oxygen gas. The proton exchange membrane water electrolyzers constructed based on this catalyst achieve a current density of 1.0 A cm −2 at a low cell voltage of 1.80 V. This research indicates that graphdiyne has the ability to manipulate the electronic spin states of electrocatalysts.
Ping et al. (Wed,) studied this question.
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