Developing efficient chemical modification technologies for upgrading classic non-noble metal based electrocatalysts to further meet the demands of practical water electrolysis industry is of vital challenge. Here, we propose an… Click to show full abstract
Developing efficient chemical modification technologies for upgrading classic non-noble metal based electrocatalysts to further meet the demands of practical water electrolysis industry is of vital challenge. Here, we propose an organic-inorganic dual-modulation strategy to construct a cobalt hydroxide-based electrocatalyst, MEC-17, synthesized by an eco-friendly and facile microbial-mediated vulcanization method. This electrocatalyst, modified with both 2-methylimidazole and inorganic sulfur exhibits notable oxygen evolution reaction performance, achieving an overpotential of 285.6 ± 1.7 mV and exceeding 300 h of durability at a high current density of 1000 mA cm−2. The operando characterizations and theoretical calculations reveal that sulfur dopant primarily shortens the Co−Co distances to support oxide path mechanism, while 2-methylimidazole plays a more critical role by modulating the d-band center of the Co sites, which optimizes intermediate adsorption for ensuring efficient O−O coupling. This work offers insights into the design of organic-inorganic hybrid electrocatalysts and contributes to understanding the origin of their electrocatalytic activities. Developing efficient non-precious catalysts is key to advancing water electrolysis. Here, the authors report a microbial vulcanization strategy that co-dopes cobalt hydroxide with sulfur and organic molecules to optimize O–O coupling and accelerate the electrocatalytic oxygen evolution reaction.
               
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