Adenosine triphosphate induced transition-metal phosphide nanostructures encapsulated with N, P-codoped carbon toward electrochemical water splitting

Transition metal phosphides (TMPs) have emerged as the most potential non-precious metal catalysts thanks to their high abundance, low cost and superior catalytic activity. Although numerous efforts have been devoted to gain TMPs, most of the synthetic processes are dangerous and complex as the utilization of flammable and toxic phosphorus sources. By using a novel green phosphorus source-adenosine triphosphate (ATP), we synthesized various N, P doped carbon-sealed TMPs nanostructures (TMPs@NPC) via a facile and simple solid-phase method. Benefiting from the porous nanostructure and in situ derived heteroatom-doped carbon encapsulation, as-synthesized TMPs@NPC exhibit good bifunctional catalytic performance. Notably, the Co 2 P@NPC demonstrates the superior activity and durability toward HER and OER. The Co 2 P@NPC, meanwhile, displays robust overall water electrolysis performance. Therefore, our work presents a simple, ecofriendly, and general strategy for the synthesis of TMPs encapsulated with N, P-codoped carbon nanostructures, which are also expected to show a bright future in other electrochemical applications.