Chelating adsorption-engaged synthesis of ultrafine iridium nanoparticles anchored on N-doped carbon nanofibers toward highly efficient hydrogen evolution in both alkaline and acidic media.

Developing highly efficient and stable precious metal electrocatalysts toward hydrogen evolution reaction (HER) is crucial for energy application, while it is still challenging to achieve highly dispersed ultrafine metal nanoparticles on some promising supports to synergistically promote their electrocatalytic performance. Herein, we propose a feasible chelating adsorption-engaged strategy by introducing de-doped polyaniline with abundant amino groups to immobilize ultrafine iridium (Ir) nanoparticles on their derived N-doped carbon nanofibers (Ir-NCNFs). Experimental results demonstrate that the synthesized Ir-NCNFs can effectively promote the charge transfer and expose more electrochemical active sites, which eventually accelerate the reaction kinetics. Thus, the synthesized Ir-NCNFs catalyst exhibits admirable HER activities in both alkaline and acidic conditions with overpotentials of only 23 and 8 mV, which are even superior or close to the benchmark Pt/C catalyst. Furthermore, the synthesized Ir-NCNFs catalyst also exhibits a long-term durability. This study affords a reliable means to construct high-performance supported ultrafine metal nanocatalysts for electrocatalytic applications to alleviate the growing demand for energy conversion.