Affiliation:
1. Department of Chemical Sciences and Centre for Advanced Functional Materials Indian Institute of Science Education and Research (IISER) Kolkata, Mohanpur 741246 India
2. Theoretical Sciences Unit School of Advanced Materials Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR) Bangalore 560064 India
Abstract
AbstractThe immiscibility of crystallographic facets in multi‐metallic catalysts plays a key role in driving the green H2 production by water electrolysis. The lattice mismatch between tetragonal In and face‐centered cubic (fcc) Ni is 14.9 % but the mismatch with hexagonal close‐packed (hcp) Ni is 49.8 %. Hence, in a series of Ni−In heterogeneous alloys, In is selectively incorporated in the fcc Ni. The 18–20 nm Ni particles have 36 wt % fcc phase, which increases to 86 % after In incorporation. The charge transfer from In to Ni, stabilizes the Ni0 state and In develops a fractional positive charge that favors *OH adsorption. With only 5 at% In, 153 mL h−1 H2 is evolved at −385 mV with mass activity of 57.5 A g−1 at—400 mV, 200 h stability at −0.18 V versus reversible hydrogen electrode (RHE), and Pt‐like activity at high current densities, due to the spontaneous water dissociation, lower activation energy barrier, optimal adsorption energy of OH− ions and the prevention of catalyst poisoning.