Dissolution Manufacturing Strategy for the Facile Synthesis of Nanoporous Metallic Glass Multifunctional Catalyst

Abstract

AbstractThe quest for heightened energy efficiency is inextricably linked to advancements in energy storage and conversion technologies, wherein multifunctional catalysts play a pivotal role by mitigating the slow kinetics endemic to many catalytic reactions. The intricate synthesis and bespoke design of such catalysts, however, present notable challenges. Addressing this, the present study capitalizes on a novel dissolution manufacturing strategy to engineer self‐supporting, nanoporous multifunctional electrocatalysts, circumventing the prevalent issue of customizing catalytic functionalities upon demand. This innovative approach grants the flexibility to finely tune the incorporation of active species and metalloid binders, culminating in the creation of a self‐supporting nanoporous metal glass electrocatalyst doped with RuO2 (NPMG@RuO2) with outstanding performance in alkaline media. The catalyst showcases superior electrocatalytic activity, achieving low overpotentials of 41.50 mV for the Hydrogen Evolution Reaction and 226.0 mV for Oxygen Evolution Reaction alongside sustained stability over 620 hours.These achievements are attributed to the distinct nanoporous architecture that ensures a high density of catalytic sites and mechanical strength, bolstered by the synergistic interplay between RuO2 and Pt‐based metallic glass. The findings provide a versatile template for the development of nanoporous multifunctional catalysts, signifying a leap forward in the realm of energy conversion technologies.