Single-Atomic Co–N₄ Sites with CrCo Nanoparticles for Metal–Air Battery-Driven Hydrogen Evolution

Abstract

Designing highly active and robust earth abundant trifunctional electrocatalysts for energy storage and conversion applications remain an enormous challenge. Herein, we report a trifunctional electrocatalyst (CrCo/CoN 4 @CNT-5), synthesized at low calcination temperature (550 °C), which consists of Co−N 4 single atom and CrCo alloy nanoparticles and exhibits outstanding electrocatalytic performance for the hydrogen evolution reaction, oxygen evolution reaction, and oxygen reduction reaction. The catalyst is able to deliver a current density of 10 mA cm −2 in an alkaline electrolytic cell at a very low cell voltage of ∼1.60 V. When the catalyst is equipped in a liquid rechargeable Zn−air battery, it endowed a high open-circuit voltage with excellent cycling durability and outperformed the commercial Pt/C+IrO 2 catalytic system. Furthermore, the Zn−air battery powered self-driven water splitting system is displayed using CrCo/CoN 4 @CNT-5 as sole trifunctional catalyst, delivering a high H 2 evolution rate of 168 μmol h −1 . Theoretical calculations reveal synergistic interaction between Co−N 4 active sites and CrCo nanoparticles, favoring the Gibbs free energy for H 2 evolution. The presence of Cr not only enhances the H 2 O adsorption and dissociation but also tunes the electronic property of CrCo nanoparticles to provide optimized hydrogen binding capacity to Co−N 4 sites, thus giving rise to accelerated H 2 evolution kinetics. This work highlights the importance of the presence of small quantity of Cr in enhancing the electrocatalytic activity as well as robustness of single-atom catalyst and suggests the design of the multifunctional robust electrocatalysts for long-term H 2 evolution application.