Rationally designed Ru catalysts supported on TiN for highly efficient and stable hydrogen evolution in alkaline conditions
Jia Zhao, Ricardo Urrego‐Ortiz, Nan Liao, Federico Calle‐Vallejo, Jingshan Luo
Abstract
Electrocatalysis holds the key to enhancing the efficiency and cost-effectiveness of water splitting devices, thereby contributing to the advancement of hydrogen as a clean, sustainable energy carrier. This study focuses on the rational design of Ru nanoparticle catalysts supported on TiN (Ru NPs/TiN) for the hydrogen evolution reaction in alkaline conditions. The as designed catalysts exhibit a high mass activity of 20 A mg−1Ru at an overpotential of 63 mV and long-term stability, surpassing the present benchmarks for commercial electrolyzers. Structural analysis highlights the effective modification of the Ru nanoparticle properties by the TiN substrate, while density functional theory calculations indicate strong adhesion of Ru particles to TiN substrates and advantageous modulation of hydrogen adsorption energies via particle-support interactions. Finally, we assemble an anion exchange membrane electrolyzer using the Ru NPs/TiN as the hydrogen evolution reaction catalyst, which operates at 5 A cm−2 for more than 1000 h with negligible degradation, exceeding the performance requirements for commercial electrolyzers. Our findings contribute to the design of efficient catalysts for water splitting by exploiting particle-support interactions. Designing efficient and stable electrocatalysts for water splitting is of great interest for H2 fuel production. Here, the authors present a Ru nanoparticle catalyst on TiN, achieving 20 A mg−1 Ru at 63 mV in alkaline conditions, and operating at 5 A cm−2 for over 1000 hours in an anion exchange membrane electrolyzer.