Metallic Ru-Ru Interaction in Ruthenium Oxide Enabling Durable Proton Exchange Membrane Water Electrolysis.
Guoqiang ZhaoWei GuoMinmin ShanYanyan FangGongming WangMingxia GaoYongfeng LiuHongge PanWenping SunPublished in: Advanced materials (Deerfield Beach, Fla.) (2024)
Developing efficient and robust electrocatalysts toward the oxygen evolution reaction (OER) is critical for proton exchange membrane water electrolysis (PEMWE). RuO 2 possesses intrinsically high OER activity, but the concurrent electrochemical dissolution leads to rapid deactivation. Here we report a unique RuO 2 catalyst containing metallic Ru-Ru interactions (m-RuO 2 ), which maintains stable in practical PEMWE for 100 h at 60 °C and 1 A cm -2 . Experimental and theoretical investigations suggest that the presence of Ru-Ru interactions significantly increases the energy barrier for the formation of RuO 2 (OH) 2 , which is a key intermediate for Ru dissolution, and hence substantially mitigates the electrochemical corrosion of m-RuO 2 . Meanwhile, the Ru4d band center downshifts, accordingly, ensuring the high OER activity, and the participation of lattice oxygen in the OER is also suppressed at the Ru-Ru sites, further contributing to the enhanced durability. Interestingly, such enhanced stability is also dependent on the size of metallic Ru-Ru cluster, where the energy barrier is further increased for Ru 3 , but is decreased for Ru 5 . These results highlight the significance of local coordination structure modulation on the electrochemical stability of RuO 2 and open a feasible avenue toward the development of robust OER electrocatalysts for high-performance PEMWE. This article is protected by copyright. All rights reserved.