Zhao, Hao; Ni, Baoxin; Pan, Yongyu; Li, Yuze; Li, Jun; Wang, Guoliang; Zou, Zhiqing; Jiang, Kun; Cheng, Qingqing; Zu, Lianhai; Yang, Hui

ADVANCED MATERIALS

2025, 26,

Zhao, Hao; Ni, Baoxin; Pan, Yongyu; Li, Yuze; Li, Jun; Wang, Guoliang; Zou, Zhiqing; Jiang, Kun; Cheng, Qingqing; Zu, Lianhai; Yang, Hui

Atop and multiple adsorbed hydrogen are considered as key intermediates on Pt-group metal for acidic hydrogen evolution reaction (HER), yet the role of bridge hydrogen intermediate (*Hbridge) is consistently overlooked experimentally. Herein, a Pt atomic chain modified fcc-Ru nanocrystal (Pt-Ru(fcc)) is developed with a co-crystalline structure, featuring *Hbridge intermediate bonded on the Pt-Ru pair site. Electrons leap from the pair site to *Hbridge facilitate hydrogen desorption, thus accelerating the Tafel kinetics and ensuring outstanding electrocatalytic performance, with a low overpotential (4.0 mV at 10 mA cm-2) and high turnover frequency (56.4 H2 s-1 at 50 mV). Notably, the proton exchange membrane water electrolyzer PEMWE with ultra-low loading of 10 ugPt cm-2 shows excellent activity (1.61 V at 1.0 A cm-2) and low average degradation rate (4.0 mu V h-1 over 1000 h), significantly outperforming the benchmark Pt/C. Furthermore, the PEMWE-based 80 mu m Gore membrane under identical operating conditions requires only 1.54 and 1.58 V to achieve 1.0 and 1.5 A cm-2. This finding highlights the key role of *Hbridge at the Pt-Ru interface in obtaining high HER intrinsic activity and underscores the transformative potential in designing next-generation bimetallic catalysts for clean hydrogen energy.