Interstitial-Hydrogen-Modulated Subnanometer PdPtIrCoNiH High-Entropy Hydride Nanowires for Efficient Hydrogen...

The slow Volmer step (water dissociation/formation) poses a fundamental challenge in alkaline hydrogen electrocatalysis. Here, we demonstrate that the integration of high-entropy design and interstitial hydrogen engineering in PdPtIrCoNiH₁₅ high-entropy hydride nanowires effectively overcomes this kinetic limitation. The PdPtIrCoNiH₁₅ nanowire catalyst (diameter ca. 1.21 nm) exhibits remarkable mass activities of 8.02 and 4.55 A mg_PGM^-1 at an overpotential of 0.05 V for the hydrogen oxidation reaction (HOR) in 0.1 M KOH and the hydrogen evolution reaction (HER) in 1.0 M KOH, respectively, outperforming commercial Pt/C and other control catalysts. Operando X-ray spectroscopies reveal that interstitial H induces lattice expansion in PdPtIrCoNiH₁₅ and buffers the structural distortion, which can promote water dissociation/*OH adsorption and boost catalytic activity/structural reversibility. Density functional theory (DFT) calculations reveal the gradient distribution of *H/*OH binding energy (HBE/OHBE) on the PdPtIrCoNiH₁₅ surface. The high-entropy effect and interstitial hydrogen could cause electron richness and deficiency on the Pd/Pt and Ir/Co/Ni sites, thus optimizing the HBE and OHBE on these sites, respectively. The gradient adsorption and optimized HBE/OHBE enable favorable channels for *H migration and lower the energy barrier of the Volmer step, thereby improving the catalytic activity. In an anion-exchange membrane fuel cell (AEMFC), the PdPtIrCoNiH₁₅ anode achieves a remarkable peak power density of 1.37 W cm^-2. As an AEM water electrolyzer (AEMWE) cathode, it requires only 1.626 V to reach 1 A cm^-2 and maintains a slow degradation rate of 71 μV h^-1 over 1000 h, representing one of the most active alkaline hydrogen electrocatalysts reported.