钌
催化作用
离解(化学)
铂金
铂纳米粒子
纳米颗粒
材料科学
氢
吸附
分解水
无机化学
纳米技术
物理化学
化学
有机化学
光催化
作者
Qinyu Li,Soshan Cheong,Agus R. Poerwoprajitno,Shuting Xiang,Anatoly I. Frenkel,Yuwei Yang,Nicholas M. Bedford,Sohaib Umer,Martina Lessio,Ichiro Ohnishi,Zeno Rizqi Ramadhan,Dale L. Huber,Liming Dai,Wolfgang Schuhmann,J. Justin Gooding,Richard D. Tilley
标识
DOI:10.1002/adma.202509610
摘要
Abstract The platinum‐ruthenium (PtRu) system is highly active for hydrogen evolution reaction (HER) in alkaline media with both Pt and Ru playing active roles in the water dissociation step that generates adsorbed hydrogen atoms. Precise control of the arrangement of Pt atoms on Ru nanoparticles can maximize the Pt‐Ru sites for water dissociation and Pt‐Pt sites for hydrogen production and can considerably improve HER catalytic performance. By directing the growth and distribution of Pt on Ru hourglass nanoparticles, the arrangement of Pt on Ru is controlled into forming Pt islands, small Pt clusters, and strings of a few Pt atoms. Calculations show that the unique atomic string arrangements of Pt on Ru is the thermodynamically favorable configuration. Additionally, these strings have a favorable combination of Pt‐Ru and Pt‐Pt sites, making the Pt‐string on Ru the most active catalyst with a more than fivefold increase in turnover frequency for alkaline HER compared to the Pt‐island on Ru catalyst. The results show how controlling the Pt atomic arrangement on Ru nanoparticle surfaces for the tuning of Pt‐Pt and Pt‐Ru neighboring sites can direct toward a more efficient HER mechanism and thereby significantly enhancing HER performance.
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