分解
固溶体
材料科学
傅里叶变换红外光谱
红外线的
催化作用
超短脉冲
红外光谱学
物理化学
金属
傅里叶变换
分析化学(期刊)
无机化学
热分解
化学工程
第三代
化学
热解
光谱学
固态
和频产生
化学分解
合理设计
过渡金属
作者
Junyun Gao,Jie Zheng,Hanwen Deng,Zhe Tan,Jiang Zhao,Bo Huang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-01-05
卷期号:20 (2): 2545-2555
被引量:3
标识
DOI:10.1021/acsnano.5c21319
摘要
Metallic Ir is known as the most active catalyst for room-temperature H 2 generation from N 2 H 4 decomposition. To improve N 2 H 4 -based H 2 storage technologies, the replacement of the extremely rare and high-cost Ir element is imminent but challenging because of its unique electronic structure. As one of the rational approaches for Ir replacements, immiscible Os x Pt 1– x solid solutions were synthesized. Even with low-activity elements (Os and Pt), Os 0.5 Pt 0.5 showed much higher N 2 H 4 decomposition activity than that of the pure Ir catalyst. According to the in situ Fourier transform infrared measurements and density-functional-theory calculations, the rapid N–N and N–H dissociations and H 2 formations on Os–Os, Os–Pt, and Pt–Pt sites might contribute to ultrafast H 2 generation and N 2 H 4 decomposition of Os 0.5 Pt 0.5 as pseudo-Ir.
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