脱氢
甲酸
碳化硅
胺气处理
催化作用
材料科学
化学
化学工程
碳化物
无机化学
有机化学
工程类
作者
Tianyang Hu,Ping He,Jiang Wu,Naichao Chen,Kangsai He,Qian Cai,Rui Shen,Wenchu Yuan,Litao Zhang,Xingyu Cao
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-02-21
卷期号:39 (9): 4458-4470
被引量:1
标识
DOI:10.1021/acs.energyfuels.4c05960
摘要
As an organic material with a high hydrogen storage density, formic acid is a liquid hydrogen carrier with broad research prospects. Designing highly efficient and selective dehydrogenation catalysts is key to realizing the application of formic acid dehydrogenation. In this article, ultrafine Pd particles were attached to aminated mesoporous SiC using impregnation and chemical reduction methods, providing a large number of active sites for the dissociation of HCOO*. Compared with α-SiC, β-SiC performs better in formic acid dehydrogenation. Pd@β-SiC(APTES + CIT) exhibits excellent catalytic performance for formic acid dehydrogenation. At 333 K, the initial turnover frequency (TOF initial ) reaches 9580 h –1, which is 1.68 times that of Pd@α-SiC(APTES + CIT). Density functional theory (DFT) revealed the mechanism by which Pd@SiC decomposed formic acid, demonstrating that Pd@β-SiC was more inclined to decompose formic acid. This study provides a new idea for the design of formic acid dehydrogenation catalysts.
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