选择性
纳米颗粒
羟甲基
离解(化学)
催化作用
四氢呋喃
密度泛函理论
化学
化学工程
核化学
无机化学
物理化学
有机化学
溶剂
计算化学
工程类
作者
Xiangyu Jia,Kai Yuan,Guofu Wang,Shanhui Zhu,Mei Dong,Jiamin Wang,Xiaoming Li,Weibin Fan
标识
DOI:10.1016/j.cej.2024.150482
摘要
Selective reduction of 5-hydroxymethylfurfural (HMF) to valuable 2,5-bis(hydroxymethyl)tetrahydrofuran (BHMTHF) remains a significant challenge under mild conditions. The synergistic effect between metal single atoms (SAs) and nanoparticles (NPs) can greatly enhance catalytic activity. Here, a high-performance Pd SAs catalyst supported on N-doped carbon (PdSAs/NC) was developed from Pd@UiO-66-NH2. It was found that partial Pd SAs were spontaneously restructured into Pd NPs during the reaction. Our catalyst exhibited 100% conversion of HMF and 98% selectivity towards BHMTHF at temperature as low as 0 °C. In situ FTIR spectra results and density functional theory calculations indicate that Pd SAs contribute to the C = O activation, while Pd NPs facilitated the H2 dissociation into H* atoms, resulting in synergistic catalytic activity between Pd SAs and Pd NPs.
科研通智能强力驱动
Strongly Powered by AbleSci AI