Modulating the microenvironment of AuPd nanoparticles using metal-organic frameworks for selective methane oxidation

被引:9
|
作者
Sui, Jianfei [1 ]
Gao, Ming-Liang [1 ]
Liu, Chengyuan [2 ]
Pan, Yang [2 ]
Meng, Zheng [1 ]
Yuan, Daqiang [3 ]
Jiang, Hai-Long [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Natl Synchrotron Radiat Lab NSRL, Hefei 230029, Anhui, Peoples R China
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
关键词
CATALYTIC CONVERSION; COPPER; OXYGEN; CH3OH; CH4;
D O I
10.1039/d3ta03712f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Direct and selective oxidation of methane (CH4) into methanol (CH3OH) under ambient conditions remains a grand challenge because of the high energy barrier of CH4 activation and the complicated processes involved. Herein, by incorporating AuPd alloy nanoparticles (NPs) into a series of Cu2+-doped metal-organic frameworks (MOFs), namely AuPd@Cu-UiO-66(x), efficient and direct catalytic conversion of CH4 to CH3OH can be achieved at mild temperature (70 & DEG;C) with H2O2 as an oxidant. The Cu-UiO-66 serving as the microenvironment parameter not only regulates the electronic state of AuPd NPs to improve the CH4 adsorption and activation, but also affects the generation of hydroxyl radicals (OH) in H2O2 reaction pathways, which consequently results in a volcano-type dependency of the CH3OH selectivity on the Cu contents. This work represents the first finding on achieving direct catalytic oxidation of CH4 to CH3OH under mild conditions by modulating the microenvironment of catalytic centers based on a MOF platform.
引用
收藏
页码:18733 / 18739
页数:7
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