Improved methane oxidation activity of P-doped γ-Al2O3 supported palladium catalysts by tailoring the oxygen mobility and electronic properties

被引:20
作者
Chen, Xiaohua [1 ]
Zheng, Yong [2 ]
Chen, Yelin [1 ]
Xu, Yalan [1 ]
Zhong, Fulan [2 ]
Zhang, Wen [1 ]
Xiao, Yihong [2 ]
Zheng, Ying [1 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci, Fujian Prov Key Lab Adv Mat Oriented Chem Engn, Fuzhou 350007, Fujian, Peoples R China
[2] Fuzhou Univ, Natl Engn Res Ctr Chem Fertilizer Catalyst, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Electronic structure; Methane oxidation; Oxygen mobility; Phosphorus-doped; Pd/Al2O3; CH4; OXIDATION; ELECTROCATALYTIC PERFORMANCES; HYDROTHERMAL STABILITY; ALUMINA CATALYST; COMBUSTION; TEMPERATURE; REACTIVITY; CO; ACTIVATION; BEHAVIOR;
D O I
10.1016/j.ijhydene.2019.08.237
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
Micro-mesoporous P-doped gamma-Al2O3 with cluster morphology was obtained via an efficient ultrasound-assisted sol-gel process and taken as carrier to construct palladium catalysts for methane oxidation. It was revealed that the structure and properties of catalysts were significantly influenced by the phosphorus precursors with diverse valence and acidity. Dissimilar reducibility of surface hydroxyl and oxygen species is observed in the catalysts derived from different phosphorus sources, indicating the difference in the oxygen mobility and the capacity of the catalysts to convert intermediate CO. The behavior of charge-transfer transition and d-d transition, the transfer ability of electrons from palladium particles into the antibonding 2 pi* orbitals of CO, together with the surface acidity and electronic density of palladium species was likewise tailored, which demonstrated the metal-support interaction could be tuned, making palladium species behave with diverse status and electronic structures. The optimized properties cooperatively provided an enhancement in catalytic performance of P-containing catalysts. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:27772 / 27783
页数:12
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