Design of yolk-shell structured PdSn@Pd@HCS nanocatalysts for efficient direct synthesis of H2O2

被引:6
作者
Tian, Wei [1 ]
Dong, Yonggang [1 ]
Qin, Hong [2 ]
Luo, Ziming [3 ]
Lin, Qian [1 ]
Chen, Zheng [1 ]
Pan, Hongyan [1 ]
Shi, Yongyong [1 ]
Wang, Keliang [4 ]
机构
[1] Guizhou Univ, Sch Chem & Chem Engn, Guizhou Key Lab Green Chem & Clean Energy Technol, Guiyang 550025, Guizhou, Peoples R China
[2] Wengfu Grp Co LTD, Guiyang 550005, Guizhou, Peoples R China
[3] Tianfu Chem Co LTD, Qiannan 558000, Guizhou, Peoples R China
[4] Liupanshui Normal Univ, Liupanshui 553004, Guizhou, Peoples R China
关键词
Direct synthesis; Hydrogen peroxide; Palladium catalyst; Bimetallic; Yolk-shell; HYDROGEN-PEROXIDE; SELECTIVE OXIDATION; CATALYSTS; PALLADIUM; HALIDE; OXYGEN; GOLD; O-2; H-2; NANOPARTICLES;
D O I
10.1016/j.mcat.2023.113376
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
The direct synthesis of hydrogen peroxide (DSHP) from hydrogen and oxygen is a green synthesis method with a high atomic economy. However, H2O2 selectivity and productivity remain a key challenge, the O-O bonds are easily broken with supported Pd catalysts to produce water. Herein, we report the synthesis of bimetallic catalyst PdSn@Pd@HCS by adapting reversed-phase micellar and galvanic replacement reaction. The novel bimetallic yolk-shell structure catalysts exhibit excellent catalytic performance, the selectivity and productivity of H2O2 reaching 98% and 4899 mmol/g(Pd)center dot h(-1), respectively. Theoretical calculations reveal that the presence of Sn inside the bimetallic alloy can enhance the ligand effect and optimize the electronic structure of the surface Pd atoms, weakening the adsorption ability of O-2 molecules and inhibiting the dissociation of O-O bonded species, resulting in the enhancement of H2O2 selectivity and productivity. This work provides the groundwork for bimetallic yolk-shell structure catalysts to achieve the efficient synthesis of H2O2.
引用
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页数:12
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