Alloyed Pt-Sn nanoparticles on hierarchical nitrogen-doped carbon nanocages for advanced glycerol electrooxidation

被引:10
|
作者
Jiang, Jietao [1 ]
Zhou, Liqi [2 ]
Xu, Fengfei [1 ]
Chen, Guanghai [1 ]
Liu, Xiaoyu [1 ]
Shen, Zhen [1 ]
Yang, Lijun [1 ]
Wu, Qiang [1 ]
Wang, Xizhang [1 ]
Hu, Zheng [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Jiangsu Prov Lab Nanotechnol, Nanjing 210023, Peoples R China
[2] Nanjing Univ, Coll Engn & Appl Sci & Collaborat Innovat Ctr Adv, Natl Lab Solid State Microstruct, Jiangsu Key Lab Artificial Funct Mat, Nanjing 210093, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Pt3Sn alloy; hierarchical nitrogen-doped carbon nanocages; glycerol electrooxidation; anti-poisoning; C-C bond cleavage; ETHANOL OXIDATION; PD NANOPARTICLES; HIGH-PERFORMANCE; ETHYLENE-GLYCOL; CATALYSTS; ELECTROCATALYSTS; NANOCUBES; GRAPHENE; ACID;
D O I
10.1007/s12274-023-6288-4
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
Glycerol is an alternative sustainable fuel for fuel cells, and efficient electrocatalyst is crucial for glycerol oxidation reaction (GOR). The promising Pt catalysts are subject to the inadequate capability of C-C bond cleavage and the susceptibility to poisoning. Herein, Pt-Sn alloyed nanoparticles are immobilized on hierarchical nitrogen-doped carbon nanocages (hNCNCs) by convenient ethylene glycol reduction and subsequent thermal reduction. The optimal Pt3Sn/hNCNC catalyst exhibits excellent GOR performance with a high mass activity (5.9 A.mg(Pt)(-1)), which is 2.7 and 5.4 times higher than that of Pt/hNCNC and commercial Pt/C, respectively. Such an enhancement can be mainly ascribed to the increased anti-poisoning and C-C bond cleavage capability due to the Pt3Sn alloying effect and Sn-enriched surface, the high dispersion of Pt3Sn active species due to N-participation, as well as the high accessibility of Pt3Sn active species due to the three-dimensional (3D) hierarchical architecture of hNCNC. This study provides an effective GOR electrocatalyst and convenient approach for catalyst preparation.
引用
收藏
页码:4055 / 4061
页数:7
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