A high-performance PdZn alloy catalyst obtained from metal-organic framework for methanol steam reforming hydrogen production

被引:50
作者
Zeng, Zilong [1 ]
Liu, Guoliang [2 ]
Geng, Jiafeng [1 ]
Jing, Dengwei [1 ]
Hong, Xinlin [2 ]
Guo, Liejin [1 ]
机构
[1] Xi An Jiao Tong Univ, Int Res Ctr Renewable Energy, State Key Lab Multiphase Flow Power Engn, Xian 710049, Shaanxi, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic-framework; Hydrogen; Methanol steam reforming; PdZn alloy; Oxygen vacancy; ADSORPTION; TIO2(110); STABILITY; EFFICIENT; DEFECTS; PD/ZNO; CO2;
D O I
10.1016/j.ijhydene.2019.07.195
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
Methanol steam reforming (MSR) is deemed to be an effective way for hydrogen production and Pd/ZnO catalyst were found to exhibit high activity in this reaction. However, their activities are strongly related to the preparations methods. In most cases, these catalysts are synthesized by impregnation or co-precipitation methods, aiming to change the dispersion and stability of Pd nanoparticle to get better performance. Here we report an efficient Pd/ZnO catalyst that was synthesized with zeolitic imidazolate framework-8 (ZIF-8) as the precursor, on which Pd ions was supported after NaHB4 reduction. Typically, when the catalyst reduced at 300 degrees C for 2 h, the methanol conversion could reach 97-98% and the CO2 selectivity is around 86.3% under the reaction condition of 0.1 MPa, water/CH3OH = 1.2:1 (mol ratio), WHSVmethanol = 43152ml/g(cat)*h, catalyst = 0.1 g, our catalyst was found to show much better performance than other Pd@ZnO catalysts prepared by other methods, especially in terms of selectivity which is particularly important for hydrogen fuel cell application considering that Pt electrode could be poisoned by even trace amount of CO. It turned out that the large surface area, enough holes, evenly distributed PdZn alloy activity sites and abundant oxygen vacancies lead to the overall excellent performance of our catalyst. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:24387 / 24397
页数:11
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