Palladium nanoclusters decorated partially decomposed porous ZIF-67 polyhedron with ultrahigh catalytic activity and stability on hydrogen generation
Chongbei Wu,
Jingya Guo,
Jifang Zhang,
Yanchun Zhao,
Jianniao Tian,
Tayirjan Taylor Isimjan and
Xiulin Yang
Renewable Energy, 2019, vol. 136, issue C, 1064-1070
Abstract:
Metal-organic frameworks have attracted extensively attentions due to their unique structural properties such as high porosity, good crystallinity, and three-dimensional networking. However, to the best of our knowledge, there is no report concerning the application of partially decomposed metal-organic frameworks based catalyst for sodium borohydride hydrolysis for H2 generation. Herein, the partially decomposed cobalt-based zeolitic imidazolate frameworks supported Pd nanoclusters are fabricated by evaporation solvent assisted method followed by subsequent annealing under H2 atmosphere. Our results show that catalytic performance of the designed catalyst can be largely improved by optimizing the Pd loading and the annealing temperatures. The optimized catalyst exhibits a high catalytic activity towards hydrolysis of alkalized sodium borohydride with a specific H2 generation rate of 20.6 l min−1 mgPd−1 and turnover frequency of 495.0 mol min−1 molPd−1 at 25 °C, which is the highest reported so far among the similar catalysts. Moreover, the resulted catalyst also demonstrates a high level of stability. Based on structural characterization and experimental optimization, the extraordinary performance of the fabricated catalyst is mainly contributed to the synergetic effect of highly dispersed Pd nanoclusters with partially decomposed cobalt-based zeolitic imidazolate frameworks.
Keywords: Metal-organic frameworks; Partially decomposed; Pd nanoclusters; Hydrogen generation; Synergetic effect (search for similar items in EconPapers)
Date: 2019
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Citations: View citations in EconPapers (4)
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Persistent link: https://EconPapers.repec.org/RePEc:eee:renene:v:136:y:2019:i:c:p:1064-1070
DOI: 10.1016/j.renene.2018.09.070
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