Self-Supported Pt@Ni2P for Controllable Hydrogen Release from Ammonia-Borane Hydrolysis

被引:16
作者
Asim, Muhammad [1 ,2 ]
Maryam, Bushra [3 ]
Liu, Xianhua [3 ]
Pan, Lun [1 ,2 ]
Shi, Chengxiang [1 ,2 ]
Zou, Ji-Jun [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Minist Educ, Tianjin 300072, Peoples R China
[2] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
[3] Tianjin Univ, Sch Environm Sci & Engn, Tianjin 300072, Peoples R China
关键词
NICKEL FOAM; NI FOAM; GENERATION; CATALYST; DEHYDROGENATION; EVOLUTION; CLUSTERS;
D O I
10.1021/acs.iecr.3c01055
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Thechemical storage of hydrogen is well accomplished by ammoniaborane. However, a significant barrier to utilizing ammonia boranepractically is developing extraordinarily effective and inexpensivecatalysts that propel hydrogen evolution from it. In this work, thecatalyst Pt@Ni2P/nickel foam (NF) is synthesized by embeddingplatinum (Pt) nanoparticles over self-supported Ni2P/NF.Pt@Ni2P/NF enables a high synergetic effect between Ptnanoparticles and Ni2P/NF, boosting the hydrolysis of ammoniaborane. The catalyst Pt@Ni2P/NF activity enriches 3.0-foldcompared to Ni2P/NF and 25.5-fold compared to pristineNi(2)P. X-ray photoelectron spectroscope analysis revealsthat embedding Pt nanoparticles over self-supported Ni2P generates a strong interaction between (Ni2P/NF)(& delta;+) and (Pt)(& delta;-). The chemical kineticresults reveal that the activation energy and turnover frequency ofPt@Ni2P/NF are calculated to be 31.0 kJ mol(-1) and 63.2 min(-1) for 0.13 M AB. This study demonstratesa reliable method used to develop active sites of (Ni2P)(& delta;+) and (Pt)(& delta;-) for ammonia-boranehydrolysis. The controllable hydrogen release and facile on/off characteristicof the catalyst demonstrate a feasible way to boost the catalyticperformance by constructing a two-dimensional (2D) structure.
引用
收藏
页码:10951 / 10960
页数:10
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