CoB supported on Ag-activated TiO2 as a highly active catalyst for hydrolysis of alkaline NaBH4 solution

被引:67
作者
Shen, Xiaochen [1 ]
Wang, Qing [1 ]
Wu, Qingquan [1 ]
Guo, Siqi [1 ]
Zhang, Zhengyan [1 ]
Sun, Ziyang [1 ]
Liu, Baishu [1 ]
Wang, Zhibin [2 ]
Zhao, Bin [1 ]
Ding, Weiping [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China
关键词
CoB; Ag activated TiO2; Electroless deposition; NaBH4; Hydrogen generation; HYDROGEN STORAGE PROPERTIES; RENEWABLE ENERGY-SYSTEMS; B AMORPHOUS ALLOY; SODIUM-BOROHYDRIDE; RU COMPOSITE; GENERATION; KINETICS; NANOPARTICLES; NANOCLUSTERS; FABRICATION;
D O I
10.1016/j.energy.2015.07.075
中图分类号
O414.1 [热力学];
学科分类号
摘要
In this study, a series of TiO2 (activated by Ag) supported CoB catalysts were synthesized using electroless deposition method. Compared to the unsupported CoB catalyst, the COB/Ag-TiO2 catalysts showed much better catalytic activity and higher stability on hydrolysis of NaBH4 in alkaline aqueous solution and the catalysts were insensitive to air oxidation. The optimistic loading amount of CoB was 2.8 wt% and its hydrogen generation rate reached 6294 mL min(-1) (g Co)(-1) in 1 wt% NaBH4 + 5 wt% NaOH solution at 293 K. The catalytic activity was comparable to some noble catalysts and could retain nearly 70% after 5 cycles. The catalysts were studied by varies techniques and the results revealed that the dispersion of CoB was improved and the CoB/Ag-TiO2 catalysts possessed distinct porous structure which could promote the diffusion of reactants/products. The surface composition and the electron transfer effects between the Co-0 with B-0 and Ag-0 could also affect the catalytic activity. Under the current experimental conditions, the specific activation energy of 2.8CoB/Ag-TiO2 catalyst was determined as 44 kJ mol(-1) and the kinetic equation was also deduced. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:464 / 474
页数:11
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