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作 者:Xiaoqiong Du Chao Liu Cheng Du Ping Cai Gongzhen Cheng Wei Luo
机构地区:[1]College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China [2]Key laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071, China
出 处:《Nano Research》2017年第8期2856-2865,共10页纳米研究(英文版)
基 金:This work was financially supported by the National Natural Science Foundation of China (No. 21571145), the Creative Research Groups of Hubei Province (No. 2014CFA007), and Large-scale Instrument and Equipment Sharing Foundation of Wuhan University.
摘 要:The safe and efficient storage and release of hydrogen is one of the key technological challenges for the fuel cell-based hydrogen economy. Hydrazine monohydrate has attracted considerable attention as a safe and convent chemical hydrogen-storage material. Herein, we report the facile synthesis of NiPt-CeOx nanocomposites supported by three-dimensional nitrogen-doped graphene hydrogels (NGHs) via a simple one-step co-reduction synthesis method. These catalysts were composition-dependent for hydrogen generation from an alkaline solution of hydrazine. (NisPt5)I-(CeOx)0.B/NGH exhibited the highest catalytic activity, with 100% hydrogen selectivity and turnover frequencies of 408 h^-1 at 298 K and 3,064 h^-1 at 323 K. These superior catalytic performances are attributed to the electronic structure of the NiPt centers, which was modified by the electron interaction between NiPt and CeOx and the strong metal-support interaction between NiPt-CeOx and the NGH.The safe and efficient storage and release of hydrogen is one of the key technological challenges for the fuel cell-based hydrogen economy. Hydrazine monohydrate has attracted considerable attention as a safe and convent chemical hydrogen-storage material. Herein, we report the facile synthesis of NiPt-CeOx nanocomposites supported by three-dimensional nitrogen-doped graphene hydrogels (NGHs) via a simple one-step co-reduction synthesis method. These catalysts were composition-dependent for hydrogen generation from an alkaline solution of hydrazine. (NisPt5)I-(CeOx)0.B/NGH exhibited the highest catalytic activity, with 100% hydrogen selectivity and turnover frequencies of 408 h^-1 at 298 K and 3,064 h^-1 at 323 K. These superior catalytic performances are attributed to the electronic structure of the NiPt centers, which was modified by the electron interaction between NiPt and CeOx and the strong metal-support interaction between NiPt-CeOx and the NGH.
关 键 词:nitrogen-doped graphene hydrogels NiPt-CeOx hydrogen storage HYDRAZINE
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