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Deposition of Fe-Ni nanoparticles on polyethyleneimine-decorated graphene oxide and application in catalytic dehydrogenation of ammonia boraneElectronic supplementary information (ESI) available: Raman, UV-Vis spectra, TEM images and XPS of PEI-GO composites, Ra of AFM micrographs, TEM images of the crystallization of the NPs, effect of the Fe to Ni ratio on the dehydrogenation, a comparison between GO and AC as the support, the valence state of Fe and Ni, et al. See DOI: 10.1039/c2jm31000g

Ammonia borane (AB) is one of the most promising hydrogen storage materials due to its high hydrogen content and outstanding environmental stability and non-toxicity, which has stimulated substantial effort devoted to developing highly efficient dehydrogenation catalysts. Transition metal nanopartic...

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Main Authors: Zhou, Xiaohui, Chen, Zhongxin, Yan, Danhua, Lu, Hongbin
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Chen, Zhongxin
Yan, Danhua
Lu, Hongbin
description Ammonia borane (AB) is one of the most promising hydrogen storage materials due to its high hydrogen content and outstanding environmental stability and non-toxicity, which has stimulated substantial effort devoted to developing highly efficient dehydrogenation catalysts. Transition metal nanoparticles (NPs) such as iron (Fe) and nickel (Ni) are quite attractive due to their advantages in cost, catalytic activity and recycling capability. However, their magnetism and strong aggregation propensity make it a challenge to develop them into highly efficient dehydrogenation catalysts. We propose a method to resolve this issue, in which a weak, branched polyelectrolyte, polyethyleneimine (PEI), is utilized to assist the deposition of Fe-Ni NPs on graphene oxide (GO). These Fe-Ni NPs are prepared by a simple co-reduction method of metal precursors with sodium borohydride under ambient conditions. The content of PEI attached on GO significantly affects the morphology and size of resulting Fe-Ni NPs. For the high PEI content, where most of metal ions are confined within the PEI layer attached on GO, the homogeneous nucleation and growth in the bulk solution are suppressed so that small, amorphous Fe-Ni NPs (∼3 nm in diameter) are formed. Compared to the Fe-Ni NPs directly deposited on GO, these NPs on PEI-decorated GO reveal a dehydrogenation rate of 982 ml min −1 g −1 at 293 K for the hydrolysis of AB, which is 18 times faster than that of the former and nearly comparable to that of the platinum catalyst deposited on carbon under the same conditions. The present work demonstrates the validity of using PEI molecules attached on GO to control the deposition and morphology of Fe and Ni NPs, which is favorable for developing high performance graphene-based dehydrogenation catalysts.
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We propose a method to resolve this issue, in which a weak, branched polyelectrolyte, polyethyleneimine (PEI), is utilized to assist the deposition of Fe-Ni NPs on graphene oxide (GO). These Fe-Ni NPs are prepared by a simple co-reduction method of metal precursors with sodium borohydride under ambient conditions. The content of PEI attached on GO significantly affects the morphology and size of resulting Fe-Ni NPs. For the high PEI content, where most of metal ions are confined within the PEI layer attached on GO, the homogeneous nucleation and growth in the bulk solution are suppressed so that small, amorphous Fe-Ni NPs (∼3 nm in diameter) are formed. Compared to the Fe-Ni NPs directly deposited on GO, these NPs on PEI-decorated GO reveal a dehydrogenation rate of 982 ml min −1 g −1 at 293 K for the hydrolysis of AB, which is 18 times faster than that of the former and nearly comparable to that of the platinum catalyst deposited on carbon under the same conditions. 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The content of PEI attached on GO significantly affects the morphology and size of resulting Fe-Ni NPs. For the high PEI content, where most of metal ions are confined within the PEI layer attached on GO, the homogeneous nucleation and growth in the bulk solution are suppressed so that small, amorphous Fe-Ni NPs (∼3 nm in diameter) are formed. Compared to the Fe-Ni NPs directly deposited on GO, these NPs on PEI-decorated GO reveal a dehydrogenation rate of 982 ml min −1 g −1 at 293 K for the hydrolysis of AB, which is 18 times faster than that of the former and nearly comparable to that of the platinum catalyst deposited on carbon under the same conditions. 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We propose a method to resolve this issue, in which a weak, branched polyelectrolyte, polyethyleneimine (PEI), is utilized to assist the deposition of Fe-Ni NPs on graphene oxide (GO). These Fe-Ni NPs are prepared by a simple co-reduction method of metal precursors with sodium borohydride under ambient conditions. The content of PEI attached on GO significantly affects the morphology and size of resulting Fe-Ni NPs. For the high PEI content, where most of metal ions are confined within the PEI layer attached on GO, the homogeneous nucleation and growth in the bulk solution are suppressed so that small, amorphous Fe-Ni NPs (∼3 nm in diameter) are formed. Compared to the Fe-Ni NPs directly deposited on GO, these NPs on PEI-decorated GO reveal a dehydrogenation rate of 982 ml min −1 g −1 at 293 K for the hydrolysis of AB, which is 18 times faster than that of the former and nearly comparable to that of the platinum catalyst deposited on carbon under the same conditions. The present work demonstrates the validity of using PEI molecules attached on GO to control the deposition and morphology of Fe and Ni NPs, which is favorable for developing high performance graphene-based dehydrogenation catalysts.</abstract><doi>10.1039/c2jm31000g</doi><tpages>11</tpages></addata></record>
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title Deposition of Fe-Ni nanoparticles on polyethyleneimine-decorated graphene oxide and application in catalytic dehydrogenation of ammonia boraneElectronic supplementary information (ESI) available: Raman, UV-Vis spectra, TEM images and XPS of PEI-GO composites, Ra of AFM micrographs, TEM images of the crystallization of the NPs, effect of the Fe to Ni ratio on the dehydrogenation, a comparison between GO and AC as the support, the valence state of Fe and Ni, et al. See DOI: 10.1039/c2jm31000g
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