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镍纳米颗粒分散的多壁碳纳米管中的储氢

Hydrogen storage in ni nanoparticle-dispersed multiwalled carbon nanotubes.

作者信息

Kim Hyun-Seok, Lee Ho, Han Kyu-Sung, Kim Jin-Ho, Song Min-Sang, Park Min-Sik, Lee Jai-Young, Kang Jeung-Ku

机构信息

Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong, Yuseong-gu, Daejeon, South Korea, Samsung Electronics Co. Ltd., San 24, Giheung, Yongin, South Korea.

出版信息

J Phys Chem B. 2005 May 12;109(18):8983-6. doi: 10.1021/jp044727b.

DOI:10.1021/jp044727b
PMID:16852070
Abstract

Hydrogen storage properties of mutiwalled carbon nanotubes (MWCNTs) with Ni nanoparticles were investigated. The metal nanoparticles were dispersed on MWCNTs surfaces using an incipient wetness impregnation procedure. Ni catalysts have been known to effectively dissociate hydrogen molecules in gas phase, providing atomic hydrogen possible to form chemical bonding with the surfaces of MWCNTs. Hydrogen desorption spectra of MWCNTs with 6 wt % of Ni nanoparticles showed that approximately 2.8 wt % hydrogen was released in the range of 340-520 K. In Kissinger's plot to evaluate the nature of interaction between hydrogen and MWCNTs with Ni nanoparticles, the hydrogen desorption activation energy was measured to be as high as approximately 31 kJ/mol.H(2), which is much higher than the estimates of pristine SWNTs. C-H(n)() stretching vibrations after hydrogenation in FTIR further supported that hydrogen molecules were dissociated when bound to the surfaces of MWCNTs. During cyclic hydrogen absorption/desorption, there was observed no significant decay in hydrogen desorption amount. The hydrogen chemisorption process facilitated by Ni nanopaticles could be suggested as an effective reversible hydrogen storage method.

摘要

研究了负载镍纳米颗粒的多壁碳纳米管(MWCNT)的储氢性能。采用初湿浸渍法将金属纳米颗粒分散在MWCNT表面。已知镍催化剂能有效分解气相中的氢分子,提供可与MWCNT表面形成化学键的氢原子。含有6 wt%镍纳米颗粒的MWCNT的氢脱附光谱表明,在340 - 520 K范围内释放了约2.8 wt%的氢。在基辛格曲线中评估氢与负载镍纳米颗粒的MWCNT之间的相互作用性质时,测得氢脱附活化能高达约31 kJ/mol·H₂,远高于原始单壁碳纳米管的估计值。FTIR氢化后的C - H(n)拉伸振动进一步证明,氢分子在与MWCNT表面结合时发生了解离。在循环吸氢/脱附过程中,未观察到氢脱附量有明显衰减。由镍纳米颗粒促进的氢化学吸附过程可被认为是一种有效的可逆储氢方法。

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