Characterization of Nickel Oxide Nanoparticles for Hydrogen Adsorption with External Electric Fifled

The Minerals, Metals and Materials Society
Zheng Zhang Xiang Sun Zhiwei Peng Jiann-Yang Hwang
Organization:
The Minerals, Metals and Materials Society
Pages:
7
File Size:
1262 KB
Publication Date:
Jan 1, 2012

Abstract

"Nickel oxide nanoparticles were synthesized using sodium dodecyl sulfate as the surfactant and urea as the hydrolyzing agent and different calcination temperatures and time were selected for preparation. Nitrogen adsorption (BET), X-ray diffraction (XRD) and scanning electron microscope (SEM) were subsequently used to characterize the prepared samples. The effect of an external electric field on hydrogen adsorption over a prepared nickel oxide was carried out. The electric filed was introduced by a piezoelectric element, which is capable of autogenously generating charges under hydrogen pressure. Increased hydrogen adsorption was obtained from this study, which indicated a stronger interaction between the adsorbent surface and hydrogen.IntroductionMetal oxide has attracted great attention for adsorption because of their wide application in catalysis [1-7], gas storage [8,9] and sensors [10,11]. However, with respect to the usage in hydrogen adsorption, few research outcomes have been reported [12,13], since there remains the difficult task of synthesizing highly porous metal oxides with unsaturated metal centers, which account for the strong interaction with hydrogen [14,15]. Nickel oxides are polar materials with an intrinsic dipole moment. The external applied electric field could further enhance the dipole moment so that the hydrogen could be more strongly adsorbed."
Citation

APA: Zheng Zhang Xiang Sun Zhiwei Peng Jiann-Yang Hwang  (2012)  Characterization of Nickel Oxide Nanoparticles for Hydrogen Adsorption with External Electric Fifled

MLA: Zheng Zhang Xiang Sun Zhiwei Peng Jiann-Yang Hwang Characterization of Nickel Oxide Nanoparticles for Hydrogen Adsorption with External Electric Fifled. The Minerals, Metals and Materials Society, 2012.

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