首页> 外文学位 >Charge induced enhancement of adsorption for hydrogen storage materials.
【24h】

Charge induced enhancement of adsorption for hydrogen storage materials.

机译:电荷诱导的储氢材料吸附增强。

获取原文
获取原文并翻译 | 示例

摘要

The rising concerns about environmental pollution and global warming have facilitated research interest in hydrogen energy as an alternative energy source. To apply hydrogen for transportations, several issues have to be solved, within which hydrogen storage is the most critical problem. Lots of materials and devices have been developed; however, none is able to meet the DOE storage target.;The primary issue for hydrogen physisorption is a weak interaction between hydrogen and the surface of solid materials, resulting negligible adsorption at room temperature. To solve this issue, there is a need to increase the interaction between the hydrogen molecules and adsorbent surface.;In this study, intrinsic electric dipole is investigated to enhance the adsorption energy. The results from the computer simulation of single ionic compounds with hydrogen molecules to form hydrogen clusters showed that electrical charge of substances plays an important role in generation of attractive interaction with hydrogen molecules. In order to further examine the effects of static interaction on hydrogen adsorption, activated carbon with a large surface area was impregnated with various ionic salts including LiCl, NaCl, KCl, KBr, and NiCl2 and their performance for hydrogen storage was evaluated by using a volumetric method. Corresponding computer simulations have been carried out by using DFT (Density Functional Theory) method combined with point charge arrays. Both experimental and computational results prove that the adsorption capacity of hydrogen and its interaction with the solid materials increased with electrical dipole moment.;Besides the intrinsic dipole, an externally applied electric field could be another means to enhance hydrogen adsorption. Hydrogen adsorption under an applied electric field was examined by using porous nickel foil as electrodes. Electrical signals showed that adsorption capacity increased with the increasing of gas pressure and external electric voltage. Direct measurement of the amount of hydrogen adsorption was also carried out with porous nickel oxides and magnesium oxides using the piezoelectric material PMN-PT as the charge supplier due to the pressure. The adsorption enhancement from the PMN-PT generated charges is obvious at hydrogen pressure between 0 and 60 bars, where the hydrogen uptake is increased at about 35% for nickel oxide and 25% for magnesium oxide. Computer simulation reveals that under the external electric field, the electron cloud of hydrogen molecules is pulled over to the adsorbent site and can overlap with the adsorbent electrons, which in turn enhances the adsorption energy;Experiments were also carried out to examine the effects of hydrogen spillover with charge induced enhancement. The results show that the overall storage capacity in nickel oxide increased remarkably by a factor of 4.
机译:对环境污染和全球变暖的日益关注促使人们对氢能作为替代能源的研究产生了兴趣。为了将氢用于运输,必须解决几个问题,其中氢的存储是最关键的问题。已经开发了许多材料和设备;氢物理吸附的主要问题是氢与固体材料表面之间的弱相互作用,导致室温下的吸附可忽略不计。为了解决这个问题,需要增加氢分子与吸附剂表面之间的相互作用。在本研究中,研究了固有电偶极子以提高吸附能。计算机模拟单个离子化合物与氢分子形成氢簇的结果表明,物质的电荷在与氢分子产生有吸引力的相互作用中起着重要作用。为了进一步检查静态相互作用对氢吸附的影响,用各种离子盐(包括LiCl,NaCl,KCl,KBr和NiCl2)浸渍了具有大表面积的活性炭,并通过使用体积比来评估了它们的储氢性能。方法。通过使用DFT(密度泛函理论)方法结合点电荷阵列进行了相应的计算机模拟。实验和计算结果均表明,氢的吸附容量及其与固体材料的相互作用随电偶极矩的增加而增加。除了本征偶极,外加电场可能是增强氢吸附的另一种方法。通过使用多孔镍箔作为电极检查在施加的电场下的氢吸附。电信号表明,随着气体压力和外部电压的增加,吸附量增加。由于压力,还使用压电材料PMN-PT作为电荷提供者,使用多孔的氧化镍和氧化镁直接测量了氢的吸附量。 PMN-PT产生的电荷在0至60 bar的氢气压力下具有明显的吸附增强作用,其中氧化镍和氧化镁的吸氢量分别增加约35%和25%。计算机仿真表明,在外电场作用下,氢分子的电子云被拉到吸附位,并可以与吸附电子重叠,从而提高了吸附能;还进行了实验研究氢的作用。电荷诱导增强的溢出效应。结果表明,氧化镍的总存储容量显着增加了4倍。

著录项

  • 作者

    Sun, Xiang.;

  • 作者单位

    Michigan Technological University.;

  • 授予单位 Michigan Technological University.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 196 p.
  • 总页数 196
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号