Emerging concepts in solid-state hydrogen storage: the role of nanomaterials design

被引:128
作者
Reardon, Hazel [1 ]
Hanlon, James M. [1 ]
Hughes, Robert W. [1 ]
Godula-Jopek, Agata [2 ]
Mandal, Tapas K. [1 ,3 ]
Gregory, Duncan H. [1 ]
机构
[1] Univ Glasgow, Sch Chem, W CHEM, Glasgow, Lanark, Scotland
[2] EADS Innovat Works Energy & Prop, D-81663 Munich, Germany
[3] Indian Inst Technol Roorkee, Dept Chem, Roorkee 247667, Uttar Pradesh, India
基金
英国工程与自然科学研究理事会;
关键词
METAL-ORGANIC FRAMEWORKS; BORON-NITRIDE NANOTUBES; HIGH-CAPACITY HYDROGEN; HIGH-SURFACE-AREA; INTRINSIC MICROPOROSITY PIMS; MILLED MAGNESIUM HYDRIDE; HCL-TREATED POLYANILINE; HIGH H-2 ADSORPTION; ELECTRONIC-STRUCTURE; LITHIUM AMIDE;
D O I
10.1039/c2ee03138h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This perspective highlights the state-of-the-art solid-state hydrogen storage and describes newly emerging routes towards meeting the practical demands required of a solid-state storage system. The article focuses both on the physical and chemical aspects of hydrogen storage. Common to both classes of storage material is the concept of nanostructure design to tailor kinetics and thermodynamics; whether this be control of functionalised porosity or crystalline growth on the nanoscale. In the area of chemical storage, different processing and nanostructuring techniques that have been employed to overcome the barriers of slow kinetics will be discussed in addition to new chemical systems that have emerged. The prospects of porous inorganic solids, coordination polymers (metal organic frameworks; MOFs) and other polymeric matrices for physical storage of hydrogen will be highlighted. Additionally the role of inorganic nanostructures as evolving materials "intermediate" between physical and chemical storage systems will be discussed and their place within the fine thermodynamic balance for optimum hydrogen uptake and release considered.
引用
收藏
页码:5951 / 5979
页数:29
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