Temporal and spatial imaging of hydrogen storage materials: watching solvent and hydrogen desorption from aluminium hydride by transmission electron microscopy

2008 ◽  
pp. 4448 ◽  
Author(s):  
Shane D. Beattie ◽  
Terry Humphries ◽  
Louise Weaver ◽  
G. Sean McGrady
Scanning ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-12 ◽  
Author(s):  
Jianding Li ◽  
Jincheng Xu ◽  
Bo Li ◽  
Liqing He ◽  
Huaijun Lin ◽  
...  

Mg-based materials are regarded as one of the most promising candidates for hydrogen storage. In order to clarify the relationship between the structures and properties as well as to understand the reaction and formation mechanisms, it is beneficial to obtain useful information about the size, morphology, and microstructure of the studied materials. Herein, the use of scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques for the representation of Mg-based hydrogen storage materials is described. The basic principles of SEM and TEM are presented and the characterizations of the size, morphology observation, phase and composition determination, and formation and reaction mechanisms clarification of Mg-based hydrogen storage materials are discussed. The applications of advanced SEM and TEM play significant roles in the research and development of the next-generation hydrogen storage materials.


2013 ◽  
Vol 724-725 ◽  
pp. 1021-1024
Author(s):  
Shi Xue Zhou ◽  
Qian Qian Zhang ◽  
Nai Fei Wang ◽  
Zong Ying Han ◽  
Wei Xian Ran ◽  
...  

Magnesium-based hydrogen storage materials were prepared by reactive milling of magnesium under hydrogen atmosphere with crystallitic carbon, prepared from anthracite coal, as milling aid. The XRD analysis shows that in the presence of 30 wt.% of crystallitic carbon, the Mg easily hydrided into β-MgH2of crystal grain size 29.7 nm and a small amount of γ-MgH2after 3 h of milling under 1 MPa H2. The enthalpy and entropy changes of the hydrogen desorption reaction are 42.7 kJ/mol and 80.7 J/mol K, respectively, calculated by the vant Hoff equation from thep-C-Tdata in 300-380°C.


Nanoscale ◽  
2015 ◽  
Vol 7 (11) ◽  
pp. 4811-4819 ◽  
Author(s):  
Xin Chen ◽  
Chang Li ◽  
Hongling Cao

In situ wet cells for transmission electron microscopy (TEM) and scanning transmission electron microscopy (STEM) allow studying structures and processes in a liquid environment with high temporal and spatial resolutions, and have been attracting increasing research interests in many fields.


2009 ◽  
Vol 289-292 ◽  
pp. 167-174
Author(s):  
Jiri Cermak ◽  
Lubomir Kral

Mg-rich alloys of the binary system Mg-Ni are prospective hydrogen-storage materials. In the present study, desorption characteristics of hydrided Mg2Ni intermetalic and hydrided Mg/Mg2Ni eutectic mixture were investigated. Structure of experimental materials during the hydrogenation was observed by SEM. Three modifications of (Mg2Ni)Hx (x ~ 4) were prepared differing in the ratio of two low-temperature phases f = LT2/LT1: with (i) f >1, (ii) f ~ 1 and with (iii) f <1. Evolution of the ratio f during hydrogen desorption was checked by XRD. It was found that the micro-twinned phase LT2 is not desirable in hydrogen-storage materials containing Mg2Ni intermetallic. Diffusion coefficient of hydrogen in LT2 is about 20 times lower than in LT1.


Rare Metals ◽  
2020 ◽  
Author(s):  
Xiao-Sheng Liu ◽  
Hai-Zhen Liu ◽  
Ning Qiu ◽  
Yan-Bing Zhang ◽  
Guang-Yao Zhao ◽  
...  

Author(s):  
G. G. Shaw

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.


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