Enhanced hydrogen generation by solid-state thermal decomposition of NaNH2–NaBH4 composite promoted with Mg–Co–B catalyst

2017 ◽  
Vol 32 (6) ◽  
pp. 1203-1209 ◽  
Author(s):  
Ying Bai ◽  
Zi-wei Pei ◽  
Feng Wu ◽  
Jian-hu Yang ◽  
Chuan Wu

Abstract

MRS Bulletin ◽  
1994 ◽  
Vol 19 (11) ◽  
pp. 28-30 ◽  
Author(s):  
C.N.R. Rao ◽  
Ram Seshadri

By virtue of their unique structures, fullerenes exhibit novel chemical transformations. Particularly pertinent to this article are the interesting properties exhibited by fullerenes in the solid state. These molecules are spherical or near-spherical in shape. Molecules with high point-group symmetry, which are not bound strongly in the solid state, tend to crystallize into structures with long-range periodicity of the molecular centers of mass, but the molecular orientations are random or even dynamically disordered. When dynamically disordered, themolecules rotate about some preferred axis. C60 and C70 satisfy the criteria for such orientationally disordered solids and exhibit rich phase behavior in the solid state. Since C60 has high electron affinity, it forms anion salts with alkali and alkaline-earth metals as well as with strong organic donor molecules. With tetrakis dimethylaminoethylene (TDAE), which is a very powerful electron donor, C60 forms a 1:1 solid that is ferromagnetic. C60-TDAE is the molecular organic ferromagnet with the highest Tc (of 16 K) known to date. Some of the alkali and alkaline-earth fullerides, on the other hand, show superconductivity, with transition temperatures going up to 33K. We shall briefly examine some of these solid-state properties.


2015 ◽  
Vol 245 ◽  
pp. 86-92 ◽  
Author(s):  
O.V. Netskina ◽  
A.M. Ozerova ◽  
O.V. Komova ◽  
G.V. Odegova ◽  
V.I. Simagina

2006 ◽  
Vol 41 (12) ◽  
pp. 2219-2225 ◽  
Author(s):  
K.G. Kanade ◽  
Jin-OoK Baeg ◽  
U.P. Mulik ◽  
D.P. Amalnerkar ◽  
B.B. Kale

2020 ◽  
Vol 73 (8) ◽  
pp. 794
Author(s):  
Aliyu M. Ja'o ◽  
Derek A. Wann ◽  
Conor D. Rankine ◽  
Matthew I. J. Polson ◽  
Sarah L. Masters

The molecular structure of morpholine borane complex has been studied in the solid state and gas phase using single-crystal X-ray diffraction, gas electron diffraction, and computational methods. Despite both the solid-state and gas-phase structures adopting the same conformation, a definite decrease in the B–N bond length of the solid-state structure was observed. Other structural variations in the different phases are presented and discussed. To explore the hydrogen storage potential of morpholine borane, the potential energy surface for the uncatalyzed and BH3-catalyzed pathways, as well as the thermochemistry for the hydrogen release reaction, were investigated using accurate quantum chemical methods. It was observed that both the catalyzed and uncatalyzed dehydrogenation pathways are favourable, with a barrier lower than the B–N bond dissociation energy, thus indicating a strong propensity for the complex to release a hydrogen molecule rather than dissociate along the B–N bond axis. A minimal energy requirement for the dehydrogenation reaction has been shown. The reaction is close to thermoneutral as demonstrated by the calculated dehydrogenation reaction energies, thus implying that this complex could demonstrate potential for future on-board hydrogen generation.


MRS Bulletin ◽  
2018 ◽  
Vol 43 (10) ◽  
pp. 775-781 ◽  
Author(s):  
Fang Hao ◽  
Fudong Han ◽  
Yanliang Liang ◽  
Chunsheng Wang ◽  
Yan Yao

Abstract


2019 ◽  
Vol 4 (28) ◽  
pp. 8365-8371
Author(s):  
José Pérez ◽  
José L. Serrano ◽  
Gregorio Sánchez ◽  
Pedro Lozano ◽  
Ivan da Silva ◽  
...  

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