Abstract:The dehydrogenated microstructure of the lithium borohydride-yttrium hydride (LiBH4-YH3) composite obtained at 350°C under 0.3 MPa of hydrogen and static vacuum was investigated by transmission electron microscopy combined with a focused ion beam technique. The dehydrogenation reaction between LiBH4 and YH3 into LiH and YB4 takes place under 0.3 MPa of hydrogen, which produces YB4 nano-crystallites that are uniformly distributed in the LiH matrix. This microstructural feature seems to be beneficial for rehydro… Show more
“…These mostly amorphous higher borane byproducts are quite stable thermodynamically, and they seem to be more difficult to rehydrogenate than the competing metal borides. Another issue is the influence of the hydrogen back/partial pressure on the formation of the dodecaboranes instead of metal borides [231][232][233]. When the dehydrogenation reaction occurs below a critical hydrogen partial pressure at a given temperature, it tends to form dodecaborane, which seems not to readily react with the metal hydrides to form metal borides.…”
The research on complex hydrides for hydrogen storage was initiated by the discovery of Ti as a hydrogen sorption catalyst in NaAlH 4 by Boris Bogdanovic in 1996. A large number of new complex hydride materials in various forms and combinations have been synthesized and characterized, and the knowledge regarding the properties of complex hydrides and the synthesis methods has grown enormously since then. A significant portion of the research groups active in the field of complex hydrides is collaborators in the International Energy Agreement Task 32. This paper reports about the important issues in the field of complex hydride research, i.e. the synthesis of borohydrides, the thermodynamics of complex hydrides, the effects of size and confinement, the hydrogen sorption mechanism and the complex hydride composites as well as the properties of liquid complex hydrides. This paper is the result of the collaboration of several groups and is an excellent summary of the recent achievements.
“…These mostly amorphous higher borane byproducts are quite stable thermodynamically, and they seem to be more difficult to rehydrogenate than the competing metal borides. Another issue is the influence of the hydrogen back/partial pressure on the formation of the dodecaboranes instead of metal borides [231][232][233]. When the dehydrogenation reaction occurs below a critical hydrogen partial pressure at a given temperature, it tends to form dodecaborane, which seems not to readily react with the metal hydrides to form metal borides.…”
The research on complex hydrides for hydrogen storage was initiated by the discovery of Ti as a hydrogen sorption catalyst in NaAlH 4 by Boris Bogdanovic in 1996. A large number of new complex hydride materials in various forms and combinations have been synthesized and characterized, and the knowledge regarding the properties of complex hydrides and the synthesis methods has grown enormously since then. A significant portion of the research groups active in the field of complex hydrides is collaborators in the International Energy Agreement Task 32. This paper reports about the important issues in the field of complex hydride research, i.e. the synthesis of borohydrides, the thermodynamics of complex hydrides, the effects of size and confinement, the hydrogen sorption mechanism and the complex hydride composites as well as the properties of liquid complex hydrides. This paper is the result of the collaboration of several groups and is an excellent summary of the recent achievements.
“…We first tested nanoparticle opals [30] as a model of a solid undeformable object for the encapsulation [31] . A diluted solution of polystyrene nanoparticles (1 μm in diameter) was drop cast and dried on a cover glass pre-coated with Au film (Figure 3a).…”
Section: Resultsmentioning
confidence: 99%
“…Graphene oxide encapsulation of immiscible liquids on a solid substrate represents another interesting class of practically important deformable objects [31] demonstrating very different results as compared to encapsulated solid objects. As a model system, we used mercury that has poor wettability to most interfaces due to its high surface tension, leading to the well-known challenges in collecting toxic Hg spills.…”
Section: Resultsmentioning
confidence: 99%
“…Figure 9a shows an STEM image of E. coli bacteria on a 50 nm thick polyimide TEM grid encapsulated by graphene oxide (right panel) and uncovered (left panel). The central image comprises both encapsulated and non-encapsulated regions [31] . Figure 9d exemplifies our approach to fix and image a grass pollen in STEM mode.…”
We demonstrate a technique for facile encapsulation and adhesion of micro- and nano objects on arbitrary substrates, stencils, and micro structured surfaces by ultrathin graphene oxide membranes via a simple drop casting of graphene oxide solution. A self-assembled encapsulating membrane forms during the drying process at the liquid-air and liquid-solid interfaces and consists of a water-permeable quasi-2D network of overlapping graphene oxide flakes. Upon drying and interlocking between the flakes, the encapsulating coating around the object becomes mechanically robust, chemically protective, and yet highly transparent to electrons and photons in a wide energy range, enabling microscopic and spectroscopic access to encapsulated objects. The characteristic encapsulation scenarios were demonstrated on a set of representative inorganic and organic micro and nano-objects and microstructured surfaces. Different coating regimes can be achieved by controlling the pH of the supporting solution, and the hydrophobicity and morphology of interfaces. Several specific phenomena such as compression of encased objects by contracting membranes as well as hierarchical encapsulations were observed. Finally, electron as well as optical microscopy and analysis of encapsulated objects along with the membrane effect on the image contrast formation, and signal attenuation are discussed
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