The microstrain-accompanied structural phase transition from h-MoO₃ to α-MoO₃ investigated by in situ X-ray diffraction

• Zeqian Zhang,
• Honglong Shi,
• Boxiang Zhuang,
• Minting Luo and
• Zhenfei Hu

Beilstein J. Nanotechnol. 2023, 14, 692–700, doi:10.3762/bjnano.14.55

• Sciences, Beijing, 100190, China 10.3762/bjnano.14.55 Abstract In situ X-ray diffraction indicates that the structural phase transition from h-MoO3 to α-MoO3 is a first-order transition with a phase transition temperature range of 378.5–443.1 °C. The linear coefficients of thermal expansion of h-MoO3 are

• α-MoO3 is still unclear. Here, to reveal the features of the structural phase transition from h-MoO3 to α-MoO3, we performed in situ X-ray diffraction experiments at temperatures ranging from 30 to 450 °C. The Rietveld refinement results indicate water molecules at the (0 0 0.25) site inside the

• α-MoO3 To observe the crystal structure evolution of h-MoO3 induced by temperature, a thoroughly powdered sample was used to perform in situ X-ray diffraction measurements during heating from 30 to 450 °C, as shown in Figure 1a. At 30 °C, all diffraction peaks can be well indexed to the hexagonal

On the transformation of “zincone”-like into porous ZnO thin films from sub-saturated plasma enhanced atomic layer deposition

• Alberto Perrotta,
• Julian Pilz,
• Stefan Pachmajer,
• Antonella Milella and
• Anna Maria Coclite

Beilstein J. Nanotechnol. 2019, 10, 746–759, doi:10.3762/bjnano.10.74

• is targeted, since its crystal growth and texture affect the optical and (piezo)electrical properties of the material [64][65][66]. The crystallinity of the pristine zincone-like layers and its evolution during and after calcination were monitored using in situ X-ray diffraction (XRD) and grazing

Hydrogen-induced plasticity in nanoporous palladium

• Markus Gößler,
• Eva-Maria Steyskal,
• Markus Stütz,
• Norbert Enzinger and
• Roland Würschum

Beilstein J. Nanotechnol. 2018, 9, 3013–3024, doi:10.3762/bjnano.9.280

• introduction. In situ X-ray diffraction experiments pointed towards a reduced lattice constant for PdHα [38] when it appeared again during desorption. In the course of the desorption-induced phase transition the lattice constant of the α-phase increases with the growing amount of PdHα (lattice-constant

Vapor-phase-synthesized fluoroacrylate polymer thin films: thermal stability and structural properties

• Paul Christian and
• Anna Maria Coclite

Beilstein J. Nanotechnol. 2017, 8, 933–942, doi:10.3762/bjnano.8.95

• homopolymer, but does not lead to the formation of crystalline domains in the cross-linked films. Likely, with a lower cross-linker fraction, some degree of crystallinity might be preserved. To gain further insight into the thermally induced structural changes of p-PFDA films, in situ X-ray diffraction

• are shifted along the y-axis (intensity). (b) Temperature-dependent in situ X-ray diffraction measurements of crystalline p-PFDA at a rate of 2 °C/min, with Tm and Tc denoting the onset of melting and of crystallisation at 76 and 69 °C, respectively. In situ spectroscopic ellipsometry data depicting

In situ observation of deformation processes in nanocrystalline face-centered cubic metals

• Aaron Kobler,
• Christian Brandl,
• Horst Hahn and
• Christian Kübel

Beilstein J. Nanotechnol. 2016, 7, 572–580, doi:10.3762/bjnano.7.50

• File 1, Figure S11a). Previous in situ X-ray diffraction studies revealed reversible diffraction peak broadening in a loading–unloading cycle in NC Ni, which indicates the suppression of a build-up of a residual dislocation network during deformation in the nanograins [30]. Here the accumulation of

Manganese oxide phases and morphologies: A study on calcination temperature and atmospheric dependence

• Matthias Augustin,
• Daniela Fenske,
• Ingo Bardenhagen,
• Anne Westphal,
• Martin Knipper,
• Thorsten Plaggenborg,
• Joanna Kolny-Olesiak and
• Jürgen Parisi

Beilstein J. Nanotechnol. 2015, 6, 47–59, doi:10.3762/bjnano.6.6

• the different manganese oxides via one route facilitates assigning actual structure–property relationships. The oxidation process related to the different MnOx species was observed by in situ X-ray diffraction (XRD) measurements showing time- and temperature-dependent phase transformations occurring

• performance for the mesoporous α-Mn2O3 species. Keywords: electrocatalytic activity; in situ X-ray diffraction; manganese glycolate; manganese oxide nanoparticles; mesoporous α-Mn2O3; Introduction Manganese oxides are a class of inexpensive compounds with a high potential for nanostructuring, which makes