The Study of Crystallization Process of As-deposited Amorphous Phase Change Materials by in-situ Annealing Experiments

2003 ◽  
Author(s):  
Zhaohui Fan ◽  
Lisha Wang ◽  
Yingguo Peng ◽  
Noel T. Nuhfer ◽  
David E. Laughlin ◽  
...  
2003 ◽  
Author(s):  
Zhaohui Fan ◽  
Lisha Wang ◽  
Yingguo Peng ◽  
Noel T. Nuhfer ◽  
David E. Laughlin ◽  
...  

2018 ◽  
Vol 51 (6) ◽  
pp. 1691-1705 ◽  
Author(s):  
Frédéric Fillot ◽  
Chiarra Sabbione ◽  
François Pierre ◽  
Françoise Hippert ◽  
Pierre Noé

The phase change from the amorphous to crystalline state which occurs upon thermal annealing in prototypical Ge2Sb2Te5 and nitrogen-doped Ge2Sb2Te5 phase-change-materials (PCM) thin films is studied by concomitant, complementary and combined in situ and ex situ X-ray diffraction (XRD) and X-ray reflectivity (XRR) techniques. It is demonstrated that combined in situ X-ray scattering techniques allow accurate investigation and clarification of the structural, morphological and mechanical variations occurring in the films upon crystallization. The crystallization process is correlated with volume shrinkage (densification and thickness reduction) and with structural change with a tensile strain build-up. The comparison of Ge2Sb2Te5 and nitrogen-doped Ge2Sb2Te5 reveals a significant slowdown of the crystallization process, induced by the incorporation of nitrogen. However, the mechanisms involved in the phase change are not strongly modified by the incorporation; rather, the crystallization process is inhibited because of the presence of nitrogen. In this way, different stages of the crystallization process can be observed. The combined XRD/XRR analysis gives new insights on the stress components built up in phase-change materials. First, at the early stage of crystallization, a large hydrostatic tensile stress builds up in the PCM thin film. Afterwards, concomitant grain growth, viscous flow, densification and thickness accommodation are observed, which lead to a partial stress relaxation in the PCM films. This combined characterization technique offers a new approach that may further our understanding of the phase change involved.


2013 ◽  
Vol 815 ◽  
pp. 367-370 ◽  
Author(s):  
Xiao Qiu Song ◽  
Yue Xia Li ◽  
Jing Wen Wang

Hexadecane microcapsule phase change materials were prepared by the in-situ polymerization method using hexadecane as core materials, urea-formaldehyde resin and urea-formaldehyde resin modified with melamine as shell materials respectively. Effect of melamine on the properties of microcapsules was studied by FTIR, biomicroscopy (UBM), TGA and HPLC. The influences of system concentration, agitation speed and mass ratio of wall to core were also investigated. The results indicated that hexadecane was successfully coated by the two types of shell materials. The addition of melamine into the urea-formaldehyde resin microcapsule reduced microcapsule particle size and microencapsulation efficiency. The influences of factors such as system concentration, agitation speed and mass ratio of wall to core to different wall materials microcapsules presented different variety trends of the microcapsule particle size.


2015 ◽  
Vol 118 (13) ◽  
pp. 135707 ◽  
Author(s):  
Matthias Kaes ◽  
Manuel Le Gallo ◽  
Abu Sebastian ◽  
Martin Salinga ◽  
Daniel Krebs

2020 ◽  
Vol 6 (2) ◽  
pp. eaay6726 ◽  
Author(s):  
Si-Xu Peng ◽  
Yudong Cheng ◽  
Julian Pries ◽  
Shuai Wei ◽  
Hai-Bin Yu ◽  
...  

Relaxation processes are decisive for many physical properties of amorphous materials. For amorphous phase-change materials (PCMs) used in nonvolatile memories, relaxation processes are, however, difficult to characterize because of the lack of bulk samples. Here, instead of bulk samples, we use powder mechanical spectroscopy for powder samples to detect the prominent excess wings—a characteristic feature of β-relaxations—in a series of amorphous PCMs at temperatures below glass transitions. By contrast, β-relaxations are vanishingly small in amorphous chalcogenides of similar composition, which lack the characteristic features of PCMs. This conclusion is corroborated upon crossing the border from PCMs to non-PCMs, where β-relaxations drop substantially. Such a distinction implies that amorphous PCMs belong to a special kind of covalent glasses whose locally fast atomic motions are preserved even below the glass transitions. These findings suggest a correlation between β-relaxation and crystallization kinetics of PCMs, which have technological implications for phase-change memory functionalities.


2013 ◽  
Vol 28 (9) ◽  
pp. 1139-1147 ◽  
Author(s):  
Jennifer Luckas ◽  
Daniel Krebs ◽  
Stephanie Grothe ◽  
Josef Klomfaß ◽  
Reinhard Carius ◽  
...  

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