Phase transitions in Ge–Te phase change materials studied by time-resolved x-ray diffraction

2009 ◽  
Vol 95 (14) ◽  
pp. 143118 ◽  
Author(s):  
Simone Raoux ◽  
Becky Muñoz ◽  
Huai-Yu Cheng ◽  
Jean L. Jordan-Sweet
2009 ◽  
Vol 1160 ◽  
Author(s):  
Simone Raoux ◽  
Cyril Cabral ◽  
Lia Krusin-Elbaum ◽  
Jean L. Jordan-Sweet ◽  
Martin Salinga ◽  
...  

AbstractThe crystallization behavior of Ge-Sb phase change materials with variable Ge:Sb ratio X between 0.079 and 4.3 was studied using time-resolved x-ray diffraction, differential scanning calorimetry, x-ray reflectivity, optical reflectivity and resistivity vs. temperature measurements. It was found that the crystallization temperature increases with Ge content from about 130 °C for X = 0.079 to about 450 °C for X = 4.3. For low X, Sb x-ray diffraction peaks occurred during a heating ramp at lower temperature than Ge diffraction peaks. For X = 1.44 and higher, Sb and Ge peaks occurred at the same temperature. Mass density change upon crystallization and optical and electrical contrast between the phases show a maximum for the eutectic alloy with X = 0.17. The large change in materials properties with composition allows tailoring of the crystallization properties for specific application requirements.


2021 ◽  
Vol 129 (9) ◽  
pp. 095102
Author(s):  
Ann-Katrin U. Michel ◽  
Felix Donat ◽  
Aurelia Siegfried ◽  
Olesya Yarema ◽  
Hanbing Fang ◽  
...  

2008 ◽  
Vol 1072 ◽  
Author(s):  
Yuan Zhang ◽  
Simone Raoux ◽  
Daniel Krebs ◽  
Leslie E. Krupp ◽  
Teya Topuria ◽  
...  

ABSTRACTPhase change nanodot arrays were fabricated using self-assembly diblock copolymer template PS-b-PMMA (polystyrene-poly (methyl-methacrylate)) and studied by time resolved X-ray diffraction. The size of the nanodots was less than 15nm in diameter with 40nm spacing. This method is quite flexible regarding the patterned materials, and can be used on different substrates. The crystallization behavior of small scale phase change nanodot arrays was studied for different materials, such as Ge15Sb85, Ge2Sb2Te5 and Ag and In doped Sb2Te. It was found that the nanodots had higher crystallization temperatures compared to their corresponding blanket films and crystallized over a broader temperature range.


1996 ◽  
Vol 20 (4) ◽  
pp. 469-482 ◽  
Author(s):  
Rumiana Tenchova ◽  
Boris Tenchov ◽  
Hans-JÜRgen Hinz ◽  
Peter J. Quinn

2004 ◽  
pp. 309-342 ◽  
Author(s):  
Hervé Cailleau ◽  
Eric Collet ◽  
Marylise Buron-Le Cointe ◽  
Marie-Hélène Lemée-Cailleau ◽  
Shin-ya Koshihara

2008 ◽  
Vol 1072 ◽  
Author(s):  
Simone Raoux ◽  
Jean L. Jordan-Sweet ◽  
Andrew J. Kellock

ABSTRACTWe have investigated the crystallization behavior of phase change materials as a function of their thickness. Thin films of variable thickness between 1 and 50nm of the phase change materials Ge2Sb2Te5 (GST), N-doped GST (N-GST), Ge15Sb85 (GeSb), Sb2Te, and Ag and In doped Sb2Te (AIST) were deposited by magnetron sputtering, and capped in situ by a 10nm thick Al2O3 film to prevent oxidation. The crystallization behavior of the films was studied using time-resolved X-ray diffraction. For each material we observed a constant crystallization temperature Tx that was comparable to bulk values for films thicker than 10 nm, and an increased Tx when the film thickness was reduced below 10 nm. The thinnest films that showed XRD peaks were 2 nm for GST and N-GST, 1.5 nm for Sb2Te and AgIn-Sb2Te, and 1.3 nm for GeSb. The observed increase in the phase transition temperature with reduced film thickness and the fact that very thin films still show clear phase change properties are indications that Phase Change Random Access Memory technology can be scaled down to several future technology nodes.


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