Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005, China.
Proc Natl Acad Sci U S A. 2011 Jun 28;108(26):10410-4. doi: 10.1073/pnas.1107464108. Epub 2011 Jun 13.
Ge(2)Sb(2)Te(5) (GST) is a technologically very important phase-change material that is used in digital versatile disks-random access memory and is currently studied for the use in phase-change random access memory devices. This type of data storage is achieved by the fast reversible phase transition between amorphous and crystalline GST upon heat pulse. Here we report pressure-induced reversible crystalline-amorphous and polymorphic amorphous transitions in NaCl structured GST by ab initio molecular dynamics calculations. We have showed that the onset amorphization of GST starts at approximately 18 GPa and the system become completely random at approximately 22 GPa. This amorphous state has a cubic framework (c-amorphous) of sixfold coordinations. With further increasing pressure, the c-amorphous transforms to a high-density amorphous structure with trigonal framework (t-amorphous) and an average coordination number of eight. The pressure-induced amorphization is investigated to be due to large displacements of Te atoms for which weak Te-Te bonds exist or vacancies are nearby. Upon decompressing to ambient conditions, the original cubic crystalline structure is restored for c-amorphous, whereas t-amorphous transforms to another amorphous phase that is similar to the melt-quenched amorphous GST.
碲化锗锑(GST)是一种非常重要的技术相变材料,用于数字通用磁盘随机存取存储器,目前正在研究用于相变随机存取存储器设备。这种数据存储是通过在热脉冲作用下 GST 非晶态和晶态之间的快速可逆相转变来实现的。在这里,我们通过从头算分子动力学计算报告了 NaCl 结构 GST 中压致可逆的晶态-非晶态和多晶非晶转变。我们已经表明,GST 的非晶化起始于大约 18 GPa,并且系统在大约 22 GPa 时完全变成随机状态。这种非晶态具有六配位的立方框架(c-非晶态)。随着压力的进一步增加,c-非晶态转变为具有三角框架(t-非晶态)和八配位的高密度非晶结构。压致非晶化是由于 Te 原子的大位移引起的,其中存在较弱的 Te-Te 键或附近有空位。在减压至环境条件下,c-非晶态恢复为原始的立方晶态,而 t-非晶态转变为另一种与熔体淬火非晶态 GST 相似的非晶相。