Yusa Hitoshi, Tsuchiya Taku, Sata Nagayoshi, Ohishi Yasuo
Advanced Nano Materials Laboratory (ANML), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba 305-0044, Japan.
Inorg Chem. 2009 Aug 17;48(16):7537-43. doi: 10.1021/ic9001253.
In situ X-ray diffraction experiments using a laser-heated diamond anvil cell revealed a novel dense phase with the Gd(2)S(3) structure stabilizing in Sc(2)O(3) at pressures over 19 GPa. Although no phase transformation was induced during room-temperature compression up to 31 GPa, the C rare earth sesquioxide structure transformed into the B rare earth sesquioxide structure at 10 GPa after laser annealing and subsequently into the Gd(2)S(3) structure at 19 GPa. Neither the A rare earth sesquioxide structure nor the U(2)S(3) structure was found in Sc(2)O(3). Static density functional lattice energy calculations demonstrated that the C structure prefers Gd(2)S(3) over U(2)S(3) as the post phase. Sc(2)O(3) is the second sesquioxide, after In(2)O(3), to crystallize into a Gd(2)S(3) structure at high pressures and high temperatures.
利用激光加热金刚石对顶砧池进行的原位X射线衍射实验表明,在压力超过19吉帕时,具有Gd₂S₃结构的新型致密相在Sc₂O₃中稳定存在。尽管在室温下压缩至31吉帕的过程中未引发相变,但激光退火后,C型稀土三氧化物结构在10吉帕时转变为B型稀土三氧化物结构,随后在19吉帕时转变为Gd₂S₃结构。在Sc₂O₃中未发现A型稀土三氧化物结构和U₂S₃结构。静态密度泛函晶格能计算表明,作为后续相,C结构相比于U₂S₃更倾向于Gd₂S₃。Sc₂O₃是继In₂O₃之后,第二种在高温高压下结晶为Gd₂S₃结构的三氧化物。