立方氮化硼单晶-金刚石薄膜异质p-n结

 在Si中掺杂N型片状立方氮化硼单晶的(111)面上,利用热灯丝化学气相沉积方法生长了掺B的p型金刚石薄膜,从而制得了立方氮化硼单晶-金刚石薄膜异质p-n结,测试了该p-n结的V-A特性,结果表明其整流特性良好。     

High pressure electrical transport behavior in SrF_2 nanoplates

The charge transport behavior of strontium fluoride nanocrystals has been investigated by in situ impedance measurement up to 35 GPa.It was found that the parameters changed discontinuously at each phase transition.The charge carriers in SrF_2 nanocrystals include both F~-ions and electrons.In the Fm3 m phase,pressure makes the electronic transport easier,while makes it more difficult in the Pnma phase.The defects at grain boundaries dominate the electronic transport process.Pressure could make the charge-discharge processes in the Fm3 m phase much easier,but make it more difficult in the Pnma phase.     

Effects of high pressure on the Raman and fluorescence emission spectra of two novel 1,3,4-oxadiazole derivatives

The effects of pressure on the fluorescence emission and Raman spectra of 1,4-bis[（4-methyloxyphenyl）-1,3,4-oxadiazolyl]- 2,5-bisheptyloxyphenylene （OXD-2） and on the fluorescence emission spectra of 1,4-bis[（4-methylphenyl）- 1,3,4-oxadiazolyl]phenylene （OXD-1） are investigated using a diamond anvil cell. With the increase of pressure, the intensity of the fluorescence emission increases and reaches maxima at 13GPa for OXD-1 and at 9.6GPa for OXD-2. The effect of pressure on the peak position of the emission shows a similar trend, red shift with the increase of pressure. But at higher pressures, the intensity of emission drops down dramatically. The Raman spectra of OXD-2 indicate that there appears a structural change at ca 3GPa.     

Structural Phase Transformations of ZnS Nanocrystalline Under High Pressure

In-situ energy dispersive x-ray diffraction on ZnS nanocrystalline was carried out under high pressure by using a diamond anvil cell. Phase transition of wurtzite of 10nm ZnS to rocksalt occurred at 16.0GPa, which was higher than that of the bulk materials. The structures of ZnS nanocrystalline at different pressures were built by using materials studio and the bulk modulus, and the pressure derivative of ZnS nanocrystalline were derived by fitting the equation of Birch-Murnaghan. The resulting modulus was higher than that of the corresponding bulk material, which indicates that the nanomaterial has higher hardness than its bulk materials.     

不同粒径纳米晶硫化锌的高压结构相变研究

 应用原位能量色散X射线散射和金刚石对顶砧技术，对纳米晶ZnS进行了高压结构相变研究。初始相为纤锌矿结构的10 nm和3 nm硫化锌分别在16.0 GPa和16.7 GPa时转变为岩盐矿结构，相变压力均高于纤锌矿结构的体材料硫化锌。该相变为一可逆的结构相变。应用大型科学计算软件Materials Studio（MS）计算了纳米晶ZnS的状态方程，根据Birch-Murnaghan方程拟合了纳米晶ZnS的零压体模量，得到的零压体模量高于相应体材料的零压体模量，表明纳米晶ZnS较难压缩。     

氧化镓的同步辐射研究

 利用金刚石对顶砧（DAC）高压装置产生高压，使用体积比为16∶3∶1的甲醇、乙醇和水混合液作为传压介质，通过原位高压同步辐射技术对氧化镓的高压行为进行了研究（0～42.5 GPa）。实验发现在室温下13.3 GPa压力附近，单斜结构的氧化镓发生了结构相变，变成三角结构。相变后镓离子由原来同时位于由氧离子围成的四面体和八面体的中心位置变成只位于八面体的中心位置。卸压后的X射线衍射谱表明，氧化镓又恢复为单斜结构，该相变为可逆相变。     

Phase Transition Behavior of LiCr 0.35 Mn0.65O2 under High Pressure by Electrical Conductivity Measurement

The electrical conductivity of powdered LiCr 0.35 Mn0.65O2 is measured under high pressure up to 26.22 GPa in the temperature range 300-413 K by using a diamond anvil cell. It is found that both conductivity and activation enthalpy change discontinuously at 5.36 GPa and 21.66 GPa. In the pressure range 1.10-5.36 GPa, pressure increases the activation enthalpy and reduces the carrier scattering, which finally leads to the conductivity increase. In the pressure ranges 6.32-21.66 GPa and 22.60-26.22 GPa, the activation enthalpy decreases with pressure increasing, which has a positive contribution to electrical conductivity increase. Two pressure-induced structural phase transitions are found by in-situ x-ray diffraction under high pressure, which results in the discontinuous changes of conductivity and activation enthalpy.     

高温高压下β相硼的电导率测量

 硼在高压下具有复杂的结构和多样的物理性质,对其结构和性质的深入研究具有很重要的意义,一直引起理论和实验研究领域的关注。高压下进行电学性质测量是获得物质物理性质的有效手段,利用集成在金刚石对顶砧上的微电路,在高压下和两个不同温度范围内对β相硼进行了电导率测量,分析了导电机制随压力的变化规律。在0～28.1 GPa范围内,β相硼的电导率随着压力的增大是逐渐增大的,卸压后样品的电导率不能回到最初的状态,是一个不可逆的变化过程;由室温到423 K的范围内,β硼的电导率随着温度的不断增加有明显的上升趋势,并且随着压力的升高,电导率变化逐渐加快。此外,对样品在14.5 GPa和18.6 GPa压力下,用溅射到金刚石对顶砧上的氧化铝薄膜做绝热层,对样品进行了激光加热实验,最高温度达到2 224 K,电导率随着温度的上升而增大,结果显示,β相硼的电学特征仍然属于半导体的特征范围内。     

利用电导率测量方法研究不同粒径ZnS高压相变过程

利用在金刚石对顶砧上集成的金属电极,对不同粒径的ZnS材料进行了高压原位电导率测量. 粒径为2 μm的体材料ZnS在15 GPa时,电导率迅速增大5个数量级,表明体材料ZnS此时发生了从闪锌矿到岩盐矿的结构相变. 而粒径6 nm的纳米材料ZnS的结构相变压力为21 GPa. 电导率测量结果还表明纳米 ZnS比体材料ZnS还具有更宽的迟滞区间.     

金刚石对顶砧原位电导率测量系统

 在金刚石对顶砧中进行原位高温高压电阻测量时,由于受到绝热层的限制,从而达不到理想的温度条件。采用普通的粉末绝热材料,会给电极的引入造成很大困难,而且不规则的电阻丝使电阻测量很难精确量化。利用溅射镀膜方法,在对顶砧的砧面上镀氧化铝膜作绝热层,溅射的金属钼膜作电极材料,成功地完成了高温高压条件下原位电阻的测量。利用此装置,测量了铁镁硅酸盐(Mg_0.875,Fe_0.125)₂SiO₄在高温高压环境下（31~35 GPa,1 500~3 400 K）的电导率,得到了样品的导电粒子激活能,发现其激活能随着压强的升高而增大,与低压低温（小于15 GPa,低于1 200 K）条件相比,其激活体积和激活能都明显减小。