用先磁控溅射多层金属膜预置层后硫化的方法成功制备出CZGe_xT_(1-x)S薄膜,并主要研究了Ge含量对于该薄膜光电学性能的影响。分别采用X射线衍射仪、X射线能量色散谱仪、拉曼光谱仪、扫描电子显微镜,紫外-可见-近红外分光光度计和霍尔效...用先磁控溅射多层金属膜预置层后硫化的方法成功制备出CZGe_xT_(1-x)S薄膜,并主要研究了Ge含量对于该薄膜光电学性能的影响。分别采用X射线衍射仪、X射线能量色散谱仪、拉曼光谱仪、扫描电子显微镜,紫外-可见-近红外分光光度计和霍尔效应测量仪对不同Ge含量的CZGe_xT_(1-x)S薄膜的物相结构、元素比例、表面形貌、光学带隙以及电学性能进行了表征与分析。结果表明随着Ge含量的升高,晶粒尺寸不断长大,光学带隙从1.52上升至2.12 e V。同时,Ge替换Sn可减少薄膜内的缺陷,所制备的CZGe S薄膜的载流子浓度与迁移率分别为1.99×1018cm-3与9.712 cm2/Vs。展开更多
Roman scattering measurement of ( 1 - x ) GeS2-x Ga2S3 system glasses was conducted in order to understand the microstructural change caused by the addition of Ga2S3 . According to the change of Raman spectra with t...Roman scattering measurement of ( 1 - x ) GeS2-x Ga2S3 system glasses was conducted in order to understand the microstructural change caused by the addition of Ga2S3 . According to the change of Raman spectra with the addition of Ga2S3, two main structural transformations were deduced : the gradual enhancement of ethane- like structural units S3 Ge- GeS3 ( 250 cm ^- 1) and S3 Ga- GaS3 (270 cm ^- 1 ) and the appearance of charge imbalanced units [ Ga2 S2 ( S1/2 )4 ]^2- and [Ga( S1/2 )4 ]^- . And this change of structural aspect seems to give as a clue to understanding the cause of the increased rare-earth solubility.展开更多
文摘用先磁控溅射多层金属膜预置层后硫化的方法成功制备出CZGe_xT_(1-x)S薄膜,并主要研究了Ge含量对于该薄膜光电学性能的影响。分别采用X射线衍射仪、X射线能量色散谱仪、拉曼光谱仪、扫描电子显微镜,紫外-可见-近红外分光光度计和霍尔效应测量仪对不同Ge含量的CZGe_xT_(1-x)S薄膜的物相结构、元素比例、表面形貌、光学带隙以及电学性能进行了表征与分析。结果表明随着Ge含量的升高,晶粒尺寸不断长大,光学带隙从1.52上升至2.12 e V。同时,Ge替换Sn可减少薄膜内的缺陷,所制备的CZGe S薄膜的载流子浓度与迁移率分别为1.99×1018cm-3与9.712 cm2/Vs。
文摘Roman scattering measurement of ( 1 - x ) GeS2-x Ga2S3 system glasses was conducted in order to understand the microstructural change caused by the addition of Ga2S3 . According to the change of Raman spectra with the addition of Ga2S3, two main structural transformations were deduced : the gradual enhancement of ethane- like structural units S3 Ge- GeS3 ( 250 cm ^- 1) and S3 Ga- GaS3 (270 cm ^- 1 ) and the appearance of charge imbalanced units [ Ga2 S2 ( S1/2 )4 ]^2- and [Ga( S1/2 )4 ]^- . And this change of structural aspect seems to give as a clue to understanding the cause of the increased rare-earth solubility.