对B+注入的n on p平面结和分子束外延 (MBE)技术原位铟掺杂的n+ n p台面异质结的碲镉汞 (HgCdTe)长波光伏探测器暗电流进行了对比分析 .与n on p平面结器件相比 ,原位掺杂的n+ n p台面异质结器件得到较高的零偏动态阻抗 面积值 (R0 A) ...对B+注入的n on p平面结和分子束外延 (MBE)技术原位铟掺杂的n+ n p台面异质结的碲镉汞 (HgCdTe)长波光伏探测器暗电流进行了对比分析 .与n on p平面结器件相比 ,原位掺杂的n+ n p台面异质结器件得到较高的零偏动态阻抗 面积值 (R0 A) .通过与实验数据拟合 ,从理论上计算了这两种结构的器件在不同温度下的R0 A和在不同偏压下的暗电流 。展开更多
Preparation of a high flux of hydrogen molecules in a specific vibrationally excited state is the major prerequisite and challenge in scattering experiments that use vibrationally excited hydrogen molecules as the tar...Preparation of a high flux of hydrogen molecules in a specific vibrationally excited state is the major prerequisite and challenge in scattering experiments that use vibrationally excited hydrogen molecules as the target. The widely used scheme of stimulated Raman pumping suffers from coherent population return which severely limits the excitation efficiency. Re- cently we successfully transferred D2 molecules in the molecular beam from （v=0, J=0） to （v=1, J=0） level, with the scheme of Stark-induced adiabatic Raman passage. As high as 75% of the excitation efficiency was achieved. This excitation technique promise to be a unique tool for crossed beam and beam-surface scattering experiments which aim to reveal the role of vibrational excitation of hydrogen molecules in the chemical reaction.展开更多
文摘对B+注入的n on p平面结和分子束外延 (MBE)技术原位铟掺杂的n+ n p台面异质结的碲镉汞 (HgCdTe)长波光伏探测器暗电流进行了对比分析 .与n on p平面结器件相比 ,原位掺杂的n+ n p台面异质结器件得到较高的零偏动态阻抗 面积值 (R0 A) .通过与实验数据拟合 ,从理论上计算了这两种结构的器件在不同温度下的R0 A和在不同偏压下的暗电流 。
文摘Preparation of a high flux of hydrogen molecules in a specific vibrationally excited state is the major prerequisite and challenge in scattering experiments that use vibrationally excited hydrogen molecules as the target. The widely used scheme of stimulated Raman pumping suffers from coherent population return which severely limits the excitation efficiency. Re- cently we successfully transferred D2 molecules in the molecular beam from （v=0, J=0） to （v=1, J=0） level, with the scheme of Stark-induced adiabatic Raman passage. As high as 75% of the excitation efficiency was achieved. This excitation technique promise to be a unique tool for crossed beam and beam-surface scattering experiments which aim to reveal the role of vibrational excitation of hydrogen molecules in the chemical reaction.
