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Measurement of Photoelectron Behavior in K_4Ru(CN)_6 Doped AgCl Emulsion

机译:K_4Ru(CN)_6掺杂AgCl乳液中光电子行为的测量

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Photoelectron decay characteristics in latent image formation process directly reflect photographic efficiency of silver halide crystals. Dopants can be substitutionally incorporated into AgX crystals and influence the photoelectron action by introducing appropriate electron traps. Long photoelectron lifetime can improve the photographic efficiency of intrinsic or unsensitized grains. In general, AgCl are intrinsic or unsensitized emulsion. Cubic AgCl microcrystals doped with K_4Ru(CN)_6 were measured by microwave absorption and dielectric-spectrum technique. Measurement of the photoelectron decay process as a function of doping position and concentration can provide important information about the electronic properties. The experimental results show the photoelectron decay time at room temperature is more or less longer than undoped samples. The photoelectron decay time increases with the doping concentration increasing and with the doping position closer to the core except for position 30%Ag and over high concentration 3.21 X 10~(-5) mol/molAg. When doping position is 30%Ag, the photoelectron decay time reaches its maximum at the doping concentration of 1.5 X10~(-5) mol/molAg. At doping concentration 3.21 X10~(-5) mol/molAg, the photoelectron decay time reaches its maximum at the doping position 60%Ag. Through studying the photoelectron decay behavior, we can know the doping can improve the image quality of AgCl emulsion.
机译:潜像形成过程中的光电子衰减特性直接反映了卤化银晶体的照相效率。可以将掺杂剂替代地掺入AgX晶体中,并通过引入适当的电子陷阱来影响光电子作用。较长的光电子寿命可以提高本征或未感光颗粒的照相效率。通常,AgCl是本征或未敏化的乳液。通过微波吸收和介电谱技术测量了掺杂有K_4Ru(CN)_6的立方AgCl微晶。作为掺杂位置和浓度的函数的光电子衰减过程的测量可以提供有关电子性质的重要信息。实验结果表明,室温下的光电子衰减时间比未掺杂的样品更长或更短。除掺杂位置30%Ag和高浓度3.21 X 10〜(-5)mol / molAg外,光电子的衰变时间随掺杂浓度的增加和掺杂位置的靠近核心而增加。当掺杂位置为Ag的30%时,在1.5 X10〜(-5)mol / molAg的掺杂浓度下,光电子衰减时间达到最大值。在掺杂浓度为3.21 X10〜(-5)mol / molAg时,在60%Ag掺杂位置光电子衰减时间达到最大值。通过研究光电子的衰减行为,我们可以知道掺杂可以改善AgCl乳剂的图像质量。

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