检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:邓叶[1] 王晓东[2] 朱彦旭[1] 曹伟伟[1] 刘飞飞[1] 杜志娟[1] 于宁[1]
机构地区:[1]北京工业大学电控学院光电子技术实验室,北京100124 [2]中国人民武警部队学院基础部,河北廊坊065000
出 处:《光电子.激光》2014年第8期1511-1515,共5页Journal of Optoelectronics·Laser
基 金:国家自然科学基金(61107026;61204011);北京市自然科学基金(4112006);北京市教委科研计划(KM201210005004)资助项目
摘 要:为了更好实现ZnO材料在光电器件方面的应用,研究了Ag/Au和n-ZnO薄膜的欧姆接触。通过半导体特性分析系统测出欧姆接触的I-V特性曲线和采用挖补圆盘法测试了欧姆接触的接触电阻率,研究了退火温度对接触特性的影响。利用俄歇电子能谱(AES)研究了欧姆接触的微观结构,比较了不同的金属电极的反射特性。结果表明,Ag(50nm)/Au(100nm)和n-ZnO薄膜的欧姆接触在退火温度为500℃时最好,欧姆接触电阻率仅为5.2×10-4Ω·cm-2,且其反射特性比其它金属电极好。In order to realize the ZnO materials better in the application of the photoelectric devices, this paper studies the Ag/Au ohmic contact to n-ZnO thin films. Semiconductor characteristic analysis system is used to measure the I-V characteristic curve. Dig disc method is used to test the ohmic contact resistance rate. They reflect the influence of annealing temperature on the contact characteristics. Auger electron spectroscopy (AES) is used to study the microscopic structure of ohmic contact finally. The results show that Ag (50 nm)/Au (100 nm) ohmic contact to n-ZnO thin film is the best when annealing tem- perature is 500 ℃. The as-deposited Ag/Au scheme shows a specific contact resistivity of 2.3 × 10-2 Ω · cm-2. And the lowest specific contact resistivity is 5.2 × 10-4 Ω · cm-2. The specific contact resis- tivity shows a decreasing tendency with the annealing temperature up to 500 ℃. However, for the sample annealed above 600 ℃, the I-V curves reveal the characteristics of local bending,which shows rectifica- tion trends. Interface diffusions and reactions induced by annealing treatment are found to be responsible for the decrease of ohmic contact resistivity and the rectification trends. The reflection of Ag/Au charac- teristic is better than that with other metal depositions.
分 类 号:TN432.2[电子电信—微电子学与固体电子学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.49