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:聂祚仁[1,2] 左铁镛[1,2] 周美玲[1,2] 王亦曼[1,2] 王金淑[1,2] 张久兴[1,2]
机构地区:[1]北京工业大学材料科学与工程学院 [2]北京真空电子技术研究所
出 处:《中国稀土学报》1999年第2期135-139,共5页Journal of the Chinese Society of Rare Earths
基 金:国家重点基础研究专项基金
摘 要:对稀土氧化物体系La2O3中O1s的超高温原位XPS进行研究,着重讨论了MoLa2O3阴极激活过程中温度变化导致表面氧状态改变的过程,并初步分析其对电子发射性能的影响。高温1300℃以上,存在两类不同氧种的氧,低结合能端(Eb=53000eV)的氧是表面晶格氧,高结合能端(Eb=53200eV)的氧为吸附氧;大量的高温吸附氧应是La2O3中晶格氧分离造成。The acitivation processes of MoLa2O3 model cathode specimens were systematically investigated with insitu high temperature XPS/AES analyses. The oxygen species produced during the processes were characterized at different temperature. The results show that there exist two kinds of oxygen ions after activation(above 1300 ), the surface lattice oxygen with lower binding energy(Eb=53000 eV) and the adsorbed oxygen with higher binding energy(Eb=53200 eV) which should be dissociated from the lattice oxygen of La2O3. It may be concluded that La2O3 is partly reduced to LaOx(x<3/2) with the dissociation of lattice oxygen. And the oxygen may play a favorable or unfavorable role to emission depending upon its relative quantity and relative position in the surface adsorption.
关 键 词:稀土 氧化镧 钼 热阴极 电子发射 真空阴极材料
分 类 号:TN103[电子电信—物理电子学]
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:216.73.216.145