铁电性
矫顽力
俘获
材料科学
兴奋剂
凝聚态物理
电场
极化(电化学)
去极化
电容器
电荷(物理)
电压
硅
光电子学
分析化学(期刊)
电介质
化学
电气工程
物理
内分泌学
物理化学
工程类
生物
医学
量子力学
色谱法
生态学
作者
Taehwan Jung,Jaemin Shin,Changhwan Shin
标识
DOI:10.1088/1361-6641/abbf0f
摘要
Abstract The shift of coercive voltage ( V c ) during cycling is investigated on ferroelectric (FE) silicon-doped hafnium oxide thin films with different (i) Si concentrations in HfO 2 , (ii) thickness of the ferroelectric layer ( T FE ), and (iii) thickness of the interface layer ( T IL ). We find that the depolarization field ( E dep ) and charge trapping are two major root-causes for the shift of coercive voltage. The increased remanent polarization ( P r ) with cycling of up to 10 5 causes a strong E dep , which leads to a higher voltage for polarization switching. On the other hand, the trapped charge improves the charge compensation, and then it suppresses the V c shift due to E dep : in the case of Si doping content, T FE , and T IL , the difference in the magnitude of V c increases by 4.5%, 0.5% and 3% while the difference in E dep increases by 5%, 8% and 15%, respectively. To investigate the rate of charge trapping, the defect band energy level is extracted by two-state NMP theory incorporated into a ‘Comphy’ tool. These results suggest that the strategy discussed above is a promising approach to designing FE-HfO 2 devices.
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