论文标题
金属卤化物钙钛矿设备的空间充电限量的当前测量的有效性窗口
The Validity Window of Space-Charge-Limited Current Measurements of Metal Halide Perovskite Devices
论文作者
论文摘要
通过分析Mott-Gurney(MG)定律预测的单极设备的电流密度 - 电压(JV)关系,使用了空间充电的电流(SCLC)测量值来估计电荷载体的迁移率和半导体的电子陷阱密度。然而,由于移动离子缺陷,在测量过程中将SCLC测量的解释是有问题的,因此在测量过程中将其重新分布到设备中的静电场。为了克服这一点,最近提出了一种SCLC测量方案,该方案通过探测叠加在背景偏置上的毫秒电压脉冲过程中的电流来最大程度地减少离子电荷重新分布。在这里,我们使用移动离子的漂移扩散模拟来评估MG法律对分析标准和新协议合资型测量的有效性。我们模拟了具有不同移动离子密度不同的理想化钙钛矿设备,并将它们与典型接触材料的模拟和测量进行了比较。我们发现,MG定律的有效性区域仅限于移动离子密度低于该设备平衡荷载载流子密度(<10^17 cm-3的400 nm厚碘化碘化物碘化物膜)和带注射/提取障碍<= 0.1 eV的接触。后一个限制可以通过增加设备厚度来部分克服,而以前的限制不能。这限制了钙钛矿层组成和可行的接触材料的范围,这些材料可以可靠地通过MG定律进行分析。诸如估算从明显电压发作到无陷阱SCLC政权的陷阱密度之类的方法也应进行严格审查,因为它们依赖于与MG法律相同的潜在无效假设。我们的结果表明,从SCLC提取金属卤化物钙钛矿材料的有意义和准确的值可能具有挑战性,或者通常是不可能的。
Space-charge-limited current (SCLC) measurements are used to estimate charge carrier mobilities and electronic trap densities of semiconductors by analysing the current density-voltage (JV) relationship for unipolar devices predicted by the Mott-Gurney (MG) law. However, the interpretation of SCLC measurements for metal-halide perovskites is problematic due to mobile ionic defects which redistribute to screen electrostatic fields in devices during measurements. To overcome this, an SCLC measurement protocol was recently suggested that minimises ionic charge redistribution by probing the current during millisecond voltage pulses superimposed on a background bias. Here, we use drift-diffusion simulations with mobile ions to assess the validity of the MG law for analysing both the standard and new protocol JV measurements. We simulated idealised perovskite devices with differing mobile ion densities and compared them with simulations and measurements of devices with typical contact materials. We found the validity region for the MG law is limited to perovskites with mobile ion densities lower than the device's equilibrium charge carrier density (<10^17 cm-3 for 400 nm thick methylammonium lead iodide films) and contacts with injection/extraction barriers <=0.1 eV. The latter limitation can be partially overcome by increasing the device thickness, whereas the former limitation cannot. This restricts the range of perovskite layer compositions and viable contact materials that can be reliably analysed with the MG law. Approaches such as estimating trap densities from the apparent voltage onset to trap-free SCLC regime should also be critically reviewed since they rely on the same potentially invalid assumptions as the MG law. Our results demonstrate that extracting meaningful and accurate values for metal halide perovskite material properties from SCLC maybe challenging, or often not possible.