Peña-Camargo, F.; Thiesbrummel, J.; Hempel, H.; Musiienko, A.; Le Corre, V.M.; Diekmann, J.; Warby, J.; Unold, T.; Lang, F.; Neher, D.; Stolterfoht, M.: Revealing the doping density in perovskite solar cells and its impact on device performance. Applied Physics Express 9 (2022), p. 021409/1-11
10.1063/5.0085286
Open Access Version
Abstract:
Traditional inorganic semiconductors can be electronically doped with high precision. Conversely, there is still conjecture regarding the assessment of the electronic doping density in metal-halide perovskites, not to mention of a control thereof. This paper presents a multifaceted approach to determine the electronic doping density for a range of different lead-halide perovskite systems. Optical and electrical characterization techniques, comprising intensity-dependent and transient photoluminescence, AC Hall effect, transfer-length-methods, and charge extraction measurements were instrumental in quantifying an upper limit for the doping density. The obtained values are subsequently compared to the electrode charge per cell volume under short-circuit conditions (Vbi/𝑒𝑉), which amounts to roughly 1016 cm−3. This figure of merit represents the critical limit below which doping-induced charges do not influence the device performance. The experimental results consistently demonstrate that the doping density is below this critical threshold (∼1012 cm−3, which means ≪ Vbi/𝑒𝑉) for all common lead-based metal-halide perovskites. Nevertheless, although the density of doping-induced charges is too low to redistribute the built-in voltage in the perovskite active layer, mobile ions are present in sufficient quantities to create space-charge-regions in the active layer, reminiscent of doped pn-junctions. These results are well supported by drift–diffusion simulations, which confirm that the device performance is not affected by such low doping densities.