• Corre, Vincent Le

Abstract

<jats:p> 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 ([Formula: see text]), which amounts to roughly 10<jats:sup>16</jats:sup> cm<jats:sup>−3</jats:sup>. 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 (∼10<jats:sup>12</jats:sup> cm<jats:sup>−3</jats:sup>, which means ≪ [Formula: see text]) 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. </jats:p>

Topics

• density
• perovskite
• impedance spectroscopy
• photoluminescence
• simulation
• extraction
• semiconductor