Congcong Wu

Impact of Capacitive Effect and Ion Migration on the Hysteretic Behavior of Perovskite Solar Cells.

In the past five years, perovskite solar cells (PSCs) based on organometal halide perovskite have exhibited extraordinary photovoltaic (PV) performance. However, the PV measurements of PSCs have been widely recognized to depend on voltage scanning condition (hysteretic current density-voltage [J-V] behavior), as well as on voltage treatment history. In this study, we find that varied PSC responses are attributable to two causes. First, capacitive effect associated with electrode polarization provides a slow transient non-steady-state photocurrent that modifies the J-V response. Second, modification of interfacial barriers induced by ion migration can modulate charge-collection efficiency so that it causes a pseudo-steady-state photocurrent, which changes according to previous voltage conditioning. Both phenomena are strongly influenced by ions accumulating at outer interfaces, but their electrical and PV effects are different. The time scale for decay of capacitive current is on the order of seconds, whereas the slow redistribution of mobile ions requires several minutes.

High efficiency planar-type perovskite solar cells with negligible hysteresis using EDTA-complexed SnO 2

Even though the mesoporous-type perovskite solar cell (PSC) is known for high efficiency, its planar-type counterpart exhibits lower efficiency and hysteretic response. Herein, we report success in suppressing hysteresis and record efficiency for planar-type devices using EDTA-complexed tin oxide (SnO2) electron-transport layer. The Fermi level of EDTA-complexed SnO2 is better matched with the conduction band of perovskite, leading to high open-circuit voltage. Its electron mobility is about three times larger than that of the SnO2. The record power conversion efficiency of planar-type PSCs with EDTA-complexed SnO2 increases to 21.60% (certified at 21.52% by Newport) with negligible hysteresis. Meanwhile, the low-temperature processed EDTA-complexed SnO2 enables 18.28% efficiency for a flexible device. Moreover, the unsealed PSCs with EDTA-complexed SnO2 degrade only by 8% exposed in an ambient atmosphere after 2880 h, and only by 14% after 120 h under irradiation at 100 mW cm−2.The development of high efficiency planar-type perovskite solar cell has been lagging behind the mesoporous-type counterpart. Here Yang et al. modify the oxide based electron transporting layer with organic acid and obtain planar-type cells with high certified efficiency of 21.5% and decent stability.

Fabrication of Lead‐Free (CH3NH3)3Bi2I9 Perovskite Photovoltaics in Ethanol Solvent

The toxicity of lead present in organohalide perovskites and the hazardous solvent systems used for their synthesis hinder the deployment of perovskite solar cells (PSCs). Herein, an environmentally friendly route toward bismuth-based, lead-free (CH3 NH3 )3 Bi2 I9 perovskites that utilize ethanol as the solvent is described. Using this method, dense and homogeneous microstructures were obtained, compared to the porous, rough microstructures obtained using dimethylformamide. Photovoltaic performances were enhanced, with an open-circuit voltage of 0.84 V measured.

Quasi-Two-Dimensional Halide Perovskite Single Crystal Photodetector

The robust material stability of the quasi-two-dimensional (quasi-2D) metal halide perovskites has opened the possibility for their usage instead of three-dimensional (3D) perovskites. Further, devices based on large area single crystal membranes have shown increasing promise for photoelectronic applications. However, growing inch-scale quasi-2D perovskite single crystal membranes (quasi-2D PSCMs) has been fundamentally challenging. Here we report a fast synthetic method for synthesizing inch-scale quasi-2D PSCMs, namely (C4H9NH3) n(CH3NH3) n-1Pb nI3 n+1 (index n = 1, 2, 3, 4, and ∞), and demonstrate their application in a single-crystal photodetector. A quasi-2D PSCM has been grown at the water-air interface where spontaneous alignment of alkylammonium cations and high chemical potentials enable uniform orientation and fast in-plane growth. Structural, optical, and electrical characterizations have been conducted as a function of quantum well thickness, which is determined by the index n. It is shown that the photodetector based on the quasi-2D PSCM with the smallest quantum well thickness ( n = 1) exhibits a strikingly low dark current of ∼10-13 A, higher on/off ratio of ∼104, and faster response time in comparison to those of photodetectors based on quasi-2D PSCMs with larger quantum well thickness ( n > 1). Our study paves the way toward the merging the gap between single crystal devices and the emerging quasi-2D perovskite materials.