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 (CHNH) (CHNH) PbI (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 A, higher on/off ratio of ∼10, 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.
Surface defects have been a key constraint for perovskite photovoltaics. Herein, 1,3‐dimethyl‐3‐imidazolium hexafluorophosphate (DMIMPF6) ionic liquid (IL) is adopted to passivate the surface of a formamidinium‐cesium lead iodide perovskite (Cs0.08FA0.92PbI3) and also reduce the energy barrier between the perovskite and hole transport layer. Theoretical simulations and experimental results demonstrate that Pb‐cluster and Pb‐I antisite defects can be effectively passivated by [DMIM]+ bonding with the Pb2+ ion on the perovskite surface, leading to significantly suppressed non‐radiative recombination. As a result, the solar cell efficiency was increased to 23.25 % from 21.09 %. Meanwhile, the DMIMPF6‐treated perovskite device demonstrated long‐term stability because the hydrophobic DMIMPF6 layer blocked moisture permeation.
We have developed a kind of high-yield synthesis strategy for silver nanowires by a two-step injection polyol method. Silver nanowires and polyethylene oxide (PEO) (M(w) = 900,000) were prepared in a homogeneous-coating ink. Wet composite films with different thicknesses were fabricated on a PET substrate by drawn-down rod-coating technology. Silver nanowires on PET substrates present a homogeneous distribution under the assistance of PEO. Then PEO was thermally removed in situ at a relatively low temperature attributed to its special thermal behavior under atmospheric conditions. As-prepared metallic nanowire films on PET substrates show excellent stability and a good combination of conductivity and light transmission. A layer of transparent poly(ethersulfones) (PESs) was further coated on silver nanowire networks by the same coating method to prevent the shedding and corrosion of silver nanowires. Sandwich-structured flexible transparent films were obtained and displayed excellent electromagnetic interference (EMI) shielding effectiveness.
Solution processability of photoactive halide perovskites differentiates them from traditional inorganic semiconducting materials that require multiple post-processing steps such as thermal/vacuum/blow- & solvent-assistant treatment. Here we report a technical breakthrough...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.