Namchul Cho

High-Performance and Environmentally Stable Planar Heterojunction Perovskite Solar Cells Based on a Solution-Processed Copper-Doped Nickel Oxide Hole-Transporting Layer

An effective approach to significantly increase the electrical conductivity of a NiOx hole-transporting layer (HTL) to achieve high-efficiency planar heterojunction perovskite solar cells is demonstrated. Perovskite solar cells based on using Cu-doped NiOx HTL show a remarkably improved power conversion efficiency up to 15.40% due to the improved electrical conductivity and enhanced perovskite film quality. General applicability of Cu-doped NiOx to larger bandgap perovskites is also demonstrated in this study.

Suppressed Charge Recombination in Inverted Organic Photovoltaics via Enhanced Charge Extraction by Using a Conductive Fullerene Electron Transport Layer

Conductive fullerene electron-transporting layers (ETLs) are developed to facilitate the solution processing of highly efficient inverted OSCs with power conversion efficiency (PCE) reaching 9.6%. Its high conductivity also allows devices to be fabricated independently of the ETL thickness (up to ca. 50 nm). Transient photovoltage (TPV) measurements are used to shed light on how these conductive ETLs help suppress charge recombination in solar cells.

Anode modification of inverted polymer solar cells using graphene oxide

A simple method has been developed to modify the anode interface of inverted bulk-heterojunction (BHJ) polymer solar cells by spin-coating a thin layer of graphene oxide (GO) on top of the organic active layer. The device with GO exhibited a remarkable improvement in power conversion efficiency compared to devices without any interfacial layer, indicating that GO can effectively modify the BHJ/metal anode interface to facilitate efficient hole collection. The dependence of the device performance on the GO layer thickness was also investigated showing an optimum performance from a GO thickness of ∼2–3 nm.

Fabrication of a bunch of sub-30-nm nanofibers inside microchannels using photopolymerization via a long exposure technique

Experimental studies on the fabrication of sub-30-nm nanofibers using two-photon initiated photopolymerization (TPP) have been carried out. To generate nanofibers at the interior region of microstructures, a photopolymerization method involving a long laser-exposure technique (LET) is proposed. A multitude of nanofibers with a notably high resolution (about 22nm) in TPP were produced using the LET. Furthermore, it is also demonstrated that thin interconnecting networks were created regularly in a weakly polymerized region existing around the boundary of a densely polymerized voxel, allowing for the creation of various embossing patterns. By controlling the distance between adjacent voxels or lines, a selective generation of nanofibers in a local area is possible, which leads to the fabrication of high-functional filters and mixers. Embossing patterns and microchannels including nanofibers inside were fabricated by the LET so as to demonstrate the practical feasibility of this approach. These sub-30-nm nan...

n-Doping of thermally polymerizable fullerenes as an electron transporting layer for inverted polymer solar cells

A novel [6,6]-phenyl-C61-butyric acid methyl styryl ester (PCBM-S) was synthesized and employed as an electron transporting interfacial layer for bulk heterojunction polymer solar cells with an inverted device configuration. After the deposition of PCBM-S film from solution, the styryl groups of PCBM-S were polymerized by post-thermal treatment to form a robust film which is resistive to common organic solvents. This allows the solution processing of upper bulk heterojunction film without eroding the PCBM-S layer. Additionally, the PCBM-S was n-doped with decamethylcobaltocene (DMC) to increase the conductivity of the film, which resulted in a significantly improved power conversion efficiency from 1.24% to 2.33%. The improved device performance is due to the decrease of series resistance and improved electron extraction property of the n-doped PCBM-S film.

Photopatternable quantum dots forming quasi-ordered arrays.

We have functionalized core-shell CdSe/ZnS quantum dots (QDs) with a photosensitive monolayer, rendering them solution processable and photopatternable. Upon exposure to ultraviolet radiation, films composed of this material were found to polymerize, forming interconnected arrays of QDs. The photoluminescence properties of the nanocrystal films increased with photocuring. The material was found to be suitable for spin casting and was used as the active layer in a green electroluminescent device. The electroluminescence efficiency of devices containing a photocured active layer was found to be largely enhanced when compared to devices containing nonphotocured active layers. The material also showed excellent adhesion to both organic and inorganic substrates because of the unique combination of a siloxane and a photopatternable layer as ligands. The pristine functionalized nanocrystals could easily be used for two-dimensional patterning on organic and inorganic substrates. The photopatternable quantum dots were uniformly dispersed into a photopolymerizable resin to fabricate QD embedded three-dimensional microstructures.

In situ doping and crosslinking of fullerenes to form efficient and robust electron-transporting layers for polymer solar cells

Efficient electron-transporting layers (ETLs) with a stable conductive fullerene doped into a thermally crosslinkable fullerene matrix have been developed for inverted polymer solar cells (PSCs). The improved electrical conductivity and solvent resistance of these ETLs have significantly enhanced the performance of PSCs.

Pure crystal orientation and anisotropic charge transport in large-area hybrid perovskite films

Controlling crystal orientations and macroscopic morphology is vital to develop the electronic properties of hybrid perovskites. Here we show that a large-area, orientationally pure crystalline (OPC) methylammonium lead iodide (MAPbI3) hybrid perovskite film can be fabricated using a thermal-gradient-assisted directional crystallization method that relies on the sharp liquid-to-solid transition of MAPbI3 from ionic liquid solution. We find that the OPC films spontaneously form periodic microarrays that are distinguishable from general polycrystalline perovskite materials in terms of their crystal orientation, film morphology and electronic properties. X-ray diffraction patterns reveal that the film is strongly oriented in the (112) and (200) planes parallel to the substrate. This film is structurally confined by directional crystal growth, inducing intense anisotropy in charge transport. In addition, the low trap-state density (7.9 × 1013 cm−3) leads to strong amplified stimulated emission. This ability to control crystal orientation and morphology could be widely adopted in optoelectronic devices.

Double Charged Surface Layers in Lead Halide Perovskite Crystals

Understanding defect chemistry, particularly ion migration, and its significant effect on the surfaces optical and electronic properties is one of the major challenges impeding the development of hybrid perovskite-based devices. Here, using both experimental and theoretical approaches, we demonstrated that the surface layers of the perovskite crystals may acquire a high concentration of positively charged vacancies with the complementary negatively charged halide ions pushed to the surface. This charge separation near the surface generates an electric field that can induce an increase of optical band gap in the surface layers relative to the bulk. We found that the charge separation, electric field, and the amplitude of shift in the bandgap strongly depend on the halides and organic moieties of perovskite crystals. Our findings reveal the peculiarity of surface effects that are currently limiting the applications of perovskite crystals and more importantly explain their origins, thus enabling viable surface passivation strategies to remediate them.

Morphology evolution by controlling solvent-solute interactions using a binary solvent in bulk heterojunction solar cells

Improved power conversion efficiency of poly(indacenodithiophene-co-phananthrene-quinoxaline) (PIDT-PhanQ)/[6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) based bulk- heterojunction (BHJ) solar cells was achieved upon adding tetrahydrofuran (THF) as a co-solvent to 1,2-dichlorobenzene (DCB). This reasonably large enhancement is achieved due to THF changes the morphology in the active layer by reducing the solvent-solute interaction. The Flory-Huggins interaction parameter and cohesive energy densities for PIDT-PhanQ and PD71BM with different solvents were further studied to understand the underlying phase separation mechanism in BHJ films.