Jaehoon Ryu

Size-controlled SiO2 nanoparticles as scaffold layers in thin-film perovskite solar cells

Perovskite-based solar cells have received much recent research attention for renewable-energy applications because of their high efficiency and long-term stability. Here, we report perovskite solar cells formed using a scaffold layer composed of size-controlled SiO2 nanoparticles (NPs). The infiltration of perovskite into the scaffold layer depended strongly on the size of the SiO2 NPs. We investigated the effects of scaffold layers comprised of SiO2 NPs that were 15, 30, 50, 70, and 100 nm in diameter on the properties of perovskite films. The performance of perovskite solar cells based on 50 nm diameter SiO2 NPs exhibited a current density (Jsc) of 16.4 mA cm−2, a open-circuit voltage (Voc) of 1.05 V, and a power-conversion efficiency (PCE) of 11.45%, which represent a significant improvement compared with perovskite solar cells fabricated using a TiO2 scaffold layer, where Jsc = 17.3 mA cm−2, Voc = 0.94 V, and the PCE was 10.29%.

SiO2/TiO2 based hollow nanostructures as scaffold layers and Al-doping in the electron transfer layer for efficient perovskite solar cells

Perovskite solar cells (PSCs) have been developed intensively recently due to their excellent efficiency. In this study, PSCs were fabricated using a hollow structure as a scaffold layer and Al doped TiO2 (Al-TiO2) as a compact layer. The hollow structure showed effective loading of perovskite (CH3NH3PbI3Cl3−x) on the working electrode of the PSCs. In particular, using SiO2/TiO2 hollow nanoparticles (STHNPs) instead of TiO2 hollow nanoparticles (THNPs) as insulators improved the open circuit voltage, because STHNPs did not allow photogenerated electrons to transfer easily from the perovskite. Al-TiO2 compact layers synthesized using a low temperature procedure (≤150 °C) promoted electron extraction and reduced the recombination, leading to enhanced power conversion efficiency (PCE). An optimum PCE of 14.7% was achieved for PSCs based on STHNP scaffold layers with Al doping in the electron transfer layer.

A graphene quantum dots based fluorescent sensor for anthrax biomarker detection and its size dependence

Graphene quantum dots (GQDs) with two different diameters were modified with a EuIII-macromolecule complex and applied in dual emission fluorescent sensors for detection of Bacillus anthracis spores. The Eu-GQD sensors exhibited a morphology of ultrafine particles, increased surface-to-volume ratio, enhanced dispersibility, and extraordinary sensitivity. The 3 nm Eu-GQDs showed three emission bands, which are ascribed to the emission from the blue GQDs (435 nm) and the red [(Eu)-(DPA)] complex (593 nm and 616 nm). Accordingly, incorporation of the GQDs as a non-interfering internal calibration makes it possible for use as a ratiometric sensor. The time dependent fluorescence response study revealed that the reaction was complete within 8 s, thus enabling rapid detection of B. anthracis spores. It is noteworthy that the Eu-GQD sensors exhibited an extraordinary limit of detection (LOD) of ca. 10 pM towards B. anthracis, which is six orders of magnitude smaller than the infectious dose of the spores (60 μM). Furthermore, the selectivity study indicates that Eu-GQD sensors have an outstanding selectivity of 103-fold for DPA over competing aromatic ligands.

Highly porous nanostructured polyaniline/carbon nanodots as efficient counter electrodes for Pt-free dye-sensitized solar cells

We report a novel method for synthesizing highly porous polyaniline (PANI) using carbon nanodots (CNDs) as a nucleating agent and demonstrate their use as counter electrodes (CEs) for dye-sensitized solar cells (DSSCs). CNDs surrounded with aniline act as efficient nuclei in the polymerization reaction. CNDs disrupt undesirable secondary growth reactions leading to the formation of an agglomerated structure, and organize the highly porous PANI structures with a large surface area (43.6 m2 g−1). Moreover, the presence of CNDs in the polymerization mixture facilitates generation of head-to-tail dimers, and enhances the degree of para-coupling in the molecular structure of PANI. As a result of these nucleation effects, the fabricated PANI-CND films exhibit an increased electrical conductivity of ca. 774 S cm−1. When used as a CE in DSSCs, PANI-CND CEs exhibit a superior power conversion efficiency (η = 7.45%) to those of conventional platinum (η = 7.37%) and pristine PANI CEs (η = 5.60%).

Large Grain-Based Hole-Blocking Layer-Free Planar-Type Perovskite Solar Cell with Best Efficiency of 18.20%

There remains tremendous interest in perovskite solar cells (PSCs) in the solar energy field; the certified power conversion efficiency (PCE) now exceeds 20%. Along with research focused on enhancing PCE, studies are also underway concerning PSC commercialization. It is crucial to simplify the fabrication process and reduce the production cost to facilitate commercialization. Herein, we successfully fabricated highly efficient hole-blocking layer (HBL)-free PSCs through vigorously interrupting penetration of hole-transport material (HTM) into fluorine-doped tin oxide by a large grain based-CH3NH3PbI3 (MAPbI3) film, thereby obtaining a PCE of 18.20%. Our results advance the commercialization of PSCs via a simple fabrication system and a low-cost approach in respect of mass production and recyclability.

Paintable Carbon-Based Perovskite Solar Cells with Engineered Perovskite/Carbon Interface Using Carbon Nanotubes Dripping Method

Paintable carbon electrode-based perovskite solar cells (PSCs) are of particular interest due to their material and fabrication process costs, as well as their moisture stability. However, printing the carbon paste on the perovskite layer limits the quality of the interface between the perovskite layer and carbon electrode. Herein, an attempt to enhance the performance of the paintable carbon-based PSCs is made using a modified solvent dripping method that involves dripping of the carbon nanotubes (CNTs), which is dispersed in chlorobenzene solution. This method allows CNTs to penetrate into both the perovskite film and carbon electrode, facilitating fast hole transport between the two layers. Furthermore, this method is results in increased open circuit voltage (Voc ) and fill factor (FF), providing better contact at the perovskite/carbon interfaces. The best devices made with CNT dripping show 13.57% power conversion efficiency and hysteresis-free performance.

Selective growth of layered perovskites for stable and efficient photovoltaics

Perovskite solar cells (PSCs) are promising alternatives toward clean energy because of their high-power conversion efficiency (PCE) and low materials and processing cost. However, their poor stability under operation still limits their practical applications. Here we design an innovative approach to control the surface growth of a low dimensional perovskite layer on top of a bulk three-dimensional (3D) perovskite film. This results in a structured perovskite interface where a distinct layered low dimensional perovskite is engineered on top of the 3D film. Structural and optical properties of the stack are investigated and solar cells are realized. When embodying the low dimensional perovskite layer, the photovoltaic cells exhibit an enhanced PCE of 20.1% on average, when compared to pristine 3D perovskite. In addition, superior stability is observed: the devices retain 85% of the initial PCE stressed under one sun illumination for 800 hours at 50 °C in an ambient environment.

Highly efficient perovskite solar cells incorporating NiO nanotubes: increased grain size and enhanced charge extraction

Perovskite solar cells (PSCs) have greatly improved through optimizing the morphology and charge extraction of the perovskite film. To increase the efficiency, we have developed a new method of adding NiO nanotubes (NTs) to the perovskite precursor solution. The NiO NTs promoted the growth of perovskite grains during annealing and facilitated charge extraction. The increase in the grain size improved the crystallinity of the perovskite film and reduced the grain boundaries that could trap charge. Additionally, the NiO NTs located between the grain boundaries transferred holes, which prevented charge recombination. The efficiency of the PSCs increased due to the improved crystallinity and charge extraction of the perovskite film. Devices incorporating the NiO NTs exhibited power conversion efficiencies of 19.3 and 12.82% for planar-type and carbon-based PSCs, respectively.

Synthesis of Hierarchical Silica/Titania Hollow Nanoparticles and Their Enhanced Electroresponsive Activity

Wrinkled silica nanoparticle (WSN)-based hollow SiO2/TiO2 nanoparticles (W-HNPs) with hierarchically arrayed internal surfaces were prepared via the combination of sol-gel, TiO2 coating, and etching of core template techniques. The hierarchical internal surface of W-HNPs was attained using WSNs as a core template. Compared with SiO2 sphere-templated hollow SiO2/TiO2 nanoparticles (S-HNPs) with flat inner surfaces, W-HNPs displayed distinctive surface areas, TiO2 loading amounts, and dielectric properties arising from the hierarchical internal surface. The unique properties of W-HNPs were further investigated as an electrorheological (ER) material. W-HNP-based ER fluids exhibited ca. 1.9-fold enhancement in the ER efficiency compared to that of S-HNP-based ER fluids. Such enhancement was attributed to the unique inner surface of W-HNPs, which effectively enhanced the polarizability by increasing the number of charge accumulation sites, and to the presence of the high-dielectric TiO2. This study demonstrated the advantages, in terms of practical ER applications, of hollow nanomaterials having uniquely arrayed internal spaces.

Size effects of a graphene quantum dot modified-blocking TiO2 layer for efficient planar perovskite solar cells

Research on the addition of suitable materials into perovskite solar cells (PSCs) for improved performance is as important as the fabrication of efficient perovskite films themselves. An attempt to enhance the performance of planar-type perovskite solar cells was performed by introducing graphene quantum dots (GQDs) onto a blocking TiO2 layer via O2 plasma treatment. Furthermore, the bandgap of the GQDs was tuned through their size control and the effects of the GQD size on cell performance were explored. The GQDs can induce fast electron extraction and the formation of the improved perovskite quality. The devices with appropriately sized-GQDs showed an average of 10% enhancement compared with those of cells without GQDs and achieved 19.11% as the best power conversion efficiency (PCE). Furthermore, GQDs contributed to the reduction in the extent of current–voltage hysteresis, which was attributed to the planar structure.