Dong-Ho Kim

Ultrasmooth, extremely deformable and shape recoverable Ag nanowire embedded transparent electrode.

Transparent electrodes have been widely used in electronic devices such as solar cells, displays, and touch screens. Highly flexible transparent electrodes are especially desired for the development of next generation flexible electronic devices. Although indium tin oxide (ITO) is the most commonly used material for the fabrication of transparent electrodes, its brittleness and growing cost limit its utility for flexible electronic devices. Therefore, the need for new transparent conductive materials with superior mechanical properties is clear and urgent. Ag nanowire (AgNW) has been attracting increasing attention because of its effective combination of electrical and optical properties. However, it still suffers from several drawbacks, including large surface roughness, instability against oxidation and moisture, and poor adhesion to substrates. These issues need to be addressed before wide spread use of metallic NW as transparent electrodes can be realized. In this study, we demonstrated the fabrication of a flexible transparent electrode with superior mechanical, electrical and optical properties by embedding a AgNW film into a transparent polymer matrix. This technique can produce electrodes with an ultrasmooth and extremely deformable transparent electrode that have sheet resistance and transmittance comparable to those of an ITO electrode.

Highly Efficient Organic Hole Transporting Materials for Perovskite and Organic Solar Cells with Long‐Term Stability

Small molecules based on N-atom-linked phenylcarbazole-fluorene as the main scaffold, end-capped with spirobifluorene derivatives, are developed as organic hole-transporting materials for highly efficient perovskite solar cells (PSCs) and bulk heterojunction (BHJ) inverted organic solar cells (IOSCs). The CzPAF-SBF-based devices show remarkable device performance with excellent long-term stability in PSCs and BHJ IOSCs with a maximum PCE of 17.21% and 7.93%, respectively.

Graphene-based gas sensor: metal decoration effect and application to a flexible device

Roles of metal nanoparticles (NPs) on graphene-based devices were investigated in terms of gas-sensing characteristics of NO2 and NH3, and flexible gas sensing was also realized for future applications. The synergistic combination of metal NPs and graphene modulates the electronic properties of graphene, leading to enhancement of selectivity and sensitivity in gas-sensing characteristics. Introduction of palladium (Pd) NPs on the graphene accumulates hole carriers of graphene, resulting in the gas sensor being sensitized by NH3 gas molecular adsorption. In contrast, aluminum (Al) NPs deplete hole carriers, which dramatically improves NO2 sensitivity. Furthermore, the sensitivity of flexible graphene-based gas sensors was also enhanced via the same approach, even after 104 bending cycles and was maintained after 3 months.

Potassium Incorporation for Enhanced Performance and Stability of Fully Inorganic Cesium Lead Halide Perovskite Solar Cells

Thermally unstable nature of hybrid organic-inorganic perovskites has been a major obstacle to fabricating the long-term operational device. A cesium lead halide perovskite has been suggested as an alternative light absorber, due to its superb thermal stability. However, the phase instability and poor performance are hindering the further progress. Here, cesium lead halide perovskite solar cells with enhanced performance and stability are demonstrated via incorporating potassium cations. Based on Cs0.925K0.075PbI2Br, the planar-architecture device achieves a power conversion efficiency of 10.0%, which is a remarkable record in the field of inorganic perovskite solar cells. In addition, the device shows an extended operational lifetime against air. Our research will stimulate the development of cesium lead halide perovskite materials for next-generation photovoltaics.

High Efficiency Inorganic/Organic Hybrid Tandem Solar Cells

Hybrid tandem solar cells comprising an inorganic bottom cell and an organic top cell have been designed and fabricated. The interlayer combination and thickness matching were optimized in order to increase the overall photovoltaic conversion efficiency. A maximum power conversion efficiency of 5.72% was achieved along with a V(oc) of 1.42 V, reaching as high as 92% of the sum of the subcell V(oc) values.

Highly flexible and transparent conducting silver nanowire/ZnO composite film for organic solar cells

High efficiency and flexible inverted organic solar cells have been fabricated using solution-processed silver nanowire/zinc oxide composite transparent electrodes. The transparent electrodes showed a low sheet resistance of ∼13 Ω·sq−1 and high transmittance of ∼93% as well as superior mechanical flexibility. Power conversion efficiencies of ∼7.57% and ∼7.21% were achieved for devices fabricated on glass and plastic substrate, respectively. Moreover, the flexible devices did not show any degradation in their performance even after being folded with a radius of ∼480 μm.

Photophysical properties and photoisomerization processes of Methyl Red embedded in rigid polymer

The photophysical properties of Methyl Red molecules embedded in a poly(methyl methacrylate) (PMMA) matrix were investigated with photoinduced absorption, absorption kinetics, steady-state, and time-resolved luminescence spectroscopy. The excited singlet (S(1)) state lifetimes for trans and cis isomers of Methyl Red in PMMA at room temperature have been measured as 35 and 420 ps, respectively. The excited triplet (T(1)) state energy level and its lifetime at 77 K were also obtained. A slow trans-cis isomerization process having a time constant of a few hundred seconds was observed for the illuminated Methyl Red in rigid polymer. Based on measured photophysical properties and dynamic processes, an energy-level diagram for Methyl Red molecules in rigid polymer is introduced to explain these observations.

Self-assembled monolayer as an interfacial modification material for highly efficient and air-stable inverted organic solar cells

Organic solar cells with inverted structures can greatly improve photovoltaic stability. This paper reports a method to lower the work function of indium tin oxide (ITO) in inverted organic solar cells by modification with ultrathin 3-aminopropyltriethoxysilane (APTES) monolayers. The device studies showed that the resulting photovoltaic efficiencies were significantly increased from 0.64% to 4.83% with the use of the APTES monolayer, which could be attributed to the dramatic enhancement in the open-circuit voltage and fill factor. The effective electron selectivity in the case of the APTES-modified ITO could be attributed to the reduction of the work function of ITO as a result of the electron-donating nature of the amine groups in the APTES monolayer. The power conversion efficiency of the unencapsulated inverted organic solar cells with APTES-modified ITO remained above 80% of their original values even after storage in air for thirty days. Our results provide a promising approach to improve the performance of highly efficient and air-stable inverted organic solar cells.

Unveiling the Crystal Formation of Cesium Lead Mixed-Halide Perovskites for Efficient and Stable Solar Cells

Thermal instability of organic-inorganic hybrid perovskites will be an inevitable hurdle for commercialization. Recently, all-inorganic cesium lead halide perovskites, in particular, CsPbI2Br, have emerged as thermally stable and efficient photovoltaic light absorbers. However, the fundamental properties of this material have not been studied in detail. The crystal formation behavior of CsPbI2Br is investigated by examining the surface morphology, crystal structure, and chemical state of the perovskite films. We discover a previously uncharacterized feature that the formation of black polymorph through optimal annealing temperature proves to be critical to both solar cell efficiency and phase stability. Our optimized planar heterojunction solar cell exhibits a J-V scan efficiency of 10.7% and open-circuit voltage of 1.23 V, which far outperforms the preceding literature.

Nanostructured plasmonic substrates for use as SERS sensors

Plasmonic nanostructures strongly localize electric fields on their surfaces via the collective oscillations of conducting electrons under stimulation by incident light at a certain wavelength. Molecules adsorbed onto the surfaces of plasmonic structures experience a strongly enhanced electric field due to the localized surface plasmon resonance (LSPR), which amplifies the Raman scattering signal obtained from these adsorbed molecules. This phenomenon is referred to as surface-enhanced Raman scattering (SERS). Because Raman spectra serve as molecular fingerprints, SERS has been intensively studied for its ability to facilely detect molecules and provide a chemical analysis of a solution. Further enhancements in the Raman intensity and therefore higher sensitivity in SERS-based molecular analysis have been achieved by designing plasmonic nanostructures with a controlled size, shape, composition, and arrangement. This review paper focuses on the current state of the art in the fabrication of SERS-active substrates and their use as chemical and biosensors. Starting with a brief description of the basic principles underlying LSPR and SERS, we discuss three distinct nanofabrication methods, including the bottom-up assembly of nanoparticles, top-down nanolithography, and lithography-free random nanoarray formation. Finally, typical applications of SERS-based sensors are discussed, along with their perspectives and challenges.