Changsoon Cho

Au@Ag Core–Shell Nanocubes for Efficient Plasmonic Light Scattering Effect in Low Bandgap Organic Solar Cells

In this report, we propose a metal-metal core-shell nanocube (NC) as an advanced plasmonic material for highly efficient organic solar cells (OSCs). We covered an Au core with a thin Ag shell as a scattering enhancer to build Au@Ag NCs, which showed stronger scattering efficiency than Au nanoparticles (AuNPs) throughout the visible range. Highly efficient plasmonic organic solar cells were fabricated by embedding Au@Ag NCs into an anodic buffer layer, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), and the power conversion efficiency was enhanced to 6.3% from 5.3% in poly[N-9-hepta-decanyl-2,7-carbazole-alt-5,5-(4,7-di-2-thienyl-2,1,3-benzothiadiazole)] (PCDTBT):[6,6]-phenyl C71-butyric acid methyl ester (PC70BM) based OSCs and 9.2% from 7.9% in polythieno[3,4-b]thiophene/benzodithiophene (PTB7):PC70BM based OSCs. The Au@Ag NC plasmonic PCDTBT:PC70BM-based organic solar cells showed 2.2-fold higher external quantum efficiency enhancement compared to AuNPs devices at a wavelength of 450-700 nm due to the amplified plasmonic scattering effect. Finally, we proved the strongly enhanced plasmonic scattering efficiency of Au@Ag NCs embedded in organic solar cells via theoretical calculations and detailed optical measurements.

Highly Transparent Au-Coated Ag Nanowire Transparent Electrode with Reduction in Haze

Ag nanowire transparent electrode has excellent transmittance and sheet resistance, yet its optical haze still needs to be improved in order for it to be suitable for display applications. Ag nanowires are known to have high haze because of the geometry of the nanowire and the high light scattering characteristic of the Ag. In this study, a Au-coated Ag nanowire structure was proposed to reduce the haze, where a thin layer of Au was coated on the surface of the Ag nanowires using a mild [Au(en)2]Cl3 galvanic displacement reaction. The mild galvanic exchange allowed for a thin layer of Au coating on the Ag nanowires with minimal truncation of the nanowire, where the average length and the diameter were 13.0 μm and 60 nm, respectively. The Au-coated Ag nanowires were suspended in methanol and then electrostatically sprayed on a flexible polycarbonate substrate that revealed a clear reduction in haze with a 2-4% increase in total transmittance, sheet resistance ranges of 80-90%, and 8.8-36.8 Ohm/sq. Finite difference time domain simulations were conducted for Au-coated Ag nanowires that indicated a significant reduction in the average scattering from 1 to 0.69 for Au layer thicknesses of 0-10 nm.

Highly Efficient Top‐Illuminated Flexible Polymer Solar Cells with a Nanopatterned 3D Microresonant Cavity

Top-illuminated flexible polymer solar cells with 3D micoresonant cavity provide not only powerful light-trapping but also electrical enhancement, resulting in significant enhancement of power efficiency (26.4%). Capping layer (CL) enhanced the transmittance of the transparent electrodes, increasing electric field intensity in the photoactive layer by forming microresonant cavity, and the nano-pattern on the rear electrodes caused significant enhancement to the Jsc by improving light absorption and charge collection.

Efficient Organic Photovoltaics Utilizing Nanoscale Heterojunctions in Sequentially Deposited Polymer/fullerene Bilayer

A highly efficient sequentially deposited bilayer (SD-bilayer) of polymer/fullerene organic photovoltaic (OPV) device is developed via the solution process. Herein, we resolve two essential problems regarding the construction of an efficient SD-bilayer OPV. First, the solution process fabrication of the SD-bilayer is resolved by incorporating an ordering agent (OA) to the polymer solution, which improves the ordering of the polymer chain and prevents the bottom-layer from dissolving into the top-layer solution. Second, a non-planar heterojunction with a large surface area is formed by the incorporation of a heterojunction agent (HA) to the top-layer solution. Poly[[9-(1-octylnonyl)-9H-carbazole-2,7-diyl]-2,5-thiophenediyl-2,1,3-benzothiadiazole-4,7-diyl-2,5-thiophenediyl] (PCDTBT) is used for the bottom-layer and phenyl-C71-butyric-acid-methyl ester (PC70BM) is used for the top-layer. The SD-bilayer OPV produced utilizing both an OA and HA exhibits a power conversion efficiency (PCE) of 7.12% with a high internal quantum efficiency (IQE). We believe our bilayer system affords a new way of forming OPVs distinct from bulk heterojunction (BHJ) systems and offers a chance to reconsider the polymers that have thus far shown unsatisfactory performance in BHJ systems.

Nanoimprinting-induced nanomorphological transition in polymer solar cells: enhanced electrical and optical performance.

We have investigated the effects of a directly nanopatterned active layer on the electrical and optical properties of inverted polymer solar cells (i-PSCs). The capillary force in confined molds plays a critical role in polymer crystallization and phase separation of the film. The nanoimprinting process induced improved crystallization and multidimensional chain alignment of polymers for more effective charge transfer and a fine phase-separation between polymers and [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) to favor exciton dissociation and increase the generation rate of charge transfer excitons. Consequently, the power conversion efficiency with a periodic nanostructure was enhanced from 7.40% to 8.50% and 7.17% to 9.15% in PTB7 and PTB7-Th based i-PSCs, respectively.

Efficient light trapping in inverted polymer solar cells by a randomly nanostructured electrode using monodispersed polymer nanoparticles

The randomly nanotextured back electrode provides a simple and efficient route for enhancing photocurrent in polymer solar cells (PSCs) by light trapping, which can increase light absorption within a finite thickness of the active layer. In this study, we incorporated mono-disperse 60 nm polystyrene nanoparticles (PS NPs) into a 50 nm thick poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) anode buffer layer (ABL) to create a randomly nanotextured back electrode with 10 nm height variations in inverted-type PSCs. The roughened interface between the PS NP-PEDOT:PSS ABL and the Ag electrode scatters light in the visible range, leading to efficient light trapping within the device and enhanced light absorption in the active layer. Inverted PSCs with randomly nanotextured electrodes (φ(NP) = 0.31) showed short-circuit current density (J(SC)) and power conversion efficiency (PCE) values that were 15% higher than those of control devices with flat electrodes. External quantum efficiency, reflectance, and optical light scattering as a function of ϕ(NP) were examined to determine the origin of the enhancement in J(SC) and PCE.

Enhancement of growth and lipid production from microalgae using fluorescent paint under the solar radiation.

Solar radiation has intensity that is too high to inhibit microalgae activity and is composed of wide light spectrum including ultraviolet (UV) range which cannot be utilized for microalgae. For these reasons, the modification of solar radiation is required for effective microalgae cultivation, and to do that, fluorescent paint was used for not only blocking excessive solar energy but also converting UV to visible light. With fluorescent aqueous layer, microalgae was protected from photoinhibition and could grow well, but there was difference in growth and lipid accumulation efficiencies depending on the color; maximum dry weight of 1.7 g/L was achieved in red paint, whereas best lipid content of 30% was obtained in blue one. This phenomenon was due to the different light spectrum made by colors. With simple process using fluorescent paint, modification of light was successfully done and allowing microalgae to grow under strong radiation such as solar radiation.

Multi-scale and angular analysis of ray-optical light trapping schemes in thin-film solar cells: Micro lens array, V-shaped configuration, and double parabolic trapper

An efficient light trapping scheme is a key to enhancing the power conversion efficiency (PCE) of thin-film photovoltaic (PV) cells by compensating for the insufficient light absorption. To handle optical components from nano-scale to micro-scale seamlessly, a multi-scale optical simulation is carefully designed in this study and is used to qualitatively analyze the light trapping performances of a micro lens array (MLA), a V-shaped configuration, and the newly proposed scheme, which is termed a double parabolic trapper (DPT) according to both daily and annual movement of the sun. DPT has the potential to enhance the PCE significantly, from 5.9% to 8.9%, for PCDTBT:PC(70)BM-based polymer solar cells by perfectly trapping the incident light between two parabolic PV cells.

Self-Supplied Nano-Fusing and Transferring Metal Nanostructures via Surface Oxide Reduction

Here, we demonstrate that chemical reduction of oxide layers on metal nanostructures fuses junctions at nanoscale to improve the opto-electrical performance, and to ensure environmental stability of the interconnected nanonetwork. In addition, the reducing reaction lowers the adhesion force between metal nanostructures and substrates, facilitating the detachment of them from substrates. Detached metal nanonetworks can be easily floated on water and transferred onto various substrates including hydrophobic, floppy, and curved surfaces. Utilizing the detached metal nanostructures, semitransparent organic photovoltaics is fabricated, presenting the applicability of proposed reduction treatment in the device applications.

Surface plasmon assisted high performance top-illuminated polymer solar cells with nanostructured Ag rear electrodes

Highly efficient plasmonic Ag rear electrodes in top-illuminated PSCs employing MoO3/Ag (13 nm)/MoO3 stacks as top transparent electrodes were successfully demonstrated, resulting in the significant enhancement of solar cell performance with a PCE of up to 7.18%. The hemispherical Ag nanostructured arrays effectively concentrate incident light within the photoactive layer in addition to contributing to extended stability with a robust structure.