Wearable electronics represent a significant paradigm shift in consumer electronics since they eliminate the necessity for separate carriage of devices. In particular, integration of flexible electronic devices with clothes, glasses, watches, and skin will bring new opportunities beyond what can be imagined by current inflexible counterparts. Although considerable progresses have been seen for wearable electronics, lithium rechargeable batteries, the power sources of the devices, do not keep pace with such progresses due to tenuous mechanical stabilities, causing them to remain as the limiting elements in the entire technology. Herein, we revisit the key components of the battery (current collector, binder, and separator) and replace them with the materials that support robust mechanical endurance of the battery. The final full-cells in the forms of clothes and watchstraps exhibited comparable electrochemical performance to those of conventional metal foil-based cells even under severe folding-unfolding motions simulating actual wearing conditions. Furthermore, the wearable textile battery was integrated with flexible and lightweight solar cells on the battery pouch to enable convenient solar-charging capabilities.

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.

In this report, plasmonic effects in organic photovoltaic cells (OPVs) are systematically analyzed using size-controlled silver nanoparticles (AgNPs, diameter: 10 ~ 100 nm), which were incorporated into the anodic buffer layer, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS). The optical properties of AgNPs tuned by size considerably influence the performance levels of devices. The power conversion efficiency (PCE) was increased from 6.4% to 7.6% 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-OPVs and from 7.9% to 8.6% in polythieno[3,4-b]thiophene/benzodithiophene (PTB7):PC70BM based-OPVs upon embedding the AgNPs. The external quantum efficiency (EQE) was significantly enhanced by the absorption enhancement due to the plasmonic scattering effect. Finally, we verified the origin of the size-dependent plasmonic forwarding scattering effect of the AgNPs by visualizing the scattering field with near-field optical microscopy (NSOM) and through analytic optical simulations.

Polymer solar cells are attracting attention as next-generation energy sources. Scalable deposition techniques of high-quality organic films should be guaranteed to realize highly efficient polymer solar cells in large areas for commercial viability. Herein, we introduce an ultrafast, scalable, and versatile process for forming high-quality organic films on an aqueous substrate by utilizing the spontaneous spreading phenomenon. This approach provides easy control over the thickness of the films by tuning the spreading conditions, and the films can be transferred to a variety of secondary substrates. Moreover, the controlled Marangoni flow and ultrafast removal of solvent during the process cause the films to have a uniform, high-quality nanomorphology with finely separated phase domains. Polymer solar cells were fabricated from a mixture of polymer and fullerene derivatives on an aqueous substrate by using the proposed technique, and the device exhibited an excellent power conversion efficiency of 8.44 %. Furthermore, a roll-to-roll production system was proposed as an air-processable and scalable commercial process for fabricating organic devices.

Stretchable organic solar cells (SOSCs) are attracting considerable attention as an off-grid power source for wearable electronics, including biosensors, electronic skins, and stretchable displays. Although SOSCs possess promising properties such as high power-per-weight output and strong durability under repetitive tensile strains, they remain proof of concept, as they do not satisfy the required performance for wearable electronics. Reconciling high power conversion efficiency (PCE) and reasonable stretchability is a difficult task. This study reports intrinsically SOSCs of over 11% by integrating multiple stretchable layers with strong bindings. Our SOSC achieved impressive stretchability; it maintained over 74% of the initial PCE when subjected to 10% strain for 1,000 cycles. Particularly, high-performance and mechanical endurance demonstrate that SOSCs are one step closer toward practical utilization in wearable electronics.