Optical Manipulation of Incident Light for Enhanced Photon Absorption in Ultrathin Organic Photovoltaics.

We attempted to improve the photon absorption of the photoactive layer in organic photovoltaic (OPV) devices by device engineering without changing their thickness. Soft nanoimprinting lithography was used to introduce a 1D grating pattern into the photoactive layer. The increase in photocurrent caused by the propagating surface plasmon-polariton mode was quantitatively analyzed by measuring the external quantum efficiency in transverse magnetic and transverse electric modes. In addition, the introduction of an ultrathin substrate with a refractive index of 1.34 improved photon absorption by overcoming the mismatched optical impedance at the air/substrate interface. As a result, the power conversion efficiency (PCE) of an ultrathin OPV with a 400 nm grating period was 8.34%, which was 11.6% higher than that of an unpatterned ultrathin OPV, and the PCE was 3.2 times higher at a low incident light angle of 80°, indicating very low incident light angle dependence.

Ultra-Flexible Organic Solar Cell Based on Indium-Zinc-Tin Oxide Transparent Electrode for Power Source of Wearable Devices.

We have developed a novel structure of ultra-flexible organic photovoltaics (UFOPVs) for application as a power source for wearable devices with excellent biocompatibility and flexibility. Parylene was applied as an ultra-flexible substrate through chemical vapor deposition. Indium-zinc-tin oxide (IZTO) thin film was used as a transparent electrode. The sputtering target composed of 70 at.% In2O3-15 at.% ZnO-15 at.% SnO2 was used. It was fabricated at room temperature, using pulsed DC magnetron sputtering, with an amorphous structure. UFOPVs, in which a 1D grating pattern was introduced into the hole-transport and photoactive layers were fabricated, showed a 13.6% improvement (maximum power conversion efficiency (PCE): 8.35%) compared to the reference device, thereby minimizing reliance on the incident angle of the light. In addition, after 1000 compression/relaxation tests with a compression strain of 33%, the PCE of the UFOPVs maintained a maximum of 93.3% of their initial value.

Ultra-Flexible Organic Photovoltaics with Low-Temperature Deposited IZTO on a Cyclic Polymer Substrate Having Excellent Mechanical Properties.

In this study, ultra-flexible organic photovoltaics (OPVs) with a new device structure are developed as a power source for ultra-flexible wearable devices with excellent biocompatibility. To fabricate ultra-flexible OPVs with excellent mechanical properties, we develop an ultra-flexible substrate with a bilayer structure based on polymers and transparent conducting oxides. An amorphous perfluorinated polymer (cyclic transparent optical polymer, CYTOP) is introduced as an ultra-flexible substrate by a solution process. An indium zinc tin oxide (IZTO) transparent electrode possessing an amorphous structure is fabricated via pulsed DC magnetron sputtering at room temperature using a target containing 80 atom % In2O3-10 atom % ZnO-10 atom % SnO2. Ultra-flexible OPVs with a one-dimensional (1D) grating pattern are fabricated on the buffer layer and photoactive layer. These OPVs exhibit an increase of 12% in power conversion efficiency (PCE) (maximum PCE: 8.52%) compared to the reference, thereby minimizing reliance on the incident angle of light. In addition, even after 1000 compression/relaxation tests with a compression strain of 33%, the PCE of the ultra-flexible OPVs is maintained up to 94.8% of its initial value.

Ultra-Flexible Organic Photovoltaics with Nanograting Patterns Based on CYTOP/Ag Nanowires Substrate.

In this study, we developed a method for fabricating ultrathin polymer substrates that can be used in ultra-flexible organic photovoltaics (OPVs) via a non-vacuum process using cyclic transparent optical polymer. In addition, a Ag nanowire network layer was used as a transparent electrode in a solution process. All processes were conducted on large area via spin coating. The power conversion efficiency (PCE) of the ultra-flexible OPV improved by 6.4% compared to the PCE of the ITO/Glass-based OPV. In addition, the PCE of the OPV increased to 10.12% after introducing nanostructures in the ZnO and photoactive layers. We performed 1000 cycles of compression/relaxation tests to evaluate the mechanical properties of the ultra-flexible OPV, after which, the PCE remained at 67% of the initial value. Therefore, the developed OPV system is suitable as a power source for portable devices.

Porphyrin-Containing Polymer as a Superior Blue Light-Absorbing Additive To Afford High- Jsc Ternary Solar Cells.

Integrating an additional component featuring complementary light absorption into binary polymer solar cells is a superior tactic to ameliorate solar cell efficiency and stability. An appropriate additive not only extends the absorption range but may also facilitate charge separation and transport processes. In this work, we elucidate the effects of incorporating a porphyrin-containing conjugated polymer (PPor-1), which displays absorption in 350-500 nm, into binary PTB7-Th:4TIC and PTB7-Th:ITIC blends, affording devices with an average power conversion efficiency approaching 9%. We successfully demonstrate that PPor-1 can be incorporated as an additive to impart improved Jsc (up to 19.1 mA cm-2).

Self-powered ultra-flexible electronics via nano-grating-patterned organic photovoltaics.

Next-generation biomedical devices1-9 will need to be self-powered and conformable to human skin or other tissue. Such devices would enable the accurate and continuous detection of physiological signals without the need for an external power supply or bulky connecting wires. Self-powering functionality could be provided by flexible photovoltaics that can adhere to moveable and complex three-dimensional biological tissues1-4 and skin5-9. Ultra-flexible organic power sources10-13 that can be wrapped around an object have proven mechanical and thermal stability in long-term operation13, making them potentially useful in human-compatible electronics. However, the integration of these power sources with functional electric devices including sensors has not yet been demonstrated because of their unstable output power under mechanical deformation and angular change. Also, it will be necessary to minimize high-temperature and energy-intensive processes10,12 when fabricating an integrated power source and sensor, because such processes can damage the active material of the functional device and deform the few-micrometre-thick polymeric substrates. Here we realize self-powered ultra-flexible electronic devices that can measure biometric signals with very high signal-to-noise ratios when applied to skin or other tissue. We integrated organic electrochemical transistors used as sensors with organic photovoltaic power sources on a one-micrometre-thick ultra-flexible substrate. A high-throughput room-temperature moulding process was used to form nano-grating morphologies (with a periodicity of 760 nanometres) on the charge transporting layers. This substantially increased the efficiency of the organophotovoltaics, giving a high power-conversion efficiency that reached 10.5 per cent and resulted in a high power-per-weight value of 11.46 watts per gram. The organic electrochemical transistors exhibited a transconductance of 0.8 millisiemens and fast responsivity above one kilohertz under physiological conditions, which resulted in a maximum signal-to-noise ratio of 40.02 decibels for cardiac signal detection. Our findings offer a general platform for next-generation self-powered electronics.

Effects of Inserting Thiophene as a π-Bridge on the Properties of Naphthalene Diimide-alt-Fused Thiophene Copolymers.

On the basis of naphthalene diimide (NDI) units connected to thiophene (T), thienothiophene (TT), or dithienothiophene (DTT) units via a thiophene π-bridge, three new copolymers-PDTNDI-T, PDTNDI-TT, and PDTNDI-DTT, respectively-were synthesized and used in the fabrication of all-polymer solar cells (all-PSCs). The relationships between the structures of the polymers and their optoelectronic properties and photovoltaic performances as electron acceptors in all-PSCs were investigated in detail. As the number of copolymerized heteroaromatic rings in the DTNDI-based polymers increased, the power conversion efficiencies of the resulting all-PSCs were found to decrease. This decreasing trend in the photovoltaic performance is opposite to the results reported previously for NDI-based polymers lacking the thiophene π-bridge and naphthodithiophene diimide-based polymers. In addition, the three polymers were found to exhibit distinct molecular orientations: a face-on orientation for PDTNDI-T and edge-on orientations for PDTNDI-TT and PDTNDI-DTT. Our results indicate that large fused aromatic rings are not necessarily advantageous in the design of NDI-based polymers containing π-conjugated bridges.

Synthesis and characterization of a fluorene-quinoxaline copolymer for light-emitting applications.

A conjugated copolymer based on 9,9-dioctyl-fluorene and 2,3-bis(4-(hexyloxy)phenyl) quinoxaline has been synthesized by the palladium-catalyzed Suzuki coupling reaction. The synthesized polymer was soluble in common organic solvents such as chloroform, THF, and toluene and had good film properties. The polymer was analyzed by 1H-NMR spectroscopy, UV-vis spectroscopy, GPC, TGA, DSC, and cyclic voltammetry. It had very good thermal properties with high decomposition and glass transition temperatures, 420 degrees C and 159 degrees C respectively, and a low band gap of 2.51 eV. The polymer LEDs (ITO/PEDOT:PSS/polymer/LiF/Ca/Al) showed pure green light emission with maximum peaks at 502 nm and CIE coordinates of x = 0.28 and y = 0.55. The turn-on voltage of the polymer device was 7 V and the maximum brightness was 10.16 cd/m2 at 14 V. The maximum luminescence efficiency of the polymer was 0.0011 cd/A at 11 V.