A Flexible Loudspeaker Using the Movement of Liquid Metal Induced by Electrochemically Controlled Interfacial Tension.

A flexible liquid metal loudspeaker (LML) is demonstrated consisting of a gallium-based eutectic liquid metal (Galinstan) and basic aqueous electrolyte (NaOH(aq) ). The LML is driven by liquid metal motion induced by the electrochemically controlled interfacial tension of the Galinstan in NaOH(aq) electrolyte under an applied alternating current (AC) voltage. The fabricated LML produces sound waves in the human audible frequency band with a sound pressure level of ≈40-50 dB at 1 cm from the device and exhibits mechanical stability under bending deformation with a bending radius of 3 mm. Various sounds can be generated with the LML from a single tone to piano notes and human voices. To understand the underlying mechanism of sound generation by the LML, motion analyses, sound measurements, and electrical characterization are conducted at various frequencies. For the first time, this work suggests a new type of liquid metal-based electrochemically driven sound generator in the field of flexible acoustic devices that can be applied to future wearable electronics.

Highly Durable and Flexible Transparent Electrode for Flexible Optoelectronic Applications.

A highly-durable, highly-flexible transparent electrode (FTE) is developed by applying a composite made of a thin metal grid and a doped conducting polymer onto a colorless polyimide-coated NOA63 substrate. The proposed FTE exhibits a transparency of 90.7% at 550 nm including the substrate and a sheet resistance of 30.3 Ω/sq and can withstand both moderately high-temperature annealing (∼180 °C) and acidic solution (70 °C, pH 0.3) processes without performance degradation. The fabricated FTE yielded good mechanical stability under 10 000 cycles of bending deformations at a bending radius less than 1 mm without degradation of electrical conductivity. The high durability of the proposed FTE allows for the fabrication of flexible energy harvesting devices requiring harsh conditions, such as highly flexible perovskite solar cells (FPSCs) with a steady-state power conversion efficiency (PCE) of 12.7%. Notably, 93% of the original PCE is maintained after 2000 bending cycles at an extremely small bending radius of 1.5 mm. The FPSCs installed on curved surfaces of commercial devices drive them under various environments. The applicability of the proposed FTE is further confirmed via the fabrication of a flexible perovskite light-emitting diode. The proposed FTE demonstrates great potential for applications in the field of flexible optoelectronic devices.

Highly Conductive, Stretchable, and Transparent PEDOT:PSS Electrodes Fabricated with Triblock Copolymer Additives and Acid Treatment.

Here, we report on a highly conductive, stretchable, and transparent electrode of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) fabricated via modification with triblock copolymer, poly(ethylene glycol)- block-poly(propylene glycol)- block-poly(ethylene glycol) (PEO20-PPO70-PEO20, Pluronic P123), and post-treatment with sulfuric acid. The fabricated electrode exhibits high transparency (89%), high electrical conductivity (∼1700 S/cm), and minimal change in resistance (∼4%) under repetitive stretch-release cycles at 40% tensile strain after stabilization. P123 acts as a secondary dopant and plasticizer, resulting in enhanced electrical conductivity and stretchability of PEDOT:PSS. Furthermore, after sulfuric acid post-treatment, P123 helps the electrode to maintain its stretchability. A successful demonstration of the stretchable interconnection was shown by stretching the P123-modified PEDOT:PSS electrodes, which were connected with light-emitting diodes (LEDs) in series. Finally, a stretchable and transparent touch sensor consisting of our fabricated electrodes and an LED array and stretchable semitransparent supercapacitor were presented, suggesting a great potential of our electrodes in the application to various deformable devices.

Discrete photoelectrodes with dyes having different absorption wavelengths for efficient cobalt-based tandem dye-sensitised solar cells.

A pn-tandem dye-sensitised solar cell (pn-DSSC) employing a set of sensitisers with complementary absorption spectra and a less-corrosive cobalt-based electrolyte is presented. We applied three organic sensitisers (denoted C343, DCBZ, and SQ) featuring different absorption wavelengths for the p-DSSC, while keeping the n-DSSC sensitiser (denoted DCA10CN2) constant. Characterisation of the Co+2/+3-based DSSC devices revealed that SQ dye, with a longer absorption wavelength, showed broader spectra and increased photocurrent activity in the visible and near-infrared region compared to the other two devices with C343 and DCBZ in the pn-DSSCs. As a result, the short-circuit current density increased significantly to 4.00 mA cm-2, and the devices displayed overall power conversion efficiencies of as high as 1.41%, which is comparable to that of the best pn-DSSCs in the literature. Our results demonstrate that complementary absorption between the two photoelectrodes is important for enhancing the photovoltaic performance of pn-DSSCs.

Enhanced Charge Collection with Passivation Layers in Perovskite Solar Cells.

The Al2 O3 passivation layer is beneficial for mesoporous TiO2 -based perovskite solar cells when it is deposited selectively on the compact TiO2 surface. Such a passivation layer suppressing surface recombination can be formed by thermal decomposition of the perovskite layer during post-annealing.

Ionic polarization-induced current-voltage hysteresis in CH3NH3PbX3 perovskite solar cells.

CH3NH3PbX3 (MAPbX3) perovskites have attracted considerable attention as absorber materials for solar light harvesting, reaching solar to power conversion efficiencies above 20%. In spite of the rapid evolution of the efficiencies, the understanding of basic properties of these semiconductors is still ongoing. One phenomenon with so far unclear origin is the so-called hysteresis in the current-voltage characteristics of these solar cells. Here we investigate the origin of this phenomenon with a combined experimental and computational approach. Experimentally the activation energy for the hysteretic process is determined and compared with the computational results. First-principles simulations show that the timescale for MA(+) rotation excludes a MA-related ferroelectric effect as possible origin for the observed hysteresis. On the other hand, the computationally determined activation energies for halide ion (vacancy) migration are in excellent agreement with the experimentally determined values, suggesting that the migration of this species causes the observed hysteretic behaviour of these solar cells.

Stretchable Active Matrix Temperature Sensor Array of Polyaniline Nanofibers for Electronic Skin.

A stretchable polyaniline nanofiber temperature sensor array with an active matrix consisting of single-walled carbon nanotube thin-film transistors is demonstrated. The integrated temperature sensor array gives mechanical stability under biaxial stretching of 30%, and the resultant spatial temperature mapping does not show any mechanical or electrical degradation.

Charge Transfer Dynamics from Organometal Halide Perovskite to Polymeric Hole Transport Materials in Hybrid Solar Cells.

Organometal halide perovskites have emerged as promising next-generation solar cell technologies presenting outstanding efficiencies. However, many questions concerning their working principles remain to be answered. Here, we present a detailed study of hole transfer dynamics into polymeric hole transporting materials (HTMs), poly(triarylamine) (PTAA), poly(3-hexylthiophee-2,5-diyl (P3HT), and poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7-(2,1,3-benzothiadiazole) (PCPDTBT). The hole transfer dynamics are shown to occur on a time scale of thousands of picoseconds, being orders of magnitude slower compared to hole transfer involving commonly used Spiro-OMeTAD as HTM.

Efficient perovskite solar cells with 13.63 % efficiency based on planar triphenylamine hole conductors.

A new type of hole transporting material (HTMs) with an incorporated planar amine or triphenylamine as a core unit have been prepared. The two amine derivatives were demonstrated to be efficient hole transporting materials in fabricating solid-state organic-inorganic hybrid solar cells. Perovskite-based solar cells with a planar amine derivative gave a short circuit photocurrent density (Jsc) of 20.98 m Acm(-2), an open circuit voltage (Voc) of 0.972 V, and a fill factor of 0.67, corresponding to an overall conversion efficiency of 13.63 %. The photovoltaic performance is comparable to that of the standard spiro-OMeTAD. Moreover, the device showed good stability under light soaking for 500 h. These HTMs hold promise to replace the expensive spiro-OMeTAD because of their high efficiency, excellent stability, synthesis from simple and inexpensive materials.

Strong Photocurrent Amplification in Perovskite Solar Cells with a Porous TiO2 Blocking Layer under Reverse Bias.

We investigate two different types of TiO2 blocking layer (BL) deposition techniques commonly used in solid-state methylammonium lead triiodide perovskite (MaPbI3)-based solar cells. Although these BLs lead to similar photovoltaic device performance, their structure and blocking capability is actually very different. In one case, the "blocking" layer is porous, allowing an intimate contact of the perovskite with the fluorine-doped tin-dioxide (FTO)-covered glass substrate serving as transparent electron collector. This interface between the perovskite and the FTO shows rectifying behavior. Reverse biasing of such a solar cell allows the determination of the valence-band position of the MaPbI3 and the theoretical maximum attainable photovoltage. We show that under reverse bias strong photocurrent amplification is observed, permitting the cell to work as a high-gain photodetector at low voltage. Without BL, the solar-cell performance decreased, but the photocurrent amplification increased. At 1 V reverse bias, the photocurrent amplification is above a factor of 10 for AM 1.5 solar light and over 100 for lower light intensities.

Sb(2)Se(3) -sensitized inorganic-organic heterojunction solar cells fabricated using a single-source precursor.

The photovoltaic performance of Sb2 Se3 -sensitized heterojunction solar cells, which were fabricated by a simple deposition of Sb2 Se3 on mesoporous TiO2 by an approach that features multiple cycles of spin coating with a single-source precursor solution and thermal decomposition, is reported. Poly[2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7(2,1,3-benzothioadiazole)] was used as the hole-transporting material. The most efficient cell exhibited a short-circuit current density of 22.3 mA cm(-2) , an open-circuit voltage of 304.5 mV, and a fill factor of 47.2 %, yielding a power conversion efficiency of 3.21 % under standard test conditions (irradiation of 1000 W m(-2) , air mass=1.5 G). The results of this study imply that the developed approach has a high potential as a simple and effective route for the fabrication of efficient and inexpensive solar cells.

Urchinlike nanostructure of single-crystalline nanorods of Sb2S3 formed at mild reaction condition.

Urchinlike nanostructure of well-defined Sb(2)S(3) crystals of 3-4 µm in length and 30-150 nm in diameter oriented along [001] direction have been produced at a mild reaction temperature of 90 °C from SbCl(3) and S-methyl 3-phenyldithiocarbazate [C(6)H(5)NHNHC(S)SMe] in ethylene glycol medium. During the reaction, the amorphous Sb(2)S(3) spheres of 1.4 µm in diameter were formed at early reaction stage and then crystalline nanorods were continuously grown at the surface of Sb(2)S(3) spheres while transforming their morphology into urchinlike structure. The urchinlike Sb(2)S(3) was composed of single-crystalline Sb(2)S(3) nanorods, belong to the orthorhombic phase with cell parameters a = 11.307 Å, b = 11.278 Å, c = 3.847 Å and absorbed the light up to 750 nm-wavelength region. The urchinlike Sb(2)S(3) architecture was applied to the photoelectrochemical cell.

Panchromatic photon-harvesting by hole-conducting materials in inorganic-organic heterojunction sensitized-solar cell through the formation of nanostructured electron channels.

Additional photon-harvesting by hole transporting materials in Sb(2)S(3)-sensitized solar cell is demonstrated through the formation of electron channels in the hole transporter such as P3HT (poly(3-hexylthiophene)) and PCPDTBT(poly(2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7(2,1,3-benzothiadiazole)) that can act as both a hole conductor and light absorber. As a result, the short-circuit current density is improved with an increment in overall efficiency. These findings provide new insights into use of light-absorbing conjugated polymers as a hole conductor in the inorganic-organic heterojunction sensitized solar cells.

Enhancing the device performance of Sb2S3-sensitized heterojunction solar cells by embedding Au nanoparticles in the hole-conducting polymer layer.

Performance of Sb(2)S(3)-sensitized heterojunction solar cells is enhanced by embedding Au nanoparticles in the poly-3-hexylthiophene (P3HT) hole-conducting polymer layer. The improved charge transfer/transport at the Sb(2)S(3)/P3HT/Au interface by extended interface area of the P3HT/Au counter electrode and the re-absorption of the backscattering light from the embedded Au nanoparticles enhanced the device performance: J(sc) 11.0 to 12.8 mA cm(-2), V(oc) 606 to 626 mV, fill factor (FF) 60.5 to 61.2%, and power conversion efficiency (η) 4.0 to 4.9%. Simultaneous enhancement of V(oc), J(sc), and FF in Au nanoparticle-embedded systems is mainly attributed to the improved charge collection efficiency and light harvesting efficiency of Sb(2)S(3) due to the improved charge transfer/transport in the Sb(2)S(3)/P3HT/Au interface.

From flat to nanostructured photovoltaics: balance between thickness of the absorber and charge screening in sensitized solar cells.

Nanoporous metal oxide electrodes provide a high internal area for dye anchoring in dye-sensitized solar cells, but the thickness required to extinguish the solar photons also enhances recombination at the TiO(2)/electrolyte interface. The high extinction coefficient of inorganic semiconductor absorber should allow the reduction of the film thickness, improving the photovoltage. Here we study all-solid semiconductor sensitized solar cells, in the promising TiO(2)/Sb(2)S(3)/P3HT configuration. Flat and nanostructured cells have been prepared and analyzed, developing a cell performance model, based on impedance spectroscopy results, that allows us to determine the impact of the reduction of metal oxide film thickness on the operation of the solar cell. Decreasing the effective surface area toward the limit of flat samples produces a reduction in the recombination rate, increasing the open circuit potential, V(oc), while providing a significant photocurrent. However, charge compensation problems as a consequence of inefficient charge screening in flat cells increase the hole transport resistance, lowering severely the cell fill factor. The use of novel structures balancing recombination and hole transport will enhance solid sensitized cell performance.

Improvement of external quantum efficiency depressed by visible light-absorbing hole transport material in solid-state semiconductor-sensitized heterojunction solar cells.

A mesoporous (mp)-TiO(2)/Sb(2)S(3)/P3HT [poly(3-hexylthiophene)] heterojunction solar cell displays reduced external quantum efficiency (EQE) at a wavelength of approximately 650 nm. This loss in EQE is due to incomplete charge carrier transport because the transportation of charge carriers generated in P3HT by the absorption of light into Sb(2)S(3) was inefficient, and consequently, the carriers recombined. The depression of the EQE was greatly relieved by introducing the porous structure formed by thermal decomposition of 2,2'-azobisisobutyronitrile (AIBN) into the P3HT layer.

Toward interaction of sensitizer and functional moieties in hole-transporting materials for efficient semiconductor-sensitized solar cells.

Sb(2)S(3)-sensitized mesoporous-TiO(2) solar cells using several conjugated polymers as hole-transporting materials (HTMs) are fabricated. We found that the cell performance was strongly correlated with the chemical interaction at the interface of Sb(2)S(3) as sensitizer and the HTMs through the thiophene moieties, which led to a higher fill factor (FF), open-circuit voltage (V(oc)), and short-circuit current density (J(sc)). With the application of PCPDTBT (poly(2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7(2,1,3-benzothiadiazole)) as a HTM in a Sb(2)S(3)-sensitized solar cell, overall power conversion efficiencies of 6.18, 6.57, and 6.53% at 100, 50, and 10% solar irradiation, respectively, were achieved with a metal mask.

Quantum-dot-sensitized solar cells fabricated by the combined process of the direct attachment of colloidal CdSe quantum dots having a ZnS glue layer and spray pyrolysis deposition.

We were able to attach CdSe quantum dots (QDs) having a ZnS inorganic glue layer directly to a mesoporous TiO(2) (mp-TiO(2)) surface by spray coating and thermal annealing. Quantum-dot-sensitized solar cells based on CdSe QDs having ZnS as the inorganic glue layer could easily transport generated charge carriers because of the intimate bonding between CdSe and mp-TiO(2). The application of spray pyrolysis deposition (SPD) to obtain additional CdSe layers improved the performance characteristics to V(oc) = 0.45 V, J(sc) = 10.7 mA/cm(2), fill factor = 35.8%, and power conversion efficiency = 1.7%. Furthermore, ZnS post-treatment improved the device performance to V(oc) = 0.57 V, J(sc) = 11.2 mA/cm(2), fill factor = 35.4%, and power conversion efficiency = 2.2%.

Performance enhancement through post-treatments of CdS-sensitized solar cells fabricated by spray pyrolysis deposition.

The CdS-sensitized solar cells (CdS-SSC) were fabricated by spray pyrolysis deposition (SPD) method. The performance of the cells was greatly improved through post-treatments that included thermal oxidation at 500 degrees C for 30 min in an air atmosphere and subsequent chemical etching by 40 mM aqueous HCl solution at room temperature for 30 min, as compared to as-deposited CdS-SSC. The CdS-SSC in a I(-)/I(3)(-) electrolyte system was resulted in the improvement of J(sc) (3.3 --> 5.2 mA/cm(2)), V(oc) (697 --> 758 mV), FF (41.4% --> 46.9%), and (0.95% --> 1.84%). Similarly, the efficiency of CdS-SSC in a noncorrosive polysulfide electrolyte system was also enhanced by the proposed thermal oxidation and etching process. The increase in the cell efficiency is attributed to the reduced charge recombination among sensitizer themselves through the mitigation of overaggregated CdS sensitizers deposited by SPD.

High-performance nanostructured inorganic-organic heterojunction solar cells.

We report all solid-state nanostructured inorganic-organic heterojunction solar cells fabricated by depositing Sb(2)S(3) and poly(3-hexylthiophene) (P3HT) on the surface of a mesoporous TiO(2) layer, where Sb(2)S(3) acts as an absorbing semiconductor and P3HT acts as both a hole conductor and light absorber. These inorganic-organic light harvesters perform remarkably well with a maximum incident-photon-to-current efficiency (IPCE) of 80% and power conversion efficiency of 5.13% under air-mass 1.5 global (AM 1.5G) illumination with the intensity of 100 mW cm(-2). These devices are highly stable under room light in air, even without encapsulation. The present findings offer novel directions for achieving high-efficiency solid-state solar cells by hybridization of inorganic-organic light harvesters and hole transporters.