Compositionally Graded Bulk Heterojunction Devices and Methods of Manufacturing The Same

Systems and methods are described to form compositionally graded BHJ structures utilizing solvent-fluxing techniques. In implementations, the systems and methods described herein involve a high boiling point additive, a solution of a polymer donor and an acceptor, a substrate material, a working solvent, and a flux solvent for formation of compositionally graded BHJ structures

Compositionally Graded Bulk Heterojunction Devices and Methods of Manufacturing The Same

Systems and methods are described to form compositionally graded BHJ structures utilizing solvent-fluxing techniques. In implementations, the systems and methods described herein involve a high boiling point additive, a solution of a polymer donor and an acceptor, a substrate material, a working solvent, and a flux solvent for formation of compositionally graded BHJ structures

From M-ary Query to Bit Query: a new strategy for efficient large-scale RFID identification

The tag collision avoidance has been viewed as one of the most important research problems in RFID communications and bit tracking technology has been widely embedded in query tree (QT) based algorithms to tackle such challenge. Existing solutions show further opportunity to greatly improve the reading performance because collision queries and empty queries are not fully explored. In this paper, a bit query (BQ) strategy based Mary query tree protocol (BQMT) is presented, which can not only eliminate idle queries but also separate collided tags into many small subsets and make full use of the collided bits. To further optimize the reading performance, a modified dual prefixes matching (MDPM) mechanism is presented to allow multiple tags to respond in the same slot and thus significantly reduce the number of queries. Theoretical analysis and simulations are supplemented to validate the effectiveness of the proposed BQMT and MDPM, which outperform the existing QT-based algorithms. Also, the BQMT and MDPM can be combined to BQMDPM to improve the reading performance in system efficiency, total identification time, communication complexity and average energy cost

Polymer aggregation correlated transition from Schottky-junction to bulk heterojunction organic solar cells

The fullerene-based organic Schottky-junction solar cells have recently attracted intensive research interest because of their unique electrical performance, such as significant photocurrent generation from excitons created in fullerenes and large open-circuit voltage (VOC) output induced by high Schottky-barrier height between the anode and the fullerene acceptor. This manuscript reports another remarkably appealing advantage that the fullerene-based Schottky-junction solar cells are more stable than the bulk heterojunction counterparts. The better stability is likely due to mitigative polymer photo-oxidation and/or little morphological change of active film in the aged Schottky-junction devices. The transition from Schottky-junction to bulk heterojunction appears at polymer donor loading ratio of 20–25 wt.% by examining the variation in the VOC with increased loading ratio of the poly(3-hexylthiophene) donor. Multiple experimental evidences, including the absorbance spectrum measurement, photoluminescence study, active film morphology characterization, and charge mobility measurement, conclusively reveal that the transition from Schottky-junction to bulk heterojunction is correlated to the polymer donor aggregation in the active films

Polymer aggregation correlated transition from Schottky-junction to bulk heterojunction organic solar cells

The fullerene-based organic Schottky-junction solar cells have recently attracted intensive research interest because of their unique electrical performance, such as significant photocurrent generation from excitons created in fullerenes and large open-circuit voltage (VOC) output induced by high Schottky-barrier height between the anode and the fullerene acceptor. This manuscript reports another remarkably appealing advantage that the fullerene-based Schottky-junction solar cells are more stable than the bulk heterojunction counterparts. The better stability is likely due to mitigative polymer photo-oxidation and/or little morphological change of active film in the aged Schottky-junction devices. The transition from Schottky-junction to bulk heterojunction appears at polymer donor loading ratio of 20–25 wt.% by examining the variation in the VOC with increased loading ratio of the poly(3-hexylthiophene) donor. Multiple experimental evidences, including the absorbance spectrum measurement, photoluminescence study, active film morphology characterization, and charge mobility measurement, conclusively reveal that the transition from Schottky-junction to bulk heterojunction is correlated to the polymer donor aggregation in the active films

Efficiency Enhancement in Polymer Solar Cells With a Polar Small Molecule Both at Interface and in the Bulk Heterojunction Layer

The polar molecules, including ferroelectric materials with large dipole moments, have been applied as interfacial layers to increase the efficiency of organic solar cells by increasing the bounded charge separation, tuning the energy levels, etc. Here, we report a small polar molecule 2-cyano-3- (4-(diphenylamino) phenyl)acrylic acid (TPACA) that can be either blended in the active layer or at the polymer/electrode interface to increase the efficiency of organic solar cell devices after poling. It is found that the built-in potential of the device is increased by 0.2 V after poling under negative bias. Blending TPACA into the active layer has shown to be a universal method to increase the efficiency of polymer solar cells. The efficiency is increased by 30–90% for all the polymer:fullerene systems tested, with the highest efficiency reaching 7.83% for the poly[4,8-bis-(2-ethyl-hexyl-thiophene-5-yl)-benzo[1,2-b:4,5-b’]dithiophene-2,6-diyl]-alt-[2-(2’-ethyl-hexanoyl)-thieno[3,4-b]thiophen-4,6-diyl]: [6,6]-phenyl-C71 -butyric acid methyl ester (PBDTTT-CT:PC70BM) system

Improving the sensitivity of a near-infrared nanocomposite photodetector by enhancing trap induced hole injection

We report the enhancement of the photoconductive gain of nanocomposite near-infrared photodetectors by a zinc oxide nanoparticles (ZnO NPs) rich surface at the nanocomposite/cathode interface. An argon plasma etching process was used to remove polymer at the surface of nanocomposite films, which resulted in a ZnO NPs rich surface. The other way is to spin-coat a thin layer of ZnO NPs onto the nanocomposite layer. The ZnO NPs rich surface, which acts as electron traps to induce secondary hole injection under reverse bias, increased hole injection, and thus the external quantum efficiency by 2–3 times. The darkcurrent declined one order of magnitude simultaneously as a result of etching the top nanocomposite layer. The specific detectivity at 800 nm was increased by 7.4 times to 1.11x1010 Jones due to the simultaneously suppressed noise and enhanced gain

Improving the sensitivity of a near-infrared nanocomposite photodetector by enhancing trap induced hole injection

We report the enhancement of the photoconductive gain of nanocomposite near-infrared photodetectors by a zinc oxide nanoparticles (ZnO NPs) rich surface at the nanocomposite/cathode interface. An argon plasma etching process was used to remove polymer at the surface of nanocomposite films, which resulted in a ZnO NPs rich surface. The other way is to spin-coat a thin layer of ZnO NPs onto the nanocomposite layer. The ZnO NPs rich surface, which acts as electron traps to induce secondary hole injection under reverse bias, increased hole injection, and thus the external quantum efficiency by 2–3 times. The darkcurrent declined one order of magnitude simultaneously as a result of etching the top nanocomposite layer. The specific detectivity at 800 nm was increased by 7.4 times to 1.11x1010 Jones due to the simultaneously suppressed noise and enhanced gain

Non-wetting surface-driven high-aspect-ratio crystalline grain growth for efficient hybrid perovskite solar cells

Large-aspect-ratio grains are needed in polycrystalline thin-film solar cells for reduced charge recombination at grain boundaries; however, the grain size in organolead trihalide perovskite (OTP) films is generally limited by the film thickness. Here we report the growth of OTP grains with high average aspect ratio of 2.3–7.9 on a wide range of non-wetting hole transport layers (HTLs), which increase nucleus spacing by suppressing heterogeneous nucleation and facilitate grain boundary migration in grain growth by imposing less drag force. The reduced grain boundary area and improved crystallinity dramatically reduce the charge recombination in OTP thin films to the level in OTP single crystals. Combining the high work function of several HTLs, a high stabilized device efficiency of 18.3% in low-temperature-processed planar-heterojunction OTP devices under 1 sun illumination is achieved. This simple method in enhancing OTP morphology paves the way for its application in other optoelectronic devices for enhanced performance. Includes supplementary materials

Unraveling the hidden function of a stabilizer in a precursor in improving hybrid perovskite film morphology for high efficiency solar cells

The morphology of the organometal trihalide perovskite (OTP) plays a critical role in the performance of solar cell devices. Nevertheless it has been frequently reported that the morphology of OTP films tends to be different in different laboratories even with the same film preparation procedure, which makes it very difficult to compare and understand the material and device physics. Here, we unravel a critical role of the H3PO2 stabilizer in HI, which has been largely ignored, in controlling the morphology of the perovskite films. The H3PO2 stabilizer in HI solution introduces MAH2PO2 impurities into the synthesized MAI (non-purified MAI) by reacting with methylamine (MA) aqueous solution. MAH2PO2 impurities can slow down the overall crystallization process of perovskite by forming an intermediate phase of Pb(H2PO2)2. Both MAH2PO2 and Pb(H2PO2)2 impede the fast reaction of PbI2 and MAI, resulting in highly uniform and smooth perovskite films with larger grain sizes. The recrystallization of non-purified MAI can remove the MAH2PO2 impurity and form purified MAI, which however results in rough and non-uniform perovskite films. Uniform and smooth perovskite films can also be obtained by directly adding artificially synthesized MAH2PO2 into the purified MAI precursor. This study also suggests Pb(H2PO2)2 to be a new precursor to formhigh quality perovskite films