Flexible solar cells based on PCBM/P3HT heterojunction

[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) / poly (3-hexylthiophene) (P3HT) heterojunction has not only the absorption in ultraviolet light for PCBM,but also the absorption in visible light for P3HT, which widens the incident light harvest range, improving the photoelectrical response of hybrid solar cell effectively.Using conducting polymers blend heterojunetion consisting of C60 derivatives PCBM and P3HT as charge carrier transferring medium to replace I3-/I- redox electrolyte and dye, a novel flexible solar cell was fabricated in this study.The influence of PCBM/P3HT mass ratio on the photovoltaic performance of the solar cell was also studied.flexible solar cell achieved a light-to-electric energy conversion efficiency of 1.04%, an open circuit voltage fill factor (FF) of 0.46.     

Effect of fullerene doping on the electrical properties of P3HT/PCBM layers

Poly (3-hexylthiophene-2, 5-diyl) (P3HT) and its blend with Phenyl-C₆₁-Butyric acid-Methyl-Ester (PCBM) and fullerene (C₆₀) thin films were prepared and their electrical properties for memory applications were studied. Due to doping, a sharp decrease in the resistance for a P3HT:PCBM:C₆₀ device was observed at around 70 °C which makes it useful for thermal switching applications. Addition of C₆₀ to P3HT:PCBM blend gave a high value for R_RESET/R_SET in thermal switching. For bias switching, threshold voltage reduces to 1.4 V from 25 V with the addition of C₆₀ to P3HT layer.     

Effect of Trace Solvent on the Morphology of P3HT:PCBM Bulk Heterojunction Solar Cells

The performance of bulk‐heterojunction (BHJ) solar cells is strongly correlated with the nanoscale structure of the active layer. Various processing techniques have been explored to improve the nanoscale morphology of the BHJ layer, e.g., by varying the casting solvent, thermal annealing, solvent annealing, and solvent additives. This paper highlights the role of residual solvent in the “dried” BHJ layer, and the effect of residual solvents on PCBM diffusion and ultimately the stability of the morphology. We show that solvent is retained within the BHJ film despite prolonged heat treatment, leading to extensive phase separation, as demonstrated by the growth in the size and quantity of PCBM agglomerates. The addition of a small volume fraction of nitrobenzene to the casting solution inhibits the diffusion of PCBM in the dry film, resulting in smaller PCBM agglomerates, and improves the fill factor of the BHJ device to 0.61 without further tempering. The addition of nitrobenzene also increases the P3HT crystalline content, while increasing the onset temperature for melting of P3HT side chains and backbone. The melting temperature for PCBM is also higher with the nitrobenzene additive present.     

Bismuth Doping–Induced Stable Seebeck Effect Based on MAPbI3 Polycrystalline Thin Films

In this article, the thermoelectric properties of a Bi‐doped CH₃NH₃PbI₃ (MAPbI₃) perovskite thin film are studied. Bi‐doped MAPbI₃ thin film samples are fabricated, and it is found that Bi doping could greatly enhance the stability and thermoelectric properties of MAPbI₃. The Bi dopant located at the grain boundaries to modify the carrier channel near grain boundaries, which is observed via scanning electron microscopy and atomic force microscopy, efficiently reduces ion migration and facilitates charge transport. In addition, the Bi dopant can also passivate the defects in bulk MAPbI₃, increasing the polarization effect of MAPbI₃ which is demonstrated by the capacitance‐frequency measurement, thus greatly enhancing the mobility of Bi‐doped MAPbI₃. In addition, Bi‐doped MAPbI₃ leads to grain size reduction; the small size effect not only effectively hinders the MAPbI₃'s crystal phase transition from the tetragonal phase to the cubic phase, but it could also make the structure of MAPbI₃ more stable. Especially, the Seebeck voltage variation of Bi‐doped perovskite was less than that of the undoped one, meaning Bi doping would lead to a much more stable state in MAPbI₃ thin films. The results show that Bi‐doped MAPbI₃ is a promising approach to develop high stable thermoelectric and photovoltaic properties in organic–inorganic hybrid perovskite materials.     

Hybrid photovoltaic structures based on amorphous silicon and P3HT:PCBM/PEDOT:PSS polymer semiconductors

Hybrid thin film photovoltaic structures, based on hydrogenated silicon (Si:H), organic poly(3-hexythiophene):methano-fullerenephenyl-C61-butyric-acid-methyl-ester (P3HT:PCBM) and poly(3,4ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) films, have been fabricated. Organic semiconductor thin films were deposited by spin-coating technique and were exposed to radio frequency plasma enhanced chemical vapor deposition (RF PECVD) of Si:H films at deposition temperature T_d = 160 °C. Different types of structures have been investigated: H1) ITO/(p)SiC:H /P3HT:PCBM/(n) Si:H, H2) ITO/PEDOT:PSS/(i)Si:H/(n) Si:H and H3) ITO/PEDOT:PSS/P3HT:PCBM/(i)Si:H/(n)Si:H. Short circuit current density spectral response and current-voltage characteristics were measured for diagnostic of the photovoltaic performance. The current density spectral dependence of hybrid structures which contains organic layers showed improved response (50–80%) in high photon energy range (hν ≈ 3.1–3.5 eV) in comparison with Si:H reference structure. An adjustment in the absorbing layer thickness and in the contact material for ITO/PEDOT:PSS/(i)Si:H/(n)Si:H structure, resulted in a remarkably high short circuit current density (as large as 17.74 mA/cm²), an open circuit voltage of 640 mV and an efficiency of 3.75%.     

Effects of PCBM concentration on the electrical properties of the Au/P3HT:PCBM/n-Si (MPS) Schottky barrier diodes

In this study, the gold/poly(3-hexylthiophene):[6,6]-phenyl C61 butyric acid methyl ester/n-type silicon (Au/P3HT:PCBM/n-Si) metal–polymer–semiconductor (MPS) Schottky barrier diodes (SBDs) were investigated in terms of the effects of PCBM concentration on the electrical parameters. The forward and reverse bias current–voltage (I–V) characteristics of the Au/P3HT:PCBM/n-Si MPS SBDs fabricated by using the different P3HT:PCBM mass ratios were studied in the dark, at room temperature. The main electrical parameters, such as ideality factor (n), barrier height (Φ_B0), series resistance (R_s), shunt resistance (R_sh), and density of interface states (N_ss) were determined from I–V characteristics for the different P3HT:PCBM mass ratios (2:1, 6:1 and 10:1) used diodes. The values of n, R_s, Φ_B0, and N_ss were reduced, while the carrier mobility and current were increased, by increasing the PCBM concentration in the P3HT:PCBM organic blend layer. The ideal values of electrical parameters were obtained for 2:1 P3HT:PCBM mass ratio used diode. This shows that the electrical properties of MPS diodes strongly depend on the PCBM concentration of the P3HT:PCBM organic layer. Moreover, increasing the PCBM concentration in P3HT:PCBM organic blend layer improves the quality of the Au/P3HT:PCBM/n-Si (MPS) SBDs which enables the fabrication of high-quality electronic and optoelectronic devices.     

Role of structural order at the P3HT/C60 heterojunction interface

The influence of structural order on the electronic and optical properties of C₆₀/P3HT bulk heterojunctions (BHJs) was studied using first principles DFT and TDDFT methods. The electronic levels alignment between the two phases in the BHJs is mainly controlled by the interfacial dipole moment that shifts the P3HT electronic levels towards higher binding energies with respect to C₆₀ levels. An increasing order translates into an increasing P3HT domains size, for which we considered different stacks of P3HT oligomers. A significant decrease of both the electronic (HOMO_P3HT–LUMO_C60) and the optical (HOMO_P3HT–LUMO_P3HT) band gap is observed with an increasing P3HT domain size. TDDFT approach was used to identify the orbitals involved in the electronic transitions, and to reveal that the reduction of the BHJ optical band gap cannot simply be predicted from the variation of the rrP3HT band gap. The lowest electronic transition in rrP3HT becomes optically forbidden due to the formation of H-aggregates.     

Novel magnetic field sensor based on magnetic fluids infiltrated dual-core photonic crystal fibers

Novel magnetic field sensor based on magnetic fluids infiltrated dual-core Photonic Crystal Fibers (PCFs) is proposed in this paper. Inside the cross-section of the designed PCFs, the two fiber cores filled with magnetic fluids (Fe₃O₄) are separated by an air hole, and then form two independent waveguides with mode coupling. The mode coupling under different magnetic field strength is investigated theoretically. A novel and simple magnetic field sensing system is proposed and its sensing performances have been studied numerically. The results show that the magnetic field sensor with 15-cm PCFs has a large sensing range and high sensitivity of 4.80 pm/Oe. It provides a new feasible method to design PCF-based magnetic field sensor.     

基于P3HT/PCBM异质结界面太阳能电池的理论及实验研究

根据整数电荷转移(ICT)模型理论分析基于P3HT为给体PCBM为受体的异质结界面,认为不同等效功函数衬底和电荷传输状态产生不同D/A界面特性。采用增加P3HT缓冲层PCBM缓冲层的方法,制备不同复合层本体异质结结构光伏器件,研究活性膜内组分变化对器件开路电压和短路电流密度的影响。结果表明增加缓冲层使器件的短路电流密度明显提高,从3.96mA/cm2分别增加到4.51mA/cm2和4.70mA/cm2,但对开路电压影响不大。     

Effects of incorporation of copper sulfide nanocrystals on the performance of P3HT: PCBM based inverted solar cells

It has been reported that performance of bulk heterojunction organic solar cells can be improved by incorporation of an additive like metal and semiconducting nanoparticles in the active layer. Here in, we have synthesized Cu₂S nanocrystals (NCs) by chemical route and studied its dispersion in poly (3-hexylthiophene) [6, 6]-phenyl C61-butyric acid methyl ester (P3HT: PCBM) matrix. Variation in the performance parameters with change in the concentration of Cu₂S NCs into the P3HT: PCBM matrix has also been studied and it was found that the inverted geometry device with concentration of 20 wt% of Cu₂S NCs and having the structure ITO/ZnO (NPs)/P3HT: PCBM:Cu₂S NCs/MoO₃/Al has shown maximum efficiency of 3.39% which is more than 100% increase in comparison with devices without Cu₂S NCs. Photoluminescence measurements studies unveiled that the incorporation of Cu₂S NCs into a P3HT: PCBM matrix has helped in quenching photoluminescence which suggests more effective exciton dissociation at the interfaces between the P3HT and PCBM domains. The Nyquist plots obtained from impedance spectroscopy at 1 V bias in the dark has suggested the effective lifetime and global mobilities for P3HT: PCBM as 0.267 ms and 1.17 × 10⁻³ cm²/V-S and for P3HT: PCBM:Cu₂S NCs (20 wt%) systems as 0.156 ms and 2.02 × 10⁻³ cm²/V-S respectively. Based on observed photoluminescence quenching, calculated effective lifetime and global mobility, we have tried to explain the possible reason for improvement in the efficiency with the very well dispersion of Cu₂S NCs into the P3HT: PCBM matrix.     

P3HT/PCBM Bulk Heterojunction Solar Cells: Impact of Blend Composition and 3D Morphology on Device Performance

The performance of polymer solar cells (PSC) strongly depends on the 3D morphological organization of the donor and acceptor compounds within the bulk heterojunction active layer. The technique of electron tomography is a powerful tool for studying 3D morphology of the layers composed of poly(3‐hexylthiophene) (P3HT) and a fullerene derivative ([6,6]‐phenyl‐C61‐butyric acid methyl ester; PCBM), especially to quantify the amount and distribution of fibrillar P3HT nanocrystals throughout the volume of the active layer. In this study, electron tomography is used to characterize P3HT/PCBM layers with different blend compositions, both before and after thermal annealing. The power conversion efficiency of the corresponding PSCs is strongly dependent on the overall crystallinity of P3HT and the way P3HT crystals are distributed throughout the thickness of the active layer.     

基于磁通元电场叠加法的涡旋电场计算

提出用磁通元电场叠加法求解涡旋电场,利用该方法推导出了空间旋转平面区域产生的涡旋电场的时域表达式,验证了磁通元电场叠加法求解涡旋电场的正确性。     

LD端面泵浦变热传导系数Nd:YAG晶棒温场特性

为了解决激光二极管泵浦激光晶体产生的热效应问题,对激光晶体内的温升进行了解析分析与定量计算。通过对激光二极管端面泵浦激光晶体工作特点的分析,建立了符合实际工作情况的热模型。考虑到晶体材料热传导系数受其宏观温度变化的影响,应用常数变易法以及特征函数法得到了变热传导系数Nd:YAG晶体棒在端面泵浦情况下温度场的一般表达式。定量计算了激光二极管超高斯分布泵浦光阶次、泵浦功率、光斑尺寸以及晶棒半径对其温度场分布的影响。研究结果表明:使用输出功率为60 W的激光二极管端面泵浦掺钕离子质量分数1.0%的Nd:YAG晶棒,若耦合入射的3阶超高斯光束泵浦光斑半径为400μm,晶棒半径为1.5 mm,长度为8 mm时,Nd:YAG棒内最大温升为343.9℃;而将其热导率视为定值时,晶体的最大温升只有222.7℃。研究结果为正确计算Nd:YAG晶体温度场分布提供了方法,并为提高全固态Nd:YAG激光器性能提供了理论依据。     

Effects of a magnetic field on the copper metallization using the electroplating process

We investigated the effects of a magnetic field on the electroplated copper films for the ULSI processes. The magnetic field was induced vertical to the electrodes and varied ranging from 0 to 600 G. The electroplating process was performed with on-off square pulse current source. The variation of the magnetic field vertical to the electrodes affected the deposition rate of the electroplated copper film, step coverage and gap filling in trench. As the intensity of the magnetic field increased, the deposition rate of the copper film increased, and also the resistance of electromigration increased. However, the magnetic field did not affect resistivity and surface morphology of the electroplated Cu film. At higher intensity of the magnetic field, good step coverage was obtained.     

Modular construction of P3HT/PCBM planar-heterojunction solar cells by lamination allows elucidation of processing–structure–function relationships

Contrary to polymer solar cells with bulk-heterojunction active layers, devices with planar-heterojunction active layers allow the decoupling of active layer phase separation from constituent crystallization, and their relative influence on device performance. We fabricated planar-heterojunction devices by first processing the electron donor and electron acceptor in isolation; they were subsequently laminated across the donor–acceptor interface to establish electrical contact. Thermal annealing was intentionally avoided after lamination to maintain the pristine charge transfer interface. Lamination thus obviates the need for solvent orthogonality; more importantly, it provides independent process tuning of individual organic semiconductor layers, ultimately allowing control over constituent structural development. We found the short-circuit current density of planar-heterojunction solar cells comprising poly(3-hexyl thiophene), P3HT, and [6,6]-phenyl-C₆₁-butyric acid methyl ester, PCBM, as the electron donor and acceptor, respectively, to be generally independent of the annealing history of P3HT. On the contrary, thermal annealing PCBM prior to lamination mainly led to a reduction in short-circuit current density. This deterioration is correlated with the development of preferentially oriented PCBM crystals that hinders electron transport in the vertical direction.     

The Effect of Ageing on Exciton Dynamics,Charge Separation,and Recombination in P3HT/PCBM Photovoltaic Blends

A study of how light‐induced degradation influences the fundamental photophysical processes in the active layer of poly(3‐hexylthiophene)/[6,6]‐phenyl C₆₁‐butyric acid methyl ester (P3HT/PCBM) solar cells is presented. Non‐encapsulated samples are systematically aged by exposure to AM 1.5 illumination in the presence of dry air for different periods of time. The extent of degradation is quantified by the relative loss in the absorption maximum of the P3HT, which is varied in the range 0% to 20%. For degraded samples an increasing loss in the number of excitons within the P3HT domains is observed with longer ageing periods. This loss occurs rapidly, within the first 15 ps after photoexcitation. A more pronounced decrease in the population of polarons than excitons is observed, which also occurs on a timescale of a few picoseconds. These observations, complemented by a quantitative analysis of the polaron and exciton population dynamics, unravel two primary loss mechanisms for the performances of aged P3HT/PCBM solar cells. One is an initial ultrafast decrease in the polaron generation, apparently not related to the exciton diffusion to the polymer/fullerene interface; the second, less significant, is a loss in the exciton population within the photoexcited P3HT domains. The steady‐state photoinduced absorption spectra of degraded samples exhibits the appearance of a signal ascribed to triplet excitons, which is absent for non‐degraded samples. This latter observation is interpreted considering the formation of degraded sites where intersystem crossing and triplet exciton formation is more effective. The photovoltaic characteristics of same blends are also studied and discussed by comparing the decrease in the overall power conversion efficiency of solar cells.     

Correlation between ultrafast transient photomodulation spectroscopy and organic photovoltaic solar cell efficiency based on RR-P3HT/PCBM blends

Ultrafast transient spectroscopy was applied to various films of regio-regular polythiophene (RR-P3HT, donor-D) and C₆₀ derivative (PCBM, acceptor-A) blends, in conjunction with organic photovoltaic (OPV) solar cell fabrication and evaluation based on the same blends, for investigating the existence of a correlation between the device efficiency and the transient photophysics characteristics. For our transient spectroscopy measurements we used the ps pump–probe transient photomodulation (PM) technique having a unique probe spectral range in the mid-IR (0.25–1.05 eV). We found that the transient PM spectra contain photoinduced absorption bands of excitons in the donor polymer, charge transfer excitons (CTE) at the D–A interfaces, and free polarons. We compared the relative density of photogenerated CTE in D–A blends having various D–A weight ratio with the photocurrent density of fabricated solar cells based on the same blends. We found that the dissociation of CTE into free charges correlates well with the optoelectronic measurements of the corresponding solar cell. The more efficient CTE dissociation occurs in films having the optimum D–A weight ratio (which is 1.2:1 for the P3HT/PCBM system) that shows the highest OPV power conversion efficiency; this is due to the lowest CTE binding energy for this blend that results from the most suitable D- and A- grain sizes. We also show that the exciton lifetime is the shortest for the optimum blend, and this helps boosting the device efficiency by reducing energy loss.     

Two-dimensional Braille readers based on electrorheological fluid valves controlled by electric field

Holes filled with electrorheological fluids (ERF) are used to form the Braille symbols or a relief in array manipulators. Matrix of holes is made from the fabric-based copper laminate. Voltage applied to upper and lower coppered surfaces of the plate, creates electric field, which controls ERF viscosity. Three methods to form a relief are investigated: (a) using an elastic membrane, covering the holes; (b) dielectric pins moving in the holes; and (c) metallic pins moving in the holes. Electric field in a hole of the matrix is calculated as the electric field in a hole of the plane capacitor. When voltage upon electrodes is kept uniform, the mean electric field in the electrorheological fluid with metallic pins becomes 1.7, with dielectric pins mean electric field being 1.25 times stronger than in the electrorheological fluid with the membrane. In the case of metallic pins, the mean electric field near the electrodes is considerably stronger than in the case of dielectric pins. In the points situated not further than 0.25 of the hole height in the direction of the hole axis, the mean electric field is 3 times stronger than in the hole without the pin. The controlling voltage can be decreased using multilayer copper laminate valves, composed of some fabric-based plates in the opposite directions of the electric field in the neighboring plates.     

Improved room-temperature thermoelectric characteristics in F4TCNQ-doped CNT yarn/P3HT composite by controlled doping

High room-temperature thermoelectric performance is important for low-grade waste heat power generation as there are plenty of heat thrown away uselessly in our daily life, most of which are below 100 °C. However, most of the thermoelectric materials are limited to high temperature application. In this work, room-temperature thermoelectric power factor of carbon nanotube (CNT) yarn is improved by controlled doping, which is achieved by making composite with poly 3-hexylthiophene −2, 5-diyl (P3HT) followed by doping with 2, 3, 5, 6-tetrafluo-7, 7, 8, 8-tetracyanoquinodimethane (F4TCNQ). The temperature-dependent Seebeck coefficient based on power–law model suggests that P3HT shifts the Fermi energy of CNT yarn towards the valence band edge, and reduces the ionic scattering and carrier relaxation time. As a result, the Seebeck coefficient is increased while the variation of Seebeck coefficient with temperature is reduced, and hence, the room-temperature thermoelectric power factor is improved. With controlled doping, the power factor of CNT yarn/P3HT composite reaches to 1640–2160 μW m⁻¹K⁻² at the temperature range of 25–100 °C, which is higher than that of CNT yarn alone.     

Free Energy Control of Charge Photogeneration in Polythiophene/Fullerene Solar Cells: The Influence of Thermal Annealing on P3HT/PCBM Blends

The function of organic solar cells is based upon charge photogeneration at donor/acceptor heterojunctions. In this paper, the origin of the improvement in short circuit current of poly(3‐hexylthiophene)/6,6‐phenyl C₆₁‐butyric acid methyl ester (P3HT/PCBM) solar cells with thermal annealing is examined. Transient absorption spectroscopy is employed to demonstrate that thermal annealing results in an approximate two‐fold increase in the yield of dissociated charges. The enhanced charge generation is correlated with a decrease in P3HT's ionization potential upon thermal annealing. These observations are in excellent quantitative agreement with a model in which efficient dissociation of the bound radical pair into free charges is dependent upon the bound radical state being thermally hot when initially generated, enabling it to overcome its coulombic binding energy. These observations provide strong evidence that the lowest unoccupied molecular orbital (LUMO) level offset of annealed P3HT/PCBM blends may be only just sufficient to drive efficient charge generation in polythiophene‐based solar cells. This has important implications for current strategies to optimize organic photovoltaic device performance based upon the development of smaller optical bandgap polymers.