Towards thinner and low bowing silicon solar cells: form the boron and aluminum co‐doped back surface field with thinner metallization film

Using thinner wafers can largely reduce the cost of silicon solar cells. One obstacle of using thinner wafers is that few methods can provide good dopant concentration for the back surface field (BSF) and good ohmic contact while generated only in low bowing. In this paper, we have demonstrated the screening–printing B and Al (B/Al) mixture metallization film technique, making use of the screen‐printing technique and the higher solubility of B in silicon to form a B/Al‐BSF. This technique can raise the carrier concentration in the BSF by more than one order of magnitude and reduce the back surface recombination at a low firing temperature (≤800 °C). We have also shown that through the new technique, the metallization paste thickness at the rear could be reduced largely, which however did not degrade the solar cell efficiency. All these efforts are aiming for pushing forward the application of thinner wafers. Copyright © 2011 John Wiley & Sons, Ltd.     

Fused-ring acceptors based on quinoxaline unit for highly efficient single-junction organic solar cells with low charge recombination

Two non-fullerene small molecule acceptors (TFQ-F and TFQ-Cl) based on quinoxaline unit were designed and synthesized for efficient organic solar cells (OSCs). These two acceptors showed intense absorption up to 900 nm and high thermal stabilities with decomposition temperatures over 360 °C due to their fused-ring skeletons. TFQ-F and TFQ-Cl are the A-D-A′-D-A type acceptors (A/A′ for acceptor unit and D for donor unit). TFQ-F and TFQ-Cl have the same D-A′-D fragment, which was flanked with different ending groups. The effect of different ending groups on their photophysical properties, electrochemical behaviors, micro-structures and charge recombination properties of active layers, and device performance were investigated systematically. PM6 with the complementary absorption to the two acceptors was used as the donor material. The pristine PM6:TFQ-F blend films displayed the optimal morphologies as revealed by AFM and TEM measurement. Organic solar cells based on PM6:TFQ-Cl blend film showed high J_SC of 25.19 mA/cm² and PCE of 13.2%. The Voc, J_SC and PCE for PM6:TFQ-F film based device were 0.857 V, 23.70 mA/cm² and 13.51%, respectively. The dependence of V_OC/J_SC on various light intensities indicated that PM6:TFQ-F/Cl based device had low charge recombination.     

Dual Additive for Simultaneous Improvement of Photovoltaic Performance and Stability of Perovskite Solar Cell

Additive engineering is one of the most efficient approaches to improve not only photovoltaic performance but also phase stability of formamidinium (FA)-based perovskite. Chlorine-based additives, such as methylammonium chloride (MACl), have been in general used to improve phase stability of FAPbI₃, which however often leads to loss of open-circuit voltage V_oc, accompanied by instability of the perovskite phase due to the volatile nature of the MA cation. A dual additive strategy for improving V_oc and thereby the overall efficiency are reported here. The mixing ratio of MACl to CsCl is varied from [MACl]/[CsCl] = 4 to 1, where V_oc increases with decreasing the ratio and best performance is achieved from [MACl]/[CsCl] = 2. As compared to the single source of MACl, the addition of CsCl reduces trap density and increases resistance against charge recombination, which is responsible for the increased V_oc. Moreover, defect passivation achieved by dual additive enables better stability than the single additive MACl as confirmed by long-term stability tests with unencapsulated devices for 50 days under relative humidity of about 40% at room temperature. The best power conversion efficiency of 23.22% is achieved by dual additive, which is higher than that for single additive of MACl or CsCl.     

全光纤电流互感器λ/4波片制作工艺

根据全光纤电流互感器（FOCT）的光路结构及其工作原理,分析了/4波片的制作效果对FOCT的影响,研究了/4波片的制作工艺,得出了影响波片制作效果的主要因素。通过选择合适的材料和工艺方法,获得了性能优异的全光纤/4波片。试验结果表明:该方法制作的波片提高了FOCT的性能,使其满足了0.2 S级测量用电子式电流互感器的准确度要求。     

Nongeminate and Geminate Recombination in PTB7:PCBM Solar Cells

A combination of transient photovoltage (TPV), voltage dependent charge extraction (CE), and time delayed collection field (TDCF) measurements is applied to poly[[4,8‐bis[(2‐ethylhexyl)oxy]benzo[1,2‐b:4,5‐b']dithiophene‐2,6‐diyl] [3‐fluoro‐2‐[(2‐ethylhexyl)carbonyl] thieno[3,4‐b]thiophenediyl]] (PTB7):[6,6]‐phenyl‐C71‐butyric acid (PC₇₁BM) bulk heterojunction solar cells to analyze the limitations of photovoltaic performance. Devices are processed from pure chlorobenzene (CB) solution and a subset is optimized with 1,8‐diiodooctane (DIO) as co‐solvent. The dramatic changes in device performance are discussed with respect to the dominating loss processes. While in the devices processed from CB solution severe geminate and nongeminate recombination is observed, the use of DIO facilitates efficient polaron pair dissociation and minimizes geminate recombination. Thus, from the determined charge carrier decay rate under open circuit conditions and the voltage dependent charge carrier densities n(V), the nongeminate loss current J_loss of the samples with DIO alone enables the reconstruction of the current/voltage (j/V) characteristics across the whole operational voltage range. Geminate and nongeminate losses are considered to describe the j/V response of cells prepared without additive, but lead to a clearly overestimated device performance. The deviation between measured and reconstructed j/V characteristics is attributed to trapped charges in isolated domains of pure fullerene phases.     

红光照射联合伐昔洛韦护理治疗糖尿病合并带状疱疹的疗效观察

目的:探讨红光照射联合伐昔洛韦护理治疗糖尿病合并带状疱疹的疗效。方法:将96例糖尿病合并带状疱疹患者随机分为观察组和对照组,各48例。两组均采取相同的护理干预,对照组给予口服伐昔洛韦,观察组在对照组治疗的基础上采用红光治疗仪病灶部位照射。结果:观察组在水疱结痂、疼痛缓解和疼痛基本消失时间与对照组相比明显缩短。结论:红光照射联合伐昔洛韦及护理治疗糖尿病合并带状疱疹起效快,疗效显著。     

退火对Al2O3薄膜结构和发光性能的影响

氧化铝(Al2O3)薄膜具有许多优良的物理化学性能,在机械、光学及微电子等高科技领域有着广泛应用,一直受到人们的高度关注.但Al2O3具有多种物相形态,性质差别很大.因此研究不同结构对其发光性能的影响在Al2O3实际应用中有着重要意义.本文采用射频磁控溅射技术在单晶硅衬底上制备了Al2O3薄膜,并在氮气中进行了不同温度的退火,对比了退火前后薄膜的结构和光致发光特性.观察到了在384nm和401nm附近的两个荧光峰,这两个发光峰都是由色心引起的.随着退火温度的升高,Al2O3薄膜的结晶质量变好,同时荧光峰峰位发生了相应的变化,强度也发生了明显的变化.     

Photon-assisted capacitance–voltage study of organic metal–insulator–semiconductor capacitors

The results are reported of a detailed investigation into the photoinduced changes that occur in the capacitance–voltage (C–V) response of an organic metal–insulator–semiconductor (MIS) capacitor based on the organic semiconductor poly(3-hexylthiophene), P3HT. During the forward voltage sweep, the device is driven into deep depletion but stabilizes at a voltage-independent minimum capacitance, C_min, whose value depends on photon energy, light intensity and voltage ramp rate. On reversing the voltage sweep, strong hysteresis is observed owing to a positive shift in the flatband voltage, V_FB, of the device. A theoretical quasi-static model is developed in which it is assumed that electrons photogenerated in the semiconductor depletion region escape geminate recombination following the Onsager model. These electrons then drift to the P3HT/insulator interface where they become deeply trapped thus effecting a positive shift in V_FB. By choosing appropriate values for the only disposable parameter in the model, an excellent fit is obtained to the experimental C_min, from which we extract values for the zero-field quantum yield of photoelectrons in P3HT that are of similar magnitude, 10^?5 to 10^?3, to those previously deduced for π-conjugated polymers from photoconduction measurements. From the observed hysteresis we deduce that the interfacial electron trap density probably exceeds 10¹⁶ m^?2. Evidence is presented suggesting that the ratio of free to trapped electrons at the interface depends on the insulator used for fabricating the device.     

High efficiency and non-color-changing orange organic light emitting diodes with red and green emitting layers

We report a high performance orange organic light-emitting diode (OLED) where red and green phosphorescent dyes are doped in an exciplex forming co-host as separate red and green emitting layers (EMLs). The OLED shows a maximum external quantum efficiency (EQE) of 22.8%, a low roll-off of efficiency with an EQE of 19.6% at 10,000 cd/m², and good orange color with a CIE coordinate of (0.442, 0.529) and no color change from 1000 to 10,000 cd/m². The exciplex forming co-host system distributes the recombination zone all over the EMLs and reduces the triplet exciton quenching processes.     

Identifying a Threshold Impurity Level for Organic Solar Cells: Enhanced First‐Order Recombination Via Well‐Defined PC84BM Traps in Organic Bulk Heterojunction Solar Cells

Small amounts of impurity, even one part in one thousand, in polymer bulk heterojunction solar cells can alter the electronic properties of the device, including reducing the open circuit voltage, the short circuit current and the fill factor. Steady state studies show a dramatic increase in the trap‐assisted recombination rate when [6,6]‐phenyl C₈₄ butyric acid methyl ester (PC₈₄BM) is introduced as a trap site in polymer bulk heterojunction solar cells made of a blend of the copolymer poly[N‐9″‐hepta‐decanyl‐2,7‐carbazole‐alt‐5,5‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothiadiazole) (PCDTBT) and the fullerene derivative [6,6]‐phenyl C₆₁ butyric acid methyl ester (PC₆₀BM). The trap density dependent recombination studied here can be described as a combination of bimolecular and Shockley–Read–Hall recombination; the latter is dramatically enhanced by the addition of the PC₈₄BM traps. This study reveals the importance of impurities in limiting the efficiency of organic solar cell devices and gives insight into the mechanism of the trap‐induced recombination loss.