The p recombination layer in tunnel junctions for micromorph tandem solar cells

A new tunnel recombination junction is fabricated for n–i–p type micromorph tandem solar cells. We insert a thin heavily doped hydrogenated amorphous silicon (a-Si:H) p + recombination layer between the n a-Si:H and the p hydrogenated nanocrystalline silicon (nc-Si:H) layers to improve the performance of the n–i–p tandem solar cells. The effects of the boron doping gas ratio and the deposition time of the p-a-Si:H recombination layer on the tunnel recombination junctions have been investigated. The current-voltage characteristic of the tunnel recombination junction shows a nearly ohmic characteristic, and the resistance of the tunnel recombination junction can be as low as 1.5 ·cm 2 by using the optimized p-a-Si:H recombination layer. We obtain tandem solar cells with open circuit voltage V oc = 1.4 V, which is nearly the sum of the V oc s of the two corresponding single cells, indicating no V oc losses at the tunnel recombination junction.     

Rubrene作电子传输层的异质结有机太阳能电池

以Rubrene为电子传输层(ETL),制备了结构为ITO/MoO3(5nm)/Rubrene(50nm)/C60(45nm)/Rubrene(0,3,5.5,9.5nm)/Al(130nm)的有机太阳能电池.与没有ETL的器件相比,含5.5nmRubrene的电池的开路电压、填充因子、功率转换效率分别从0.68V,0.488,0.315%增加到0.86V,0.574,0.490%.实验结果分析表明:热的Al原子直接沉积在C60上,破坏了C60层,形成高功函数的C60/Al阴极,弱化内建电场,降低电池性能;当插入ETL后,C60层得到保护,热的Al原子沉积破坏了Rubrene层,形成了缺陷态能级,提高电池的内建电场,促进了电子的传输.进一步的单电子电池实验表明,缺陷态能级低于C60的最低未占据分子轨道.     

Improved efficiency of small-molecular (S-M) tandem organic solar cells (TOSCs) by employing low work function alloy nanoparticle intermediate layer

We improved the power conversion efficiency (PCE) of the small molecular (S-M) tandem organic solar cells (TOSCs) by employing different low work function alloy nanoparticle intermediate layers. The enhancement of the PCE was mainly attributed to the gap states formed at the interface between the buffer layer and alloy nanoparticle intermediate layer. The gap states result in the disappearance of the electron injection barrier. Compared with the planar heterojunction (PHJ) TOSCs with single Ag nanoparticle intermediate layer, the PCE of the PHJ TOSC with the Mg-Ag alloy nanoparticle intermediate layer exhibits an enhancement of 7.5%. Moreover, the Mg-Ag alloy nanoparticle intermediate layer was also employed in the bulk-heterojunction (BHJ) TOSCs. Compared with the PHJ TOSCs, the PCE of the BHJ TOSCs with Mg-Ag alloy nanoparticle intermediate layer is doubled and achieves a value of 5.54%.     

MoO3/Ag/Al/ZnO intermediate layer for inverted tandem polymer solar cells

We report an MoO3/Ag/Al/ZnO intermediate layer connecting two identical bulk heterojunction subcells with a poly(3-hexylthiophene) and [6,6]-phenyl-C61-butyric acid methyl ester(P3HT and PCBM) active layer for inverted tandem polymer solar cells. The highly transparent intermediate layer with an optimized thickness realizes an Ohmic contact between the two subcells for effective charge extraction and recombination. A maximum power conversion efficiency of 3.76% is obtained for the tandem cell under 100 mW/cm2 illumination, which is larger than that of a single cell(3.15%).The open-circuit voltage of the tandem cell(1.18 V) approaches double that of the single cell(0.61 V).     

MoO3/Ag/AI/ZnO intermediate layer for inverted tandem polymer solar cells

We report an MoO3/Ag/Al/ZnO intermediate layer connecting two identical bulk heterojunction subcells with a poly（3-hexylthiophene） and [6,6]-phenyl-C61-butyric acid methyl ester （P3HT and PCBM） active layer for inverted tan- dem polymer solar cells. The highly transparent intermediate layer with an optimized thickness realizes an Ohmic contact between the two subcells for effective charge extraction and recombination. A maximum power conversion efficiency of 3.76% is obtained for the tandem cell under 100 mW/cm2 illumination, which is larger than that of a single cell （3.15%）. The open-circuit voltage of the tandem cell （1.18 V） approaches double that of the single cell （0.61 V）.     

Ca/Alq3 hybrid cathode buffer layer for the optimization of organic solar cells based on a planar heterojunction

Use of efficient anode cathode buffer layer (CBL) is crucial to improve the efficiency of organic photovoltaic cells. Here we show that using a double CBL, Ca/Alq₃, allows improving significantly cell performances. The insertion of Ca layer facilitates electron harvesting and blocks hole collection, leading to improved charge selectivity and reduced leakage current, whereas Alq₃ blocks excitons. After optimisation of this Ca/Alq₃ CBL using CuPc as electron donor, it is shown that it is also efficient when SubPc is substituted to CuPc in the cells. In that case we show that the morphology of the SubPc layer, and therefore the efficiency of the cells, strongly depends on the deposition rate of the SubPc film. It is necessary to deposit slowly (0.02 nm/s) the SubPc films because at higher deposition rate (0.06 nm/s) the films are porous, which induces leakage currents and deterioration of the cell performances. The SubPc layers whose formations are kinetically driven at low deposition rates are more uniform, whereas those deposited faster exhibit high densities of pinholes.     

Theory study on the properties of thiadiazole polymer donors for organic solar cells

In this work, the properties of [1,2,5] thiadiazolo [3,4‐c] pyridine ‐alt‐cyclopenta [2,1‐b:3,4‐b′] dithiophene (PT‐CDT) and [1,2,5] thiadiazolo [3,4‐c] pyridine‐6‐carbonitrile‐alt‐cyclopenta [2,1‐b:3,4‐b′] dithiophene (PCNT‐CDT) as donors were investigated by means of Density Functional Theory. The electronic properties and optical absorption properties were discussed, and hole‐transfer properties of donors were studied by Marcus electron transfer theory. The results indicate that the linear structure of PCNT‐CDT and PT‐CDT is more stable than the spiral structure of PCNT‐CDT and PT‐CDT; the absorption peak in visible region of PCNT‐CDT is stronger and wider, and the absorption spectrum is more matchable to solar spectrum than PT‐CDT, while the maximum absorption wavelength of PCNT‐CDT has an obvious red shift; the two designed materials show strong intramolecular and intermolecular charge transfer properties; PCNT‐CDT owns a large open‐circuit voltage and low reorganization energy, as well as high hole mobility. Therefore, the newly designed PCNT‐CDT can be a potential donor material of organic solar cell. Copyright © 2013 John Wiley & Sons, Ltd.     

石墨烯衍生物作为有机太阳能电池界面材料的研究进展

本文综述了石墨烯及其衍生物作为界面材料在有机太阳能电池中的应用, 包括作为阳极界面层、阴极界面层和叠层电池中间层等方面. 氧化石墨烯由于较好的透光性, 易于分散在水溶液中与溶液加工等优点已被应用在有机太阳能电池中. 对氧化石墨烯作为阳极界面层的研究包括通过部分还原或掺杂提高其导电性、通过引入高负电性原子提高其表面功函数, 以及通过与其他材料复合提高性能等. 同时, 本文综述了石墨烯衍生物及复合材料作为有机太阳能电池阴极界面层和叠层电池中间层的研究. 最后本文展望了石墨烯及其衍生物在有机太阳能电池与有机无机复合钙钛矿太阳能电池中的应用前景.     

Numerical study of InGaN tandem solar cells with intermediate bands

Theoretical investigations of InGaN tandem solar cells with intermediate bands (IBs) have been conducted through calculating the diode equation taking into account the radiative and nonradiative recombination currents. The calculated maximum ef?ciencies of the double‐junction cell with one IB in each subcell are 57.85% and 68.37% under AM1.5G one‐sun and 46000‐sun illuminations, respectively. It has also been observed that the combined device with the top‐cell bandgaps of 2.9–3.4 eV (2.6–3.4 eV for full concentration) may have an opportunity to realize the application of over 50% efficiency. We suggest that the optimized width of the IB layer be designed in the range of 1–6 μm if its absorption coefficient is 10⁴–10⁵ cm^–1 in the IB region.     

Nongeminate recombination in organic bulk heterojunction solar cells: Contribution of exciton–polaron interaction

A new model to explain nongeminate recombination in organic bulk heterojunction solar cells is presented. We suggest that the annihilation of excitons on charge carriers at the interface between donor and acceptor phases competes with the bimolecular recombination of Coulombically bound electron–hole pairs. The exciton–polaron interaction gives visible contribution to the reduction of Langevin recombination. An analytical formula, which describes the reduction prefactor, has been derived. We demonstrate that exciton–charge carrier interactions cause an increase of the recombination order. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

p-n 型GaInP2/GaAs叠层太阳电池研究

报道了对p-n型 GaInP2/GaAs叠层太阳电池的研究结果.采用低压金属有机物化学气相沉积工艺制备电池样品.通过对GaInP2顶电池中场助收集效应的计算机模拟，提出用p+p-n-n+结构取代常用的p+n 结构，显著改善了GaInP2顶电池和GaInP2/GaAs叠层太阳电池的光伏性能，使其光电转换效率(Eff)分别达到14.26% 和23.82% (AM0, 25℃, 2×2cm2). 关键词： 场助收集效应 镓铟磷 砷化镓 叠层太阳电池     

p-n型GaInP_2/GaAs叠层太阳电池研究

报道了对p n型GaInP2 GaAs叠层太阳电池的研究结果 .采用低压金属有机物化学气相沉积工艺制备电池样品 .通过对GaInP2 顶电池中场助收集效应的计算机模拟 ,提出用p p- n- n 结构取代常用的p n结构 ,显著改善了GaInP2 顶电池和GaInP2 GaAs叠层太阳电池的光伏性能 ,使其光电转换效率 (Eff)分别达到 14 2 6 %和 2 3 82 %(AM0 ,2 5℃ ,2× 2cm2 )     

ZnO电子传输层对于反型结构聚合物太阳电池光浴效应的影响

采用金属氧化物电子传输层(ETL)的聚合物光伏器件在制备完成之初通常性能表现低下, J-V曲线呈异常“S”形. 当器件受白光持续照射后, 该不良状况会逐渐好转, 此过程称为光浴(light-soaking). 光浴现象普遍被认为是ETL界面问题所致. 从器件结构着手, 研究了ZnO 纳米颗粒ETL相邻的两个界面在光浴问题上的作用. 制备了功能层相同的(电极除外)正型、反型器件及复合ETL结构器件, 发现光浴现象仅出现于包含ZnO/ITO界面的反型器件中, 证明该界面是导致光浴现象的主要原因. 分析认为: ZnO颗粒表面O₂吸附形成的电子陷阱增加了ITO/ZnO势垒厚度, 使得光生电子无法逾越而成为空间电荷积累, 从而导致器件初始性能不佳. 器件经光照后, ETL内部受激而生的空穴电子对填补了ZnO缺陷, 提升了ETL的电荷选择性并减小了界面势垒厚度, 被束缚的光生电子得以隧穿至ITO电极, 反型器件性能最终得以改善.     

Effect of NaCl doped into Bphen layer on the performance of tandem organic light-emitting diodes

To improve the performance of tandem organic light-emitting diodes （OLEDs）, we study the novel NaCl as n-type dopant in Bphen：NaCl layer. By analyzing their relevant energy levels and cartier transporting characteristics, we discuss the mechanisms of the effective charge generation layer （CGL） of Bphen：NaCl （6 wt%）/MoO3. In addition, we use the Bphen：NaC1 （20 wt%） layer as the electron injection layer （ELL） combining the CGL to further improve the performance of tandem device. For this tandem device, the maximal current efficiency of 9.32 cd/A and the maximal power efficiency of 1.93 lm/W are obtained, which are enhanced approximately by 2.1 and 1.1 times compared with those of the single- emissive-unit device respectively. We attribute this improvement to the increase of electron injection ability by introducing of Bphen：NaCl layer. Moreover, the CGL is almost completely transparent in the visible light region, which is also important to achieve an efficient tandem OLEDs.     

有机共混结构叠层太阳电池的研究进展

有机太阳电池由于质轻、价廉、柔性,受到人们的广泛关注.单个有机材料只能吸收部分太阳光,叠层结构的太阳电池将不同吸收带隙的有机材料通过中间层连接起来,既能充分吸收太阳光,又能提高太阳电池的开路电压或短路电流.本文综述了近年来有机共混结构叠层太阳电池的研究进展,介绍了各种叠层有机太阳电池的结构、原理及性能,阐述了国内外有机叠层太阳电池研究的现状及存在问题,为高性能有机太阳电池的研究提供有价值的参考.     

Photoconductivity as loss mechanism in organic solar cells

We observe that the reverse current under illumination in solar cells containing C₆₀ and ZnPc is dominated by a photoshunt. This shunt, not present in the dark, causes a linear current–voltage relation under illumination showing no saturation. Although observable in bulk heterojunctions, this effect is more pronounced in the presence of a pristine C₆₀ layer. An internal quantum efficiency larger than unity under an applied negative voltage and in the spectral range where C₆₀ absorbs identifies charges which are injected in addition to those photogenerated. The photoshunt is also present in the power‐generating region and represents a loss mechanism limiting the fill factor in particular for flat heterojunction devices. (© 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Influence of optical interference and carrier lifetime on the short circuit current density of organic bulk heterojunction solar cells

Based on simple analytical equations, short circuit current density (J_SC) of the organic bulk heterojunction solar cells has been calculated. It is found that the optical interference effect plays a very important role in the determination of J_SC; and obvious oscillatory behaviour of J_SC was observed as a function of thickness. At the same time, the influence of the carrier lifetime on J_SC also cannot be neglected. When the carrier lifetime is relatively short, J_SC only increases at the initial stage and then decreases rapidly with the increase of active layer thickness. However, for a relatively long carrier lifetime, the exciton dissociation probability must be considered, and J_SC behaves wave-like with the increase of active layer thickness. The validity of this model is confirmed by the experimental results.     

给体-受体型有机太阳电池光敏层的优化设计

针对有机给体-受体型异质结薄膜太阳电池，基于薄膜中的光学干涉效应和激子扩散理论建立模型，定量分析了有机层厚度对太阳电池性能的影响，通过限制有机光敏层厚度来控制由光学干涉效应引起的局部光子密度(光强度)的分布，进而优化有机层的吸收效率和激子扩散效率，以此达到提高器件光伏效率的目的.并通过实验进行了验证. 关键词： 有机太阳电池 给体-受体 优化设计 激子     

Device simulation of quasi-two-dimensional perovskite/silicon tandem solar cells towards 30%-efficiency

Perovskite/silicon (Si) tandem solar cells have been recognized as the next-generation photovoltaic technology with efficiency over 30% and low cost. However, the intrinsic instability of traditional three-dimensional (3D) hybrid perovskite seriously hinders the lifetimes of tandem devices. In this work, the quasi-two-dimensional (2D) (BA)₂(MA)_n-1Pb_nI_3n+1 (n=1, 2, 3, 4, 5) (where MA denotes methylammonium and BA represents butylammonium), with senior stability and wider bandgap, are first used as an absorber of semitransparent top perovskite solar cells (PSCs) to construct a four-terminal (4T) tandem devices with a bottom Si-heterojunction cell. The device model is established by Silvaco Atlas based on experimental parameters. Simulation results show that in the optimized tandem device, the top cell (n=4) obtains a power conversion efficiency (PCE) of 17.39% and the Si bottom cell shows a PCE of 11.44%, thus an overall PCE of 28.83%. Furthermore, by introducing a 90-nm lithium fluoride (LiF) anti-reflection layer to reduce the surface reflection loss, the current density (J_sc) of the top cell is enhanced from 15.56 mA/cm² to 17.09 mA/cm², the corresponding PCE reaches 19.05%, and the tandem PCE increases to 30.58%. Simultaneously, in the cases of n=3, 4, and 5, all the tandem PCEs exceed the limiting theoretical efficiency of Si cells. Therefore, the 4T quasi-2D perovskite/Si devices provide a more cost-effective tandem strategy and long-term stability solutions.     

钙钛矿/硅异质结叠层太阳电池:光学模拟的研究进展

近几年,钙钛矿/硅异质结叠层太阳电池发展迅速,效率已经从13.7％提升到29.1％.由于叠层电池器件的制作工艺复杂,而叠层太阳电池中的光学损失对转换效率的影响很大,所以通过光学模拟进而获得高效电池至关重要.本文首先从商业软件和自建模型两方面概述了光学模拟的方法,接着从反射损失和寄生吸收两方面针对光学模拟研究进展进行了总...