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Reducing burn-in loss in organic photovoltaics by enhancing the morphological and interfacial stability (Conference Presentation) 通过提高形态和界面稳定性来减少有机光伏电池的烧蚀损失(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2531612
Kyungkon Kim
With rapid advances in the development of new conjugated polymers, non-fullerene acceptors, the power conversion efficiency (PCE) of OPVs has been increased over 14%. However, a major drawback for the commercialization of OPVs is their long-term stability under continuous operation. Especially, OPVs suffer from a rapid decrease in PCE during initial device operation, which is known as the “burn-in loss”. It is considered that the origin of the burn-in loss is mainly related with the instability of the BHJ morphology and/or interface rather than the photooxidation of the photoactive layer. We find that the photoactive layer prepared by a sequential solution deposition is more stable than that prepared by blend solution deposition. We also find that the burn-in loss is closely related with stability of photoactive layer / electron transporting layer interface.
随着新型共轭聚合物、非富勒烯受体的快速发展,OPVs的功率转换效率(PCE)提高了14%以上。然而,opv商业化的一个主要缺点是其在连续运行下的长期稳定性。特别是,opv在初始设备运行期间遭受PCE快速下降的影响,这被称为“老化损失”。认为烧蚀损耗的来源主要与BHJ形态和/或界面的不稳定性有关,而与光活性层的光氧化无关。我们发现顺序溶液沉积法制备的光活性层比混合溶液沉积法制备的光活性层更稳定。我们还发现,烧蚀损耗与光活性层/电子传递层界面的稳定性密切相关。
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引用次数: 0
Semi-transparent organic solar cells for greenhouse application (Conference Presentation) 用于温室的半透明有机太阳能电池(会议介绍)
Pub Date : 2019-09-10 DOI: 10.1117/12.2529997
Yuan Xiong, Eshwar Ravishankar, Jennifer E. Swift, H. Ade, Ronald E Booth, Melodi Charles, Reece Henry, B. O’Connor, J. Rech, C. Saravitz, H. Sederoff, L. Ye, W. You
Semi-transparent Organic Solar Cells for Greenhouse ApplicationYuan Xiong1*, Eshwar Ravishankar2, Jennifer Swift3, Harald Ade1*, Ronald Booth2, Melodi Charles4, Reece Henry1, Brendan O’Connor2, Jeromy James Rech5, Carole Saravitz3, Heike Sederoff4, Long Ye1, Wei You51. Department of Physics, Organic and Carbon Electronics Lab (ORaCEL), North Carolina State University, Raleigh, NC 27695, USA2. Department of Mechanical and Aerospace Engineering and ORaCEL, North Carolina State University, Raleigh, NC 27695, USA 3. Department of Plant Biology, North Carolina State University, Raleigh, NC 27695, USA4. Department of Plant and Microbial Biology, North Carolina State University, Raleigh, NC 27695, USA 5. Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USAE-mail: yxiong8@ncsu.edu; hwade@ncsu.edu Semitransparent organic solar cells (ST-OSCs) show great potential in building-integrated photovoltaics due to the advantages in solution processability, flexibility, and transparency. Herein, we present a systematic study on the application of high-performance ST-OSC filters in a greenhouse by utilizing three representative systems with different spectral responses, namely, FTAZ:PC71BM[1], FTAZ:IT-M[2, 3], and PTB7-Th:IEICO-4F[4]. Specifically, the cultivation of red leaf lettuce is conducted in a controlled environment growth chamber, which is possible to duplicate any climate, and under different ST-OSC filters. In principle, the ST-OSCs absorb a portion of the solar spectrum for power generation and lettuce utilizes the penetrated light for photosynthesis. Furthermore, we quantitatively investigate the leaf area and number profiles, plant biomass, and photosynthetic rate under the as-prepared ST-OSC filters treatments. On the base of statistical analysis after the growth cycle, we can identify the best ST-OSC for plant growth. These results thus pave the way to integrate ST-OSCs with greenhouses. [1] S. C. Price, A. C. Stuart, L. Yang, H. Zhou, W. You, Journal of the American Chemical Society 2011, 133, 4625.[2] L. Ye, Y. Xiong, Q. Zhang, S. Li, C. Wang, Z. Jiang, J. Hou, W. You, H. Ade, Advanced Materials 2018, 30, 1705485.[3] Y. Xiong, L. Ye, A. Gadisa, Q. Zhang, J. J. Rech, W. You, H. Ade, Advanced Functional Materials 2019, 29, 1806262.[4] X. Song, N. Gasparini, L. Ye, H. Yao, J. Hou, H. Ade, D. Baran, ACS Energy Letters 2018, 3, 669.
应用于温室的透明有机太阳能电池:袁雄1*,Eshwar Ravishankar2, Jennifer swif3, Harald Ade1*, Ronald Booth2, Melodi Charles4, Reece Henry1, Brendan O 'Connor2, jerome James Rech5, Carole Saravitz3, Heike Sederoff4,叶龙1,优伟51。北卡罗来纳州立大学物理系,有机与碳电子实验室(ORaCEL),北卡罗来纳州罗利27695,美国a22 .北卡罗来纳州立大学机械与航空航天工程系与ORaCEL,美国北卡罗来纳州罗利27695美国北卡罗来纳州立大学植物生物系,罗利276954 .北卡罗来纳州立大学植物与微生物学系,北卡罗来纳州罗利27695北卡罗来纳大学教堂山分校化学系,美国北卡罗来纳教堂山27599 e -mail: yxiong8@ncsu.edu;hwade@ncsu.edu半透明有机太阳能电池(ST-OSCs)由于其在溶液可加工性、灵活性和透明度方面的优势,在建筑集成光伏发电中显示出巨大的潜力。本文采用FTAZ:PC71BM[1]、FTAZ:IT-M[2,3]和PTB7-Th:IEICO-4F[4]三个具有代表性的光谱响应系统,系统研究了高性能ST-OSC滤波器在温室中的应用。具体而言,红叶莴苣的培养是在可控环境的生长室内进行的,可以复制任何气候,并在不同的ST-OSC过滤器下进行。原则上,ST-OSCs吸收一部分太阳光谱用于发电,生菜利用穿透的光进行光合作用。此外,我们定量研究了制备的ST-OSC过滤器处理下的叶面积和叶数分布、植物生物量和光合速率。在生长周期结束后的统计分析基础上,我们可以确定植物生长的最佳ST-OSC。这些结果为将ST-OSCs与温室相结合铺平了道路。[1] s c价格,a·c·斯图亚特·l·杨h .周w .你,2011年美国化学学会杂志》,133年,4625年。[2]叶磊,熊艳,张强,李树生,王超,蒋志强,侯建军,游伟,阿德红,2018 .[3]熊艳,叶丽丽,张强,李建军,尤伟,阿德华,高性能材料,2019,29 (4):662 - 662 .[4]宋晓霞,叶丽丽,姚海燕,侯俊杰,艾德H.,巴兰D.,能源工程学报,2018,36,669。
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引用次数: 2
Rational strategies to stabilize the morphology of non-fullerene organic solar cells (Conference Presentation) 稳定非富勒烯有机太阳能电池形态的合理策略(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2529990
Huawei Hu, L. Ye, Masoud Ghasemi, Nrup Balar, J. Rech, W. You, Samuel J. Stuard, B. O’Connor, H. Ade
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引用次数: 0
Aqueous processing of Ag-nanowire electrodes on top of semi-transparent perovskite solar cells (Conference Presentation) 半透明钙钛矿太阳能电池顶部银纳米线电极的水处理(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2529331
T. Gahlmann, K. Brinkmann, C. Tückmantel, T. Becker, Junjie He, Johannes Bahr, C. Kreusel, T. Riedl
Aqueous dispersions of silver nanowires state an environmentally friendly avenue for highly conductive, yet transparent top electrodes for semi-transparent perovskite solar cells. However, for the well-known chemical instability of halide perovskites upon exposure to water, there are no reports of successful aqueous processing on top of perovskite devices. Here, we show that electron extraction layers of AZO/SnOx [1,2], with the SnOx grown by low temperature atomic layer deposition, provide outstanding protection layers, which even afford the spray coating of AgNW electrodes (sheet resistance Rsh =15 Ohm/sq and a transmittance of 90%) from water-based dispersions without damage to the perovskite.The layer sequence of the inverted cells is ITO/PTAA/perovskite/PCBM/AZO/SnOx/top-electrode. In devices without the ALD SnOx, aqueous spray processing decomposes the perovskite layers. Interestingly, the direct interface of Ag-NW/SnOx comprises a Schottky barrier, with characteristics strongly dependent on the charge carrier density of the SnOx. For a carrier density below 10^18 cm^-3, S-shaped J-V characteristics are found, that successively vanish upon UV-light soaking. For our low-T SnOx with 10^16 cm^-3, the insertion of a thin interfacial layer with a high charge carrier density (10^20 cm^-3), e.g. 10nm of ITO, is found to afford high performance semitransparent PSCs with an efficiency of 15%. Most importantly, compared to ITO electrodes Ag-NW based electrodes provide a key to achieve a higher transmittance in the IR, which is desirable for tandem Si/PSCs. [1] K. Brinkmann et al., Nat. Commun. 8, 13938 (2017).[2] L. Hoffmann et al. ACS Applied Mater. & Interfaces 10, 6006 (2018).
银纳米线的水分散体为半透明钙钛矿太阳能电池的高导电性、透明顶电极提供了一条环保的途径。然而,众所周知,卤化物钙钛矿在暴露于水时具有化学不稳定性,目前还没有在钙钛矿装置上成功进行水处理的报道。在这里,我们证明了AZO/SnOx的电子萃取层[1,2],通过低温原子层沉积生长的SnOx,提供了出色的保护层,甚至可以在水基分散体中喷涂AgNW电极(片电阻Rsh =15欧姆/平方,透射率为90%),而不会损坏钙钛矿。倒置电池层序为ITO/PTAA/钙钛矿/PCBM/AZO/SnOx/顶电极。在没有ALD SnOx的设备中,水喷雾处理会分解钙钛矿层。有趣的是,Ag-NW/SnOx的直接界面包括一个肖特基势垒,其特性强烈依赖于SnOx的载流子密度。当载流子密度小于10^18 cm^-3时,发现s形J-V特性,在紫外线照射下逐渐消失。对于我们的10^16 cm^-3的低t SnOx,发现插入具有高载流子密度(10^20 cm^-3)的薄界面层,例如10nm的ITO,可以提供具有15%效率的高性能半透明psc。最重要的是,与ITO电极相比,Ag-NW电极提供了在IR中实现更高透射率的关键,这对于串联Si/ psc是理想的。[1]王晓明,王晓明,王晓明,等。中国生物医学工程学报,2017,32 (2).[2]L. Hoffmann等。ACS应用材料。与接口10,6006(2018)。
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引用次数: 0
Morphology, microstructure and stability in perovskite photovoltaics (Conference Presentation) 钙钛矿光伏电池的形态、微观结构和稳定性(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2530213
M. McLachlan
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引用次数: 0
Novel materials and process toward commercialization of perovskite solar cells (Conference Presentation) 钙钛矿太阳能电池商业化的新材料和新工艺(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2529907
H. Jung
All solid-state solar cells based on organometal trihalide perovskite absorbers have already achieved distinguished power conversion efficiency (PCE) to over 23% and further improvements are expected up to 25%. These novel organometal halide perovskite absorbers which possess exceptionally strong and broad light absorption enable to approach the performances of the best thin film technologies. To commercialize these great solar cells, there are many bottlenecks such as long-term stability, large scale fabrication process, and environmental issues. In this presentation, we introduce our recent efforts to improve long term stability and solve environmental issues, which will facilitate commercialization of Perovskite photovoltaic system. For examples, we introduce a recycling technology of perovskite solar cells, which will facilitate the commercialization as well as solve the environmental issues of perovskite solar cells. Also, we are going to show new interfacial layers and highly crystalline SnO2 nanoparticle layers for electron transport layer. Also, we will show a large scale coating methodology for enabling large size module fabrication by using a new solvent extractor, anisole. Also, stability issue of perovskite materials regarding charge generation and extraction will be discussed.
所有基于有机金属三卤化物钙钛矿吸收剂的固态太阳能电池已经实现了超过23%的卓越功率转换效率(PCE),并且有望进一步提高到25%。这些新型有机金属卤化物钙钛矿吸收剂具有超强和广泛的光吸收能力,使其接近最佳薄膜技术的性能。要使这种大型太阳能电池商业化,还面临着长期稳定性、大规模制造过程、环境问题等诸多瓶颈。在本报告中,我们介绍了我们最近在提高长期稳定性和解决环境问题方面所做的努力,这将促进钙钛矿光伏系统的商业化。例如,我们引入了钙钛矿太阳能电池的回收技术,这将促进钙钛矿太阳能电池的商业化,并解决钙钛矿太阳能电池的环境问题。此外,我们还将展示用于电子传输层的新的界面层和高度结晶的SnO2纳米颗粒层。此外,我们将展示一种大规模的涂层方法,通过使用一种新的溶剂萃取剂,茴香醚,来实现大尺寸模块的制造。此外,还将讨论钙钛矿材料在电荷产生和萃取方面的稳定性问题。
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引用次数: 0
New molecular design towards high performance single junction organic solar cell (Conference Presentation) 面向高性能单结有机太阳能电池的新分子设计(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2542105
Y. Zou
Recently, non-fullerene n-type organic semiconductors (n-OS) have attracted significant attention as acceptors in organic photovoltaics (OPVs) due to their great potential to realize high power conversion efficiencies (PCEs). In this regard, a rational design of central fused ring unit of the n-OS molecules is crucial to maximize the state-of-the-art PCEs. Here, we report a new class of n-OS acceptor, Y series, that employ a ladder-type electron-deficient-core-based central fused ring to fine tune its absorption and energy levels. Among these new acceptors, the Y6-based OPVs exhibit a high efficiency of 15.7 % (both in conventional or inverted structures), and a certified efficiency of 14.9 % by an inverted structure. The electron-deficient-core-based fused ring reported in this work opens a new way in the molecular design of high performance n-OS acceptors for OPVs. References:[1] Nat. Commun., 2019, 10: 570[2] Adv.Mater., 2019, 31: 1807577[3] Joule, 2019, 4:1140-1151
近年来,非富勒烯n型有机半导体(n-OS)由于具有实现高功率转换效率(pce)的巨大潜力,作为有机光伏(opv)的受体受到了广泛关注。在这方面,合理设计n-OS分子的中心熔环单元对于最大限度地提高最先进的pce至关重要。在这里,我们报告了一类新的n-OS受体,Y系列,它采用阶梯型电子亏缺核为基础的中心熔接环来微调其吸收和能级。在这些新型受体中,y6基opv的效率高达15.7%(无论是在常规结构还是倒置结构下),倒置结构下的效率为14.9%。本文报道的基于电子缺陷核的熔合环为opv高性能n-OS受体的分子设计开辟了一条新途径。参考文献:[1]Nat. common。[2]中国机械工程,2019,10:570。[3]焦耳学报,2019,31:1807577
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引用次数: 0
Exciton binding energy and dielectric effect in small molecular and polymeric photovoltaic materials (Conference Presentation) 小分子和聚合物光伏材料中的激子结合能和介电效应(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2528570
S. Tsang
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引用次数: 0
The crucial role of end group planarity for fused-ring electron acceptors in organic solar cells (Conference Presentation) 有机太阳能电池中融合环电子受体端基平面度的关键作用(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2529500
J. Rech, N. Bauer, David Dirkes, J. Kaplan, Huotain Zhang, Zhengxing Peng, L. Ye, Shubin Liu, H. Ade, F. Gao, W. You
Newly developed fused-ring electron acceptors (FREAs) have proven to be an effective class of materials for extending the absorption window and boosting the efficiency of organic photovoltaics (OPVs). While numerous FREA small molecules have been developed, there is surprisingly little structural diversity among high performance FREAs in literature. For example, of the high efficiency electron acceptors reported, the vast majority utilize derivatives of 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile (INCN) as the acceptor moiety. It has been postulated that the high electron mobility exhibited by FREA molecules with INCN end groups is a result of close π-π stacking between the neighboring planar INCN groups, forming an effective charge transport pathway between molecules. To explore this as a design rationale for electron acceptors, we synthesized a new fused-ring electron acceptor, IDTCF, which has methyl substituents out of plane to the conjugated acceptor backbone. These methyl groups hinder packing and expand the π-π stacking distance by ~ 1 A, but this change doesn’t affect the optical or electrochemical properties of the individual acceptor molecule. Overall, our results show that intermolecular interactions (especially π-π stacking between end groups) play a crucial role in performance of FREAs. We demonstrated that the planarity of the acceptor unit is of paramount importance as even minor deviations in end group distance are enough to disrupt crystallinity and cripple device performance.
新开发的熔环电子受体(FREAs)已被证明是一类有效的材料,可以延长吸收窗口和提高有机光伏(opv)的效率。虽然已经开发了许多FREA小分子,但在文献中,高性能FREA的结构多样性却很少。例如,在报道的高效电子受体中,绝大多数是利用2-(3-氧-2,3-二氢茚-1-乙基)丙二腈(INCN)衍生物作为受体部分。假设具有INCN端基的FREA分子表现出的高电子迁移率是相邻平面INCN基团之间紧密π-π堆积的结果,形成了分子间有效的电荷传输途径。为了探索这作为电子受体的设计原理,我们合成了一种新的融合环电子受体IDTCF,它的甲基取代基与共轭受体主链平面外。这些甲基阻碍了填充并使π-π堆积距离扩大了~ 1a,但这种变化并不影响单个受体分子的光学或电化学性质。总的来说,我们的研究结果表明分子间相互作用(特别是端基之间的π-π堆叠)在FREAs的性能中起着至关重要的作用。我们证明了受体单元的平面性是至关重要的,因为即使端基距离的微小偏差也足以破坏结晶度并削弱器件性能。
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引用次数: 0
The role of donor-acceptor interfacial charge-transfer (CT) electronic states in photoelectric energy conversion in organic solar cells (Conference Presentation) 有机太阳能电池中供体-受体界面电荷转移(CT)电子态在光电能量转换中的作用(会议报告)
Pub Date : 2019-09-10 DOI: 10.1117/12.2528967
Xian-Kai Chen
A critical component of any donor-acceptor (D-A) bulk heterojunction organic solar cell is the appearance of inter-molecular charge-transfer (CT) electronic states at their D-A interfaces. These electronic states play a determining role in the photo-physical processes that transform the energy of the absorbed sunlight into electrical power. Here, through integrated multiscale theoretical simulations, we have illustrated how factors such as the details of the molecular packing at the D-A interfaces, the electronic polarization effects, and the extent of electron/hole delocalization around the interface impact the nature of the CT states. Moreover, we have also discussed how the hybridization between the CT and local-exciton (LE) states impacts the spectroscopy characteristics of D-A blends, the recombination rates and consequently the voltage losses, which need to be minimized.
任何供体-受体(D-A)体异质结有机太阳能电池的一个关键组成部分是其D-A界面上分子间电荷转移(CT)电子态的出现。这些电子态在将吸收的太阳光转化为电能的光物理过程中起着决定性的作用。在这里,通过集成的多尺度理论模拟,我们说明了诸如D-A界面上分子堆积的细节、电子极化效应以及界面周围电子/空穴离域的程度等因素如何影响CT态的性质。此外,我们还讨论了CT态和局域激子(LE)态之间的杂化如何影响D-A共混物的光谱特性、复合速率以及因此需要最小化的电压损失。
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引用次数: 0
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Organic, Hybrid, and Perovskite Photovoltaics XX
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