共查询到20条相似文献,搜索用时 31 毫秒
1.
Side Chain Optimization of Naphthalenediimide–Bithiophene‐Based Polymers to Enhance the Electron Mobility and the Performance in All‐Polymer Solar Cells
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Wonho Lee Changyeon Lee Hojeong Yu Dong‐Jun Kim Cheng Wang Han Young Woo Joon Hak Oh Bumjoon J. Kim 《Advanced functional materials》2016,26(10):1543-1553
Tuning the side chains of conjugated polymers is a simple, yet effective strategy for modulating their structural and electrical properties, but their impact on n‐type conjugated polymers has not been studied extensively, particularly in the area of all‐polymer solar cells (all‐PSCs). Herein, the effects of side chain engineering of P(NDI2OD‐T2) polymer (also known as Polyera Activink N2200) are investigated, which is the most widely used n‐type polymer in all‐PSCs and organic field‐effect transistors (OFETs), on their structural and electronic properties. A series of naphthalenediimide‐bithiophene‐based copolymers (P(NDIR‐T2)) is synthesized, with different side chains (R) of 2‐hexyldecyl (2‐HD), 2‐octyldodecyl (2‐OD), and 2‐decyltetradecyl (2‐DT). The P(NDI2HD‐T2) exhibits more noticeable crystalline behaviors than P(NDI2OD‐T2) and P(NDI2DT‐T2), thereby facilitating superior 3D charge transport. For example, the P(NDI2HD‐T2) shows the highest OFET electron mobility (1.90 cm2 V?1 s?1). Also, a series of all‐PSCs is produced using different electron donors of PTB7‐Th, PTB7, and PPDT2FBT. The P(NDI2HD‐T2) based all‐PSCs produce much higher power conversion efficiency (PCE) irrespective of the electron donors. In particular, the PTB7‐Th:P(NDI2HD‐T2) forms highly ordered, strong face‐on interchain stackings, and has better intermixed bulk‐heterojunction morphology, producing the highest PCE of 6.11% that has been obtained by P(NDIR‐T2) based all‐PSCs to date. 相似文献
2.
Shift of the Branching Point of the Side‐Chain in Naphthalenediimide (NDI)‐Based Polymer for Enhanced Electron Mobility and All‐Polymer Solar Cell Performance
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
《Advanced functional materials》2018,28(39)
The branching point of the side‐chain of naphthalenediimide (NDI)‐based conjugated polymers is systematically controlled by incorporating four different side‐chains, i.e., 2‐hexyloctyl (P(NDI1‐T)), 3‐hexylnonyl (P(NDI2‐T)), 4‐hexyldecyl (P(NDI3‐T)), and 5‐hexylundecyl (P(NDI4‐T)). When the branching point is located farther away from the conjugated backbones, steric hindrance around the backbone is relaxed and the intermolecular interactions between the polymer chains become stronger, which promotes the formation of crystalline structures in thin film state. In particular, thermally annealed films of P(NDI3‐T) and P(NDI4‐T), which have branching points far away from the backbone, possess more‐developed bimodal structure along both the face‐on and edge‐on orientations. Consequently, the field‐effect electron mobilities of P(NDIm‐T) polymers are monotonically increased from 0.03 cm2 V−1 s−1 in P(NDI1‐T) to 0.22 cm2 V−1 s−1 in P(NDI4‐T), accompanied by reduced activation energy and contact resistance of the thin films. In addition, when the series of P(NDIm‐T) polymers is applied in all‐polymer solar cells (all‐PSCs) as electron acceptor, remarkably high‐power conversion efficiency of 7.1% is achieved along with enhanced current density in P(NDI3‐T)‐based all‐PSCs, which is mainly attributed to red‐shifted light absorption and enhanced electron‐transporting ability. 相似文献
3.
Alkoxy‐Functionalized Thienyl‐Vinylene Polymers for Field‐Effect Transistors and All‐Polymer Solar Cells
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Hui Huang Nanjia Zhou Rocio Ponce Ortiz Zhihua Chen Stephen Loser Shiming Zhang Xugang Guo Juan Casado J. Teodomiro López Navarrete Xinge Yu Antonio Facchetti Tobin J. Marks 《Advanced functional materials》2014,24(19):2782-2793
π‐conjugated polymers based on the electron‐neutral alkoxy‐functionalized thienyl‐vinylene (TVTOEt) building‐block co‐polymerized, with either BDT (benzodithiophene) or T2 (dithiophene) donor blocks, or NDI (naphthalenediimide) as an acceptor block, are synthesized and characterized. The effect of BDT and NDI substituents (alkyl vs alkoxy or linear vs branched) on the polymer performance in organic thin film transistors (OTFTs) and all‐polymer organic photovoltaic (OPV) cells is reported. Co‐monomer selection and backbone functionalization substantially modifies the polymer MO energies, thin film morphology, and charge transport properties, as indicated by electrochemistry, optical spectroscopy, X‐ray diffraction, AFM, DFT calculations, and TFT response. When polymer P7 is used as an OPV acceptor with PTB7 as a donor, the corresponding blend yields TFTs with ambipolar mobilities of μe = 5.1 × 10?3 cm2 V–1 s–1 and μh = 3.9 × 10?3 cm2 V–1 s–1 in ambient, among the highest mobilities reported to date for all‐polymer bulk heterojunction TFTs, and all‐polymer solar cells with a power conversion efficiency (PCE) of 1.70%, the highest reported PCE to date for an NDI‐polymer acceptor system. The stable transport characteristics in ambient and promising solar cell performance make NDI‐type materials promising acceptors for all‐polymer solar cell applications. 相似文献
4.
A Synergetic Effect of Molecular Weight and Fluorine in All‐Polymer Solar Cells with Enhanced Performance
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Shanshan Chen Yujin An Gitish K. Dutta Yiho Kim Zhi‐Guo Zhang Yongfang Li Changduk Yang 《Advanced functional materials》2017,27(2)
A synergetic effect of molecular weight (Mn) and fluorine (F) on the performance of all‐polymer solar cells (all‐PSCs) is comprehensively investigated by tuning the Mn of the acceptor polymer poly((N,N′‐bis(2‐octyldodecyl)‐naphthalene‐1,4,5,8‐bis(dicarboximide)‐2,6‐diyl)‐alt‐5,5′‐(2,2′‐bithiophene)) (P(NDI2OD‐T2)) and the F content of donor polymer poly(2,3‐bis‐(3‐octyloxyphenyl)quinoxaline‐5,8‐dyl‐alt‐thiophene‐2,5‐diyl). Both Mn and F variations strongly influence the charge transport properties and morphology of the blend films, which have a significant impact on the photovoltaic performance of all‐PSCs. In particular, the effectiveness of high Mn in increasing power conversion efficiency (PCE) can be greatly improved by the devices based on optimum F content, reaching a PCE of 7.31% from the best all‐PSC combination. These findings enable us to further understand the working principles of all‐PSCs with a view on achieving even higher power conversion efficiency in the future. 相似文献
5.
Recently Advanced Polymer Materials Containing Dithieno[3,2‐b:2′,3′‐d]phosphole Oxide for Efficient Charge Transfer in High‐Performance Solar Cells
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Kwang Hun Park Yu Jin Kim Gi Back Lee Tae Kyu An Chan Eon Park Soon‐Ki Kwon Yun‐Hi Kim 《Advanced functional materials》2015,25(26):3991-3997
Two novel semiconducting polymers based on benzodithiophene and dithienophosphole oxide (DTP) units are designed and synthesized. A novel electron‐deficient DTP moiety is developed. Surprisingly, the introduction of DTP units brings highly polarizable characteristics, which is beneficial for the photocurrent in solar cells. Thus, the donor–acceptor type of conjugated polymers based on this novel acceptor has superior charge transfer properties and highly efficient PL quenching efficiencies. As a result, polymer solar cells (PSCs) with high power conversion efficiencies of 6.10% and 7.08% are obtained from poly(3,5‐didodecyl‐4‐phenylphospholo[3,2‐b:4,5‐b']dithiophene–4‐oxide‐alt‐4,8‐bis(5‐decylthiophen‐2‐yl)benzo[1,2‐b:4,5‐b']dithiophene) (PDTP–BDTT) and PDTP–4‐oxide‐alt‐4,8‐bis(5‐decylselenophen‐2‐yl)benzo[1,2‐b:4,5‐b']dithiophene) (PDTP–BDTSe), respectively, when the photoactive layer is processed with the 1,8‐octanedithiol (ODT) additive. The PDTP–BDTSe copolymer is now the best performing DTP‐based material for PSCs. Using the polarizable unit strategy determined in this study for the molecular design of conjugated polymers is expected to greatly advance the development of organic electronic devices. 相似文献
6.
Correlated Donor/Acceptor Crystal Orientation Controls Photocurrent Generation in All‐Polymer Solar Cells
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Marcel Schubert Brian A. Collins Hannah Mangold Ian A. Howard Wolfram Schindler Koen Vandewal Steffen Roland Jan Behrends Felix Kraffert Robert Steyrleuthner Zhihua Chen Konstantinos Fostiropoulos Robert Bittl Alberto Salleo Antonio Facchetti Frédéric Laquai Harald W. Ade Dieter Neher 《Advanced functional materials》2014,24(26):4068-4081
New polymers with high electron mobilities have spurred research in organic solar cells using polymeric rather than fullerene acceptors due to their potential of increased diversity, stability, and scalability. However, all‐polymer solar cells have struggled to keep up with the steadily increasing power conversion efficiency of polymer:fullerene cells. The lack of knowledge about the dominant recombination process as well as the missing concluding picture on the role of the semi‐crystalline microstructure of conjugated polymers in the free charge carrier generation process impede a systematic optimization of all‐polymer solar cells. These issues are examined by combining structural and photo‐physical characterization on a series of poly(3‐hexylthiophene) (donor) and P(NDI2OD‐T2) (acceptor) blend devices. These experiments reveal that geminate recombination is the major loss channel for photo‐excited charge carriers. Advanced X‐ray and electron‐based studies reveal the effect of chloronaphthalene co‐solvent in reducing domain size, altering domain purity, and reorienting the acceptor polymer crystals to be coincident with those of the donor. This reorientation correlates well with the increased photocurrent from these devices. Thus, efficient split‐up of geminate pairs at polymer/polymer interfaces may necessitate correlated donor/acceptor crystal orientation, which represents an additional requirement compared to the isotropic fullerene acceptors. 相似文献
7.
Competitive Absorption and Inefficient Exciton Harvesting: Lessons Learned from Bulk Heterojunction Organic Photovoltaics Utilizing the Polymer Acceptor P(NDI2OD‐T2)
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Zhi Li Jason D. A. Lin Hung Phan Alexander Sharenko Christopher M. Proctor Peter Zalar Zhihua Chen Antonio Facchetti Thuc‐Quyen Nguyen 《Advanced functional materials》2014,24(44):6989-6998
Organic solar cells utilizing the small molecule donor 7,7′‐(4,4‐bis(2‐ethylhexyl)‐4H‐silolo[3,2‐b:4,5‐b′]dithiophene‐2,6‐diyl)bis(6‐fluoro‐4‐(5′‐hexyl‐[2,2′‐bithiophen]‐5‐yl)benzo[c][1,2,5] thiadiazole) (p‐DTS(FBTTh2)2 and the polymer acceptor poly{[N,N′‐bis(2‐octyldodecyl)‐1,4,5,8‐naphthalenedicarboximide‐2,6‐diyl]‐alt‐5,5′‐(2,2′‐bithiophene)}(P(NDI2OD‐T2)) are investigated and a power conversion efficiency of 2.1% is achieved. By systematic study of bulk heterojunction (BHJ) organic photovoltaic (OPV) quantum efficiency, film morphology, charge transport and extraction and exciton diffusion, the loss processes in this blend is revealed compared to the blend of [6,6]‐phenyl‐C71‐butyric acid methyl ester (PC71BM) and the same donor. An exciton diffussion study using Förster resonant energy transfer (FRET) shows the upper limit of the P(NDI2OD‐T2) exciton diffusion length to be only 1.1 nm. The extremely low exciton diffusion length of P(NDI2OD‐T2), in combination with the overlap in donor and acceptor absorption, is then found to significantly limit device performance. These results suggest that BHJ OPV devices utilizing P(NDI2OD‐T2) as an acceptor material will likely be limited by its low exciton diffusion length compared to devices utilizing functionalized fullerene acceptors, especially when P(NDI2OD‐T2) significantly competes with the donor molecule for photon absorption. 相似文献
8.
[6, 6]‐Phenyl‐C61‐butyric acid methyl ester (PC60BM) is the widely used acceptor material in polymer solar cells (PSCs). Nevertheless, the low LUMO energy level and weak absorption in visible region are its two weak points. For enhancing the solar light harvest, the soluble C70 derivative PC70BM has been used as acceptor instead of PC60BM in high efficiency PSCs in recent years. But, the LUMO level of PC70BM is the same as that of PC60BM, which is too low for the PSCs based on the polymer donors with higher HOMO level, such as poly (3‐hexylthiophene) (P3HT). Here, a new soluble C70 derivative, indene‐C70 bisadduct (IC70BA), is synthesized with high yield of 58% by a one‐pot reaction of indene and C70 at 180 °C for 72 h. The electrochemical properties and electronic energy levels of the fullerene derivatives are measured by cyclic voltammetry. The LUMO energy level of IC70BA is 0.19 eV higher than that of PC70BM. The PSC based on P3HT with IC70BA as acceptor shows a higher Voc of 0.84 V and higher power conversion efficiency (PCE) of 5.64%, while the PSC based on P3HT/PC60BM and P3HT/PC70BM displays Voc of 0.59 V and 0.58 V, and PCE of 3.55% and 3.96%, respectively, under the illumination of AM1.5G, 100 mW cm?2. The results indicate that IC70BA is an excellent acceptor for the P3HT‐based PSCs and could be a promising new acceptor instead of PC70BM for the high performance PSCs based on narrow bandgap conjugated polymer donor. 相似文献
9.
Miscibility and morphology of the active layers have significant influence on the photovoltaic performance of polymer solar cells (PSCs). Chemical strategies, especially molecular structure design, have been proven to be crucial for polymer donor materials. In this work, two wide bandgap D-A copolymer donors composed of tripropylsilyl substituted bithienyl-benzodithiophene as donor (D) unit and dialkyl substituted bithiazole as acceptor (A) unit were designed and synthesized. By introducing thiophene π-bridges into the backbone, the miscibility and morphological properties of the materials are effectively tuned, leading to tremendous progress in power conversion efficiency from 0.95% to 10.73% with m-ITIC as the acceptor. The results demonstrate that manipulating molecular distortion can be an effective strategy to regulate molecular self-assembly behavior of the polymer donors and achieve excellent aggregation properties, blend miscibility, and photovoltaic performance of the PSCs. 相似文献
10.
The Impact of Sequential Fluorination of π‐Conjugated Polymers on Charge Generation in All‐Polymer Solar Cells
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Kakaraparthi Kranthiraja Seonha Kim Changyeon Lee Kumarasamy Gunasekar Vijaya Gopalan Sree Bhoj Gautam Kenan Gundogdu Sung‐Ho Jin Bumjoon J. Kim 《Advanced functional materials》2017,27(29)
The performance of all‐polymer solar cells (all‐PSCs) is often limited by the poor exciton dissociation process. Here, the design of a series of polymer donors ( P1 – P3 ) with different numbers of fluorine atoms on their backbone is presented and the influence of fluorination on charge generation in all‐PSCs is investigated. Sequential fluorination of the polymer backbones increases the dipole moment difference between the ground and excited states (Δµge) from P1 (18.40 D) to P2 (25.11 D) and to P3 (28.47 D). The large Δµge of P3 leads to efficient exciton dissociation with greatly suppressed charge recombination in P3 ‐based all‐PSCs. Additionally, the fluorination lowers the highest occupied molecular orbital energy level of P3 and P2 , leading to higher open‐circuit voltage (VOC). The power conversion efficiency of the P3 ‐based all‐PSCs (6.42%) outperforms those of the P2 and P1 (5.00% and 2.65%)‐based devices. The reduced charge recombination and the enhanced polymer exciton lifetime in P3 ‐based all‐PSCs are confirmed by the measurements of light‐intensity dependent short‐circuit current density (JSC) and VOC, and time‐resolved photoluminescence. The results provide reciprocal understanding of the charge generation process associated with Δµge in all‐PSCs and suggest an effective strategy for designing π‐conjugated polymers for high performance all‐PSCs. 相似文献
11.
Nonfullerene Polymer Solar Cells based on a Perylene Monoimide Acceptor with a High Open‐Circuit Voltage of 1.3 V
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Youdi Zhang Xia Guo Bing Guo Wenyan Su Maojie Zhang Yongfang Li 《Advanced functional materials》2017,27(10)
Nonfullerene polymer solar cells (PSCs) are fabricated with a perylene monoimide‐based n‐type wide‐bandgap organic semiconductor PMI‐F‐PMI as an acceptor and a bithienyl‐benzodithiophene‐based wide‐bandgap copolymer PTZ1 as a donor. The PSCs based on PTZ1:PMI‐F‐PMI (2:1, w/w) with the treatment of a mixed solvent additive of 0.5% N ‐methyl pyrrolidone and 0.5% diphenyl ether demonstrate a very high open‐circuit voltage (V oc) of 1.3 V with a higher power conversion efficiency (PCE) of 6%. The high V oc of the PSCs is a result of the high‐lying lowest unoccupied molecular orbital (LUMO) of ?3.42 eV of the PMI‐F‐PMI acceptor and the low‐lying highest occupied molecular orbital (HOMO) of ?5.31 eV of the polymer donor. Very interestingly, the exciton dissociation efficiency in the active layer is quite high, even though the LUMO and HOMO energy differences between the donor and acceptor materials are as small as ≈0.08 and 0.19 eV, respectively. The PCE of 6% is the highest for the PSCs with a V oc as high as 1.3 V. The results indicate that the active layer based on PTZ1/PMI‐F‐PMI can be used as the front layer in tandem PSCs for achieving high V oc over 2 V. 相似文献
12.
Fluorinated and Alkylthiolated Polymeric Donors Enable both Efficient Fullerene and Nonfullerene Polymer Solar Cells
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Guangjun Zhang Xiaopeng Xu Zhaozhao Bi Wei Ma Dongsheng Tang Ying Li Qiang Peng 《Advanced functional materials》2018,28(10)
In this work, four donor (D)–acceptor (A) copolymers based on benzodithiophene (BDT) and benzothiadiazole (BT) with different alkylthiolated and/or fluorinated side chains are developed for efficient fullerene and nonfullerene polymer solar cells (PSCs). The synergistic effect of sulfuration and fluorination on the optical absorption, energy level, crystallinity, carrier mobility, blend morphology, and photovoltaic performance is investigated systematically. By incorporating sulfur atoms onto the side chains, a little blueshifted but significantly increased absorption can be obtained for PBDTS‐FBT compared to PBDT‐FBT . On the other side, a little more blueshifted but much stronger absorption and much lower‐lying highest occupied molecular orbital (HOMO) level can be realized for PBDTF‐FBT when introducing fluorine atoms instead of sulfur atoms. With the combination of both fluorination and sulfuration strategies, PBDTS‐FBT exhibits the best absorption ability, lowest HOMO energy level, and highest crystallinity, which make PBDTSF‐FBT devices show the highest power conversion efficiency (PCE) of 10.69% in fullerene PSCs and 11.66% in nonfullerene PSCs. The PCE of 11.66% is the best value for PSCs based on BT‐containing copolymer donors reported so far. The results indicate that fluorination and sulfuration have a synergistically positive effect on the performance of D–A photovoltaic copolymers and their solar cell devices. 相似文献
13.
Huanxiang Jiang Xiaoming Li Jianing Wang Shanlin Qiao Yong Zhang Nan Zheng Weichao Chen Yonghai Li Renqiang Yang 《Advanced functional materials》2019,29(34)
Ternary polymer solar cells (PSCs) are one of the most promising device architectures that maintains the simplicity of single‐junction devices and provides an important platform to better tailor the multiple performance parameters of PSCs. Herein, a ternary PSC system is reported employing a wide bandgap polymeric donor (PBTA‐PS) and two small molecular nonfullerene acceptors (labeled as LA1 and 6TIC). LA1 and 6TIC keep not only well‐matched absorption profiles but also the rational crystallization properties. As a result, the optimal ternary PSC delivers a state of the art power conversion efficiency (PCE) of 14.24%, over 40% higher than the two binary devices, resulting from the prominently increased short‐circuit current density (Jsc) of 22.33 mA cm?2, moderate open‐circuit voltage (Voc) of 0.84 V, and a superior fill factor approaching 76%. Notably, the outstanding PCE of the ternary PSC ranks one of the best among the reported ternary solar cells. The greatly improved performance of ternary PSCs mainly derives from combining the complementary properties such as absorption and crystallinity. This work highlights the great importance of the rational design of matched acceptors toward highly efficient ternary PSCs. 相似文献
14.
Xi Fan Chaohua Cui Guojia Fang Jinzhao Wang Songzhan Li Fei Cheng Hao Long Yongfang Li 《Advanced functional materials》2012,22(3):585-590
Polymer solar cells (PSCs) with poly(3‐hexylthiophene) (P3HT) as a donor, an indene‐C70 bisadduct (IC70BA) as an acceptor, a layer of indium tin oxide modified by MoO3 as a positive electrode, and Ca/Al as a negative electrode are presented. The photovoltaic performance of the PSCs was optimized by controlling spin‐coating time (solvent annealing time) and thermal annealing, and the effect of the spin‐coating times on absorption spectra, X‐ray diffraction patterns, and transmission electron microscopy images of P3HT/IC70BA blend films were systematically investigated. Optimized PSCs were obtained from P3HT/IC70BA (1:1, w/w), which exhibited a high power conversion efficiency of 6.68%. The excellent performance of the PSCs is attributed to the higher crystallinity of P3HT and better a donor–acceptor interpenetrating network of the active layer prepared under the optimized conditions. In addition, PSCs with a poly(3,4‐ethylenedioxy‐thiophene):poly(styrenesulfonate) (PEDOT:PSS) buffer layer under the same optimized conditions showed a PCE of 6.20%. The results indicate that the MoO3 buffer layer in the PSCs based on P3HT/IC70BA is superior to that of the PEDOT:PSS buffer layer, not only showing a higher device stability but also resulting in a better photovoltaic performance of the PSCs. 相似文献
15.
Huiliang Sun Bin Liu Chang Woo Koh Yujie Zhang Jianhua Chen Yang Wang Peng Chen Bao Tu Maoyao Su Hang Wang Yumin Tang Yongqiang Shi Han Young Woo Xugang Guo 《Advanced functional materials》2019,29(42)
The aggregation/crystallinity of classic n‐type terpolymers based on naphthalene diimide and perylene diimide is challenging to tune due to their rigid and extended cores, leading to suboptimal film morphology. A new strategy for developing high‐performance n‐type terpolymers by incorporating imide‐functionalized heteroarenes is reported here to balance crystallinity and miscibility without sacrificing charge carrier mobilities. The introduction of thienopyrroledione (TPD) into the copolymer f‐BTI2‐FT results in a series of terpolymers BTI2‐xTPD having distinct TPD content. The irregular backbone reduces crystallinity, yielding improved miscibility with the polymer donor. More importantly, TPD triggers noncovalent S?O interactions, increasing backbone planarity and in‐chain charge transport. Such interactions also promote face‐on polymer packing. As a result, all‐polymer solar cells (all‐PSCs) based on BTI2‐30TPD achieve an optimal power conversion efficiency (PCE) of 8.28% with a small energy loss (0.53 eV). This efficiency is substantially higher than that of TPD (4.4%) or a BTI2‐based copolymer (6.8%) and is also the highest for additive‐free all‐PSCs based on a terpolymer acceptor. Moreover, the BTI2‐30TPD cell exhibits excellent stability with the PCE retaining 90% of its initial value after 400 h of aging. The results demonstrate that random polymerization using imide‐functionalized heteroarenes is a powerful approach to develop terpolymer acceptors toward efficient and stable all‐polymer solar cell PSCs. 相似文献
16.
Alkylsilyl Functionalized Copolymer Donor for Annealing‐Free High Performance Solar Cells with over 11% Efficiency: Crystallinity Induced Small Driving Force
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Bin Huang Lie Chen Xiufen Jin Dong Chen Yongkang An Qian Xie Yun Tan Hui Lei Yiwang Chen 《Advanced functional materials》2018,28(20)
The contradiction between enlarging the offset between energy levels of donor/acceptor and the required driving force for exciton split leads to a trade‐off between open circuit voltage (VOC) and short circuit current density (JSC), which is a big challenge for development of high performance polymer solar cells (PSCs). Some advanced works reported the PSCs with low photon energy loss (Eloss) and small driving force, but the correlation of molecular structures of light‐harvesting system and driving force is still unclear. In this work, a new alkylsilyl functionalized copolymer donor PBDS‐T (PBDST: poly[(2,6trialkylsilyl thiophen2yl)benzo[1,2b:4,5b′]dithiophene))alt(5,5(1′,3′di2thienyl5′,7′bis(2ethylhexyl)benzo[1′,2′c:4′,5′c′]dithiophene4,8dione))]) with low‐lying energy levels was designed for efficient PSCs. By monitoring the Photoluminescence quenching of the bulk and bilayer heterojunctions, small driving forces, ?EHOMO of 0.15 eV and ?ELUMO of 0.22 eV were founded to allow for efficient charge transfer, which were observed to correlate with the crystalline PBDS‐T and the optimal morphology in PBDS‐T:ITIC (ITIC: 3,9bis(2methylene(3(1,1dicyanomethylene)indanone))5,5,11,11tetrakis(4hexylphenyl)dithieno[2,3d:2′,3′d′]sindaceno[1,2b:5,6b′]dithiophene). Simultaneously improved VOC, JSC and small Eloss boosted the PCE over 11%, which is one of the highest values for annealing‐free device. These results shield a light on precise design of a light‐harvesting system with small driving force to simultaneously improve the VOC and JSC for highly efficient PSCs. 相似文献
17.
Self‐Doping Fullerene Electrolyte‐Based Electron Transport Layer for All‐Room‐Temperature‐Processed High‐Performance Flexible Polymer Solar Cells
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Jingwen Zhang Rongming Xue Guiying Xu Weijie Chen Guo‐Qing Bian Changan Wei Yaowen Li Yongfang Li 《Advanced functional materials》2018,28(13)
To achieve high‐performance large‐area flexible polymer solar cells (PSCs), one of the challenges is to develop new interface materials that possess a thermal‐annealing‐free process and thickness‐insensitive photovoltaic properties. Here, an n‐type self‐doping fullerene electrolyte, named PCBB‐3N‐3I, is developed as electron transporting layer (ETL) for the application in PSCs. PCBB‐3N‐3I ETL can be processed at room temperature, and shows excellent orthogonal solvent processability, substantially improved conductivity, and appropriate energy levels. PCBB‐3N‐3I ETL also functions as light‐harvesting acceptor in a bilayer solar cell, contributing to the overall device performance. As a result, the PCBB‐3N‐3I ETL‐based inverted PSCs with a PTB7‐Th:PC71BM photoactive layer demonstrate an enhanced power conversion efficiency (PCE) of 10.62% for rigid and 10.04% for flexible devices. Moreover, the device avoids a thermal annealing process and the photovoltaic properties are insensitive to the thickness of PCBB‐3N‐3I ETL, yielding a PCE of 9.32% for the device with thick PCBB‐3N‐3I ETL (61 nm). To the best of one's knowledge, the above performance yields the highest efficiencies for the flexible PSCs and thick ETL‐based PSCs reported so far. Importantly, the flexible PSCs with PCBB‐3N‐3I ETL also show robust bending durability that could pave the way for the future development of high‐performance flexible solar cells. 相似文献
18.
Xiangyue Meng Wenqing Zhang Zhan'ao Tan Yongfang Li Yihan Ma Taishan Wang Li Jiang Chunying Shu Chunru Wang 《Advanced functional materials》2012,22(10):2187-2193
The efficiency of polymer solar cells (PSCs) can be essentially enhanced by improving the performance of electron‐acceptor materials, including by increasing the lowest unoccupied molecular orbital (LUMO) level, improving the optical absorption, and tuning the material solubility. Here, a new soluble C70 derivative, dihydronaphthyl‐based C70 bisadduct (NC70BA), is synthesized and explored as acceptor in PSCs. The NC70BA has high LUMO energy level that is 0.2 eV higher than [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM), and displays broad light absorption in the visible region. Consequently, the PSC based on the blend of poly(3‐hexylthiophene) (P3HT) and NC70BA shows a high open‐circuit voltage (Voc = 0.83 V) and a high power conversion efficiency (PCE = 5.95%), which are much better than those of the P3HT:PCBM‐based device (Voc = 0.60 V; PCE = 3.74%). Moreover, the amorphous nature of NC70BA effectively suppresses the thermally driven crystallization, leading to high thermal stability of the P3HT:NC70BA‐based solar cell devices. It is observed that the P3HT:NC70BA‐based device retains 80% of its original PCE value against thermal heating at 150 °C over 20 h. The results unambiguously indicate that the NC70BA is a promising acceptor material for practical PSCs. 相似文献
19.
Fullerene‐Free Polymer Solar Cells with Open‐Circuit Voltage above 1.2 V: Tuning Phase Separation Behavior with Oligomer to Replace Polymer Acceptor
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Yingying Fu Bei Wang Jianfei Qu Yang Wu Wei Ma Yanhou Geng Yanchun Han Zhiyuan Xie 《Advanced functional materials》2016,26(32):5922-5929
This study has proposed to use a well‐defined oligomer F4TBT4 to replace its analogue polymer as electron acceptor toward tuning the phase separation behavior and enhancing the photovoltaic performance of all‐polymer solar cells. It has been disclosed that the oligomer acceptor favors to construct pure and large‐scale phase separation in the polymer:oligomer blend film in contrast to the polymer:polymer blend film. This gets benefit from the well‐defined structure and short rigid conformation of the oligomer that endows it aggregation capability and avoids possible entanglement with the polymer donor chains. The charge recombination is to some extent suppressed and charge extraction is also improved. Finally, the P3HT:F4TBT4 solar cells not only output a high VOC above 1.2 V, but also achieve a power conversion efficiency of 4.12%, which is two times higher than the P3HT:PFTBT solar cells and is comparable to the P3HT:PCBM solar cells. The strategy of constructing optimum phase separation with oligomer to replace polymer opens up new prospect for the further improvement of the all‐polymer solar cells. 相似文献
20.
Highly Efficient Inverted Organic Solar Cells Through Material and Interfacial Engineering of Indacenodithieno[3,2‐b]thiophene‐Based Polymers and Devices
下载免费PDF全文
![点击此处可从《Advanced functional materials》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Jeremy J. Intemann Kai Yao Yong‐Xi Li Hin‐Lap Yip Yun‐Xiang Xu Po‐Wei Liang Chu‐Chen Chueh Fei‐Zhi Ding Xi Yang Xiaosong Li Yiwang Chen Alex K.‐Y. Jen 《Advanced functional materials》2014,24(10):1465-1473
A synergistic approach combining new material design and interfacial engineering of devices is adopted to produce high efficiency inverted solar cells. Two new polymers, based on an indacenodithieno[3,2‐b]thiophene‐difluorobenzothiadiazole (PIDTT‐DFBT) donor–acceptor (D–A) polymer, are produced by incorporating either an alkyl thiophene (PIDTT‐DFBT‐T) or alkyl thieno[3,2‐b]thiophene (PIDTT‐DFBT‐TT) π‐bridge as spacer. Although the PIDTT‐DFBT‐TT polymer exhibits decreased absorption at longer wavelengths and increased absorption at higher energy wavelengths, it shows higher power conversion efficiencies in devices. In contrast, the thiophene bridged PIDTT‐DFBT‐T shows a similar change in its absorption spectrum, but its low molecular weight leads to reduced hole mobilities and performance in photovoltaic cells. Inverted solar cells based on PIDTT‐DFBT‐TT are explored by modifying the electron‐transporting ZnO layer with a fullerene self‐assembled monolayer and the MoO3 hole‐transporting layer with graphene oxide. This leads to power conversion efficiencies as high as 7.3% in inverted cells. PIDTT‐DFBT‐TT's characteristic strong short wavelength absorption and high efficiency suggests it is a good candidate as a wide band gap material for tandem solar cells. 相似文献