共查询到20条相似文献,搜索用时 31 毫秒
1.
Dr. Gang Zhang Vincent Lami Dr. Frank Rominger Prof.Dr. Yana Vaynzof Prof.Dr. Michael Mastalerz 《Angewandte Chemie (International ed. in English)》2016,55(12):3977-3981
A new class of rigid twisted truxenone oligomers with an enlarged π backbone has been established by oxidative dimerization reactions. The resulting extended conjugated systems have large extinction coefficients and low‐lying LUMO levels and show good solubility in common organic solvents, thus making them attractive compounds as new electron acceptors in organic electronics. Their suitability as electron acceptors has been demonstrated in bulk‐heterojunction organic solar cells with 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) as the donor material. 相似文献
2.
《化学:亚洲杂志》2017,12(12):1286-1290
Three kinds of nonconjugated rigid perylene bisimide (PBI) derivatives based on a triptycene core were designed, synthesized and characterized. The unique three‐dimensional (3D) conformation of triptycene could enable formation of polymer with the favorable morphology for organic polymer solar cells (PSCs) by relieving the self‐aggregation of rigid PBI units. The low‐lying LUMO energy levels of these compounds demonstrated that they are very suitable for use as acceptors in organic solar cells. A higher power conversion efficiency (PCE) of 6.15 % was obtained for the blend film using the compound with two PBI units ( T‐2 ) as the acceptor and commercial poly[[4,8‐bis[5‐(2‐ethylhexyl)thiophene‐2‐yl]benzo[1,2‐b :4,5‐b ′]dithiophene‐2,6‐diyl][3‐fluoro‐2‐[(2‐ethylhexyl)‐carbonyl]thieno[3,4‐b ]thiophenediyl]] (PCE‐10) as the electron donor. 相似文献
3.
Optimized domain size and enlarged D/A interface by tuning intermolecular interaction in all‐polymer ternary solar cells 下载免费PDF全文
Rui Zhang Hua Yang Ke Zhou Jidong Zhang Jiangang Liu Xinhong Yu Rubo Xing Yanchun Han 《Journal of Polymer Science.Polymer Physics》2016,54(18):1811-1819
The selection of sensitizer and its existence in the blend films are important to the performance of all‐polymer ternary solar cells. Herein, all‐polymer ternary solar cell devices, which used poly[4,8‐bis(5‐(2‐ethylhexyl)thiophen‐2‐yl)benzo[1,2‐b:4,5‐b′] dithiophene‐alt‐3‐fluorothieno[3,4‐b]thiophene‐2‐carboxy‐late] (PTB7‐Th) as donor, poly[[N,N‐bis(2‐octyldodecyl)‐napthalene‐1,4,5,8‐bis(dicarboximide)?2,6‐diyl]‐alt‐5, 5′‐(2,2′‐bithiophene)] (N2200) as acceptor and poly[N?900‐hepta‐decanyl‐2,7‐carbazole‐alt‐5,5‐(40,70‐di‐2‐thienyl‐20,10,30‐benzothiadiazole) (PCDTBT) as sensitizer, are successfully demonstrated. The intermolecular interaction between donor PTB7‐Th and sensitizer PCDTBT may lead to aggregation of PTB7‐Th which decreases domain sizes and enlarges D/A effective interface area. In addition, the PCDTBT molecules also extend light absorption and cascaded energy levels of the ternary blend system. As a result, with 15% PCDTBT we get a power conversion efficiency of 5.11%, almost 20% higher than control device due to more favored exciton dissociation and higher charge transport efficiency. This study reveals a promising way to achieve high efficiency all‐polymer solar cells using a low‐band gap polymer PCDTBT. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 1811–1819 相似文献
4.
《Journal of Polymer Science.Polymer Physics》2018,56(10):814-820
Thin‐film polymer solar cell consisting of [6,6]‐phenyl‐C71‐butyric acid methyl ester (PC71BM) and 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) demonstrates elastic stretchability with the aid of a high boiling point additive, 1,8‐diiodooctane (DIO). The usage of DIO not only helps to form uniformly distributed nanocrystalline grains, but may also create free volumes between the nano‐grains that allow for relative sliding between the nano‐grains. The relative sliding can accommodate large external deformation. Large dichroic ratios of the optical absorption of both PC71BM and PTB7 were observed under large‐strain deformation, indicating reorientation of the nanocrystalline PC71BM and PTB7 polymer chains along stretching direction. The dichroic ratio decreases to nearly 1.0 as the blend was relaxed to 0% strain. Therefore, the nanometer‐size grain blending morphology provides an approach to impart stretchability to organic semiconductors that are otherwise un‐stretchable. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018 , 56, 814–820 相似文献
5.
A‐D‐A Type Small Molecules Based on Boron Dipyrromethene for Solution‐Processed Organic Solar Cells 下载免费PDF全文
Liangang Xiao Dr. Hongda Wang Ke Gao Dr. Lisheng Li Chang Liu Prof. Dr. Xiaobin Peng Prof. Dr. Wai‐Yeung Wong Prof. Dr. Wai‐Kwok Wong Dr. Xunjin Zhu 《化学:亚洲杂志》2015,10(7):1513-1518
The unique properties of boron dipyrromethene (BODIPY) dyes including facile synthesis, high absorption coefficients, and delocalized molecular orbitals as well as excellent photochemical and thermal stability, make them promising as materials for organic solar cells. Accordingly, in this study three A‐D ‐A structural small molecules of BDTT‐BODIPY, FL‐BODIPY, and TT‐BODIPY have been synthesized, in which two BODIPY acceptor units are symmetrically conjugated to 4,8‐bis(5‐(2‐ethylhexyl) thiophen‐2‐yl)benzo[1,2‐b:4,5‐b]dithiophene (BDTT), 9,9‐dioctyl‐9H‐fluorene (FL), and thieno[3,2‐b]thiophene (TT) donor cores, respectively. The manipulation of the structural parameters significantly improves the performances of the BHJ OSCs, which show power conversion efficiencies of 4.75 %, 1.51 %, and 1.67 % based on [6,6]‐phenyl C71‐butyric acid methyl ester (PC71BM) as the acceptor material and BDTT‐BODIPY, FL‐BODIPY, and TT‐BODIPY as the donor materials, respectively. 相似文献
6.
Yunli Han Lie Chen Yiwang Chen 《Journal of polymer science. Part A, Polymer chemistry》2013,51(2):258-266
A new liquid crystalline (LC) acceptor monomer 2,5‐bis[4‐(4′‐cyanobiphenyloxy)dodecyl]‐3,6‐dithiophen‐2‐yl‐pyrrolo[3,4‐c]pyrrole‐1,4‐dione (TDPPcbp) was synthesized by incorporating cyanobiphenyl mesogens into diketopyrrolopyrrole (DPP). The monomer was copolymerized with bis(2‐ethylhexyloxy)benzo[1,2‐b:4,5‐b′] dithiophene (BDT) and N‐9′‐heptadecanylcarbazole (CB) donors to obtain donor–acceptor alternating copolymers poly[4,8‐bis(2‐ethylhexyloxy)benzo[1,2‐b:4,5‐b′]dithiophene‐alt‐3,6‐bis(thiophen‐5‐yl)‐2,5‐bis[4‐(4′‐cyanobiphenyloxy)dodecyl]‐2,5‐dihydropyrrolo[3,4‐c]pyrrole‐1,4‐dione] (PBDTDPPcbp) and poly[N‐9′‐heptadecanyl‐2,7‐carbazole‐alt‐3,6‐bis(thiophen‐5‐yl)‐2,5‐bis[4‐(4′‐cyano‐biphenyloxy)dodecyl]‐2,5‐dihydropyrrolo[3, 4‐c]pyrrole‐1,4‐dione] (PCBTDPPcpb) with reduced band gap, respectively. The LC properties of the copolymers, the effects of main chain variation on molecular packing, optical properties, and energy levels were analyzed. Incorporating the mesogen cyanobiphenyl units not only help polymer donors to pack well through mesogen self‐organization but also push the fullerene acceptor to form optimized phase separation. The bulk heterojunction photovoltaicdevicesshow enhanced performance of 1.3% for PBDTDPPcbp and 1.2% for PCBTDPPcbp after thermal annealing. The results indicate that mesogen‐controlled self‐organization is an efficient approach to develop well‐defined morphology and to improve the device performance. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
7.
《Journal of polymer science. Part A, Polymer chemistry》2018,56(17):1978-1988
New donor–π–acceptor (D–π–A) type conjugated copolymers, poly[(4,8‐bis((2‐hexyldecyl)oxy)benzo[1,2‐b:4,5‐b′]dithiophene)‐alt‐(2,5‐bis(4‐octylthiophen‐2‐yl)thiazolo[5,4‐d]thiazole)] (PBDT‐tTz), and poly[(4,8‐bis((2‐hexyldecyl)oxy)benzo[1,2‐b:4,5‐b′]dithiophene)‐alt‐(2,5‐bis(6‐octylthieno[3,2‐b]thiophen‐2‐yl)thiazolo[5,4‐d]thiazole)] (PBDT‐ttTz) were synthesized and characterized with the aim of investigating their potential applicability to organic photovoltaic active materials. While copolymer PBDT‐tTz showed a zigzagged non‐linear structure by thiophene π‐bridges, PBDT‐ttTz had a linear molecular structure with thieno[3,2‐b]thiophene π‐bridges. The optical, electrochemical, morphological, and photovoltaic properties of PBDT‐tTz and PBDT‐ttTz were systematically investigated. Furthermore, bulk heterojunction photovoltaic devices were fabricated by using the synthesized polymers as p‐type donors and [6,6]‐phenyl‐C71‐butyric acid methyl ester as an n‐type acceptor. PBDT‐ttTz showed a high power conversion efficiency (PCE) of 5.21% as a result of the extended conjugation arising from the thienothiophene π‐bridges and enhanced molecular ordering in the film state, while PBDT‐tTz showed a relatively lower PCE of 2.92% under AM 1.5 G illumination (100 mW/cm2). © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 1978–1988 相似文献
8.
Hua Tan Xianping Deng Junting Yu Jianhua Chen Kaixuan Nie Ying Huang Yu Liu Yafei Wang Meixiang Zhu Weiguo Zhu 《Journal of polymer science. Part A, Polymer chemistry》2013,51(5):1051-1057
Two donor/acceptor (D/A)‐based benzo[1,2‐b:4,5‐b′]dithiophene‐alt‐2,3‐biphenyl quinoxaline copolymers of P 1 and P 2 were synthesized pending different functional groups (thiophene or triphenylamine) in the 4‐positions of phenyl rings. Their thermal, photophysical, electrochemical, and photovoltaic properties, as well as morphology of their blending films were investigated. The poly(4,8‐bis((2‐ethyl‐hexyl)oxy)benzo[1,2‐b:4,5‐b'] dithiophene)‐alt‐(2,3‐bis(4′‐bis(N,N‐bis(4‐(octyloxy) phenylamino)‐ 1,1′‐biphen‐4‐yl)quinoxaline) ( P 2) exhibited better photovoltaic performance than poly(4,8‐bis((2‐ethylhexyl)oxy)benzo[1,2‐b:4,5‐b'] dithiophene)‐alt‐(2,3‐bis(4‐(5‐octylthiophen‐2‐yl)phenyl)quinoxaline) ( P 1) in the bulk‐heterojunction polymer solar cells with a configuration of ITO/PEDOT:PSS/polymers: [6,6]‐phenyl‐C71‐butyric acid methyl ester (PC71BM)/LiF/Al. A power conversion efficiency of 3.43%, an open‐circuit voltage of 0.80 V, and a short‐circuit current of 9.20 mA cm?2 were achieved in the P 2‐based cell under the illumination of AM 1.5, 100 mW cm?2. Importantly, this power conversion efficiency level is 2.29 times higher than that in the P 1‐based cell. Our work indicated that incorporating triphenylamine pendant in the D/A‐based polymers can greatly improved the photovoltaic properties for its resulting polymers. 相似文献
9.
B. Hari Babu Chengkun Lyu Hongwei Zhang Zhihao Chen Fenghong Li Lin Feng Xiao‐Tao Hao 《中国化学》2020,38(8):817-822
Interfacial engineering is expected to be a feasible strategy to improve the charge transport properties of the hole transport layer (HTL), which is of crucial importance to boost the device performance of organic solar cells (OSCs). In this study, two types of alcohol soluble materials, 2,3,5,6‐tetrafluoro‐7,7,8,8‐tetracyanoquinodimethane (F4‐TCNQ) and di‐tetrabutylammoniumcis–bis(isothiocyanato)bis (2,2’‐bipyridyl‐4,4’‐dicarboxylato) ruthenium(II) (N719) dye were selected as the dopant for HTL. The doping of F4‐TCNQ and N719 dye in poly (ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) with and without integrating a graphene quantum‐dots (G‐QDs) layer has been explored in poly[[2,6′‐4‐8‐di(5‐ethylhexylthienyl)benzo[1,2‐b:3,3‐b]dithiophene][3‐fluoro‐2[(2‐ethylhexyl)carbonyl]thieno[3,4‐b]thio‐phenediyl:(2,2′‐((2Z,2′Z)‐(((4,4,9, 9‐tetrakis(4‐hexylphenyl)‐4,9‐dihydro‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene‐2,7‐diyl)bis(4‐((2‐ethylhexyl)oxy)thiophene‐5,2‐diyl))bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (PTB7‐Th:IEICO‐4F) OSCs. The power conversion efficiency of the non‐fullerene OSCs has been increased to 10.12% from 8.84%. The influence of HTL modification on the nano‐morphological structures and photophysical properties is analyzed based on the comparative studies performed on the control and modified devices. The use of chemical doping and bilayer strategy optimizes the energy level alignment, nanomorphology, hole mobility, and work‐function of HTL, leading to considerable reduction of the leakage current and recombination losses. Our work demonstrates that the doping of HTL and the incorporation of G‐QDs layer to constitute a bilayer HTL is an promising strategy to fabricate high performance non‐fullerene polymer solar cells 相似文献
10.
Seulki Song Gang‐Young Lee Chan Eon Park Taiho Park 《Journal of polymer science. Part A, Polymer chemistry》2013,51(2):372-382
Three classes of quinoxaline (Qx)‐based donor–acceptor (D–A)‐type copolymers, poly[thiophene‐2,5‐diyl‐alt‐2,3‐bis(4‐(octyloxy)phenyl‐quinoxaline‐5,8‐diyl] P(T‐Qx), poly{4,8‐bis(2‐ethylhexyloxy)benzo[1,2‐b:4,5‐b′]dithiophene‐2,6‐diyl‐alt‐2,3‐bis(4‐(octyloxy)phenyl‐quinoxaline‐5,8‐diy} P(BDT‐Qx), and poly{4,8‐bis(2‐ethylhexyloxy)benzo[1,2‐b:4,5‐b′]dithiophene‐2,6‐diyl‐alt‐(5′,8′‐di‐2‐thienyl‐2,3‐bis(4‐octyloxyl)phenyl)‐quinoxaline‐5,5‐diyl} P(BDT‐DTQx), were synthesized via a Stille coupling reaction. The Qx unit was functionalized at the 2‐ and 3‐positions with 4‐(octyloxy)phenyl to provide good solubility and to reduce the steric hindrance. The absorption spectra of the Qx‐containing copolymers could be tuned by incorporating three different electron‐donating moieties. Among these, P(T‐Qx) acted as an electron donor and yielded a high‐performance solar cell by assuming a rigid planar structure, confirmed by differential scanning calorimetry, UV–vis spectrophotometer, and density functional theory study. In contrast, the P(BDT‐Qx)‐based solar cell displayed a lower power conversion efficiency (PCE) with a large torsional angle (34.7°) between the BDT and Qx units. The BDT unit in the P(BDT‐DTQx) backbone acted as a linker and interfered with the formation of charge complexes or quinoidal electronic conformations in a polymer chain. The PCEs of the polymer solar cells based on these copolymers, in combination with [6,6]‐phenyl C70 butyric acid methyl ester (PC71BM), were 3.3% [P(T‐Qx)], 1.9% [P(BDT‐Qx)], and 2.3% [P(BDT‐DTQx)], respectively, under AM 1.5G illumination (100 mW cm?2). © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
11.
In Hwan Jung Jinyoung Yu Eunjae Jeong Jinseck Kim Sooncheol Kwon Hoyoul Kong Kwanghee Lee Prof. Han Young Woo Prof. Hong‐Ku Shim Prof. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(12):3743-3752
We have synthesized four types of cyclopentadithiophene (CDT)‐based low‐bandgap copolymers, poly[{4,4‐bis(2‐ethylhexyl)‐4H‐cyclopenta[2,1‐b:3,4‐b′]dithiophene‐2,6‐diyl}‐alt‐(2,2′‐bithiazole‐5,5′‐diyl)] ( PehCDT‐BT ), poly[(4,4‐dioctyl‐4H‐cyclopenta[2,1‐b:3,4‐b′]dithiophene‐2,6‐diyl)‐alt‐(2,2′‐bithiazole‐5,5′‐diyl)] ( PocCDT‐BT ), poly[{4,4‐bis(2‐ethylhexyl)‐4H‐cyclopenta[2,1‐b:3,4‐b′]dithiophene‐2,6‐diyl}‐alt‐{2,5‐di(thiophen‐2‐yl)thiazolo[5,4‐d]thiazole‐5,5′‐diyl}] ( PehCDT‐TZ ), and poly[(4,4‐dioctyl‐4H‐cyclopenta[2,1‐b:3,4‐b′]dithiophene‐2,6‐diyl)‐alt‐{2,5‐di(thiophen‐2‐yl)thiazolo[5,4‐d]thiazole‐5,5′‐diyl}] ( PocCDT‐TZ ), for use in photovoltaic applications. The intramolecular charge‐transfer interaction between the electron‐sufficient CDT unit and electron‐deficient bithiazole (BT) or thiazolothiazole (TZ) units in the polymeric backbone induced a low bandgap and broad absorption that covered 300 nm to 700–800 nm. The optical bandgap was measured to be around 1.9 eV for PehCDT‐BT and PocCDT‐BT , and around 1.8 eV for PehCDT‐TZ and PocCDT‐TZ . Gel permeation chromatography showed that number‐average molecular weights ranged from 8000 to 14 000 g mol?1. Field‐effect mobility measurements showed hole mobility of 10?6–10?4 cm2 V?1 s?1 for the copolymers. The film morphology of the bulk heterojunction mixtures with [6,6]phenyl‐C61‐butyric acid methyl ester (PCBM) was also examined by atomic force microscopy before and after heat treatment. When the polymers were blended with PCBM, PehCDT‐TZ exhibited the best performance with an open circuit voltage of 0.69 V, short‐circuit current of 7.14 mA cm?2, and power conversion efficiency of 2.23 % under air mass (AM) 1.5 global (1.5 G) illumination conditions (100 mW cm?2). 相似文献
12.
Enhancement of the Photovoltaic Performance of CH3NH3PbI3 Perovskite Solar Cells through a Dichlorobenzene‐Functionalized Hole‐Transporting Material 下载免费PDF全文
Jin‐Wook Lee Sungmin Park Dr. Min Jae Ko Dr. Hae Jung Son Prof. Nam‐Gyu Park 《Chemphyschem》2014,15(12):2595-2603
A dichlorobenzene‐functionalized hole‐transporting material (HTM) is developed for a CH3NH3PbI3‐based perovskite solar cell. Notwithstanding the similarity of the frontier molecular orbital energy levels, optical properties, and hole mobility between the functionalized HTM [a polymer composed of 2′‐butyloctyl‐4,6‐dibromo‐3‐fluorothieno[3,4‐b]thiophene‐2‐carboxylate (TT‐BO), 3′,4′‐dichlorobenzyl‐4,6‐dibromo‐3‐fluorothieno[3,4‐b]thiophene‐2‐carboxylate (TT‐DCB), and 2,6‐bis(trimethyltin)‐4,8‐bis(2‐ethylhexyloxy)benzo[1,2‐b:4,5‐b′]dithiophene (BDT‐EH), denoted PTB‐DCB21] and the nonfunctionalized polymer [a polymer composed of thieno[3,4‐b]thiophene (TT) and benzo[1,2‐b:4,5‐b′]dithiophene (BDT), denoted PTB‐BO], a higher power conversion efficiency for PTB‐DCB21 (8.7 %) than that for PTB‐BO (7.4 %) is achieved because of a higher photocurrent and voltage. The high efficiency is even obtained without including additives, such as lithium bis(trifluoromethanesulfonyl)imide and/or 4‐tert‐butylpyridine, that are commonly used to improve the conductivity of the HTM. Transient photocurrent–voltage studies show that the PTB‐DCB21‐based device exhibits faster electron transport and slower charge recombination; this might be related to better interfacial contact through intermolecular chemical interactions between the perovskite and the 3,4‐dichlorobenzyl group in PTB‐DCB21. 相似文献
13.
Vellaiappillai Tamilavan Kyung Hwan Roh Rajalingam Agneeswari Dal Yong Lee Shinuk Cho Youngeup Jin Sung Heum Park Myung Ho Hyun 《Journal of polymer science. Part A, Polymer chemistry》2014,52(24):3564-3574
Pyrrolo[3,4‐c]pyrrole‐1,3(2H,5H)‐dione (DPPD)‐based large band gap polymers, P(BDT‐TDPPDT) and P(BDTT‐TDPPDT), are prepared by copolymerizing electron‐rich 4,8‐bis(2‐ethylhexyloxy)benzo[1,2‐b:4,5‐b′]dithiophene (BDT) or 4,8‐bis(5‐(2‐ethylhexyl)thiophen‐2‐yl)benzo[1,2‐b:4,5‐b′]dithiophene (BDTT) unit with novel electron deficient 2,5‐dioctyl‐4,6‐di(thiophen‐2‐yl)pyrrolo[3,4‐c]pyrrole‐1,3(2H,5H)‐dione (TDPPDT) unit. The absorption bands of polymers P(BDT‐TDPPDT) and P(BDTT‐TDPPDT) cover the region from 300 to 600 nm with an optical band gap of 2.11 eV and 2.04 eV, respectively. The electrochemical study illustrates that the highest occupied/lowest unoccupied molecular orbital energy levels of P(BDT‐TDPPDT) and P(BDTT‐TDPPDT) are ?5.39 eV/?3.28 eV and ?5.44 eV/?3.40 eV, respectively. The single layer polymer solar cell (PSC) fabricated with a device structure of ITO/PEDOT:PSS/P(BDT‐TDPPDT) or P(BDTT‐TDPPDT):PC70BM+DIO/Al offers a maximum power conversion efficiency (PCE) of 6.74% and 6.57%, respectively. The high photovoltaic parameters such as fill factor (~72%), open circuit voltage (Voc, ~0.90 V), incident photon to collected electron efficiency (~76%), and PCE obtained for the PSCs made from polymers P(BDT‐TDPPDT) and P(BDTT‐TDPPDT) make them as promising large band gap polymeric candidates for PSC application. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3564–3574 相似文献
14.
Chinna Bathula Sachin Badgujar Chang Eun Song In‐Nam Kang Shinuk Cho Jong‐Cheol Lee Won Suk Shin Sang‐Jin Moon Sang Kyu Lee 《Journal of polymer science. Part A, Polymer chemistry》2014,52(3):305-312
A “zigzag” naphthodithiophene‐based copolymer, poly[4,9‐bis(2‐ethylhexyloxy)naphtho[1,2‐b:5,6‐b′]dithiophene‐2,7‐diyl‐alt‐1,3‐(5‐heptadecan‐9‐yl)‐4H‐thieno[3,4‐c]pyrrole‐4,6‐dione] (P1) is synthesized and its properties are compared to “linear” naphthodithiophene‐based copolymer, poly[4,9‐bis(2‐ethylhexyloxy)naphtho[2,3‐b:6,7‐d′]dithiophene‐2,7‐diyl‐alt‐1,3‐(5‐heptadecan‐9‐yl)‐4H‐thieno[3,4‐c]pyrrole‐4,6‐dione] (P2). The field‐effect carrier mobilities and the optical, electrochemical, and photovoltaic properties of the copolymers are systematically investigated. The results suggest that the backbone of the copolymer structure significantly influences the band gap, electronic energy levels, carrier mobilities, and photovoltaic properties of the resultant thin films. In this work, the zigzag naphtho[1,2‐b:5,6‐b′]dithiophene‐based copolymer displays a good hole mobility and a high open‐circuit voltage; however, polymer solar cells in which the linear naphtho[2,3‐b;6,7‐d′]dithiophene‐based copolymer is used as the electron donor material perform better than the cells prepared using the zigzag naphtho[1,2‐b:5,6‐b′]dithiophene‐based copolymer. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 305–312 相似文献
15.
《Journal of polymer science. Part A, Polymer chemistry》2018,56(14):1528-1535
Two new random terpolymers containing 4,8‐bis(5‐(2‐ethylhexyl)thiophen‐2‐yl)benzo[1,2‐b:4,5‐b′]dithiophene (BDT) as a donating unit, methyl‐3‐thiophenecarboxylate (3MT) as a weak accepting unit, and the more electron‐deficient benzo[c][1,2,5]thiadiazole (BTz) or 5,5′‐bis(2‐ethylhexyl)‐4H,4′H‐1,1′‐bithieno[3,4‐c]pyrrole‐4,4′,6,6′(5H,5′H)‐tetraone (BiTPD) unit as a third monomer (respectively yielding 3MTB and 3MTT ) were synthesized in order to achieve improved physical and optoelectronic properties relative to the 3MT‐Th copolymer bearing only BDT and 3MT. The UV–vis absorption spectra and optical bandgap energies of these terpolymers were broader and smaller than those of the 3MT‐Th copolymer. In thin films, the terpolymers displayed the face‐on polymer chain orientation, indicating that the BTz or BiTPD unit in the terpolymer backbones did not affect the molecular arrangement on the substrate. In comparison with 3MT‐Th ‐based polymer solar cells (PSCs) as control devices, the PSCs employing blend films of these terpolymers as the donor and 2,2′‐[[6,6,12,12‐Tetrakis(4‐hexylphenyl)‐6,12‐dihydrodithieno[2,3‐d:2′,3′‐d′]‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene‐2,8‐diyl]bis[methylidyne(3‐oxo‐1H‐indene‐2,1(3H)‐diylidene)]]bis[propanedinitrile] (ITIC) as the acceptor exhibited higher power conversion efficiencies (>8.0%) for the same device configuration. In addition, the 3MTB‐ and 3MTT‐ based PSC devices displayed excellent shelf‐life even after aging for over 1000 h. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 1528–1535 相似文献
16.
Jinjun Shao Jingjing Chang Gaole Dai Chunyan Chi 《Journal of polymer science. Part A, Polymer chemistry》2014,52(17):2454-2464
A pyromellitic diimide building block, 2,6‐bis(2‐decyltetradecyl)?4,8‐di(thiophen‐2‐yl)pyrrolo[3,4‐f]isoindole‐1,3,5,7(2H,6H)‐tetraone ( 4 ), is synthesized. Based on this building block and other electron‐rich units such as 2,2′‐bithiophene, thieno[3,2‐b]thiophene and 4,8‐bis(dodecyloxy)benzo[1,2‐b:4,5‐b′]dithiophene, three conjugated polymers P1 , P2 , and P3 are prepared in good yield via Stille coupling polymerization. These new copolymers have good solubility in common organic solvents and exhibit good thermal stability. The optical, electrochemical, and thermal properties of these polymers P1–P3 are carefully investigated, and their applications in solution‐processed organic field‐effect transistors are also studied. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 2454–2464 相似文献
17.
Cyclometalated Pt complex based random terpolymers as electron acceptors for all polymer solar cells
《Journal of polymer science. Part A, Polymer chemistry》2018,56(1):105-115
Various molar ratios of platinum complexes were introduced into the conjugated backbone of the well‐studied poly[[N,N′‐bis(2‐octyldodecyl)‐naphthalene‐1,4,5,8‐bis(dicarboximide)‐2,6‐diyl]‐alt‐5,5′‐(2,2′‐bithiophene)](PNDIT2) acceptor polymer through random terpolymer approach. Terpolymers PNDIT2Ptx (x = 1, 2 and 5) exhibited slightly higher melting point (Tm), crystallization temperature, HOMO and LUMO energy levels than the control PNDIT2 copolymer due to the introduction of small amount of weaker electron‐withdrawing bulky rigid Pt complex instead of strong electron‐withdrawing flexible naphthalene diimide. When blended them with poly[[2,6′‐4,8‐di(5‐ethylhexylthienyl)benzo[1,2‐b;3,3‐b] dithiophene] [3‐fluoro‐2[(2‐ethylhexyl)carbonyl]thieno[3,4‐b]thiophenediyl]] (PTB7‐Th) in all polymer solar cells, enhanced power conversion efficiency of 4.51% (3.74%) was obtained in terpolymer PNDIT2Pt1 based device compared to 3.88% (3.24%) of the control PNDIT2 at the same inverted (conventional) device conditions. The enhancement was probably ascribed to higher hole and electron transport ability and more efficient charge separation. To the best of our knowledge, this is the first example of random terpolymer acceptors based on heavy metal complexes. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 105–115 相似文献
18.
Tailorable PC71BM Isomers: Using the Most Prevalent Electron Acceptor to Obtain High‐Performance Polymer Solar Cells
下载免费PDF全文
Xin‐Xing Zhan Xin Zhang Si‐Min Dai Shu‐Hui Li Xu‐Zhai Lu Dr. Lin‐Long Deng Prof. Su‐Yuan Xie Prof. Rong‐Bin Huang Prof. Lan‐Sun Zheng 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(52):18709-18713
Despite being widely used as electron acceptor in polymer solar cells, commercially available PC71BM (phenyl‐C71‐butyric acid methyl ester) usually has a “random” composition of mixed regioisomers or stereoisomers. Here PC71BM has been isolated into three typical isomers, α‐, β1‐ and β2‐PC71BM, to establish the isomer‐dependent photovoltaic performance on changing the ternary composition of α‐, β1‐ and β2‐PC71BM. Mixing the isomers in a ratio of α/β1/β2=8:1:1 resulted in the best power conversion efficiency (PCE) of 7.67 % for the polymer solar cells with PTB7:PC71BM as photoactive layer (PTB7=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]]). The three typical PC71BM isomers, even though sharing similar LUMO energy levels and light absorption, render starkly different photovoltaic performances with average‐performing PCE of 1.28–7.44 % due to diverse self‐aggregation of individual or mixed PC71BM isomers in the otherwise same polymer solar cells. 相似文献
19.
Prakash Sista Mahesh P. Bhatt Ashton R. Mccary Hien Nguyen Jing Hao Michael C. Biewer Mihaela C. Stefan 《Journal of polymer science. Part A, Polymer chemistry》2011,49(10):2292-2302
Poly{4,8‐bis(4‐decylphenylethynyl)benzo[1,2‐b:4,5‐b′]dithiophene} ( P1 ) homopolymer and poly{4,8‐bis(4‐decylphenylethynyl)benzo[1,2‐b:4,5‐b′]dithiophene ‐alt‐thiophene} ( P2 ) alternating copolymer have been synthesized by Stille coupling polymerization. The field‐effect mobilities of both polymers were measured on both untreated and silane‐treated OFET devices. Various silanes were selected to allow an incremental increase in the hydrophobicity of the silicon dioxide dielectric. A direct correlation was observed between the hydrophobicity of the silicon dioxide dielectric surface and the enhancement of the field‐effect mobilities. The highest mobilities for both polymers were measured on the OFET devices treated with heptadecafluoro‐1,1,2,2‐tetrahydro‐decyl‐1‐trimethoxysilane (FS) which generated the most hydrophobic surface. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
20.
Performance Enhancement of Bulk Heterojunction Solar Cells with Direct Growth of CdS‐Cluster‐Decorated Graphene Nanosheets 下载免费PDF全文
Kai Yuan Prof. Dr. Lie Chen Dr. Licheng Tan Prof. Dr. Yiwang Chen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(20):6010-6018
Two‐dimensional graphene–CdS (G–CdS) semiconductor hybrid nanosheets were synthesized in situ by graphene oxide (GO) quantum wells and a metal–xanthate precursor through a one‐step growth process. Incorporation of G–CdS nanosheets into a photoactive film consisting of poly[4,8‐bis‐(2‐ethyl‐hexyl‐thiophene‐5‐yl)‐benzo[1,2‐b:4,5‐b]dithiophene‐2,6‐diyl]‐alt‐[2‐(2‐ethyl‐hexanoyl)‐thieno[3,4‐b]thiophen‐4,6‐diyl] (PBDTTT‐C‐T) and [6,6]‐phenyl C70 butyric acid methyl ester (PC70BM) effectively decreases the exciton lifetime to accelerate exciton dissociation. More importantly, the decreasing energy levels of PBDTTT‐C‐T, PC70BM, and G–CdS produces versatile heterojunction interfaces of PBDTTT‐C‐T:PC70BM, PBDTTT‐C‐T:G–CdS, and PBDTTT‐C‐T:PC70BM:G–CdS; this offers multi‐charge‐transfer channels for more efficient charge separation and transfer. The charge transfer in the blend film also depends on the G–CdS nanosheet loadings. In addition, G–CdS nanosheets improve light utilization and charge mobility in the photoactive layer. As a result, by incorporation of G–CdS nanosheets into the active layer, the power‐conversion efficiency of inverted solar cells based on PBDTTT‐C‐T and PC71BM is improved from 6.0 % for a reference device without G–CdS nanosheets to 7.5 % for the device with 1.5wt % G–CdS nanosheets, due to the dramatically enhanced short‐circuit current. Combined with the advantageous mechanical properties of the PBDTTT‐C‐T:PC70BM:G–CdS active layer, the novel CdS‐cluster‐decorated graphene hybrid nanomaterials provide a promising approach to improve the device performance. 相似文献