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1.
Dithieno[2,3‐d:2',3'‐d']benzo[1,2‐b:4,5‐b']dithiophene (DTBDAT)‐based copolymers for high‐performance organic solar cells 下载免费PDF全文
Yung Jin Yoon Yun‐Ji Lee Soon‐Ki Kwon Jin Young Kim Yun‐Hi Kim 《Journal of polymer science. Part A, Polymer chemistry》2016,54(19):3182-3192
P(BDT‐TCNT) and P(DTBDAT‐TCNT) , which has an extended conjugation length, were designed and synthesized for applications in organic solar cell (OSCs). The solution absorption maxima of P(DTBDAT‐TCNT) with the extended conjugation were red‐shifted by 5–15 nm compared with those of P(BDT‐TCNT) . The optical band gaps and highest occupied molecular orbital (HOMO) energy levels of both P(BDT‐TCNT) and P(DTBDAT‐TCNT) were similar. The structure properties of thin films of these materials were characterized using grazing‐incidence wide‐angle X‐ray scattering and tapping‐mode atomic force microscopy, and charge carrier mobilities were characterized using the space‐charge limited current method. OSCs were formed using [6,6]‐phenyl‐C71‐butyric acid methyl ester (PC71BM) as the electron acceptor and 3% diphenylether as additive suppress aggregation. OSCs with P(BDT‐TCNT) as the electron donor exhibited a power conversion efficiency (PCE) of 4.10% with a short‐circuit current density of JSC = 9.06 mA/cm2, an open‐circuit voltage of VOC = 0.77 V, and a fill factor of FF = 0.58. OSCs formed using P(DTBDAT‐TCNT) as the electron donor layer exhibited a PCE of 5.83% with JSC = 12.2 mA/cm2, VOC = 0.77 V, and FF = 0.62. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3182–3192 相似文献
2.
Yue Wang Chunyu Xu Chong Wang Yutong Yan Qianqian Sun Xiaoling Ma Fujun Zhang 《Journal of polymer science. Part A, Polymer chemistry》2022,60(6):968-974
Recombining the advantages on photovoltaic parameters of two binary-organic photovoltaics (OPVs) into one ternary cell is an efficient strategy for selecting materials, in addition to the absorption spectra complementary among the used materials. The binary-OPVs with J71:BTP-4F-12 exhibit a power conversion efficiency (PCE) of 11.70%, along with a short-circuit-current-density (JSC) of 23.61 mA cm−2, an open-circuit-voltage (VOC) of 0.841 V and a fill factor (FF) of 58.99%. Although the relatively low PCE of 10.92% and JSC of 16.59 mA cm−2 are achieved in J71:ITIC-based binary-OPVs, the VOC of 0.935 V and FF of 70.40% are impressive compared with J71:BTP-4F-12-based OPVs. Optimal ternary-OPVs are achieved with J71:BTP-4F-12:ITIC as active layers by weight ratio of 1:0.48:0.72, delivering a markedly increased PCE of 13.05% with a VOC of 0.903 V, a JSC of 21.27 mA cm−2 and a FF of 68.20%. An over 11.5% PCE improvement is obtained by recombining the advantages of binary-OPVs into ternary-OPVs with ITIC as photon harvesting reinforcing agent and morphology regulator. The good compatibility between BTP-4F-12 and ITIC provides large room to well optimize their relative content for achieving the well balanced three key photovoltaic parameters of ternary-OPVs. 相似文献
3.
Highly Efficient Dye‐Sensitized Solar Cells Based on Panchromatic Ruthenium Sensitizers with Quinolinylbipyridine Anchors 下载免费PDF全文
Hsiu‐Hsuan Yeh Hsin‐Pei Wu Yun Chi John N. Clifford Emilio Palomares Shih‐Hung Liu Pi‐Tai Chou Gene‐Hsiang Lee 《Angewandte Chemie (International ed. in English)》2014,53(1):178-183
Panchromatic RuII sensitizers TF‐30–TF‐33 bearing a new class of 6‐quinolin‐8‐yl‐2,2′‐bipyridine anchor were synthesized and tested under AM1.5 G simulated solar irradiation. Their increased π conjugation relative to that of the traditional 2,2′:6′,2′′‐terpyridine‐based anchor led to a remarkable improvement in absorptivity across the whole UV–Vis–NIR spectral regime. Furthermore, the introduction of a bulky tert‐butyl substituent on the quinolinyl fragment not only led to an increase in the JSC value owing to the suppression of dye aggregation, but remarkably also resulted in no loss in VOC in comparison with the reference sensitizer containing a tricarboxyterpyridine anchor. The champion sensitizer in DSC devices was found to be TF‐32 with a performance of JSC=19.2 mA cm?2, VOC=740 mV, FF=0.72, and η=10.19 %. This 6‐quinolin‐8‐yl‐2,2′‐bipyridine anchor thus serves as a prototype for the next generation of RuII sensitizers with any tridentate ancillary. 相似文献
4.
A Photoelectrochemical Solar Cell Consisting of a Cadmium Sulfide Photoanode and a Ruthenium–2,2′‐Bipyridine Redox Shuttle in a Non‐aqueous Electrolyte 下载免费PDF全文
Yosuke Kageshima Hiromu Kumagai Tsutomu Minegishi Prof. Jun Kubota Prof. Kazunari Domen 《Angewandte Chemie (International ed. in English)》2015,54(27):7877-7881
A photoelectrochemical (PEC) cell consisting of an n‐type CdS single‐crystal electrode and a Pt counter electrode with the ruthenium–2,2′‐bipyridine complex [Ru(bpy)3]2+/3+ as the redox shuttle in a non‐aqueous electrolyte was studied to obtain a higher open‐circuit voltage (VOC) than the onset voltage for water splitting. A VOC of 1.48 V and a short‐circuit current (ISC) of 3.88 mA cm?2 were obtained under irradiation by a 300 W Xe lamp with 420–800 nm visible light. This relatively high voltage was presumably due to the difference between the Fermi level of photo‐irradiated n‐type CdS and the redox potential of the Ru complex at the Pt electrode. The smooth redox reaction of the Ru complex with one‐electron transfer was thought to have contributed to the high VOC and ISC. The obtained VOC was more than the onset voltage of water electrolysis for hydrogen and oxygen generation, suggesting prospects for application in water electrolysis. 相似文献
5.
Ram B. Ambre Gao‐Fong Chang Manoj R. Zanwar Prof. Ching‐Fa Yao Prof. Eric Wei‐Guang Diau Dr. Chen‐Hsiung Hung 《化学:亚洲杂志》2013,8(9):2144-2153
A series of porphyrin sensitizers that featured two electron‐donating groups and dual anchoring groups that were connected through a porphine π‐bridging unit have been synthesized and successfully applied in dye‐sensitized solar cells (DSSCs). The presence of electron‐donating groups had a significant influence on their spectroscopic, electrochemical, and photovoltaic properties. Overall, the dual anchoring groups gave tunable electronic properties and stronger attachment to TiO2. These new dyes were readily synthesized in a minimum number of steps in gram‐scale quantities. Optical and electrochemical data confirmed the advantages of these dyes for use as sensitizers in DSSCs. Porphyrins with electron‐donating amino moieties provided improved charge separation and better charge‐injection efficiencies for the studied dual‐push–pull dyes. Attenuated total reflectance–Fourier‐transform infrared (ATR‐FTIR) and X‐ray photoelectron spectroscopy of the porphyrin dyes on TiO2 suggest that both p‐carboxyphenyl groups are attached onto TiO2, thereby resulting in strong attachment. Among these dyes, cis-Zn2BC2A , with two electron‐donating 3,6‐ditertbutyl‐phenyl‐carbazole groups and dual‐anchoring p‐carboxyphenyl groups, showed the highest efficiency of 4.07 %, with JSC=9.81 mA cm?2, VOC=0.63 V, and FF=66 %. Our results also indicated a better photostability of the studied dual‐anchored sensitizers compared to their mono‐anchored analogues under identical conditions. These results provide insight into the developments of a new generation of high‐efficiency and thermally stable porphyrin sensitizers. 相似文献
6.
Suhee Song Sung Heum Park Youngeup Jin Jina Park Joo Young Shim Il Kim Heesoo Lee Kwanghee Lee Hongsuk Suh 《Journal of polymer science. Part A, Polymer chemistry》2010,48(20):4567-4573
A series of new semiconducting polymers based on 4,4‐dihexyl‐4H‐cyclopenta[2,1‐b:3,4‐b′]dithiophene, 2,2‐dihexyl‐2H‐benzimidazole, and thiophene units was synthesized. The polymers show good solubility at room temperature in organic solvents owing to long alkyl chain in new acceptor, 2,2‐dihexyl‐2H‐benzimidazole. The advantage of dihexyl‐2H‐benzimidazole compared to the benzothiadiazole is to improve the solubility of the polymer. It was found that these polymers can finely be tuned for photovoltaic application by adjusting the contents ratio of the dihexyl‐2H‐benzimidazole unit. The spectra of the solid films show absorption bands with maximum peaks in the range of 421–577 nm and the absorption onsets at 588–683 nm, corresponding to band gaps of 2.11–1.82 eV. The devices with PCPDTDTHBI‐1 :PC71BM showed an open‐circuit voltage (VOC) of 0.46 V, a short‐circuit current density (JSC) of 3.83 mA/cm2, and a fill factor of 0.36, giving a power conversion efficiency of 0.64%. Decrease of the dihexyl‐2H‐benzimidazole contents in the polymers induced red‐shift of the UV absorptions, and increased VOC and JSC values, to improve the efficiency of organic photovoltaics. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
7.
First‐Generation Subporphyrinatoboron(III) Sensitizers Surpass the 10 % Power Conversion Efficiency Threshold 下载免费PDF全文
Dr. Graeme Copley Daesub Hwang Prof. Dr. Dongho Kim Prof. Dr. Atsuhiro Osuka 《Angewandte Chemie (International ed. in English)》2016,55(35):10287-10291
Subporphyrinatoboron(III) (SubB) sensitizers were synthesized for use in dye‐sensitized solar cells (DSSCs). The prototype, which comprises a sterically demanding 3,5‐di‐tert‐butylphenyl scaffold, a meso‐ethynylphenyl spacer, and a cyanoacrylic acid anchoring group, achieved an open‐circuit voltage VOC of 836 mV, short‐circuit current density JSC of 15.3 mA cm?2, fill factor of 0.786, and a photon‐to‐current conversion efficiency of 10.1 %. Such astonishing figures suggest that a bright future lies ahead for SubB in the realm of DSSCs. 相似文献
8.
Pedro Atienzar Dr. Maite Navarro Dr. Avelino Corma Prof. Dr. Hermenegildo Garcia Prof. Dr. 《Chemphyschem》2009,10(1):252-256
Ti/MCM‐41 is a well‐known heterogeneous catalyst for alkene epoxidation with organic peroxides. This titanosilicate contains isolated titanium atoms forming part of a framework of mesoporous silica whose structure is formed by parallel hexagonal channels 3.2 nm in diameter. The surface area and porosity of Ti/MCM‐41 are about 880 m2 g?1 and 0.70 cm3 g?1, respectively. These values are among the highest for any material. Herein, we show that Ti/MCM‐41 exhibits photovoltaic activity. Dye‐sensitized solar cells using mesoporous Ti/MCM‐41 (2.8–5.7 % Ti content) as active layer, black dye N3 as photosensitizer and I3?/I? in methoxyacetonitrile as electrolyte exhibit a VOC, JSC and FF of 0.44 V, 0.045 mA cm?2 and 0.33, respectively. These values compare well against 0.75 V, 4.1 mA cm?2 and 0.64, respectively, measured for analogous solar cells using conventional P‐25 TiO2. However, the specific current density (JSC/Ti atom) for the Ti/MCM‐41 is very similar to that of P25 TiO2. 相似文献
9.
Yuan Liu Qian Xiu Lifen Xiao Hui Huang Lihui Guo Lirong Zhang Hailiang Zhang Songting Tan Chaofan Zhong 《先进技术聚合物》2011,22(12):2583-2591
Two novel side chain polymeric metal complexes (PFT‐Cd and PFT‐Zn) have been designed, synthesized, and characterized. These polymers were found to be good thermally stable and high glass transitions temperature, which indicate that these polymers could be applied as photovoltaic materials for dye‐sensitized solar cells (DSSCs). The obtained polymers exhibited good photovoltaic property. The DSSCs based on the PFT‐Cd and PFT‐Zn exhibited a maximum solar‐to‐electricity conversion efficiency (η) up to 3.37% (Jsc = 7.27 mA/cm2, Voc = 0.67 V, and FF = 0.69) and 3.01% (Voc = 0.72 V, Jsc = 6.10 mA/cm2, FF = 0.69) under simulated AM 1.5 G solar irradiation (90–95 mW/cm2). The result shows that these novel materials are suitable for the dye‐sensitized solar cells. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
10.
Benjamin Schulze Douglas G. Brown Dr. Kiyoshi C. D. Robson Christian Friebe Dr. Michael Jäger Dr. Eckhard Birckner Prof. Dr. Curtis P. Berlinguette Prof. Dr. Ulrich S. Schubert 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(42):14171-14180
A series of heteroleptic bis(tridentate) RuII complexes featuring N^C^N‐cyclometalating ligands is presented. The 1,2,3‐triazole‐containing tridentate ligands are readily functionalized with hydrophobic side chains by means of click chemistry and the corresponding cyclometalated RuII complexes are easily synthesized. The performance of these thiocyanate‐free complexes in a dye‐sensitized solar cell was tested and a power conversion efficiency (PCE) of up to 4.0 % (Jsc=8.1 mA cm?2, Voc=0.66 V, FF=0.70) was achieved, while the black dye ((NBu4)3[Ru(Htctpy)(NCS)3]; Htctpy=2,2′:6′,2′′‐terpyridine‐4′‐carboxylic acid‐4,4′′‐dicarboxylate) showed 5.2 % (Jsc=10.7 mA cm?2, Voc=0.69 V, FF=0.69) under comparable conditions. When co‐adsorbed with chenodeoxycholic acid, the PCE of the best cyclometalated dye could be improved to 4.5 % (Jsc=9.4 mA cm?2, Voc=0.65 V, FF=0.70). The PCEs correlate well with the light‐harvesting capabilities of the dyes, while a comparable incident photon‐to‐current efficiency was achieved with the cyclometalated dye and the black dye. Regeneration appeared to be efficient in the parent dye, despite the high energy of the highest occupied molecular orbital. The device performance was investigated in more detail by electrochemical impedance spectroscopy. Ultimately, a promising RuII sensitizer platform is presented that features a highly functionalizable “click”‐derived cyclometalating ligand. 相似文献
11.
Dr. Hai‐Feng Xiang Dr. Stephen Sin‐Yin Chui Prof. V. A. L. Roy Prof. Chi‐Ming Che 《化学:亚洲杂志》2011,6(12):3223-3229
Organic photovoltaic (OPV) cells using metal(II) (Pt, Pd, Cu, and Ni) chelates of 8‐hydroxyquinoline (Hq) or 5,7‐dimethyl‐8‐hydroxy‐quinoline (HMe2q) as an electron donor were fabricated by vacuum deposition. The bis(5,7‐dimethyl‐8‐hydroxyquinolinato)platinum(II) [Pt(Me2q)2]‐based OPVs showed the best performance with an open voltage (VOC) of 0.42 V, a short circuit current density (JSC) of 14.8 mA cm?2, and a maximum power conversion efficiency (ηP) of 2.4 %. The X‐ray single‐crystal structures together with the grazing incidence X‐ray diffraction (GIXRD) data of thin film samples reveal that the peripheral methyl substituent(s) and platinum(II) ion are essential for the high degree of film crystallinity resulting in improved performance of the as‐fabricated field‐effect transistors (FETs) and OPV cells. 相似文献
12.
In Taek Choi Dr. Myung Jong Ju Sang Hyun Song Sang Gyun Kim Dr. Dae Won Cho Prof. Dr. Chan Im Prof. Dr. Hwan Kyu Kim 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(46):15545-15555
The Y‐shaped, low molecular mass, hole‐conductor (HC), acidic coadsorbents 4‐{3,7‐bis[4‐(2‐ethylhexyloxy)phenyl]‐10H‐phenothiazin‐10‐yl}benzoic acid ( PTZ1 ) and 4‐{3,7‐bis[4‐(2‐ethylhexyloxy)phenyl]‐10H‐phenothiazin‐10‐yl}biphenyl‐4‐carboxylic acid ( PTZ2 ) were developed. Owing to their tuned and negative‐shifted HOMO levels (vs. NHE), they were used as HC coadsorbents in dye‐sensitized solar cells (DSSCs) to improve cell performance through desired cascade‐type hole‐transfer processes. Their detailed functions as HC coadsorbents in DSSCs were investigated to obtain evidence for the desired cascade‐type hole‐transfer processes. They have multiple functions, such as preventing π–π stacking of dye molecules, harvesting light of shorter wavelengths, and faster dye regeneration. By using PTZ2 as the tailor‐made HC coadsorbent on the TiO2 surface with the organic dye NKX2677, an extremely high conversion efficiency of 8.95 % was achieved under 100 mW cm?2 AM 1.5G simulated light (short‐circuit current JSC=16.56 mA cm?2, open‐circuit voltage VOC=740 mV, and fill factor of 73 %). Moreover, JSC was increased by 13 %, VOC by 27 % and power‐conversion efficiency by 49 % in comparison to an NKX2677‐based DSSC without an HC coadsorbent. This is due to the HC coadsorbent having a HOMO energy level well matched to that of the NKX‐2677 dye to induce the desired cascade‐type hole‐transfer processes, which are associated with a slower charge recombination, fast dye regeneration, effective screening of liquid electrolytes, and an induced negative shift of the quasi‐Fermi level of the electrode. Thus, this new class of Y‐shaped, low molecular weight, organic, HC coadsorbents based on phenothiazine carboxylic acid derivatives hold promise for highly efficient organic DSSCs. 相似文献
13.
Chi‐Wei Tu Ken‐Yen Liu An‐Ting Chien Ming‐Huei Yen Ting Hsiang Weng Kuo‐Chuan Ho King‐Fu Lin 《Journal of polymer science. Part A, Polymer chemistry》2008,46(1):47-53
Poly(n‐isopropylacrylamide) (PNIPAAm) and its nanocomposite with exfoliated montmorillonite (MMT) were prepared by soap‐free emulsion polymerization and individually applied to gel the electrolyte systems for the dye‐sensitized solar cells (DSSCs). Each exfoliated MMT nanoplatelet had a thickness of ~ 1 nm, carried ~ 1.8 cation/nm2, and acted like a two‐dimensional electrolyte. The DSSC with the LiI/I2/tertiary butylpyridine electrolyte system gelled by this polymer nanocomposite had higher short‐circuit current density (Jsc) compared to that gelled by the neat PNIPAAm. The former has a Jsc of 12.6 mA/cm2, an open circuit voltage (Voc) of 0.73 V, and a fill factor (FF) of 0.59, which harvested 5.4% electricity conversion efficiency (η) under AM 1.5 irradiation at 100 mW/cm2, whereas the latter has Jsc = 7.28 mA/cm2, Voc = 0.72 V, FF = 0.60, and η = 3.17%. IPCE of the nanocomposite‐gelled DSSC were also improved. Electrochemical impedance spectroscopy of the DSSCs revealed that the nanocomposite‐gelled electrolytes significantly decreased the impedances in three major electric current paths of DSSCs, that is, the resistance of electrolytes and electric contacts, impedance across the electrolytes/dye‐coated TiO2 interface, and Nernstian diffusion within the electrolytes. The results were also consistent with the increased molar conductivity of nanocomposite‐gelled electrolytes. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 47–53, 2008 相似文献
14.
Lirong Zhang Minh‐Ngoc Ha Guanghui Sun Yuehui Fan Guanlin Zhang Yuhong Wang Guanzhong Lu 《中国化学会会志》2013,60(11):1371-1379
In this work, high‐performance dye‐sensitized solar cells (DSSCs) based on new low‐cost visible nickel complex dye (VisDye), TiO2 nanoparticle/nanotube composites electrodes, carbon nanoparticles counter electrodes, and ionic liquids electrolytes have been fabricated. The electronic structure, optical spectroscopy, and electrochemical properties of the VisDye were studied. Experimental results indicate that it is beneficial to improve the electron transport and power conversion efficiency using the nickel complex VisDye and TiO2 nanoparticle/nanotube composites. Under optimized conditions, the solar energy conversion efficiencies were measured. The short‐circuit current density (JSC), the open‐circuit voltage (VOC), the fill factor (FF), and the overall efficiency (η) of the DSSCs are 10.01 mA/cm2, 516 mV, 0.68, and 3.52%, respectively. This study demonstrates that the combination of new VisDye with TiO2 nanoparticle/nanotube composites electrodes and carbon nanoparticles counter electrodes provide a way to fabricate highly efficient dye‐sensitized solar cells in low‐cost production. 相似文献
15.
Min Ju Cho Jangwon Seo Kyung Hwan Kim Dong Hoon Choi Paras N. Prasad 《Macromolecular rapid communications》2012,33(2):146-151
A new donor‐acceptor copolymer, containing benzodithiophene (BDT) and methyl thiophene‐3‐carboxylate (3MT) units, is designed and synthesized for polymer solar cells (PSCs). The 3MT unit is used as an electron acceptor unit in this copolymer to provide a lower highest occupied molecular orbital (HOMO) level for obtaining polymer solar cells with a higher open‐circuit voltage (VOC). The resulting bulk heterojunction PSC made of the copolymer and [6,6]‐phenyl‐C71‐butyric acid methyl ester (PC71BM) exhibits a power conversion efficiency (PCE) up to 4.52%, a short circuit current (JSC) of 10.5 mA·cm‐2, and a VOC of 0.86 V. 相似文献
16.
Manxi Zhou Min Wang Lei Zhu Zhenqing Yang Chao Jiang Dapeng Cao Qifang Li 《Macromolecular rapid communications》2015,36(24):2156-2161
The theoretical calculations are used to find that D–π–A–π–A style conjugated polymer PC‐TBTBT is more efficient for solar cells application than the D–π–A analog PC‐TBT because the D–π–A–π–A structure has a narrower band gap and higher molar absorption coefficient and redshift spectrum. Motivated by the theoretical prediction, 5,6‐bis(octyloxy)‐2,1,3‐benzothiadiazole and 2,7‐carbazole are adopted to synthesize the D–π–A–π–A style PC‐TBTBT (Mw = 31.1 kDa) and D–π–A analog PC‐TBT (Mw = 87.5 kDa) by Suzuki coupling reaction. Experimental results confirm that D–π–A–π–A PC‐TBTBT ‐based solar cell shows a power conversion efficiency (PCE) of 4.74% with high VOC of 0.99 V and enhanced JSC of 9.70 mA cm−2. The PCE and JSC achieve improvements of 17% and 26%, respectively, compared to the D–π–A PC‐TBT ‐based solar cell.
17.
Lifen Xiao Yuan Liu Qian Xiu Lirong Zhang Lihui Guo Hailiang Zhang Chaofan Zhong 《Journal of polymer science. Part A, Polymer chemistry》2010,48(9):1943-1951
Two novel main chain polymeric metal complexes containing 8‐hydroxyquinoline europium complexes and phenylethyl or fluorene units: 1,4‐Dioctyloxy‐2,5‐bis[2‐(8‐hydroxyquinoline)‐vinyl]‐benzene Eu(III) (3) and 2,7‐bis[2‐(8‐hydroxyquinoline)‐vinyl]‐9,9′‐diocthylfluorene Eu(III) (4) with donor–acceptor‐π‐conjugated structure (D‐π‐A) have been synthesized and investigated as dye sensitizers for dye‐sensitized solar cells dyes (DSSCs). They have been determined and studied by FT‐IR, TGA, DSC, GPC, Elemental analysis, UV–vis absorption spectroscopy, photoluminescence spectroscopy, cyclic voltammetry, and application in dye‐sensitized solar cells (DSSCs) as dye sensitizers. On the basis of optimized dye and molecular structure, they have shown solar‐to‐electricity conversion efficiency 2.25% for 3 (Jsc = 4.77 mA cm?2, Voc = 630 mV, FF = 0.75) and 3.04% for 4 (Jsc = 6.33 mA cm?2, Voc = 640 mV, FF = 0.75), under the illumination of AM1.5G, 100 mW/cm2. The IPCE of 3 and 4 are 30% and 46% at 400 nm, respectively. Besides, they showed good stabilities with thermal decomposition temperatures at 280 °C and 225 °C, respectively, which are suitable for DSSCs. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1943–1951, 2010 相似文献
18.
Mingjian Yuan Andrew H. Rice Christine K. Luscombe 《Journal of polymer science. Part A, Polymer chemistry》2011,49(3):701-711
The synthesis of four alternating copolymers using benzo[2,1‐b;3,4‐b′]dithiophene (BDP) as the common donor unit is presented. Before the synthesis, theoretical calculations that we performed predicted that the incorporation of BDP, which consists of fused dithiophene units with a benzene ring, into these polymers would produce a low‐lying highest occupied molecular orbital (HOMO) energy level. Low‐lying HOMO levels are desirable to produce high open circuit voltages (VOC) in organic bulk heterojunction (BHJ) photovoltaic devices. The polymers' structural characterization, as well as the preliminary results of their performance in BHJ devices, using (6,6)‐phenyl C61‐butyric acid methyl ester as the electron acceptor, is presented. The VOC values follow the expected trend: increasing with decreasing HOMO level of the polymer. High VOC values of 0.81 and 0.82 V have been obtained from two polymers: PBDPBT and PBDPDPP. The initial power conversion efficiency achieved in these unoptimized devices was 1.11% because of relatively low JSC values. The variation observed in the JSC values between the four polymers is discussed. Device performance is expected to increase with optimization of processing conditions for the devices. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
19.
Sang Kyu Lee Nam Sung Cho Shinuk Cho Sang‐Jin Moon Jae Kwan Lee Guillermo C. Bazan 《Journal of polymer science. Part A, Polymer chemistry》2009,47(24):6873-6882
Novel series of conjugated copolymers, incorporating cyclopentadithiophene (CPDT) and the biselenophene ( R‐CPDT‐Se2 ), were synthesized by Pd‐catalyzed Stille coupling polymerization. The optical, electrochemical, field‐effect carrier mobilities, and photovoltaic properties of the R‐CPDT‐Se2 were investigated and compared with cyclopentadithiophene (CPDT) and the bithiophene ( EHex‐CPDT‐T2 ). The highest hole mobility of thin film transistor devices fabricated with new p‐type polymer semiconductors, Oct‐CPDT‐Se2 , was 1.3 × 10?3 cm2/Vs with an on/off ratio of about 105. The maximum power conversion efficiency of polymer solar cell fabricated with the blend of EHex‐CPDT‐Se2 /C71‐PCBM reached 1.86% with an open circuit voltage (VOC) of 0.55 V, a short circuit current density (Jsc) of 7.27 mA/cm2, and a fill factor (FF) of 0.47 under AM 1.5G irradiation (100 mW/cm2). © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2009 相似文献
20.
Xue Gong Cuihong Li Zhen Lu Guangwu Li Qiang Mei Tao Fang Zhishan Bo 《Macromolecular rapid communications》2013,34(14):1163-1168
The synthesis, characterization, and photophysical and photovoltaic properties of two anthracene‐containing wide‐band‐gap donor and acceptor (D–A) alternating conjugated polymers ( P1 and P2 ) are described. These two polymers absorb in the range of 300–600 nm with a band gap of about 2.12 eV. Polymer solar cells with P1 :PC71BM as the active layer demonstrate a power conversion efficiency (PCE) of 2.23% with a high Voc of 0.96 V, a Jsc of 4.4 mA cm−2, and a comparable fill factor (FF) of 0.53 under simulated solar illumination of AM 1.5 G (100 mW cm−2). In addition, P2 :PC71BM blend‐based solar cells exhibit a PCE of 1.42% with a comparable Voc of 0.89 V, a Jsc of 3.0 mA cm−2, and an FF of 0.53.