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Efficient non-fullerene polymer solar cells enabled by side-chain conjugated thieno[3,4-c]pyrrole-4,6-dione-based polymer and small molecular acceptors

机译:通过侧链共轭噻吩并[3,4-c]吡咯-4,6-二酮基聚合物和小分子受体实现的高效非富勒烯聚合物太阳能电池

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The application of non-fullerene (NF) acceptors in bulk-heterojunction (BHJ) polymer solar cells (PSCs) is a promising approach to overcome the inherent drawbacks of fullerene derivatives-based acceptors. In PSCs, complementary absorption as well as matched molecular energy levels between the low bandgap acceptordonor-acceptor (A-D-A) small molecular acceptor and medium/wide bandgap polymer donor is crucial to achieve high power conversion efficiency (PCE). Alternating polymers based on benzodithiophene (BDT) electron-donating segment and thieno[3,4-dpyrrole-4,6-dione (TPD) electron-withdrawing segment own medium bandgap and low-lying highest occupied molecular orbital (HOMO) energy level, leading to presentable photovoltaic properties with fullerene derivatives. To probe into the performances of TPD-based polymers in NF-PSCs, two TPD-based polymers containing alkoxy or alkylthienyl modified benzo[1,2-b:4,5-131 dithiophene (BDT) were synthesized and adopted as electron-donors and blended with A-D-A-type electron-acceptor 2,2'-[[6,6,12,12-tetrakis(4- hexylphenyl)-s-indacenodithieno [3, 2-b] thiophene] methylidyne(3-oxo-1H-indene- 2,1(3H)-diylidene)]] bis(propanedinitrile) (ITIC) to fabricate the corresponding photovoltaic devices. The two-dimensional conjugated polymer PBDTT-TPD shows enhanced extinction coefficient, deeper HOMO energy level and better hole transport performance, resulting in improved PCE of 6.17%. To further boost the performances of the polymers, a small molecular acceptor 2,2'4(2Z,2'Z)-((4,4,9,9-tetrahexyl-4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene-2,7-diyl) bis(methanylylidene))bis(3-oxo-2,3-dihydro-IH-indene-2,1-diylidene))dimalononitrile (IDIC) with down-shifted energy level was also used to blend with the two polymers in PSCs. Despite the opencircuit voltage (V-OC) of the PBDTT-TPD:IDIC-based device is slightly decreased, the short-circuit current density (J(SC)) and fill factor (FF) are simultaneously improved, yielding an promising PCE of 7.15%. These results indicate that two-dimensional conjugated TPD-based polymers can be potential application as medium bandgap polymeric donor to match with small molecular acceptors having suitable molecular energy levels to get high efficiency in PSCs.
机译:非富勒烯(NF)受体在体异质结(BHJ)聚合物太阳能电池(PSC)中的应用是克服基于富勒烯衍生物的受体固有缺点的一种有前途的方法。在PSC中,低带隙受体供体-受体(A-D-A)小分子受体与中/宽带隙聚合物供体之间的互补吸收以及匹配的分子能级对于实现高功率转换效率(PCE)至关重要。基于苯并二噻吩(BDT)供电子链段和噻吩并[3,4-dpyrrole-4,6-dione(TPD)吸电子链段的交替聚合物具有中等带隙和低位的最高占据分子轨道(HOMO)能级,导致富勒烯衍生物具有合适的光伏性能。为了探讨基于TPD的聚合物在NF-PSC中的性能,合成了两种含烷氧基或烷基噻吩基改性的苯并[1,2-b:4,5-131二噻吩(BDT)的TPD聚合物,并将其用作电子给体并与ADA型电子受体2,2'-[[6,6,12,12-四(4-己基苯基)-s-吲哚并二噻吩并[3,2-b]噻吩]亚甲基(3-oxo-1H -茚-2,1(3H)-二亚甲基)]]双(丙腈)(ITIC)来制造相应的光电器件。二维共轭聚合物PBDTT-TPD显示出更高的消光系数,更深的HOMO能级和更好的空穴传输性能,从而使PCE改善了6.17%。为了进一步提高聚合物的性能,使用了小分子受体2,2'4(2Z,2'Z)-((4​​,4,9,9-四己基-4,9-二氢-s-indaceno [1, 2-b:5,6-b']二噻吩-2,7-二基)双(亚甲叉基))双(3-氧代-2,3-二氢-IH-茚-2,1-二亚叉基))二甲基腈(IDIC能量水平下移的)也用于与PSC中的两种聚合物共混。尽管基于PBDTT-TPD:IDIC的器件的开路电压(V-OC)有所降低,但短路电流密度(J(SC))和填充因子(FF)却同时得到了改善,产生了有希望的PCE 7.15%。这些结果表明,基于二维共轭TPD的聚合物可以作为中带隙聚合物供体,与具有合适分子能级的小分子受体相匹配,从而在PSC中获得高效率。

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