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Cofacial Versus Coplanar Arrangement in Centrosymmetric Packing Dimers of Dipolar Small Molecules: Structural Effects on the Crystallization Behaviors and Optoelectronic Characteristics

机译:偶极小分子中心对称堆积二聚体的界面对共面排列:对结晶行为和光电特性的结构影响

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Two D-pi-A-A molecules (MIDTP and TIDTP) composed of an electron-rich ditolylamino group (D) and an electron-deficient 5-dicyanovinylenylpyrimidine (A-A) fragment bridged together with indeno[1,2-b]thiophene (IDT) were synthesized. These molecules provide an opportunity to examine in-depth the impact of side-chain variations (methyl vs p-tolyl) on the crystallization behaviors, solid-state morphology, physical properties, and optoelectronic characteristics relevant for practical applications. X-ray analyses on single-crystal structures indicate that methyl-substituted MIDTP forms coplanar antiparallel dimers via C-H center dot center dot center dot S interactions and organizes into an ordered slip-staircase arrays. In contrast, p-tolyl-bearing TIDTP shows cofacial centrosymmetric dimers via pi-pi interactions and packs into a less-ordered layered structures. The X-ray diffraction analyses upon thermal treatment are consistent with a superior crystallinity of MIDTP, as compared to that of TIDTP. This difference indicates a greater propensity to organization by introduction of the smaller methyl group versus the bulkier p-tolyl group. The increased propensity for order by MIDTP facilitates the crystallization of MIDTP in both solution-processed and vacuum-deposited thin films. MIDTP forms solution-processed single-crystal arrays that deliver OFET hole mobility of 6.56 x 10(-4) cm(2) V-1 s(-1), whereas TIDTP only forms amorhpous films that gave lower hole mobility of 1.34 x 10(-5) cm(2) V-1 s(-1). MIDTP and TIDTP were utilized to serve as donors together with C-70 as acceptor in the fabrication of small-molecule organic solar cells (SMOSCs) with planar heterojunction (PHJ) or planar-mixed heterojunction (PMHJ) device architectures. OPV devices based on higher crystalline MIDTP delivered power conversion efficiencies (PCEs) of 2.5% and 4.3% for PHJ and PMHJ device, respectively, which are higher than those of TIDTP-based cells. The improved PCEs of MIDTP-based devices are attributed to better hole-transport character.
机译:两个D-pi-AA分子(MIDTP和TIDTP)由富电子的二甲苯基氨基基团(D)和缺电子的5-二氰基炔基嘧啶(AA)片段与茚并[1,2-b]噻吩(IDT)桥连而成被合成。这些分子为深入研究侧链变化(甲基对对甲苯基)对实际应用中相关的结晶行为,固态形态,物理性质和光电特性的影响提供了机会。对单晶结构的X射线分析表明,甲基取代的MIDTP通过C-H中心点中心点中心点S相互作用形成共面反平行二聚体,并组织成有序的阶梯状楼梯阵列。相反,带有对甲苯基的TIDTP通过pi-pi相互作用显示出界面中心对称的二聚体,并堆积成较少顺序的分层结构。与TIDTP相比,热处理后的X射线衍射分析与MIDTP的优异结晶度是一致的。这种差异表明与引入较小的对甲苯基相比,引入较小的甲基具有更大的组织倾向。 MIDTP的有序化倾向的增加促进了溶液处理和真空沉积薄膜中MIDTP的结晶。 MIDTP形成溶液处理的单晶阵列,其OFET空穴迁移率达到6.56 x 10(-4)cm(2)V-1 s(-1),而TIDTP仅形成非晶膜,其空穴迁移率较低,为1.34 x 10 (-5)厘米(2)V-1 s(-1)。在具有平面异质结(PHJ)或平面混合异质结(PMHJ)器件架构的小分子有机太阳能电池(SMOSC)的制造中,MIDTP和TIDTP与C-70一起用作受体。基于较高的晶体MIDTP的OPV器件,PHJ和PMHJ器件的功率转换效率(PCE)分别为2.5%和4.3%,高于基于TIDTP的电池的功率转换效率。基于MIDTP的设备的改进的PCE归因于更好的空穴传输特性。

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