首页> 外文期刊>Organic Electronics >Supramolecular donor-acceptor structures via orienting predeveloped fibrillar poly(3-hexylthiophene) crystals on bared/functionalized/grafted reduced graphene oxide with novel thiophenic constituents
【24h】

Supramolecular donor-acceptor structures via orienting predeveloped fibrillar poly(3-hexylthiophene) crystals on bared/functionalized/grafted reduced graphene oxide with novel thiophenic constituents

机译:通过将预先开发的原纤维状聚(3-己基噻吩)晶体定向在带有新型噻吩成分的裸露/官能化/接枝还原氧化石墨烯上的超分子供体-受体结构

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Reduced graphene oxide (rGO) and its derivatives functionalized with 2-thiophene acetic acid (rGO-f-TAA) and grafted with poly (3-dodecylthiophene) (rGO-g-P3DDT) and poly C3-thiophene ethanol) (rGO-g-PTEt) were prepared to design the donor-acceptor supramolecular structures based on the regioregular poly (3-hex-ylthiophene) (P3HT). The P3HT nanofibers, which were pre-grown in a separate system and possessed the n-stacked P3HT backbones in the length of fibrils, were perpendicular to the rGO surface in the solution and, consequently, they inclined onto the substrate during solvent evaporation. Through this inclination, the orientation of P3HT chains changed from face-on to edge-on. In rGO-f-TAA systems, for either short (80 nm) or long (420 nm) P3HT nanofibers, the P3HT nanofibers were attached from their sides onto the rGO. The appearance of (020) and (002) spots in selected area electron diffraction (SAED) patterns proved a fixed edge-on orientation even after solvent evaporation. Functionalization of rGO surface with 2-thiophene acetic acid altered the tethering tendency of P3HT chains from the thiophenic rings to the hexyl side chains. Via grafting the rGO with P3DDT and PTEt, the tethered P3HT nanofibers were perpendicularly fixed onto its surface with a face-on orientation having (002) and (100) spots even after solvent evaporation, resulting in the conductivity range of 9.9-10.9 S/cm. The pre-developed large single crystals were also employed to construct the donor-acceptor supramolecules with edge-on oriented P3HTs. Further tethering of P3HT fibrils onto the rGO based micron sheets reflected a red-shifting and more intensified A_(0-2), A_(0-1), and A_(0-0) peaks in the ultraviolet-visible spectra. A quenching in the photoluminescence spectra was observed in longer preparation time (18 h) based on the charge transferring from donor (P3HT) to acceptor (rGO derivatives).
机译:还原的氧化石墨烯(rGO)及其衍生物经2-噻吩乙酸(rGO-f-TAA)功能化并接枝有聚(3-十二烷基噻吩)(rGO-g-P3DDT)和聚C3-噻吩乙醇(rGO-g -PTEt)的设计是基于区域规则的聚(3-己基噻吩)(P3HT)设计供体-受体超分子结构。 P3HT纳米纤维在一个单独的系统中预先生长,并在原纤维长度上具有n个堆叠的P3HT主链,它们垂直于溶液中的rGO表面,因此,它们在溶剂蒸发过程中向基材倾斜。通过这种倾斜,P3HT链的方向从面朝边变为边沿。在rGO-f-TAA系统中,对于短(80 nm)或长(420 nm)的P3HT纳米纤维,P3HT纳米纤维从其侧面附着到rGO上。即使在溶剂蒸发后,在选定区域电子衍射(SAED)图案中出现的(020)和(002)点也被证明具有固定的边沿取向。用2-噻吩乙酸对rGO表面进行功能化改变了P3HT链的束缚趋势,从噻吩环到己基侧链。通过将rGO与P3DDT和PTEt接枝,即使在溶剂蒸发后,系留的P3HT纳米纤维也以面对面的方向垂直固定在其表面上,该表面具有(002)和(100)点,即使如此,其电导率范围仍为9.9-10.9 S /厘米。预开发的大型单晶也被用于构建具有边缘定向P3HTs的供体-受体超分子。 P3HT原纤维在基于rGO的微米片上的进一步束缚反映了红移,并且在紫外可见光谱中出现了更强的A_(0-2),A_(0-1)和A_(0-0)峰。基于电荷从供体(P3HT)转移至受体(rGO衍生物)的较长制备时间(18 h),观察到了光致发光光谱的猝灭。

著录项

  • 来源
    《Organic Electronics》 |2018年第1期|243-256|共14页
  • 作者单位

    Institute of Polymeric Materials and Faculty of Polymer Engineering, Sahand University of Technology, Tabriz, Iran;

    Chemical Engineering Department, Faculty of Engineering, Azarbaijan Shahid Madani University, Tabriz, Iran;

    Institute of Polymeric Materials and Faculty of Polymer Engineering, Sahand University of Technology, Tabriz, Iran;

    Department of Chemistry, Payame Noor University, Tehran, Iran;

    Department of Chemistry, Payame Noor University, Tehran, Iran;

    Chemical Engineering Department, Faculty of Engineering, Azarbaijan Shahid Madani University, Tabriz, Iran;

    Department of Chemistry, Payame Noor University, Tehran, Iran;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    rGO; Functionalization; Grafting; Supramolecule; Orientation;

    机译:rGO;功能化;嫁接;超分子;取向;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号