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Organic-inorganic hybrid solar cells via electropolymerization.

机译:通过电聚合的有机-无机混合太阳能电池。

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摘要

Integrating polymers with inorganic nanostructures is difficult due to wetting and surface energy considerations. We developed an electropolymerization method to grow conformal polymers on high aspect ratio nanostructures. Our method is shown to improve the polymer filling rate inside the nanostructures and can be used in the development of efficient hybrid solar cells. As an example, we have studied the hybrid system of electropolymerized polythiophene (e-PT) on a variety of conductive (Au and ITO) and semiconductive substrates (Si, Ge, ZnO). In particular, e-PT/ZnO hybrid structure can be further developed into organic photovoltaics (OPV). Although unsubstituted PT is not the ideal polymer material for high efficiency solar cells, it is an excellent choice for studying basic bonding and morphology in hybrid structures. We find that e-PT is covalently bound to the polar ZnO planar substrate via a Zn-S bond, adopting an upright geometry. By contrast, no strong covalent bonding was observed between e-PT and ZnO nanorods that consist of non-polar ZnO surfaces predominantly.;Energy level alignment at interfaces is critical for fundamental understanding and optimization of OPV as band offsets of the donor and acceptor materials largely determine the open circuit voltage (Voc) of the device. Using ultraviolet photoemission spectroscopy (UPS) and inverse photoemission spectroscopy (IPS), we examined the correlation between energy alignment and photovoltaic properties of a model hybrid solar cell structure incorporating undoped electrodeposited polythiophene (e-PT) films on ZnO planar substrates. The electrolyte anion (BF4-, PF6 -, ClO4- or CF3SO3 -) used in the electrodeposition solution was found to exert a strong influence on the neutral e-PT film morphology and adhesion, the band alignment at the interface, and ultimately the photovoltaic behavior. The interfacial dipole lowers polythiophene energy levels, increasing the theoretical and actual Voc in polythiophene/ZnO photovoltaics.;Our electropolymerization approach to integrate the organic and inorganic phases aims at understanding the chemistry at the interface, and the electronic and morphological properties of the system. This work should be generally applicable to other conjugated polymers and nanostructures, and it contributes to an understanding of organic-inorganic interfaces and electronic structures that may be advantageous to a range of electronic/photonic applications.
机译:由于湿润和表面能的考虑,将具有无机纳米结构的聚合物整合是困难的。我们开发了一种电聚合方法,可以在高长径比的纳米结构上生长保形聚合物。我们的方法显示可以提高纳米结构内部的聚合物填充率,可用于开发高效的混合太阳能电池。例如,我们研究了在各种导电(Au和ITO)和半导电衬底(Si,Ge,ZnO)上电聚合聚噻吩(e-PT)的混合系统。特别地,e-PT / ZnO杂化结构可以进一步发展为有机光伏(OPV)。尽管未取代的PT并不是高效太阳能电池的理想聚合物材料,但它是研究混合结构中基本键合和形态的绝佳选择。我们发现e-PT通过Zn-S键共价键合到极性ZnO平面基板,采用直立的几何形状。相比之下,在e-PT和主要由非极性ZnO表面组成的ZnO纳米棒之间未观察到牢固的共价键。;界面上的能级对齐对于供体和受体材料的能带偏移对OPV的基本理解和优化至关重要。在很大程度上决定了设备的开路电压(Voc)。使用紫外光发射光谱法(UPS)和逆向光发射光谱法(IPS),我们检查了在ZnO平面基板上结合了未掺杂电沉积聚噻吩(e-PT)膜的模型混合太阳能电池结构的能量对准与光伏性能之间的相关性。发现电沉积溶液中使用的电解质阴离子(BF4-,PF6-,ClO4-或CF3SO3-)对中性e-PT膜的形貌和附着力,界面处的能带排列以及最终的光伏产生强烈影响行为。界面偶极子降低了聚噻吩的能级,增加了聚噻吩/ ZnO光伏中的理论和实际Voc 。;我们将有机相和无机相结合的电聚合方法旨在了解界面的化学性质以及系统的电子和形态特性。这项工作通常应适用于其他共轭聚合物和纳米结构,并且有助于理解有机-无机界面和电子结构,这可能对一系列电子/光子应用有利。

著录项

  • 作者

    Feng, Wenchun.;

  • 作者单位

    Rutgers The State University of New Jersey - New Brunswick.;

  • 授予单位 Rutgers The State University of New Jersey - New Brunswick.;
  • 学科 Chemistry Biochemistry.;Energy.;Engineering Materials Science.;Chemistry Physical.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 196 p.
  • 总页数 196
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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