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Exciton generation and dissociation mechanisms in organic bulk heterojunction solar cell materials.

机译:有机体异质结太阳能电池材料中激子的产生和离解机理。

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摘要

Characterization of the optical and electrical properties of organic solar cell materials is of prime importance to organic solar cell design. This thesis describes the use of capacitive photocurrent measurements to study the exciton generation and dissociation mechanisms of organic solar cell materials. The emphasis is on the study of the methanofullerene derivatives (e.g., PCBM) which act as the electron acceptor material. This is because much work has already been done studying electron donating polymers used in organic solar cells (in an effort to enhance their absorbance coefficient), but less information is available on the acceptor material.;Illumination of light at the PCBM ground state singlet exciton causes a sharp decrease in the photovoltage, while illumination at the ground state MDMO-PPV exciton shows no change. A direct pathway of recombination of above gap generated charge carriers was identified. Photovoltage bleaching results suggests that excitation at the PCBM ground singlet state exciton increases the recombination rate of higher energy excitations, either by acting as a recombination center or by forcing higher energy carriers into short lived states that recombine before reaching the contacts. The fact that the photovoltage bleaching correlates with the ground state PCBM singlet exciton suggests that charge dissociation from PCBM preferentially generates long-lived localized states.;Capacitive photocurrent measurements were then performed on isolated methanofullerene derivatives, with the polymer donor material absent. Several low energy transitions were resolved in the optical spectroscopy of methanofullerene derivatives. These low energy states lay below the optical energy band-gap of these materials, so that their presence was unexpected. It was determined that the low energy states overlapped with the plasmon state of the highly conducting substrates (Indium Tin Oxide) which were in close proximity with the PCBM. Plasmon states in ITO have been observed previously, but the results presented in this thesis are unique in that this is the first evidence of charge transfer from the plasmon state of ITO to a high electron affinity fullerene derivative.;The results show the evidence of charge transfer from PCBM to ITO over a broad wavelength range of 400 -- 2400 nm (3 eV -- 0.5 eV). Few materials have been observed to have absorbance and charge transfer over such a large range of energies in the infra-red regime. These results open a new direction for development of organic solar cell design with higher power conversion efficiencies.;In the blend films of MDMO-PPV: PCBM, the charge generation rate in PCBM was discovered to be much higher than would be expected from the absorbance cross-section. This observation led to design of a photovoltage bleaching experiment to examine the charge generation mechanism. Here the effect of illumination by a tunable light source on the open circuit photovoltage of a MDMO-PPV: PCBM bulk heterojunction solar cell was measured.
机译:有机太阳能电池材料的光学和电学特性的表征对于有机太阳能电池设计至关重要。本文介绍了使用电容式光电流测量技术来研究有机太阳能电池材料的激子产生和解离机理。重点在于研究用作电子受体材料的亚甲基富勒烯衍生物(例如PCBM)。这是因为已经进行了大量研究以研究有机太阳能电池中使用的给电子聚合物(以提高吸光系数),但是受主材料的信息较少。; PCBM基态单重态激子的光照明导致光电压急剧下降,而基态MDMO-PPV激子的照明没有变化。鉴定了上述空位产生的载流子重组的直接途径。光电压漂白的结果表明,通过充当复合中心或通过迫使较高能量的载流子进入短寿命状态(在到达触点之前重新结合),PCBM基态单态激子的激发提高了高能激发的复合率。光电压漂白与基态PCBM单线态激子相关的事实表明,电荷从PCBM上解离会优先生成长寿命的局部态。然后,在不存在聚合物供体材料的情况下,对孤立的甲基富勒烯衍生物进行了电容性光电流测量。在亚甲基富勒烯衍生物的光谱学中解决了几个低能跃迁。这些低能态位于这些材料的光能带隙以下,因此它们的存在是出乎意料的。已确定低能态与与PCBM紧邻的高导电衬底(氧化铟锡)的等离激元态重叠。以前已经观察到了ITO中的等离子态,但是本文提出的结果是独特的,因为这是电荷从ITO的等离振子态转移到高电子亲和性富勒烯衍生物的第一个证据。在400-2400 nm(3 eV-0.5 eV)的宽波长范围内从PCBM转移到ITO。在红外条件下,几乎没有材料在如此大的能量范围内具有吸收和电荷转移。这些结果为具有更高功率转换效率的有机太阳能电池设计的发展开辟了新的方向。;在MDMO-PPV的共混膜:PCBM中,发现PCBM中的电荷产生速率比吸收率预期的要高得多。横截面。该观察结果导致设计了光电压漂白实验以检查电荷产生机理。在此,测量了可调谐光源对MDMO-PPV:PCBM体异质结太阳能电池的开路光电压的影响。

著录项

  • 作者

    Shah, Hemant M.;

  • 作者单位

    University of Louisville.;

  • 授予单位 University of Louisville.;
  • 学科 Engineering Electronics and Electrical.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 130 p.
  • 总页数 130
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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