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Pulse radiolysis studies on charge carriers in conjugated polymers

机译:共轭聚合物中载流子的脉冲辐解研究

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The charged states of the conjugated polymers poly(2-methoxy,5-(2'-ethylhexyloxy)-p- phenylenevinylene) (MEH-PPV) and poly(2,5-pyridinediyl) (PPY) have been studied by pulse radiolysis. Following pulse radiolysis of argon-saturated solutions of MEH-PPV in chloroform, a new absorption is seen to grow in over a few hundred microseconds. This has a principal absorption at 1.43 eV and a weaker, low energy band (less than or equal to 0.80 eV), and is assigned to the positive one-electron charge state (positive polaron) of MEH-PPV. The slow absorption decay is unaffected by oxygen. Negative charge states (negative polarons), with absorptions around 1.4 eV, are produced upon pulse radiolysis of MEH-PPV in argon-saturated solutions in tetrahydrofuran (THF) or benzonitrile. A small solvatochromic shift is observed. In contrast to the behavior of the positive polaron, the MEH-PPV negative charge carriers decay fairly rapidly, and are readily quenched by molecular oxygen. Previous results on chemically produced positive and negative charge states of conjugated polymers and oligomers are discussed on the basis of these assignments, and comparison is made with theoretical calculations. Using benzophenone as a charge scavenger, pulse radiolysis of formic acid is shown to generate one-electron reducing species. Various derivatives of PPY, including a regioregular polymer (rPPY) and a hexyl substituted compound (HPPY) have been studied by pulse radiolysis in formic acid solution. With rPPY, new absorptions are observed at 2.59 and 1.40 eV, and are assigned to the one-electron reduced species. These are strongly quenched by molecular oxygen. With HPPY, the lower energy transition is broadened to give a maximum below 1.21 eV and a shoulder at 1.65 eV. The differences between rPPY and HPPY are interpreted on the basis of differences in the rigidity of the polymer. The relevance of these assignments to the identification of charged species in photoinduced absorption measurements is indicated. (C) 2000 American Institute of Physics. [S0021-9606(00)51206-9]. [References: 87]
机译:已经通过脉冲放射分解研究了共轭聚合物聚(2-甲氧基,5-(2'-乙基己氧基)-对苯撑亚乙烯基)(MEH-PPV)和聚(2,5-吡啶二基)(PPY)的带电态。在MEH-PPV的氩气饱和溶液在氯仿中进行脉冲辐解后,新的吸收量会在几百微秒内增长。它具有1.43 eV的主吸收和较弱的低能带(小于或等于0.80 eV),并被分配给MEH-PPV的正单电子电荷态(正极化子)。缓慢的吸收衰减不受氧的影响。 MEH-PPV在四氢呋喃(THF)或苄腈中的氩饱和溶液中进行脉冲辐射分解后,会产生约1.4 eV的负电荷态(负极化子)。观察到小的溶剂化变色。与正极化子的行为相反,MEH-PPV负电荷载流子相当快地衰减,并容易被分子氧淬灭。在这些分配的基础上,讨论了化学合成的共轭聚合物和低聚物的正电荷和负电荷状态的先前结果,并与理论计算进行了比较。使用二苯甲酮作为电荷清除剂,显示了甲酸的脉冲辐射分解可生成单电子还原物种。已经通过在甲酸溶液中进行脉冲辐射分解研究了PPY的各种衍生物,包括区域规则聚合物(rPPY)和己基取代的化合物(HPPY)。使用rPPY时,在2.59和1.40 eV处观察到新的吸收,并将其分配给单电子还原的物质。这些被分子氧强烈淬灭。借助HPPY,较低的能量跃迁变宽到最大,使最大能量低于1.21 eV,而肩峰为1.65 eV。 rPPY和HPPY之间的差异是基于聚合物刚性的差异来解释的。指出了这些分配与光诱导吸收测量中带电物质的鉴定的相关性。 (C)2000美国物理研究所。 [S0021-9606(00)51206-9]。 [参考:87]

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