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Charge-carrier relaxation dynamics in highly ordered poly(p-phenylene vinylene): Effects of carrier bimolecular recombination and trapping

机译:高度有序的聚对亚苯基亚乙烯基中的载流子弛豫动力学:载流子双分子重组和俘获的影响

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We have studied the charge-carrier relaxation dynamics in highly ordered poly(p-phenylene vinylene) over a broad time range using fast (t > 100 ps)transient photoconductivity measurements. The carrier density was also monitored (t > 100 fs) by means of photoinduced absorption probed at the infrared active vibrational modes. We find that promptly upon charge-carrier photogeneration, the initial polaron dynamics is governed by bimolecular recombination, while later in the subnanosecond time regime carrier trapping gives rise to an exponential decay of the photocurrent. The more sensitive transient photocurrent measurements indicate that in the low excitation regime, when the density of photocarriers is comparable to that of the trapping states (~10~(16) cm~(-3)), carrier hopping between traps along with transport via extended states determines the carrier relaxation, a mechanism that is manifested by a long-lived photocurrent "tail." This photocurrent tail is reduced by lowering the temperature and/or by increasing the excitation density. Based on these data; we develop a comprehensive kinetic model that takes into account the bipolar charge transport, the free-carrier bimolecular recombination, the carrier trapping, and the carrier recombination involving free and trapped carriers.
机译:我们已经使用快速(t> 100 ps)瞬态光电导率测量在很宽的时间范围内研究了高度有序的聚对亚苯基亚乙烯基中的载流子弛豫动力学。还通过以红外主动振动模式探测的光诱导吸收来监测载流子密度(t> 100 fs)。我们发现,在电荷载流子光生化后,迅速的初始极化子动力学受双分子复合作用的控制,而在随后的亚纳秒时间范围内,载流子的俘获引起光电流的指数衰减。更为敏感的瞬态光电流测量结果表明,在低激发态下,当载流子的密度与俘获态(〜10〜(16)cm〜(-3))相当时,陷阱之间的载流子跃迁以及通过扩展态决定了载流子弛豫,这种机制通过长寿命的光电流“尾巴”来体现。通过降低温度和/或通过增加激发密度来减少该光电流尾部。基于这些数据;我们开发了一个综合的动力学模型,该模型考虑了双极性电荷传输,自由载流子双分子重组,载流子俘获以及涉及自由载流子和俘获载流子的载流子重组。

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