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共振电子附着于四氰基对苯二醌二甲烷。

Resonance electron attachment to tetracyanoquinodimethane.

作者信息

Pshenichnyuk Stanislav A, Modelli Alberto, Lazneva Eleonora F, Komolov Alexei S

机构信息

Institute of Molecule and Crystal Physics, Ufa Research Centre, Russian Academy of Sciences , Prospeκt Oktyabrya 151, 450075 Ufa, Russia.

出版信息

J Phys Chem A. 2014 Aug 28;118(34):6810-8. doi: 10.1021/jp505841c. Epub 2014 Aug 14.

Abstract

Resonance interaction of low energy (0-14 eV) electrons with gas-phase 7,7,8,8-tetracyanoquinodimethane (TCNQ) was investigated using dissociative electron attachment (DEA) spectroscopy. Spectral features associated with formation of long-lived TCNQ molecular negative ions are detected at incident electron energies of 0.3, 1.3, and 3.0 eV. A variety of negative fragments is observed around 4 eV, and slow (microseconds) dissociative decay channels are detected at about 3 eV, in competition with simple re-emission of the captured electron. The average electron detachment time from the TCNQ(-) negative ions formed at 3 eV was evaluated to be 250 μs. The experimental findings are interpreted with the support of density functional theory (DFT) calculations of the empty orbital energies, scaled with an empirical equation, and by comparison with earlier electron transmission spectroscopy (ETS) data. A possible mechanism for the unusual formation of long-lived molecular anions above zero energy (up to 3 eV) is briefly discussed. The present results on the interactions between electrons and isolated TCNQ molecules could give more insight into processes observed in TCNQ adsorbates under conditions of excess negative charge. In particular, electron-stimulated surface reactions are hypothesized, likely occurring when condensed TCNQ molecules are exposed to electron beam irradiation.

摘要

采用离解电子附着(DEA)光谱研究了低能(0 - 14电子伏特)电子与气相7,7,8,8 - 四氰基对苯二醌二甲烷(TCNQ)的共振相互作用。在0.3、1.3和3.0电子伏特的入射电子能量下,检测到与长寿命TCNQ分子负离子形成相关的光谱特征。在4电子伏特左右观察到各种负离子碎片,在约3电子伏特处检测到缓慢(微秒级)的离解衰变通道,这与捕获电子的简单再发射相互竞争。在3电子伏特形成的TCNQ(-)负离子的平均电子脱离时间估计为250微秒。实验结果通过对空轨道能量进行密度泛函理论(DFT)计算(用经验方程进行标度)并与早期电子传输光谱(ETS)数据进行比较来解释。简要讨论了在零能量以上(高达3电子伏特)形成长寿命分子阴离子的异常机制。目前关于电子与孤立TCNQ分子之间相互作用的结果可以更深入地了解在过量负电荷条件下TCNQ吸附物中观察到的过程。特别是,推测了电子激发的表面反应,这可能在凝聚态TCNQ分子暴露于电子束辐照时发生。

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