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Optical and electrical characterization of thin films based on anthracene polyether polymers

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Optical and electrical characterization of thin films based on anthracene polyether polymers

Auteurs : RBID : Pascal:13-0188207

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English descriptors

Abstract

Two new anthracene derivatives were characterized to improve the optoelectronic properties of π-conjugated anthracene polymers. The optical properties of the polymers were investigated by UV-visible absorption and photoluminescence (PL) spectroscopy. The energy bandgaps of anthracene-based polyether thin films were in the range 2.8-2.97 eV. Green emission (504 nm) was observed for anthracene/bisphenol A (An-BPA) and green-yellow emission (563 nm) for anthracene/fluorinated bisphenol A. (An-BPAF) Organic diodes formed by sandwiching anthracene layers between indium-tin oxide (ITO) and aluminum contacts were characterized. The dc electrical properties of ITO/anthracene derivatives/Al diodes were studied using current-voltage measurements and showed ohmic behavior at low voltage. The conduction mechanism seems to be a space-charge-limited current with exponential trap distribution at high applied bias voltage. The ac electrical transport of the anthracene derivatives was studied as a function of frequency (100 Hz-10 MHz) and applied bias in impedance spectroscopy analyses. We interpreted Cole-Cole plots in terms of the equivalent circuit model as a single parallel resistance and a capacitance network in series with a relatively small resistance. The evolution of the electrical parameters deduced from fitting of the experimental data is discussed. The conduction mechanism revealed by I-V characteristics is in agreement with the impedance spectroscopy results.

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Pascal:13-0188207

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<term>Cole Cole model</term>
<term>Conjugated polymer</term>
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<term>Sandwich structures</term>
<term>Space-charge-limited conduction</term>
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<term>Traps</term>
<term>Ultraviolet spectra</term>
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<div type="abstract" xml:lang="en">Two new anthracene derivatives were characterized to improve the optoelectronic properties of π-conjugated anthracene polymers. The optical properties of the polymers were investigated by UV-visible absorption and photoluminescence (PL) spectroscopy. The energy bandgaps of anthracene-based polyether thin films were in the range 2.8-2.97 eV. Green emission (504 nm) was observed for anthracene/bisphenol A (An-BPA) and green-yellow emission (563 nm) for anthracene/fluorinated bisphenol A. (An-BPAF) Organic diodes formed by sandwiching anthracene layers between indium-tin oxide (ITO) and aluminum contacts were characterized. The dc electrical properties of ITO/anthracene derivatives/Al diodes were studied using current-voltage measurements and showed ohmic behavior at low voltage. The conduction mechanism seems to be a space-charge-limited current with exponential trap distribution at high applied bias voltage. The ac electrical transport of the anthracene derivatives was studied as a function of frequency (100 Hz-10 MHz) and applied bias in impedance spectroscopy analyses. We interpreted Cole-Cole plots in terms of the equivalent circuit model as a single parallel resistance and a capacitance network in series with a relatively small resistance. The evolution of the electrical parameters deduced from fitting of the experimental data is discussed. The conduction mechanism revealed by I-V characteristics is in agreement with the impedance spectroscopy results.</div>
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<s5>22</s5>
</fC03>
<fC03 i1="23" i2="3" l="FRE">
<s0>Anthracène</s0>
<s2>NK</s2>
<s5>23</s5>
</fC03>
<fC03 i1="23" i2="3" l="ENG">
<s0>Anthracene</s0>
<s2>NK</s2>
<s5>23</s5>
</fC03>
<fC03 i1="24" i2="X" l="FRE">
<s0>Ether polymère</s0>
<s2>NK</s2>
<s5>24</s5>
</fC03>
<fC03 i1="24" i2="X" l="ENG">
<s0>Ether polymer</s0>
<s2>NK</s2>
<s5>24</s5>
</fC03>
<fC03 i1="24" i2="X" l="SPA">
<s0>Eter polímero</s0>
<s2>NK</s2>
<s5>24</s5>
</fC03>
<fC03 i1="25" i2="X" l="FRE">
<s0>Polymère conjugué</s0>
<s5>25</s5>
</fC03>
<fC03 i1="25" i2="X" l="ENG">
<s0>Conjugated polymer</s0>
<s5>25</s5>
</fC03>
<fC03 i1="25" i2="X" l="SPA">
<s0>Polímero conjugado</s0>
<s5>25</s5>
</fC03>
<fC03 i1="26" i2="X" l="FRE">
<s0>Dérivé de l'anthracène</s0>
<s5>26</s5>
</fC03>
<fC03 i1="26" i2="X" l="ENG">
<s0>Anthracene derivatives</s0>
<s5>26</s5>
</fC03>
<fC03 i1="26" i2="X" l="SPA">
<s0>Antraceno derivado</s0>
<s5>26</s5>
</fC03>
<fC03 i1="27" i2="3" l="FRE">
<s0>Composé du fluor</s0>
<s5>27</s5>
</fC03>
<fC03 i1="27" i2="3" l="ENG">
<s0>Fluorine compounds</s0>
<s5>27</s5>
</fC03>
<fC03 i1="28" i2="X" l="FRE">
<s0>Oxyde d'indium</s0>
<s5>28</s5>
</fC03>
<fC03 i1="28" i2="X" l="ENG">
<s0>Indium oxide</s0>
<s5>28</s5>
</fC03>
<fC03 i1="28" i2="X" l="SPA">
<s0>Indio óxido</s0>
<s5>28</s5>
</fC03>
<fC03 i1="29" i2="3" l="FRE">
<s0>Aluminium</s0>
<s2>NC</s2>
<s5>29</s5>
</fC03>
<fC03 i1="29" i2="3" l="ENG">
<s0>Aluminium</s0>
<s2>NC</s2>
<s5>29</s5>
</fC03>
<fC03 i1="30" i2="3" l="FRE">
<s0>Matériau dopé</s0>
<s5>46</s5>
</fC03>
<fC03 i1="30" i2="3" l="ENG">
<s0>Doped materials</s0>
<s5>46</s5>
</fC03>
<fC03 i1="31" i2="3" l="FRE">
<s0>7867</s0>
<s4>INC</s4>
<s5>56</s5>
</fC03>
<fC03 i1="32" i2="3" l="FRE">
<s0>7840R</s0>
<s4>INC</s4>
<s5>57</s5>
</fC03>
<fC03 i1="33" i2="3" l="FRE">
<s0>8235C</s0>
<s4>INC</s4>
<s5>58</s5>
</fC03>
<fC03 i1="34" i2="3" l="FRE">
<s0>8105L</s0>
<s4>INC</s4>
<s5>59</s5>
</fC03>
<fC03 i1="35" i2="3" l="FRE">
<s0>ITO</s0>
<s4>INC</s4>
<s5>82</s5>
</fC03>
<fC03 i1="36" i2="3" l="FRE">
<s0>Modèle Cole Cole</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="36" i2="3" l="ENG">
<s0>Cole Cole model</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fN21>
<s1>168</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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