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Analysis of the degradation mechanism of ITO-free organic solar cells under UV radiation

Identifieur interne : 000196 ( Main/Repository ); précédent : 000195; suivant : 000197

Analysis of the degradation mechanism of ITO-free organic solar cells under UV radiation

Auteurs : RBID : Pascal:14-0046849

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English descriptors

Abstract

This work reports on the stability of encapsulated ITO-free bulk heterojunction organic solar cells (BHJ-OSC) under UV radiation in ambient air with the layer sequence Cr/Al/Cr/photoactive layer (PAL)/ poly (3, 4-ethylenedioxythiophene) poly (styrenesulfonate) (PEDOT:PSS)/metal-grid. The PAL consisted of poly(3-hexylthiophene) (P3HT) as a donor and (6,6)-phenyl-C60 butyric acid methyl ester (PCBM) as an acceptor. BHJ-OSC with this setup showed remarkable stability under continuous illumination (1000 W/ m2) with a low UV content. In contrast, the devices degraded significantly under UV radiation which was characterized by a reduction in fill factor and short-circuit current density. Additional experiments revealed an increase of the sheet resistance of the PEDOT:PSS layer which was interestingly much more pronounced in pure PEDOT:PSS samples as compared to samples where a PAL was deposited underneath. In addition, current extraction by linear increasing voltage (CELIV) measurements indicated a decrease of the effective charge carrier mobility of the PAL. Numerical simulations based on the experimentally determined parameters showed good agreement of the solar cell performance as a function of UV exposure duration. This suggests that the increase of the sheet resistance of the polymeric hole contact and to a lesser extent the change of the effective mobility of the PAL are the main factors governing the deterioration of the photovoltaic performance upon UV exposure. A comparison to devices with a setup ITO/ZnO/PAL/PEDOT:PSS and a full metallization showed clearly improved UV stability, although the absorption of UV in the PAL is very similar. This further supports our interpretation that the degradation of the PAL plays a very minor role. The issue with the degradation of the PEDOT:PSS can easily be solved by incorporating an UV-filter into the device or preferably the use of UV-stabilized PEDOT:PSS formulations.

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Pascal:14-0046849

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<term>Ambient atmosphere</term>
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<term>Charge carrier mobility</term>
<term>Comparative study</term>
<term>Damaging</term>
<term>Degradation</term>
<term>Ester</term>
<term>Experimental study</term>
<term>Fill factor</term>
<term>Fullerene compounds</term>
<term>Fullerenes</term>
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<term>Long term</term>
<term>Metal grid</term>
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<term>Numerical simulation</term>
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<term>Performance evaluation</term>
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<term>Sheet resistivity</term>
<term>Short circuit currents</term>
<term>Solar cell</term>
<term>Styrenesulfonate polymer</term>
<term>Thiophene derivative polymer</term>
<term>Tin addition</term>
<term>Ultraviolet radiation</term>
<term>Voltage measurement</term>
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<term>Endommagement</term>
<term>Dégradation</term>
<term>Addition étain</term>
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<term>Hétérojonction</term>
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<div type="abstract" xml:lang="en">This work reports on the stability of encapsulated ITO-free bulk heterojunction organic solar cells (BHJ-OSC) under UV radiation in ambient air with the layer sequence Cr/Al/Cr/photoactive layer (PAL)/ poly (3, 4-ethylenedioxythiophene) poly (styrenesulfonate) (PEDOT:PSS)/metal-grid. The PAL consisted of poly(3-hexylthiophene) (P3HT) as a donor and (6,6)-phenyl-C
<sub>60</sub>
butyric acid methyl ester (PCBM) as an acceptor. BHJ-OSC with this setup showed remarkable stability under continuous illumination (1000 W/ m
<sup>2</sup>
) with a low UV content. In contrast, the devices degraded significantly under UV radiation which was characterized by a reduction in fill factor and short-circuit current density. Additional experiments revealed an increase of the sheet resistance of the PEDOT:PSS layer which was interestingly much more pronounced in pure PEDOT:PSS samples as compared to samples where a PAL was deposited underneath. In addition, current extraction by linear increasing voltage (CELIV) measurements indicated a decrease of the effective charge carrier mobility of the PAL. Numerical simulations based on the experimentally determined parameters showed good agreement of the solar cell performance as a function of UV exposure duration. This suggests that the increase of the sheet resistance of the polymeric hole contact and to a lesser extent the change of the effective mobility of the PAL are the main factors governing the deterioration of the photovoltaic performance upon UV exposure. A comparison to devices with a setup ITO/ZnO/PAL/PEDOT:PSS and a full metallization showed clearly improved UV stability, although the absorption of UV in the PAL is very similar. This further supports our interpretation that the degradation of the PAL plays a very minor role. The issue with the degradation of the PEDOT:PSS can easily be solved by incorporating an UV-filter into the device or preferably the use of UV-stabilized PEDOT:PSS formulations.</div>
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<s0>This work reports on the stability of encapsulated ITO-free bulk heterojunction organic solar cells (BHJ-OSC) under UV radiation in ambient air with the layer sequence Cr/Al/Cr/photoactive layer (PAL)/ poly (3, 4-ethylenedioxythiophene) poly (styrenesulfonate) (PEDOT:PSS)/metal-grid. The PAL consisted of poly(3-hexylthiophene) (P3HT) as a donor and (6,6)-phenyl-C
<sub>60</sub>
butyric acid methyl ester (PCBM) as an acceptor. BHJ-OSC with this setup showed remarkable stability under continuous illumination (1000 W/ m
<sup>2</sup>
) with a low UV content. In contrast, the devices degraded significantly under UV radiation which was characterized by a reduction in fill factor and short-circuit current density. Additional experiments revealed an increase of the sheet resistance of the PEDOT:PSS layer which was interestingly much more pronounced in pure PEDOT:PSS samples as compared to samples where a PAL was deposited underneath. In addition, current extraction by linear increasing voltage (CELIV) measurements indicated a decrease of the effective charge carrier mobility of the PAL. Numerical simulations based on the experimentally determined parameters showed good agreement of the solar cell performance as a function of UV exposure duration. This suggests that the increase of the sheet resistance of the polymeric hole contact and to a lesser extent the change of the effective mobility of the PAL are the main factors governing the deterioration of the photovoltaic performance upon UV exposure. A comparison to devices with a setup ITO/ZnO/PAL/PEDOT:PSS and a full metallization showed clearly improved UV stability, although the absorption of UV in the PAL is very similar. This further supports our interpretation that the degradation of the PAL plays a very minor role. The issue with the degradation of the PEDOT:PSS can easily be solved by incorporating an UV-filter into the device or preferably the use of UV-stabilized PEDOT:PSS formulations.</s0>
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<s5>02</s5>
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<s5>02</s5>
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<s5>03</s5>
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<s5>04</s5>
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<s5>05</s5>
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<s5>09</s5>
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<s5>09</s5>
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<s5>10</s5>
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<s5>10</s5>
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<s5>12</s5>
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<s5>13</s5>
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<s0>Sheet resistivity</s0>
<s5>13</s5>
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<s5>15</s5>
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</fC03>
<fC03 i1="16" i2="X" l="SPA">
<s0>Movilidad portador carga</s0>
<s5>16</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE">
<s0>Simulation numérique</s0>
<s5>17</s5>
</fC03>
<fC03 i1="17" i2="X" l="ENG">
<s0>Numerical simulation</s0>
<s5>17</s5>
</fC03>
<fC03 i1="17" i2="X" l="SPA">
<s0>Simulación numérica</s0>
<s5>17</s5>
</fC03>
<fC03 i1="18" i2="X" l="FRE">
<s0>Cellule solaire</s0>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="X" l="ENG">
<s0>Solar cell</s0>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="X" l="SPA">
<s0>Célula solar</s0>
<s5>18</s5>
</fC03>
<fC03 i1="19" i2="X" l="FRE">
<s0>Evaluation performance</s0>
<s5>19</s5>
</fC03>
<fC03 i1="19" i2="X" l="ENG">
<s0>Performance evaluation</s0>
<s5>19</s5>
</fC03>
<fC03 i1="19" i2="X" l="SPA">
<s0>Evaluación prestación</s0>
<s5>19</s5>
</fC03>
<fC03 i1="20" i2="X" l="FRE">
<s0>Métallisation</s0>
<s5>20</s5>
</fC03>
<fC03 i1="20" i2="X" l="ENG">
<s0>Metallizing</s0>
<s5>20</s5>
</fC03>
<fC03 i1="20" i2="X" l="SPA">
<s0>Metalización</s0>
<s5>20</s5>
</fC03>
<fC03 i1="21" i2="X" l="FRE">
<s0>Long terme</s0>
<s5>21</s5>
</fC03>
<fC03 i1="21" i2="X" l="ENG">
<s0>Long term</s0>
<s5>21</s5>
</fC03>
<fC03 i1="21" i2="X" l="SPA">
<s0>Largo plazo</s0>
<s5>21</s5>
</fC03>
<fC03 i1="22" i2="X" l="FRE">
<s0>Oxyde d'indium</s0>
<s5>22</s5>
</fC03>
<fC03 i1="22" i2="X" l="ENG">
<s0>Indium oxide</s0>
<s5>22</s5>
</fC03>
<fC03 i1="22" i2="X" l="SPA">
<s0>Indio óxido</s0>
<s5>22</s5>
</fC03>
<fC03 i1="23" i2="X" l="FRE">
<s0>Thiophène dérivé polymère</s0>
<s2>NK</s2>
<s5>23</s5>
</fC03>
<fC03 i1="23" i2="X" l="ENG">
<s0>Thiophene derivative polymer</s0>
<s2>NK</s2>
<s5>23</s5>
</fC03>
<fC03 i1="23" i2="X" l="SPA">
<s0>Tiofeno derivado polímero</s0>
<s2>NK</s2>
<s5>23</s5>
</fC03>
<fC03 i1="24" i2="X" l="FRE">
<s0>Styrènesulfonate polymère</s0>
<s2>NK</s2>
<s5>24</s5>
</fC03>
<fC03 i1="24" i2="X" l="ENG">
<s0>Styrenesulfonate polymer</s0>
<s2>NK</s2>
<s5>24</s5>
</fC03>
<fC03 i1="24" i2="X" l="SPA">
<s0>Estireno sulfonato polímero</s0>
<s2>NK</s2>
<s5>24</s5>
</fC03>
<fC03 i1="25" i2="3" l="FRE">
<s0>Mélange polymère</s0>
<s5>25</s5>
</fC03>
<fC03 i1="25" i2="3" l="ENG">
<s0>Polymer blends</s0>
<s5>25</s5>
</fC03>
<fC03 i1="26" i2="X" l="FRE">
<s0>Fullerènes</s0>
<s5>26</s5>
</fC03>
<fC03 i1="26" i2="X" l="ENG">
<s0>Fullerenes</s0>
<s5>26</s5>
</fC03>
<fC03 i1="27" i2="X" l="FRE">
<s0>Acide butyrique</s0>
<s2>NK</s2>
<s5>27</s5>
</fC03>
<fC03 i1="27" i2="X" l="ENG">
<s0>Butyric acid</s0>
<s2>NK</s2>
<s5>27</s5>
</fC03>
<fC03 i1="27" i2="X" l="SPA">
<s0>Butírico ácido</s0>
<s2>NK</s2>
<s5>27</s5>
</fC03>
<fC03 i1="28" i2="X" l="FRE">
<s0>Ester</s0>
<s5>28</s5>
</fC03>
<fC03 i1="28" i2="X" l="ENG">
<s0>Ester</s0>
<s5>28</s5>
</fC03>
<fC03 i1="28" i2="X" l="SPA">
<s0>Ester</s0>
<s5>28</s5>
</fC03>
<fC03 i1="29" i2="3" l="FRE">
<s0>Composé du fullerène</s0>
<s5>29</s5>
</fC03>
<fC03 i1="29" i2="3" l="ENG">
<s0>Fullerene compounds</s0>
<s5>29</s5>
</fC03>
<fC03 i1="30" i2="X" l="FRE">
<s0>Oxyde de zinc</s0>
<s5>30</s5>
</fC03>
<fC03 i1="30" i2="X" l="ENG">
<s0>Zinc oxide</s0>
<s5>30</s5>
</fC03>
<fC03 i1="30" i2="X" l="SPA">
<s0>Zinc óxido</s0>
<s5>30</s5>
</fC03>
<fC03 i1="31" i2="X" l="FRE">
<s0>ITO</s0>
<s4>INC</s4>
<s5>82</s5>
</fC03>
<fC03 i1="32" i2="X" l="FRE">
<s0>C60</s0>
<s4>INC</s4>
<s5>83</s5>
</fC03>
<fC03 i1="33" i2="X" l="FRE">
<s0>ZnO</s0>
<s4>INC</s4>
<s5>84</s5>
</fC03>
<fN21>
<s1>055</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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