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    <subfield code="2">doi</subfield>
    <subfield code="a">10.1016/j.dyepig.2022.110310</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">128723</subfield>
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    <subfield code="a">ART-2022-128723</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Duerto, I.</subfield>
    <subfield code="0">(orcid)0000-0001-9690-9662</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Enhancing the temporal stability of DSSCs with novel vinylpyrimidine anchoring and accepting group</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2022</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Three compounds based on aniline, thiophene and vinylpyrimidine as anchoring group have been prepared and studied as light harvesting units for dye-sensitized solar cells (DSSCs). They comprise thiophenyl p-spacer systems with one or two thiophenes (AT-Pyri, ATT-Pyri) and aniline as donor which is functionalized, in one case, with an hydroxyl group (HO-AT-Pyri). The bithiophene based dye (ATT-Pyri) shows higher extinction coefficients and smaller transition energy, as well as broader absorption spectrum. Thus, despite lower dye uptake, devices based on one thiophene and with the hydroxyl group (HO-AT-Pyri) have slightly higher power conversion efficiencies (¿) as compared with the analogous dye without this group (AT-Pyri). However, the best performing device is based on the dye with bithiophene bridge (ATT-Pyri) when a co-adsorbent is added to avoid the aggregation of the dye. The photovoltaic parameters of cells based on these vinylpyrimidine dyes are enhanced over 1000 h, especially for ATT-Pyri devices, which reach a ¿ = 6, 4%. © 2022 The Authors</subfield>
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    <subfield code="u">http://creativecommons.org/licenses/by-nc-nd/3.0/es/</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sarasa, S.</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Barrios, D.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-1466-5719</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Orduna, J.</subfield>
    <subfield code="0">(orcid)0000-0003-3514-2570</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Villacampa, B.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-9814-0834</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Blesa, M. -J</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-7193-1732</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">2013</subfield>
    <subfield code="2">765</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Orgánica</subfield>
    <subfield code="c">Área Química Orgánica</subfield>
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    <subfield code="1">2003</subfield>
    <subfield code="2">395</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Física Materia Condensa.</subfield>
    <subfield code="c">Área Física Materia Condensada</subfield>
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    <subfield code="g">203, 110310 (2022),  -</subfield>
    <subfield code="p">Dyes pigm.</subfield>
    <subfield code="t">Dyes and Pigments</subfield>
    <subfield code="x">0143-7208</subfield>
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