Charge transfer (CT) crystals exhibit unique electronic and magnetic properties with interesting applications. We present a rational and easy guide which allows to foresee the effective charge transfer co-crystal production and that is based on the comparison of the frontier molecular orbital (MO) energies of a donor and acceptor couple. For the sake of comparison, theoretical calculations have been carried out by using the cheap and fast PM6 semiempirical Hamiltonian and pure HF/cc-pVTZ level of the theory. The results are then compared with experimental results obtained both by chemical (bromine and iodine were used as the acceptor) and electrochemical doping (exploiting an original experimental set-up by this laboratory: the electrochemical transistor). Infra-red vibrational experimental results and theoretically calculated spectra are compared to assess both the effective donor-acceptor (D/A) charge-transfer and transport mechanism (giant IRAV polaron signature). XPS spectra have been collected (carbon (1 s) and iodine (3d5/2)) signals, yielding further evidence of the effective formation of the CT anthracene:iodine complex.The ElectrochemicaTransistor set-up proposed in this paper features the peculiar characteristics that a suitable functionalized materials acts both as the working electrode (in an electrochemical cell) and the gate (in the transistor source/gate/drain layout). Allowing for simultaneous potential control and electrical impedance measurement of the working/gate (anthracene is used as working/gate electrode). image

Charge‐Transfer Complexes: Halogen‐Doped Anthracene as a Case of Study / Gilioli, Simone; Giovanardi, Roberto; Ferrari, Camilla; Montecchi, Monica; Gemelli, Andrea; Severini, Andrea; Roncaglia, Fabrizio; Carella, Alberta; Rossella, Francesco; Vanossi, Davide; Marchetti, Andrea; Carmieli, Raanan; Pasquali, Luca; Fontanesi, Claudio. - In: CHEMISTRY-A EUROPEAN JOURNAL. - ISSN 0947-6539. - (2024), pp. 1-6. [10.1002/chem.202400519]

Charge‐Transfer Complexes: Halogen‐Doped Anthracene as a Case of Study

Gilioli, Simone;Giovanardi, Roberto;Ferrari, Camilla;Montecchi, Monica;Severini, Andrea;Roncaglia, Fabrizio;Carella, Alberta;Rossella, Francesco;Vanossi, Davide;Marchetti, Andrea;Pasquali, Luca;Fontanesi, Claudio
2024

Abstract

Charge transfer (CT) crystals exhibit unique electronic and magnetic properties with interesting applications. We present a rational and easy guide which allows to foresee the effective charge transfer co-crystal production and that is based on the comparison of the frontier molecular orbital (MO) energies of a donor and acceptor couple. For the sake of comparison, theoretical calculations have been carried out by using the cheap and fast PM6 semiempirical Hamiltonian and pure HF/cc-pVTZ level of the theory. The results are then compared with experimental results obtained both by chemical (bromine and iodine were used as the acceptor) and electrochemical doping (exploiting an original experimental set-up by this laboratory: the electrochemical transistor). Infra-red vibrational experimental results and theoretically calculated spectra are compared to assess both the effective donor-acceptor (D/A) charge-transfer and transport mechanism (giant IRAV polaron signature). XPS spectra have been collected (carbon (1 s) and iodine (3d5/2)) signals, yielding further evidence of the effective formation of the CT anthracene:iodine complex.The ElectrochemicaTransistor set-up proposed in this paper features the peculiar characteristics that a suitable functionalized materials acts both as the working electrode (in an electrochemical cell) and the gate (in the transistor source/gate/drain layout). Allowing for simultaneous potential control and electrical impedance measurement of the working/gate (anthracene is used as working/gate electrode). image
2024
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Charge‐Transfer Complexes: Halogen‐Doped Anthracene as a Case of Study / Gilioli, Simone; Giovanardi, Roberto; Ferrari, Camilla; Montecchi, Monica; Gemelli, Andrea; Severini, Andrea; Roncaglia, Fabrizio; Carella, Alberta; Rossella, Francesco; Vanossi, Davide; Marchetti, Andrea; Carmieli, Raanan; Pasquali, Luca; Fontanesi, Claudio. - In: CHEMISTRY-A EUROPEAN JOURNAL. - ISSN 0947-6539. - (2024), pp. 1-6. [10.1002/chem.202400519]
Gilioli, Simone; Giovanardi, Roberto; Ferrari, Camilla; Montecchi, Monica; Gemelli, Andrea; Severini, Andrea; Roncaglia, Fabrizio; Carella, Alberta; R...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1347386
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