Surface Polarization Drives Photoinduced Charge Separation at the P3HT/Water Interface

التفاصيل البيبلوغرافية
العنوان: Surface Polarization Drives Photoinduced Charge Separation at the P3HT/Water Interface
المؤلفون: Paolo Salvatori, Sergio Brovelli, Hong Li, Alessandro Mattoni, Francesco Bruni, Guglielmo Lanzani, Sebastiano Bellani, Maria Ilenia Saba, Maria Rosa Antognazza, Filippo De Angelis, Beatriz Santiago Gonzalez, Jean-Luc Brédas, Edoardo Mosconi
المساهمون: Mosconi, E, Salvatori, P, Saba, M, Mattoni, A, Bellani, S, Bruni, F, SANTIAGO GONZALEZ, B, Antognazza, M, Brovelli, S, Lanzani, G, Li, H, Brédas, J, De Angelis, F
المصدر: ACS Energy Letter 1 (2016): 454–463. doi:10.1021/acsenergylett.6b00197
info:cnr-pdr/source/autori:Edoardo Mosconi+?, Paolo Salvatori+?, Maria Ilenia Saba§, Alessandro Mattoni§, Sebastiano Bellani??, Francesco Bruni#, Beatriz Santiago Gonzalez#, Maria Rosa Antognazza*?, Sergio Brovelli#, Guglielmo Lanzani??, Hong Li?, Jean-Luc Brédas?, Filippo De Angelis*+?/titolo:Surface Polarization Drives Photoinduced Charge Separation at the P3HT%2FWater Interface/doi:10.1021%2Facsenergylett.6b00197/rivista:ACS Energy Letter/anno:2016/pagina_da:454/pagina_a:463/intervallo_pagine:454–463/volume:1
بيانات النشر: American Chemical Society (ACS), 2016.
سنة النشر: 2016
مصطلحات موضوعية: Materials Chemistry2506 Metals and Alloys, P3HT, Surface Polarization, Analytical chemistry, Energy Engineering and Power Technology, 02 engineering and technology, Electrolyte, ING-IND/22 - SCIENZA E TECNOLOGIA DEI MATERIALI, 010402 general chemistry, 01 natural sciences, Chemistry (miscellaneous), Renewable Energy, Sustainability and the Environment, Fuel Technology, Ion, Materials Chemistry, Renewable Energy, Polarization (electrochemistry), Bioelectronics, Aqueous solution, Sustainability and the Environment, Chemistry, 021001 nanoscience & nanotechnology, 0104 chemical sciences, Indium tin oxide, P3HT/Water Interface, Organic semiconductor, Photoinduced charge separation, Chemical physics, 0210 nano-technology
الوصف: Hybrid devices employing organic semiconductors interfaced with an aqueous solution represent a new frontier in bioelectronics and energy applications. Understanding of the energetics and photoinduced processes occurring at the organic/water interface is fundamental for further progress. Here, we investigate the interfacial electronic structure of poly-3-hexylthiophene (P3HT) sandwiched between an indium tin oxide (ITO) electrode and a liquid water electrolyte. The aqueous solution is found to polarize the polymer outermost layers, which together with the polymer p-(photo) doping by dissolved oxygen localizes photogenerated electrons at the P3HT/water interface, while holes can be transferred to the ITO electrode. Under illumination, the polymer/water interface is negatively charged, attracting positive ions from the electrolyte solution and perturbing the ion distribution in the aqueous solution. The observed mechanism is of general character and could underlie the behavior of a variety of devices characterized by an organic/water interface, such as prosthetic devices for artificial vision and organic-based systems for photoelectrochemical applications.
تدمد: 2380-8195
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f11f01ee710eee235fbfffc45393b707Test
https://doi.org/10.1021/acsenergylett.6b00197Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....f11f01ee710eee235fbfffc45393b707
قاعدة البيانات: OpenAIRE