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dc.contributor.authorGrzibovskis, Raitis
dc.contributor.authorVembris, Aivars
dc.date.accessioned2020-08-19T17:44:17Z
dc.date.available2020-08-19T17:44:17Z
dc.date.issued2018
dc.identifier.issn0022-2461
dc.identifier.urihttps://dspace.lu.lv/dspace/handle/7/52430
dc.descriptionFinancial support provided by Scientific Research Project for Students and Young Researchers Nr. SJZ2015/20 realized at the Institute of Solid State Physics, University of Latvia, is greatly acknowledged. This work has been supported by the Latvian State Research Program on Multifunctional Materials IMIS2. Jennifer Mann from Physical Electronics is greatly acknowledged for providing UPS data.en_US
dc.description.abstractUltraviolet photoelectron spectroscopy (UPS) is commonly used method for energy level determination using planar heterojunction samples in either metal/organic or organic/organic systems. Only some attempts have been made in the study of bulk heterojunction systems. Photoemission yield spectroscopy (PYS) could be applied as a method for organic compound–organic compound interface studies in bulk heterojunction samples. Contrary to the UPS, PYS method does not require ultra-high vacuum, which simplifies experiment setup. Also, scanning depth of PYS is in the range of tens of nanometers, which allows studying deeper layers of the sample instead of only surface layer. In this work, poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-phenyl C61 butyric acid methyl ester (PCBM) bulk heterojunction thin films were studied as a model system. A mass ratio between P3HT and PCBM in the system was varied from 1:0 to 1:50. Ionization energy dependence on this ratio was studied using two methods: UPS and PYS. To study the influence of the sample morphology on the PYS measurements and obtainable results, phase-separated and homogeneously distributed samples were prepared for analyses. P3HT ionization energy shift of 0.40 eV was observed in the samples made from chloroform solution. Experiments showed the need for a low degree of phase separation between P3HT and PCBM to observe P3HT ionization energy shift using PYS. On the contrary, no ionization energy shift of P3HT was observed in the UPS measurements for the same systems.en_US
dc.description.sponsorshipLatvian State Research Program IMIS2; ISSP UL Scientific Research Project for Students and Young Researchers No. SJZ2015/20; Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART²en_US
dc.language.isoengen_US
dc.publisherSpringer New York LLCen_US
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/739508/EU/Centre of Advanced Material Research and Technology Transfer/CAMART²en_US
dc.relation.ispartofseriesJournal of Materials Science;53 (10)
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES:Physicsen_US
dc.subjectphotoemission yield spectroscopyen_US
dc.subjectultraviolet photoelectron spectroscopyen_US
dc.subjectinterfaceen_US
dc.subjectionization energyen_US
dc.subjectorganic materialsen_US
dc.subjectthin filmsen_US
dc.titleEnergy level determination in bulk heterojunction systems using photoemission yield spectroscopy: case of P3HT:PCBMen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.identifier.doi10.1007/s10853-018-2050-9


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