A complex study of the dependence of the reduced graphite oxide electrochemical behavior on the annealing temperature and the type of electrolyte

dc.contributorAalto-yliopistofi
dc.contributorAalto Universityen
dc.contributor.authorIurchenkova, A. A.en_US
dc.contributor.authorLobiak, Egor V.en_US
dc.contributor.authorKobets, Anna A.en_US
dc.contributor.authorKolodin, Alexey N.en_US
dc.contributor.authorStott, Ashen_US
dc.contributor.authorSilva, Ravi P.en_US
dc.contributor.authorFedorovskaya, Ekaterina O.en_US
dc.contributor.departmentDepartment of Chemistry and Materials Scienceen
dc.contributor.groupauthorElectrochemical Energy Conversionen
dc.contributor.organizationNovosibirsk State Universityen_US
dc.contributor.organizationRAS - Nikolaev Institute of Inorganic Chemistry, Siberian Branchen_US
dc.contributor.organizationUniversity of Surreyen_US
dc.date.accessioned2021-01-25T10:16:32Z
dc.date.available2021-01-25T10:16:32Z
dc.date.embargoinfo:eu-repo/date/embargoEnd/2023-01-19en_US
dc.date.issued2021-02-20en_US
dc.description.abstractIn this work we investigate the influence of thermal treatment of reduced graphite oxide (RGO) on its functional composition and electrochemical performance. It is found that carboxyl, carbonyl, hydroxyl and epoxy groups are present on the RGO surface, witch when subject to thermal annealing in the temperature range 230-250°C can be controllably modified. In the process of thermal annealing, we show the formation of quinoid groups due to an increase in the number of defects. Decrease of the number of layers in RGO material and the quantity of oxygen-containing functional groups (OCFG) also occurs. With increase in annealing temperature, sequential removal of OCFG occurs as follows: carboxyl (250°C-600°C), hydroxyl (600°C-800°C), carbonyl and quinoid (700°C-1000°C). Electrochemical measurements over a wide range of pH values of the buffer electrolytes is possible to correlate the peaks in the cyclic voltammogram curves with the redox reactions of oxygen-containing functional groups as a function of applied potential. Peaks correlated with specific redox reactions which are identified as two-electron. The dependence of the specific capacities of materials on the electrolyte type has been studied. Highest capacitance was detected in 1M NaOH at a scan rate 2 mVs−1 and is equal to 210 Fg−1.en
dc.description.versionPeer revieweden
dc.format.extent12
dc.format.mimetypeapplication/pdfen_US
dc.identifier.citationIurchenkova, A A, Lobiak, E V, Kobets, A A, Kolodin, A N, Stott, A, Silva, R P & Fedorovskaya, E O 2021, 'A complex study of the dependence of the reduced graphite oxide electrochemical behavior on the annealing temperature and the type of electrolyte', Electrochimica Acta, vol. 370, 137832. https://doi.org/10.1016/j.electacta.2021.137832en
dc.identifier.doi10.1016/j.electacta.2021.137832en_US
dc.identifier.issn0013-4686
dc.identifier.issn1873-3859
dc.identifier.otherPURE UUID: b575547b-aae6-4e58-92e7-4ba9f8814f6cen_US
dc.identifier.otherPURE ITEMURL: https://research.aalto.fi/en/publications/b575547b-aae6-4e58-92e7-4ba9f8814f6cen_US
dc.identifier.otherPURE LINK: http://www.scopus.com/inward/record.url?scp=85099691794&partnerID=8YFLogxK
dc.identifier.otherPURE FILEURL: https://research.aalto.fi/files/55338844/CHEM_Iurchenkova_et_al_A_complex_study_of_the_dependence_Electrochimica_Acta.pdfen_US
dc.identifier.urihttps://aaltodoc.aalto.fi/handle/123456789/102235
dc.identifier.urnURN:NBN:fi:aalto-202101251545
dc.language.isoenen
dc.publisherElsevier
dc.relation.ispartofseriesElectrochimica Actaen
dc.relation.ispartofseriesVolume 370en
dc.rightsopenAccessen
dc.subject.keywordgraphite oxideen_US
dc.subject.keywordreduced graphite oxideen_US
dc.subject.keywordsupercapacitoren_US
dc.subject.keywordFourier transform infrared spectroscopyen_US
dc.subject.keywordX-ray photoelectron spectroscopyen_US
dc.subject.keywordcyclic voltammetryen_US
dc.titleA complex study of the dependence of the reduced graphite oxide electrochemical behavior on the annealing temperature and the type of electrolyteen
dc.typeA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessäfi
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