Khizar Hayat Khan, Aneesa Zafar, Haroon Rashid, Iftikhar Ahmad, Gul Shahzada Khan and Hazrat Hussain
{"title":"Enhancing lithium-ion conductivity: impact of hausmannite nanofiller on PVDF–HFP/PEG blend nanocomposite polymer electrolytes","authors":"Khizar Hayat Khan, Aneesa Zafar, Haroon Rashid, Iftikhar Ahmad, Gul Shahzada Khan and Hazrat Hussain","doi":"10.1039/D4MA00694A","DOIUrl":null,"url":null,"abstract":"<p >A new series of PVDF–HFP/PEG-based nanocomposite polymer electrolytes (NCPEs) have been fabricated using hausmannite (Mn<small><sub>3</sub></small>O<small><sub>4</sub></small>) nanoparticles as the nanofiller and LiClO<small><sub>4</sub></small> as the lithium-ion source <em>via</em> the solvent casting method. A pristine PVDF–HFP NCPE sample with 2 wt% nanofiller was also prepared for comparison. The Mn<small><sub>3</sub></small>O<small><sub>4</sub></small> nanoparticles were synthesized by the precipitation method using CTAB as a templating agent and MnCl<small><sub>2</sub></small>·4H<small><sub>2</sub></small>O as the precursor. FTIR spectroscopy showed that while pristine PVDF–HFP forms a nonpolar α-phase, the incorporation of salt and nanofiller induced a mixed β and γ crystal phase, indicating interaction between the matrix and additives. Surface morphology studies showed that the NCPEs had a denser surface than pristine PVDF–HFP, with no PEG spherulite formation detected in polarized optical micrographs. Electrochemical impedance spectroscopy revealed that the 2% blend NCPE exhibited the highest ion conductivity of 3.1 × 10<small><sup>−4</sup></small> S cm<small><sup>−1</sup></small> at 80 °C, an order of magnitude higher than the pristine NCPE (5.1 × 10<small><sup>−5</sup></small> S cm<small><sup>−1</sup></small>). Temperature-dependent ion conductivity followed Arrhenius behavior, indicating a thermally activated ion hopping mechanism. The dielectric relaxation peak shifted to higher frequency with increasing temperature, suggesting faster ion dynamics and improved conductivity.</p>","PeriodicalId":18242,"journal":{"name":"Materials Advances","volume":" 24","pages":" 9613-9625"},"PeriodicalIF":5.2000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ma/d4ma00694a?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Advances","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ma/d4ma00694a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
A new series of PVDF–HFP/PEG-based nanocomposite polymer electrolytes (NCPEs) have been fabricated using hausmannite (Mn3O4) nanoparticles as the nanofiller and LiClO4 as the lithium-ion source via the solvent casting method. A pristine PVDF–HFP NCPE sample with 2 wt% nanofiller was also prepared for comparison. The Mn3O4 nanoparticles were synthesized by the precipitation method using CTAB as a templating agent and MnCl2·4H2O as the precursor. FTIR spectroscopy showed that while pristine PVDF–HFP forms a nonpolar α-phase, the incorporation of salt and nanofiller induced a mixed β and γ crystal phase, indicating interaction between the matrix and additives. Surface morphology studies showed that the NCPEs had a denser surface than pristine PVDF–HFP, with no PEG spherulite formation detected in polarized optical micrographs. Electrochemical impedance spectroscopy revealed that the 2% blend NCPE exhibited the highest ion conductivity of 3.1 × 10−4 S cm−1 at 80 °C, an order of magnitude higher than the pristine NCPE (5.1 × 10−5 S cm−1). Temperature-dependent ion conductivity followed Arrhenius behavior, indicating a thermally activated ion hopping mechanism. The dielectric relaxation peak shifted to higher frequency with increasing temperature, suggesting faster ion dynamics and improved conductivity.