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  <titleInfo>
    <title>Morphological control of ternary composite innickel-cobalt-manganese system and enhancing surface of porous carbon using sunlight for energy storage application</title>
  </titleInfo>
  <name type="personal">
    <namePart>Ling Jin Kiong</namePart>
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    <dateIssued encoding="marc">2024</dateIssued>
    <copyrightDate encoding="marc">2024</copyrightDate>
    <issuance>monographic</issuance>
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  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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  <physicalDescription>
    <extent>xxiv, 240 pages : illustrations ; 30 cm.</extent>
  </physicalDescription>
  <abstract>Energy storage devices under lithium-ion battery and electrochemical capacitor storage  modes are currently commercial; however, increasing their performance indicators such  as specific energy and power as well as the charge-discharge cycle lifetime is an  ongoing research topic. Often composite materials containing two or more components  are required to serve a device functionality; and in the case of energy storage devices,  composites of two ternary metal oxide have never been examined as an anode. Besides,  the volume changes (isotropic/anisotropic) of transition metal oxide composite anode  could significantly impact the cycling stability and need to be investigated. For the  porous carbon cathode, capability of enhancing the surface of carbon through surface  modification technique that does not depend on high temperature annealing and toxic  chemical is equally important. Electrolyte modification for wider electrochemical  potential window and inducing redox reaction (either bulk or surface-limited) is equally  important to achieve improved specific energy and power. Herein, ternary metal oxide  system consisting of nickel, cobalt, and manganese with two different morphologies  (one-dimensional fiber and three-dimensional octahedron) were synthesized,  characterized, and compared. For the first time, the formation of octahedron was  achieved through electrospinning technique during this study. The nickel-cobaltmanganese system (regardless of the morphology) could offer specific capacity &gt;1000  mAh/g at a current density of 100 mA/g. During charge-discharge cycling, the quasianisotropic volume changes of octahedrons significantly maintained the crystal  structure of the nickel-cobalt-manganese system, leading to a superior capacity  retention of 72.1%, compared to 24.1% capacity retention in fibers. On the other hand,  the surface of the porous carbon was treated with 20 seconds of focused sunlight under  mild vacuum conditions. Trapped moisture was released under illumination as steam,  creating an environment identical to the physical activation process, etching the surface  and enhanced porosity. The treated porous carbon leads to 50% enhancement on its  electrochemical performance. Using this solar activation process, a procedure to regain  95% of the electrochemical properties of degraded carbon electrode was also  established. Regarding the electrolyte modification, a carbon symmetric supercapacitor  with 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid as the electrolyte  offered a 4-fold improvement in specific energy as compared to the aqueous electrolyte  (2M potassium hydroxide), owing to its exceptional high operating voltage of 3V.  Addition of lithium perchlorate at a concentration of 0.5M doubled the specific energy  of the symmetric device. Addition of lithium salts also induced surface redox reaction  on the metal oxide electrode, enhancing its specific energy by an order of magnitude.  Thus, this study presents advanced electrochemical energy storage devices with  improved performance indicators by appropriately tailoring the materials properties of  anode, cathode, and electrolyte.</abstract>
  <targetAudience authority="marctarget">specialized</targetAudience>
  <note type="statement of responsibility">Ling Jin Kiong</note>
  <note>Faculty of Industrial Management</note>
  <note>Thesis (Doctor of Philosophy) -- Universiti Malaysia Pahang – 2023</note>
  <note>Includes bibliographical references</note>
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    <name type="corporate">
      <namePart>Faculty of Industrial Management</namePart>
    </name>
    <topic>Dissertations</topic>
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  <subject authority="lcsh">
    <topic>Universities and colleges</topic>
    <topic>Dissertations</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Theses</topic>
    <topic>Dissertations</topic>
  </subject>
  <identifier type="isbn">THE0009894 (Local)</identifier>
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    <recordCreationDate encoding="marc">240726</recordCreationDate>
    <recordChangeDate encoding="iso8601">20251125110909.0</recordChangeDate>
    <languageOfCataloging>
      <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
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