MARC details
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04197nam a2200361 i 4500 |
| 003 - CONTROL NUMBER IDENTIFIER |
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MY-KuUP |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
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20251125110753.0 |
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t||||fr|||| 000 0 |
| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION |
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ta |
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230720t20232023my a|||fr|||| 000 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
THE0009668 (Local) |
| Qualifying information |
Hardback |
| 040 ## - CATALOGING SOURCE |
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| Original cataloging agency |
UMP |
| Language of cataloging |
eng |
| Transcribing agency |
UMP |
| Description conventions |
rda |
| 090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN) |
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| Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) |
FIST .S86 2023 r Thesis |
| 100 1# - MAIN ENTRY--PERSONAL NAME |
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| Personal name |
Vaishak, Sunil, |
| Relator term |
author. |
| 245 10 - TITLE STATEMENT |
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| Title |
Surface engineering of commercial activated carbon for improving the charge storability of electrochemical capacitors / |
| Statement of responsibility, etc. |
Sunil Vaishak |
| 264 ## - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE |
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| Place of production, publication, distribution, manufacture |
Kuantan, Pahang : |
| Name of producer, publisher, distributor, manufacturer |
UMP, |
| Date of production, publication, distribution, manufacture, or copyright notice |
2023 |
| 264 ## - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE |
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| Date of production, publication, distribution, manufacture, or copyright notice |
©2023 |
| 300 ## - PHYSICAL DESCRIPTION |
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| Extent |
xiii, 120 p. : |
| Other physical details |
illustration |
| Dimensions |
30 cm. + |
| Accompanying material |
1 CD-ROM |
| 336 ## - CONTENT TYPE |
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| Source |
rdacontent |
| Content type term |
text |
| 336 ## - CONTENT TYPE |
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| Source |
rdacontent |
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text |
| 337 ## - MEDIA TYPE |
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| Source |
rdamedia |
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unmediated |
| 337 ## - MEDIA TYPE |
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| Source |
rdamedia |
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computer |
| 338 ## - CARRIER TYPE |
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| Source |
rdacarrier |
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volume |
| 338 ## - CARRIER TYPE |
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| Source |
rdacarrier |
| Carrier type term |
computer disc |
| 347 ## - DIGITAL FILE CHARACTERISTICS |
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| Source |
rda |
| File type |
text file |
| Encoding format |
PDF |
| 500 ## - GENERAL NOTE |
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| General note |
Faculty of Industrial Sciences and Technology |
| 502 ## - DISSERTATION NOTE |
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| Dissertation note |
Thesis (Master of Science) -- Universiti Malaysia Pahang – 2023 |
| 504 ## - BIBLIOGRAPHY, ETC. NOTE |
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| Bibliography, etc. note |
Supercapacitors based on activated carbon are the representatives of sustainable devices among electrochemical energy storage devices because of their renewable electrode materials, eco-friendliness, longer life cycle and superior charge-discharge rate capabilities. However, to expand their commercial value, their current energy densities should be made comparable with the market leading Lithium-ion batteries. One of the approaches to increase the energy density is by maximizing the number of pores to incorporate more ions. A majority of the research on supercapacitors demonstrated excellent laboratory-scale results through improving porosity, where the mass loading of such electrodes has a staggering difference from the industrial standards. These factors predominantly suppressed the initiatives to lift the biomass-derived carbon-based electrodes into the commercial picture. To address this issue, the present thesis focuses on expanding the electrochemical properties of commercial activated carbon derived from palm kernel shells by engineering its porosity in an eco-friendly and cost-effective manner. Herein, we employ the nitric acid refluxing method for the activation purpose, which, unlike the conventional routes, not only limits the usage of harsh chemicals, but also enables recyclability. We have optimized the performance of the electrode materials by refluxing the activated carbon for various acid to precursor ratios and refluxing duration. The electrochemical performances of the resulting materials were examined in a three-electrode system configuration in 1 M sodium sulphate electrolyte. The specific capacitance of the optimum sample was increased ~110% following a significant reduction in Warburg impedance. To understand the physicochemical alterations introduced upon refluxing, the as-synthesized carbon samples were characterized using X-ray Diffraction, Fourier Transform Infrared Spectroscopy, Scanning ElectronMicroscopy, Energy Dispersive Spectroscopy, and gas adsorption measurements. With~75% increment, a highest surface area of ~722 m2·g-1 was recorded for the 72 hoursrefluxed sample, which aligns with the increased electrochemical performance incorresponding electrodes. Further, supercapacitor devices were fabricated using thisoptimized sample by varying the mass loading (~3, ~6, ~9, ~12, and ~14 mg·cm2), andthe electrochemical properties were studied. All the fabricated devices achieved apotential window of 1.8 V in 1 M sodium sulphate. The highest mass loaded (~14 mg·cm-2)device fabricated using the prepared material has delivered a maximum arealcapacitance of ~494 mF·cm-2, an energy density of ~13 mWh·cm-3, and a maximumpower density of ~2189 mW·cm-3. The current research thereby demonstrates anenvironmentally friendly and economic approach for engineering the porosity ofcommercial activated carbon to enhance the charge storability for practical applications. |
| 610 20 - SUBJECT ADDED ENTRY--CORPORATE NAME |
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| Corporate name or jurisdiction name as entry element |
Faculty of Industrial Sciences and Technology |
| General subdivision |
Dissertations |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Universities and colleges |
| General subdivision |
Dissertations |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Theses |
| General subdivision |
Dissertations |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) |
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| Source of classification or shelving scheme |
Library of Congress Classification |
| Koha item type |
Thesis |