Synthesis And Electrochemical Behavior Of Lifepo4/C With Air-Electrode For Aqueous Lithium Ion Battery

An aqueous rechargeable lithium ion battery (ARLB) has become a great solution to overwhelm the cost and safety issue of the conventional lithium ion battery with organic electrolyte. Recently, the in situ carbon layer was proven to avoid any direct contact between the nanoparticles and the environm...

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Main Author: Alias, Nurhaswani
Format: Thesis
Language:English
Published: 2015
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Online Access:http://eprints.usm.my/40948/1/NURHASWANI_BINTI_ALIAS_24_pages.pdf
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spelling my-usm-ep.409482018-07-09T02:32:40Z Synthesis And Electrochemical Behavior Of Lifepo4/C With Air-Electrode For Aqueous Lithium Ion Battery 2015 Alias, Nurhaswani TN Mining Engineering. Metallurgy An aqueous rechargeable lithium ion battery (ARLB) has become a great solution to overwhelm the cost and safety issue of the conventional lithium ion battery with organic electrolyte. Recently, the in situ carbon layer was proven to avoid any direct contact between the nanoparticles and the environment, including O2 and H2O. This help to achieve high capacity battery with improved capacity retention in aqueous environment. A citric acid assisted sol-gel method is employed in this study to prepare carbon-coated lithium iron phosphate (LiFePO4/C) using different calcination temperatures (500–800 °C). The phase structure and elemental analyses confirmed the orthorhombic crystal structure of LiFePO4 surrounded by different amounts of carbon layer. The morphologies and physical absorption results proved the porous structure of LiFePO4/C with a mesoporous range. The calcination temperature influences the crystallite size, impurity phase, and surface area as the LiFePO4/C calcined at 700 °C offered the optimum properties. This finding was supported by the electrochemical behavior of LiFePO4/C in the ARLB system with an air-electrode. The LiFePO4/C calcined at 700 °C showed the highest current response for cyclic voltammetry and the lowest impedance (6.11 Ω) with a good discharge capacity (83 mA h g−1 at 1.0 C). In addition, good cycling stability was achieved as the LiFePO4/C maintained a discharge capacity of approximately 90 mA h g−1 within 30 cycles at 0.5 C. By contrast, bare LiFePO4, which was calcined at the same calcination temperature (700 °C), exhibited poor electrochemical performance with high capacity fading (45 % within 30 cycles at 0.5 C) because of high 2 impedance (18.98 Ω). The rate capability of the LiFePO4/C calcined at 700 °C was also compared with that of a platinum counter electrode; the air-electrode still showed better cycling behavior. 2015 Thesis http://eprints.usm.my/40948/ http://eprints.usm.my/40948/1/NURHASWANI_BINTI_ALIAS_24_pages.pdf application/pdf en public masters Universiti Sains Malaysia Pusat Pengajian Kejuruteraan Bahan dan Sumber Mineral
institution Universiti Sains Malaysia
collection USM Institutional Repository
language English
topic TN Mining Engineering
Metallurgy
spellingShingle TN Mining Engineering
Metallurgy
Alias, Nurhaswani
Synthesis And Electrochemical Behavior Of Lifepo4/C With Air-Electrode For Aqueous Lithium Ion Battery
description An aqueous rechargeable lithium ion battery (ARLB) has become a great solution to overwhelm the cost and safety issue of the conventional lithium ion battery with organic electrolyte. Recently, the in situ carbon layer was proven to avoid any direct contact between the nanoparticles and the environment, including O2 and H2O. This help to achieve high capacity battery with improved capacity retention in aqueous environment. A citric acid assisted sol-gel method is employed in this study to prepare carbon-coated lithium iron phosphate (LiFePO4/C) using different calcination temperatures (500–800 °C). The phase structure and elemental analyses confirmed the orthorhombic crystal structure of LiFePO4 surrounded by different amounts of carbon layer. The morphologies and physical absorption results proved the porous structure of LiFePO4/C with a mesoporous range. The calcination temperature influences the crystallite size, impurity phase, and surface area as the LiFePO4/C calcined at 700 °C offered the optimum properties. This finding was supported by the electrochemical behavior of LiFePO4/C in the ARLB system with an air-electrode. The LiFePO4/C calcined at 700 °C showed the highest current response for cyclic voltammetry and the lowest impedance (6.11 Ω) with a good discharge capacity (83 mA h g−1 at 1.0 C). In addition, good cycling stability was achieved as the LiFePO4/C maintained a discharge capacity of approximately 90 mA h g−1 within 30 cycles at 0.5 C. By contrast, bare LiFePO4, which was calcined at the same calcination temperature (700 °C), exhibited poor electrochemical performance with high capacity fading (45 % within 30 cycles at 0.5 C) because of high 2 impedance (18.98 Ω). The rate capability of the LiFePO4/C calcined at 700 °C was also compared with that of a platinum counter electrode; the air-electrode still showed better cycling behavior.
format Thesis
qualification_level Master's degree
author Alias, Nurhaswani
author_facet Alias, Nurhaswani
author_sort Alias, Nurhaswani
title Synthesis And Electrochemical Behavior Of Lifepo4/C With Air-Electrode For Aqueous Lithium Ion Battery
title_short Synthesis And Electrochemical Behavior Of Lifepo4/C With Air-Electrode For Aqueous Lithium Ion Battery
title_full Synthesis And Electrochemical Behavior Of Lifepo4/C With Air-Electrode For Aqueous Lithium Ion Battery
title_fullStr Synthesis And Electrochemical Behavior Of Lifepo4/C With Air-Electrode For Aqueous Lithium Ion Battery
title_full_unstemmed Synthesis And Electrochemical Behavior Of Lifepo4/C With Air-Electrode For Aqueous Lithium Ion Battery
title_sort synthesis and electrochemical behavior of lifepo4/c with air-electrode for aqueous lithium ion battery
granting_institution Universiti Sains Malaysia
granting_department Pusat Pengajian Kejuruteraan Bahan dan Sumber Mineral
publishDate 2015
url http://eprints.usm.my/40948/1/NURHASWANI_BINTI_ALIAS_24_pages.pdf
_version_ 1747820846128300032