Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent
Li1-xNi1+xO2 powder was synthesized by polymerised complex method using malonic acid as a chelating agent. The carboxylate precursor was calcined in the temperature range 650-800°C for 14-48 h. The TG curves of malonic acid, lithium acetate dihydrate, nickel acetate tetrahydrate and the precursor we...
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th-cmuir.6653943832-50192014-08-30T02:56:04Z Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent Thongtem T. Thongtem S. Li1-xNi1+xO2 powder was synthesized by polymerised complex method using malonic acid as a chelating agent. The carboxylate precursor was calcined in the temperature range 650-800°C for 14-48 h. The TG curves of malonic acid, lithium acetate dihydrate, nickel acetate tetrahydrate and the precursor were studied at 29.52-600°C. The FTIR spectra of the precursor without and with 650-800°C calcination were used to explain the vibrational bonding. At 750°C and above, only Li 1-xNi1+xO2phase was detected. The maximum [I(003/I(104)] and minimum [I(006+102)/I (101)] intensity ratios of the XRD spectra were used to determine the optimum temperature and time of calcination for preparation of Li 1-xNi1+xO2 powder. In addition, formation mechanism of Li1-xNi1+xO2 is proposed. The content of nickel, lithium, Ni3+/(Ni3+ + Ni2+) and mean oxidation state of nickel at 650-800°C were determined and they show very good agreement. The SEM micrograph is also used to explain the morphology of the powder. © 2004 Elsevier Ltd and Techna Group S.r.l. All rights reserved. 2014-08-30T02:56:04Z 2014-08-30T02:56:04Z 2005 Article 02728842 10.1016/j.ceramint.2004.05.007 CINND http://www.scopus.com/inward/record.url?eid=2-s2.0-10444219580&partnerID=40&md5=1749384900fdbc27405b5aaba1ba7988 http://cmuir.cmu.ac.th/handle/6653943832/5019 English |
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Li1-xNi1+xO2 powder was synthesized by polymerised complex method using malonic acid as a chelating agent. The carboxylate precursor was calcined in the temperature range 650-800°C for 14-48 h. The TG curves of malonic acid, lithium acetate dihydrate, nickel acetate tetrahydrate and the precursor were studied at 29.52-600°C. The FTIR spectra of the precursor without and with 650-800°C calcination were used to explain the vibrational bonding. At 750°C and above, only Li 1-xNi1+xO2phase was detected. The maximum [I(003/I(104)] and minimum [I(006+102)/I (101)] intensity ratios of the XRD spectra were used to determine the optimum temperature and time of calcination for preparation of Li 1-xNi1+xO2 powder. In addition, formation mechanism of Li1-xNi1+xO2 is proposed. The content of nickel, lithium, Ni3+/(Ni3+ + Ni2+) and mean oxidation state of nickel at 650-800°C were determined and they show very good agreement. The SEM micrograph is also used to explain the morphology of the powder. © 2004 Elsevier Ltd and Techna Group S.r.l. All rights reserved. |
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Thongtem T. Thongtem S. |
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Thongtem T. Thongtem S. Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent |
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Thongtem T. Thongtem S. |
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Thongtem T. |
title |
Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent |
title_short |
Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent |
title_full |
Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent |
title_fullStr |
Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent |
title_full_unstemmed |
Synthesis of Li1-xNi1+xO2 using malonic acid as a chelating agent |
title_sort |
synthesis of li1-xni1+xo2 using malonic acid as a chelating agent |
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2014 |
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http://www.scopus.com/inward/record.url?eid=2-s2.0-10444219580&partnerID=40&md5=1749384900fdbc27405b5aaba1ba7988 http://cmuir.cmu.ac.th/handle/6653943832/5019 |
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