Enhancement of the Desorption Properties of LiAlH<sub>4</sub> by the Addition of LaCoO<sub>3</sub>

The high hydrogen storage capacity (10.5 wt.%) and release of hydrogen at a moderate temperature make LiAlH<sub>4</sub> an appealing material for hydrogen storage. However, LiAlH<sub>4</sub> suffers from slow kinetics and irreversibility. Hence, LaCoO<sub>3</sub>...

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Main Authors: Noratiqah Sazelee, Nurul Amirah Ali, Mohammad Ismail, Sami-Ullah Rather, Hisham S. Bamufleh, Hesham Alhumade, Aqeel Ahmad Taimoor, Usman Saeed
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Materials
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Online Access:https://www.mdpi.com/1996-1944/16/11/4056
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author Noratiqah Sazelee
Nurul Amirah Ali
Mohammad Ismail
Sami-Ullah Rather
Hisham S. Bamufleh
Hesham Alhumade
Aqeel Ahmad Taimoor
Usman Saeed
author_facet Noratiqah Sazelee
Nurul Amirah Ali
Mohammad Ismail
Sami-Ullah Rather
Hisham S. Bamufleh
Hesham Alhumade
Aqeel Ahmad Taimoor
Usman Saeed
author_sort Noratiqah Sazelee
collection DOAJ
description The high hydrogen storage capacity (10.5 wt.%) and release of hydrogen at a moderate temperature make LiAlH<sub>4</sub> an appealing material for hydrogen storage. However, LiAlH<sub>4</sub> suffers from slow kinetics and irreversibility. Hence, LaCoO<sub>3</sub> was selected as an additive to defeat the slow kinetics problems of LiAlH<sub>4</sub>. For the irreversibility part, it still required high pressure to absorb hydrogen. Thus, this study focused on the reduction of the onset desorption temperature and the quickening of the desorption kinetics of LiAlH<sub>4</sub>. Here, we report the different weight percentages of LaCoO<sub>3</sub> mixed with LiAlH<sub>4</sub> using the ball-milling method. Interestingly, the addition of 10 wt.% of LaCoO<sub>3</sub> resulted in a decrease in the desorption temperature to 70 °C for the first stage and 156 °C for the second stage. In addition, at 90 °C, LiAlH<sub>4</sub> + 10 wt.% LaCoO<sub>3</sub> can desorb 3.37 wt.% of H<sub>2</sub> in 80 min, which is 10 times faster than the unsubstituted samples. The activation energies values for this composite are greatly reduced to 71 kJ/mol for the first stages and 95 kJ/mol for the second stages compared to milled LiAlH<sub>4</sub> (107 kJ/mol and 120 kJ/mol for the first two stages, respectively). The enhancement of hydrogen desorption kinetics of LiAlH<sub>4</sub> is attributed to the in situ formation of AlCo and La or La-containing species in the presence of LaCoO<sub>3</sub>, which resulted in a reduction of the onset desorption temperature and activation energies of LiAlH<sub>4</sub>.
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spelling doaj.art-a9de5791b79e479c955fc97df07557a82023-11-18T08:09:39ZengMDPI AGMaterials1996-19442023-05-011611405610.3390/ma16114056Enhancement of the Desorption Properties of LiAlH<sub>4</sub> by the Addition of LaCoO<sub>3</sub>Noratiqah Sazelee0Nurul Amirah Ali1Mohammad Ismail2Sami-Ullah Rather3Hisham S. Bamufleh4Hesham Alhumade5Aqeel Ahmad Taimoor6Usman Saeed7Energy Storage Research Group, Faculty of Ocean Engineering Technology and Informatics, Universiti Malaysia Terengganu, Kuala Nerus 21030, Terengganu, MalaysiaEnergy Storage Research Group, Faculty of Ocean Engineering Technology and Informatics, Universiti Malaysia Terengganu, Kuala Nerus 21030, Terengganu, MalaysiaEnergy Storage Research Group, Faculty of Ocean Engineering Technology and Informatics, Universiti Malaysia Terengganu, Kuala Nerus 21030, Terengganu, MalaysiaDepartment of Chemical and Materials Engineering, King Abdulaziz University, P.O. Box 80204, Jeddah 21589, Saudi ArabiaDepartment of Chemical and Materials Engineering, King Abdulaziz University, P.O. Box 80204, Jeddah 21589, Saudi ArabiaDepartment of Chemical and Materials Engineering, King Abdulaziz University, P.O. Box 80204, Jeddah 21589, Saudi ArabiaDepartment of Chemical and Materials Engineering, King Abdulaziz University, P.O. Box 80204, Jeddah 21589, Saudi ArabiaDepartment of Chemical and Materials Engineering, King Abdulaziz University, P.O. Box 80204, Jeddah 21589, Saudi ArabiaThe high hydrogen storage capacity (10.5 wt.%) and release of hydrogen at a moderate temperature make LiAlH<sub>4</sub> an appealing material for hydrogen storage. However, LiAlH<sub>4</sub> suffers from slow kinetics and irreversibility. Hence, LaCoO<sub>3</sub> was selected as an additive to defeat the slow kinetics problems of LiAlH<sub>4</sub>. For the irreversibility part, it still required high pressure to absorb hydrogen. Thus, this study focused on the reduction of the onset desorption temperature and the quickening of the desorption kinetics of LiAlH<sub>4</sub>. Here, we report the different weight percentages of LaCoO<sub>3</sub> mixed with LiAlH<sub>4</sub> using the ball-milling method. Interestingly, the addition of 10 wt.% of LaCoO<sub>3</sub> resulted in a decrease in the desorption temperature to 70 °C for the first stage and 156 °C for the second stage. In addition, at 90 °C, LiAlH<sub>4</sub> + 10 wt.% LaCoO<sub>3</sub> can desorb 3.37 wt.% of H<sub>2</sub> in 80 min, which is 10 times faster than the unsubstituted samples. The activation energies values for this composite are greatly reduced to 71 kJ/mol for the first stages and 95 kJ/mol for the second stages compared to milled LiAlH<sub>4</sub> (107 kJ/mol and 120 kJ/mol for the first two stages, respectively). The enhancement of hydrogen desorption kinetics of LiAlH<sub>4</sub> is attributed to the in situ formation of AlCo and La or La-containing species in the presence of LaCoO<sub>3</sub>, which resulted in a reduction of the onset desorption temperature and activation energies of LiAlH<sub>4</sub>.https://www.mdpi.com/1996-1944/16/11/4056LiAlH<sub>4</sub>LaCoO<sub>3</sub>solid-state hydrogen storagemetal oxide
spellingShingle Noratiqah Sazelee
Nurul Amirah Ali
Mohammad Ismail
Sami-Ullah Rather
Hisham S. Bamufleh
Hesham Alhumade
Aqeel Ahmad Taimoor
Usman Saeed
Enhancement of the Desorption Properties of LiAlH<sub>4</sub> by the Addition of LaCoO<sub>3</sub>
Materials
LiAlH<sub>4</sub>
LaCoO<sub>3</sub>
solid-state hydrogen storage
metal oxide
title Enhancement of the Desorption Properties of LiAlH<sub>4</sub> by the Addition of LaCoO<sub>3</sub>
title_full Enhancement of the Desorption Properties of LiAlH<sub>4</sub> by the Addition of LaCoO<sub>3</sub>
title_fullStr Enhancement of the Desorption Properties of LiAlH<sub>4</sub> by the Addition of LaCoO<sub>3</sub>
title_full_unstemmed Enhancement of the Desorption Properties of LiAlH<sub>4</sub> by the Addition of LaCoO<sub>3</sub>
title_short Enhancement of the Desorption Properties of LiAlH<sub>4</sub> by the Addition of LaCoO<sub>3</sub>
title_sort enhancement of the desorption properties of lialh sub 4 sub by the addition of lacoo sub 3 sub
topic LiAlH<sub>4</sub>
LaCoO<sub>3</sub>
solid-state hydrogen storage
metal oxide
url https://www.mdpi.com/1996-1944/16/11/4056
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