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Experimental and DFT investigation of LiFePO₄/graphene composites prepared via shear exfoliation route

International Journal of Renewable Energy Development : JRED · Vol. 15 No. 2 (2026) · hlm. 266–277

DOI
10.61435/ijred.2026.61976
ISSN
2252-4940
Terbit
2026-03-01
Penerbit
Center of Biomass & Renewable Energy (CBIORE)
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-sa/4.0

Abstrak

The performance of LiFePO₄ (LFP) cathodes was successfully enhanced by incorporating two types of graphene obtained through green and low-cost liquid shear exfoliation processes. Commercial LFP was combined with few-layer graphene (FLG) and very few-layer graphene (VFLG), with compositions ranging from 0-4 wt.%. LFP, LFP/FLG, and LFP/VFLG, were characterized using electrochemical impedance spectroscopy (EIS), charge–discharge (CD), XRD, FTIR, and FESEM–EDX. Density functional theory (DFT) calculations were further employed to probe the electronic structure of LFP and an idealized LFP(001)/pristine-graphene interface as a baseline model for interfacial electronic coupling. DFT indicated interfacial charge redistribution and the emergence of C-2p π-derived states near the Fermi level, resulting in bandgap narrowing relative to pristine LFP and suggesting an additional electronic percolation pathway at the interface. Experimentally, EIS showed that VFLG reduced charge-transfer resistance and increased effective electrochemical conductivity, while FLG addition was associated with improved interfacial charge-transfer behavior inferred from EIS. CD tests at 0.5 C showed that the 4 wt.% FLG and 4 wt.% VFLG electrodes delivered the highest specific capacities of 29.98 mAh/g and 44.66 mAh/g, corresponding to increases of 81.9% and 170.5% compared to bare LFP. XRD and FTIR confirmed that LFP phase integrity was maintained, and FESEM–EDX revealed a uniform particle distribution with well-dispersed graphene networks. Overall, these results demonstrated that shear-exfoliated graphene effectively improved electronic connectivity and charge-transfer behavior in LFP cathodes, supported by consistent electrochemical measurements and electronic-structure insights from DFT.

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  • Indonesia Open University
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  • United Arab Emirates University
  • Ming Chi University of Technology
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Rekan penulisOrganisasiArtikel bersama
Zhong‐Tao JiangMurdoch University5
Yola Bertilsya HendriRiau University5
Sentot Budi RahardjoSebelas Maret University2
Nurma Yunita IndriyantiSebelas Maret University2
Desi HeltinaRiau University2
Endang SusilowatiSebelas Maret University2
EvelynAtma Jaya Catholic University of Indonesia2
ChairulAfiliasi tidak diketahui2
Dhina FebryzaRiau University2
Hussein Ali Jan MiranUniversity of Baghdad2
Lina MahardianiSebelas Maret University2
Alpahmi Aji SatriaSebelas Maret University1
SutarnoAfiliasi tidak diketahui1
HarjanaSebelas Maret University1
Fais Nurul HadiCharles Darwin University1
Riezky Maya ProbosariSebelas Maret University1
Fatma WidyastutiSebelas Maret University1
SajidanAfiliasi tidak diketahui1
SUTIKNOState University of Semarang1
FadloliIndonesia Open University1
Dimas FahrudinSebelas Maret University1
Sarwanto SarwantoSebelas Maret University1
S. S. SauliUniversity of Technology Malaysia1
Q. QiaoLuAfiliasi tidak diketahui1
Murwani Dewi WijayantiSebelas Maret University1
Sri MulyaniIndonesia University of Education1
Inas SausanIndonesia Open University1
Yayan SetiawanAfiliasi tidak diketahui1
Raihan Daffansyah SinagaAfiliasi tidak diketahui1

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Sumber metadata: OAI-PMH (metadata jurnal) https://ijred.cbiore.id/index.php/ijred/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en-US">Experimental and DFT investigation of LiFePO₄/graphene composites prepared via shear exfoliation route</dc:title>
	<dc:creator>Amri, Amun</dc:creator>
	<dc:creator>Mawaddah, Mawaddah</dc:creator>
	<dc:creator>Alfatlian, Alfatlian</dc:creator>
	<dc:creator>Sunarno, Sunarno</dc:creator>
	<dc:creator>Murdiya, Fri</dc:creator>
	<dc:creator>Assylzhan, Mazhibayev</dc:creator>
	<dc:creator>Jumbri, Khairulazhar</dc:creator>
	<dc:creator>Altarawneh, Mohammednoor</dc:creator>
	<dc:creator>Yang, Chun-Chen</dc:creator>
	<dc:creator>Saputro, Sulistyo</dc:creator>
	<dc:creator>Rahman, M Mahbubur</dc:creator>
	<dc:subject xml:lang="en-US">LiFePO4 cathode; Graphene composite; Electrochemical performances; DFT</dc:subject>
	<dc:description xml:lang="en-US">The performance of LiFePO₄ (LFP) cathodes was successfully enhanced by incorporating two types of graphene obtained through green and low-cost liquid shear exfoliation processes. Commercial LFP was combined with few-layer graphene (FLG) and very few-layer graphene (VFLG), with compositions ranging from 0-4 wt.%. LFP, LFP/FLG, and LFP/VFLG, were characterized using electrochemical impedance spectroscopy (EIS), charge–discharge (CD), XRD, FTIR, and FESEM–EDX. Density functional theory (DFT) calculations were further employed to probe the electronic structure of LFP and an idealized LFP(001)/pristine-graphene interface as a baseline model for interfacial electronic coupling. DFT indicated interfacial charge redistribution and the emergence of C-2p π-derived states near the Fermi level, resulting in bandgap narrowing relative to pristine LFP and suggesting an additional electronic percolation pathway at the interface. Experimentally, EIS showed that VFLG reduced charge-transfer resistance and increased effective electrochemical conductivity, while FLG addition was associated with improved interfacial charge-transfer behavior inferred from EIS. CD tests at 0.5 C showed that the 4 wt.% FLG and 4 wt.% VFLG electrodes delivered the highest specific capacities of 29.98 mAh/g and 44.66 mAh/g, corresponding to increases of 81.9% and 170.5% compared to bare LFP. XRD and FTIR confirmed that LFP phase integrity was maintained, and FESEM–EDX revealed a uniform particle distribution with well-dispersed graphene networks. Overall, these results demonstrated that shear-exfoliated graphene effectively improved electronic connectivity and charge-transfer behavior in LFP cathodes, supported by consistent electrochemical measurements and electronic-structure insights from DFT.</dc:description>
	<dc:publisher xml:lang="en-US">Center of Biomass &amp; Renewable Energy (CBIORE)</dc:publisher>
	<dc:date>2026-03-01</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en-US"></dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://ijred.cbiore.id/index.php/ijred/article/view/61976</dc:identifier>
	<dc:identifier>10.61435/ijred.2026.61976</dc:identifier>
	<dc:source xml:lang="en-US">International Journal of Renewable Energy Development; Vol 15, No 2 (2026): March 2026; 266-277</dc:source>
	<dc:source>2252-4940</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://ijred.cbiore.id/index.php/ijred/article/view/61976/pdf</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2026 The Author(s). Published by Centre of Biomass and Renewable Energy (CBIORE)</dc:rights>
	<dc:rights xml:lang="en-US">https://creativecommons.org/licenses/by-sa/4.0</dc:rights>
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