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Diff Summary

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Visual Assets

这是实际图表资产输出,不是审计层重新推断。

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1figureDocling Figure 11missing_caption0.55[201.74, 410.5, 334.56, 168.78]
2figureFig. 14direct_caption_ref0.82[39.05, 271.2, 518.3, 436.69]Fig. 1. (a) Schematic illustrating the suppression of surface degradation (Mn dissolution, O2 evolution, and rock-salt phase transformation) by the carbon-coated LiFePO4 (C-LFP) layer. (b) X-ray diffraction (XRD) pattern of pristine Li-rich Mn-based layered oxide (LMR); the inset highlights superlattice reflections (20 -23 ◦ ). (c) XRD patterns of samples with various C-LFP loadings. (d) Comparison of LMR@F2.0 with the corresponding physical mixture (LMR + 2.0 wt% C-LFP).
3figureFig. 25direct_caption_ref0.82[39.28, 391.82, 515.49, 296.03]Fig. 2. Field-emission scanning electron microscopy (FE-SEM) images of the (a) hydroxide precursor and (b) pristine LMR revealing a hierarchical structure composed of spherical secondary and granular primary particles. (c -f) Surface FE-SEM images of LMR@F0.5 -;2.0 demonstrating the formation of a discrete islandlike coating morphology progressively densifying with increasing C-LFP loading. (g) Cross-sectional FE-SEM image and (h) corresponding energy-dispersive X-ray spectroscopy (EDS) line profile of LMR@F0.75. (i -l) EDS elemental mappings of Fe (red) obtained for LMR@F0.5 -;2.0. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
4figureFig. 36direct_caption_ref0.82[38.6, 56.38, 517.79, 317.71]Fig. 3. (a) Initial charge -discharge voltage profiles recorded at 0.1C. (b) Results of rate capability tests. (c) Capacity retention and coulombic efficiency evolution during 200 cycles at 0.5C. Charge -discharge voltage profiles of (d) pristine LMR and (e) LMR@F0.75 at selected cycles (initial, 1st, 50th, 100th, 150th, and 200th). (f) Evolution of average discharge voltage over 200 cycles.
5figureFig. 47direct_caption_ref0.82[39.4, 55.85, 518.05, 311.52]Fig. 4. (a) Volume resistivities of different electrode. (b -d) Li-ion diffusion coefficients ( D Li + ) as functions of voltage determined during discharge: (b) full voltage range, (c) magnified view of the 3.2 -3.5 V region showing enhanced kinetics near the LFP activation potential, and (d) the 3.6 -4.0 V region. Nyquist plots of LMR half-cells recorded (e) in the fresh state (at open-circuit voltage) and (f) after the third initial cycle.
6figureFig. 59direct_caption_ref0.82[39.74, 54.63, 515.75, 435.71]Fig. 5. (a -l) High-resolution transmission electron microscopy (HRTEM) analysis of electrodes after three initial cycles. Low-magnification images of a single particle of (a) pristine LMR and (g) LMR@F0.75. (b, h) HRTEM images focusing on the near-surface region. (c, d) Magnified lattice image and corresponding fast Fourier transform (FFT) pattern of the pristine LMR surface revealing the formation of a degraded rock-salt phase ( Fm 3 m ). (e, f) Magnified lattice image and FFT pattern of pristine LMR bulk showing the original layered structure ( R 3 m ). (i, j) Magnified lattice image and FFT pattern of the LMR@F0.75 surface confirming the preservation of the Li2MnO3-like superlattice structure ( C 2/ m ). (k, l) Magnified lattice image and FFT pattern of the LMR@F0.75 bulk ( R 3 m ). (m, n) In situ differential electrochemical mass spectrometry profiles showing O2 and CO2 evolution during the first charge. (o) Differential scanning calorimetry curves of charged cathodes.

Excluded Blocks

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[37.59, 168.03, 419.45, 46.81]Decoupling activation from passivation in high-rate Li-rich Mn-based layered oxides through the construction of a conductive LiFePO4 island architectureDecoupling activation from passivation in high-rate Li-rich Mn-based layered oxides through the construction of a conductive LiFePO4 island architecture
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[201.99, 375.28, 125.99, 6.4]G R A P H I C A L A B S T R A C TG R A P H I C A L A B S T R A C T
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[37.59, 394.76, 135.36, 25.68]A scalable solvent-free mechanofusion process constructs discrete LiFePO4 island architectures on LMR surfaces.A scalable solvent-free mechanofusion process constructs discrete LiFePO4 island architectures on LMR surfaces.
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[37.59, 423.95, 135.37, 25.69]This unique insular coating decouples bulk activation from surface passivation to suppress inherent voltage decay.This unique insular coating decouples bulk activation from surface passivation to suppress inherent voltage decay.
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[37.59, 227.09, 422.38, 37.94]Eunki Kim a,1 , Joo-Hyung Kim b,1 , Joon Ha Chang c,1 , Juhyoung Kim a,d , Jun Ho Shin a,e , Junhee Lee a,e , Garam Lee a,f , Ho Jin Lee a,g , Kwangjin Park h,* , Dong Wook Kim a,** , San Moon a,***Eunki Kim a,1 , Joo-Hyung Kim b,1 , Joon Ha Chang c,1 , Juhyoung Kim a,d , Jun Ho Shin a,e , Junhee Lee a,e , Garam Lee a,f , Ho Jin Lee a,g , Kwangjin Park h,* , Dong Wook Kim a,** , San Moon a,***
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[202.0, 81.66, 357.8, 132.94]Although Li-rich Mn-based layered oxides (LMRs) exhibit high specific capacities ( > 250 mAh g 1 ) through anionic redox activity and are therefore promising next-generation cathode materials for high-energy Li-ion batteries, their commercialization is severely hindered by voltage fading, structural degradation, and safety concerns arising from surface instability. To address these problems, we deposited an insular protective layer of carbon-coated LiFePO4 (C-LFP) nanoparticles on LMR secondary particles using a scalable solvent-free mechanofusion strategy. The optimal coating (C-LFP loading = 0.75 wt%) notably enhanced electrochemical performance, resulting in a capacity retention of 60.7% at 3C (cf. 38% for pristine LMR) and 93.43% after 200 cycles at 0.5C while suppressing voltage fading. According to the proposed synergistic mechanism, C-LFP provided electronic conductivity exceeding that of bare LMR, the insular morphology preserved direct electron transport pathways, and the nanoscale C-LFP particle size enabled rapid Li-ion transport and shortened diffusion lengths. The C-LFP coating prevented the formation of highly resistive rock-salt degradation layers, maintained a low interfacial impedance, and suppressed Mn dissolution ( > 95% reduction) and O2 evolution. Thus, this work demonstrates that rationally designed surface modification can unlock the full potential of LMR cathodes for next-generation energy storage applications.Although Li-rich Mn-based layered oxides (LMRs) exhibit high specific capacities ( > 250 mAh g 1 ) through anionic redox activity and are therefore promising next-generation cathode materials for high-energy Li-ion batteries, their commercialization is severely hindered by voltage fading, structural degradation, and safety concerns arising from surface instability. To address these problems, we deposited an insular protective layer of carbon-coated LiFePO4 (C-LFP) nanoparticles on LMR secondary particles using a scalable solvent-free mechanofusion strategy. The optimal coating (C-LFP loading = 0.75 wt%) notably enhanced electrochemical performance, resulting in a capacity retention of 60.7% at 3C (cf. 38% for pristine LMR) and 93.43% after 200 cycles at 0.5C while suppressing voltage fading. According to the proposed synergistic mechanism, C-LFP provided electronic conductivity exceeding that of bare LMR, the insular morphology preserved direct electron transport pathways, and the nanoscale C-LFP particle size enabled rapid Li-ion transport and shortened diffusion lengths. The C-LFP coating prevented the formation of highly resistive rock-salt degradation layers, maintained a low interfacial impedance, and suppressed Mn dissolution ( > 95% reduction) and O2 evolution. Thus, this work demonstrates that rationally designed surface modification can unlock the full potential of LMR cathodes for next-generation energy storage applications.
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[37.59, 694.24, 253.44, 49.15]Eunki Kim: Writing -original draft, Methodology, Investigation, Formal analysis, Data curation. Joo-Hyung Kim: Visualization, Investigation, Conceptualization. Joon Ha Chang: Visualization, Methodology, Investigation. Juhyoung Kim: Methodology, Investigation. Jun Ho Shin: Methodology, Investigation. Junhee Lee: Methodology,Eunki Kim: Writing -original draft, Methodology, Investigation, Formal analysis, Data curation. Joo-Hyung Kim: Visualization, Investigation, Conceptualization. Joon Ha Chang: Visualization, Methodology, Investigation. Juhyoung Kim: Methodology, Investigation. Jun Ho Shin: Methodology, Investigation. Junhee Lee: Methodology,
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[306.59, 140.58, 253.42, 28.23]The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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[306.6, 308.62, 253.43, 101.42]Cathode -electrolyte interphase (CEI), carbon-coated LiFePO4 (CLFP), carbon nanotube (CNT), differential electrochemical mass spectrometry (DEMS), differential scanning calorimetry (DSC), energydispersive X-ray spectroscopy (EDS), electric vehicle (EV), fieldemission scanning electron microscopy (FE-SEM), fast Fourier transform (FFT), galvanostatic intermittent titration technique (GITT), highresolution transmission electron microscopy (HRTEM), LiFePO4 (LFP), Li-ion battery (LIB), Li-rich Mn-based layered oxide (LMR), polyvinylidenedifluoride (PVDF), transition metal (TM), X-ray diffraction (XRD).Cathode -electrolyte interphase (CEI), carbon-coated LiFePO4 (CLFP), carbon nanotube (CNT), differential electrochemical mass spectrometry (DEMS), differential scanning calorimetry (DSC), energydispersive X-ray spectroscopy (EDS), electric vehicle (EV), fieldemission scanning electron microscopy (FE-SEM), fast Fourier transform (FFT), galvanostatic intermittent titration technique (GITT), highresolution transmission electron microscopy (HRTEM), LiFePO4 (LFP), Li-ion battery (LIB), Li-rich Mn-based layered oxide (LMR), polyvinylidenedifluoride (PVDF), transition metal (TM), X-ray diffraction (XRD).
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[224.72, 33.45, 145.08, 11.73]Journal of Power Sources 671 (2026) 239599Journal of Power Sources 671 (2026) 239599
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[228.42, 63.48, 140.65, 7.31]Contents lists available at ScienceDirectContents lists available at ScienceDirect
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[219.29, 87.36, 158.93, 12.79]Journal of Power SourcesJournal of Power Sources
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[195.48, 119.22, 206.54, 6.67]journal homepage: www.elsevier.com/locate/jpowsourjournal homepage:
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[37.59, 273.05, 448.21, 15.96]a Department of Advanced Battery Research Center, Korea Research Institute of Chemical Technology (KRICT), 141 Gajeongro, Yueong, Daejeon, 34114, Republic of Koreaa Department of Advanced Battery Research Center, Korea Research Institute of Chemical Technology (KRICT), 141 Gajeongro, Yueong, Daejeon, 34114, Republic of Korea
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[37.59, 290.17, 362.56, 7.4]b Department of Materials Engineering and Convergence Technology, Gyeongsang National University, Jinju, 52828, Republic of Koreab Department of Materials Engineering and Convergence Technology, Gyeongsang National University, Jinju, 52828, Republic of Korea
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[37.59, 298.73, 359.78, 7.4]c Department of Materials Science and Engineering, Korea National University of Transportation, Chumgju, 27469, Republic of Koreac Department of Materials Science and Engineering, Korea National University of Transportation, Chumgju, 27469, Republic of Korea
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[37.59, 307.29, 276.21, 7.4]d Department of Material Science and Engineering, Yonsei University, Seoul, 03722, Republic of Koread Department of Material Science and Engineering, Yonsei University, Seoul, 03722, Republic of Korea
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[37.59, 315.85, 324.86, 7.4]e Department of Chemical Engineering, Hanyang University, 222, Wangsimni-ro, Seongdong-gu, Seoul, Republic of Koreae Department of Chemical Engineering, Hanyang University, 222, Wangsimni-ro, Seongdong-gu, Seoul, Republic of Korea
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[37.59, 324.47, 333.53, 7.4]f Department of Materials Science and Engineering, Korea University, 145, Anam-ro, Seongbuk-gu, Seoul, Republic of Koreaf Department of Materials Science and Engineering, Korea University, 145, Anam-ro, Seongbuk-gu, Seoul, Republic of Korea
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[37.59, 333.03, 239.14, 7.4]g Department of Chemistry, Pusan National University, Busan, 46241, Republic of Koreag Department of Chemistry, Pusan National University, Busan, 46241, Republic of Korea
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[37.59, 341.59, 401.45, 7.4]h Department of Mechanical Engineering, Gachon University, 1342 Sungnamdaero, Sujeong-Gu, Sungnam Si, Gyeonggi-do, 13120, Republic of Koreah Department of Mechanical Engineering, Gachon University, 1342 Sungnamdaero, Sujeong-Gu, Sungnam Si, Gyeonggi-do, 13120, Republic of Korea
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[37.59, 375.28, 69.91, 6.4]H I G H L I G H T SH I G H L I G H T S
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[41.61, 634.57, 399.17, 6.58]This article is part of a special issue entitled: MDB 2025 : Progresses and Challenges published in Journal of Power Sources.This article is part of a special issue entitled: MDB 2025 : Progresses and Challenges published in Journal of Power Sources.
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[42.63, 644.15, 78.79, 6.58]* Corresponding author.* Corresponding author.
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[42.63, 653.73, 82.36, 6.58]** Corresponding author.** Corresponding author.
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[42.63, 663.26, 85.99, 6.58]*** Corresponding author.*** Corresponding author.
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[43.71, 680.69, 159.27, 8.31]1 These authors contributed equally to this work.1 These authors contributed equally to this work.
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[49.55, 672.84, 370.79, 6.58]E-mail addresses: ydmj79@gachon.ac.kr (K. Park), dongwook@krict.re.kr (D.W. Kim), san82@krict.re.kr (S. Moon).E-mail addresses: ydmj79@gachon.ac.kr (K. Park), dongwook@krict.re.kr (D.W. Kim), san82@krict.re.kr (S. Moon).
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[37.59, 699.43, 158.54, 6.58]https://doi.org/10.1016/j.jpowsour.2026.239599
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[37.52, 714.7, 110.87, 11.73]Available online 11 February 2026Available online 11 February 2026
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[37.59, 708.95, 322.41, 6.58]Received 9 December 2025; Received in revised form 29 January 2026; Accepted 7 February 2026Received 9 December 2025; Received in revised form 29 January 2026; Accepted 7 February 2026
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[37.52, 724.32, 522.04, 11.73]0378-7753/© 2026 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license ( http://creativecommons.org/licenses/by/4.0/ ).0378-7753/© 2026 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license ( ).
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[37.59, 36.99, 461.87, 5.85]E. Kim et al.E. Kim et al.
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[433.38, 33.66, 124.91, 10.42]Journal of Power Sources 671 (2026) 239599Journal of Power Sources 671 (2026) 239599
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[37.59, 64.26, 78.1, 6.4]A R T I C L E I N F OA R T I C L E I N F O
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[202.0, 64.26, 56.72, 6.4]A B S T R A C TA B S T R A C T
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[37.59, 83.2, 59.2, 57.27]Keywords: Li-rich layered oxide LiFePO4 coating Mechanofusion Voltage fading Surface stabilization High-energy cathodeKeywords: Li-rich layered oxide LiFePO4 coating Mechanofusion Voltage fading Surface stabilization High-energy cathode
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[37.59, 247.11, 60.25, 7.31]1. Introduction1. Introduction
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[306.6, 487.71, 98.06, 7.31]2. Experimental methods2. Experimental methods
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[306.6, 508.63, 81.33, 7.31]2.1. Materials synthesis2.1. Materials synthesis
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[306.6, 529.55, 196.82, 7.31]2.1.1. Synthesis of Li-rich Mn-based layered oxide (LMR)2.1.1. Synthesis of Li-rich Mn-based layered oxide (LMR)
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[296.21, 754.46, 3.59, 10.42]22
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[433.38, 33.66, 124.91, 10.42]Journal of Power Sources 671 (2026) 239599Journal of Power Sources 671 (2026) 239599
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[37.59, 36.99, 461.87, 5.85]E. Kim et al.E. Kim et al.
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[37.59, 76.4, 199.65, 7.31]2.1.2. Preparation of carbon-coated LiFePO4 nanoparticles2.1.2. Preparation of carbon-coated LiFePO4 nanoparticles
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[37.59, 275.17, 128.43, 7.31]2.1.3. Mechanofusion coating process2.1.3. Mechanofusion coating process
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[37.59, 422.23, 105.97, 7.31]2.2. Materials characterization2.2. Materials characterization
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[37.59, 443.2, 179.22, 7.31]2.2.1. Structural and morphological characterization2.2.1. Structural and morphological characterization
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[37.59, 641.91, 133.52, 7.31]2.2.2. Electrochemical characterization2.2.2. Electrochemical characterization
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[306.6, 532.21, 157.07, 7.31]2.2.3. Chemical and thermal stability analysis2.2.3. Chemical and thermal stability analysis
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[433.38, 33.66, 124.91, 10.42]Journal of Power Sources 671 (2026) 239599Journal of Power Sources 671 (2026) 239599
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[306.59, 55.49, 98.62, 7.31]3. Results and discussion3. Results and discussion
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[306.59, 76.41, 229.26, 7.31]3.1. Synthesis and characterization of LFP-coated LMR (LMR@Fx)3.1. Synthesis and characterization of LFP-coated LMR (LMR@Fx)
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[37.59, 717.45, 522.2, 25.69]Fig. 1. (a) Schematic illustrating the suppression of surface degradation (Mn dissolution, O2 evolution, and rock-salt phase transformation) by the carbon-coated LiFePO4 (C-LFP) layer. (b) X-ray diffraction (XRD) pattern of pristine Li-rich Mn-based layered oxide (LMR); the inset highlights superlattice reflections (20 -23 ◦ ). (c) XRD patterns of samples with various C-LFP loadings. (d) Comparison of LMR@F2.0 with the corresponding physical mixture (LMR + 2.0 wt% C-LFP).Fig. 1. (a) Schematic illustrating the suppression of surface degradation (Mn dissolution, O2 evolution, and rock-salt phase transformation) by the carbon-coated LiFePO4 (C-LFP) layer. (b) X-ray diffraction (XRD) pattern of pristine Li-rich Mn-based layered oxide (LMR); the inset highlights superlattice reflections (20 -23 ◦ ). (c) XRD patterns of samples with various C-LFP loadings. (d) Comparison of LMR@F2.0 with the corresponding physical mixture (LMR + 2.0 wt% C-LFP).
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[306.59, 233.73, 148.48, 7.31]3.2. Enhanced electrochemical performance3.2. Enhanced electrochemical performance
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[37.59, 698.35, 522.18, 44.79]Fig. 2. Field-emission scanning electron microscopy (FE-SEM) images of the (a) hydroxide precursor and (b) pristine LMR revealing a hierarchical structure composed of spherical secondary and granular primary particles. (c -f) Surface FE-SEM images of LMR@F0.5 -;2.0 demonstrating the formation of a discrete islandlike coating morphology progressively densifying with increasing C-LFP loading. (g) Cross-sectional FE-SEM image and (h) corresponding energy-dispersive X-ray spectroscopy (EDS) line profile of LMR@F0.75. (i -l) EDS elemental mappings of Fe (red) obtained for LMR@F0.5 -;2.0. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)Fig. 2. Field-emission scanning electron microscopy (FE-SEM) images of the (a) hydroxide precursor and (b) pristine LMR revealing a hierarchical structure composed of spherical secondary and granular primary particles. (c -f) Surface FE-SEM images of LMR@F0.5 -;2.0 demonstrating the formation of a discrete islandlike coating morphology progressively densifying with increasing C-LFP loading. (g) Cross-sectional FE-SEM image and (h) corresponding energy-dispersive X-ray spectroscopy (EDS) line profile of LMR@F0.75. (i -l) EDS elemental mappings of Fe (red) obtained for LMR@F0.5 -;2.0. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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[433.38, 33.66, 124.91, 10.42]Journal of Power Sources 671 (2026) 239599Journal of Power Sources 671 (2026) 239599
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[37.59, 36.99, 461.87, 5.85]E. Kim et al.E. Kim et al.
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[37.59, 384.16, 522.16, 25.69]Fig. 3. (a) Initial charge -discharge voltage profiles recorded at 0.1C. (b) Results of rate capability tests. (c) Capacity retention and coulombic efficiency evolution during 200 cycles at 0.5C. Charge -discharge voltage profiles of (d) pristine LMR and (e) LMR@F0.75 at selected cycles (initial, 1st, 50th, 100th, 150th, and 200th). (f) Evolution of average discharge voltage over 200 cycles.Fig. 3. (a) Initial charge -discharge voltage profiles recorded at 0.1C. (b) Results of rate capability tests. (c) Capacity retention and coulombic efficiency evolution during 200 cycles at 0.5C. Charge -discharge voltage profiles of (d) pristine LMR and (e) LMR@F0.75 at selected cycles (initial, 1st, 50th, 100th, 150th, and 200th). (f) Evolution of average discharge voltage over 200 cycles.
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[306.59, 425.18, 244.54, 17.8]3.3. Synergistic promotional effects of C-LFP islands on electrochemical reaction kinetics3.3. Synergistic promotional effects of C-LFP islands on electrochemical reaction kinetics
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[37.59, 379.39, 522.21, 25.74]Fig. 4. (a) Volume resistivities of different electrode. (b -d) Li-ion diffusion coefficients ( D Li + ) as functions of voltage determined during discharge: (b) full voltage range, (c) magnified view of the 3.2 -3.5 V region showing enhanced kinetics near the LFP activation potential, and (d) the 3.6 -4.0 V region. Nyquist plots of LMR half-cells recorded (e) in the fresh state (at open-circuit voltage) and (f) after the third initial cycle.Fig. 4. (a) Volume resistivities of different electrode. (b -d) Li-ion diffusion coefficients ( D Li + ) as functions of voltage determined during discharge: (b) full voltage range, (c) magnified view of the 3.2 -3.5 V region showing enhanced kinetics near the LFP activation potential, and (d) the 3.6 -4.0 V region. Nyquist plots of LMR half-cells recorded (e) in the fresh state (at open-circuit voltage) and (f) after the third initial cycle.
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[37.59, 673.32, 203.54, 7.31]3.4. Elucidating the multifunctional stabilization mechanism3.4. Elucidating the multifunctional stabilization mechanism
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[37.59, 501.68, 522.2, 57.32]Fig. 5. (a -l) High-resolution transmission electron microscopy (HRTEM) analysis of electrodes after three initial cycles. Low-magnification images of a single particle of (a) pristine LMR and (g) LMR@F0.75. (b, h) HRTEM images focusing on the near-surface region. (c, d) Magnified lattice image and corresponding fast Fourier transform (FFT) pattern of the pristine LMR surface revealing the formation of a degraded rock-salt phase ( Fm 3 m ). (e, f) Magnified lattice image and FFT pattern of pristine LMR bulk showing the original layered structure ( R 3 m ). (i, j) Magnified lattice image and FFT pattern of the LMR@F0.75 surface confirming the preservation of the Li2MnO3-like superlattice structure ( C 2/ m ). (k, l) Magnified lattice image and FFT pattern of the LMR@F0.75 bulk ( R 3 m ). (m, n) In situ differential electrochemical mass spectrometry profiles showing O2 and CO2 evolution during the first charge. (o) Differential scanning calorimetry curves of charged cathodes.Fig. 5. (a -l) High-resolution transmission electron microscopy (HRTEM) analysis of electrodes after three initial cycles. Low-magnification images of a single particle of (a) pristine LMR and (g) LMR@F0.75. (b, h) HRTEM images focusing on the near-surface region. (c, d) Magnified lattice image and corresponding fast Fourier transform (FFT) pattern of the pristine LMR surface revealing the formation of a degraded rock-salt phase ( Fm 3 m ). (e, f) Magnified lattice image and FFT pattern of pristine LMR bulk showing the original layered structure ( R 3 m ). (i, j) Magnified lattice image and FFT pattern of the LMR@F0.75 surface confirming the preservation of the Li2MnO3-like superlattice structure ( C 2/ m ). (k, l) Magnified lattice image and FFT pattern of the LMR@F0.75 bulk ( R 3 m ). (m, n) In situ differential electrochemical mass spectrometry profiles showing O2 and CO2 evolution during the first charge. (o) Differential scanning calorimetry curves of charged cathodes.
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[37.59, 76.74, 54.38, 7.31]4. Conclusion4. Conclusion
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[37.59, 673.32, 161.94, 7.31]CRediT authorship contribution statementCRediT authorship contribution statement
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[306.59, 55.49, 253.41, 49.15]Investigation. Garam Lee: Methodology, Investigation. Ho Jin Lee: Methodology, Investigation. Kwangjin Park: Validation, Supervision. Dong Wook Kim: Validation, Supervision. San Moon: Writing -review & editing, Writing -original draft, Visualization, Validation, Supervision, Project administration, Funding acquisition, Conceptualization.Investigation. Garam Lee: Methodology, Investigation. Ho Jin Lee: Methodology, Investigation. Kwangjin Park: Validation, Supervision. Dong Wook Kim: Validation, Supervision. San Moon: Writing -review & editing, Writing -original draft, Visualization, Validation, Supervision, Project administration, Funding acquisition, Conceptualization.
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[306.59, 119.66, 128.59, 7.31]Declaration of competing interestDeclaration of competing interest
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[306.59, 182.76, 73.84, 7.31]AcknowledgementsAcknowledgements
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[306.59, 203.68, 253.43, 70.07]This research was supported by the National Research Council of Science & Technology (NST) grant by the Korea government (MSIT) ( No. GTL24011 -000), the Materials and Components Technology Development Program (grant no. 2410004404 and 2410005140) funded by the Ministry of Trade, Industry & Energy (MOTIE, Korea) and project No. SS2222 -20 funded by Korea Research Institute of Chemical Technology (KRICT).This research was supported by the National Research Council of Science & Technology (NST) grant by the Korea government (MSIT) ( No. GTL24011 -000), the Materials and Components Technology Development Program (grant no. 2410004404 and 2410005140) funded by the Ministry of Trade, Industry & Energy (MOTIE, Korea) and project No. SS2222 -20 funded by Korea Research Institute of Chemical Technology (KRICT).
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[306.59, 287.7, 32.47, 7.31]GlossaryGlossary
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[306.6, 423.99, 128.57, 7.31]Appendix A. Supplementary dataAppendix A. Supplementary data
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[306.6, 444.91, 253.41, 17.8]Supplementary data to this article can be found online at https://doi. org/10.1016/j.jpowsour.2026.239599.Supplementary data to this article can be found online at org/10.1016/j.jpowsour.2026.239599.
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[306.6, 476.31, 63.51, 7.31]Data availabilityData availability
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[318.56, 497.23, 140.32, 7.31]Data will be made available on request.Data will be made available on request.
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[433.38, 33.66, 124.91, 10.42]Journal of Power Sources 671 (2026) 239599Journal of Power Sources 671 (2026) 239599
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[294.42, 754.46, 7.18, 10.42]1111