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      "caption": "Fig. 1. (a) Crystal structure of trigonal LiMO2 ( R -3m) and (b) monoclinic Li2MnO3 ( C 2/ m ). Reproduced from Ref. [27] with permission from American Chemical Society. (c) XRD patterns of Li1.2Ni0.13Co0.13Mn0.54O2+ d synthesized from two different precursors (C for conventional precursor and H for hierarchically structured precursor). Reproduced from Ref. [27] with permission from American Chemical Society. (d) Structural scheme showing the honeycomb pattern consisting of Li@Mn6 superstructure units in LMR layered oxide. Reproduced from Ref. [29]) with permission from Royal Society of Chemistry.",
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      "caption": "Fig. 2. (a) Initial charging-discharging profiles of Li2MnO3, LiNi0.5Mn0.5O2 and Li1.2Ni0.2Mn0.6O2. (b) The 1st and 2nd CV curves of Li1.2Ni0.2Mn0.6O2 in (a). Reproduced from Ref. [35] with permission from American Chemical Society. (c) p DOS of O 2 p orbitals and Mn 3 d orbitals in Li2MnO3 and the corresponding oxygen environment model. Reproduced from Ref. [47] with permission from Springer Nature. (d) Cycling performance of Li1.2Ni0.13Co0.13Mn0.54O2 synthesized by two different synthesis methods at 0.1 C in the voltage range of 2.0-4.8 V. (e) The corresponding capacity-voltage profiles of the re-synthesized Li1.2Ni0.13Co0.13Mn0.54O2 in (d). Reproduced from Ref. [53] with permission from Elsevier. (f) Schematic representation for the structural transformation of trigonal LiMO2 component ( R -3m) and monoclinic Li2MnO3 component ( C 2/ m ) in Li1.2Ni0.1Mn0.525Co0.175O2 during cycling. Reproduced from Ref. [54] with permission from American Chemical Society. (g) Selected area electron diffraction (SAED) pattern obtained along [0001] zone axis of Li1.2Co0.1Mn0.55Ni0.15O2 cathode at the charging voltage of 4.5 V. (h) Schematic diagram of TM migration in Li1.2Co0.1Mn0.55Ni0.15O2 cathode when holding at 4.5 V. Reproduced from Ref. [55] with permission from Royal Society of Chemistry.",
      "caption_preview": "Fig. 2. (a) Initial charging-discharging profiles of Li2MnO3, LiNi0.5Mn0.5O2 and Li1.2Ni0.2Mn0.6O2. (b) The 1st and 2nd CV curves of Li1.2Ni0.2Mn0.6O2 in (a). Reproduced from Ref. [35] with permission from American Chem…",
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      "caption": "Fig. 4. (a) Schematic illustration of the formation of porous Li1.2Ni0.18Co0.08Mn0.54O2. Reproduced from Ref. [68] with permission from Royal Society of Chemistry. (b) Schematic illustration of the synthesizing route for 3D Li1.2Ni0.2Mn0.6O2 and the morphological evolution. Reproduced from Ref. [69] with permission from American Chemical Society. (c) SEM image of Li1.2Ni0.2Mn0.6O2 oxide. Reproduced from Ref. [70] with permission from American Chemical Society.",
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      "caption": "Fig. 5. (a) Schematic illustration of ice-template coprecipitation method to synthesize Li1.2Ni0.2Mn0.6O2 with hierarchical mesopore structure. (b) The rate performance of Li1.2Ni0.2Mn0.6O2 synthesized by freeze drying (M1) and vacuum drying (M2). Reproduced from Ref. [73] with permission from American Chemical Society. (c) Schematic diagram of building nano-porous structures in Li1.144Ni0.136Co0.136Mn0.544O2. Reproduced from Ref. [74] with permission from American Chemical Society. (d) Schematic diagram to show various structure defects in Li1.143Ni0.136Co0.136Mn0.544O2. (e) TEM image to show nano-defects (stacking faults and cationic mixing) in the Li1.143Ni0.136Co0.136Mn0.544O2. (f) Comparison for the average voltage of highly crystalline Li1.143Ni0.136Co0.136Mn0.544O2 cathode (Pristine-LrLO) and defect abundant sample (NDA-LrCO-5) during cycling at 0.1 C. Reproduced from Ref. [75] with permission from Elsevier. (g) Schematic diagram of the element gradient distribution in LMR cathodes. (h) SEM image of Li1.2Mn0.44Co0.04Ni0.32O2 with element gradient distribution and (i) EDS line scanning along the marked line in (h). Reproduced from Ref. [80] with permission from Elsevier.",
      "caption_preview": "Fig. 5. (a) Schematic illustration of ice-template coprecipitation method to synthesize Li1.2Ni0.2Mn0.6O2 with hierarchical mesopore structure. (b) The rate performance of Li1.2Ni0.2Mn0.6O2 synthesized by freeze drying …",
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      "caption": "Fig. 6. (a) XRD patterns of Li1.2Ni0.13Co0.13Mn0.54O2 and Li1.17Na0.03[Ni0.13Co0.13Mn0.54]O2. (b) The cycling performance of Li1.2Ni0.13Co0.13Mn0.54O2 and Li1.17Na0.03[Ni0.13Co0.13Mn0.54]O2 at the current density of 100 mA g \u0000 1 . Reproduced from Ref. [84] with permission from Royal Society of Chemistry. (c) Schematic diagram of pristine LMR, LMR with surface-doped with Na (Na-LMR) and LMR with homogenously Na doping (Na/SDS-LMR) before cycling and after 200 cycles. Reproduced from Ref. [85] with permission from Wiley-VCH. (d) Schematic illustration for the structure of Mg-doped Li1.4Mg0.1[Mn0.75Ni0.25]O2+ r . (e) The rate performance of Mg-doped Li1.4Mg0.1[Mn0.75Ni0.25]O2+ r . Reproduced from Ref. [88] with permission from Royal Society of Chemistry. (f) Schematic diagram of Na and F co-doping in Li1.2Ni0.2Mn0.6O2 cathode. (g) The cycling performance of Li1.2Ni0.2Mn0.6O2 cathode (LNMO), Na doped LNMO cathode (Na-LNMO), F doped LNMO cathode (F-LNMO) and Na and F co-doped LNMO cathode (Na&FLNMO) at 0.1 C in the voltage range of 2.0-4.8 V. Reproduced from Ref. [95] with permission from Elsevier.",
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      "caption": "Fig. 7. (a) Schematic diagram of Al2O3 coated Li1.2Ni0.20Co0.08Mn0.52O2. (b) The capacity-voltage profiles of Al2O3 coated Li1.2Ni0.20Co0.08Mn0.52O2 in different cycles. Reproduced from Ref. [102] with permission from Elsevier. (c) Schematic illustration of different oxygen migration model in bare and SnO2 coated Li1.2Ni0.13Co0.13Mn0.54O2 (filled with oxygen vacancies at the surface). Reproduced from Ref. [103] with permission from Elsevier. (d) Schematic diagram for the surficial structure of AlPO4 coated LMR oxide. (e) The Coulombic efficiency of the LMR oxides coated with different ALD cycles of AlPO4 during long-term cycling. Reproduced from Ref. [104] with permission from Elsevier.",
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      "caption": "Fig. 8. (a) Illustration of the Li3PO4 coating process at the surface of Li1.2Ni0.2Mn0.6O2 through annealing at different temperatures. (b) TEM image of Li3PO4 coating layer. Reproduced from Ref. [107] with permission from Elsevier. (c) The cycling performance of the Li1.2Ni0.13Co0.13Mn0.54O2 cathode coated with different contents of Al2O3 and polyacene at 0.2 C (APL is short for double-shelled of Al2O3 and polyacene, and the number represents different amount of polyacene). Reproduced from Ref. [115] with permission from Royal Society of Chemistry. (d) Schematic diagram of the detailed synthetic process of the LMR cathode coated with a sandwich-like carbon@spinel@layered@spinel@carbon shell. Reproduced from Ref. [116] with permission from Elsevier. (e) Cycle performance of uncoated Li1.2Ni0.13Co0.13Mn0.54O2 (LR) and Mg2TiO4 coated Li1.2Ni0.13Co0.13Mn0.54O2 (LR@MTO) at 2 C. Reproduced from Ref. [117] with permission from John Wiley and Sons.",
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}