2021
DOI: 10.1016/j.inoche.2020.108434
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Synthesis of Li1.5Ni0.25Mn0.75O2.5 cathode material via carbonate co-precipitation method and its electrochemical properties

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Cited by 19 publications
(19 citation statements)
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“…The irregular primary particles agglomerate into a loose and porous structure, favoring easy Li-ion diffusion and electrolyte infiltration into the bulk phase. The smaller particles also allow faster intercalation and deintercalation of Li + in the Li-rich NMO cathode, thus finally instigating better charge and discharge properties, particularly at high rate cycling. , The elemental distribution in the NMO sample was further investigated by energy-dispersive spectroscopy (EDS) elemental mapping. The elemental mapping is displayed in Figure .…”
Section: Resultsmentioning
confidence: 99%
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“…The irregular primary particles agglomerate into a loose and porous structure, favoring easy Li-ion diffusion and electrolyte infiltration into the bulk phase. The smaller particles also allow faster intercalation and deintercalation of Li + in the Li-rich NMO cathode, thus finally instigating better charge and discharge properties, particularly at high rate cycling. , The elemental distribution in the NMO sample was further investigated by energy-dispersive spectroscopy (EDS) elemental mapping. The elemental mapping is displayed in Figure .…”
Section: Resultsmentioning
confidence: 99%
“…After this, the dried powder was mixed with lithium carbonate (Li 2 CO 3 ) and then calcined at 950 °C for 10 h to obtain the final product. Excess Li 2 CO 3 (3%) was added to compensate for its loss at high-temperature heating. , …”
Section: Methodsmentioning
confidence: 99%
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“…In this regard, layered lithium-rich mixed transition metal oxides existing as solid solutions between Li­[Li 1/3 Mn 2/3 ]­O 2 (Li 2 MnO 3 ) and LiMO 2 (M = Mn, Co, and Ni) are considered to be the most prospective contenders for next-generation high-energy LIBs. Lithium manganese rich oxides (LMRO) exhibit higher specific capacities of >250 mAh g –1 as well as energy densities of ∼1000 Wh kg –1 over a wide voltage range owing to the coexistence of the layered LiMO 2 phase (with space group R 3̅ m ) and the Li 2 MnO 3 (having C 2/ m phase). However, the introduction of LMRO in commercial cells remains hindered by several fatal drawbacks, such as severe capacity and voltage fading during cycling owing to structural instability. The phase transition from layered to spinel structure detrimentally affects the crystal stability when the LMRO cathode is charged to 4.8 V. Surface coating with inert phases and ion doping are the two main strategies adopted to alleviate the capacity and voltage fading of LMRO based cathode materials. …”
Section: Water Based Binders For Various Cathode Materials In Libsmentioning
confidence: 99%
“…To compensate for the lithium loss during the high-temperature calcination, an extra 3 wt % of Li 2 CO 3 was added. 34 The scheme for the synthesis of the cathode material is given in Figure 1.…”
Section: Introductionmentioning
confidence: 99%