2021
DOI: 10.1007/s10008-021-04995-x
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Mg-doped Li-rich vanadium phosphate Li9V3(P2O7)3(PO4)2 as cathode for lithium-ion batteries: electrochemical performance and lithium storage mechanism

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Cited by 4 publications
(4 citation statements)
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“…Moreover, after 500 cycles the capacity retention of NP-1 and NP-5 are 69.3% and 65.7% respectively, which means neither a small amount of PO 4− doped in NP-1 nor a large amount of PO 4− doped in NP-5 are helpful to stabilize the structure. 45 Clearly, NP-3 also shows a great discharge capacity at 0.5 and 5C in Figure S6 in the Supporting Information. NP-3 clearly shows a higher discharge capacity of 193.4 mAh g −1 after 200 cycles at 0.5C and 126.17 mAh g −1 after 600 cycles at 5C.…”
Section: Resultsmentioning
confidence: 96%
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“…Moreover, after 500 cycles the capacity retention of NP-1 and NP-5 are 69.3% and 65.7% respectively, which means neither a small amount of PO 4− doped in NP-1 nor a large amount of PO 4− doped in NP-5 are helpful to stabilize the structure. 45 Clearly, NP-3 also shows a great discharge capacity at 0.5 and 5C in Figure S6 in the Supporting Information. NP-3 clearly shows a higher discharge capacity of 193.4 mAh g −1 after 200 cycles at 0.5C and 126.17 mAh g −1 after 600 cycles at 5C.…”
Section: Resultsmentioning
confidence: 96%
“…Figure c shows that NP-3 delivers a high discharge capacity of 211.5 mAh g –1 at 1C; it still can reach 159.5 mAh g –1 with a capacity retention of 75%, even after 500 cycles, which is much better than Co-free LLO fade to 143.6 mAh g –1 with the capacity retention of 65%. Moreover, after 500 cycles the capacity retention of NP-1 and NP-5 are 69.3% and 65.7% respectively, which means neither a small amount of PO 4– doped in NP-1 nor a large amount of PO 4– doped in NP-5 are helpful to stabilize the structure . Clearly, NP-3 also shows a great discharge capacity at 0.5 and 5C in Figure S6 in the Supporting Information.…”
Section: Results and Discussionmentioning
confidence: 99%
“…The smaller radius of Ni 2+ will make the lattice structure of the pristine NVP phase smaller with successful substitution of Ni 2+ for V 3+ . In previous studies, we have found that sodium ions are mainly diffused in the internal space with a curved trajectory, and thus the compressive structure of VO 6 octahedrons by Ni 2+ doping can widen the space for Na + migration. Furthermore, the replacement of Ni 2+ for V 3+ will lead to the stoichiometric oxidation of V 3+ to V 4+ due to the charge imbalance of Ni 2+ and V 3+ , which largely enhances the electronic conductivity of the NVP structure by charge compensation. , As V 4+ has a smaller radius ( r = 0.58 Å), the formation of mixed valence (V 4+ /V 3+ ) would facilitate structural aberration. The faintly twisted lattice structure may induce some structural defects that may be beneficial for electrochemical reactions.…”
Section: Resultsmentioning
confidence: 99%
“…[6][7][8][9] Its unique kagome lattice structure has made it a subject of study for exploring interplay among various physical properties, with recent findings shedding light on its magnetic and transport properties. [5,10,11] Some researchers reported on the lowtemperature magnetism of Li 9 Fe 3 (P 2 O 7 ) 3 (PO 4 ) 2 (S = 5/2), which exhibits an antiferromagnetic long-range order developing at T N = 1.3 K and a crossover from a paramagnet to a classical spin-liquid phase at approximately 5 K. [10] Additionally, the weak magnetic interaction allows for the observa-tion of the 1/3 magnetization plateau under a stable field near B = 4.75 T, providing valuable opportunities to explore classical and quantum fluctuations effects with zero and applied fields of the Heisenberg antiferromagnetic model. Another material in this family, Li 9 V 3 (P 2 O 7 ) 3 (PO 4 ) 2 (S = 1), exhibits distinct properties.…”
Section: Introductionmentioning
confidence: 99%