2019
DOI: 10.1016/j.jpowsour.2019.227260
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Co3O4 nanospheres composed of highly interconnected nanoparticles for boosting Li-Ion storage

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Cited by 23 publications
(8 citation statements)
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“…Such small differences in the reduction/oxidation peak locations between Co 3 O 4 /GC 350 and Co 3 O 4 /GC 450 are related to the insertion of Li + ions into the Co 3 O 4 structure, involving the different concentrations of lithium ions and their polarization. Such a phenomenon is also observed in other reported Co 3 O 4 electrode materials. Moreover, the integral areas of corresponding oxidation and reduction peaks are nearly not changed in the following second to fifth cycles, which indicates that the graphitic carbon-encapsulated Co 3 O 4 /GC composites prepared from the waste poplar branch template present well electrochemical reversibility and cycling stability.…”
Section: Resultssupporting
confidence: 58%
See 1 more Smart Citation
“…Such small differences in the reduction/oxidation peak locations between Co 3 O 4 /GC 350 and Co 3 O 4 /GC 450 are related to the insertion of Li + ions into the Co 3 O 4 structure, involving the different concentrations of lithium ions and their polarization. Such a phenomenon is also observed in other reported Co 3 O 4 electrode materials. Moreover, the integral areas of corresponding oxidation and reduction peaks are nearly not changed in the following second to fifth cycles, which indicates that the graphitic carbon-encapsulated Co 3 O 4 /GC composites prepared from the waste poplar branch template present well electrochemical reversibility and cycling stability.…”
Section: Resultssupporting
confidence: 58%
“…Figure c,d presents the galvanostatic charge/discharge profiles for the first five cycles of Co 3 O 4 /GC 350 and Co 3 O 4 /GC 450 electrodes during 0.01–3.0 V at 0.1 A g –1 . The first discharge profiles of Co 3 O 4 /GC 350 and Co 3 O 4 /GC 450 electrodes display voltage platforms at 1.08 and 1.11 V, while the discharge platforms for the subsequent four cycles shift to near 1.34 and 1.32 V. In comparison, the charge platforms in the first cycles of the two electrodes are basically stable at about 2.0 V, while the charge platforms for the next four cycles shift to near 2.04 and 2.06 V. The reasons for such small differenced in voltage platform values are similar to those for CV curves. The first discharge/charge-specific capacities of Co 3 O 4 /GC 350 and Co 3 O 4 /GC 450 are 1036.7/704.3 and 1201.2/864.1 mA h g –1 with Coulombic efficiencies of 67.9 and 71.9%, respectively. The initial capacity loss is mainly caused by the decomposition of the electrolyte during the first discharge process, the formation of the SEI film, and the incomplete deintercalation of Li + ions. , In comparison, the discharge capacities of Co 3 O 4 /GC 350 and Co 3 O 4 /GC 450 electrodes in the following second/third cycles are basically stable at 743.2/732.4 and 907.9/906.9 mA h g –1 , respectively.…”
Section: Resultsmentioning
confidence: 98%
“…Due to the capacity of biomass-derived graphitic carbon being about 130 mA h g –1 at 1 A g –1 (Figure S2), the introduction of biomass-derived graphitic carbon can contribute to the capacity of Co 3 O 4 -based nanocomposites in LIBs . During the first cathodic scan, both Co 3 O 4 /C-1 and Co 3 O 4 /C-2 electrodes show a strong cathodic peak at 0.70 and 0.67 V, ascribed to the reduction of Co 3+ ions to Co 0 , decomposition of electrolyte, and formation of amorphous Li 2 O and SEI films. , At the first anodic scan, the CV curves of Co 3 O 4 /C-1 and Co 3 O 4 /C-2 electrodes display a wide oxidation peak at 2.06 and 2.10 V, which are assigned to the oxidation of Co 0 to Co 3+ ions and the formation of Co 3 O 4 , as well as the decomposition of Li 2 O . Therefore, they have the same redox reaction mechanism: Co 3 O 4 + 8Li + + 8e – ↔ 4Li 2 O + 3Co.…”
Section: Resultsmentioning
confidence: 99%
“…13,48 At the first anodic scan, the CV curves of Co 3 O 4 /C-1 and Co 3 O 4 /C-2 electrodes display a wide oxidation peak at 2.06 and 2.10 V, which are assigned to the oxidation of Co 0 to Co 3+ ions and the formation of Co 3 O 4 , as well as the decomposition of Li 2 O 34. Therefore, they have the same redox reaction mechanism: Co 3 O 4 + 8Li + + 8e − ↔ 4Li 2 O + 3Co.…”
mentioning
confidence: 99%
“…Aimed at handling the above-mentioned problems, the construction of protective layer with carbonaceous component is accounted as an appealing approach, which can improve the electrochemical properties of anode materials [12][13][14]. Nevertheless, the presence of carbonaceous materials can not only suppress the capacity of Co 3 O 4 but also make the preparation process complex [15]. Hence, it is highly desirable to design Co 3 O 4 with suitable architectures to obtain high capacity and long-term cycling performance.…”
Section: Introductionmentioning
confidence: 99%