2011
DOI: 10.1016/j.jpowsour.2010.10.031
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Investigation on porous MnO microsphere anode for lithium ion batteries

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Cited by 213 publications
(176 citation statements)
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“…This can be ascribed to the content of metallic Co increasing with the cycling process. 50 The results further conrm that the metallic Co cannot be fully converted to CoS 2 , which is the origin of the irreversible capacity loss of the CoS 2 electrode material.…”
Section: 4748mentioning
confidence: 89%
“…This can be ascribed to the content of metallic Co increasing with the cycling process. 50 The results further conrm that the metallic Co cannot be fully converted to CoS 2 , which is the origin of the irreversible capacity loss of the CoS 2 electrode material.…”
Section: 4748mentioning
confidence: 89%
“…When the annealing temperature was increased to 700 C and above, the two samples have obviously sharp diffraction peaks, especially the MnO-800 sample. We noticed that all the four samples have a small board peak (2q ¼ [20][21][22][23][24][25][26][27][28][29][30] that might indicate to a certain amount of carbon. 16 Meanwhile, we noticed that the SEM images of the MnO-500, MnO-600 and MnO-700 samples maintain typical fusiform shape just as the MnCO 3 precursor in Fig.…”
Section: Resultsmentioning
confidence: 91%
“…Porous MnO materials can be synthesized by templated or non-templated methods, such as co-precipitation [35], hydrothermal, solvothermal [36], sol-gel and deposition processes [37]. Among these synthesis method, The co-precipitation method is more simple than the above mentioned processes and is suitable for large-scale production in commercial fields.…”
Section: Introductionmentioning
confidence: 99%
“…Among these synthesis method, The co-precipitation method is more simple than the above mentioned processes and is suitable for large-scale production in commercial fields. Zhong et al [35] synthesized porous MnO/C microspheres which delivered a reversible capacity of 600 mAh·g -1 at a rate of 400 mA·g -1 . This porous MnO particles were obtained with MnCO 3 as the precursor through a co-precipitation method, and carbon was coated by chemical vapor deposition.…”
Section: Introductionmentioning
confidence: 99%
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