TY - JOUR
T1 - Controlled synthesis of Sb nanostructures and their conversion to CoSb 3 nanoparticle chains for li-ion battery electrodes
AU - Zhu, Jixin
AU - Sun, Ting
AU - Chen, Junsong
AU - Shi, Wenhui
AU - Zhang, Xiaojun
AU - Lou, Xiongwen
AU - Mhaisalkar, Subodh
AU - Hng, Huey Hoon
AU - Boey, Freddy
AU - Ma, Jan
AU - Yan, Qingyu
PY - 2010/9/28
Y1 - 2010/9/28
N2 - Nanostructured Sb was prepared through a simple polyol process. Either Sb nanoparticles (Sb NP) or nanowires (Sb NW) were obtained by adjusting the concentration of surfactant. Electrochemical analyses revealed that the resultant Sb crystals displayed high charge storage capacities as Li-ion battery electrodes and relatively poor cycling retention during the charge-discharge process. For instance, the capacity was 560-584 mA h/g during the second cycle, which decreased to 120-200 mA h/g during the 70th cycle at a rate of 0.2 C. Thus, Sb NPs were reacted with Co precursors to form one-dimensional (1-D) NP chains wrapped in a polyvinyl pyridine layer, and the length of the NP chains could be adjusted by varying the concentration of polyvinyl pyridine. Through a controlled annealing process, the polyvinyl pyridine layer was converted to amorphous carbon, which led to the formation of 1-D core-shell structures with CoSb3 NP chains entrapped in the carbon layer. Although CoSb 3 NP chains with a carbon shell displayed a lower initial charge storage capacity than Sb nanostructures, improved cycling performance was observed. The capacity was 468 mA h/g during the second cycle, which dropped to 421 mA h/g during the 70th cycle at a rate of 0.2 C. Compared to CoSb 3 produced via other techniques, CoSb3/C NP chains displayed higher cycling stability, because of the presence of a carbon buffer layer.
AB - Nanostructured Sb was prepared through a simple polyol process. Either Sb nanoparticles (Sb NP) or nanowires (Sb NW) were obtained by adjusting the concentration of surfactant. Electrochemical analyses revealed that the resultant Sb crystals displayed high charge storage capacities as Li-ion battery electrodes and relatively poor cycling retention during the charge-discharge process. For instance, the capacity was 560-584 mA h/g during the second cycle, which decreased to 120-200 mA h/g during the 70th cycle at a rate of 0.2 C. Thus, Sb NPs were reacted with Co precursors to form one-dimensional (1-D) NP chains wrapped in a polyvinyl pyridine layer, and the length of the NP chains could be adjusted by varying the concentration of polyvinyl pyridine. Through a controlled annealing process, the polyvinyl pyridine layer was converted to amorphous carbon, which led to the formation of 1-D core-shell structures with CoSb3 NP chains entrapped in the carbon layer. Although CoSb 3 NP chains with a carbon shell displayed a lower initial charge storage capacity than Sb nanostructures, improved cycling performance was observed. The capacity was 468 mA h/g during the second cycle, which dropped to 421 mA h/g during the 70th cycle at a rate of 0.2 C. Compared to CoSb 3 produced via other techniques, CoSb3/C NP chains displayed higher cycling stability, because of the presence of a carbon buffer layer.
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U2 - 10.1021/cm101663w
DO - 10.1021/cm101663w
M3 - Article
AN - SCOPUS:77957069964
SN - 0897-4756
VL - 22
SP - 5333
EP - 5339
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 18
ER -