阳极
复合数
材料科学
碳化
化学工程
磷
锂(药物)
炭黑
碳纤维
电化学
涂层
石墨
纳米技术
化学
复合材料
电极
冶金
扫描电子显微镜
天然橡胶
物理化学
内分泌学
工程类
医学
作者
Ziqiang Cheng,Penglong Chen,Shuang Gu,Gengchang Lai,Chan Ke,Xiaoxiao Feng,Xue‐Feng Yu,Jiahong Wang
标识
DOI:10.1016/j.jpowsour.2023.233650
摘要
Black phosphorus (BP) has attracted extensive attention in high-rate lithium-ion batteries due to its high theoretical capacity and moderate lithiation potential. However, the large volume expansion and the low conductivity of BP nanostructures in the electrochemical cycle have inhibited the rate performance and long-term cycle stability. In this paper, by combining the glucose-assisted ball-milling and carbonization method, a black-phosphorus/carbon (BP@C) composite anodic material is developed, in which the nano-sized BP nanoparticles are homogeneously embedded in the amorphous carbon matrix. Both the phosphorus-oxygen-carbon bonds and the phosphorus-carbon bonds improve the cross-link between BP and the surface-coated carbon matrix. The unique well-embedded structure promotes the cycling stability and the rate performance of BP@C. The composite shows a high discharge specific capacity of about 1881 mAh g−1 at 0.1 A g−1, the specific capacity at 4 A g−1 is about 63% of the low current capacity, and the discharge specific capacity retains 1130 mAh g−1 after 300 charge-discharge cycles at 0.5 A g−1. Moreover, the significant role of the active unsaturated groups for building the well-embedded composite is further revealed. These results indicate that dual regulation of surface coating and structure optimization offers great potential for further optimizing phosphorus-based anode materials.
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