阳极
碳化
材料科学
热解
钠
水热碳化
钠离子电池
碳纤维
石墨烯
电化学
微观结构
纳米技术
化学工程
化学
法拉第效率
电极
复合材料
扫描电子显微镜
冶金
工程类
物理化学
复合数
作者
Yu Jin,Shixiong Sun,Mingyang Ou,Yi Liu,Chenyang Fan,Xueping Sun,Jian Peng,Yuyu Li,Yuegang Qiu,Peng Wei,Zhi Deng,Yue Xu,Jiantao Han,Yunhui Huang
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2018-04-26
卷期号:1 (5): 2295-2305
被引量:117
标识
DOI:10.1021/acsaem.8b00354
摘要
Hard carbon (HC) is one of the most promising anode materials for sodium-ion batteries (SIBs) due to its suitable potential and high reversible capacity. At the same time, the correlation between carbon local structure and sodium-ion storage behavior is not clearly understood. In this paper, the two series of HC materials with perfect spherical morphology and tailored microstructures were designed and successfully produced using resorcinol formaldehyde (RF) resin as precursor. Via hydrothermal self-assembly and controlled pyrolysis, RF is a flexible precursor for high-purity carbon with a wide range of local-structure variation. Using these processes, one series of five representative RF-based HC nanospheres with varying degrees of graphitization were obtained from an RF precursor at different carbonization temperatures. The other series of HC materials with various microscopic carbon layer lengths and shapes was achieved by carbonizing five RF precursors with different cross-linking degrees at a single carbonization condition (1300 °C and 2 h). On the basis of the microstructures, unique electrochemical characteristics, and atomic pair distribution function (PDF) analyses, we proposed a new model of "three-phase" structural for HC materials and found triregion Na-ion storage behavior: chemi-/physisorption, intercalation between carbon layers, and pore-filling, derived from the HC phases, respectively. These results enable new understanding and insight into the sodium storage mechanism in HC materials and improve the potential for carbon-based SIB anodes.
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