材料科学
聚吡咯
化学工程
多孔性
壳体(结构)
聚苯乙烯
碳纤维
形态学(生物学)
热解
纳米技术
聚合
复合材料
复合数
聚合物
工程类
生物
遗传学
作者
Ruilong Cai,Yinsong Si,Bo You,Min Chen,Limin Wu
标识
DOI:10.1021/acsami.0c02980
摘要
Yolk-shell carbon nanospheres (YSCNs) have raised a great deal of interest due to the synergistic advantages over their counterparts. However, it is still difficult to precisely regulate the morphology, porosity, and composition of YSCNs. Here, N-doped porous YSCNs were synthesized via an in situ self-activation by pyrolysis of polypyrrole encapsulated hyper-cross-linked polystyrene (HPS@PPy) core-shell nanospheres, followed by a mild air activation treatment. During the self-activation process, the polypyrrole shell of HPS@PPy provided a confinement effect for the morphology transformation from the core-shell to the yolk-shell structure. The air activation exhibited simultaneous control over porosity and composition. The preparation parameters, such as shell thickness and air activation conditions, were modified to optimize the structure and surface composition of YSCNs to achieve optimal electrochemical performances.
科研通智能强力驱动
Strongly Powered by AbleSci AI