4.8 Article

Hyper-Cross-Linking Mediated Self-Assembly Strategy To Synthesize Hollow Microporous Organic Nanospheres

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 9, Issue 40, Pages 35209-35217

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.7b08657

Keywords

hollow microporous organic nanospheres; polylactide-b-polystyrene diblock copolymers; hyper-cross-linking; self-assembly; carbon nanospheres; nanocomposite materials

Funding

  1. National Natural Science Foundation of China [51273066, 21574042]
  2. Shanghai Pujiang Program [13PJ1402300]
  3. Large Instruments Open grant Foundation of East China Normal University

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Hollow microporous organic nanospheres (H-MONs) are prepared by using polylactide-b-polystyrene diblock copolymers (PLA-b-PS) as the precursor via a hyper-cross-linking mediated self-assembly strategy, in which the hyper-cross linking PS block forms the microporous organic shell framework, and the degradable PLA block produces the hollow mesoporous core structure. The formation mechanism, morphology, and porosity parameters of the resulting H-MONs are systematically investigated. Moreover, based on the hyper-cross-linking generated rigid microporous organic frameworks, hollow microporous carbon nanospheres (H-MCNs) can be achieved by further pyrolysis progress. The obtained H-MCNs as electrode materials of a supercapacitor exhibit excellent electrochemical performance with specific capacitances of up to 145 F g(-1) at 0.2 A g(-1), with almost no capacitance loss even after 5000 cycles at 10 A More especially, H-MONs can be further act as nanoreactors for the synthesis of Fe3O4 nanoparticles within hollow cores to construct magnetic core-shell Fe3O4@H-MONs nanocomposite materials. Our strategy represents a new avenue for the preparation of hollow morphology-controlled microporous organic polymers with various potential applications.

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