TY - JOUR
T1 - Hyper-Cross-Linking Mediated Self-Assembly Strategy to Synthesize Hollow Microporous Organic Nanospheres
AU - He, Zidong
AU - Zhou, Minghong
AU - Wang, Tianqi
AU - Xu, Yang
AU - Yu, Wei
AU - Shi, Buyin
AU - Huang, Kun
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/10/11
Y1 - 2017/10/11
N2 - 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 gâ'1 at 0.2 A gâ'1, with almost no capacitance loss even after 5000 cycles at 10 A gâ'1. 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.
AB - 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 gâ'1 at 0.2 A gâ'1, with almost no capacitance loss even after 5000 cycles at 10 A gâ'1. 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.
KW - carbon nanospheres
KW - hollow microporous organic nanospheres
KW - hyper-cross-linking
KW - nanocomposite materials
KW - polylactide-b-polystyrene diblock copolymers
KW - self-Assembly
UR - https://www.scopus.com/pages/publications/85031292629
U2 - 10.1021/acsami.7b08657
DO - 10.1021/acsami.7b08657
M3 - 文章
C2 - 28926693
AN - SCOPUS:85031292629
SN - 1944-8244
VL - 9
SP - 35209
EP - 35217
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 40
ER -