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Pre‐Polymerization Enables Controllable Synthesis of Nanosheet‐Based Porphyrin Polymers towards High‐Performance Li‐Ion Batteries
Author(s) -
Han Zhuolei,
Ai Yan,
Jiang Xiaolin,
You Yuxiu,
Wei Facai,
Luo Hao,
Cui Jing,
Bao Qinye,
Fu Jianwei,
He Qingguo,
Liu Shaohua,
Cheng Jiangong
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202001943
Subject(s) - porphyrin , nanosheet , materials science , polymerization , polymer , stacking , chemical engineering , lithium (medication) , nanotechnology , organic chemistry , chemistry , composite material , medicine , endocrinology , engineering
The precise regulation of nucleation growth and assembly of polymers is still an intriguing goal but an enormous challenge. In this study, we proposed a pre‐polymerization strategy to regulate the assembly and growth of polymers by facilely controlling the concentration of polymerization initiator, and thus obtained two kinds of different nanosheet‐based porphyrin polymer materials using tetrakis‐5,10,15,20‐(4‐aminophenyl) porphyrin (TAPP) as the precursor. Notably, due to the π–π stacking and doping of TAPP during the preparation process, the obtained PTAPP‐nanocube material exhibits a high intrinsic bulk conductivity reaching 1.49×10 −4  S m −1 . Profiting from the large π‐conjugated structure of porphyrin units, closely stacked layer structure and excellent conductivity, the resultant porphyrin polymers, as electrode materials for lithium ion batteries, deliver high specific capacity (≈650 mAh g −1 at the current density of 100 mA g −1 ), excellent rate performance and long‐cycle stability, which are among the best reports of porphyrin polymer‐based electrode materials for lithium‐ion batteries, to the best of our knowledge. Therefore, such a pre‐polymerization approach would provide a new insight for the controllable synthesis of polymers towards custom‐made architecture and function.

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