scholarly journals Incorporation of hydrogen‐bonding units into polymeric semiconductors toward boosting charge mobility, intrinsic stretchability, and self‐healing ability

SmartMat ◽  
2021 ◽  
Author(s):  
Xiaobo Yu ◽  
Cheng Li ◽  
Chenying Gao ◽  
Xisha Zhang ◽  
Guanxin Zhang ◽  
...  
2019 ◽  
Vol 157 ◽  
pp. 1-13 ◽  
Author(s):  
L. Guadagno ◽  
L. Vertuccio ◽  
C. Naddeo ◽  
E. Calabrese ◽  
G. Barra ◽  
...  

Author(s):  
Liangliang Xia ◽  
Ming Zhou ◽  
Hongjun Tu ◽  
wen Zeng ◽  
xiaoling Yang ◽  
...  

The preparation of room-temperature self-healing polymeric materials with good healing efficiency and high mechanical strength is challenging. Two processes are essential to realise the room-temperature self-healing of materials: (a) a...


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Jaebin Nam ◽  
Eunsoo Kim ◽  
Rajeev K.K. ◽  
Yeonho Kim ◽  
Tae-Hyun Kim

Abstract A ureido-pyrimidinone (UPy)-functionalized poly(acrylic acid) grafted with poly(ethylene glycol)(PEG), designated PAU-g-PEG, was developed as a high performance polymer binder for Si anodes in lithium-ion batteries. By introducing both a ureido-pyrimidinone (UPy) unit, which is capable of self-healing through dynamic hydrogen bonding within molecules as well as with Si, and an ion-conducting PEG onto the side chain of the poly(acrylic acid), this water-based self-healable and conductive polymer binder can effectively accommodate the volume changes of Si, while maintaining electronic integrity, in an electrode during repeated charge/discharge cycles. The Si@PAU-g-PEG electrode retained a high capacity of 1,450.2 mAh g−1 and a Coulombic efficiency of 99.4% even after 350 cycles under a C-rate of 0.5 C. Under a high C-rate of 3 C, an outstanding capacity of 2,500 mAh g−1 was also achieved, thus demonstrating its potential for improving the electrochemical performance of Si anodes.


2018 ◽  
Vol 30 (36) ◽  
pp. 1802792 ◽  
Author(s):  
Ryota Tamate ◽  
Kei Hashimoto ◽  
Tatsuhiro Horii ◽  
Manabu Hirasawa ◽  
Xiang Li ◽  
...  

2019 ◽  
Vol 7 (9) ◽  
pp. 1475-1493 ◽  
Author(s):  
Sovan Lal Banerjee ◽  
Thomas Swift ◽  
Richard Hoskins ◽  
Stephen Rimmer ◽  
Nikhil K. Singha

In this investigation, we report a non-covalent (ionic interlocking and hydrogen bonding) strategy of self-healing in a covalently crosslinked organic–inorganic hybrid nanocomposite hydrogel, with specific emphasis on tuning its properties fitting into a muscle mimetic material.


2020 ◽  
Vol 393 ◽  
pp. 124685 ◽  
Author(s):  
Ren'ai Li ◽  
Ting Fan ◽  
Guangxue Chen ◽  
Hujun Xie ◽  
Bin Su ◽  
...  

2019 ◽  
Vol 52 (5) ◽  
pp. 410-431 ◽  
Author(s):  
Xun Lu ◽  
Min Xu ◽  
Ye-ming Sheng ◽  
Zhi-peng Li ◽  
Han-mo Li

It is urgent for polyurethane (PU) damping materials to broaden the effective damping range. Based on the designability of PU, this study is focused on the role of long dangling chain, wherein prepared by the reaction of polyethylene glycol monomethyl ether with toluene-2,4-diisocyanate. Notably, the introduction of long dangling chain not only makes the dangling chain longer and enhances the intermolecular interaction but also equips the dangling chain with strong polar carbamate group, bringing about more excellent compatibility of the soft and hard segments and lower degree of microphase separation under the condition of hydrogen bonding. The results show that the damping performance increases with the synergistic effect of significant hydrogen bonding and decreased degree of microphase separation, and the effective damping temperature range (tan δ ≥ 0.3) can exceed 150°C (−50°C to 100°C). Simultaneously, the addition of long dangling chains endows PU with self-healing property, the self-healing rate of system reaches maximum 70% with shore A hardness of 15 because of the synergistic effect above with the addition of 60% dangling chain, which extends the service life of PU damping materials.


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