Quadruple Hydrogen Bonded Nanocarbon Networks for High Performance Dispersant-Free Conducting Pastes

2014 ◽  
Vol 1700 ◽  
pp. 91-95
Author(s):  
Joong Tark Han ◽  
Jeong In Jang ◽  
Sua Choi ◽  
Seon Hee Seo ◽  
Seung Yol Jeong ◽  
...  

ABSTRACTColloidal dispersion of nanocarbon (NC) materials in dilute solutions or pastes is prerequisite for applications of NC-based electrodes from flexible electronics and flexible conducting fibers to electrochemical devices. Here, we show a straightforward method for fabricating NC suspensions with >10% weight concentrations in absence of organic dispersants. The method involves introducing supramolecular quadruple hydrogen bonding motifs into the NC materials without sacrificing the electrical conductivity.

2016 ◽  
Vol 52 (39) ◽  
pp. 6597-6600 ◽  
Author(s):  
Xue Huang ◽  
Yan-Chao Zhao ◽  
Bao-Hang Han

A rigid triptycene derivative with three 2-ureido-4[1H]-pyrimidinone (UPy) terminals was employed to construct a supramolecular hydrogen-bonded organic polymer (HOP-1).


2020 ◽  
Vol 117 (44) ◽  
pp. 27154-27161
Author(s):  
Sijie Wan ◽  
Xiang Li ◽  
Yanlei Wang ◽  
Ying Chen ◽  
Xi Xie ◽  
...  

Titanium carbide (Ti3C2Tx) MXene has great potential for use in aerospace and flexible electronics due to its excellent electrical conductivity and mechanical properties. However, the assembly of MXene nanosheets into macroscopic high-performance nanocomposites is challenging, limiting MXene’s practical applications. Here we describe our work fabricating strong and highly conductive MXene sheets through sequential bridging of hydrogen and ionic bonding. The ionic bonding agent decreases interplanar spacing and increases MXene nanosheet alignment, while the hydrogen bonding agent increases interplanar spacing and decreases MXene nanosheet alignment. Successive application of hydrogen and ionic bonding agents optimizes toughness, tensile strength, oxidation resistance in a humid environment, and resistance to sonication disintegration and mechanical abuse. The tensile strength of these MXene sheets reaches up to 436 MPa. The electrical conductivity and weight-normalized shielding efficiency are also as high as 2,988 S/cm and 58,929 dB∙cm2/g, respectively. The toughening and strengthening mechanisms are revealed by molecular-dynamics simulations. Our sequential bridging strategy opens an avenue for the assembly of other high-performance MXene nanocomposites.


2019 ◽  
Vol 6 (5) ◽  
pp. 611-617 ◽  
Author(s):  
Qiang Chen ◽  
Xiaoshi Su ◽  
Edvinas Orentas ◽  
Qixun Shi

A novel design of highly preorganized bicyclic monomers, based on quadruple hydrogen bonding motifs, is proposed to access noncovalent cavitands with large internal volumes and interesting shapes.


RSC Advances ◽  
2015 ◽  
Vol 5 (79) ◽  
pp. 64240-64246 ◽  
Author(s):  
Mustafa Supur ◽  
Ayhan Yurtsever ◽  
Ümit Akbey

N,N′-di(2-(trimethylammoniumiodide)ethylene) perylenediimide (TAIPDI), forming extensive π-stacks through the strong π–π interactions of large π-planes, was isolated in the hydrogen-bonding milieu of polyvinyl alcohol (PVA) from aqueous solutions.


2009 ◽  
Vol 11 (19) ◽  
pp. 4342-4345 ◽  
Author(s):  
Yosuke Hisamatsu ◽  
Naohiro Shirai ◽  
Shin-ichi Ikeda ◽  
Kazunori Odashima

2018 ◽  
Vol 16 (24) ◽  
pp. 4429-4432
Author(s):  
Dong-Hui Wang ◽  
Deng-Jie Zhu ◽  
Wen Ding ◽  
Min Xue ◽  
Yong Yang

A hydrogen bonded luminescent supramolecular network from HTPE and CTPE can be further tuned.


2018 ◽  
Vol 9 (44) ◽  
pp. 5395-5401 ◽  
Author(s):  
Shaobo Tan ◽  
Ye Sha ◽  
Tianyu Zhu ◽  
Md Anisur Rahman ◽  
Chuanbing Tang

A photoresponsive quadruple hydrogen-bonded supramolecular polymer was constructed using photochromic azobenzene and ureidopyrimidinone motifs.


2021 ◽  
Author(s):  
Thufail M. Ismail ◽  
Neetha Mohan ◽  
P. K. Sajith

Interaction energy (Eint) of hydrogen bonded complexes of nitroxide radicals can be assessed in terms of the deepest minimum of molecular electrostatic potential (Vmin).


Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1908
Author(s):  
Hai Li ◽  
Sooman Lim

Self-polarized piezoelectric devices have attracted significant interest owing to their fabrication processes with low energy consumption. Herein, novel poling-free piezoelectric nanogenerators (PENGs) based on self-polarized polyvinylidene difluoride (PVDF) induced by the incorporation of different surface-modified barium titanate nanoparticles (BTO NPs) were prepared via a fully printing process. To reveal the effect of intermolecular interactions between PVDF and NP surface groups, BTO NPs were modified with hydrophilic polydopamine (PDA) and hydrophobic 1H,1H,2H,2H-perfluorodecyltriethoxysilane (PFDTES) to yield PDA-BTO and PFD-BTO, respectively. This study demonstrates that the stronger hydrogen bonding interactions existed in PFD-BTO/PVDF composite film comparative to the PDA-BTO/PVDF composite film induced the higher β-phase formation (90%), which was evidenced by the XRD, FTIR and DSC results, as well as led to a better dispersion of NPs and improved mechanical properties of composite films. Consequently, PFD-BTO/PVDF-based PENGs without electric poling exhibited a significantly improved output voltage of 5.9 V and power density of 102 μW cm−3, which was 1.8 and 2.9 times higher than that of PDA-BTO/PVDF-based PENGs, respectively. This study provides a promising approach for advancing the search for high-performance, self-polarized PENGs in next-generation electric and electronic industries.


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