Lightweight carbon materials of effective electromagnetic interference (EMI) shielding have attracted increasing interest because of rapid development of smart communication devices. To meet the requirement in portable electronic devices, flexible shielding materials with ultrathin characteristic have been pursued for this purpose. In this work, we demonstrated a facile strategy for scalable fabrication of flexible all-carbon networks, where the insulting polymeric frames and interfaces have been well eliminated. Microscopically, a novel carbon nanofiber-graphene nanosheet-carbon nanofiber (CNF-GN-CNF) heterojunction, which plays the dominant role as the interfacial modifier, has been observed in the as-fabricated networks. With the presence of CNF-GN-CNF heterojunctions, the all-carbon networks exhibit much increased electrical properties, resulting in the great enhancement of EMI shielding performance. The related mechanism for engineering the CNF interfaces based on the CNF-GN-CNF heterojunctions has been discussed. Implication of the results suggests that the lightweight all-carbon networks, whose thickness and density are much smaller than other graphene/polymer composites, present more promising potential as thin shielding materials in flexible portable electronics.
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http://dx.doi.org/10.1021/am502103u | DOI Listing |
Nanomaterials (Basel)
October 2024
School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, China.
It is difficult for carbonaceous materials to combine a large specific surface area with flexibility. Here, a flexible all-carbon nanoarchitecture based on the in situ growth of nanoporous graphene within "skeletal-capillary" carbon nanotube (CNT) networks has been achieved by a chemical vapor deposition (CVD) process. Multi-path long-range conductivity is established, and the porous graphene provides a large specific surface area for charge storage.
View Article and Find Full Text PDFNanomaterials (Basel)
September 2024
Department of Chemistry and Physics, Prairie View A&M University, Prairie View, TX 77446, USA.
Carbon nanotubes (CNTs) are often regarded as semi-rigid, all-carbon polymers. However, unlike conventional polymers that can form 3D networks such as hydrogels or elastomers through crosslinking in solution, CNTs have long been considered non-crosslinkable under mild conditions. This perception changed with our recent discovery of UV-defluorination-driven direct crosslinking of CNTs in solution.
View Article and Find Full Text PDFNanoscale
October 2024
School of Science, Harbin Institute of Technology, Shenzhen 518055, PR China.
J Am Chem Soc
September 2024
State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China.
To date, it remains challenging to precisely and efficiently construct structurally intriguing polycarbocycles with densely packed stereocenters in organic synthesis. Niduterpenoid B, a naturally occurring ERα inhibitor, exemplifies this complexity with its intricate polycyclic network comprising 5 cyclopentane and 1 cyclopropane rings, featuring 13 contiguous stereocenters, including 4 all-carbon quaternary centers. In this work, we describe the first total synthesis of niduterpenoid B using a structural reorganization strategy.
View Article and Find Full Text PDFJ Am Chem Soc
August 2024
Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Institute of Frontier Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Qingdao 266237, P.R. China.
Lithium-sulfur (Li-S) batteries enable a promising high-energy-storage system while facing practical challenges regarding lithium dendrites and lithium polysulfides (LiPSs) shuttling. Herein, a fascinating SOH-functionalized graphdiyne (SOGDY) was developed by grafting SOH onto GDY to modify the separator in Li-S batteries. It realizes structure-retained material transformation, that is, SOGDY retains the crystalline all-carbon network and uniform subnanopores from the initial GDY.
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