In Situ Room-Temperature Cross-Linked Highly Branched Biopolymeric Binder Based on the Diels-Alder Reaction for High-Performance Silicon Anodes in Lithium-Ion Batteries.

ACS Appl Mater Interfaces

Department of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Shanghai Key Laboratory of Electrical Insulation and Thermal Aging, Shanghai Jiao Tong University, Shanghai 200240, China.

Published: December 2021

Silicon (Si) is an auspicious anode material in next-generation lithium-ion batteries due to its exceptional theoretical gravimetric capacity, environmental friendliness, and high natural abundance. However, the practical application of Si anodes remains a "must-solve" challenge because of its drastic capacity fading that results from the inherent property of drastic volume expansion of Si during repeated lithiation and delithiation. Developing binders employed in robust electrodes has been considered an economical and practical method to affect the electrochemical performance of Si-based electrodes. Some natural polymers have demonstrated good adhesive properties with Si-active materials. However, they have limited capacity to keep the structural integrity of electrodes because the network structures solely based on weak hydrogen bonds are susceptible to deformation during cycling. Herein, we develop an covalently cross-linked three-dimensional (3D) supramolecular network and apply it to the Si electrode to improve cycling performance. This network architecture is constructed using furan-modified branched arabinoxylan of corn fiber gum (CFG) and an ionically conductive cross-linker of maleimido-poly(ethylene glycol) (PEG) through the Diels-Alder reaction. The maleimide groups in PEG can react spontaneously with the furan groups in CFG at room temperature without any other stimulation, thus forming strong covalent bonds in the network. The cross-linked CFG-PEG binder has demonstrated robust adhesive properties with Si-active materials and the current collector. The branching of CFG and functional groups of PEG are conducive to improving the lithium-ion conductivity in the silicon anode, resulting in excellent rate performances. The Si anode with a cross-linked CFG-PEG binder exhibits superior cycling stability. As a result, an cross-linking 3D network as a novel binder has a great potential for fabricating an advanced Si anode in next-generation Li-ion batteries.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.1c16196DOI Listing

Publication Analysis

Top Keywords

diels-alder reaction
8
lithium-ion batteries
8
adhesive properties
8
properties si-active
8
si-active materials
8
groups peg
8
cross-linked cfg-peg
8
cfg-peg binder
8
network
5
situ room-temperature
4

Similar Publications

Aza-[4 + 2]-cycloaddition of benzocyclobutenones into isoquinolinone derivatives enabled by photoinduced regio-specific C-C bond cleavage.

Nat Commun

December 2024

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu, 610064, China.

The activation of C-C bond of benzocyclobutenones under mild reaction conditions remains a challenge. We herein report a photoinduced catalyst-free regio-specific C1-C8 bond cleavage of benzocyclobutenones, enabling the generation of versatile ortho-quinoid ketene methides for aza-[4 + 2]-cycloaddition with imines, which offers a facile route to isoquinolinone derivatives, including seven family members of protoberberine alkaloids, gusanlung A, B, D, 8-oxotetrahydroplamatine, tetrahydrothalifendine, tetrahydropalmatine, and xylopinine. Furthermore, the catalytic enantioselective version of this strategy is also realized by merging synergistic photocatalysis and chiral Lewis acid catalysis.

View Article and Find Full Text PDF

Three-component diels-alder reaction through palladium carbene migratory insertion enabled dearomative C(sp)-H bond activation.

Nat Commun

December 2024

Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research, Ministry of Education of China, Key Laboratory of the Assembly and Application of Organic Functional Molecules of Hunan Province, College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha, Hunan, 410081, China.

Owning to the versatile nature in participation of Diels-Alder (D-A) reactions, the development of efficient approaches to generate active ortho-quinodimethanes (o-QDMs) has gained much attention. However, a catalytic method involving coupling of two readily accessible components to construct o-QDMs is lacking. Herein, we describe a palladium carbene migratory insertion enabled dearomative C(sp)-H activation to form active o-QDM species through the cross-coupling of N-tosylhydrazones with aryl halides.

View Article and Find Full Text PDF

Steering acidic oxygen reduction selectivity of single-atom catalysts through the second sphere effect.

Nat Commun

December 2024

Center of Artificial Photosynthesis for Solar Fuels and Department of Chemistry, School of Science, Westlake University, Hangzhou, China.

Natural enzymes feature distinctive second spheres near their active sites, leading to exquisite catalytic reactivity. However, incumbent synthetic strategies offer limited versatility in functionalizing the second spheres of heterogeneous catalysts. Here, we prepare an enzyme-mimetic single Co-N atom catalyst with an elaborately configured pendant amine group in the second sphere via 1,3-dipolar cycloaddition, which switches the oxygen reduction reaction selectivity from the 4e to the 2e pathway under acidic conditions.

View Article and Find Full Text PDF

Although the Diels-Alder reaction (DA) has garnered significant attention due to its numerous advantages, its long reaction time is a drawback. Herein, we investigated the effects of polarity difference on DA using Layer-by-Layer (LbL) films comprising polycationic polyallylamine hydrochloride and polyanionic poly (styrenesulfonic acid-co-furfuryl methacrylate) [poly (SS--FMA)] as the reaction environment. First, furan composition in poly (SS--FMA) was adjusted to be 19 mol% to achieve good water solubility and layer deposition.

View Article and Find Full Text PDF

In this study, Diels-Alder reaction was performed to sulfolene and endo/exo-diacetate compounds. After a series of reactions, new conduritol A and F analogs containing oxo-bridge and naphthalene rings in their structures were synthesized. To the starting compound, bromination, elimination, singlet oxygen reaction, acetylation, selective oxidation with osmium tetroxide (OsO), and m-chloroperbenzoic acid (m-CPBA), re-acetylation, and finally hydrolysis of the compounds by NH(g)/MeOH reactions were carried out.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!