Polymer Crosslinking Research Articles

Characterization of Secondary Structure and Thermal Stability by Biophysical Methods of the D-alanyl,D-alanine Ligase B Protein from Escherichia coli.

Peptidoglycan (PG) is a key structural component of the bacterial cell wall and interruption of its biosynthesis is a validated target for antimicrobials. Of the enzymes involved in PG biosynthesis, D-alanyl,D-alanine ligase B (DdlB) is responsible for the condensation of two alanines, forming D-Ala-D-Ala, which is required for subsequent extracellular transpeptidase crosslinking of the mature peptidoglycan polymer. We aimed at the biophysical characterization of recombinant Escherichia coli DdlB (EcDdlB), considering parameters of melting temperature (Tm), calorimetry and Van't Hoff enthalpy changes of denaturation ( ΔHUcal and ΔHUvH ), as well as characterization of elements of secondary structure at three different pHs. DdlB was overexpressed in E. coli BL21 and purified by affinity chromatography. Thermal stability and structural characteristics of the purified enzyme were analyzed by circular dichroism (CD), differential scanning calorimetry and fluorescence spectroscopy. The stability of EcDdlB increased with proximity to its pI of 5.0, reaching the maximum at pH 5.4 with Tm and ΔHUvH U of 52.68 ºC and 484 kJ.mol-1, respectively. Deconvolutions of the CD spectra at 20 ºC showed a majority percentage of α-helix at pH 5.4 and 9.4, whereas for pH 7.4, an equal contribution of β-structures and α-helices was calculated. Thermal denaturation process of EcDdlB proved to be irreversible with an increase in β-structures that can contribute to the formation of protein aggregates. Such results will be useful for energy minimization of structural models aimed at virtual screening simulations, providing useful information in the search for drugs that inhibit peptidoglycan synthesis.

A Review on various methods for the Cross-linking of Polymers

Cross-Linking the carbon atoms suffices to transform such material intoa superior material that may be resistant to temperature, pressure, corrosion, and that can be used in a variety of applications. Cross Linking is a stabilization process in polymer chemistry which leads to multidimensional extension of polymeric chain resulting in network structure. Cross-link is a bond which links one polymer chain to other. It can be ionic or covalent. Cross Linking changes a liquid polymer into ‘solid’ or ‘gel’ by restricting the ability of movement. When polymer chains are linked together by cross-links, they lose some of their ability to move as individual polymer chains. A liquid polymer (where the chains are freely flowing) can be turned into a ‘solid’ or ‘gel’ by cross-Linking the chains together. Cross Linking increases the molecular mass of a polymer. Cross-linked polymers are important because they are mechanically strong and resistant to heat, wear and attack by solvents. Cross-link property has been used to improve the insolubility, mechanical strength, stiffness, and rigidity of polymer microbeads having potential applications in solid-phase synthesis, solid-phase extraction, and biomedical fields. Hydrogels represents a class of high-water content polymers with physical or chemical crosslinks. Their physical properties are similar to soft tissues. A popular approach to attaining controlled drug delivery from polymer-based systemsinvolves the use of cross-linkers. In order to improve the properties of polymers specific toothier applications, they can be modified by either physical cross-linkers (high pressure, irradiation) or chemical cross-linkers (glutraldehyde, genipin).Therefore, synthesis of polymer with desired cross-linker (hydrophilic/hydrophobic/rigid/flexible) and concentration of cross-linker (cross-link density) is an important.Polyethylene (PE) once cross linked is advantageously employed in the fabrication of blanket insulation for electrical and telephone wires, pipes for the transport of cold and hot liquids, prostheses for the human body. In the present review, chemical cross-Linking by free-radical, condensation, UV radiation, and small-molecule cross-Linking are discussed in details.

Effects of Hydrothermal Aging on the Breakdown Voltage of Polyesterimide

Polymers have always played a big role in the insulation of electrical machines and have been the focus of several studies when they are subjected to different stresses. The humidity and temperature are the main constraints that degrade the insulating performance of the materials when they act together causing hydrothermal aging of the polymers. This study deals with the influence of hydrothermal aging on the breakdown voltage of polyesterimide which is known as one of the most important factors which define the electrical insulation performance of the polymer. The breakdown test was executed under AC and DC voltage. A statistical analysis of breakdown data was carried out using the two-parameter Weibull distribution. According to the findings, the breakdown voltage changes with aging time. Its rise is due to a polymer crosslinking by thermal action, causing a reduction of the mean-free path of charge carriers decreasing their mobility. The decline is attributed to the material plasticization after water penetration into the polymer matrix at the beginning of aging, which is a physical effect. Eventually, the chemical effect reflects the hydrolysis reaction, which destroys the hydrogenous links of the polymer. The breakdown voltage under the DC ramp is higher than that obtained under the AC ramp. The DC breakdown voltage depends on the polarity of the applied electrical field. The polymer degradation is characterized by a change in color and the crumbling of samples.

Fabrication of Self-Oscillating Gels by Polymer Crosslinking Method and Analysis on Their Autonomous Swelling-Deswelling Behaviors.

We have developed a new methodology for fabricating self-oscillating gels by a post-polymerization crosslinking. The method enables us to make the self-oscillating gels easily just by mixing two kinds of polymer solutions at room temperature with fast gelation. Moreover, the polymer crosslinking method has the advantage that the self-oscillating gels could be fabricated from well-defined linear polymers. We revealed that the dynamic swelling-deswelling behavior of the gels was simply affected by the net amount of the catalyst for the Belousov–Zhabotinsky reaction in the whole gels, although the equilibrium swelling behavior was influenced by the properties of the constituent linear polymers. Our results offer the opportunity to access the origin of the dynamic and equilibrium behavior of materials by the hierarchical assembly as well as enable easy microfabrication of the self-oscillating gel.

Hydrogel-Based Adsorbent Material for the Effective Removal of Heavy Metals from Wastewater: A Comprehensive Review.

Water is a vital resource that is required for social and economic development. A rapid increase in industrialization and numerous anthropogenic activities have resulted in severe water contamination. In particular, the contamination caused by heavy metal discharge has a negative impact on human health and the aquatic environment due to the non-biodegradability, toxicity, and carcinogenic effects of heavy metals. Thus, there is an immediate need to recycle wastewater before releasing heavy metals into water bodies. Hydrogels, as potent adsorbent materials, are a good contenders for treating toxic heavy metals in wastewater. Hydrogels are a soft matter formed via the cross-linking of natural or synthetic polymers to develop a three-dimensional mesh structure. The inherent properties of hydrogels, such as biodegradability, swell-ability, and functionalization, have made them superior applications for heavy metal removal. In this review, we have emphasized the recent development in the synthesis of hydrogel-based adsorbent materials. The review starts with a discussion on the methods used for recycling wastewater. The discussion then shifts to properties, classification based on various criteria, and surface functionality. In addition, the synthesis and adsorption mechanisms are explained in detail with the understanding of the regeneration, recovery, and reuse of hydrogel-based adsorbent materials. Therefore, the cost-effective, facile, easy to modify and biodegradable hydrogel may provide a long-term solution for heavy metal removal.

Carbene-Mediated Polymer Cross-Linking with Diazo Compounds by C–H Activation and Insertion

Carbene-Mediated Polymer Cross-Linking with Diazo Compounds by C–H Activation and Insertion

Role of Polymer Concentration and Crosslinking Density on Release Rates of Small Molecule Drugs.

Over the past few years, researchers have demonstrated the use of hydrogels to design drug delivery platforms that offer a variety of benefits, including but not limited to longer circulation times, reduced drug degradation, and improved targeting. Furthermore, a variety of strategies have been explored to develop stimulus-responsive hydrogels to design smart drug delivery platforms that can release drugs to specific target areas and at predetermined rates. However, only a few studies have focused on exploring how innate hydrogel properties can be optimized and modulated to tailor drug dosage and release rates. Here, we investigated the individual and combined roles of polymer concentration and crosslinking density (controlled using both chemical and nanoparticle-mediated physical crosslinking) on drug delivery rates. These experiments indicated a strong correlation between the aforementioned hydrogel properties and drug release rates. Importantly, they also revealed the existence of a saturation point in the ability to control drug release rates through a combination of chemical and physical crosslinkers. Collectively, our analyses describe how different hydrogel properties affect drug release rates and lay the foundation to develop drug delivery platforms that can be programmed to release a variety of bioactive payloads at defined rates.

A reaction–diffusion model for grayscale digital light processing 3D printing

Digital light processing (DLP) 3D printing is an additive manufacturing process that utilizes light patterns to photopolymerize a liquid resin into a solid. Due to the accuracy of modern digital micromirror devices (DMD) and recent advances in resin chemistry, it is now possible to create functionally graded structures using different light intensity values, also known as grayscale DLP (g-DLP). Different intensities of light lead to differences in the polymer crosslinking density after curing, which ultimately produces a part with gradients of material properties. However, g-DLP is a complicated process. First, the DLP printing is a highly coupled chemical and physical process that involves light propagation, chemical reactions, species diffusion, heat transfer, volume shrinkage, and changes in mechanical behaviors of the curing resin. Second, in g-DLP, light gradients create strong in plane gradients of chemical species concentrations in the curing liquid resin due to the strong dependence of light intensity on the rate of monomer crosslinking. Furthermore, light gradients through the depth create concentration gradients due to the degree of cure dependent light absorption and the use of photoabsorbers. These complex physical features of the printing process must be understood in order to properly control printing parameters such as light exposure time, printing speed, and grayscale variations to achieve accurate mechanical properties. In this paper, a photopolymerization reaction–diffusion model is developed and used in conjunction with experiments to investigate the coupled effects of light propagation, chemical reaction rates, and species diffusion during g-DLP 3D printing. The model is implemented numerically utilizing the finite difference method and simulation results are compared to experimental findings of simple printed structures. The agreement between experimental and model predictions of simple quantities of interest, such as geometric feature sizes, shows that the model can capture the overcure due to free-radical and other species diffusion during printing when grayscale patterns are employed. This model lays the groundwork for future extensions that can incorporate more complex coupled physics such as heat transfer, volume shrinkage, and material property evolution, which are critically important in utilizing g-DLP 3D printing for the fabrication of high-performance parts which excellent geometric and material property tolerances.

A Review on Various Methods for the Cross-linking of Polymers

Cross-Linking the carbon atoms suffices to transform such material intoa superior material that may be resistant to temperature, pressure, corrosion, and that can be used in a variety of applications. Cross Linking is a stabilization process in polymer chemistry which leads to multidimensional extension of polymeric chain resulting in network structure. Cross-link is a bond which links one polymer chain to other. It can be ionic or covalent. Cross Linking changes a liquid polymer into ‘solid’ or ‘gel’ by restricting the ability of movement. When polymer chains are linked together by cross-links, they lose some of their ability to move as individual polymer chains. A liquid polymer (where the chains are freely flowing) can be turned into a ‘solid’ or ‘gel’ by cross-Linking the chains together. Cross Linking increases the molecular mass of a polymer. Cross-linked polymers are important because they are mechanically strong and resistant to heat, wear and attack by solvents. Cross-link property has been used to improve the insolubility, mechanical strength, stiffness, and rigidity of polymer microbeads having potential applications in solid-phase synthesis, solid-phase extraction, and biomedical fields. Hydrogels represents a class of high-water content polymers with physical or chemical crosslinks. Their physical properties are similar to soft tissues. A popular approach to attaining controlled drug delivery from polymer-based systemsinvolves the use of cross-linkers. In order to improve the properties of polymers specific toothier applications, they can be modified by either physical cross-linkers (high pressure, irradiation) or chemical cross-linkers (glutraldehyde, genipin).Therefore, synthesis of polymer with desired cross-linker (hydrophilic/hydrophobic/rigid/flexible) and concentration of cross-linker (cross-link density) is an important.Polyethylene (PE) once cross linked is advantageously employed in the fabrication of blanket insulation for electrical and telephone wires, pipes for the transport of cold and hot liquids, prostheses for the human body. In the present review, chemical cross-Linking by free-radical, condensation, UV radiation, and small-molecule cross-Linking are discussed in details.

Characterization of a Radiofluorogenic Polymer for Low-Energy Electron Beam Penetration Depth Visualization.

Low-energy (80–300 keV) electron beam accelerators are gaining in importance in the radiation processing industry due to their ease of use and wide range of applications (e.g. product surface sterilizations or polymer curing and cross-linking). Due to their very low penetration depth (tens to hundreds of microns), currently used film dosimeters exhibit dose gradients over their thickness and do not resolve the dose response in the first microns of the irradiated material. Hence, the surface dose, defined as the dose in the first micron Dµ, cannot be measured directly. This study presents a polymer material as a dosimeter candidate for high-dose low-energy electron beam irradiations. The readout of the dose-dependent fluorescence intensity, originating from a pararosaniline dye reaction when irradiated, is measured using fluorescence microscopy. So far, no in-depth characterization of the material has been performed, leaving the stability and fluorescence properties of the material not fully optimized. We describe the improvements in polymer composition and the fabrication method, and characterize the material properties in terms of the thermal stability, glass transition temperature, refractive index, hardness, rheological behavior, and water affinity. All of these create a complex set of requirements a polymer needs to fulfill to become an effective dosimeter when measuring using confocal microscopy. The fluorescence readout procedure will be addressed in further studies.

Seismic performance of Unbonded Fiber-Reinforced Elastomeric Isolators (UFREI) made by recycled rubber. Influence of suboptimal crosslinking

Seismic base isolation is considered effective to reduce the vulnerability of structures and it represents an optimal retrofitting solution in terms of reliability and effectiveness. Nowadays, one of the most promising devices is the Unbonded Fiber Reinforced Elastomeric Isolator (UFREI), which is considered a low-cost device, thanks to its lightweight, easy installation, and the total absence of steel. The rubber used to assemble the devices must be vulcanized correctly to create the polymer crosslinking to be ready for structural application. All rubber mechanical properties are strongly affected by curing temperature and curing time. In this paper, a series of experimental tests and numerical analyses have been performed to investigate the influence of crosslinking on the seismic performance of UFREIs made of regenerated Ethylene Propylene Diene Monomer (EPDM) combined with glass fiber reinforcement. Two prototypes have been considered, one vulcanized correctly at 150 °C for 40 min and the other at 130 °C for 40 min. Results obtained from Finite Element (FE) cyclic shear tests analysis and nonlinear time history analyses of a preliminary structural application have shown that the devices vulcanized at 130 °C for 40 min, although having suboptimal crosslinking density, are suitable to isolate low-rise masonry buildings properly.

Silicon oxycarbide-tin nanocomposite derived from a UV crosslinked single source preceramic precursor as high-performance anode materials for Li-ion batteries

In this work, we report an innovative and facile UV light-assisted synthesis of a nanocomposite based on silicon oxycarbide (SiOC) and tin nanoparticles. SiOC ceramic matrix, containing a conductive free carbon phase, participates in lithium-ion storage, and buffers the volume changes of Li-alloying/de-alloying material. The reported synthesis procedure through a polymer-derived ceramic route involves the preparation of a single-source precursor by UV crosslinking of a preceramic polymer in the presence of a tin precursor. Pyrolysis of this starting precursor at 1000 °C leads to a homogenous distribution of tin nanoparticles (25–35 nm) within the SiOC ceramic matrix, which is crucial for electrochemical stability of the material. SiOC/Sn nanocomposite tested as an anode for Li-ion battery exhibits high reversible capacity values (603 mAh g−1 at the current density of 74.4 mA g−1), outstanding rate capability (524 mAh g−1 at 2232 mA g−1), and superior stability (494 mAh g−1 after 250 charge/discharge cycles).

Recovery of Model Pharmaceutical Compounds from Water and Organic Solutions with Alginate-Based Composite Membranes.

In this work, we combined the non-solvent induced phase separation (NIPS) and further cross-linking by cations towards the preparation of nanofiltration membranes based on sodium alginate, a biodegradable, natural polymer. Acetone, ethanol, toluene, and hexane were used as non-solvents, and cations of calcium, silver, and aluminum—for polymer cross-linking, respectively. Results showed the precipitation strength of non-solvent played a noticeable role in the membrane’s performance; for instance, the toluene permeability changed by four orders of magnitude with the decrease of precipitation strength of the non-solvent: acetone (Ptoluene = 0.1 kg∙m−2∙h−1∙bar−1) < ethanol (3 kg∙m−2∙h−1∙bar−1) < hexane (41 kg∙m−2∙h−1∙bar−1) < toluene (415 kg∙m−2∙h−1∙bar−1). It was shown that simultaneous precipitation and crosslinking in aqueous solutions AlCl3 or AgNO3 must be used in the preparation of alginate membranes for the highly selective recovery of pharmaceutical compounds from organic media. These membranes show rejection R = 90–93% of substances with MW = 626 g/mol and ethanol permeability PEtOH = 1.5–2.5 kg∙m−2∙h−1∙bar−1. For the highly selective recovery of pharmaceutical compounds from water, the method of obtaining membranes must be changed. Precipitation in toluene and then crosslinking in aqueous solutions of AlCl3 or AgNO3 must be used sequentially instead of simultaneous precipitation and crosslinking in aqueous solutions of the same inorganic salts. The permeability of such membranes varied from 0.44 to 7.8 kg∙m−2∙h−1∙bar−1 depending on the crosslinking cation in the alginate. The rejection of model substances with MW 350 and 626 g/mol were on the level of 99%. Alginate membranes can be used to solve separation problems in the pharmaceutical field, for example, to isolate antibiotics from their extractants and remove the same antibiotics from aqueous pharmaceutical waste to prevent their accumulation in the environment and the emergence of resistant genes and bacteria.

Unique Ligand Exchange Dynamics of Metal–Organic Polyhedra for Vitrimer-like Gas Separation Membranes

Unique Ligand Exchange Dynamics of Metal–Organic Polyhedra for Vitrimer-like Gas Separation Membranes

High-efficient lignin-based polymerizable macromolecular photoinitiator with UV-blocking property for visible light polymerization

Developing high-efficient visible light macromolecular photoinitiator (macro PI) with excellent initiation performance, low migration, high biosafety and multi-function is beneficial to broaden the application of photopolymer. Lignin contains chromophores which could generate free radicals under light irradiation. In this study, a lignin-based polymerizable macro PI (DAL-11ene-amine) was designed and synthesized through covalent grafting 10-undecenoyl chloride (11ene) and hydrogen donor 4-(dimethylaminobenzoic acid) ethyl ester (EDAB) into dealkaline lignin (DAL) skeleton. The structure of DAL-11ene-amine was characterized by UV–vis, FTIR, 1H NMR, GPC, and 31P NMR spectra. Under the irradiation of a 405 nm LED, DAL-11ene-amine can directly produce active species and initiate the polymerization of acrylate monomers or thiol-ene click reaction. The photoinitiation efficiency of DAL-11ene-amine is higher than that of DAL-11ene or the two-component combination of DAL-11ene and EDAB. Using DAL-11ene-amine as PI, the prepared polymer films exhibit excellent UV-blocking property. With only 0.5 wt% addition of DAL-11ene-amine, nearly 100% of UVB + UVC and the most of UVA can be blocked by the films. Moreover, DAL-11ene-amine exhibits higher migration stability and biosafety because it can be covalently linked into polymer cross-linking networks. The results indicate that DAL-11ene-amine has great application potentials in preparing environmentally friendly UV-blocking films and biosafety coatings.

Engineering Multifunctional Hydrogel-Integrated 3D Printed Bioactive Prosthetic Interfaces for Osteoporotic Osseointegration.

3D printed porous titanium alloy implants is an advanced orthopedic material for joint replacement. However, the high risk of aseptic loosening and periprosthetic infection is difficult to avoid, and the declined autophagy of osteoporosis-derived bone marrow mesenchymal stem cells (OP-BMSCs) further severely impairs the osseointegration under the osteoporotic circumstance. It is thus becoming urgently significant to develop orthopedic materials with autophagy regulation and antibacterial bioactivity. In this regard, a novel class of multifunctional hydrogel-integrated 3D printed bioactive prosthetic interfaces is engineered for in situ osseointegration in osteoporosis. The hydrogel is fabricated from the dynamic crosslinking of synthetic polymers, natural polymers, and silver nanowires to deliver autophagy-regulated rapamycin. Therefore, the resultant soft material exhibits antibacterial ability, biocompatibility, degradability, conductive, self-healing, and stimuli-responsive abilities. In vitro experiments demonstrate that the hydrogel-integrated 3D printed bioactive prosthetic interfaces can restore the declined cellular activities of OP-BMSCs by upregulating the autophagy level and show excellent antibacterial activity against S. aureus and MRSA. More remarkably, the multifunctional 3D printed bioactive prosthetic interfaces significantly improve osseointegration and inhibit infection in osteoporotic environment in vivo. This study provides an efficient strategy to develop novel prosthetic interfaces to reduce complications after arthroplasty for patients with osteoporosis.

Vulcanization degree influence on the mechanical properties of Fiber Reinforced Elastomeric Isolators made with reactivated EPDM

Rubber is well known as the basic material for some structural devices, such as seaport fenders and seismic isolators. In practice, to seismically isolate a structure it is necessary to interpose between the foundation and the superstructure a rubber device that increases the period of the superstructure, a feature that allows the structure to be "transparent" to the seismic excitation. A seismic isolator is constituted typically by a package of several rubber pads 1–2 cm thick vertically interspersed with either steel laminas or FRP dry textiles suitably treated. In this latter case the isolator is called FREI (Fiber Reinforced Elastomeric Isolator). FREIs exhibit light weight, easy installation and low cost. In this study, recycled rubber in the form of reactivated EPDM has been used to produce very low cost FREIs, combined with glass fiber reinforcement. To be ready for structural application, the rubber used must be vulcanized correctly to properly create the polymer crosslinking. However, all rubber mechanical properties are strongly affected by curing temperature and curing time. Here, the mechanical properties of a typology of FREI conceived and produced by the authors in prototypes are evaluated through a series of experimental tests and numerical computations, taking into account the different levels of vulcanization degree. Shore A hardness test, uniaxial tensile test, and relaxation test have been conducted and verified through Finite Element (FE) modeling. All collected data allow to precisely determine the curing time and temperature to use in the industrial production to obtain optimal output mechanical properties for FREIs.

Selective Laser Sintering of High-Temperature Thermoset Polymer

Thermoplastic materials such as PA12 and PA6 have been extensively employed in Selective Laser Sintering (SLS) 3D printing applications due to their printability, processability, and crystalline structure. However, thermoplastic-based materials lack polymer inter-chain bonding, resulting in inferior mechanical and thermal properties and relatively low fatigue behavior. Therefore, 3D printing of high-performance crosslinked thermosets using SLS technology is paramount to pursue as an alternative to thermoplastics. In this work, a thermoset resin was successfully 3D printed using SLS, and its thermal stability of printed parts after a multi-step post-curing process was investigated. Dimensionally stable and high glass transition temperature (Tg: ~300 °C) thermoset parts were fabricated using SLS. The polymer crosslinking mechanism during the printing and curing process was investigated through FTIR spectra, while the mechanical stability of the SLS 3D-printed thermoset was characterized through compression tests. It is found that 100% crosslinked thermoset can be 3D printed with 900% higher compressive strength than printed green parts.

Mechanically Strong and Tailorable Polyimide Aerogels Prepared with Novel Silicone Polymer Crosslinkers.

Polyimide (PI) aerogels were prepared using self-designed silicone polymer cross-linkers with multi-amino from low-cost silane coupling agents to replace conventional small-molecule cross-linkers. The long-chain structure of silicone polymers provides more crosslinking points than small-molecule cross-linkers, thus improving the mechanical properties of polyimide. To investigate the effects of amino content and degree of polymerization on the properties of silicone polymers, the different silicone polymers and their cross-linked PI aerogels were prepared. The obtained PI aerogels exhibit densities as low as 0.106 g/cm3 and specific surface areas as high as 314 m2/g, and the maximum Young’s modulus of aerogel is up to 20.9 MPa when using (T-20) as cross-linkers. The cross-linkers were an alternative to expensive small molecule cross-linkers, which can improve the mechanical properties and reduce the cost of PI aerogels.

Polyacrylic acid and β-cyclodextrin polymer cross-linking binders to enhance capacity performance of silicon/carbon composite electrodes in lithium-ion batteries

Binders play a key role in maintaining the integrity of high-capacity silicon anodes, which otherwise experience serious capacity decay during cycling caused by huge volume variation of the silicon. With an aim to developing a highly efficient polymeric binder to mitigate this capacity decay, we present a novel binder synthesized from polyacrylic acid (PAA) and polymerized β-cyclodextrin (β-CDp) for Si anodes for the lithium-ion batteries. This PAA-β-CDp binder has a 3D network structure, which provides strong adhesion between the active material and the current collector. PAA-β-CDp binder makes silicon anode achieve a specific capacity of 2326.4 mAhg−1 at the current density of 0.2 A g−1 with a capacity retention of 64.6% after 100 cycles. The experimental results show that the PAA-β-CDp binder can effectively mitigate the huge volume change and improve the capacity and cycling performance of Si anodes.