Shell Layer Research Articles

Performance of 3D printing biomimetic conch shell and pearl shell hybrid design composites under quasi-static three-point bending load

The failure process of biomimetic hybrid design composite composed of layers of conch shell and pearl shell was studied through quasi-static three-point bending experiments and numerical simulations. The biomimetic conch shell structure with inclined angles serves as the upper layer of the hybrid structure, while the biomimetic pearl shell structure with traditional brick and mud structure serves as the lower layer of the hybrid structure, forming a hybrid design structure. Four inclined angles were designed for the structural units of the conch shell, namely 15°, 30°, 45°, and 60°. Twenty-four specimens (six specimens for each inclined angle) were prepared using 3D printing technology using both soft and hard matrix materials. The influence of different inclined angles on the fracture strength, fracture toughness, and energy absorption of hybrid design structures was experimentally studied. The biomimetic hybrid design composite specimen with a notch is placed between two supporting rollers, and a loading indenter acts at mid-span. All twenty-four specimens were notched with a triangular tip and a rectangular bottom. A loading rate of 1 mm/min is used to avoid the viscoelastic effect of the composite materials. Details of the specimens, the experimental set-up and procedure are discussed in this paper. Complementary to the experimental studies, an extensive numerical investigation was carried out to study the influence of the aspect ratio of brick and mud units on the fracture initiation and failure of hybrid design structures. The causes of crack initiation and propagation, and failure modes in biomimetic hybrid design structures were postulated. These numerical findings help in reinforcing the experimental results and provide crucial information to enhance further research in this exciting area.

Molecular Design and Controlled Self-Assembly of Copolymers as Core-Shell-Corona Nanoparticles for Smarter Tumor Treatment.

Copolymer-based core-shell-corona nanoparticles have attracted more interest for tumor chemotherapy, owing to their unique multifunctionality benefiting from their unique multilevel topological structure in comparison with the conventional core-shell ones. Here, the recent progress in such core-shell-corona nanoparticle-based drug delivery systems (DDSs) in tumor chemotherapy was reviewed, focusing on additive functionality of the shell layer for controlled drug release performance from the viewpoints of the molecular design and controlled self-assembly, such as stimuli-responsive gatekeepers, independent loading of active substances, and so on. Moreover, future perspectives have been prospected for smarter tumor treatment.

Temporal control in shell-core structured nanofilm for tracheal cartilage regeneration: synergistic optimization of anti-inflammation and chondrogenesis.

Cartilage tissue engineering offers hope for tracheal cartilage defect repair. Establishing an anti-inflammatory microenvironment stands as a prerequisite for successful tracheal cartilage restoration, especially in immunocompetent animals. Hence, scaffolds inducing an anti-inflammatory response before chondrogenesis are crucial for effectively addressing tracheal cartilage defects. Herein, we develop a shell-core structured PLGA@ICA-GT@KGN nanofilm using poly(lactic-co-glycolic acid) (PLGA) and icariin (ICA, an anti-inflammatory drug) as the shell layer and gelatin (GT) and kartogenin (KGN, a chondrogenic factor) as the core via coaxial electrospinning technology. The resultant PLGA@ICA-GT@KGN nanofilm exhibited a characteristic fibrous structure and demonstrated high biocompatibility. Notably, it showcased sustained release characteristics, releasing ICA within the initial 0 to 15 days and gradually releasing KGN between 11 and 29 days. Subsequent in vitro analysis revealed the potent anti-inflammatory capabilities of the released ICA from the shell layer, while the KGN released from the core layer effectively induced chondrogenic differentiation of bone marrow stem cells (BMSCs). Following this, the synthesized PLGA@ICA-GT@KGN nanofilms were loaded with BMSCs and stacked layer by layer, adhering to a 'sandwich model' to form a composite sandwich construct. This construct was then utilized to repair circular tracheal defects in a rabbit model. The sequential release of ICA and KGN facilitated by the PLGA@ICA-GT@KGN nanofilm established an anti-inflammatory microenvironment before initiating chondrogenic induction, leading to effective tracheal cartilage restoration. This study underscores the significance of shell-core structured nanofilms in temporally regulating anti-inflammation and chondrogenesis. This approach offers a novel perspective for addressing tracheal cartilage defects, potentially revolutionizing their treatment methodologies.

A Flexible and Stretchable MXene/Waterborne Polyurethane Composite-Coated Fiber Strain Sensor for Wearable Motion and Healthcare Monitoring.

Fiber-based flexible sensors have promising application potential in human motion and healthcare monitoring, owing to their merits of being lightweight, flexible, and easy to process. Now, high-performance elastic fiber-based strain sensors with high sensitivity, a large working range, and excellent durability are in great demand. Herein, we have easily and quickly prepared a highly sensitive and durable fiber-based strain sensor by dip coating a highly stretchable polyurethane (PU) elastic fiber in an MXene/waterborne polyurethane (WPU) dispersion solution. Benefiting from the electrostatic repulsion force between the negatively charged WPU and MXene sheets in the mixed solution, very homogeneous and stable MXene/WPU dispersion was successfully obtained, and the interconnected conducting networks were correspondingly formed in a coated MXene/WPU shell layer, which makes the as-prepared strain sensor exhibit a gauge factor of over 960, a large sensing range of over 90%, and a detection limit as low as 0.5% strain. As elastic fiber and mixed solution have the same polymer constitute, and tight bonding of the MXene/WPU conductive composite on PU fibers was achieved, enabling the as-prepared strain sensor to endure over 2500 stretching-releasing cycles and thus show good durability. Full-scale human motion detection was also performed by the strain sensor, and a body posture monitoring, analysis, and correction prototype system were developed via embedding the fiber-based strain sensors into sweaters, strongly indicating great application prospects in exercise, sports, and healthcare.

Constructing micro/nano-photonics barcodes based on micro-region upconversion emission spectrum of single core-shell microcrystal

The construction of core-shell structures with different structural properties based on the epitaxial growth technique has become an effective technique for regulating the luminescence properties of micro/nanocrystals. In order to obtain richer spectral information, NaYF<sub>4</sub>:50%Yb<sup>3+</sup>/2%Tm<sup>3+</sup>@NaYF<sub>4</sub>@NaYF<sub>4</sub>:20%Yb<sup>3+</sup>/2%Er<sup>3+</sup>@NaYF<sub>4</sub>@NaYbF<sub>4</sub>:2%Er<sup>3+</sup> multilayered core-shell microcrystals are prepared by using multiple epitaxial growth through introducing surface modifiers and controlling their reaction conditions. The XRD and SEM results clearly show that the core-shell microcrystals possess a pure hexagonal crystal structure in the form of a disk. The microdesk has a thickness of about 2.32 μm and a diameter of about 28.31 μm. The upconversion luminescence characteristics of different single microcrystal structures are investigated by a confocal microspectroscopy system. In order to realize the selective excitation and emission of a single microcrystal, the spatial distribution of luminescent ions can be controlled through introducing an intermediate isolation layer. Under 980 nm laser excitation, different excitation sites of the single microdisk exhibit different upconversion emission characteristics. The significant blue (450 and 475 nm), red (648 nm) and green (524 and 540 nm) emissions are observed, which mainly originat from Tm<sup>3+</sup> and Er<sup>3+</sup> radiative transitions. Meanwhile, the red and blue upconversion emission intensities of the microcrystals are improved by using various shell layers. In addition, the luminescence and energy-transfer features of single microcrystals are explored by changing the excitation position. The experimental results demonstrate that the incorporation of NaYF<sub>4</sub> inert shells between luminescent layers can regulate luminescence and prevent ions from interacting. By utilizing the spectral fingerprint data of dopant ions in various shell layers, we create customizable micro-nano photonic barcodes and employ them for optical anti-counterfeiting detection. This study explores the use of constructed core-shell structures with luminescent tunable micron core-shell structures to acquire diverse spectral information and maintain stability through their structural properties. Thus, this core-shell structure provides a novel method for using upconversion luminescent microcrystals into micro- and nanophotonics to achieve anti-counterfeiting and display purposes.

A coaxial electrospun mat coupled with piezoelectric stimulation and atorvastatin for rapid vascularized bone regeneration.

The repair of critical bone defects caused by various clinical conditions needs to be addressed urgently, and the regeneration of large bone defects depends on early vascularization. Therefore, enhanced vascularization of artificial bone grafts may be a promising strategy for the regeneration of critical-sized bone defects. Taking into account the importance of rapid angiogenesis during bone repair and the potential of piezoelectric stimulation in promoting bone regeneration, novel coaxial electrospun mats coupled with piezoelectric materials and angiogenic drugs were fabricated in this study using coaxial electrospinning technology, with a shell layer loaded with atorvastatin (AVT) and a core layer loaded with zinc oxide (ZnO). AVT was used as an angiogenesis inducer, and piezoelectric stimulation generated by the zinc oxide was used as an osteogenesis enhancer. The multifunctional mats were characterized in terms of morphology, core-shell structure, piezoelectric properties, drug release, and mechanical properties, and their osteogenic and angiogenic capabilities were validated in vivo and ex vivo. The results revealed that the coaxial electrospun mats exhibit a porous surface morphology and nanofibers with a core-shell structure, and the piezoelectricity of the mats improved with increasing ZnO content. Excellent biocompatibility, hydrophilicity and cell adhesion were observed in the multifunctional mats. Early and rapid release of AVT in the fibrous shell layer of the mat promoted angiogenesis in human umbilical vascular endothelial cells (HUVECs), whereas ZnO in the fibrous core layer harvested bioenergy and converted it into electrical energy to enhance osteogenic differentiation of rat bone mesenchymal stem cells (BMSCs), and both modalities synergistically promoted osteogenesis and angiogenesis. Furthermore, optimal bone regeneration was achieved in a model of critical bone defects in the rat mandible. This osteogenesis-promoting effect was induced by electrical stimulation via activation of the calcium signaling pathway. This multifunctional mat coupling piezoelectric stimulation and atorvastatin promotes angiogenesis and bone regeneration, and shows great potential in the treatment of large bone defects.

Effect of interfacial electronic structure on conductivity and space charge characteristics of core-shell quantum dots/polyethylene nanocomposite insulation

To investigate the effect of the interface electronic structure of core-shell quantum dots on the conductivity and space charge characteristics of polyethylene insulation, nanocomposite insulations, namely CdSe@ZnS/LDPE and ZnSe@ZnS/LDPE, are synthesized. The study focuses on elucidating the evolution patterns of DC conductivity and space charge in the nanocomposite insulation, and analyzing the effect of the interfacial electronic structure of core-shell quantum dots on the distribution of charge traps. Comparative analysis reveals that in contrast to LDPE insulation, ZnSe@ZnS/LDPE nanocomposite insulation demonstrates a substantial reduction in DC conductivity by 47.2% and a decrease in space charge accumulation by 40.3% under the conditions of elevated temperature and strong electric field. The increase of trap energy level means an enhanced trap effect on charger carriers. According to density functional theory, the band structure characteristics of core-shell quantum dots integrated with polyethylene are computationally assessed. The findings underscore that the band misalignment at the core-shell interface and the shell-insulation interface induces shifts in the conduction band bottom and at the valence band top, respectively. These shifts impose a confinement effect on electrons and holes, with the extent of this effect escalating with the augment of the difference in band gap between the core layer and the shell layer. Consequently, this phenomenon curtails carrier migration, thereby inhibiting space charge accumulation under the conditions of elevated temperature and strong electric fields.

Multifunctional molecularly imprinted nanozymes with improved enrichment and specificity for organic and inorganic trace compounds.

Although nanozymes exhibit properties superior to those of natural enzymes and conventional engineered enzymes, the development of highly specific nanozymes remains a challenge. New yolk-shell Fe3O4 molecularly imprinted (MIP@void@Fe3O4) nanozymes with peroxidase-like activity were developed by modelling the substrate channels of natural enzymes through molecular imprinting techniques and interfacial affinity modifications in this study. To establish a platform technology for the adsorption and determination of inorganic and organic contaminants, lead ion (Pb2+) and diazinon (DIZ), respectively, were selected as imprinting templates, and a hollow mesoporous shell was synthesized. The as-prepared MIP@void@Fe3O4 nanozymes, characterized using TEM, HRTEM, SEM, FT-IR, TGA, VSM and XPS, not only affirmed the successful fabrication of a magnetic nanoparticle with a unique hollow core-shell structure but also facilitated an exploration of the interfacial bonding mechanisms between Fe3O4 and other shell layers. The enrichment of the MIP@void@Fe3O4 nanozymes due to imprinting was approximately 5 times higher than the local substrate concentration and contributed to the increased activity. Based on selective and competitive recognition experiments, the synthesized nanozymes could selectively recognize organic and inorganic targets with the lowest detection limits (LOD) of 6.6 × 10-9 ppm for Pb2+ and 5.13 × 10-11 M for DIZ. Therefore, the proposed biosensor is expected to be a potent tool for trace pollutant detection, which provides a rational design for more advanced and subtle methods to bridge the activity gap between natural enzymes and nanozymes.

Hydroquinone colorimetric sensing based on core–shell structured CoFe2O4@N-GQDs@CeO2 nanocomposites as oxidase mimics

The core–shell structured CoFe2O4@N-GQDs@CeO2 nanocomposites were successfully synthesized by co-precipitation method, and CeO2 was uniformly dispersed on the shell layer with the help of nitrogen-doped graphene quantum dots (N-GQDs).

UV-resonant magnetoplasmonic properties of chemically synthesized indium nanoparticles.

In this article, we for the first time demonstrate magnetoplasmonic properties of metallic indium (In0) nanoparticles, one of the promising non-noble metals for UV plasmonics, by using magnetic circular dichroism (MCD) spectroscopy. In0 nanoparticles are synthesized by a kinetically controlled reduction of indium salts, followed by performing centrifugation-based size selection, giving nanoparticles of 37.5 ± 9.7 or 51.6 ± 8.4 nm in diameter. These In0 nanoparticles exhibit a single extinction peak in the UV region (<300 nm), which can be attributed to localised surface plasmon resonance (LSPR), and upon increasing the particle size, the peak is red-shifted and broadened. The MCD signatures are then typical for circular magnetoplasmonic modes of metal nanospheres, and on the basis of the MCD responses, the effective mass of an electron (m*) of indium is estimated. Interestingly, although the large-sized In0 nanoparticles (51.6 nm) have a broader LSPR linewidth, the magneto-optical (MO) activity is larger than that of the smaller one (37.5 nm), which is unlike the behaviour of Ag nanospheres with high-quality-factor plasmonic performance. This can probably be due not only to the formation of stiff semiconducting (In(OH)3) shell layers on the In0 cores (= In0@In(OH)3 core-shell morphology) but also to the effect of the dielectric function of In0 that can influence the light-helicity-dependent field-induced cyclotron shift.

PtCu/Pt core/atomic-layer shell hollow octahedra for oxygen reduction and methanol oxidation electrocatalysis.

Engineering effective bifunctional electrocatalysts that outperform the benchmark Pt/C for direct methanol proton exchange membrane fuel cells is desired and challenging. Here, we designed H-PtCu/PtL OH catalysts with a sub-nanometer Pt(111) shell layer featuring Cu- and Co-vacancies, which exhibited high activity in acidic oxygen reduction and methanol oxidation reactions.

Thermally stable Pd/CeO2@SiO2 with a core-shell structure for catalytic lean methane combustion.

Noble metal catalysts exhibit high catalytic activity in lean CH4 combustion at low temperatures. However, the high surface energy of noble metal nanoparticles makes them susceptible to deactivation due to migratory-aggregation during the catalytic process. Herein, a core-shell structure with a Pd/CeO2 core and a SiO2 shell (denoted as Pd/CeO2@SiO2) was designed and prepared to enhance the thermal stability for catalytic lean CH4 combustion. A series of characterization methods demonstrated the successful encapsulation of SiO2 and the modified thermal stability. The results of activity tests indicated that Pd/CeO2@SiO2 exhibited the optimal catalytic performance. After seven runs, Pd/CeO2@SiO2 achieved 90% conversion of CH4 at 385 °C compared to Pd/CeO2 at 440 °C. The remarkable catalytic performance was attributed to the synergistic effect of strengthened metal-support interactions and the core-shell structure. On the one hand, the migration and aggregation of Pd nanoparticles were limited due to the protection of the SiO2 shell layer. On the other hand, the SiO2 shell layer further enhanced the interactions between the Pd nanoparticles and CeO2, thus promoting the formation of PdxCe1-xO2-δ solid solutions and active oxygen species, which were beneficial for the improvement of the stability and redox capacity of the catalyst.

Flexible carbon fibres with magnetic ZIF-67 as core layer and in-situ grown NiMn-LDH nanosheets as shell layer for microwaves absorption

Fabrication of high-performance microwaves absorbers by assembling multi-dimensional nanocomponents into core-shell electromagnetic structures has been shown to be a new manufacturing strategy. In this work, a novel core-shell carbon-fibres@ZIF-67@NiMn-Layered double...

Multiple narrowband whispering-gallery model and transparent display applications of spherical hyperbolic dispersive metamaterial cavity

A novel spherical hyperbolic metamaterial (HMM) cavity for enhancing color-transparent display is designed in this work. This HMM cavity consists of a silver core wrapped alternatively by several dielectric layers and silver layers. According to the effective medium theory and Mie scattering theory, we demonstrate that such an HMM cavity supports multiple whispering-gallery modes with deep subwavelength characteristics. The number of whispering-gallery modes with the same angular momentum is equal to the number of silver layers within the HMM cavity. Furthermore, we demonstrate that these excited whispering-gallery modes are capable of strongly confining the electric fields within the different dielectric shell layers, thus reducing Ohmic losses and narrowing resonance linewidths. In addition, we systematically investigate how the structure parameters affect whispering-gallery modes for an HMM cavity with 5 alternative dielectric layers and silver layers. Interestingly, by increasing the thickness of outermost dielectric layer and silver layer, the resonance wavelength of TM&lt;sub&gt;1,2&lt;/sub&gt; mode and TM&lt;sub&gt;1,3&lt;/sub&gt; mode remain nearly unchanged. However, the TM&lt;sub&gt;1,1&lt;/sub&gt; mode experiences a significant blueshift, and the intensity of the TM&lt;sub&gt;1,1&lt;/sub&gt;, TM&lt;sub&gt;1,2&lt;/sub&gt; and TM&lt;sub&gt;1,3&lt;/sub&gt; mode can be substantially tuned. Consequently, through structural optimization, the HMM cavity can support triple narrowband resonances in the red, green, and blue spectral regions. Finally, we show that the HMM cavity exhibits dipole radiation characteristics at the three resonance wavelengths, effectively confining light within an angular range from –45° to +45° relative to the incident light direction, and confirming the scattered light viewed from a wide angle. These features make the HMM cavity suitable for achieving high transparency, brightness, and wide viewing angles in full-color transparent displays.

K-X rays induced by helium-like C ions in thick target atoms of different metals

The physical process and experimental phenomena of the interaction between highly charged heavy ions and atoms are very complex, particularly in the intermediate energy region, because of the limitation of accelerator and existing theoretical analysis, less systematic researches, incomplete atomic data, and not so high accuracy. The research of celestial element X-ray data is more scarce and the research of X-ray data of celestial elements is even more scarce. Helium-like C ions with 15–55 MeV kinetic energy provided by the HI-13 MV series accelerator of the China Institute of Atomic Energy are used to bombard Fe, Ni, Nb and Mo thick targets. The HpGe detectors are used to measure the K-X ray emission, and the corresponding K-X ray emission cross sections are obtained. Due to the different ionization degrees of the shell layers of various target atoms, the branching intensity ratio of K&lt;sub&gt;&lt;i&gt;β&lt;/i&gt; &lt;/sub&gt;to K&lt;sub&gt;&lt;i&gt;α&lt;/i&gt;&lt;/sub&gt; X rays emitted by Helium-like C ions interacting with Fe and Ni target atoms decreases with the increase of the kinetic energy of the incident ions, while the branching intensity ratio of K-X rays emitted by Nb and Mo target atoms does not change significantly. The K-X ray emission cross section of target atom is calculated by using the formula of thick target cross section, and compared with the results of different theoretical models and proton. The results show that with the increase of the kinetic energy of helium-like C ions, the total emission cross section of the K&lt;sub&gt;&lt;i&gt;β&lt;/i&gt; &lt;/sub&gt;and K&lt;sub&gt;&lt;i&gt;α&lt;/i&gt;&lt;/sub&gt; X ray emitted from Fe and Ni target atoms are most consistent with the BEA correction model considering multiple ionization, and the total emission cross section of K&lt;sub&gt;&lt;i&gt;β&lt;/i&gt; &lt;/sub&gt;and K&lt;sub&gt;&lt;i&gt;α&lt;/i&gt;&lt;/sub&gt; X ray emitted from Nb and Mo target atoms are closest to the theoretical values of PWBA model. When the energy of proton is the same as that of single nucleon C ion, the cross section of K-X ray produced by proton is about three orders of magnitude smaller than that produced by helium-like C ion.

Advanced lead-free double perovskites/silica hybrid nanocrystals for highly stable light-emitting diodes

Cs2AgIn0.98Bi0.02Cl6@KIT-6 NCs were obtained by in situ assembly within KIT-6 mesoporous molecular sieves, and their fluorescence thermal stability was significantly improved benefiting from the protection of the KIT-6 shell layer.

Repercussions of the Inner Shell Layer on the Performance of Cd-Free Quantum Dots and Their Light-Emitting Diodes.

Indium phosphide (InP) and zinc selenium tellurium (ZnSeTe) quantum dots (QDs) as less toxic alternatives have received substantial attention. The structure of QDs generally consists of a QD core, inner shell layer, and outer shell layer. We reckon that the inner shell layer, especially its components and thickness, have a significant influence on the optical and electronic performances of QDs. In this Perspective, we compare optical properties of these QDs with different inner shells and summarize how typical inner shell components and thickness influence their optical properties. The impact of the inner shell on the performance of QD light-emitting diodes (QLEDs) has also been discussed. The appropriate components and thickness of the inner shell both contribute to alleviate valence or lattice mismatch, thereby enhancing the performance of QDs. We expect that this Perspective could heighten awareness of the significance and impact of the inner shell layer in QDs and facilitate further development of QDs and QLEDs.

Influence of Ho spontaneous aggregation on the coercivity and magnetic domain movement of sintered NdY-Fe-B magnets

Development of NdY-Fe-B magnets not only reduces the cost of Nd-Fe-B type magnets but also promotes the balanced utilization of rare-earth resources. However, the lower coercivity of NdY-Fe-B magnets hinders their further development. This study investigated the coercivity of NdY-Fe-B magnets via intergranular doping of Ho76Al12Ga12 powders. Although this process improved the coercivity, the remanence substantially deteriorated with the increasing content of the Ho76Al12Ga12 alloy. A coercivity of 1.37 T was achieved in a NdY-Fe-B magnet with a Ho76Al12Ga12 alloy doping of 7 wt%, showing a coercivity increment (ΔHcj) of 0.64 T compared to the original magnet. This can be attributed to the observed microstructural and elemental distributions, as well as the analysis of the magnetic domain wall movement. An abnormal Ho-biased layer is observed between the Y-rich core and the Ho-rich shell in the matrix grains, exhibiting a higher anisotropy field compared than the shell layer. Further analysis revealed that the movement of magnetic domain wall movement was obstructed by the Ho-biased layer, demonstrating a domain-wall pinning effect within the matrix grains. Additionally, the formation of a Ho-rich shell in the outer area of the 2:14:1 matrix grain and the presence of a continuous uniform grain boundary phase were found to be important for improving both coercivity and thermal stability.

Design of a novel magnetic composite catalyst with highly efficient cobalt circulation for activating peroxymonosulfate to degrade tetracycline

In this study, a magnetic CoFe2O4/Co2O3/Na-X Zeolite (CFCOZ) composite catalyst was prepared via a co-precipitation hydrothermal method. Comprehensive characterizations suggest that the porous shell layer composed of CoFe2O4 and Co2O3 nanoparticles is evenly supported on Na-X zeolite. The specific surface area of CFCOZ is 266.93 m2/g. CFCOZ was exploited to catalyze peroxymonosulfate (PMS) to degrade tetracycline (TC). Catalytic degradation experiments indicated that the TC removal rate in the PMS/CFCOZ system was higher than that in the CoFe2O4/zeolite/PMS oxidation system. The highest degradation rate reached 96.6 % ([PMS] = 1 mM, 0.2-g/L CFCOZ, [TC] = 20 mg/L, initial pH = 7, room temperature). Several influence factors were investigated, including initial solution pH, PMS concentration, and CFCOZ dosage, etc. on the TC degradation. Electron paramagnetic resonance spectroscopy and reactive species scavenging experiments showed that 1O2, SO4−, and O2− played the predominant role in the TC removal. The possible catalytic degradation mechanism was proposed. It is found that CoFe2O4 and Co2O3 could synergistically activate PMS, and enhance the circulation efficiency between Co2+ and Co3+ to promote the generation of ROS. The cyclic experiments and characterization results between the fresh and the used CFCOZ showed its continuous catalytic activity and good structural stability.

Turning Complexity into Simplicity: In Situ Synthesis of High-Performance Si@C Anode in Battery Manufacturing Process by Partially Carbonizing the Slurry of Si Nanoparticles and Dual Polymers.

For Si/C anodes, achieving excellent performance with a simple fabrication process is still an ongoing challenge. Herein, we report a green, facile and scalable approach for the in situ synthesis of Si@C anodes during the electrode manufacturing process by partially carbonizing Si nanoparticles (Si NPs) and dual polymers at a relatively low temperature. Due to the proper mass ratio of the two polymer precursors and proper carbonization temperature, the resultant Si-based anode demonstrates a typical Si@C core-shell structure and has strong mechanical properties with the aid of dual-interfacial bonding between the Si NPs core and carbon shell layer, as well as between the C matrix and the underlying Cu foil. Consequently, the resultant Si@C anode shows a high specific capacity (3458.1 mAh g-1 at 0.2 A g-1), good rate capability (1039 mAh g-1 at 4 A g-1) and excellent cyclability (77.94% of capacity retention at a high current density of 1 A g-1 after 200 cycles). More importantly, the synthesis of the Si@C anode is integrated in situ into the electrode manufacturing process and, thus, significantly decreases the cost of the lithium-ion battery but without sacrificing the electrochemical performance of the Si@C anode. Our results provide a new strategy for designing next-generation, high-capacity and cost-effective batteries.