Template Method Research Articles

Leaded Bronze Foams As Innovative Electrodes for Organic Electrosynthesis

The electrification of organic synthesis represents an outstanding green alternative to prepare valuable and fine chemicals. However, the design of electrode materials for organic electrosynthesis remains as an open field to investigate. Motivated by the superior performance of leaded bronzes as electrodes for reductive transformations,[1, 2, 3] we have developed highly porous binary and ternary leaded metal foams through the dynamic hydrogen bubble template method [4] and tested them as cathodes in the electro-organic synthesis of 2,6-dichlorobenzonitrile from 2,6-dichlorobenzaldoxime.[5]The electrocatalytic performance of the novel leaded foams was compared to the one of the planar CuSn7Pb15 leaded bronze. The novel porous leaded foams outperformed the CuSn7Pb15 electrodes in terms of chemical yield and energy efficiency. Furthermore, due to their highly crystalline surface, these materials are mechanically more stable and less prone to cathodic corrosion than flat Pb and CuSn7Pb15 electrodes.

Colloidal Templating in Catalyst Design for Thermocatalysis.

Conventional catalyst preparative methods commonly entail the impregnation, precipitation, and/or immobilization of nanoparticles on their supports. While convenient, such methods do not readily afford the ability to control collective ensemble-like nanoparticle properties, such as nanoparticle proximity, placement, and compartmentalization. In this Perspective, we illustrate how incorporating colloidal templating into catalyst design for thermocatalysis confers synthetic advantages to facilitate new catalytic investigations and augment catalytic performance, focusing on three colloid-templated catalyst structures: 3D macroporous structures, hierarchical macro-mesoporous structures, and discrete hollow nanoreactors. We outline how colloidal templating decouples the nanoparticle and support formation steps to devise modular catalyst platforms that can be flexibly tuned at different length scales. Of particular interest is the raspberry colloid templating (RCT) method which confers high thermomechanical stability by partially embedding nanoparticles within its support, while retaining high levels of reactant accessibility. We illustrate how the high modularity of the RCT approach allows one to independently control collective nanoparticle properties, such as nanoparticle proximity and localization, without concomitant changes to other catalytic descriptors that would otherwise confound analyses of their catalytic performance. We next discuss how colloidal templating can be employed to achieve spatially disparate active site functionalization while directing reactant transport within the catalyst structure to enhance selectivity in multistep catalytic cascades. Throughout this Perspective, we highlight developments in advanced characterization that interrogate transport phenomena and/or derive new insights into these catalyst structures. Finally, we offer our outlook on the future roles, applications, and challenges of colloidal templating in catalyst design for thermocatalysis.

CO2 Adsorption by CMK-3 at Low Temperatures and High Pressure to Reduce the Greenhouse Effect.

In this study, the maximum CO2 capture capacity of an ordered mesoporous carbon (CMK-3) was evaluated at high pressure (35 atm) and several temperatures (0, 10, 20, and 35 °C). CMK-3 was synthesized with the hard template method (silica SBA-15) using furfuryl alcohol and toluene as carbon sources. The CO2 adsorption isotherms were fitted to the following adsorption theories: Freundlich, Langmuir, Sips, Toth, Dubinin-Radushkevich, and Temkin. The maximum capture capacity (726.7 mg·g-1) was achieved at 0 °C and 34 atm. The results of the study of successive adsorption-desorption cycles showed that multi-cycle reversible gas capture processes could be used in optimal temperature and pressure conditions. It was determined that 0.478 g of CMK-3 would be required to reduce the CO2 concentration in 1 m3 of air to pre-industrial levels (280 ppm). The obtained results may contribute to technological developments for the mitigation of human impacts on the environment through the capture of atmospheric CO2.

Preparation of eggshell-based materials and their adsorption performance on Fe(III) in water*

Abstract If there is too much trivalent iron in the body, it will disrupt the balance of osmotic pressure inside the body, and its heavy metal properties will denature proteins. Therefore, effective management of industrial pollution source wastewater is very important for environmental protection and human’s health. Calcium carbonate particles have a good ability to adsorb trivalent iron in wastewater. The aim is to prepare porous calcium carbonate by a template method using eggshell powder, hydrochloric acid, sodium stearate, and anhydrous sodium carbonate solution as the raw materials and research the adsorption properties of porous calcium carbonate to trivalent iron. Porous calcium carbonate was prepared by a template method using eggshell powder, hydrochloric acid, sodium stearate, and anhydrous sodium carbonate solution as the raw materials. The morphology and adsorptive properties of Fe (III) of the porous calcium carbonate were analyzed by scanning electron microscope (SEM) and UV-visible spectrophotometer (UV). The best value was found between different temperatures, time, and pH. The results verified that the maximum amount of adsorption was obtained when calcination was 400°C, pH was 5, time was 60 min, and the input amount was 20 mg. The adsorption of porous calcium carbonate to Fe (III) is chemical and has a better adsorption effect.

Microwave-assisted PMS activation Ti3C2/LaFe0.5Cu0.5O3-P catalysts for efficient degradation of CIP: Enhancement of catalytic performance by phosphoric acid etching

The LaFe0.5Cu0.5O3 perovskite synthesised by MOFs template method was compounded with Mxene Ti3C2, and the novel catalyst M-Ti3C2/LFCO-P was subsequently prepared by phosphoric acid etching. This catalyst effectively induced microwave activation of peroxymonosulfate (PMS), and ciprofloxacin (CIP) was efficiently degraded with a degradation rate reaching 95.48 % within 14 min. Characterization results revealed that the MOFs template method and phosphoric acid etching increased specific surface area (from 25.91 m2/g to 142.41 m2/g) of catalyst and improved its pore size distribution. Phosphoric acid etching successfully introduced phosphorus functional groups and promoted the formation of more oxygen vacancies, thereby significantly enhancing the catalytic activity of the catalyst. The conversion of free radicals and the transformation of free radicals to non-free radicals were demonstrated. Additionally, the catalyst exhibited higher electron transfer efficiency. The catalytic reaction was primarily driven by O2– and 1O2, with OH, SO4−, and e- playing auxiliary roles. Furthermore, the degradation pathway and toxicity of CIP were also evaluated. This work provides a new perspective for improving the catalytic degradation activity of antibiotics by perovskite catalysts.

Biologically inspired shell-hollow particles for designing efficient passive all-sky radiative cooling

Passive radiation cooling (PRC), as the most promising technology to meet future cooling needs, has attracted great interest. However, there are still huge challenges in manufacturing high-efficiency and low-cost radiant coolers suitable for all-day use. Here, we report a secondary micro-nano shell-hollow structure based on blending method, inspired by the African white beetle Goliathus goliatus. Due to the difference in reflectance between the shell and the internal air, compared with the homogeneous particles, the scattered light has a changed optical path at the interface of the core (air) and the shell (SiO2), and most of the light escapes from the particles, showing strong total internal reflection. The design ingeniously deposits the nano-sized shell-hollow structure on the surface of the micron-sized shell-hollow structure, achieving high solar reflectance (95 ​%)and excellent long-wave infrared emissivity (94 ​%). Sub-ambient cooling of 7.8 and 4.7 ​°C can be achieved at night and daytime, respectively. Silica microspheres with shell and hollow structure can be prepared by soft template method, which is mature, reliable, simple and cheap.Our work provides new ideas for the design and manufacture of high-performance Passive all-day radiative cooling (PARC).

Synthesis and in vitro Biological Assessments of Novel Thiazole-Based Thiosemicarbazone Complexes

In the present work, novel heterocyclic thiazole-based thiosemicarbazone Ag(I) complexes (Hc1, Hc2, Hc3) were obtained using the template method. The structures of synthesized thiosemicarbazone compounds were determined by some spectroscopic techniques (element analysis, infrared spectra (IR), thermogravimetric analysis (TGA), organic elemental analysis, and magnetic susceptibility measurements). The biological activities of novel heterocyclic thiazole-based thiosemicarbazone Ag(I) complexes werev screenedv in vitro against selected disease-causing pathogens (Micrococcus luteus ATCC9341, Staphylococcus epidermidis ATCC12228, Bacillus cereus RSKK863, Pseudomonas aeroginosa ATCC27853, Klebsiella pneumonia ATCC27853, Enterobacter aerogenes ATCC51342, Salmonellav typhi H NCTC9018394, Shigella dysenteria NCTC2966, Proteus vulgaris RSKK96026, Candidav albicans Y-1200-NIH) were as potential antimicrobial agents. It was determined that the thiazole-based thiosemicarbazone Ag(I) complexes exhibited high or moderate antibacterial and antifungal activity.

Facile Preparation of Superhydrophobic PDMS Polymer Films with Good Mechanical Strength Based on a Wear-Resistant and Reusable Template.

In this paper, a new method involving a wear-resistant and reusable template is proposed for the preparation of high-mechanical-strength superhydrophobic polymer film based on wire electrical discharge machining (WEDM). A solid-liquid-contact-angle simulation model was established to obtain surface-texture types and sizes that may achieve superhydrophobicity. The experimental results from template preparation show that there is good agreement between the simulation and experimental results for the contact angle. The maximum contact angle on the template can reach 155.3° given the appropriate triangular surface texture and WEDM rough machining. Besides, the prepared superhydrophobic template exhibits good wear resistance and reusability. PDMS superhydrophobic polymer films were prepared by the template method, and their properties were tested. The experimental results from the preparation of superhydrophobic polymer films show that the maximum contact angle of the polymer films can be up to 154.8° and that these films have good self-cleaning and anti-icing properties, wear resistance, bending resistance, and ductility.

Temperature-Sensitive Template for Preparation of ZnO/CeO2 Composite Photocatalytic Materials and Its Catalytic Performance.

In this work, a series of thermosensitive ionic liquid functionalized polymers, PNx(IL)y, with controllable morphology and particle size were prepared by free radical polymerization. Then, using the polymer PN64(IL)8 with uniform morphology as a templating agent, the ZnO composite photocatalytic materials doped with rare earth metal Ce were prepared in combination with a microwave-assisted and templated hydrothermal reaction method. Series different Ce-doping amount photocatalytic materials ZnO-Ce-x‱ were characterized by XRD, SEM, TEM, XPS, and other methods. The results demonstrated that the templated materials PN64(IL)8 can prepare ZnO-Ce-2‱ with uniform petaloid ambulacra shape, good distribution of elements, and excellent photocatalytic performance. Photocatalytic degradation experiments of methyl orange (MO) showed that when the Ce-doping amount is only 2‱, the degradation rate of organic dyes can reach 96.5% by reacting the photocatalytic materials in water for 1 h. In addition, this kind of photocatalyst can be used for the degradation of high-concentration MO, as well as being easily recovered and effectively reused by simple filtration. Therefore, the structure of this kind of photocatalyst is controllable in the preparation process with an extremely low Ce-doping amount compared with current reports, and it has a good application prospect in the field of wastewater treatment technology.

Investigating the Potential of CO2 Nanobubble Systems for Enhanced Oil Recovery in Extra-Low-Permeability Reservoirs.

Carbon Capture, Utilization, and Storage (CCUS) stands as one of the effective means to reduce carbon emissions and serves as a crucial technical pillar for achieving experimental carbon neutrality. CO2-enhanced oil recovery (CO2-EOR) represents the foremost method for CO2 utilization. CO2-EOR represents a favorable technical means of efficiently developing extra-low-permeability reservoirs. Nevertheless, the process known as the direct injection of CO2 is highly susceptible to gas scrambling, which reduces the exposure time and contact area between CO2 and the extra-low-permeability oil matrix, making it challenging to utilize CO2 molecular diffusion effectively. In this paper, a comprehensive study involving the application of a CO2 nanobubble system in extra-low-permeability reservoirs is presented. A modified nano-SiO2 particle with pro-CO2 properties was designed using the Pickering emulsion template method and employed as a CO2 nanobubble stabilizer. The suitability of the CO2 nanobubbles for use in extra-low-permeability reservoirs was evaluated in terms of their temperature resistance, oil resistance, dimensional stability, interfacial properties, and wetting-reversal properties. The enhanced oil recovery (EOR) effect of the CO2 nanobubble system was evaluated through core experiments. The results indicate that the CO2 nanobubble system can suppress the phenomena of channeling and gravity overlap in the formation. Additionally, the system can alter the wettability, thereby improving interfacial activity. Furthermore, the system can reduce the interfacial tension, thus expanding the wave efficiency of the repellent phase fluids. The system can also improve the ability of CO2 to displace the crude oil or water in the pore space. The CO2 nanobubble system can take advantage of its size and high mass transfer efficiency, among other advantages. Injection of the gas into the extra-low-permeability reservoir can be used to block high-gas-capacity channels. The injected gas is forced to enter the low-permeability layer or matrix, with the results of core simulation experiments indicating a recovery rate of 66.28%. Nanobubble technology, the subject of this paper, has significant practical implications for enhancing the efficiency of CO2-EOR and geologic sequestration, as well as providing an environmentally friendly method as part of larger CCUS-EOR.

Synthesis of an ion-imprinted starch phosphate porous carbonaceous material removing U(VI) from wastewater: Kinetics and mechanism

Uranium enrichment and separation are important for the sustainable development of nuclear energy. In this study, reverse-phase emulsion crosslinking polymerization was used to synthesize spherical hollow porous carbon materials (II-CLSPC) with a “red blood cell” morphology after roasting. The soft template method was used to modify II-CLSPC to obtain an open pore structure, which increased its contact area. Based on this, ion imprinting was conducted to improve the selective adsorption of U(VI). A spatial site matching the size of U(VI) was formed after ion template removal, which played a crucial role in this process. Multifaceted and multilevel improvements of II-CLSPC facilitated rapid adsorption, reaching equilibrium at 40 min and a removal rate of 94.6 % (pH 5, 298 K). The pseudo-second-order kinetic model and Langmuir isothermal model indicated that the adsorption process of uranyl ions by II-CLSPC involved via monolayer chemisorption with a theoretical saturation adsorption capacity of 653.6 mg g−1. In addition, II-CLSPC exhibited excellent selectivity (KdU = 3.7 × 104 mL g−1), cyclic stability, and salt tolerance, making it a promising candidate for uranium removal from wastewater.

Eco-friendly, highly interpenetrated and slightly swollen pHEMA hydrogel foam for durable underwater superoleophobicity and emulsion separation

Despite the emergence of hydrogels as ideal candidates for preparing the superhydrophilic materials for emulsion separation, their structural stability and swelling still hinder their long-term use, mainly due to structure defects after swelling. Herein, differing from the common modification, the eco-friendly poly 2-hydroxyethyl methacrylate (pHEMA) hydrogel foam was designed and synthesized via a one-step strategy by using the high internal phase emulsion (HIPE) template method, which endowed it with a highly interpenetrated porous structure. Unlike the normal swellable hydrogels such as poly(N-isoproplyacrylamide) (PNIPAM) hydrogel, or modified hydrogel coatings, the pHEMA hydrogel foam displayed stable structure and underwater superoleophobicity after 20 d of immersion in water. The pHEMA hydrogel foam could separate different kinds of highly surfactant-stabilized oil-in-water (O/W) emulsions with a high separation efficiency of 99.3% for liquid paraffin emulsion obtained solely under gravity-driven. Additionally, it exhibited excellent antifouling performance and long-term acid/alkali tolerance over 100 h without decrease in emulsion separation efficiency (98.0%, oil/water ratio of 99:1) and permeation flux (over 2000 L·m−2·h−1) attributed to its stable bulky structure. Moreover, the pHEMA hydrogel foam demonstrated high cell viability of 96.87% and 95.96% after culturing the 3T3 clone A31 cells in the pHEMA hydrogel foam for 24 h and 48 h, respectively, indicating good biocompatibility. Hence, our work provides a new design to develop an eco-friendly bulk hydrogel foam that achieves stable structure and performance for emulsion separation.

3DOM Cu-Ce binary composite oxides for selective catalytic reduction of NO with CO

A series of 3DOM Cu-Ce catalysts for CO-SCR were prepared by a colloidal template method. Among these catalysts, 3DOM Cu1Ce1 catalyst exhibited the best CO-SCR performance (about 100 %) in the widest temperature window (450–700 ℃). Notably, this catalyst still showed excellent stability in the presence of H2O and SO2. It was found that the appropriate molar ratio of Cu and Ce could optimize the pores of Cu-Ce catalysts, and increase their specific surface area. This could contribute to the contact between reaction gas and active sites. The stronger synergistic effect between Cu and Ce could be conducive to the increase of chemisorbed oxygen, and then enhance the redox properties. These might be the key factors for the improvement of 3DOM Cu1Ce1 catalytic activity. In addition, the molar ratio of Cu to Ce had a significant influence on the adsorption of CO, which might cause the difference in the consumption of active oxygen and the formation of oxygen vacancies, thus affecting the CO-SCR performance of 3DOM Cu-Ce catalysts.

Liquid bath-assisted combustion activation preparation of nitrogen/sulfur-doped porous carbon for sodium-ion battery applications

A liquid-bath-assisted salt-template combustion activation method has been developed to overcome the shortcomings of the conventional template method, including elaborate processes and environmental pollution. Herein, N/S double-doped porous carbon material (ECSK-15) with high specific surface area (1148.60 m2 g−1) is synthesized through it for sodium-ion batteries (SIBs). Benefitting from this approach, the number of ion diffusion channels and the ion exchange rate of the product are significantly increased. When using ether-based electrolyte, after 1000 cycles at a large current density of 2 A g−1, the reversible capacity could still be maintained at 135.60 mA h g−1. The assembled full cell exhibits a high reversible capacity of 480.49 mAh g−1 at a current rate of 0.5 A g−1. The energy density is calculated to be 204.11 Wh kg−1 at a power density of 160.71 W kg−1. This work provides a porous carbon anode material with good sodium-ion storage capacity and rate performance for application in SIBs.

Platinum Cluster Decoration on Hollow Carbon Spheres for High-Efficiency Hydrogen Evolution Reaction.

Currently, platinum (Pt)/carbon support composite materials have tremendous application prospects in the hydrogen evolution reaction (HER). However, one of the primary challenges for boosting their performance is designing a substrate with the desired microstructure. Herein, the intact hollow carbon spheres (HCSs) were prepared via template method. Based on the morphology variation of the as-prepared HCSs-x, we conjectured that the polydopamine (PDA) core was generated first and then slowly grew into a complete overburden (SiO2@PDA). Afterward, Pt atomic clusters were anchored on the outer shells of HCSs-4 to construct composite electrocatalysts (Pty/HCSs-4) by a chemical reduction method. Due to the low charge-transfer resistance, the HCSs have a large electrochemical surface area and provide a continuous electron transport pathway, boosting the atom utilization efficiency during hydrogen production and release. The synthesized Pt2.5/HCSs-4 electrocatalysts exhibit excellent HER activity in acidic media, which can be ascribed to the compositional modulation and delicate structural design. Specifically, when the overpotential is 10 A g-1, the overpotential can achieve 92 mV. This work opens a new route to fabricate Pt-based electrocatalysts and brings a new understanding of the formation mechanism of HCSs.

Bacterial Blocking and Repair of Intestinal Defects With Well-Alighed Lamellar MXene/Polyvinyl Alcohol Hydrogels Prepared by Bidirectional Freezing Method

To explore the bacterial blocking effect of oriented multilayer MXene/polyvinyl alcohol (PVA) nanocomposite hydrogels and their effect on the repair of intestinal defects. MXene/PVA nanocomposite hydrogels were prepared using the traditional freezing method and the bidirectional freezing ice template method. The structures of the different hydrogels were observed using scanning electron microscopy (SEM) and micro-CT reconstruction. The rheological properties of the hydrogels were measured using a dynamic rheometer, and their mechanical properties were assessed using a universal testing machine. The burst pressure of the hydrogels was determined through burst experiments, and bacterial colony growth was observed by the osmosis method to assess the bacteria blocking ability of the hydrogels in vitro. A rat model of cecal perforation was established, and the hydrogels were used for intestinal repair. Gram staining was performed to observe in vivo the bacterial blocking ability of the hydrogels, HE staining was performed to observe the intestinal inflammation, and CD31 and CD68 immunofluorescence staining and proliferating cell nuclear antigen (PCNA) staining were performed to observe the repair effect of the hydrogels on intestinal defects. SEM and micro-CT reconstruction revealed that the hydrogel prepared by the traditional freezing method exhibited a random porous structure, while the hydrogel prepared by the bidirectional freezing method showed an oriented multilayer structure. Rheological and tensile tests indicated that the oriented hydrogel had superior mechanical properties, and the burst pressure of the oriented multilayer hydrogel was as high as 27 kPa, significantly higher than that of the non-oriented hydrogel (P<0.001). Bacterial colony growth was observed by the osmosis method and it was found that, compared with the non-oriented hydrogel, the oriented multilayer hydrogel could effectively prevent the infiltration of Escherichia coli and Staphylococcus aureus in vitro. Gram staining results showed that the oriented multilayer hydrogel could effectively block intestinal bacteria from entering the abdominal cavity in vivo. HE staining results showed that the oriented multilayer hydrogel could effectively reduce intestinal inflammation in vivo. CD31 and CD68 immunofluorescence staining and PCNA staining results showed that the oriented multilayer hydrogel had a repairing effect on intestinal defects in vivo. The oriented multilayer hydrogel prepared by bidirectional freezing effectively prevents bacterial infiltration and reduces intestinal inflammation.

Double emulsion templates for efficient production of phase change microcapsules

The utilization of phase change materials (PCMs) in thermal storage technology exhibits great potential for various applications in thermal management and latent heat storage systems. However, leakage of organic PCMs hinders its practical application. Encapsulation of PCMs in microcapsules with polymer shells can prevent PCM leakage while improving heat transfer and stability. In this study, shell monomers were introduced as an immiscible third phase into the traditional o/w two-phase emulsion system, and the formed three-phase complex emulsion was dynamically reconfigured to exhibit a core–shell encapsulated conformation induced by interfacial tension, resulting in the formation of a thermodynamically stable double emulsion. Microcapsules with 1,6-hexanediol diacrylate (HDDA) shells were successfully prepared using this double emulsion as a template. The emulsion configuration is of significant advantage in promoting stable encapsulation of the phase change material in the shell material, resulting in fast and efficient encapsulation and improved utilization of the phase change material. Phase change microcapsules with different phase change temperatures were prepared and characterized using n-octadecane (C18), methyl stearate (Mes), n-eicosane (C20) and n-docosane (C22) as phase change materials, respectively. Results show that the prepared microcapsules are spherically integrated, with smooth surfaces and obvious core–shell structures, and the enthalpies of phase transition of C18, Mes, C20 and C22 microcapsules are as high as 171.86, 122.37, 165.77 and 178.69 J/g, respectively. These microcapsules exhibit excellent thermal stability and durability and the encapsulation efficiencies exceed 99.7 % at different phase change temperatures. Furthermore, the potential applications of PCM microcapsules in the field of temperature regulation were also demonstrated. This double-emulsion template method provides a straightforward, rapid and scalable approach for the mass production of microcapsules with different core–shell compositions.

Hierarchical Magnetic Carbon Nanoflowers for Ultra-Efficient Electromagnetic Wave Absorption.

Porous carbon nanomaterials are widely applied in the electromagnetic wave absorption (EMWA) field. Among them, an emerging flower-like carbon nanomaterial, termed carbon nanoflowers (CNFs), has attracted tremendous research attention due to their unique hierarchical flower-like structure. However, the design of flower-like carbon nanomaterials with different magnetic cores for EMWA has rarely been reported. Herein, a general template method is proposed to achieve a set of high-quality magnetic CNFs, namely Co@Void@CNFs, CoNi@CNFs, and Ni@CNFs. The prepared magnetic CNFs have highly accessible surface area and internal space, rich heteroatom content, multi-scale pore system, and uniform and highly dispersed magnetic nanoparticles, as a result, deliver superior EMWA performance. Specifically, when the thickness is 2.6mm, the Co@Void@CNFs exhibit a maximum refection loss (RLmax) of -56.6dB and an effective absorption bandwidth (EAB) from 8.0 to 12.1GHz covering the whole X band. The CoNi@CNFs have an RLmax of up to -57.6dB and a wide EAB of 5.6GHz at just 1.9mm. For the Ni@CNFs, possess an ultra-broad EAB of 6.1GHz, covering the entire Ku band at 2.0mm. Overall, the hierarchical magnetic carbon nanoflowers proposed here offer new insights toward realizing multifunctional integrated carbon nanomaterials for EMWA.

Natural shellac-based microcapsules as lipase carriers for recyclable efficient Pickering interfacial biocatalysis

Enzyme is an important class of catalyst. However, the efficiency of enzyme-catalyzed reactions is constrained by the limited contact between the enzyme and its substrate. In this study, to overcome this challenge, lipase-loaded microcapsules were prepared from natural shellac and nanoparticles using the emulsion template method. These microcapsules can perform dual roles as stabilizers and enzyme carriers to construct a water-in-oil Pickering interfacial biocatalytic system. The results showed that the hydrolytic conversion of the microcapsules could reach 90% within 20 min, which was significantly higher than that of the traditional biphasic system. The catalytic activity was influenced by the oil-to-water volume ratio and the microcapsule content. The microcapsules remained highly catalytic efficiency even after storage for three months or seven cycles of reuse. These microcapsules were prepared without the use of any cross-linkers or harsh solvents. This green and efficient catalytic system has great application prospects in the food industry.

Multi‐Interfacial Heterostructure Design of Carbon Fiber/Silicone Rubber‐Oriented Composites for Microwave Absorption and Thermal Management

AbstractIn order to ensure the operation and longevity of electronic devices, the design of multifunctional composites integrating microwave absorption (MA) and thermal conduction has become the key to solving the problem. However, the superior MA properties and thermal conductivity are usually incompatible in the blend system. In this study, a modified carbon fiber/silicone rubber‐oriented structure is designed based on the multiscale design concept of heterostructures with multiple interfaces. The forward deposition‐reverse growth mechanism is utilized at the microscopic level to construct multi‐interfacial heterogeneous structures on the surface of 1D carbon fibers (CFs). The magneto‐electric coupling network of the multi‐interfacial heterostructure induces interfacial polarization and enhances MA properties and heat transfer. Subsequently, the structural design of the modified CFs is carried out on a macroscopic scale using the ice template method. The directionally aligned modified CFs/silicone rubber aerogel composites are obtained by backfilling with silicone rubber (SR). The samples achieved an effective absorption bandwidth of 4.41 GHz and a maximum reflection loss of −42.29 dB with ultra‐thin thickness (1.3 mm). The thermal conductivity of the sample is improved to 200% compared to pure silicone rubber. The composites with directional alignment have promising applications in lightweight and flexible electronic packaging.