Porous Spheres Research Articles

Regulating Li2S Deposition and Accelerating Conversion Kinetics through Intracavity ZnS toward Low-Temperature Lithium-Sulfur Batteries.

The uncontrolled deposition behavior and sluggish conversion kinetics of the discharging product (solid Li2S) severely deteriorate the electrochemical performance of lithium-sulfur (Li-S) batteries, especially under high S loading and low-temperature conditions. Herein, a multifunctional S cathode host consisting of ZnS nanoparticles (NPs) confined in hollow porous carbon spheres (ZnS@HPCS) is synthesized via a unique capillary force-driven melting-diffusion strategy. The porous carbon shell of ZnS@HPCS provides a space-confined reservoir for soluble polysulfides and solid Li2S, while the intracavity ZnS NPs trap polysulfides, induce Li2S inside deposition, and accelerate conversion kinetics. Thus, Li-S batteries with ZnS@HPCS-S cathodes exhibit excellent electrochemical performance at both room and low temperatures (-40 °C) and high reversible capacities under high S loading (5.2 mg cm-2). Furthermore, Li2S nucleation/deposition, in situ Raman, and theoretical analyses reveal the underlying mechanism. This work offers fundamental insights into regulating Li2S deposition and designing S hosts for high-performance Li-S batteries.

Electrocatalytic oxygen reduction on nitrogen-doped porous carbon spheres prepared with resorcinol–phenolsulfonic acid–formaldehyde mixed resins

Abstract The resorcinol–phenolsulfonic acid–formaldehyde (RxPS1–xF) mixed resin spheres were prepared by the high-temperature hydrothermal synthesis. Pyrolysis of the resin spheres under NH3 atmosphere produced small, porous, conductive N-doped carbon spheres. These carbon spheres promoted electrocatalytic oxygen reduction reaction (ORR) with almost 100% four-electron reduction selectivity, and their performance was comparable to that of the state-of-the-art Pt/C catalyst.

Alkalized MQDs/Bi2S3 Porous Structure for Efficient Photocatalytic CO2 Reduction

AbstractFinding effective and specific catalytic materials for the transformation of carbon dioxide into fuel is indisputably a significant challenge. In this study, 3D porous sphere structure MXene quantum dot/Bi2S3 (MBS) composites were prepared using electrostatic self‐assemblage of protonated Bismuth sulphide nanoparticles (Bi2S3 NSs) with Ti3C2(OH)2 QDs (MQDs‐OH). The optimized MBS material demonstrates an excellent narrow band gap (Eg=1.24 V (vs. NHE)) and high selectivity and efficiency in catalyzing CH3OH, delivering impressive yields of up to 694.7 μmol/g. This study may lead to a new approach to the development of multidimensional photocatalysts for CH3OH production by adsorption of atmospheric CO2.

Hierarchical porous carbon spheres using nano-ZnO as a template to remove benzene and ethyl acetate

The treatment of volatile organic compounds emitted from the paint and coatings industry is a challenge. In this study, porous carbon spheres (PCSs) with a diameter of about 1mm were successfully prepared via the phase inversion followed by charring with nano-ZnO as the template to adsorb VOCs. Nano-ZnO prepared in situ was adapted to tailor the structure and chemical properties of PCSs, and commercial nano-ZnO was used for comparison. The resultant PCSs possessed a high surface area and favorable hierarchical porous structure. Adsorption of benzene and ethyl acetate from the paint and coatings industry can be used to evaluate the adsorption properties of PCS. Due to the doping of different amount of in-situ nano-ZnO, the specific surface area increased and the pore size decreased, which accelerated the mass transfer and had a good adsorption effect. In particular, the adsorption capacity of PCSs-2 to benzene reached 459.6mg/g. At the same time, due to the abundance of oxygen-containing functional groups on the PCSs surface, hydrogen bonds could be formed with polar molecules, thus achieving a good adsorption effect on polar VOCs. The simultaneous adsorption mechanism of benzene and ethyl acetate was also defined. These results suggested that PCS would be ideal for the removal of VOCs from the paint and coatings industry.

Hydrangea-like MnO2@sulfur-doped porous carbon spheres with high packing density for high-performance supercapacitor

Hydrangea-like MnO2@sulfur-doped porous carbon spheres with high packing density for high-performance supercapacitor

Transient Dynamics of a Porous Sphere in a Linear Fluid

This article describes the unsteady translational motion of a porous sphere with slip-surface in a quiescent viscous fluid. Apart from its radius a and density ρs , the particle is characterized by its permeability parameter γ , slip-length l and effective viscosity-ratio ϵ for interior flow. The Reynolds number for the system is assumed to be small leading to negligible convective contribution, though the transient inertia for both the liquid and the solid is comparable to viscous forces. The resulting linearized but unsteady flow-equations for both inside and outside the porous domain are solved in time-invariant frequency domain by satisfying appropriate boundary conditions. The analysis ultimately renders frequency-dependent hydrodynamic friction for the suspended body. The frictional coefficient is computed under both low and high frequency limit for different values of γ, l and ϵ so that the findings can be compared to known results with impermeable surface. Moreover, the parametric exploration shows that the sphere acts like a no-slip body even with non-zero l if aγ ≫ 1/√ϵ . Scaling arguments from a novel boundary layer theory for flow inside porous media near interfaces explain this rather unexpected observation. Also, computed fluid resistance is incorporated in equation of motion for the particle to determine its time-dependent velocity response to a force impulse. This transient response shows wide variability with ρs, γ, l and ϵ insinuating the significance of the presented study. Consequently, the paper concludes that slip and permeability should be viewed as crucial features of submicron particles if unexpected variability is to be explained in nano-scale phenomena like nano-fluidic heat conduction or viral transmission. Thus, the theory and findings in this paper will be immensely useful in modeling of nano-particle dynamics.

Controlled fabrication of hierarchical porous carbon nanospheres with high doped nitrogen content for high-performance adsorbent of biomacromolecule

Constructing nitrogen-doped porous carbons with high specific surface area, rapid mass transfer channels, and positive charge is a crucial requirement for high-performance adsorbents. Herein, by the kinetic self-assembly synthesis strategy, we prepared nitrogen-doped hierarchical porous carbon spheres (N-HPCS) with adjustable pore structure, high specific surface area, and high nitrogen doping content (8.88 %). By using ethylenediamine as an assisted polymerization and assembly agent, the hydrolysis and condensation rate of tetraethyl orthosilicate (TEOS) as the silica source and the condensation rate of 3-aminophenol and formaldehyde as the phenolic resin precursor were controlled by adjusting ammonia volume as the alkaline catalyst to tune kinetic self-assembly of silica and phenolic resin components, thus achieving their simultaneous or sequential nucleus and growth. After carbonization and selective silica etching, three types of carbon nanospheres with center-radial pores, hollow center-radial pores and hollow structure were obtained. High nitrogen doping content endowed the nanospheres with positive charge. Through adsorption experiments on the bovine serum albumin (BSA) and Hemoglobin (Hb) as typical biological macromolecules, hollow carbon nanospheres with center-radial pores exhibited excellent adsorption performance for BSA(622.34 mg g−1) and Hb(759.96 mg g−1). Our fabricated N-HPCS may become a potential candidate for high-performance adsorption materials.

High quality factor, monodisperse micron-sized random lasers based on porous PLGA spheres.

Miniature random lasers with high quality factor are crucial for applications in barcoding, bioimaging, and on-chip technologies. However, achieving monodisperse and size-tunable biocompatible random lasers has been a significant challenge. In this study, we employed poly(lactic-co-glycolic) acid (PLGA), a biocompatible material approved for medical use, as the base material for random lasers. By integrating a dye-doped PLGA solution with a microfluidic system, we successfully fabricated monodisperse and miniature dye-doped PLGA spheres with tunable sizes ranging from 25 to 52 µm. Upon optical pulse excitation, these spheres exhibited strong random lasing emission at 610-640 nm with a threshold of approximately 22 µJ·mm-2. The lasing modes demonstrated a spectral linewidth of 0.2 nm, corresponding to a quality factor of 3100. Fourier transform analysis of the lasing emission revealed fundamental cavity lengths, providing insights into the properties of the random lasers.

Synthesis of Porous Red Mud/Slag-Based Spherical Geopolymers for Efficient Methylene Blue and Ni2+ Removal from Water.

To reuse red mud and slag wastes as raw materials, a green type of porous spherical red mud/slag-based geopolymer (RSG) was synthesized by utilizing suspension curing and foaming techniques. Because methylene blue (MB) and nickel ion (Ni2+) were common and difficult to treat in wastewater, the adsorption characteristics of MB and Ni2+, as well as the phase and microstructure of the porous RSG spheres prior to and after adsorption, were thoroughly investigated. The porous RSG spheres showed a stable and mesoporous structure with a BET surface area of 31.36 m2/g. The spheres achieved the maximum removal efficiencies of 99.81% (MB) and 99.01% (Ni2+) at dosages of 16 and 10 g/L, respectively. The pseudo-second-order kinetic model and the Langmuir model could match the adsorption data of these spheres, with predicted maximum adsorption capacity (Qmax) values of 19.88 mg/g for MB and 12.39 mg/g for Ni2+, respectively. After three adsorption-desorption cycles, porous RSG spheres demonstrated good recycling capability with removal efficiencies of 98.10% (MB) and 54.60% (Ni2+). The spheres were also effective in adsorbing additional dyes (methyl orange (MO), crystal violet (CV), and malachite green (MG)) and heavy metal ions (Cd2+, Pb2+, Zn2+, and Cu2+). The spheres have potential use in water treatment.

Postoperative Outcomes of Enucleation without Closure of the Conjunctiva

Purpose: To evaluate the long-term outcomes of enucleation without conjunctival closure in a large patient cohort. Methods: A retrospective chart review was conducted from January 2011 to January 2024, examining 144 eyes of 143 patients who underwent enucleation without conjunctival closure by a single oculoplastic surgeon. Data collected included patient demographics, indications for surgery, implant types, and complications. Results: This study included 144 eyes from 143 patients undergoing enucleation without conjunctival closure. Patients had a mean age of 46.47 years (SD: 19.76; range: 4–92 years), with a mean follow-up of 14.66 months (range: 2–142 months). Indications for enucleation included blind painful eyes for a variety of reasons (e.g., endophthalmitis, end-stage glaucoma, irreparable corneal graft failure, irreparable corneal melt, and intraocular tumors, etc.) which was the most common reason in our practice (72.92%). Porous polyethylene spheres (86.11%) and polymethyl methacrylate spheres (13.89%) were the primary implants used, with no observed implant complications. Three cases (2.08%) developed conjunctival cysts post-trauma. Conclusions: Enucleation without conjunctival closure in an otherwise normal eye with no evidence of severe conjunctival shrinkage appears to be a safe and effective procedure with a low complication rate comparable to traditional techniques involving suture-based conjunctival approximation. Meticulous closure of Tenon’s capsule may be sufficient to prevent implant-related complications. This approach could potentially reduce surgical time and simplify the enucleation procedure without compromising patient outcomes.

Phosphorus and Nitrogen Dual-Doped Hollow Porous Carbon Spheres toward Enhanced Cycling Stability of Room-Temperature Na-S Batteries.

Development of room-temperature sodium-sulfur (RT Na-S) batteries with satisfactory cycling life and rate capability remains challenging due to the unfavorable electric conductivity from S species, sluggish redox kinetics of S conversion, and serious shuttle effects of sodium polysulfides (NaPSs). To address these issues, a phosphorus and nitrogen dual-doped hollow porous carbon sphere (PN-HPCs) is synthesized as the S hosts, which enhances the electric conductivity, ion diffusion, and conversion of polysulfides. Such a hollow hierarchically porous structure is beneficial to accommodate the volume variations of S species and shorten the ion/electron transfer distances during electrochemical reaction process. As a result, the S@PN-HPCs600 cathode delivers noticeable cycling performance (313 mAh g-1 after 4500 cycles at 5.0 C, and capacity degeneration of only 0.01% per cycle) and rate capability (646.4 mAh g-1@1.0 and 527.5 mAh g-1@3.0 C). This work presents an efficient strategy based on structural confinement and dual-heteroatom doping engineering for long-life RT Na-S batteries.

Biomass-derived N-doping porous carbon spheres by N2 plasma for lithium-ion batteries

Biomass-derived N-doping porous carbon spheres by N2 plasma for lithium-ion batteries

Revealing Energy Density in Porous Carbon Supercapacitors Using Hydroquinone Sulfonic Acid as Cathodic and Alizarin Red S as Anodic Redox Electrolytes.

Exploration of innovative strategies aiming to boost energy densities of supercapacitors without sacrificing the power density and long-term stability is of great importance. Herein, highly porous nitrogen-doped carbon spheres (NPCS) are decorated onto the graphite sheets (GSs) through a hydrothermal route, followed by a chemical activation. The capacitive performance of the NPCS is then enhanced by hydroquinone sulfonic acid (HSQA) incorporation in both cathodic electrolyte and electrode materials. Later, NPCS are decorated with polypyrrole (PPY), in which HSQA takes a versatile role as conjugated polymer dopant and cathodic redox additive. The capacitive performance of the negative electrodes is enhanced by incorporating of alizarin red S (ARS) as anodic redox additive. Finally, PPY(HQSA)@NPCS-GS//NPCS-GS asymmetric supercapacitor is assembled and tested in dual redox electrolyte system containing HQSA-cathodic and ARS-anodic electrolytes. This device delivers a remarkable energy density of 60.37 Wh kg-1, which is close or even better than lead acid batteries. Thus, the present work provides a novel pathway to develop high energy supercapacitors using redox active electrolytes for next-generation energy storage applications.

Joule heating synthesis for single-atomic Fe sites on porous carbon spheres and armchair-type edge defect engineering dominated oxygen reduction reaction performance

Single-atom catalysts (SACs) embedded in heteroatom-doped carbon are the most promising oxygen reduction reaction (ORR) electrocatalysts. However, the expeditious and facile synthesis of high-performance SACs with Fe-Nx active sites and identifying the role of edge-type defect at the atomic level in carbon support are essential but remain challenging. Herein, Joule heating is applied to anchor Fe single atoms on newly defect rich porous carbon spheres (Fe-N-DCSs) in milliseconds. Fe-N-DCSs achieves exceptional ORR performance, with a half-wave potential (E1/2) of 0.90 V and E1/2 lost of only 20 mV after 30,000 cycles in 0.1 M KOH, and superior Zn-air batteries performances. Density functional theory calculations establish that armchair-type edge defects decorated Fe-N4 active sites boost the desorption of OH* and diminish the ORR overpotential. This work not only provides a speedy route for the fabrication of SACs but also presents new insights into the excellent ORR activity.

Core-shell cobalt-iron@N-doped carbon: A high-performance cathode material for lithium-sulfur batteries.

Lithium-sulfur batteries hold great promise as energy storage systems, but the shuttle effect of lithium polysulfides (LiPS) and large volume variation limit their capacity and cycle life. We have developed CoFe alloy wrapped in N-doped porous carbon spheres (e-CF@NC) with a core-shell structure through simple copolymerization and pyrolysis. The nitrogen-doped porous carbon shell provides electron and ion transport channels and more active sites for electrolyte ion adsorption. The high chemically stable carbon can limit the segregation of polysulfides, further improving the battery cycling stability. Besides, the inside CoFe alloy particles catalyze the conversion between LiPS and Li2S, speeding up reaction kinetics and reducing solvation of active sites. Consequently, lithium-sulfur batteries with e-CF@NC-2 as the cathode display a high initial specific capacity of 1146 mA h g-1 at 0.1 C, excellent rate performance (891 mA h g-1 at 1 C, 741 mA h g-1 at 2 C), and satisfied cycle stability (average capacity decay rate of 0.033% per cycle at 1 C for 300 cycles), demonstrating significant application potential.

Axial modulation of catalysis mechanism via charge-asymmetric for enhanced electrocatalytic performance toward hydrogen and oxygen evolution reactions

Designing efficient, stable, and nonprecious metal bifunctional catalysts is warranted for realizing the industrial application of electrocatalytic overall water splitting. Herein, we report a new catalyst (CoFe/SNC) for the HER and OER. The active site of catalysis composed of two charge-asymmetric Co/Fe atoms could axial modulation of the catalysis mechanism, thus improving the kinetics of the HER and OER. Moreover, the use of hollow porous carbon spheres as catalyst support not only enhances the distribution of Co/Fe atoms but also improves the mass transfer during the HER and OER processes. Therefore, the CoFe/SNC displays a good alkaline HER and OER activity with a small overpotential of 96.2 mV and 285.8 mV at 10 mA cm−2, respectively. Theoretical calculations reveal that the Fe atoms with optimal absorption energy for the hydrogen intermediate and the Co centers with a reduced energy barrier for the rate-determining step are the active sites for HER and OER, respectively. Additionally, the synergistic effect of Co/Fe dual-atoms could effectively optimize the intermediate adsorption of Co/Fe-N4 sites and improve the barriers of HER and OER activity and stability. This study provides valuable insight for designing bifunctional alkaline water-splitting electrocatalysts.

Promoting nitrogen-doped porous phosphorus spheres for high-rate lithium storage

Phosphorus anode has shown great potential for the high-rate and high-energy–density lithium-ion batteries. Nevertheless, it still suffers from possible electrode cracking, ion-transport restrictions, and active-particle decomposition resulting from repeated alloying/de-alloying. To address the aforementioned issues, a nitrogen-doped flower-like porous phosphorus (f-P) sphere has been developed. The abundant micro-mesopores facilitate ion diffusion and enhance the internal bonding strength of the electrode. Concurrently, the doped nitrogen promotes the generation of a favorable solid electrolyte interphase constructed by fast-ion-conductors. As a result, the f-P exhibits a high-rate capacity of 735mAh g−1 at 20 A g−1 and maintains high Coulombic efficiencies over 900 cycles at 10 A g−1. Furthermore, coin full-cells comprising the f-P anode and lithium cobalt oxide cathode demonstrate stable operation at a high current density of 6 mA cm−2. The combination of a porous structure and doping strategy represents a viable approach for strengthening the durability of electrodes and optimizing the ion transport kinetics of advanced alloy anode materials.

Attaining superior performance in an aqueous hybrid supercapacitor based on N-Doped highly porous carbon spheres and N-S dual doped Co3O4

Cobalt oxide (Co3O4) has seen a significant interest for its application as an electrode for supercapacitors, due to its cost-effectiveness, high theoretical capacitance and outstanding redox activity. However, Co3O4 exhibits poor electrical conductivity and cycle life restricting its high-power energy storage applications. High porosity carbons are materials of choice for applications in electric double layer charge storage but suffer from poor energy densities due to limited charge storage capabilities. Here we propose a hierarchical functionalization strategy to develop N, S co-doped Co3O4 and N doped high porosity carbon micro-spheres for efficient and durable hybrid supercapacitor. Benefiting from the structural eminence, improved electrical conductivity and high quantity of N content, the heteroatom enriched N, S co-doped Co3O4 and N doped porous carbon spheres demonstrates superior electrochemical performance. Moreover, hybrid supercapacitor cell with N, S co-doped Co3O4 as a cathode and N doped porous carbon spheres as anode deliver a high specific energy of 52 Wh kg-1 at power density of 1462 W kg-1 coupled with the capacity retention of 95 % after 5,000 charge-discharge cycles.Therefore, by improving both anode and cathode simultaneously can be considered an effective approach to enhance energy storage capabilities of hybrid supercapacitors while maintain exceptionally high-power densities.

Enhanced flame retardancy and thermal insulation of epoxy resins composites incorporated with ammonium polyphosphate and ionic liquids loaded CuO-ZnO hollow spheres

Epoxy resin, as a thermosetting polymer material with good performance, has been limited in application due to its high flammability. In this investigation, porous CuO-ZnO hollow spheres (CZHS) were prepared by a hydrothermal method. By incorporation with ionic liquids loaded CuO-ZnO hollow spheres (CZHS@Ils) and ammonium polyphosphate (APP) into epoxy resin (EP) matrix, a new composite flame retardant material, named as EP/7.5APP/1.5CZHS@ILs, was developed for improvement of their thermal insulation and flame retardancy. The thermal conductivity of EP/7.5APP/1.5CZHS@ILs was measured to be 0.0197 W m −1 K −1, which is lesser than that of APP incorporated epoxy resin (EP/APP), demonstrating good thermal insulation capability. The flame retardancy were assessed using the limiting oxygen index (LOI) test, the Vertical flame testing (UL-94) test, and the cone calorimeter (CC) test. The results obtained from LOI test show that the EP/7.5APP/1.5CZHS@ILs has good flame retardancy with a LOI value of up to 28, better than that of pure EP which has a LOI value of 19.2. Moreover, a V-0 level of the EP/7.5APP/1.5CZHS@ILs was observed from the UL-94 test. The peak heat release rate (PHRR) was reduced to 257.9 kW m−2, which is 74.8 % lower than that of the pure EP. Such results are attributed to the synergy effect of CZHS@ILs and APP which offers the epoxy resin excellent flame retardancy. Taking advantages of the excellent thermal insulation, flame retardancy and better mechanical properties, the as-resulted EP/7.5APP/1.5CZHS@ILs may hold great potential for future thermal insulation and flame-retardant applications of energy saving building.

Microporous tungsten oxide spheres coupled with Ti3C2Txnanosheets for high-volumetric capacitance supercapacitors.

In the contemporary landscape of technological advancements, the burgeoning demand for portable electronics and flexible wearable devices has necessitated the development of energy storage systems with superior volumetric performance. Tungsten oxide (WO3), known for its high density and theoretical capacitance, is a promising electrode material for supercapacitors. However, low conductivity and poor cycling stability are still the key bottlenecks for its application. Herein, a novel composite comprising hollow porous WO3 spheres (HPWS) derived by template method was electrostatic self-assembled on the surface of the Ti3C2Tx nanosheets. The resulting electrodes exhibited ultra-high volumetric capacitance of 1930 F cm-3 at 1 A g-1 and rate capability of 46% at 50 A g-1, attributed to enhanced ion accessibility from microporous structure and electron transport from conductive network of Ti3C2Tx even at a high packing density of 3.86 g cm-3. Utilizing HPWS/Ti3C2Tx as the negative electrode and porous carbon as the positive electrode, the assembled asymmetric supercapacitor achieved an energy density of 31 Wh kg-1 at a power density of 650 W kg-1 with over 107% capacitance retention after 5000 cycles. This work provides a promising approach for developing next-generation supercapacitors with ultra-high volumetric capacitance.