Intervention-Free Graphitization of Carbon Microspheres from a Non-Graphitizing Polymer at Low Temperature: Nanopores as Dynamic Nanoreactors.

Graphitizability of organic precursors is the topic of numerous investigations due to the wide applications of graphitic materials in the industry and emerging technologies of supercapacitors, batteries, etc. Most polymers, such as polydivinyl benzene (PDVB) are classified as non-graphitizings that do not convert to Graphite even after heating to 3000℃. Here, for the first time, the development of graphitic structure in the hierarchal porous sulfonated-PDVB microspheres without employing specific equipment or additives like metal catalysts, organic ingredients, or graphite particles, at 1100°C is reported. The abnormal additive-free graphitic structure formation is confirmed by Raman spectroscopy (ID/IG = 0.87), high-resolution transmission electron microscopy (HRTEM), and selected area diffraction patterns (SAED), as well as x-ray diffraction patterns (XRD), while preservation of aromatic compounds from the carbonization is detected by Fourier transform infrared (FTIR) analysis. Polymer evolution from room temperature to 1100°C is also studied by FTIR, Raman spectroscopy, and XRD techniques. Based on the obtained results, it is suggested that the hierarchal and complicated ink-bottle pore network with a high surface area besides super micropores in the sulfonated-PDVB microspheres has served as nano-sized reaction media. These pores, hereafter referred as "dynamic nanoreactors", are expected to have confined the in-situ produced thermal decomposition products containing broken bond benzene rings, while changing dimensionally and structurally during the designed carbonization regime. This confinement has led to the benzene rings fusion at 250°C, a remarkable extension of them at 450°C, their growth to graphene sheets at 900°C and finally, the stacking of curved graphene layers at 1100°C. The results of this research put stress on the capability of nanopores as nanoreactors to facilitate reactions of decomposition products at low temperatures and ambient pressures to form stacked layers of graphene; A transformation that normally requires catalysts and very high pressures for only specific polyaromatic hydrocarbons.

Solvothermal Synthesis and Pyrolysis Toward Heteroatom-Doped Carbon Microspheres for Zinc-Ion Hybrid Capacitors.

Heteroatom-doped porous carbon materials have investigated to promote the energy density of zinc-ion hybrid capacitors (ZICs). Yet, the quest for high-performance carbon materials or cathodes brings to light the question of which dopants facilitate fast energy storage kinetics and various types of pseudocapacitive reactions. Investigation of carbon materials with precise quantitative dopants as the key variable represents an effective appropriate approach to comprehending the intricate role of dopants in energy storage areas. Here, a straightforward solvothermal strategy is demonstrated for a variety of pristine and iron-incorporated polymer microspheres, used as precursors for durable spherical carbons intended for cathode applications in ZICs. The strategy effectively governs the incorporation of dopants within the carbon materials, whilewhile maintaining consistent morphology, microtexture, and pore structure across different carbon variations. The synergistic effect of various dopants enhance the pseudocapacitance and facilitate the ion storage process. In consequence, the optimal cathode delivers considerable capacity (178.8 mAh g-1 at 0.5 A g-1), good energy density (120.2 Wh kg-1 at 336 W kg-1), and excellent cycling stability (101.5% capacity retention at 35 000 cycles). The demonstration showcases a viable method for crafting carbon materials with precise dopants to accommodate the zinc anode, thus enabling high-capacity and high-energy ZICs.

Innovative Wearable Electronics: Next-Generation Nitrogen-Doped Lutetium-Carbon Microspheres Composites for Robust Energy Harvesting.

In the quest to advance wearable electronics, this study presents a novel method using nitrogen-doped lutetium-carbon microspheres (N, Lu-CMS) for high-performance piezoelectric energy harvesting. The synthesis of N, Lu-CMS begins with the polymerization of sucrose, followed by the preparation of N, Lu-CMS metal complexes through the incorporation of lutetium (III) nitrate hydrate and thiourea, yielding a black powder product. The wearable electronic device is designed with a silicon rubber (SR) matrix, reinforced with 0D fillers such as N, Lu-CMS, or molybdenum disulfide (MoS2). Mechanical testing revealed a significant improvement in compressive modulus, reaching 3.7 MPa (N, Lu-CMS) at a concentration of 3 parts per hundred rubber (phr). Electromechanical assessments demonstrated efficient energy conversion, while biomechanical analysis, including thumb pressing tests, showed a notable increase in output voltage, peaking at ≈285 mV (N, Lu-CMS) at 3 phr. This research provides a foundation for future engineering applications, particularly in electronic packaging for wearable electronics and smart devices, underscoring the significant impact of N, Lu-CMS in this emerging field. The surface power density achieved is 0.026 nW cm- 2 (N, Lu-CMS) and 0.0056 nW cm- 2 (Hybrid). Lastly, the conversion efficiency is 6.26% for N, Lu-CMS, and 1.05% for the hybrid system.

Synthesis and Properties of Carbon Microspheres from Waste Office Paper.

As a kind of biomass resource, waste office paper can be used as a carbon precursor to prepare carbon materials. In this work, carbon microspheres with regular shape, uniform particle size and high carbon content were successfully prepared from waste office paper via a hydrothermal synthesis method with sulfuric acid as the catalyst. The effects of reaction temperature and sulfuric acid dosage on the morphology of the carbon microspheres were studied. The formation mechanism of the carbon microspheres was investigated by analyzing the structure and composition of the products. The results show that the hydrolysis of cellulose in waste paper under hydrothermal conditions was the key for the formation of carbon microspheres. The temperature of hydrothermal reaction and the use of sulfuric acid can affect the morphology of carbon microspheres. The carbon microspheres synthesized at 210 °C with 10 mL sulfuric acid have the best surface morphology, with uniform particle size and higher dispersion. Cyclic voltammetry and electrochemical impedance spectroscopy show that the carbon microspheres have good capacitance performance and can be used in capacitors. This study provides a low-cost precursor for carbon microspheres as well as a new method for the recycle of waste paper.

Carbon Microsphere-Supported Metallic Nickel Nanoparticles as Novel Heterogeneous Catalysts and Their Application for the Reduction of Nitrophenol.

Nickel nanoparticles are gaining increasing attention in catalysis due to their versatile catalytic action. A novel, low-cost and facile method was developed in this work to synthesize carbon microsphere-supported metallic nickel nanoparticles (Ni-NP/C) for heterogeneous catalysis. The synthesis was based on carbonizing a polystyrene-based cation exchange resin loaded with nickel ions at temperatures between 500 and 1000 °C. The decomposition of the nickel-organic framework resulted in both Ni-NP and carbon microsphere formation. The phase composition, morphology and surface area of these Ni-NP/C microspheres were characterized by powder X-ray diffraction, Raman spectroscopy, scanning electron microscopy and BET analysis. Elemental nickel was found to be the only metal containing phase; fcc-Ni coexisted with hcp-Ni at carbonization temperatures between 500 and 700 °C, and fcc-Ni was the only metallic phase at 800-1000 °C. Graphitization and carbon nanotube formation were observed at high temperatures. The catalytic activity of Ni-NP/C was tested in the reduction of 4-nitrophenol to 4-aminophenol by sodium borohydride, and Ni-NP/C was proved to be an efficient catalyst in this reaction. The relatively easy and scalable synthetic method, as well as the easy separation and catalytic activity of Ni-NP/C, provide a viable alternative to existing nickel nanocatalysts in future applications.

Application of Carbon-Microsphere-Modified Electrodes for Electrochemistry of Hemoglobin and Electrocatalytic Sensing of Trichloroacetic Acid.

By using the hydrothermal method, carbon microspheres (CMS) were fabricated and used for electrode modification. The characteristics of CMS were investigated using various techniques. The biocompatible sensing platform was built by immobilizing hemoglobin (Hb) on the micrometer-sized CMS-modified electrode with a layer of chitosan membrane. On the cyclic voltammogram, a couple of quasi-reversible cathodic and anodic peaks appeared, showing that direct electrochemistry of Hb with the working electrode was achieved. The catalytic reduction peak currents of the bioelectrode to trichloroacetic acid was established in the linear range of 2.0~70.0 mmol·L(-1) accompanied by a detection limit of 0.30 mmol·L(-1) (3σ). The modified electrode displayed favorable sensitivity, good reproducibility and stability, which suggests that CMS is promising for fabricating third-generation bioelectrochemical sensors.

Nitrogen-doped hollow carbon sphere composite Mn3O4 as an advanced host for lithium-sulfur battery.

As the most promising advanced energy storage system, lithium-sulfur batteries (LSBs) are highly favored by the researchers because of their advantages of high energy density (2500 W h kg-1), low cost and non-pollution. However, the low conductivity, volume expansion of sulfur, and shuttle effect are still the great hindrance to the practical application of LSBs. Herein, the above problems can be addressed through the following strategies: (1) Hollow carbon microspheres with high specific surface area were constructed as sulfur hosts to increase sulfur loading while also being able to enhance the physical adsorption of polysulfides; (2) the loading of Mn3O4 particles on the basis of hollow carbon microspheres facilitates the capture and adsorption of polysulfides; (3) the hollow carbon sphere structure as a conductive network can provide more pathways for rapid electrical/ionic transport and also accelerate electrolyte wetting. Moreover, the thinner shell of hollow carbon microsphere is conducive to ion diffusion and speed up the reaction rate. Thus, the NHCS/Mn3O4/S composites exhibit a high discharge specific capacity of 1010.3 mAh g-1 at first and still maintained a reversible capacity of 269.2 mAh g-1 after 500 cycles. This work presents a facile sustainable and efficient synergistic strategy for the development of advanced LSBs.

A new sustainable filtration membrane extraction method based on nanoconfined liquid phase extraction: Determination of organochlorinated pesticides and pyrethroids in tea samples.

BACKGROUND: Pesticides are used in agricultural production for prevent and control crop diseases and pests, but it is easy to cause excessive pesticides residues in agricultural products, polluting the environment and endangering human health. Due to their unmatched and sustainable capabilities, nanoextraction procedures are becoming every day more important in Analytical Chemistry. In particular, nanoconfined liquid phase extraction has shown extraction capabilities toward polar, medium polar, and/or nonpolar substances, which can be easily modulated depending on the nanoconfined solvent used. Furthermore, this "green" technique showed excellent characteristics in terms of recoveries, extraction time (≤1 min), reliability, and versatility. (97) RESULTS: In this work, the advantages of this technique have been coupled with those of filtration membrane extraction, making use of carbon nanofibers (CnFs) growth on carbon microspheres (CµS). This substrate has been deposited on a filter, which combined with gas chromatographic mass spectrometry (GC-MS) analysis successfully employed for the nanoextraction of 30 pesticides (18 organochlorine and 12 pyrethroids) in tea samples. Under the optimized extraction conditions, the linear range with standard solutions was from 1 to 1000 ng mL-1 (R2 ≥ 0.99), the limit of detections in tea samples were in the range 0.56-17.98 µg kg-1. The accuracy of the developed method was evaluated by measuring the extraction recovery of the spiked tea samples, and recoveries between 74.41 % and 115.46 %. (119) SIGNIFICANCE: Considering the versatility of nanoconfined liquid phase extraction and the functionality of the filtration membrane extraction procedure, this new extraction method can be considered a powerful candidate for automatized high-throughput analyses of real samples. (34).

Low-strain and ultra-long cycle stability large-diameter soft carbon microsphere potassium ion anode.

Potassium-ion batteries (PIBs) with high potassium abundance, low redox potential of K/K+ and similar energy storage mechanism to lithium-ion batteries are potential candidates for large-scale energy storage in the future. However, due to the large size of K+ (1.38 Å), PIBs exhibit poor kinetics in existing commercial graphite anode materials system. Additionally, they can degrade the material structure and induce significant volume effects, leading to material fragmentation and pulverization in the process of long cycling. It is not straightforward to achieve compatibility with existing potassium anode systems, which forces us to develop new high-performance, low-strain anode materials with outstanding structural stability. Hence, nitrogen doping low-strain and large diameter soft carbon microspheres (NDCS) anodes were successfully developed to meet the demands of high-performance PIBs. Due to its large diameter and low strain characteristics, the Coulomb efficiency is as high as 98.7 %, and the capacity retention is close to 70 % after 4000 cycles at a current density of 1 A/g. Furthermore, we employed advanced computed tomography (CT) techniques to enhance the comprehension of electrochemically driven reactions from the surface to the bulk. This work provides a promising and viable technical solution for exploring PIBs anode materials with low strain and long cycling capabilities to meet the requirements of various application scenarios.

Lignin-derived sulfonate base metal-free N, S co-doped carbon microspheres doped with different nitrogen sources as catalysts for oxygen reduction reactions.

The oxygen reduction reaction (ORR) is an important step in the widespread application of metal-air batteries, so it is necessary to study and develop low-cost and efficient metal-free carbon-based catalysts to catalyze the ORR reaction. Heteroatomic doping, especially N and S co-doped carbon materials, has received much focus as a promising ORR catalyst. Meanwhile, the lignin material has high carbon content, wide source, and low price, and has wide application prospects for the preparation of carbon material catalysts. Here we report a hydrothermal­carbonation preparation method for the synthesis of carbon microspheres by utilizing lignin derivatives as carbon precursors. And a variety of N, S co-doped carbon microsphere materials were prepared by adding different nitrogen sources (urea, melamine, NH4Cl) to the microspheres. The N, S co-doped carbon microspheres (NSCMS-MLSN) catalysts achieved with NH4Cl as the nitrogen source displayed superior RR catalytic activity with high half-wave potential (E1/2 = 0.83 V vs. RHE) and current density (JL = 4.78 mA cm-2). This work provides some references on the method of preparing carbon materials co-doped with N and S and the choice of nitrogen sources.

Study on the polystyrene plastic degradation in supercritical water/CO2 mixed environment and carbon fixation of polystyrene plastic in CO2 environment.

Through the degradation of organic waste, the carbon can be extracted and converted into syngas with calorific value, and the CO2 generated can also be used after fixed. In this work, the gasification of polystyrene (PS) in supercritical water with CO2 was studied in the temperature range of 400 °C-700 °C and time range of 0-30 min. In addition, PS containing only carbon and hydrogen can react with CO2 to generate CO in CO2 atmosphere. Therefore, the degradation of PS plastics in CO2 atmosphere was also studied. The results showed that PS plastic was hardly gasified at 400 °C, and as the temperature rose, the liquid composition changed. In supercritical water, under certain feedstock conditions, reacting for 20 min, the carbon conversion efficiency of PS plastic reached 47.6% at 700 °C. Under all CO2 atmosphere conditions in this experiment, the highest proportion of CO2 consumed by PS degradation was 12.5%. Moreover, the higher the temperature, the smaller the average diameter of carbon microspheres in the solid product. The morphology of carbon microsphere was also related to the reaction time, and the main change came from the gasification of carbon microspheres and the precipitation and adhesion of carbon element in liquid product.

Natural Polysaccharide Strengthened Hydrogel Electrolyte and Biopolymer Derived Carbon for Durable Aqueous Zinc Ion Storage.

Aqueous zinc-ion hybrid supercapacitors (ZHSCs) represent one of the current research subjects because of their flame retardancy, ease of manufacturing, and exceptional roundtrip efficiency. With the evolution into real useful energy storage cells, the bottleneck factors of the corrosion and dendrite growth problems must be properly resolved for largely boosting their cycling life and energy efficiency. Herein, a natural polysaccharide strengthened hydrogel electrolyte (denoted as PAAm/agar/Zn(CF3SO3)2) was engineered by designing an asymmetric dual network of covalently cross-linked polyacrylamide (denoted as PAAm) and physically cross-linked loose polysaccharide (e.g., agar) followed by intense uptake of Zn(CF3SO3)2 aqueous electrolyte. In this polymeric matrix, the PAAm chains are responsible for constructing the soft domains to immobilize the water molecules, and the agar component boosts the mechanical performance (by using its inherent reversible sacrificial bonds) and favors the electrolyte ion transport. Due to these reasons, the as-designed hydrogel electrolyte effectively inhibits the zinc dendrite growth, realizes the uniform Zn deposition, and affords a satisfactory ionic conductivity of 1.55 S m-1, excellent tensile strength (78.9 kPa at 507.7% stretchable), and high compression strength (118.0 kPa at 60.0% strain). Additionally, a biopolymer-derived N-doped carbon microsphere cathode material with a highly interconnected porous carbonaceous network (denoted as NC) was also synthesized, which delivers a high capacity of 92.8 mAh g-1, along with superb rate capability and long duration cycling lifespan (95.4% retention for 10000 cycles) in the aqueous Zn//NC ZHSC. More notably, with integrated merits of the PAAm/agar/Zn(CF3SO3)2 hydrogel electrolyte and NC, the as-built quasi-solid-state ZHSC achieves a high specific capacity of 73.4 mAh g-1 and superior energy density of 61.3 Wh kg-1 together with excellent cycling stability for 10000 cycles. This work demonstrated favorable practicability in the structural design of the hydrogel electrolytes and electrode materials for advanced ZHSC applications.

In situ constructed honeycomb-like NiFe2O4@Ni@C composites as efficient electromagnetic wave absorber.

Rational excogitation of microstructure and chemical constituents is a superior means of constructing electromagnetic wave (EMW) absorption materials with high performance. In this study, a kind of honeycomb-like NiFe2O4@Ni@C composite is prepared via an uncomplicated polymerization, pyrolysis and etching. Porous structure and internal cavity of NiFe2O4@Ni@C contribute to the numerous reflection and scattering of EMW. The strong ferromagnetic resonance of NiFe2O4 core and the multiple relaxation processes of porous carbon shell strongly promote the EMW loss. Additionally, the synergistic effect can improve impedance matching. The results demonstrate that the minimum reflection loss (RL) of honeycomb-like NiFe2O4@Ni@C composites is -65.33 dB at 13.63 GHz. The effective absorption bandwidth (EAB) is 3.68 GHz when the matching thickness is 4.95 mm. The mechanism of EMW dissipation of the honeycomb-like NiFe2O4@Ni@C composites is attributed to multiple reflections and scattering, conductive loss, interfacial polarization and ferromagnetism resonance. This work provides a tactic for the excogitation and synthesis of a low cost, light weight and efficient EMW absorber.

Activated Carbon Microsphere from Sodium Lignosulfonate for Cr(VI) Adsorption Evaluation in Wastewater Treatment.

In this study, activated carbon microsphere (SLACM) was prepared from powdered sodium lignosulfonate (SL) and polystyrene by the Mannich reaction and ZnCl2 activation, which can be used to remove Cr(VI) from the aqueous solution without adding any binder. The SLACM was characterized and the batch experiments were conducted under different initial pH values, initial concentrations, contact time durations and temperatures to investigate the adsorption performance of Cr(VI) onto SLACM. The results indicated that the SLACM surface area and average pore size were 769.37 m2/g and 2.46 nm (the mesoporous material), respectively. It was found that the reduced initial pH value, the increased temperature and initial Cr(VI) concentration were beneficial to Cr(VI) adsorption. The maximum adsorption capacity of Cr(VI) on SLACM was 227.7 mg/g at an initial pH value of 2 and the temperature of 40 °C. The adsorption of SLACM for Cr(VI) mainly occurred during the initial stages of the adsorption process. The adsorption kinetic and isotherm experimental data were thoroughly described by Elovich and Langmuir models, respectively. SL could be considered as a potential raw material for the production of activated carbon, which had a considerable potential for the Cr(VI) removal from wastewater.

Waste biomass valorization through production of xylose-based porous carbon microspheres for supercapacitor applications.

Sequential potassium hydroxide (KOH)-phosphoric acid (H3PO4) activation was applied to biomass waste to fabricate activated carbon microspheres (mCMs) with a controllable porous structure. Carbon microspheres (CMs) were first synthesized from xylose using a bottom-up approach of hydrothermal carbonization. Sequential KOH and H3PO4 activation was applied to the CMs in a KOH-carbon solid reaction. This created pores, which were further enlarged by adsorption of H3PO4. The KOH:carbon (C) and H3PO4:C molar ratios, and the H3PO4 heating rate and activation time, were varied to investigate the effect on average pore size and pore distribution. A uniform porous structure was formed without destruction of the spherical shape, and an almost 700-fold increase in surface area was obtained over the non-activated CMs. Following activation with H3PO4, phosphorous groups were found to be present at the surface of the carbon microspheres. The mCM was tested as a supercapacitor electrode and was shown to have a maximum specific capacitance of up to 277F g-1. A Ragone plot showed the maximum power density to be 173.88 W Kg-1. This increased specific capacitance was attributed to the increase in surface area and the presence of phosphorous-containing acid sites on the material surface.

Green synthesis of aluminum-hydrochar for the selective isomerization of glucose to fructose.

Hydrochar microspheres supported Al catalysts with hierarchically porous structure (Al/HPHMs) for glucose to fructose isomerization were fabricated. Superior catalytic selectivity (93.3%) and fructose yield (32.6%) were achieved in aqueous under 160 °C for 20 min. Hierarchically porous structure was formed after KHCO3 and K2CO3 activation and the roles of KHCO3 and K2CO3 in controlling the Al phase and tailoring morphology of hydrochar supported Al were evaluated. The major active sites were characterized as Al hydroxides including ß-Al(OH)3, γ-Al(OH)3, γ-AlO(OH), Al-C-O linkages. Active sites by KHCO3 activation with high contents of Al-C-O and Al(OH)3 have better selectivity. Oxygen-containing functional groups including aluminum­oxygen groups on the hydrochar microspheres have contributed to the formation of hydrogen bond and π-π interactions between glucose and Al species. Green process synthesized aluminum-hydrochars have potential for their application as a variety of stable, recyclable, and efficient catalysts for lignocellulosic biorefining.

Corn derivative mesoporous carbon microspheres supported hydrophilic polydopamine for development of new membrane: Water treatment containing bovine serum albumin.

A new mixed matrix membrane (MMM) was prepared by incorporating biological mesoporous carbon microspheres (mCMSs) from corn starch polysaccharide-supported hydrophilic polydopamine (PDA), as a mesoporous and large-surface area filler, selective modifier, and pore-forming agent, into polyvinylidene fluoride (PVDF) matrix in presence of polyethylene glycol (PEG) as a hydrophilic agent. The structural parameters of the prepared membranes were characterized via FE-SEM, BET/BJH, XRD, FT-IR, and AFM analyses, sorption experiments, water permeability assessments, porosimetry tests, flux recovery ratio (FRR) evaluations, and contact angle measurements, with the so-called central composite design (CCD) been successfully applied for optimization and investigation of the effects of the operational parameters. The results were then applied to treat double-distilled water containing bovine serum albumin (BSA) utilizing a cross-module set-up. Based on the findings, the content of the mCMS-PDA in the PVDF matrix significantly affected the contact angle, pure water flux (PWF), FRR, and BSA removal. In this respect, the PWF of the PVDF-PEG-mCMS-PDA increased from 10.25 to 27.78 L/m2 h with increasing the mCMS-PDA content, with the peak FRR (93.84%) of the PVDF-PEG-mCMS-PDA seen at maximum surface hydrophilicity of the membrane.

Controlled microstructure and mechanical properties of Al2O3-based nanocarbon composites fabricated by electrostatic assembly method.

This work reports on the microstructure-controlled formation of interconnected carbon-layered Al2O3 ceramics using carbon nanoparticles (CNP)-alumina (Al2O3) composite particles. The Al2O3 micro-particles used in this study were obtained by granulation of nano-sized Al2O3 nanoparticles with an average diameter of 150 nm. Then, CNP-Al2O3 composite was fabricated using an electrostatic assembly method using the granulated Al2O3 and CNP. The decoration of CNP on the surface of granulated Al2O3 was investigated as a function of primary particle size and coverage percentage using a fixed amount of CNP. Notably, an interconnected layer of carbon particles at the interface of Al2O3 that resemble the grain boundaries was obtained. The mechanical properties of the samples obtained with different particle size and CNP coverage on Al2O3 particles were also investigated which presented the possibility to control the mechanical properties through microstructural design of composite ceramic materials.

Synergistic Effect of Molecular-Type Electrocatalysts with Ultrahigh Pore Volume Carbon Microspheres for Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries are regarded as potential high-energy storage devices due to their outstanding energy density. However, the low electrical conductivity of sulfur, dissolution of the active material, and sluggish reaction kinetics cause poor cycle stability and rate performance. A variety of approaches have been attempted to resolve the above issues and achieve enhanced electrochemical performance. However, inexpensive multifunctional host materials which can accommodate large quantities of sulfur and exhibit high electrode density are not widely available, which hinders the commercialization of Li-S batteries. Herein, mesoporous carbon microspheres with ultrahigh pore volume are synthesized, followed by the incorporation of Fe-N-C molecular catalysts into the mesopores, which can act as sulfur hosts. The ultrahigh pore volume of the prepared host material can accommodate up to ∼87 wt % sulfur, while the uniformly controlled spherical morphology and particle size of the carbon microspheres enable high areal/volumetric capacity with high electrode density. Furthermore, the uniform distribution of Fe-N-C (only 0.33 wt %) enhances the redox kinetics of the conversion reaction of sulfur and efficiently captures the soluble intermediates. The resulting electrode with 5.2 mg sulfur per cm2 shows excellent cycle stability and 84% retention of the initial capacity even after 500 cycles at a 3 C rate.

Highly nitrogen and sulfur dual-doped carbon microspheres for supercapacitors.

Heteroatom doping, especially dual-doped carbon materials have attracted much attention for the past few years, and have been regarded as one of the most efficient strategies to enhance the capacitance behavior of porous carbon materials. In this work, a facile two-step synthetic route was developed to fabricate nitrogen and sulfur co-doped carbon microsphere (NSCM) by using thiourea as dopant. The N/S doping content is controlled via varying the carbonization temperature. It has been proved that a suitable quantity of N and S groups could not only provide pseudo-capacitance but also promote the electron transfer for carbon materials, which ensures the further utilization of the exposed surfaces for charge storage. The optimized NSCM prepared at a carbonization temperature of 800°C (NSCM-800) achieves a capacitance of 277.1Fg-1 at a current density of 0.3Ag-1 in 6.0molL-1 KOH electrolyte, which is 71% higher than that of undoped carbon microsphere. Besides, NSCM-800 shows an excellent cycling stability, 98.2% of the initial capacitance is retained after 5,000 cycles at a current density of 3.0Ag-1.