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Manganese dioxide (MnO 2 ) with high theoretical capacitance and natural abundance has attracted great attention but is still challenging for use in supercapacitors, due to the limited conductivity and lower electron and ion migration. Here, a facile in situ growth strategy is developed to prepare heterostructural graphitized cellulose nanocrystal (GCNC)/MnO 2 with unblocked conductive networks through a hydrothermal reaction. The GCNC with highly ordered graphitic carbon layers as conductive support framework solves the agglomeration problem of MnO 2 and increases effective specific surface areas in contact with electrolyte ions. Meanwhile, the stable connection of MnOC covalent bonds enhances the interface bonding, which effectively reduces the contact resistance at the interface of heterostructural GCNC/MnO 2 and enhances the interface firmness. The resulting GCNC/MnO 2 electrode shows a remarkable specific capacitance of 528.2 F g -1 at 0.5 A g -1 . Furthermore, the symmetric supercapacitor based on GCNC/MnO 2 -15 mM exhibits high rate capability and excellent cycle stability of 100 % capacitance retention after 3000 cycles. This work provides a new path to designing high performance electrode material for sustainable energy technologies., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Techniques to improve the graphitization of lignin, the second most abundant natural polymer, are in great demand as a viable means to obtain cost-effective and less energy-intensive graphite for various applications. In this work, we report the effects of two-dimensional nanomaterials, graphene oxide (GO) and its derivative, reduced graphene oxide (RGO), used as templating agents for the graphitization of alkali-derived lignin. The hypothesis is that during heat temperature treatment, the GO additives act as a template that allows the lignin matrix to align on its basal planes through π-π interactions. In addition, possible chemical bonding between the GO additives and lignin may extend the two planar frameworks. Results from X-ray diffraction and Raman spectroscopy showed improved graphitic quality in the lignin-GO and lignin-RGO samples compared to pure lignin at 2500 °C. Transmission electron microscopy images and selected area electron diffraction patterns also revealed ordered nanostructures and defined polycrystalline patterns in the lignin-GO and lignin-RGO samples. This work presents a method to synthesize graphitic-like materials using carbon-based templates with the advantage that there is no need for further purification of the final material as in the case of transition metal catalysts.

The particulate matter and soluble organic fraction emitted by diesel engine are hazardous to environment and human health. Exploring the effect mechanism of soluble organic fraction on soot oxidation is beneficial for reducing the emissions. In this study, the effects of four different types of soluble organic fractions on the soot oxidation activity and physicochemical properties are investigated. The results show that the attachment of oxygen-containing soluble organic fractions enhances the soot oxidation and reduces the peak characteristic temperature. However, the low volatility soluble organic fractions without oxygen element inhibit soot oxidation. Additionally, the high volatility soluble organic fractions without oxygen element elicit limited effects on soot oxidation. the contents of aliphatic C-H functional groups, carbonyl CO functional groups, and carboxylic acid O-CO functional groups significantly increase after adding oxygen-containing soluble organic fractions, while the limited increase in functional groups is observed in soluble organic fractions without oxygen element. Solid soluble organic fractions adhere to soot particles in the form of small particles, leading a reduction in the initial particle size distribution, while liquid soluble organic fractions exhibit block and chain shapes around the soot particles, which makes the initial particle size distribution increasing. Moreover, the attachment of all soluble organic fractions disrupts the surface order of soot particle, leading to a decrease in soot graphitization. This study is beneficial for revealing the interaction mechanism between soot and soluble organic fractions., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Overcoming the trade-off between the graphitization of the carbon substrate and enhanced electronic metal-support interaction (EMSI) and intrinsic activity of Pt-C catalysts remains a major challenge for ensuring the durable operation of energy conversion devices. This article presents a hybrid catalyst consisting of PtFe nanoparticles and single Pt and Fe atoms supported on N-doped carbon (PtFe NPs @PtFe SAs -N-C), which exhibits improved activities in hydrogen evolution and oxygen reduction reactions (HER and ORR, respectively) and has excellent durability owing to the high graphitization, rich edge defects, and porosity of the carbon in PtFe NPs @PtFe SAs -N-C, as well as strong EMSI between the PtFe nanoparticles and edge-defective carbon embedded with Pt and Fe atoms. According to theoretical calculations, the strong EMSI optimizes the H* adsorption-desorption and facilitates the adsorption OOH*, accelerating the HER and ORR processes. A novel flow seawater-Al/acid hybrid fuel cell using the PtFe NPs @PtFe SAs -N-C cathode can serve as a high-efficiency energy conversion device that delivers a high power density of 109.5 mW cm -2 while producing H 2 at a significantly high rate of 271.6 L m -2 h -1 . Moreover, PtFe NPs @PtFe SAs -N-C exhibits a remarkable performance (high power density of 298.0 mW cm -2 and long-term durability of 1000 h) in a flow Zn-air battery., (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

2D magnets are expected to give new insights into the fundamentals of magnetism, host novel quantum phases, and foster development of ultra-compact spintronics. However, the scarcity of 2D magnets often makes a bottleneck in the research efforts, prompting the search for new magnetic systems and synthetic routes. Here, an unconventional approach is adopted to the problem, graphenization - stabilization of layered honeycomb materials in the 2D limit. Tetragonal GdAlSi, stable in the bulk, in ultrathin films gives way to its layered counterpart - graphene-like anionic AlSi layers coupled to Gd cations. A series of inch-scale films of layered GdAlSi on silicon is synthesized, down to a single monolayer, by molecular beam epitaxy. Graphenization induces an easy-plane ferromagnetic order in GdAlSi. The magnetism is controlled by low magnetic fields, revealing its 2D nature. Remarkably, it exhibits a non-monotonic evolution with the number of monolayers. The results provide a fresh platform for research on 2D magnets by design., (© 2024 Wiley‐VCH GmbH.)

In the realm of carbon fiber research, a variety of structural configurations is noted, comprising crystalline, noncrystalline, and semicrystalline forms. Recent investigations into this domain have revealed an array of intriguing phases of carbon, among which amorphous graphite is the most notable for its unique mechanical, thermal, and electrical properties that arise from its inherent topological disorders. In this study, we utilized the ReaxFF molecular dynamics (MD) simulations to investigate the carbonization and graphitization processes involved in the production of amorphous graphite from benzothiophene, a sulfur-containing polar aromatic precursor. We developed C/H/S ReaxFF force field parameters to describe the high-temperature chemistry of benzothiophene. Our investigation reveals the reaction mechanisms, providing critical insights into the underlying chemical processes toward the formation of amorphous graphite and the structural characteristics of the end products. The formation of volatile gaseous molecules and their continuous elimination led to the development of noncontinuous layered graphite structures analogous to amorphous graphite consisting of pentagons, hexagons, and heptagons. These findings offer unprecedented insights into the carbonization and graphitization processes of sulfur-containing heavy-end aromatic feedstock. This knowledge lays the groundwork for advancing synthesis methods and developing amorphous graphite materials with specific properties.

In this study, an evaluation of carbon-beam tuning and 14 C/ 12 C ratio measurements is performed to validate the graphitization process in the pre-processing procedure employed at the accelerator mass spectrometry (AMS) facility of Dongguk University in Korea. The AMS isotopic ratio data are analyzed for samples subjected to three different graphitization conditions: (1) the entire process including Fe catalyst pre-heating with a high vacuum, (2) a high vacuum without pre-heating, and (3) a low vacuum without pre-heating. High-quality isotopic ratio measurements are achieved under these conditions. The measured mean isotopic ratio values for the background samples are almost equivalent to the different graphitization condition samples, with a difference in the order of 10 -16 . Therefore, conducting measurements with or without Fe catalyst pre-heating or high vacuum conditions is equally viable. Furthermore, the simplification of the graphitization process steps reduces the processing time required to produce five samples from 8 to 4 h, thereby enhancing the daily sample throughput by a factor of two, without compromising data quality., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Yu-Seok Kim reports financial support was provided by Korea Ministry of Science and ICT. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Carbon is a critical material for existing and emerging energy applications and there is considerable global effort in generating sustainable carbons. A particularly promising area is iron-catalyzed graphitization, which is the conversion of organic matter to graphitic carbon nanostructures by an iron catalyst. In this paper, it is reported that iron-catalyzed graphitization occurs via a new type of mechanism that is called homogeneous solid-state catalysis. Dark field in situ transmission electron microscopy is used to demonstrate that crystalline iron nanoparticles "burrow" through amorphous carbon to generate multiwalled graphitic nanotubes. The process is remarkably fast, particularly given the solid phase of the catalyst, and in situ synchrotron X-ray diffraction is used to demonstrate that graphitization is complete within a few minutes., (© 2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH.)

In this study, it is analyzed how sample geometry (spheres, nanofibers, or films) influences the graphitization behavior of polyacrylonitrile (PAN) molecules. The chemical bonding and changes in the composition of these three geometries are studied at the oxidation, carbonization, and graphitization stages via scanning electron microscopy (SEM), in situ thermogravimetric-infrared (TGA-IR) analysis, elemental analysis, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The influence of molecular alignment on the graphitization of the three sample geometries is investigated using synchrotron wide-angle X-ray diffraction (WAXD) and transmission electron microscopy (TEM). The effects of molecular alignment at different draw rates during spinning are explored in detail., (© 2024 Wiley‐VCH GmbH.)

Hydrogenated diamond-like carbon (HDLC) is a promising solid lubricant for its superlubricity which can benefit various industrial applications. While HDLC exhibits notable friction reduction in macroscale tests in inert or reducing environmental conditions, ultralow friction is rarely observed at the nanoscale. This study investigates this rather peculiar dependence of HDLC superlubricity on the contact scale. To attain superlubricity, HDLC requires i) removal of ≈2 nm-thick air-oxidized surface layer and ii) shear-induced transformation of amorphous carbon to highly graphitic and hydrogenated structure. The nanoscale wear depth exceeds the typical thickness of the air-oxidized layer, ruling out the possibility of incomplete removal of the air-oxidized layer. Raman analysis of transfer films indicates that shear-induced graphitization readily occurs at shear stresses lower than or comparable to those in the nanoscale test. Thus, the same is expected to occur at the nanoscale test. However, the graphitic transfer films are not detected in ex-situ analyses after nanoscale friction tests, indicating that the graphitic transfer films are pushed out of the nanoscale contact area due to the instability of transfer films within a small contact area. Combining all these observations, this study concludes the retention of highly graphitic transfer films is crucial to achieving HDLC superlubricity., (© 2024 The Authors. Small published by Wiley‐VCH GmbH.)

Phenolic resin pyrolytic carbons were obtained by catalytic pyrolysis of phenolic resin at 500 °C, 600 °C, 700 °C, and 800 °C for 3 h in an argon atmosphere using copper nitrate as a catalyst precursor. The effects of copper salts on the pyrolysis process of phenolic resin as well as the structural evolution and oxidation resistance of phenolic resin pyrolytic carbons were studied. The results showed that copper oxide (CuO) generated from the thermal decomposition of copper nitrate was reduced to copper (Cu) by the gas generated from the thermal decomposition of the phenolic resin. Carbon nanofibers with tapered structures were synthesized by Cu catalysis of pyrolysis gas at 500-800 °C. The catalytic pyrolysis of phenolic resin with Cu increased the graphitization degree and reduced the pore volume of the phenolic resin pyrolytic carbons. The combined action improved the oxidation resistance of phenolic resin pyrolytic carbons.

While nano-crystalline diamond (NCD) is a promising engineering composite material for its unique mechanical properties, achieving the ultrahigh surface quality of NCD-based components through conventional grinding and polishing is challenging due to its exceptional hardness and brittleness. In the present work, we experimentally investigate the nanosecond laser ablation-induced graphitization characteristics of NCD, which provides a critical pretreatment method of NCD for realizing its superlative surface finish. Specifically, systematic experimental investigations of the nanosecond pulsed laser ablation of NCD are carried out, in which the characteristics of graphitization are qualitatively characterized by the Raman spectroscopy detection of the ablated area of the microhole and microgroove. Subsequently, the influence of laser processing parameters on the degree and morphological characteristics of graphitization is evaluated based on experimental data and related interpretation, from which optimized parameters for maximizing the graphitization of NCD are then identified. The findings reported in the current work provide guidance for promoting the machinability of NCD via laser irradiation-induced surface modification.

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 (I D /I G = 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., (© 2024 Wiley‐VCH GmbH.)

The complexity of biomass components leads to significant variations in the performance of biomass-based carbon dots (CDs). To shed light on this matter, this study presents a comparative analysis of the fluorescence properties of CDs using pure cellulose, lignin, and protein as models. Three CDs showed different fluorescent properties, resulting from the structure difference and carbonization behavior in the hydrothermal. The relatively gentle thermal degradation of proteins allows the macromolecular structure of amino acids to be preserved. This preservation results in a more regular lattice structure, a larger sp 2 domain size, and N-doping, which contribute to the highest quantum yield (QY) of 8.7% of the CDs. In contrast, cellulose undergoes more severe thermal degradation with large amounts of small molecules generated, resulting in the CDs with fewer surface defects, more irregular lattice structures, and lower QY. These results provide a guideline for the design of carbon dots from different biomass., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Intermetallic ordered PtCo is effective for high oxygen reduction reaction (ORR) activity and stability. However, preparing small-sized, highly ordered PtM alloys is still challenging. Herein, we report a controlled two-stage confinement strategy, in which highly ordered PtCoZn/NC nanoparticles of 5.3 nm size were prepared in a scalable process. The contradiction between the high ordering degree with the small particle size as well as the atomic migration with the space confinement was well resolved. An outstanding PEMFC performance was achieved for L1 0 -PtCoZn/NC with a high mass activity (MA) of 1.21 A/mg Pt at 0.9 V iR-free , 80.1 % MA retention after 30 k cycles in H 2 -O 2 operation, and a high mass-specific power density of 8.24 W mg -1 Pt in H 2 -Air operation with a slight loss of cell voltage@0.8 A cm -2 of 28 mV after 30 k cycles. The high performance can be ascribed to the high Pt area exposure, the enhanced Pt-Co coupling, and the prevented agglomeration in the mesoporous carbon wall. Overall, this strategy may contribute to the commercialization of fuel cells., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

This study describes computer simulations of carbonization and graphite formation, including the effects of hydrogen, nitrogen, oxygen, and sulfur. We introduce a novel technique to simulate carbonization, 'Simulation of Thermal Emission of Atoms and Molecules (STEAM)', designed to elucidate volatile outgassing and density variations in the intermediate material during carbonization. The investigation analyzes the functional groups that endure through high-temperature carbonization and examines the graphitization processes in carbon-rich materials containing non-carbon impurity elements. The physical, vibrational, and electronic attributes of impure amorphous graphite are analyzed, and the impact of nitrogen on electronic conduction is investigated., (Creative Commons Attribution license.)

Herein, three-dimensional activated graphitic carbon spheres (AGCS) were constructed by simultaneous activation-graphitization of Fe-tannic acid coordination spheres with the assistance of KOH. Nanosheets-assembled AGCS with complex intersecting channel system can expose more active sites for charge storage. Simultaneous activation-graphitization can relieve trade-off relationship between porosity and conductivity of carbon materials. Benefiting from multiple synergistic effects of large specific surface area (2069 m 2 g -1 ), abundant ion-accessible micropores (>0.78 nm), good electronic conductivity (I G /I D  = 1.11), and moderate amount of oxygen doping, the optimized AGCS-2 has favored ion and electron transfer channels. AGCS-2 based zinc-ion hybrid capacitor (ZIHC) displays a high specific capacity of 148.6 mA h g -1 (334 F g -1 ) at 0.5 A g -1 , a remarkable energy density of 119.0 W h kg -1 at 1440 W kg -1 , and superior cycling life with 96% capacity retention after 10,000 cycles. This simultaneous activation-graphitization strategy may open up a new avenue to design novel carbon spheres linking optimal pores and graphitic carbon structure for ZIHC application., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

In the present paper, a scalable, economically feasible, and continuous process for making cellulose-based carbon fibers (CFs) is described encompassing precursor spinning, precursor additivation, thermal stabilization, and carbonization. By the use of boric acid (BA) as an additive, the main drawback of cellulose-based CFs, i.e., the low carbon yield, is overcome while maintaining a high level of mechanical properties. This is demonstrated by a systematic comparison between CFs obtained from a BA-doped and an un-doped cellulose precursor within a temperature range for carbonization between 1000 and 2000 °C. The changes in chemical composition (via elemental analysis) and physical structure (via X-ray scattering) as well as the mechanical and electrical properties of the resulting CFs were investigated. It turned out that, in contrast to current opinion, the catalytic effect of boron in the formation of graphite-like structures sets in already at 1000 °C. It becomes more and more effective with increasing temperature. The catalytic effect of boron significantly affects crystallite sizes ( L a , L c ), lattice plane spacings ( d 002 ), and orientation of the crystallites. Using BA, the carbon yield increased by 71%, Young's modulus by 27%, and conductivity by 168%, reaching 135,000 S/m. At the same time, a moderate decrease in tensile strength by 25% and an increase in density of 14% are observed.

Since the discovery of laser-induced graphite/graphene, there has been a notable surge of scientific interest in advancing diverse methodologies for their synthesis and applications. This study focuses on the utilization of a pulsed Nd:YAG laser to achieve graphitization of polydopamine (PDA) deposited on the surface of titania nanotubes. The partial graphitization is corroborated through Raman and XPS spectroscopies and supported by water contact angle, nanomechanical, and electrochemical measurements. Reactive molecular dynamics simulations confirm the possibility of graphitization in the nanosecond time scale with the evolution of NH 3 , H 2 O, and CO 2 gases. A thorough exploration of the lasing parameter space (wavelength, pulse energy, and number of pulses) was conducted with the aim of improving either electrochemical activity or photocurrent generation. Whereas the 532 nm laser pulses interacted mostly with the PDA coating, the 365 nm pulses were absorbed by both PDA and the substrate nanotubes, leading to a higher graphitization degree. The majority of the photocurrent and quantum efficiency enhancement is observed in the visible light between 400 and 550 nm. The proposed composite is applied as a photoelectrochemical (PEC) sensor of serotonin in nanomolar concentrations. Because of the suppressed recombination and facilitated charge transfer caused by the laser graphitization, the proposed composite exhibits significantly enhanced PEC performance. In the sensing application, it showed superior sensitivity and a limit of detection competitive with nonprecious metal materials.

Various materials have been developed to capture volatile organic compounds (VOCs) to mitigate air pollution. However, sorbent materials with excellent resistance to water are rare. Here, several Fe/N-doped activated carbons (ACs) have been prepared to capture VOCs in humid environments. The ACs were analyzed by various characterization techniques, such as BET, SEM, XPS, XRD, FTIR, and Raman. The results showed that Fe/N doping resulted in the specific surface area of the ACs increasing by 500 to 1000 m 2  g -1 , the average pore size increasing to approximately 2 nm, improved mesoporous structure, higher graphitization, lower hydrophilicity, and polarity. The VOCs adsorption performance of the ACs was evaluated by static and dynamic adsorption experiments. The uptake of toluene and ethyl acetate by ACs was enhanced to 224 mg g -1 and 135 mg g -1 , respectively. And ACs were able to maintain 70 to 80% VOCs adsorption capacity for VOCs at 80% relative humidity. Furthermore, the microscopic mechanisms were investigated by the grand canonical Monte Carlo method (GCMC). The highly graphitized structure and the N functional groups favored the VOC adsorption process and discouraged the adsorption of water vapor. This work affirmed the dominance of Fe/N-doped carbon, which will contribute to the evolution of water-resistant VOCs adsorbent materials., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Fe-doped carbon xerogels with a highly developed graphitic structure were synthesized by a one-step sol-gel polymerization. These highly graphitic Fe-doped carbons are presented as promising dual-functional electro-Fenton catalysts to perform both the electro-reduction of O 2 to H 2 O 2 and H 2 O 2 catalytic decomposition (Fenton) for wastewater decontamination. The amount of Fe is key to the development of this electrode material, since affects the textural properties; catalyzes the development of graphitic clusters improving the electrode conductivity; and influences the O 2 -catalyst interaction controlling the H 2 O 2 selectivity but, at the same time is the catalyst for the decomposition of the electrogenerated H 2 O 2 to OH • radicals for the organic pollutants oxidation. All materials achieve the development of ORR via the 2-electron route. The presence of Fe considerably improves the electro-catalytic activity. However, a mechanism change seems to occur at around -0.5 V in highly Fe-doped samples. At potential lower than -0.5 eV, the present of Fe δ+ species or even Fe-O-C active sites favour the selectivity to 2e-pathway, however at higher potentials, Fe δ+ species are reduced favoring a O-O strong interaction enhancing the 4e-pathway. The Electro-Fenton degradation of tetracycline was analyzed. The TTC degradation is almost complete (95.13%) after 7 h of reaction without using any external Fenton-catalysts., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)

Fe single atoms and N co-doped carbon nanomaterials (Fe-N-C) are the most promising oxygen reduction reaction (ORR) catalysts to replace platinum group metals. However, high-activity Fe single-atom catalysts suffer from poor stability owing to the low graphitization degree. Here, an effective phase-transition strategy is reported to enhance the stability of Fe-N-C catalysts by inducing increased degree of graphitization and incorporation of Fe nanoparticles encapsulated by graphitic carbon layer without sacrificing activity. Remarkably, the resulted Fe@Fe-N-C catalysts achieved excellent ORR activity (E 1/2  = 0.829 V) and stability (19 mV loss after 30K cycles) in acid media. Density functional theory (DFT) calculations agree with experimental phenomena that additional Fe nanoparticles not only favor to the activation of O 2 by tailoring d-band center position but also inhibit the demetallization of Fe active center from FeN 4 sites. This work provides a new insight into the rational design of highly efficient and durable Fe-N-C catalysts for ORR., (© 2023 Wiley-VCH GmbH.)

Fabricating highly crystalline macroscopic films with extraordinary electrical and thermal conductivities from graphene sheets is essential for applications in electronics, telecommunications and thermal management. High-temperature graphitization is the only method known to date for the crystallization of all types of carbon materials, where defects are gradually removed with increasing temperature. However, when using graphene materials as precursors, including graphene oxide, reduced graphene oxide and pristine graphene, even lengthy graphitization at 3000°C can only produce graphene films with small grain sizes and abundant structural disorders, which limit their conductivities. Here, we show that high-temperature defects substantially accelerate the grain growth and ordering of graphene films during graphitization, enabling ideal AB stacking as well as a 100-fold, 64-fold and 28-fold improvement in grain size, electrical conductivity and thermal conductivity, respectively, between 2000°C and 3000°C. This process is realized by nitrogen doping, which retards the lattice restoration of defective graphene, retaining abundant defects such as vacancies, dislocations and grain boundaries in graphene films at a high temperature. With this approach, a highly ordered crystalline graphene film similar to highly oriented pyrolytic graphite is fabricated, with electrical and thermal conductivities (∼2.0 × 10 4 S cm -1 ; ∼1.7 × 10 3  W m -1 K -1 ) that are improved by about 6- and 2-fold, respectively, compared to those of the graphene films fabricated by graphene oxide. Such graphene film also exhibits a superhigh electromagnetic interference shielding effectiveness of ∼90 dB at a thickness of 10 μm, outperforming all the synthetic materials of comparable thickness including MXene films. This work not only paves the way for the technological application of highly conductive graphene films but also provides a general strategy to efficiently improve the synthesis and properties of other carbon materials such as graphene fibers, carbon nanotube fibers, carbon fibers, polymer-derived graphite and highly oriented pyrolytic graphite., (© The Author(s) 2023. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd.)

This effort aimed to explore the activation and catalytic graphitization mechanisms of non-toxic salts in converting biomass to biochar from the perspective of pyrolysis kinetics using renewable biomass as feedstock. Consequently, thermogravimetric analysis (TGA) was used to monitor the thermal behaviors of the pine sawdust (PS) and PS/KCl blends. The model-free integration methods and master plots were used to obtain the activation energy (E) values and reaction models, respectively. Further, the pre-exponential factor (A), enthalpy (ΔH), Gibbs free energy (ΔG), entropy (ΔS), and graphitization were evaluated. When the KCl content was above 50%, the presence of KCl decreased the resistance to biochar deposition. In addition, the differences in the dominant reaction mechanisms of the samples were not significant at low (α ≤ 0.5) and high (α ≥ 0.5) conversion rates. Interestingly, the lnA value showed a linearly positive correlation with the E values. The PS and PS/KCl blends possessed positive ΔG and ΔH values, and KCl was able to assist biochar graphitization. Encouragingly, the co-pyrolysis of the PS/KCl blends allows us to target-tune the yield of the three-phase product during biomass pyrolysis.

Graphitic carbon is a valuable material that can be utilized in many fields, such as electronics, energy storage and wastewater filtration. Due to the high demand for commercial graphite, an alternative raw material with lower costs that is environmentally friendly has been explored. Amongst these, an agricultural bio-waste material has become an option due to its highly bioactive properties, such as bioavailability, antioxidant, antimicrobial, in vitro and anti-inflammatory properties. In addition, biomass wastes usually have high organic carbon content, which has been discovered by many researchers as an alternative carbon material to produce graphite. However, there are several challenges associated with the graphite production process from biomass waste materials, such as impurities, the processing conditions and production costs. Agricultural bio-waste materials typically contain many volatiles and impurities, which can interfere with the synthesis process and reduce the quality of the graphitic carbon produced. Moreover, the processing conditions required for the synthesis of graphitic carbon from agricultural biomass waste materials are quite challenging to optimize. The temperature, pressure, catalyst used and other parameters must be carefully controlled to ensure that the desired product is obtained. Nevertheless, the use of agricultural biomass waste materials as a raw material for graphitic carbon synthesis can reduce the production costs. Improving the overall cost-effectiveness of this approach depends on many factors, including the availability and cost of the feedstock, the processing costs and the market demand for the final product. Therefore, in this review, the importance of biomass waste utilization is discussed. Various methods of synthesizing graphitic carbon are also reviewed. The discussion ranges from the conversion of biomass waste into carbon-rich feedstocks with different recent advances to the method of synthesis of graphitic carbon. The importance of utilizing agricultural biomass waste and the types of potential biomass waste carbon precursors and their pre-treatment methods are also reviewed. Finally, the gaps found in the previous research are proposed as a future research suggestion. Overall, the synthesis of graphite from agricultural bio-waste materials is a promising area of research, but more work is needed to address the challenges associated with this process and to demonstrate its viability at scale.

The purpose of this study is to improve the oxidation resistance of graphite blocks after graphitization at 2800 °C by introducing a curing process of phenolic resin, used as a binder to control the pore size. Using the methylene index obtained from FTIR, the curing temperature was set to 150 °C, the temperature at which cross-linking most highly occurs. Graphite blocks that had undergone curing, and were carbonized with a slow heating rate, showed increased mechanical and electrical properties. Microstructural observation confirmed that the curing process inhibited the formation of large pores in the graphite block. Therefore, the cured graphite block showed better oxidation resistance in air than a non-cured graphite block. Oxidation of the graphite block was caused by pores created by pyrolysis of the phenolic resin binder, which acted as active sites.

The anti-friction of diamond-like carbon (DLC) is achieved by a well-developed carbonaceous transfer layer, and Ti-doped DLC is developed into a robustly built-up carbonaceous transfer layer. The friction performance of DLC depends on the operating environment, e.g., ambient gas, humidity, temperature, lubricants, and mating material. In this study, we aimed to reveal the environmental sensitivities of Ti-DLC on friction characteristics. To this end, a Ti-DLC was rubbed against a steel ball, and friction behaviors were evaluated with different gas compositions, humidity, and temperature. Finally, we identified that fractional coverage of water on surfaces affected the anti-graphitization on Ti-DLC, leading to avoiding friction reduction.

The in situ free carbon generated in polymer-derived ceramics (PDCs) plays a crucial role in their unique microstructure and resultant properties. This study advances a new phenomenon of graphitization of PDCs. Specifically, whether in micro-/nanoscale films or millimeter-scale bulks, the surface/interface radically changes the fate of carbon and the evolution of PDC nanodomains, promotes the graphitization of carbon, and evolves a free carbon enriched layer in the near-surface/interface region. Affected by the enrichment behavior of free carbon in the near-surface/interface region, PDCs exhibit highly abnormal properties such as the skin behavior and edge effect of the current. The current intensity in the near-surface/interface region of PDCs is orders of magnitude higher than that in its interior. Ultrahigh conductivity of up to 14.47 S cm -1 is obtained under the action of the interface and surface, which is 5-8 orders of magnitude higher than that of the bulk prepared under the same conditions. Such surface/interface interactions are of interest for the regulation of free carbon and its resultant properties, which are the core of PDC applications. Finally, the first PDC thin-film strain gauge that can survive a butane flame with a high temperature of up to ≈1300 °C is fabricated., (© 2022 Wiley-VCH GmbH.)

The use of the ultrafast pulse is the current trend in laser processing many materials, including diamonds. Recently, the orientation of the irradiated crystal face was shown to play a crucial role in the diamond to graphite transition process. Here, we develop this approach and explore the nanostructure of the sp 2 phase, and the structural perfection of the graphite produced. The single pulse of the third harmonic of a Ti:sapphire laser (100 fs, 266 nm) was used to study the process of producing highly oriented graphite (HOG) layers on the (111) surface of a diamond monocrystal. The laser fluence dependence on ablated crater depth was analyzed, and three different regimes of laser-induced diamond graphitization are discussed, namely: nonablative graphitization, customary ablative graphitization, and bulk graphitization. The structure of the graphitized material was investigated by confocal Raman spectroscopy. A clear correlation was found between laser ablation regimes and sp 2 phase structure. The main types of structural defects that disrupt the HOG formation both at low and high laser fluencies were determined by Raman spectroscopy. The patterns revealed give optimal laser fluence for the production of perfect graphite spots on the diamond surface.

The feasibility of achieving in situ sulfur (S) and nitrogen (N) co-doped carbon nano-onions (CNOs and SN-CNOs) via a simple flame-pyrolysis technique without using sophisticated high-vacuum annealing or expensive nanodiamond-based complex processes is demonstrated for the first time. The characteristic onion-like feature of 0.34 nm remained intact with a high degree of ordering and graphitization, even though the S and N heteroatoms were co-doped simultaneously. The in situ co-doped SN-CNO demonstrated high supercapacitor device performance with a high energy density of 25 Wh kg -1 at a maximum power density of 18 kW kg -1 , maintaining 98% specific capacitance over 10,000 cycles at 10 A g -1 . These are the highest achieved device performance values of a fullerene family electrode material to date.

In this study, nitrogen self-doping layered graphitic biochar (Na-BC900) was prepared by catalytic pyrolysis of lotus leaves at 900  ° C, in the presence of NaCl catalyst, for peroxydisulfate (PDS) activation and sulfamethoxazole (SMX) degradation. NaCl as catalyst played a crucial part in the preparation of Na-BC900 and could be reused. The SMX degradation rate in Na-BC900/PDS system was 12 times higher than that in un-modified biochar (BC900)/PDS system. The excellent performance of Na-BC900 for PDS activation was attributed to its large specific surface areas (SSAs), the enhanced graphitization structure and the high graphitic N content. The quenching and electrochemical experiments, electron paramagnetic resonance (EPR) studies inferred that the radicals included SO 4 •- , • OH, O 2 •- and the non-radical processes were driven by 1 O 2 and biochar mediated electron migration. Both radical and non-radical mechanisms contributed to the removal of SMX. Additionally, this catalytic pyrolysis strategy was clarified to be scalable, which can be applied to produce multiple biomass-based biochar catalysts for restoration of polluted water bodies., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The boron carbide (B 4 C) nanoparticles doping mesophase pitch (MP) was synthesized by the in-situ doping method with tetrahydrofuran solvent, and the corresponding MP-based carbon fibers (CFs) were successfully prepared through the melt-spinning, stabilization, carbonization and graphitization processes. The structural evolution and properties of boron-containing pitches and fibers in different processes were investigated for exploring the effect of B 4 C on mechanical, electrical and thermal properties of CFs. The results showed that the B 4 C was evenly dispersed in pitch fibers to provide active sites of oxygen, resulting in a homogeneous stabilization and ameliorating the split-ting microstructures of CFs. Moreover, the thermal conductivity of B1-MP-CF prepared with 1 wt.% B 4 C increased to 1051 W/m•K, which was much higher than that of B0-MP-CF prepared without B 4 C (659 W/m•K). While the tensile strength of B 4 C-doped CFs was lower than that of pristine CFs. In addition, a linear relationship equation between the graphite microcrystallite parameter (I D /I G ) calculated from Raman spectra and the thermal conductivity (λ) calculated according to the electrical resistivity was found, which was beneficial to understand the thermal properties of CFs. Therefore, the doping B 4 C nanoparticles in MP did play a significant role in reducing the graphitization temperatures due to the boron catalytic graphitization but decreasing the mechanical properties due to the introduction of impurities.

Contact metamorphism in coal is usually characterized by a rapid, brief, and exotherm reaction that can change the geothermal gradient. In this process, coal adjacent to the intrusive body can form thermally altered coal-based graphite (TACG). In order to further study the structural changes of TACG at different distances from the intrusive body, four TACG samples were collected in the Zhuji coal mine in the Huainan Coalfield, North China, and their vitrinite reflectance and Raman spectra were measured using polarizing microscopy and Raman spectroscopy. The results showed that: (1) affected by the temperature and stress of magmatic hydrothermal intrusion, the clay minerals in the coal seams appeared distributed in strips; the occurrence of ankerite and pyrite in the coal seams near the magmatic intrusions could be due to a late magmatic hydrothermal mineralization; (2) the R max - R min correlation for the TACG samples under study showed that thermal metamorphism was the main factor leading to the graphitization of the TACG samples, without an obvious pressure effect; (3) with the increase of the graphitization process, the D- and G-band showed some similar changes, specifically, their peak positions shifted to lower wave numbers, and the full width at half maximum (FW G and FW D ) gradually decreased; the difference was that the intensity of the G-band increased, while that of the D-band decreased; (4) the graphitization degree of the TACG samples increased with the increase of the transverse size of the crystals, while the FW G and FW D values of the G- and D-band decreased; (5) in comparison to natural graphite, the TACG still presented structural defects.

Carbon nanomaterials have attracted great interest for their unique physico-chemical properties for various applications, including medicine and, in particular, drug delivery, to solve the most challenging unmet clinical needs. Graphitization is a process that has become very popular for their production or modification. However, traditional conditions are energy-demanding; thus, recent efforts have been devoted to the development of greener routes that require lower temperatures or that use waste or byproducts as a carbon source in order to be more sustainable. In this concise review, we analyze the progress made in the last five years in this area, as well as in their development as drug delivery agents, focusing on active targeting, and conclude with a perspective on the future of the field.

Carbon xerogel nanocomposites with integrated Bi and Fe particles (C–Bi–Fe) represent an interesting model of carbon nanostructures decorated with multifunctional nanoparticles (NPs) with applicability for electrochemical sensors and catalysts. The present study addresses the fundamental aspects of the catalyzed growth of nano-graphites in C–Bi–Fe systems, relevant in charge transport and thermo-chemical processes. The thermal evolution of a C–Bi–Fe xerogel is investigated using different pyrolysis treatments. At lower temperatures (~750°C), hybrid bismuth iron oxide (BFO) NPs are frequently observed, while graphitization manifests under more specific conditions such as higher temperatures (~1,050°C) and reduction yields. An in situ heating TEM experiment reveals graphitization activity between 800 and 900°C. NP motion is directly correlated with textural changes of the carbon support due to the catalyzed growth of graphitic nanoshells and nanofibers as confirmed by HR-TEM and electron tomography (ET) for the graphitized sample. An exponential growth model for the catalyst dynamics enables the approximation of activation energies as 0.68 and 0.29–0.34 eV during reduction and graphitization stages. The results suggest some similarities with the tip growth mechanism, while oxygen interference and the limited catalyst–feed gas interactions are considered as the main constraints to enhanced growth.

Aiming to investigate the impacts of n-octanol addition on the oxidation reactivity, morphology and graphitization of diesel exhaust particles, soot samples were collected from a four-cylinder turbocharged diesel engine fueled with D100 (neat diesel fuel), DO15 (85% diesel and 15% n-octanol, V/V) and DO30 (70% diesel and 30% n-octanol, V/V). All tests were conducted at two engine speeds of 1370 and 2150 r/min under a fixed torque of 125 N·m. The soot properties were characterized by thermogravimetric analyzer (TGA), transmission electron microscopy (TEM) and Raman spectroscopy (RS). The higher volatile organic fraction content, lower soot oxidation temperatures and lower activation energy from TGA results indicated that both the increasing n-octanol concentration and engine speed enhanced the soot oxidation reactivity. Additionally, quantitative analysis of TEM images showed that the soot derived from DO30 had the smallest primary particle diameters and fractal dimension, followed by those of soot produced by DO15 and D100. The RS results demonstrated that the n-octanol addition and higher engine speed led to a larger D1-FWHM (D1-full width at half maximum), A D1 /A T (area ratio of D1 band and the total spectral) and A D3 /A T (area ratio of D3 band and the total spectral) as well as a smaller L a (crystallite width), revealing a lower degree of graphitization. Furthermore, the correlations between characterization parameters of soot properties and reactivity were nonlinear., (Copyright © 2021. Published by Elsevier B.V.)

With the large-scale application and high-speed operation of electronic equipment, the thermal diffusion problem presents an increasing requirement for effective heat dissipation materials. Herein, high thermal conductive graphite films were fabricated via the graphitization of polyimide (PI) films with different amounts of chemical catalytic reagent. The results showed that chemically imidized PI (CIPI) films exhibit a higher tensile strength, thermal stability, and imidization degree than that of purely thermally imidized PI (TIPI) films. The graphite films derived from CIPI films present a more complete crystal orientation and ordered arrangement. With only 0.72% chemical catalytic reagent, the graphitized CIPI film achieved a high thermal conductivity of 1767 W·m -1 ·K -1 , which is much higher than that of graphited TIPI film (1331 W·m -1 ·K -1 ), with an increase of 32.8%. The high thermal conductivity is attributed to the large in-plane crystallite size and high crystal integrity. It is believed that the chemical imidization method prioritizes the preparation of high-quality PI films and helps graphite films achieve an excellent performance.

Carbon-based nanomaterials have been regarded as promising non-noble metal catalysts for renewable energy conversion system (e.g., fuel cells and metal-air batteries). In general, graphitic skeleton and porous structure are both critical for the performances of carbon-based catalysts. However, the pursuit of high surface area while maintaining high graphitization degree remains an arduous challenge because of the trade-off relationship between these two key characteristics. Herein, a simple yet efficient approach is demonstrated to fabricate a class of 2D N-doped graphitized porous carbon nanosheets (GPCNSs) featuring both high crystallinity and high specific surface area by utilizing amine aromatic organoalkoxysilane as an all-in-one precursor and FeCl 3 ·6H 2 O as an active salt template. The highly porous structure of the as-obtained GPCNSs is mainly attributed to the alkoxysilane-derived SiO x nanodomains that function as micro/mesopore templates; meanwhile, the highly crystalline graphitic skeleton is synergistically contributed by the aromatic nucleus of the precursor and FeCl 3 ·6H 2 O. The unusual integration of graphitic skeleton with porous structure endows GPCNSs with superior catalytic activity and long-term stability when used as electrocatalysts for oxygen reduction reaction and Zn-air batteries. These findings will shed new light on the facile fabrication of highly porous carbon materials with desired graphitic structure for numerous applications., (© 2021 The Authors. Advanced Science published by Wiley-VCH GmbH.)

This work documents the annealing effect on the thermal conductivity of nanotube film (CNTB) and carbon nanotube fiber (CNTF). The thermal properties of carbon nanotube samples are measured by using the transient electro-thermal (TET) technique, and the experimental phenomena are analyzed based on numerical simulation. During the current annealing treatment, CNTB1 always maintains the negative temperature coefficient of resistance (TCR), and its thermal diffusivity increases gradually. When the annealing current is 200 mA, it increases by 33.62%. However, with the increase of annealing current, the TCR of CNTB2 changes from positive to negative. The disparity between CNTB2 and CNTB1 suggests that they have different physical properties and even structures along their lengths. The high-level thermal diffusivity of CNTB2 and CNTF are 2.28-2.46 times and 1.65-3.85 times higher than the lower one. The results show that the decrease of the thermal diffusivity for CNTB2 and CNTF is mainly caused by enhanced Umklapp scattering, the high thermal resistance and torsional sliding during high temperature heating.

Doped diamond electrodes have attracted significant attention for decades owing to their excellent physical and electrochemical properties. However, direct experimental observation of dopant effects on the diamond surface has not been available until now. Here, low-temperature scanning tunneling microscopy is utilized to investigate the atomic-scale morphology and electronic structures of (100)- and (111)-oriented boron-doped diamond (BDD) electrodes. Graphitized domains of a few nanometers are shown to manifest the effects of boron dopants on the BDD surface. Confirmed by first-principles calculations, local density of states measurements reveal that the electronic structure of these features is characterized by in-gap states induced by boron-related lattice deformation. The dopant-related graphitization is uniquely observed in BDD (111), which explains its electrochemical superiority over the (100) facet. These experimental observations provide atomic-scale information about the role of dopants in modulating the conductivity of diamond, as well as, possibly, other functional doped materials., (© 2021 Wiley-VCH GmbH.)

Ultraflat and damage-free single-crystal diamond is a promising material for use in electronic devices such as field-effect transistors. Diamond surfaces are conventionally prepared by the chemical mechanical polishing (CMP) method, although the CMP efficiency remains a critical issue owing to the extremely high hardness of diamond. Recently, OH radicals have been demonstrated to be potentially useful for improving the CMP efficiency for diamond; however, the underlying mechanisms are still elusive. In this work, we applied our previously developed CMP-specialized tight-binding quantum chemical molecular dynamics simulator to comprehensively elucidate the CMP mechanisms of diamond assisted by OH radicals. Our simulation results indicate that the diamond surface is oxidized by reactions with OH radicals and then a concomitant surface reconstruction takes place due to the distorted and unstable nature of the oxidized diamond surface structure. Furthermore, we interestingly reveal that the reconstruction of the diamond surface ultimately leads to two distinct removal mechanisms: (i) gradual atom-by-atom removal through the desorption of gaseous molecules (e.g., CO 2 and H 2 CO 3 ) and (ii) drastic sheet-by-sheet removal through the exfoliation of graphitic ring structures. Hence, we propose that promoting the oxidation-induced graphitization of the diamond surface may provide a route to further improving the CMP efficiency.

An efficient reduction method to obtain high-quality graphene sheets from mass-producible graphene oxide is highly desirable for practical applications. Here, we report an in situ deoxidation and graphitization mechanism for graphene oxide that allows for high-quality reduced graphene oxide sheets under the low temperature condition (<300 °C) by utilizing a well-known Fischer-Tropsch reaction catalyst (CuFeO 2 ). By applying modified FTR conditions, where graphene oxide was reduced on the catalyst surface under the hydrogen-poor condition, deoxidation with much suppressed carbon loss was possible, resulting in high-quality graphene sheets. Our experimental data and density functional theory calculations proved that reduction which occurred on the CuFeO 2 surface preferentially removed adsorbed oxygen atoms in graphene oxide sheets, leaving dissociated carbon structures to be restored to a near-perfect few-layer graphene sheet. TGA-mass data revealed that GO with catalysts released 92.8% less carbon-containing gases than GO without catalysts during the reduction process, which suggests that this process suppressed carbon loss in graphene oxide sheets, leading to near-perfect graphene. The amount of oxygen related to the epoxide group in the basal plane of GO significantly decreased to near zero (from 43.84 to 0.48 at. %) in catalyst-assisted reduced graphene oxide (CA-rGO). The average domain size and the density of defects of CA-rGO were 4 times larger and 0.1 times lower than those for thermally reduced graphene oxide (TrGO), respectively. As a result, CA-rGO had a 246 and 8 times lower electrical resistance than TrGO and CVD-graphene. With these performances, CA-rGO coated paper connected to a coin-cell battery successfully lit an LED bulb, and CA-rGO itself acted as an efficient catalyst for both the hydrogen evolution reaction and the oxygen evolution reaction.

Free-standing crystalline membranes are highly desirable owing to recent developments in heterogeneous integration of dissimilar materials. Van der Waals (vdW) epitaxy enables the release of crystalline membranes from their substrates. However, suppressed nucleation density due to low surface energy has been a challenge for crystallization; reactive materials synthesis environments can induce detrimental damage to vdW surfaces, often leading to failures in membrane release. This work demonstrates a novel platform based on graphitized SiC for fabricating high-quality free-standing membranes. After mechanically removing epitaxial graphene on a graphitized SiC wafer, the quasi-two-dimensional graphene buffer layer (GBL) surface remains intact for epitaxial growth. The reduced vdW gap between the epilayer and substrate enhances epitaxial interaction, promoting remote epitaxy. Significantly improved nucleation and convergent quality of GaN are achieved on the GBL, resulting in the best quality GaN ever grown on two-dimensional materials. The GBL surface exhibits excellent resistance to harsh growth environments, enabling substrate reuse by repeated growth and exfoliation.

The dataset presented in this article is linked to the research article titled "Evolution in size and structural order for incipient soot formed at flame temperatures greater than 2100 K" [1]. The research article discusses the systematic evolution of flame formed carbon in premixed stagnation flames with flame temperatures hotter than conventional combustion applications. The effect of the growth environment on particle size, structure, composition and properties are studied. The flame temperature (1950  K < T f,max < 2250 K) and equivalence ratio (Φ = 2.4, 2.5, and 2.6) are methodically varied to analyze impact on insipient soot while maintaining a comparable particle residence time (t p ~ 15 ms). This article presents the data acquired for this systematic study. The data presented herein provides fundamental observations suitable for development of soot formation theory and modeling. Characterization of material properties and morphology are also relevant to potential applications of functional carbon nanomaterials. Raman spectra are measured for carbon films deposited from the flames, soot particle size distributions are obtained by aerosol sampling from the flames and soot radiative emissions are measured in-situ by color-ratio pyrometry. Deconvolution of Raman peaks is carried out to extract information on carbon bonding and structural order. Flame temperature is extracted from the measured color-ratio field making assumptions for the soot optical dispersion exponent., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships which have, or could be perceived to have, influenced the work reported in this article., (© 2021 The Author(s). Published by Elsevier Inc.)

The polycondensation of resorcinol and formaldehyde in a water-ethanol mixture using the adapted Stöber method was used to obtain resol resins. An optimization of synthesis conditions and the use of an appropriate stabilizer (e.g., poly(vinyl alcohol)) resulted in spherical grains. The resins were carbonized in the temperature range of 600-1050 °C and then chemically activated in an aqueous HNO 3 solution, gaseous ammonia, or by an oxidation-reduction cycle (soaking in a HNO 3 solution followed by treatment with NH 3 ). The obtained carbons were characterized by XRD, the low-temperature adsorption of nitrogen, SEM, TGA, and XPS in order to determine degree of graphitization, porosity, shape and size of particles, and surface composition, respectively. Finally, the materials were tested in phenol adsorption. The pseudo-second order model perfectly described the adsorption kinetics. A clear correlation between the micropore volume and the adsorption capacity was found. The content of graphite domains also had a positive effect on the adsorption properties. On the other hand, the presence of heteroatoms, especially oxygen groups, resulted in the clogging of the pores and a decrease in the amount of adsorbed phenol.

The occurrence of environmental endocrine disrupting chemicals (EDCs) in aquatic environments has caused extensive concern. Graphene-like magnetic sawdust biochar was synthesized using potassium ferrate (K 2 FeO 4 ) to make activated sawdust biochar and applied for the removal of 17-estradiol (E2). The characterization showed that the surface morphology of five graphene-like magnetic sawdust biochars prepared with different preparation conditions were quite different. The specific surface area and pore structure increased with the increment of K 2 FeO 4 addition. The results have shown that graphene-like magnetic sawdust biochar (1:1/900 °C) had the best removal on E2. The experimental results indicated that pseudo-first-order kinetic model and the Langmuir model could describe the adsorption process well, in which the equilibrium adsorption capacity ( q e,1 ) of 1:1/900 °C were 59.18 mg·g -1 obtained from pseudo-first-order kinetic model and the maximum adsorption capacity ( q max ) of 1:1/900 °C were 133.45 mg·g -1 obtained from Langmuir model at 298K. At the same time, lower temperatures, the presence of humic acid (HA), and the presence of NaCl could be regulated to change the adsorption reaction in order to remove E2. Adsorption capacity was decreased with the increase of solution pH because pH value not only changed the surface charge of graphene-like magnetic sawdust biochar, but also affected the E2 in the water. The possible adsorption mechanism for E2 adsorption on graphene-like magnetic sawdust biochar was multifaceted, involving chemical adsorption and physical absorption, such as H-bonding, π-π interactions, micropore filling effects, and electrostatic interaction. To sum up, graphene-like magnetic sawdust biochar was found to be a promising absorbent for E2 removal from water.

Porous carbon materials are promising candidates for anode materials in rechargeable potassium-ion batteries. However, their high surface area and low crystallinity usually cause side reactions with electrolytes and slanted charge/discharge profiles. Herein, we report the synthesis of porous carbon microspheres with highly graphitized structure and enhanced potassium-ion storage properties. The prepared carbon microspheres exhibit a low working potential of ~0.2 V, high Coulombic efficiency, and a stable reversible capacity of 292.0 mAh/g after 100 cycles, which is significantly higher than that of commercial graphite (137.5 mAh/g after 100 cycles). These desirable performances are attributed to the high crystallinity of carbon and its porous structure, which provide active sites for potassium-ion storage and alleviate the stress caused by the large volume change during the insertion and extraction of potassium ions., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Area-selective atomic layer deposition (AS-ALD) is a promising technique for fine nanoscale patterning, which may overcome the drawbacks of conventional top-down approaches for the fabrication of future electronic devices. However, conventional materials and processes often employed for AS-ALD are inadequate for conformal and rapid processing. We introduce a new strategy for AS-ALD based on molecular layer deposition (MLD) that is compatible with large-scale manufacturing. Conformal thin films of "indicone" (indium alkoxide polymer) are fabricated by MLD using INCA-1 (bis(trimethylsily)amidodiethylindium) and HQ (hydroquinone). Then, the MLD indicone films are annealed by a thermal heat treatment under vacuum. The properties of the indicone thin films with different annealing temperatures were measured with multiple optical, physical, and chemical techniques. Interestingly, a nearly complete removal of indium from the film was observed upon annealing to ca. 450 °C and above. The chemical mechanism of the thermal transformation of the indicone film was investigated by density functional theory calculations. Then, the annealed indicone thin films were applied as an inhibiting layer for the subsequent ALD of ZnO, where the deposition of approximately 20 ALD cycles (equivalent to a thickness of approximately 4 nm) of ZnO was successfully inhibited. Finally, patterns of annealed MLD indicone/Si substrates were created on which the area-selective deposition of ZnO was demonstrated.

The lack of methods to modulate intrinsic textures of carbon cathode has seriously hindered the revelation of in-depth relationship between inherent natures and capacitive behaviors, limiting the advancement of lithium ion capacitors (LICs). Here, an orientated-designed pore size distribution (range from 0.5 to 200 nm) and graphitization engineering strategy of carbon materials through regulating molar ratios of Zn/Co ions has been proposed, which provides an effective platform to deeply evaluate the capacitive behaviors of carbon cathode. Significantly, after the systematical analysis cooperating with experimental result and density functional theory calculation, it is uncovered that the size of solvated PF 6 ion is about 1.5 nm. Moreover, the capacitive behaviors of carbon cathode could be enhanced attributed to the controlled pore size of 1.5-3 nm. Triggered with synergistic effect of graphitization and appropriate pore size distribution, optimized carbon cathode (Zn - ion is about 1.5 nm. Moreover, the capacitive behaviors of carbon cathode could be enhanced attributed to the controlled pore size of 1.5-3 nm. Triggered with synergistic effect of graphitization and appropriate pore size distribution, optimized carbon cathode (Zn 90 Co 10 -APC) displays excellent capacitive performances with a reversible specific capacity of ~ 50 mAh g -1 at a current density of 5 A g -1 . Furthermore, the assembly pre-lithiated graphite (PLG)//Zn 90 Co 10 -APC LIC could deliver a large energy density of 108 Wh kg -1 and a high power density of 150,000 W kg -1 as well as excellent long-term ability with 10,000 cycles. This elaborate work might shed light on the intensive understanding of the improved capacitive behavior in LiPF 6 electrolyte and provide a feasible principle for elaborate fabrication of carbon cathodes for LIC systems.

Graphite nanoplatelets (GNPs), a functional 2D nanofiller for polymer nanocomposites, utilize natural graphite as a raw material due to its stacked graphene layers and outstanding material properties upon successful exfoliation into nano-thick sheets. However, the increasing demand for natural graphite in many industrial applications necessitates the use of graphite from waste resources. We synthesized GNPs from waste chicken feathers (WCFs) by graphitizing carbonized chicken feathers and exfoliating the graphitic carbon by high-speed homogenization and sonication. We then separated GNP from non-exfoliated carbon by centrifugation. This paper describes the morphology, chemical, and crystalline properties of WCF and its carbon derivatives, as well as the structural features of WCF-derived carbons. We obtained GNPs that have a 2D structure with huge variations in particle size and thickness. The GNP shows the presence of carbonyl groups, which are mostly attached at the edges of the stacked graphene sheets. Defects in the GNP are higher than in graphene synthesized from direct exfoliation of natural graphite but lower than in graphene oxide and reduced graphene oxide. To produce GNP of high quality from WCF, restacking of graphene sheets and concentration of carbonyls must be minimized.