N/S Co-Doped Graphene Aerogels as Superior Anode Materials for High-Rate Lithium-Ion Batteries.

The nitrogen and sulfur co-doped graphene aerogel (SNGA) was synthesized by a one-pot hydrothermal route using graphene oxide as the starting material and thiourea as the S and N source. The obtained SNGA with a three-dimensionally hierarchical structure, providing more available pathways for the transport of lithium ions. The existing form of S and N was regulated by changing the calcination temperature and thiourea doping amount. The results revealed that high temperature could decompose -SOX- functional groups and promote the transformation of C-S-C to C-S, ensuring the cyclic stability of electrode materials, and increasing the thiourea dosage amount introduced more pyridine nitrogen, improving the multiplicative performance of electrode materials. Benefiting from the synergistic effect of sulfur and nitrogen atoms, the prepared SNGA showed superior rate capability (107.8 mAh g-1 at 5 A g-1), twice more than that of GA (52.8 mAh g-1), and excellent stability (232.1 mAh g-1 at 1 A g-1 after 300 cycles), 1.85 times more than that of GA (125.6 mAh g-1). The present study provides a detailed report on thiourea as a dopant to provide a sufficient basis for SNGA and a theoretical guide for further modifying.

Construction of a type-II BiVO4/BiOI heterojunction for efficient photoelectrocatalytic degradation of ß-naphthol and coal gasification wastewater under visible-light irradiation.

Herein, a novel type-II BiVO4/BiOI (BVOI) heterojunction electrode material was successfully fabricated by using a facile two-step electrodeposition approach. The experimental results revealed that BiOI nanosheets were deposited onto the surface of BiVO4 particles successfully, with the special morphology providing more active sites, which was beneficial to the improvement of PEC performance. According to the electrochemical performance tests, it could be observed that the construction of a heterojunction effectively promoted the separation of photoinduced electron-hole pairs and increased the transfer rate of surface charges. Under visible-light irradiation, the BVOI-300 photoanode possessed the highest PEC ß-naphthol degradation rate at pH = 7, which approximately reached 82%, whose corresponding kinetic constant was 1.4 and 1.5 times higher than those of pure BiVO4 and BiOI. After five cycles, the degradation rate still remained at 64.61%. The band structure of the BVOI electrode was deduced, and the PEC mechanism of the BVOI electrode was investigated through the radical trapping quenching experiments and ESR test, which indicated that the ˙OH, h+ and ˙O2- radicals were crucial active species in the PEC ß-naphthol degradation process. For the BVOI-300 working electrode, the TOC content of coal gasification wastewater (CGW) decreased from 94.44 to 54.4 mg L-1, and the removal rate reached 42.4%. GC-MS was used to identify the organic components of coal gasification wastewater, which was expected to provide reference for remedying actual gasification wastewater containing refractory organic pollutants and offer a new development direction for the treatment of actual coal chemical wastewater.

3D chrysanthemum-like g-C3N4/TiO2 as an efficient visible-light-driven Z-scheme hybrid photocatalyst for tetracycline degradation.

Utilization of a solar-driven semiconductor as a photocatalyst to degrade antibiotic pollutants is a feasible and environmentally friendly technology. In this paper, 3D chrysanthemum-like g-C3N4/TiO2 as a visible-light-driven hybrid photocatalyst with a Z-scheme heterostructure was firstly synthesized by the in situ hydrothermal synthesis method. Experiments proved that this 3D chrysanthemum-like g-C3N4/TiO2 had better degradation performance toward tetracycline than TiO2 and g-C3N4. In particular, when optimized g-C3N4/TiO2-2 was applied for tetracycline removal (200 ml, 10 mg L-1), the corresponding degradation efficiency could reach nearly 100% within 60 min. The improved photocatalytic activity was the result of better utilization of the heterostructure-induced visible light, more efficient charge transfer in the Z-scheme heterojunction as well as stronger redox capability. The Z-scheme degradation mechanism was supported by the trapping experiments of active species and ESR radical detection, and the whole photocatalytic process was controlled by the combined action of ˙O2-, h+ and ˙OH radicals. This study may be beneficial for the design of more efficient sunlight-driven hybrid photocatalysts and their applications in wastewater treatment.

Preparation of valuable pyrolysis products from poplar waste under different temperatures by pyrolysis: Evaluation of pyrolysis products.

Poplar waste is used as feedstock to prepare valuable pyrolysis products by pyrolysis under different temperature. The bio-oil is rich in aldehyde with the maximum relative content of 47.15%, which has potential application in chemical industries. Pyrolysis temperature has significantly influenced the composition and heating value of bio-gas. The maximum heating value of bio-gas is 14.56 MJ/Nm3. Biochar is used as an adsorbent to adsorb Ag+ from aqueous solution with the adsorption capacity of 76.09 mg/g. Biochar forms the value-added Ag-Biochar composite by reduction after adsorption Ag+. While, Ag-Biochar composite can be used as catalyst for methyl orange removal with the maximum removal of 94.08%. Ag-Biochar composite is also used as lithium ion battery cathode material for energy storage with the specific capacity of 345 mAh/g. Besides, preliminary economic analysis is used to evaluate the economics of pyrolysis process with the total annual revenue of $115, 725/year.

Construction of nitrogen vacant g-C3N4 nanosheet supported Ag3PO4 nanoparticle Z-scheme photocatalyst for improved visible-light photocatalytic activity.

The superior photocatalytic activity of semiconductor-based photocatalytic materials has attracted great attention. In this work, a series of novel Ag3PO4/g-C3N4-x (APO/CNx) composites with the Z-scheme structure were fabricated through a facile precipitation method. B naphthol, a typical phenolic compound, was selected to evaluate the photocatalytic activity of all as-prepared photocatalysts. The obtained APO/CNx composites exhibited excellent photocatalytic activity for degradation of B naphthol under visible-light irradiation. Experimental results showed that the degradation rate toward B naphthol could reach to 90.5% for 180 min, which was almost 3.66 times higher than pure g-C3N4, indicating that the presence of nitrogen vacancies and Z-scheme structure could efficiently improve the photocatalytic performance of pure g-C3N4. Furthermore, the results of trapping experiments and electron spin resonance (ESR) spectroscopy manifest that •O2- and •OH radicals were the predominant active substances for B naphthol degradation, and the possible mechanism of improved photocatalytic performance was elucidated. This work will provide an innovative perspective for constructing Z-scheme photocatalysts for the application of photocatalytic in the field of wastewater treatment.

Recent Advances in Binary Colloidal Crystals for Photonics and Porous Material Fabrication.

In the past few years, binary colloidal crystals (BCCs) composed of both large and small particles have attracted considerable attention from the scientific community as an exciting alternative to single colloidal crystals (SCCs). In particular, more complex structures with diverse nanotopographies and desirable optical properties of BCCs can be obtained by various colloidal assembly methods, as compared to SCCs. Furthermore, high accuracy in crystal growth with controllable stoichiometries allows for a great deal of promising applications in the fields of both interfacial and material sciences. The visible-light diffraction property of BCCs is more superior than that of SCCs, which makes them have more promising applications in the fabrication of photonic crystals with full band gaps. On the other hand, their spherical shapes and ease of removal property make them ideal templates for ordered porous material fabrication. Hence, this perspective outlined recent advances in assembly approaches of BCCs, with an emphasis on their promising applications for advanced photonics and multifunctional porous material fabrication. Eventually, some challenging yet important issues and some future perspectives are further discussed.

Magnetic graphene-based nanocomposites as highly efficient absorbents for Cr(VI) removal from wastewater.

Due to the merits of their high adsorption and convenient separation, magnetic graphene-based composites have become a promising adsorbent in terms of wastewater treatment. However, recycling and regeneration properties of magnetic graphene-based composites are still a conundrum, which remains to be resolved. Here, Fe3O4/reduced graphene oxide (RGO) (Fe3O4/RGO) nanocomposites were synthesized by one-step solvent-thermal reduction route and used as adsorbents for water purification. It was encouraging to find that the nanocomposites possessed many intriguing properties in removing of Cr(VI) ions, including high adsorption efficiency and excellent recycling and regeneration property. The results indicated that the magnetic separation process of the Fe3O4/RGO nanocomposites only took less than 5 s and the maximum removal efficiency of Cr(VI) reached 99.9% under the optimum experimental conditions. Most significantly, the adsorption rate of Cr(VI) can still be as high as 98.13% after 10 cycles and the single recycle quality of the nanocomposites can maintain at more than 80%. As a result, the Fe3O4/RGO nanocomposites could be a potential adsorbent for removing heavy metal ions effectively, especially in environmental protection and restoration.

Effect of Cu-based metal organic framework (Cu-MOF) loaded with TiO2 on the photocatalytic degradation of rhodamine B dye.

Using copper nitrate trihydrate as the copper source, TiO2@Cu-MOF nanocomposites were prepared by a one-step crystallization method, and the effect of the amount of TiO2 loaded on the adsorption of rhodamine B was studied. X-ray diffraction (XRD), scanning electron microscope (SEM), energy spectrometer (EDS), N2 adsorption-desorption (BET), and infrared spectroscopy (FTIR) were used to characterize the microstructure and surface properties of composite materials. The results show that the composite material not only has a good degradability for rhodamine B, the decolorization rate reaches 98.03% after 120 min, but it also maintains a good cycle performance. Fitting the first-order kinetic equation to the reaction process, under the optimal conditions, R2 = 0.98, indicating that the reaction process conforms to the first-order kinetic equation. Therefore, the catalyst has good catalytic degradation and cycle performance.

A minireview on doped carbon dots for photocatalytic and electrocatalytic applications.

To date, carbon dots (CDs) or carbon quantum dots (CQDs), considered as alternatives to conventional fluorescent materials such as organic dyes and semiconductor quantum dots (QDs), have drawn significant attention from relevant researchers due to their superior properties, including nontoxicity, biocompatibility, low cost and facile synthesis, and high photoluminescence. In particular, doping heteroatoms with CDs can not only dramatically enhance the fluorescence but also greatly improve the electronic structure and doped CDs have been successfully applied in various technological fields. Herein, this minireview summarizes recent advances on the synthesis and optical properties of doped CDs and their promising applications for photocatalysis and electrocatalysis. Finally, some challenging issues as well as future perspectives of this exciting material are discussed.

Hydrothermal-template synthesis and electrochemical properties of Co3O4/nitrogen-doped hemisphere-porous graphene composites with 3D heterogeneous structure.

Despite the high capacity of Co3O4 employed in lithium-ion battery anodes, the reduced conductivity and grievous volume change of Co3O4 during long cycling of insertion/extraction of lithium-ions remain a challenge. Herein, an optimized nanocomposite, Co3O4/nitrogen-doped hemisphere-porous graphene composite (Co3O4/N-HPGC), is synthesized by a facile hydrothermal-template approach with polystyrene (PS) microspheres as a template. The characterization results demonstrate that Co3O4 nanoparticles are densely anchored onto graphene layers, nitrogen elements are successfully introduced by carbamide and the nanocomposites maintain the hemispherical porous structure. As an anode material for lithium-ion batteries, the composite material not only maintains a relatively high lithium storage capacity (the first discharge specific capacity can reach 2696 mA h g-1), but also shows significantly improved rate performance (1188 mA h g-1 at 0.1 A g-1, 344 mA h g-1 at 5 A g-1) and enhanced cycling stability (683 mA h g-1 after 500 cycles at 1 A g-1). The enhanced electrochemical properties of Co3O4/N-HPGC nanocomposites can be ascribed to the synergistic effects of Co3O4 nanoparticles, novel hierarchical structure with hemisphere-pores and nitrogen-containing functional groups of the nanomaterials. Therefore, the developed strategy can be extended as a universal and scalable approach for integrating various metal oxides into graphene-based materials for energy storage and conversion applications.

Hydrothermal Synthesis of Co3O4/ZnO Hybrid Nanoparticles for Triethylamine Detection.

Development of high performances gas sensors to monitor and detect the volatile organic compound triethylamine is of paramount importance for health and environmental protection. The Co3O4-ZnO nanoparticles composite was successfully synthesized by the one-step hydrothermal route and annealing process in this work. The gas sensitivity test results show that the composite exhibits excellent triethylamine-sensing performance at a cobalt content of 1 at%, indicating potential application for triethylamine detection. The sensor based on the Co3O4-ZnO composite had higher sensitivity to triethylamine, better selectivity, and faster response recovery rate compared with pure ZnO sensor. Combined with the structural characteristics of the characterized Co3O4-ZnO nanocomposite, the optimized triethylamine sensing performances can be ascribed to the p-n heterojunction effect between Co3O4 and ZnO, as well as the catalytic and high oxygen adsorption properties of Co3O4.

Nitrogen-Doped Porous Co3O4/Graphene Nanocomposite for Advanced Lithium-Ion Batteries.

A novel approach is developed to synthesize a nitrogen-doped porous Co3O4/anthracite-derived graphene (Co3O4/AG) nanocomposite through a combined self-assembly and heat treatment process using resource-rich anthracite as a carbonaceous precursor. The nanocomposite contains uniformly distributed Co3O4 nanoparticles with a size smaller than 8 nm on the surface of porous graphene, and exhibits a specific surface area (120 m2·g-1), well-developed mesopores distributed at 3~10 nm, and a high level of nitrogen doping (5.4 at. %). These unique microstructure features of the nanocomposite can offer extra active sites and efficient pathways during the electrochemical reaction, which are conducive to improvement of the electrochemical performance for the anode material. The Co3O4/AG electrode possesses a high reversible capacity of 845 mAh·g-1 and an excellent rate capacity of 587 mAh·g-1. Furthermore, a good cyclic stability of 510 mAh·g-1 after 100 cycles at 500 mA·g-1 is maintained. Therefore, this work could provide an economical and effective route for the large-scale application of a Co3O4/AG nanocomposite as an excellent anode material in lithium-ion batteries.

Hydrothermal Synthesis of Ultra-Light Coal-Based Graphene Oxide Aerogel for Efficient Removal of Dyes from Aqueous Solutions.

A novel carboxymethyl cellulose (CMC)-supported graphene oxide aerogel (CGOA) was fabricated from a cost-effective and abundant bituminous coal by a mild hydrothermal process and freeze-drying treatment. Such an aerogel has cross-linked graphene oxide layers supported by CMC, and therefore, displays high mechanical strength while having ultra-low density (8.257 mg·cm-3). The CGOA has a 3D interconnected porous structure, beneficial graphene framework defects and abundant oxygen-containing functional groups, which offer favorable diffusion channels and effective adsorption sites for the transport and adsorption of dye molecules. The adsorption performance of rhodamine B by an optimized CGOA shows a maximum monolayer adsorption capacity of 312.50 mg·g-1, as determined by Langmuir isotherm parameters. This CGOA exhibited a better adsorption efficiency (99.99%) in alkaline solution, and satisfactory stability (90.60%) after three cycles. In addition, adsorption experiments on various dyes have revealed that CGOA have better adsorption capacities for cationic dyes than anionic dyes.

IR spectrum simulation of molecular structure model of Shendong coal vitrinite by using quantum chemistry method.

The structure of coal needs to be understood from a molecular point of view for clean, effective and high value-added utilization of coal. In the literature, molecular structure model of Shendong coal vitrinite (SV) was established by the authors on the basis of experimental results of ultimate analysis and 13C NMR, and the calculated 13C NMR spectrum of SV model was consistent with the experimental spectrum. In order to further verify the accuracy of SV structure model established by the authors, the infrared spectrum of SV structure model was calculated using quantum chemistry semi-empirical VAMP in this thesis. The results showed that the peak shape of calculated IR spectrum of SV structure model was similar to the experiment's, but the wave number of calculated IR spectrum was obviously higher than that of experimental spectrum. According to the calculated results for model compounds by using the same method, calculated vibrational frequency was higher than that of experiment for the same functional groups. Hence, the calculated IR spectrum should be corrected. After correction the calculated IR spectrum of SV structure model matched well with the experimental spectrum. In other words, the SV structure model can truly reflect the structure characteristics of SV.

Preparation and self-assembly of uniform TiO2/SiO2 composite submicrospheres.

Monodisperse spheres of silica were uniformly coated with titania through the hydrolysis of titanium alkoxide in order to increase the refractive index of complex submicrospheres and keep their monodispersity as well as their surface morphology. On the basis of the hydrolysis of tetrabutyl orthotitanate (TBOT), a continuous-feeding procedure was used to fabricate 10-nm titania coatings on monodisperse colloidal silica submicrospheres of diameter 200 nm. The TiO2/SiO2 composite spheres were assembled to achieve structures with three-dimensional order by gravity sedimentation and vertical deposition. The complex sphere composition, quality, and morphology were characterized by different techniques.