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The aim of achieving integration of lightweight, high strength, high‐temperature resistant, and satisfactory electromagnetic (EM) wave absorption was successfully accomplished in the present study by synthesizing TiC–TiB2 fibers reinforced Si3N4 composites, which were pressureless sintered at 1650°C for 2 h. The preparation of TiC–TiB2 fibers was conducted through a chloride‐assisted carbothermic method. This work focused on investigating the effects of incorporating TiC–TiB2 fibers on the mechanical properties and EM wave absorption characteristics of the composites. The 30 wt% TiC–TiB2/Si3N4 composite displayed the bulk density of 1.89 g/cm3, bending strength of 93.11 ± 3.91 MPa, fracture toughness of 1.81 ± 0.10 MPa m1/2, minimum reflection loss of −38.87 dB, and effective absorption bandwidth of 1.43 GHz in the Ku‐band, respectively. The as‐synthesized TiC–TiB2/Si3N4 composites are promising candidates for EM wave absorbing load‐bearing materials due to their outstanding mechanical properties and microwave absorption properties. [ABSTRACT FROM AUTHOR]

In this study, a chloride-assisted boro/carbothermal reduction method was employed to prepare HfB 2 whiskers, aiming to address the challenges associated with large-scale preparation of HfB 2 whiskers and the development of high-temperature resistant electromagnetic wave absorbing materials. When the precursors were mechanically stirred, the resulting mixture underwent calcination at 1450 °C for 3 h, leading to the formation of single-phase HfB 2 whiskers. The as-synthesized HfB 2 whiskers showed exceptional resistance to oxidation at temperatures up to 700 °C. The microwave absorption performance and mechanism of the HfB 2 whiskers/paraffin composite were also investigated. The results revealed that the composite achieved a minimum reflection loss of −41.29 dB when the HfB 2 whiskers content reached 80 wt%, while the widest effective absorption bandwidth of the composite reached 3.6 GHz when the HfB 2 whiskers content increased to 82.5 wt%. This work presents a novel candidate for high-temperature resistant materials used in absorbing electromagnetic wave. [ABSTRACT FROM AUTHOR]

In this study, a chloride-assisted boro/carbothermal reduction method was employed to prepare HfB 2 whiskers, aiming to address the challenges associated with large-scale preparation of HfB 2 whiskers and the development of high-temperature resistant electromagnetic wave absorbing materials. When the precursors were mechanically stirred, the resulting mixture underwent calcination at 1450 °C for 3 h, leading to the formation of single-phase HfB 2 whiskers. The as-synthesized HfB 2 whiskers showed exceptional resistance to oxidation at temperatures up to 700 °C. The microwave absorption performance and mechanism of the HfB 2 whiskers/paraffin composite were also investigated. The results revealed that the composite achieved a minimum reflection loss of −41.29 dB when the HfB 2 whiskers content reached 80 wt%, while the widest effective absorption bandwidth of the composite reached 3.6 GHz when the HfB 2 whiskers content increased to 82.5 wt%. This work presents a novel candidate for high-temperature resistant materials used in absorbing electromagnetic wave. [ABSTRACT FROM AUTHOR]

Compared with common monoanionic high entropy ceramics, polyanionic high entropy ceramics, with better performance, are more difficult to prepare. Since transition metal carbides have high hardness and transition metal nitrides have good toughness, it is hoped that high entropy carbonitride ceramics can combine the advantages of the two. In this paper, a series of novel (Ti 0.25 Nb 0.25 Hf 0.25 Ta 0.25)C x N 1–x (x = 0.3, 0.4, 0.5, 0.6, and 0.7) high entropy ceramics were successfully synthesized for the first time using spark plasma sintering at 1850 °C with metal carbides and metal nitrides as raw materials. The phase evolution, microstructure, hardness and fracture toughness of high carbonitride entropy ceramics were investigated. X-ray diffraction indicates the ceramics with the single-phase face-centered cubic structure were successfully prepared. It was found that the high entropy ceramics sintered at 1850 °C with four cationic components have excellent performance on fracture toughness (KIC = 7.1746 MPa m1/2). With the increase of carbide proportion, the hardness of the ceramics increased, but the fracture toughness and bending strength decreased slightly. And it was found that the differences of grain size and porosity content were the main reasons for the mechanical properties difference. The excellent hardness properties, good bending strength and outstanding fracture toughness of the high entropy ceramics provide the possibility for the application of high entropy ceramics in aerospace and other applications requiring high performance. [ABSTRACT FROM AUTHOR]

Nowadays, the increasingly severe electromagnetic (EM) wave pollution requires high-performance EM wave absorbing materials. Multi-principal-element materials are acknowledged as promising for broadening the applications owing to their tunable chemistries and structures in many fields, including as EM wave absorbers. Herein, we prepared a high-entropy MXene, (Mo 0.25 Cr 0.25 Ti 0.25 V 0.25) 3 C 2 T x. Furthermore, multi-principal-element (Mo 0.25 Cr 0.25 Ti 0.25 V 0.25) 3 C 2 T x /FeCoNi and (Mo 0.25 Cr 0.25 Ti 0.25 V 0.25) 3 C 2 T x /FeCoNiCu composites were synthesized via an in-situ hydrothermal process by combining high-entropy MXene with medium-entropy magnetic alloys. In contrast with the relatively narrow effective absorption bandwidth (EAB) of (Mo 0.25 Cr 0.25 Ti 0.25 V 0.25) 3 C 2 T x MXene (2.56 GHz), (Mo 0.25 Cr 0.25 Ti 0.25 V 0.25) 3 C 2 T x /FeCoNi composite with 50 wt% MXene can attain an optimum EAB of 4.88 GHz with the matching thickness of only 1.73 mm. As for (Mo 0.25 Cr 0.25 Ti 0.25 V 0.25) 3 C 2 T x /FeCoNiCu composites, both the absorption efficiency and absorption bandwidth are significantly enhanced. The combination of multi-principal-component strategy and composite construction endows the composites with synergistic dielectric and magnetic losses, optimized impedance matching as well as enhanced attenuation ability, thus improving EM wave absorption performances. In addition, radar cross section (RCS) simulation confirms that the prepared composites have broad application prospects as radar stealth materials. [ABSTRACT FROM AUTHOR]

In view of the lack of conformal, load‐bearing, light‐weight, and high temperature‐resistant integrated wave‐absorbing composites suitable for extremely complex conditions, the gel‐casting process was successfully applied to porous Si3N4 wave‐absorbing composites in this work. A universal low‐slurry for gel casting was prepared by using two dispersants acting together (tetramethylammonium hydroxide solution and sodium lauryl sulfate), which ensured the smooth completion of the gel casting process. Combining the thermogravimetric and differential thermal gravity curves of the composite green body, reasonable parameters of the rubber discharge process are given to avoid the problem of the green body swelling and cracking. The porous TiC/Si3N4 composites were successfully prepared by holding them at 1650°C for 3 h. The bending strength, density, minimum reflection loss, absorption bandwidth, and matched thickness in the P‐band of the composites with 30 wt.% TiC addition were 54.08 ± 3.02 MPa, 1.906 g/cm3, ‐37.75 dB, 1.9 GHz, and 4.1 mm, respectively. The electromagnetic wave loss mechanisms of the composites are a combination of conductivity loss, multiple reflections and scattering, interfacial polarization, and defect polarization. [ABSTRACT FROM AUTHOR]

The TiB 2 fibers were prepared by a chloride-assisted carbothermic method accompanied with the vapor-liquid-solid (VLS) mechanism. The influences of TiO 2 , B 2 O 3 , C 12 H 22 O 11 , and calcination temperature on the yield of TiB 2 fibers were investigated. In addition, the effects of TiB 2 fibers content on the electromagnetic (EM) parameters and microwave absorption (MA) properties of TiB 2 fibers/paraffin composite was studied in detail. The TiB 2 fibers/paraffin composite showed excellent microwave absorption performance, with an optimized reflection loss (RL) of −46.63 dB at 14 GHz and a thickness of 1.5 mm. Moreover, it exhibited a broad effective absorption bandwidth (EAB) (RL < −10 dB) of 3.9 GHz, ranging from 12 to 15.9 GHz. TiB 2 fibers exhibit promising potential as materials for high-temperature applications in the field of MA. [ABSTRACT FROM AUTHOR]

In the recent years, MXenes (2D transition metal carbides, carbon nitrides and nitrides) and its precursor MAX phases have been widely investigated in electrochemical research. In this research, we successfully prepared a core-shell structured compound——Ti 3 C 2 @Ti 2 SnC/CNFs (MXene@TSC/C) as an anode material for lithium ion battery via electrospinning method. Results showed that this type of compound has a specific capacity of 288.9 mAh·g−1 at the current density of 0.4 A g−1 after 300 cycles, accompany with a retention rate of capacity of 105.4% in the rate performance test. These performances were benefit from the core-shell structured CNFs and Ti 3 C 2 MXenes. This work supported a novel way to improve the electrochemical property of MXene and MAX phases, which was expected to further explored. [ABSTRACT FROM AUTHOR]

A sol-gel method was employed for the synthesis of new High-entropy boride (HEB) powders, (Hf 0.2 Nb 0.2 Cr 0.2 Ta 0.2 Mo 0.2)B 2 , with nanoscale. The as-synthesized powders were obtained at a relatively low temperature of 1650 °C, and had small average particle size of 62.09 nm. X-ray diffraction confirmed that the (Hf 0.2 Nb 0.2 Cr 0.2 Ta 0.2 Mo 0.2)B 2 powders were hexagonal single-phase without any oxide impurities. In particular, electrochemical performance of the (Hf 0.2 Nb 0.2 Cr 0.2 Ta 0.2 Mo 0.2)B 2 powders with multiphase and high-entropy single phase were investigated using a three-electrode system. The improved electrochemical performance of the HEB powders is realized, with 27% higher in specific capacitance compared to the powders with multiphase. The HEB powders electrode exhibits a high capacitance retention of 97.03% after 5000 cycles. [ABSTRACT FROM AUTHOR]

The new inorganic material known as "high-entropy oxides" (HEOs) has a single-phase structure and is made up of several different main metal elements. It has many useful properties, including a high specific capacity, excellent cycling performance, high structural stability, and super-electronic conductivity. For lithium-ion batteries, it is viewed as a promising electrode material (LIBs). It is significant to develop high entropy oxides with different components and study their properties. Herein, Mg, Ni and Li are added to the quaternary medium entropy (CrFeMnCo)3O4. Four new spinel high entropy oxides were synthesized by glycine-nitrate SCS method at 750 °C and their material characterization and electrochemical properties were investigated respectively. The experimental results show that the four obtained samples have uniform particle size distribution. As for the electrochemical test, the capacities of the (CrFeMnCoMg)3O4 and (CrFeMnCoNi)3O4 do not decrease significantly after 800 cycles at 2000 mA·g−1. They have better cycle stability than the (CrFeMnCoMgLi)3O4 and (CrFeMnCoNiLi)3O4. As the anode of LIBs, all HEOs show excellent cycle stability and rate capability. This work provides a new strategy for designing high-entropy energy storage materials. [ABSTRACT FROM AUTHOR]

The composition and synthesis approach of high entropy ceramics have significant influences on their microstructures and mechanical properties. A new (Hf 0.2 Zr 0.2 Ta 0.2 V 0.2 Nb 0.2)B 2 high entropy diboride ceramic with excellent mechanical properties was successfully prepared by spark plasma sintering (SPS) at a relatively "low temperature" (1800 °C) in this work. The effects of two mixing strategies, grinding and ball milling, on the solid solubility of the calcined powders were studied. Furthermore, the effects of these two mixing strategies on the phase and morphology of the calcined powders and the mechanical properties of the SPS sintered ceramics were analyzed. Experimental results indicated that, compared with a single solid solution phase within the high entropy boride powders obtained by ball milling, incomplete solid-solution presented in the high entropy boride powders obtained using grinding treatment. It promoted the solid-state diffusion and in-situ reaction of the diborides in the ceramics during the sintering process, thereby improving the densification and the hardness of the high entropy diboride ceramics. By grinding treatment, (Hf 0.2 Zr 0.2 Ta 0.2 V 0.2 Nb 0.2)B 2 high entropy ceramic with a relative density of 94% and a hardness of up to 25.34 ± 1.5 GPa at an indentation load of 9.8 N was obtained at 1800 °C. This work not only expanded the family of high-entropy diboride ceramics but also proved the advantage of grinding treatment in preparation of high entropy diboride ceramics. [ABSTRACT FROM AUTHOR]

The boron nitride nanosheets (BNNSs)/aluminum nitride (AlN) composites were prepared by hot press sintering at 1600°C. The microstructure, mechanical properties, and thermal conductivity of the samples were measured, and the effect of adding BNNSs to AlN ceramics on the properties was studied. It is found that the addition of BNNSs can effectively improve the mechanical properties of AlN. When the additional amount is 1 wt%, the bending strength of the sample reaches the maximum value of 456.6 MPa, which is 23.1% higher than that of the AlN sample without BNNSs. The fracture toughness of the sample is 4.47 MPa m1/2, a 68.7% improvement over the sample without BNNSs. The composites obtained in the experiment have brilliant mechanical properties. [ABSTRACT FROM AUTHOR]

Upconversion (UC) luminescence modulation is quite important in controlling and processing light for active components of light sources, photoswitches, optical memories, and optical sensing devices. In this work, we reported one kind of novel phosphor, Ho3+/Yb3+‐doped SrBi4Ti4O15 ceramics, which displayed both strong UC luminescence and obvious photochromic (PC) reaction. The UC luminescence, PC effect, and the modulation of UC performance based on PC behavior were investigated in detail. By alternating visible light irradiation and thermal stimulus, the UC luminescence could be reversibly regulated. Meanwhile, the modulation was unveiled to tightly rely on the irradiation time and thermal treatment processes. Excellent reproducibility was also achieved. In addition, as an alternative method to thermal treatment, the manipulation of luminescence by electric field was also explored. Finally, the mechanism related to the UC luminescence manipulation was illustrated. The results indicate that these samples could be potentially utilized in optical data storage and anti‐counterfeiting security fields. [ABSTRACT FROM AUTHOR]

Due to their intriguing properties, boron nitride nanosheets (BNNSs) with large lateral size and high crystallinity have great promise for many applications. However, the quantitative exfoliation of hexagonal boron nitride (h-BN) into good quality BNNSs still remains a key challenge. Herein, we report a scalable method to exfoliate BNNSs in ionic liquids (ILs) via shear-assisted thermal treatment. Few-layer BNNSs with well-preserved structural integrity are successfully prepared by this method. The synergistic effects of strong physical adsorption and intercalation of IL molecules, chemical interactions between hydrogen fluoride (HF) and h-BN, activation energy provided by heat treatment, and shear forces generated by repetitive stirring effect contribute to the exfoliation of BNNSs. [ABSTRACT FROM AUTHOR]

Strontium has been widely used in bone repair materials due to its roles in promoting osteoclast apoptosis and enhancing osteoblast proliferation. In this work, synthesis and the effects of Sr2+ doping α-tricalcium phosphate at low-temperature was studied. The setting time and the mechanical properties of α-tricalcium phosphate were controlled by varying the content of Sr2+. The synthesized compounds were evaluated by XRD, SEM, XPS, setting time, compressive strength, SBF immersion, and colorimetric CCK-8 assay. The results showed that Sr2+ can improve the compressive strength and cell activity of calcium phosphate bone cement. [ABSTRACT FROM AUTHOR]

Nickel ferrite owns a lot of advantages as electrode materials for supercapacitor, such as high energy density and excellent theoretical capacity. Whereas, the electrochemical performances of NiFe 2 O 4 in terms of rate performance and cycle stability are not satisfactory due to the low conductivity. While carbon fiber is a kind of material with high conductivity. Hence, NiFe 2 O 4 @ slit modified hollow carbon fiber is obtained through the coaxial electrospinning method. The slits on hollow carbon fibers are beneficial to the contact of inner NiFe 2 O 4 nanoparticles with electrolyte. Results of electrochemical tests show that at a current density of 1 A/g, the specific capacitance of NiFe 2 O 4 @ slit modified hollow carbon fiber is calculated to be 225.4 F/g, higher than that of NiFe 2 O 4 nanoparticles of 134.8 F/g. Moreover, a better cycle and rate performances (100 % vs 80 %; 71.9 % vs 47.5 %) are achieved. This work displays that slit modified hollow carbon fiber can improve the electrochemical performance of NiFe 2 O 4 efficiently. [Display omitted] • Carbon fibers are introduced to enhance the rate and cycle performances of NiFe 2 O 4. • Slits are obtained utilizing Al 2 O 3 sacrificial hard templates. • Slits are beneficial to the contact of NiFe 2 O 4 and electrolyte. [ABSTRACT FROM AUTHOR]

Core-shell hierarchical structured composites have demonstrated great advantages in numerous energy storage devices. In particular, structured composites with rationally structural components and controllable morphology are the most effective in enhancing electrochemical properties. In this work, MnO 2 @NiCo 2 O 4 @Ti 3 SiC 2 /CC (carbon cloth) core-shell hierarchical structured composites were designed and successfully synthesized via electrospinning followed by a two-step hydrothermal reaction. The Ti 3 SiC 2 /CC nanofibers and core-shell nanoarrays were able to improve the specific capacitance and cycling stability. In the three-electrode system, the specific capacitance of MnO 2 @NiCo 2 O 4 @Ti 3 SiC 2 /CC was observed as 1938.2 F/g at a current density of 1 A/g, while the rate capability retention was observed as 81.7% between 1 and 10 A/g. Furthermore, a superior cycling stability was observed following 5000 cycles with a specific capacitance retention rate of 55.4%. Employing MnO 2 @NiCo 2 O 4 @Ti 3 SiC 2 /CC as the all solid-state supercapacitor positive electrode exhibited a high energy density of 58.0 W h/kg at the power density of 800 W/kg. Results demonstrate the potential of the MnO 2 @NiCo 2 O 4 @Ti 3 SiC 2 /CC as an electrode material with phenomenal electrochemical properties for supercapacitors. [ABSTRACT FROM AUTHOR]

Strontium has been widely used in bone repair materials due to its roles in promoting osteoclast apoptosis and enhancing osteoblast proliferation. In this work, synthesis and the effects of Sr2+ doping α-tricalcium phosphate at low-temperature was studied. The setting time and the mechanical properties of α-tricalcium phosphate were controlled by varying the content of Sr2+. The synthesized compounds were evaluated by XRD, SEM, XPS, setting time, compressive strength, SBF immersion, and colorimetric CCK-8 assay. The results showed that Sr2+ can improve the compressive strength and cell activity of calcium phosphate bone cement. [ABSTRACT FROM AUTHOR]

Boron nitride nanosheets (BNNSs)/magnesium oxide (MgO) composites were prepared via hot pressing. Mechanical properties of MgO ceramics were improved obviously in virtue of adding BNNSs. The bending strength of the 1 wt% BNNSs/MgO composite increased by about 85% than that of the monolithic MgO. The fracture toughness increased by 34% with the addition of 1.5 wt% BNNSs. Microstructural analyzes have shown that the toughening mechanisms are combinations of the pull-out and bridging of BNNSs, crack deflection, and crack bypassing mechanisms. The addition of a small amount of BNNSs don't destroy the excellent dielectric properties of composites. The dielectric constant of the sample doped with 1 wt% BNNSs was about 9.5 in the whole X-band and the vast majority of P-band, and the loss tangent was less than 5 × 10−3 in 10–15.8 GHz. [ABSTRACT FROM AUTHOR]

Abstract Graphene oxide (GO) is one of the most important ceramic-toughening candidates due to its outstanding physical and chemical properties. In this paper, nacre-like alumina ceramics reinforced with GO have been prepared by freeze casting followed by hot pressing. The experimental results showed that a laminated structure with homogeneous distribution of GO was obtained in the composites. Microstructural analysis, relative densities, flexural strength and fracture toughness of the samples were investigated to reveal the effect of GO. Higher flexural strength and fracture toughness (~380 MPa and ~7.5 MPa m1/2, respectively) were achieved and the multiple length-scale toughening mechanisms of composites contributed to the improved mechanical properties. The results show that it is a promising method to enhance the mechanical properties of nacre-like alumina by the addition of GO. [ABSTRACT FROM AUTHOR]

Abstract Bimetallic carbides with high activity and stability are promising potential materials for energy-storage application. However, the researches about Fe 2 MoC as electrode material on supercapacitors are comparatively weak, and the processing methods of Fe 2 MoC were also relatively few. Herein, a simple hydrothermal method, combining with carbothermic treatment at 900 °C, is explored to fabricate molybdenum iron carbon (Fe 2 MoC) successfully. Chitosan is not only a carbon source, but also a chelating agent to form bimetallic carbide rather than two separated monometallic carbide during the high-temperature treatment. Fe 2 MoC nanoparticles possessing large specific surface, high activity, stability and small resistance were the promising candidate for electrode material. Systematic electrochemical characterizations have verified the Fe 2 MoC (chitosan as carbon source) possesses a specific capacitance (97.7 F/g at a current density of 0.5 A/g), high rate capability (97.0% capacitance retention from 0.5 to 10 A/g) and cycling stability (83.9% capacitance retention after 1000 cycles) in 1 M KOH. In addition, it offers the energy density of 6.74 Wh/kg at a power density of 21 kW/kg. In view of the low-cost and excellent performance, Fe 2 MoC will hold great promise in energy-storage field for supercapacitors. [ABSTRACT FROM AUTHOR]

Well-dispersed boron nitride nanosheets (BNNSs) reinforced fused silica composites were successfully fabricated by surface modification assisted flocculation method. Surface modification can enhance the performance of flocculation process. BNNSs were homogeneously mixed with fused silica through the electrostatic interaction between hydroxylated BNNSs with negative charge and amino-modified fused silica with positive charge. The BNNSs can act as excellent nanofillers for enhancing the mechanical properties of fused silica composites. Approximately 74% and 48% increases in flexure strength and fracture toughness can be achieved for the 1.5 wt% BNNSs/fused silica composite, respectively. The toughening mechanisms were analyzed by microstructural characterization, especially for pull-out mechanism. [ABSTRACT FROM AUTHOR]

In this paper, BNNSs/Al 2 O 3 composite powder was prepared by in-situ reaction using borate nitridation method and BNNSs/Al 2 O 3 composite ceramics were prepared by hot-pressing sintering. This method achieves uniform mixing of BNNSs and Al 2 O 3 ceramic matrix and reduces the introduction of impurities in the processing process. The BNNSs/Al 2 O 3 composite ceramics have excellent bending strength (549.4 MPa), fracture toughness (5.18 MPa m1/2) and hardness (21.3 GPa). The high hardness of composite ceramics is attributed to high grain boundary strength and density. The reinforcing mechanisms of ceramics include BNNSs pull-out, BNNSs bridging, crack deflection as well as the transgranular fracture and intergranular fracture of Al 2 O 3 matrix. [ABSTRACT FROM AUTHOR]

As the precursor of MXenes (2D transition metal carbides, carbon nitrides and nitrides), MAX phase materials have attracted ever-increasing attention in electrochemical applications. In this work, we have successfully hybridized a MAX phase, Ti 2 SnC, with various ratios of carbon nanofibers (CNFs) via electrospinning. The results show that the Ti 2 SnC/CNFs compounds possess a stable lithium ion storage ability as an anode material, reaching a stable specific capacity of up to 367.5 mAh·g−1 after 500 charge/discharge cycles at the current density of 1.0 A g−1, which are drastically better than some other MAX phase materials such as Ti 3 SiC 2 and Nb 2 SnC. This strategy provides a new pathway for the improvement of the electrochemical stability of MAX phase, which has a wide application prospect. • Ti 2 SnC/CNFs was successfully prepared by an electrospinning method. • CNFs retard the volume expansion of Ti 2 SnC during the charge/discharge process. • Ti 2 SnC/CNFs performed stable lithium ion capacitance (367.5 mAh·g−1 at 1.0 A g−1). [ABSTRACT FROM AUTHOR]

MAX phase materials, the precursors of MXenes (2D transition metal carbides, carbon nitrides, and nitrides), have become increasingly popular in electrochemical applications. In this study, we have successfully prepared Ti 2 SnC with high lithium capacity via the in-situ formation of SnO 2. Results show that there are TiC nanowhiskers and SnO 2 inside the Ti 2 SnC MAX calcined at 800 ℃, and the initial specific capacity could reach 377 and 371 mAh·g−1 at high current densities of 400 mA·g−1 and 1.0 A·g−1, respectively. These values are higher than those of most MAX phase materials reported in previous studies, such as Ti 3 SiC 2 and Nb 2 SnC, but the stability and rate performance are inferior, which is a direction for the future. This paper provides a new pathway for the application of MAX phases in electrochemistry, which has more in-depth application prospects. ● Ti 2 SnC with in-situ formation of SnO 2 was successfully prepared by a calcination method. ● The Ti 2 SnC layered structure slows down the volume expansion of in-situ prepared SnO 2. ● This anode material performed a better specific capacitance, arriving at 377 mAh/g at the current density of 1.0 A/g. [ABSTRACT FROM AUTHOR]

Transitional metal nitrides (TMNs) are regarded as comparatively promising electrode materials for supercapacitor due to the high electronic conductivity, good corrosion resistance and special electron structure. Herein, in this work a heterostructure Co 2 N-Ni 3 N nanosheets-nanowires arrays grown on Ni foam (NF) are designed and synthesized by a simple hydrothermal reaction and nitriding treatment. The prepared Co 2 N-Ni 3 N/NF nanoarrays has a high electrical conductivity, abundant surface active sites, charge transfer channels and the synergy effect between each component, which makes it exhibit outstanding electrochemical performance. Electrochemical test results revealed that the areal capacitance of Co 2 N-Ni 3 N/NF was 2.17 F cm−2 at 1 mA cm−2 using a three-electrode system in 1 M KOH. Meanwhile, when the current density increases to 20 mA cm−2, it can still retain 62.21% of the original capacitance, suggesting a good rate capability. In addition, in two-electrode test with Co 2 N-Ni 3 N/NF as the positive electrode and activated carbon as the negative electrode, a maximum energy density of 145.65 μWh cm−2 is shown when the power density is 0.75 mW cm−2. And it has 85.90% capacitance retention after 5000 cycles. [Display omitted] • Unique Co 2 N-Ni 3 N nanoarray heterostructure was successfully synthesized. • Co 2 N-Ni 3 N/NF achieves an areal capacitance 2.17 F cm-2 at current density of 1 mA cm-2. • The Co 2 N-Ni 3 N/NF // AC exhibits good electrochemical performance in two-electrode tests. [ABSTRACT FROM AUTHOR]

The layered transition metal oxides are an essential class of cathode materials in sodium-ion batteries. However, the capacity decay mechanisms of many materials at a wide voltage window are still ambiguous. Therefore, research on the intrinsic structure of materials at the electronic or atomic level is of great significance to unlock the potential of more materials. In this study, a new family of layered NaNi 0.45 Mn 0.3 Ti 0.2 M 0.05 O 2 (M = Nb/Mo/Cr) has been demonstrated to combine high specific capacity (NaNi 0.45 Mn 0.3 Ti 0.2 Cr 0.05 O 2 , 12 mA g−1, 185.7 mAh g−1, 2-4.2 V) with preferable Na+ insertion/extraction activity (1920 mA g−1, 111.2 mAh g−1). The participation of Ni2+/Ni3+ and Cr3+/Cr4+/Cr6+ in the redox reaction upon cycling significantly contributes to the superior specific capacity, and the diffusion kinetics calculation indicates that the substitution of Cr for Ni can create a more suitable path with a low energy barrier for Na+ movement, which is particularly crucial for the rate performance. Besides, the unfavorable cycling stability is affected by the distortion of the crystal structure, suggesting that the Jahn-Teller effect of Mn3+/Ni3+ and the second-order Jahn-Teller effect of Nb5+/Mo6+ (d0 transition metal) together with Cr6+ migration caused by disproportionation of Cr4+ have inescapable responsibilities. Additionally, the reversible phase transition between the O3 and P3 phases upon Na+ insertion/extraction at a wide voltage window is identified by in situ XRD measurements and verified to be the key factor of the high coulombic efficiency for NMTCr. An in-depth understanding of NMTNb and NMTMo can provide new insights for material design and exploitation. The composition-structure-property relationships behind the electrochemical performance can be comprehended profoundly by coupling the experimental verification with density functional theory calculations. • A new family of layered NaNi 0.45 Mn 0.3 Ti 0.2 M 0.05 O 2 (M = Nb/Mo/Cr) has been prepared. • The participation of Ni2+/Ni3+ and Cr3+/Cr4+/Cr6+ contributes greatly to the capacity. • The substitution of Cr provided a suitable path with low energy barrier for Na+ movement. • The Jahn-Teller effect of Mn3+/Ni3+ and second-order JT effect of Nb5+/Mo6+ are discussed. [ABSTRACT FROM AUTHOR]

An innovative and convenient method has been performed to stabilize the surface of O3-type NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 composited electrode by ultrathin MgO film. There are few reports on the modification on the fabricated electrode instead of the active material powder, especially by radio frequency magnetron sputtering. Besides, the surface stability and capacity retention of MgO coated cathode are superior compared to the bare one under the high rate. The protective effect could physically enhance electrochemical performance because the MgO coating has been identified strictly. Three main reasons are discovered by investigating the mechanisms. Firstly, the MgO layer suppresses the dissolution of the active material into electrolyte; this might be the origin for more stable electrode structure. Secondly, the MgO layer boosts sodium-ion and electron transport owing to its location of the deposition. Finally, the appropriate thickness of MgO can minimize transmission resistance and SEI formation. Particularly, the half-cell constructed with NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 –MgO cathode delivers a good rate performance (80.3 and 70.3 mA h g−1 at 1200 and 1920 mA g−1) and a long cycle life (71.6 mA h g−1 at 240 mA g−1 for 300 cycles) when sputtering time is 10 s; meanwhile, the reversible discharge capacity (140.7 mA h g−1 at 12 mA g−1) with a cut-off voltage of 2–4 V is also a considerable achievement. The work provides a broad idea to apply MgO as a protective coating. • MgO film is performed via magnetron sputtering on NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 electrode. • The surface stability and capacity retention of MgO coated cathode are superior at high rate. • MgO layer boosts sodium-ion and electron transport owing to its location of deposition. • The appropriate thickness of MgO can minimize transmission resistance and SEI formation. • The NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 –MgO cell delivers 80.3 and 70.3 mA h g−1 at 1200 and 1920 mA g−1. [ABSTRACT FROM AUTHOR]

Morphology of transition metal oxide largely affects its electrochemical energy storage properties. This also applies to its composites. In this paper, NiFe 2 O 4 /Graphene nanosheets composites (NFO/GNSs) are successfully prepared by a facile hydrothermal method. NiFe 2 O 4 (NFO) in the sample exhibits a unique nanosheet morphology, vertically arranging on the graphene nanosheets (GNSs). Microscopically, NFO nanosheets interpenetrate on the surface of graphene to form a continuous network structure. The sample exhibits excellent specific capacitance and rate performance. It is worth mentioning that the specific capacitance increases to 140% after 5000 cycles, showing superior cycle stability. This may be due to the conductive network formed by NFO nanosheets and GNSs. Excellent electrochemical performance indicates excellent application prospects of materials in supercapacitor electrodes. Image 1 • Unique NiFe 2 O 4 nanosheets structure with graphene nanosheets was successfully prepared by a hydrothermal method. • NiFe 2 O 4 nanosheets/graphene performed a better specific capacitance, arriving at 464.15 F/g at current density of 1 A/g. • The network structure formed between NiFe 2 O 4 nanosheets and graphene nanosheets provides excellent cycle performance. [ABSTRACT FROM AUTHOR]

Due to the low cost and abundance of sodium, sodium-ion batteries (SIBs) show great potential as energy storage devices. As far as the current research is concerned, cathode materials are still the bottleneck for boosting the performance of SIBs. O3-type layered NaNi 0.5 Mn 0.5 O 2 is considered as an important cathode material of SIBs, but its irreversible phase transition, poor stability in air, and sluggish kinetics usually lead to reduced capacity, poor rate performance and high cost for material storage, which largely limit the large-scale application. Herein, a remarkable O3-type layered material NaNi 0.5-x Mn 0.3 Ti 0.2 Zr x O 2 (NaNMTZ, x = 0.02, 0.05), with stable phase structure has been synthesized by the solid-phase method. The partial substitution of electrochemical inactive Ti/Zr brings about higher electronic delocalization and entropy of mixing leading to enhanced structural stability. In addition, the enlarged interlayer spacing and good conductivity contribute to better rate capability. The micro-nano structure leads to faster Na+ diffusion rates and shorter diffusion paths for both ions and electrons. Therefore, NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 exhibits an initial reversible capacity of 141.4 mAh g−1 with a coulombic efficiency of 98.8% and remarkable capacity retention of 70% after 200 cycles at 0.05C, presenting better electrochemistry performance than the conventional NaNi 0.5 Mn 0.5 O 2. This study provides a new angle to design high capacity cathode materials with high rate capability and cycling stability through crystal lattice modulation. Image 1 • A remarkable O3-type layered NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 is designed as cathode material for sodium ion batteries. • The structural stability and rate performance of NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 are superior. • The higher electronic delocalization and better conductivity of NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 are provided. • The difference value about entropy of mixing between NaNi 0.5 Mn 0.5 and NaNi 0.45 Mn 0.3 Ti 0.2 Zr 0.05 O 2 is calculated. • The enlarged interlayer spacing and micro-nano structure contribute to the high rate capability. [ABSTRACT FROM AUTHOR]

Bimetallic carbides have aroused wide attention for energy-storage applications recently. In this work, one-dimensional Fe 2 MoC/CNFs (Fe 2 MoC/C nanofibers) are successfully synthesized via a facile electrospinning method for the first time. To obtain the most integrated structure between the Fe 2 MoC nanoparticles and carbon nanofibers, we explore the optimal heating rate during the carbonization treatment. Fe 2 MoC/CNFs exhibits an integrated one-dimensional structure under 800 °C with a heating rate of 5 °C/min. As revealed in the experimental results, Fe 2 MoC/CNFs possesses a high specific surface area of 196.9 m2/g, a high specific capacitance of 347.8 F/g at the current density of 1 A/g, an excellent rate capability of 91% capacitance retention from 1 A/g to 40 A/g, and shows superior cycling stability with the capacitance retention of about 85.6% and Coulombic efficiency of about 100% after 5000 cycles. An asymmetric supercapacitor coin-cell device using Fe 2 MoC/CNFs as the positive electrode displays an energy density of 14.5 Wh/kg at a power density of 300 W/kg and an outstanding cycling life of 93% retention after 5000 cycles. The impressive electrochemical performance indicates that the Fe 2 MoC/CNFs composite is a promising material for efficient supercapacitors. Image 1 • Fe 2 MoC nanofibers can be prepared via a facile electrospinning method. • Fe 2 MoC/CNFs-5 exhibits a superior rate capability and cycle stability. • ASC coin-cell device shows a promising energy and power density. [ABSTRACT FROM AUTHOR]

Uniformly dispersed boron nitride nanosheets (BNNSs) reinforced silicon nitride (Si 3 N 4) composites were prepared by surface modification assisted flocculation combined with SPS sintering. In order to improve the dispersibility of the BNNSs in the composites, the liquid phase stripped BNNSs are surface functionalized by a two-step covalently modification. The amino-modified BNNSs (NH 2 -BNNSs) and Si 3 N 4 powders have opposite surface potential, mixed evenly by electrostatic interaction during flocculation. The results showed that mechanical properties of Si 3 N 4 composites were obviously enhanced by adding NH 2 -BNNSs. The fracture toughness and bending strength of Si 3 N 4 composites added 0.75 wt% NH 2 -BNNSs were increased by 34% and 28%, respectively, compared with monolithic Si 3 N 4. Toughening mechanisms are synergistic action of the torn, pull-out or bridging of BNNSs and crack deflection mechanisms with microstructural analyzes. The dielectric properties of the Si 3 N 4 ceramics are also improved after the addition of NH 2 -BNNSs. [ABSTRACT FROM AUTHOR]

Boron nitride nanosheets (BNNSs) with relatively low dielectric constant and excellent mechanical strength were employed for fabrication of BNNSs/fused silica (FS) composites. High-temperature mechanical behavior and microstructural evolution of the composites were investigated. The addition of BNNSs can improve the mechanical properties of FS efficiently, and the reinforcement from BNNSs can be preserved during the high temperature service. The flexural strength of BNNSs/FS composites exhibited anomalous gains at certain high temperature range, which can be explained by the softening of FS matrix, the heal of defect tips, and the reinforcement from BNNSs. [ABSTRACT FROM AUTHOR]

How to deal with the brittleness of ceramic materials is always one of the hot topics in the field of materials science. Design of layered ceramics with textured structure is one of the effective methods to improve their fracture toughness. The introduction of additives as interlayer phases can balance fracture toughness and flexural strength. However, the research about addition of interlayer phases and their mechanisms in the layered ceramics is still limited. In this work, nacre-like alumina ceramics were successfully fabricated by freeze casting followed by hot pressing. Silicon nitride was incorporated as the interlayer phase, and the effect on the mechanical properties of the nacre-like alumina was investigated. The addition of silicon nitride was beneficial to improvement of interlayer bonding between the alumina layers due to formation of sialon phase, leading to increase of flexural strength but decease of fracture toughness. When the content of silicon nitride was 3.3 wt%, flexural strength and fracture toughness of the sample was 468 MPa and 6.2 MPa m1/2, respectively. Compared with the sample without silicon nitride, the flexural strength was enhanced significantly. Additionally, both flexural strength and fracture toughness were improved as compared the sample without any additives. This work can provide available references for design and fabrication of high-strength and high-toughness ceramics by properly tuning the layer structure and interlayer phase composition. [ABSTRACT FROM AUTHOR]

[Display omitted] • Three non-resonant SiOC-based meta-structures are synthesized by 3D printing. • The metamaterials achieve good impedance matching through structural design. • The reflection loss is −55.68 dB with an ultra-wideband absorption of 11.88 GHz. • The mechanisms between meta-structures and electromagnetic wave are investigated. Lightweight, wide-band ceramic-based electromagnetic (EM) absorbers have great application demand in the field of high-temperature EM wave absorption. However, it is difficult for traditional ceramic-based structural EM absorbing materials (EMAMs) to balance the contradiction between broadband absorption and good impedance matching due to resonance effect. Herein, three novel non-resonant SiOC-based triply periodic minimal surface (TPMS) meta-structures named Schoen G (SG), Schwarz D (SD) and Schwarz P (SP) with a density of 0.556 g/cm3 were successfully synthesized by digital light processing (DLP) 3D printing and polymer-derived ceramics (PDCs) method. Through the structural design of multilayer arrays and holes, three metamaterials achieve good impedance matching and broadband EM absorption. The effective absorption bandwidth (EAB) of all three meta-structures reaches 9.80 GHz (8.2–18.0 GHz) in a wide matching thickness range, covering the entire X-Ku band. In addition, the minimum reflection loss (RL min) of −55.68 dB is obtained at a matching thickness of 3.02 mm for SD meta-structure in X-band. Besides, the SG meta-structure tested by the arch method has an ultra-wide EAB of 11.88 GHz (6.12–18.0 GHz), exhibiting ultra-broadband EM absorption properties. It is significant that the intrinsic relationships between TPMS meta-structures and EM responses are explored by CST simulation. This work provides a new perspective for the design of lightweight, broadband ceramic-based EM metamaterial absorbers under high-temperature, harsh environments. [ABSTRACT FROM AUTHOR]

The microstructure and mechanical properties of (Hf 0.2 Nb 0.2 Ta 0.2 Ti 0.2 Zr 0.2)B 2 high-entropy boride (HEB) were first predicted by first-principles calculations combined with virtual crystal approximation (VCA). The results verified the suitability of VCA scheme in HEB studying. Besides, single-phase (Hf 0.2 Nb 0.2 Ta 0.2 Ti 0.2 Zr 0.2)B 2 ceramics were successfully fabricated using boro/carbothermal reduction (BCTR) method and subsequent spark plasma sintering (SPS); furthermore, the effects of different amounts of B 4 C on microstructure and mechanical properties were evaluated. Due to the addition of B 4 C and C, all samples formed single-phase solid solutions after SPS. When the excess amount of B 4 C increased to 5 wt%, the sample with fine grains exhibited superior comprehensive properties with the hardness of 18.1 ± 1.0 GPa, flexural strength of 376 ± 25 MPa, and fracture toughness of 4.70 ± 0.27 MPa m1/2. Nonetheless, 10 wt% excess of B 4 C coarsened the grains and decreased the strength of the ceramic. Moreover, the nanohardness (34.5–36.9 GPa) and Young's modulus (519–571 GPa) values with different B 4 C contents just showed a slight difference and were within ranges commonly observed in high-entropy diboride ceramics. [ABSTRACT FROM AUTHOR]

Silica is one of the most widely used ceramics due to its excellent chemical stability and dielectric property. However, its destructive brittle nature inhabits it from wider application as a functional ceramic. An improvement in toughness is a challenging topic for silica ceramic, as well as other ceramics. In the paper, silica ceramic with different types of boron nitride powders and alumina platelets was fabricated by hot-pressing. Introduction of the additives had great influence on the composites' mechanical properties and microstructure. The silica matrix composite containing micro-sized boron nitride powders possessed the best mechanical properties, including the bending strength (134.5 MPa) and the fracture toughness (1.85 Mpa·m1/2). Meanwhile, the introduction of alumina platelets combined with boron nitride nanosheets achieved an effective enhancement of fracture toughness while maintaining the bending strength. Compared with the monolithic silica, the composite with simultaneous addition of alumina platelets and boron nitride nanosheets had a fracture toughness of 2.23 Mpa·m1/2, increased by approximately 27% (1.75 Mpa·m1/2). The crack deflection and platelet pullout were contributing to enhancement of the fracture toughness. The improved mechanical properties, combined with the intrinsic excellent dielectric and chemical properties, make the silica matrix composites promising wave transparent and thermal protection materials. [ABSTRACT FROM AUTHOR]

Alumina is one of the most commonly used and researched structural ceramic because of its excellent properties. However, its intrinsic brittleness is the fatal drawback, which hinders it from wider applications. How to improve its fracture toughness as well as the bending strength is always challenging for material researchers. In this paper, alumina matrix composites were fabricated by hot-pressing, in which some additives, including zirconia, alumina platelets, and MXene, were incorporated. The influence of the introduced additives on their microstructure and mechanical properties was investigated. Compare with the monolithic alumina, both bending strength and fracture toughness of all samples were improved greatly. Incorporation of zirconia was beneficial to the mechanical properties due to the phase-transformation strengthening and toughening mechanism. While alumina platelets resulted in high fracture toughness because of the self-toughening of elongated grains. The synergistic effect of alumina platelets and MXene enormously improved the fracture toughness from 2.9 ± 0.3 MPa·m1/2 for monolithic alumina to 7.5 ± 0.4 MPa·m1/2 for the composite, which was increased by 159%. This work will provide useful references for the fabrication of high-strength and high-toughness alumina ceramics by introducing additives properly. [ABSTRACT FROM AUTHOR]

Synergic effect of graphene oxide (GO) and silicon nitride whisker (Si 3 N 4 w) on the mechanical properties of nacre-like alumina was investigated in this study. A comprehensive analysis on the composites, including microstructure, relative densities, flexural strength and fracture toughness, was carried out. The experimental results showed that, GO promoted the fracture toughness of the composites, but reduced the flexural strength slightly; while adding a certain amount of Si 3 N 4 w improved both flexural strength and fracture toughness. With the incorporation of GO and Si 3 N 4 w, the highest flexural strength reached 520 MPa and the fracture toughness reached 9.59 MPa m1/2. Microstructure observation revealed that the enhanced mechanical properties were ascribed to the synergistic toughening mechanisms induced by the nacre-like structure of alumina, GO pull-out, Si 3 N 4 w pinning and pull-out. [ABSTRACT FROM AUTHOR]

Abstract Boron nitride nanosheets (BNNSs) have attracted increasing attention in the field of two-dimensional materials. In the paper, the BNNSs/alumina composites were fabricated by a flocculation method and hot pressing. It is found that the BNNSs were dispersed uniformly in the alumina matrix by the flocculation technique via pH adjustment. The experimental results showed that with the increasing BNNSs content, the density of the composites decreased. Compared with the monolithic alumina, bending strength of the composite with 1.0 wt% BNNSs was increased by 58.6%; while the fracture toughness was increased slightly. The addition of BNNSs changed the fracture pattern, refined the grains of composites and inhibited abnormal grain growth, which contributed to the improvement of mechanical properties of the composites. [ABSTRACT FROM AUTHOR]

A facile, low-cost, and room-temperature UV-ozone (UVO) assisted solution process was employed to prepare zirconium oxide (ZrO x ) films with high dielectric properties. ZrO x films were deposited by a simple spin-coating of zirconium acetylacetonate (ZrAcAc) precursor in the environment-friendly solvent of ethanol. The smooth and amorphous ZrO x films by UVO exhibit average visible transmittances over 90% and energy bandgap of 5.7 eV. Low leakage current of 6.0 × 10 −8 A/cm 2 at 3 MV/cm and high dielectric constant of 13 (100 Hz) were achieved for ZrO x dielectrics at the nearly room temperature. Moreover, a fully room-temperature solution-processed oxide thin films transistor (TFT) with UVO assisted ZrO x dielectric films achieved acceptable performances, such as a low operating voltage of 3 V, high carrier mobility of 1.65 cm 2 V −1 s −1 , and on/off current ratio about 10 4 –10 5 . Our work indicates that simple room-temperature UVO is highly potential for low-temperature, solution-processed and high-performance oxide films and devices. [ABSTRACT FROM AUTHOR]

Objectives Emerging studies have demonstrated that micro RNAs (mi RNAs) play crucial roles in carcinogenesis of many developing human tumours. However, the functions and mechanisms of miR-297 in lung cancer have, up to now, been largely undefined. Materials and methods Here, miR-297 expression was measured in lung adenocarcinoma tissues and cell lines, using qRT- PCR. Lung adenocarcinoma cell line was treated with an miR-297 mimic. MTT and colony analysis were performed to detect cell proliferation and colony formation. The direct target gene of miR-297 was assessed by qRT- PCR, Western blotting and luciferase assays. Results We demonstrated that miR-297 expression was upregulated in lung adenocarcinomas compared to adjacent normal tissues. Expression of miR-297 was also upregulated in tested lung adenocarcinoma cell lines. Ectopic expression of miR-297 enhanced lung adenocarcinoma cell proliferation and colony formation. Furthermore, overexpression of miR-297 promoted cell migration and invasion. In addition, we identified Glypican-5 ( GPC5) as a direct target gene of miR-297 in lung adenocarcinoma cells. Expression of GPC5 was downregulated in both lung adenocarcinoma tissues and cell lines. Moreover, expression of GPC5 was inversely associated with expression of miR-297 in lung adenocarcinoma tissues. Conclusions These results suggest that miR-297 acted as an oncogenic mi RNA, partly by targeting GPC5, adenocarcinoma of the lung. [ABSTRACT FROM AUTHOR]