Facile synthesis of a carbon-rich SiAlCN precursor and investigation of its structural evolution during the polymer-ceramic conversion process

A liquid carbon-rich SiAlCN precursor is facilely synthetized by hydrosilylation between liquid polyaluminocarbosilane (LPACS) and 1,3,5,7-tetravinyl- 1,3,5,7-tetramethylcyclotetrasilazane {[CH₃(CH₂CH₂)SiNH]₄} (TeVSZ). The structural evolution during the polymer-ceramic conversion process is investigated by various methods. The results show that the main cured mechanism is β-addition on hydrosilylation, although α-addition on hydrosilylation, polymerization of vinyl groups and dehydrocoupling reaction between N–H bonds also occur during the cured process. During the pyrolysis process, dehydrogenation and dehydrocarbonation condensation reactions, transamination reactions occur, leading to formation of a three-dimensional network inorganic structure at 400–800 °C, where part of Al–O bonds convert to Al–N bonds. Then the network inorganic structure undergoes demixing and separation into amorphous SiAlCN(O) phase, where the amorphous turbostratic free carbon phase also form at 800–1200 °C. With demixing and decomposition of the amorphous carbon-rich SiAlCN(O) phase, the crystalline β-SiC and graphitic carbon start to form at about 1400 °C, the crystalline sizes of them both enlarge with increasing temperature. However, the crystal growth of β-SiC is distinctly inhibited due to existence of the rich carbon phase, tiny amounts of Al₂O₃ and AlN. In addition, a small amount of AlN can promote the formation of α-SiC at 1800 °C.     

Preparation,microstructure and ion-irradiation damage behavior of Al4SiC4-added SiC ceramics

Single-phase Al₄SiC₄ powder with a low neutron absorption cross section was synthesized and mixed with SiC powder to fabricate highly densified SiC ceramics by hot pressing. The densification of SiC ceramics was greatly improved by the decomposition of Al₄SiC₄ and the formation of aluminosilicate liquid phase during the sintering process. The resulting SiC ceramics were composed of fine equiaxed grains with an average grain size of 2.0 μm and exhibited excellent mechanical properties in terms of a high flexure strength of 593 ± 55 MPa and a fracture toughness of 6.9 ± 0.2 MPa m^1/2. Furthermore, the ion-irradiation damage in SiC ceramics was investigated by irradiating with 1.2 MeV Si⁵⁺ ions at 650 °C using a fluence of 1.1 × 10¹⁶ ions/cm², which corresponds to 6.3 displacements per atom (dpa). The evolution of the microstructure was investigated by X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. The breaking of Si–C bonds and the segregation of C elements on the irradiated surface was revealed by XPS, whereas the formation of Si–Si and C–C homonuclear bonds within the Si–C network of SiC grains was detected by Raman spectroscopy.     

A comparative study on the catalytic activities and stabilities of atomic-layered platinum on dispersed Ti0.9Cu0.1N nanoparticles supported by N-doped carbon nanotubes (N-CNTs) and reduced graphene oxide (N-rGO)

In our previous research, titanium-based nitride with high conductivity and superior corrosion resistance were developed as an ideal core material for replacing noble metal to form Pt-based core-shell catalysts by pulse electrodeposition. Meanwhile, the smaller sizes of nitride cores would also be available for pulse electrodeposition by dispersing them on carbon nanotubes (CNT). To achieve a better practice on the preparation of the Pt-based core-shell catalysts, in this work, both nitrogen-doped carbon nanotubes (N-CNT) and reduced graphene oxide (N-rGO) were used to support the copper-doped titanium nitride (Ti_0.9Cu_0.1N) cores. In the course of pulse electrodeposition, their influences as supports on the electronic states of electrodeposited Pt as well as their catalytic activities were compared. The results showed that the Pt preferred to electrodeposit on Ti_0.9Cu_0.1N cores supported by N-CNT and formed a core-shell structure. While with the same electrodeposition process, the Pt was found to be electrodeposited not only on the Ti_0.9Cu_0.1N cores supported by N-rGO with heavy aggregations but also on the N-rGO support. Raman spectroscopy analysis indicated that the higher degree of structural defects on N-rGO, as support, might have contributed to such divergence observation.     

In-situ formation of Ni (oxy)hydroxide on Ni foam as an efficient electrocatalyst for oxygen evolution reaction

A binder-free Ni (oxy)hydroxide on Ni foam was prepared through an in-situ electrochemical activation method. Ni (oxy)hydroxide is active for the oxygen evolution reaction. The Ni (oxy)hydroxide directly formed on the surface of Ni foam as a binder-free catalyst not only exhibited large electrochemically active area, but also displayed low interfacial electronic resistance and low charge transfer resistance. Therefore, the optimized Ni (oxy)hydroxide exhibits an overpotential of 288 and 370 mV at 10 and 500 mA cm⁻², respectively, in 1.0 M KOH for the oxygen evolution reaction, as well as favorable during 240 h at 100 mA cm⁻².     

Luminescence and energy transfer of color-tunable Lu_2MgAl_4SiO_(12):Eu~(2+),Ce~(3+),Mn~(2+) phosphors

Energy transfer among the co-doped activators is an efficient route to achieve color-tunable emission in inorganic phosphors.Herein,photoluminescence tuning from blue to cyan has been achieved in the Lu_2MgAl_4 SiO_(12);Eu~(2+),Ce~(3+)phosphors by varying the Ce~(3+) concentration with a fixed Eu~(2+)content.With the further introduction of a Mn~(2+)-Si4+couple into the host lattice,the emission color can be tuned to red through the energy transfer of Eu~(2+)and Mn~(2+).The luminescence properties and the energy transfer mechanism were studied in detail.The energy transfer from Eu~(2+)to Ce~(3+)is certified as a dipolequadrupole interaction with the energy transfer efficiency of 41.4% and Eu~(2+)to Mn~(2+)belongs to a dipole-dipole interaction with the energy transfer efficiency of 94.3%.The results imply that this singlephased Lu_2MgAl4 SiO_(12):Eu~(2+),Ce~(3+),Mn~(2+)phosphor has a potential prospect for application in near-UV chip pumped white light emitting diodes.     

Fabrication of RGO/Cu composites based on electrostatic adsorption

To address the issues of reduced graphene oxide (RGO) dispersion in copper (Cu) matrix and interface bonding between RGO and Cu, an electrostatic adsorption method with interface transition phase design was employed to prepare the RGO/Cu based composites. Cu-Ti alloy powder was employed to improve the combination by forming carbides at the RGO-Cu interface. It was noted that the mechanical property of 0.3wt.%RGO/Cu-Ti composite was increased by 60% compared with that of the matrix. Strengthening mechanism analysis suggested that the enhancement of the mechanical property was ascribed to the load transfer and second phase strengthening which were from the improved dispersion of RGO and the in-situ formed titanium carbide phase.     

Low-temperature diffusion bonding of Ti3Si(Al)C2 ceramic with Au interlayer

Herein, a reliable diffusion bonding of Ti₃Si(Al)C₂ ceramic is achieved by applying Au foil as an interlayer at 650 °C for 30 min with an axial pressure of 20 MPa. This novel method significantly decreases the bonding temperature, which is about 150 °C lower than the lowest bonding temperature from current research to the best of our knowledge. Maximum shear strength of 58 MPa is achieved at 650 °C among the bonding temperature range of 600 °C~800 °C. The microstructure evolution mechanism and the relationship between microstructure and mechanical property are discussed. The facile mutual diffusion of Au with de-intercalated Al and Si from Ti₃Si(Al)C₂ is considered critical in achieving sound interfacial bonding.     

轰击离子能量对V2AlC MAX相涂层结构及力学性能的影响

采用物理气相沉积（PVD）磁控溅射沉积方法,通过改变轰击离子能量制备高密度的V₂AlC涂层,并探究不同轰击离子能量对涂层结构和性能的影响。利用能谱仪测试、X射线衍射、拉曼光谱、扫描电镜、原子力显微镜对涂层的化学组成、相结构、表面与截面形貌进行分析,同时利用纳米压痕测试评价V₂AlC涂层力学性能。结果表明,提高轰击离子能量从15 eV到35 eV可以有效使得V₂AlC涂层致密化,且降低涂层表面粗糙度~50%（从~20.2 nm到~11.9 nm）,同时提高涂层的硬度~50%（从~14 GPa到~21 GPa）,与杨氏模量~20%（从~309 GPa到~363 GPa）。但当轰击离子能量升高到50 eV时,Al元素含量急剧下降,涂层由V₂AlC相转变为V₂C与VC多相混合。轰击离子能量的提高有效改善V₂AlC涂层的结构,提高V₂AlC涂层的硬度,杨氏模量,但需控制轰击离子能量改变范围才可实现结构与性能最优化。