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.

Brittle fracture is a typical mechanical characteristic of high-strength self-compacting concrete, and the research on its toughening modification remains the highlight in the engineering field. To understand the effect of toughening materials (including polymer latex powders, rubber particles, and polyethylene fibers) on the mechanical behavior of C80 high-strength self-compacting concrete under static loading, the failure mode, mechanical strength, strain field, and crack opening displacement (COD) of prepared high-strength self-compacting concrete under compressive, splitting, and flexural loads were studied based on digital image technology (DIC). The corresponding mechanism is also discussed. The results show that the hybrid of polymer latex powders, rubber particles, and polyethylene fibers can increase the crack path and inhibit the development of macrocracks in concrete, thus turning the fracture behavior of concrete from brittle to ductile. The addition of toughening materials reduced the compressive and flexural strengths of high-strength self-compacting concrete, but it increased the splitting strength. DIC showed that the incorporation of toughening materials promoted the redistribution of strain and reduced the degree of strain concentration in high-strength self-compacting concrete. The evolution of COD in high-strength self-compacting concrete can be divided into two stages, including the linear growth stage and the plastic yield stage. The linear growth stage can be extended by incorporating toughening materials. The COD and energy absorption capacity of concrete were enhanced with the addition of toughening materials, and the best enhancement was observed with the hybrid of polymer latex powders, rubber particles, and polyethylene fibers. Overall, this research provides a reference for exploring effective technical measures to improve the toughness of high-strength self-compacting concrete.

A novel method is introduced in this study for producing ceramisite coarse aggregates that are both lightweight and possess high strength. The process involves utilizing fly ash as the primary material, along with coal ash floating beads (CAFBs) that have high softening temperature and a spherical hollow structure serving as the template for forming pores. This study examined the impact of varying particle size and quantity of floating beads on the composition and characteristics of ceramisite aggregates. Results showed that the high softening temperature of floating beads provided stability to the spherical cavity structure throughout the sintering process. Furthermore, the pore structure could be effectively tailored by manipulating the size and quantity of the floating beads in the manufacturing procedure. The obtained ceramisite aggregates feature a compact outer shell and a cellular inner core with uniformly distributed pores that are isolated from each other and mostly spherical in form. They achieve a low density ranging from 723 to 855 kg/m³, a high cylinder compressive strength between 8.7 and 13.5 MPa, and minimal water absorption rates of 3.00 to 4.09%. The performance metrics of these coarse aggregates significantly exceeded the parameters specified in GB/T 17431.1-2010 standards.

Multilayer films can achieve advanced properties and a wide range of applications. The heterogeneous interface plays an important role in the performances of multilayer films. In this paper, the effects of the interface of Ba(Mg_1/3Ta_2/3)O₃/PbZr_0.52Ti_0.48O₃ (BMT/PZT) thin films on dielectric behavior and temperature stability are investigated. The heterogeneous interface structures are characterized by Auger electron spectroscopy (AES). The PZT-BMT interface is different from the BMT-PZT interface in thickness. For the PZT-BMT interface, the PZT thin films are diffused to the whole BMT layers, and the interface thickness is about 90 nm, while the BMT-PZT interface’s thickness is only about 8.6 nm. The presence of heterogeneous interfaces can improve the performances of BMT/PZT thin films and expand their applications. The dielectric constant of BBPP thin films is significantly lower than BPBP thin films, while the dielectric loss is exactly the opposite. The more interfaces there are, the greater the dielectric constant. The relationship between the electric-field-dependent dielectric constant curve and the P-E curve is established. The equivalent interface barrier of the diode is used to show that the dielectric peaks under the positive and negative voltage are different. Similarly, heterogeneous interfaces show a certain improvement in dielectric tunability and temperature stability.

Lead-free Mn²⁺-based metal halide materials are now being considered as clean candidates for backlight displays and lights due to the d–d transition, diverse components, and environmental friendliness. Therefore, efficient and stable Mn²⁺-based metal halide phosphors are in great demand for practical applications. In this work, adopting the mixed-ligand strategy, a series of [(CH₃)₄N]_2−x[(C₂H₅)₄N]_xMnCl₄ phosphors were synthesized by mechanochemical process. With the increase molar ratio of (CH₃)₄N/(C₂H₅)₄N, the phase of phosphors is transformed from orthorhombic to tetragonal. Compared to [(CH₃)₄N]₂MnCl₄ and [(C₂H₅)₄N]₂MnCl₄ phosphors, the mixed-ligand strategy significantly boosts the green emission intensity of Mn²⁺-based metal halide phosphors. The obtained [(CH₃)₄N][(C₂H₅)₄N]MnCl₄ phosphors exhibit a high photoluminescence quantum yield (PLQY) of 83.78% under 450 nm excitation, which is attributed to the modulation of the adjacent [MnCl₄]₂- distance by using the different chain length of organic cations, effectively suppressing non-radiative recombination. Additionally, the [(CH₃)₄N][(C₂H₅)₄N]MnCl₄ phosphors exhibit a green emission at 516 nm, narrow full width at half-maximum (FWHM) of 45.53 nm, and good thermal stability. The constructed white light-emitting diode (WLED) device exhibits a wide color gamut of 108.3% National Television System Committee, demonstrating the suitability of the [(CH₃)₄N][(C₂H₅)₄N]MnCl₄ phosphors as a green emitter for WLED displays and lightings. This work provides a new way to modulate the PL performance of manganese-based metal halides for application in the optoelectronic field.

Ferroelectric random access memory (FeRAM) has been regarded as a promising technology for next-generation nonvolatile storage due to its excellent data storage performance and nonvolatile storage characteristics. However, fatigue degradation properties seriously impede the development and large-scale commercial use of FeRAM. In this paper, the interaction mechanism and enhancement of ferroelectric fatigue in lead zirconate titanate (PZT) thin film are investigated by the first-principles calculations (DFT). Theoretical calculations suggest that the coupling between oxygen vacancies and 180 degrees domain walls in PZT is responsible for ferroelectric fatigue. Oxygen vacancies are more likely to be formed closer to domain wall, the "pinning" between oxygen vacancies and domain wall makes the migration of domain wall difficult, resulting in the suppression of polarization reversal and ultimately fatigue in ferroelectric thin film. The insertion of Ba(Mg1/3Nb2/3)O-3 (BMN) can absorb the oxygen vacancies in PZT and reduce the concentration of oxygen vacancies, and in doing so, the ferroelectric fatigue problem caused by the " pinning" effect of the oxygen vacancies can be eliminated. Moreover, the PZT thin films are deposited on Pt/Ti/SiO2/Si(100) by the sol-gel method with using BMN buffer layer. The remnant polarization (P-r) of PZT film decreases by 51% and the PZT/BMN film remains 85% after 10(10) cycles. Furthermore, it keeps stable even up to 10(12) cycles. This paper demonstrates that the PZT/BMN film with excellent ferroelectric and fatigue endurance possesses the promising applications in FeRAM.