Interface‐Driven Partial Dislocation Formation in 2D Heterostructures

Van der Waals (vdW) epitaxy allows the fabrication of various heterostructures with dramatically released lattice matching conditions. This study demonstrates interface‐driven stacking boundaries in WS₂ using epitaxially grown tungsten disulfide (WS₂) on wrinkled graphene. Graphene wrinkles function as highly reactive nucleation sites on WS₂ epilayers; however, they impede lateral growth and induce additional stress in the epilayer due to anisotropic friction. Moreover, partial dislocation‐driven in‐plane strain facilitates out‐of‐plane buckling with a height of 1 nm to release in‐plane strain. Remarkably, in‐plane strain relaxation at partial dislocations restores the bandgap to that of monolayer WS₂ due to reduced interlayer interaction. These findings clarify significant substrate morphology effects even in vdW epitaxy and are potentially useful for various applications involving modifying optical and electronic properties by manipulating extended 1D defects via substrate morphology control.     

考虑亚稳态的绝热毛细管模型与计算

制冷剂在通过毛细管过程中,存在一个不稳定的亚稳态流动阶段.在考虑亚稳态现象的基础上,基于两相流动的漂移流模型,建立了绝热毛细管内制冷剂流动特性的数学模型.针对工质为R134a的制冷系统开发了绝热毛细管数值模拟程序,并对漂移流模型中的3个重要参数:空隙率、漂移速度和干度进行了计算和分析.该程序在制冷系统毛细管的匹配中具有一定实用价值.     

Sol-gel synthesis of single-phase Ca5MgSi3O12: Eu, Mn phosphors for white-light emitting diodes

A novel Ca₅MgSi₃O₁₂: Eu²⁺, Mn²⁺ phosphor has been prepared by a sol-gel method. X-ray diffractometer, spectrofluorometer were used to characterize structural and optical properties of the samples. The results indicate that Ca₅MgSi₃O₁₂: Eu²⁺, Mn²⁺ phosphors show two emission bands excited by ultraviolet light. Blue (around 450 nm) and green (around 502 nm) emissions originate from Mn²⁺ and Eu²⁺, respectively. With appropriate tuning the concentration ratios of Eu²⁺ to Mn²⁺, Ca₅MgSi₃O₁₂: Eu²⁺, Mn²⁺ phosphors exhibit different hues and relative color temperatures, which have potential to act as a single-phase phosphor for white-light emitting diode.     

Reliable Piezoelectricity in Bilayer WSe2 for Piezoelectric Nanogenerators

Recently, piezoelectricity has been observed in 2D atomically thin materials, such as hexagonal‐boron nitride, graphene, and transition metal dichalcogenides (TMDs). Specifically, exfoliated monolayer MoS₂ exhibits a high piezoelectricity that is comparable to that of traditional piezoelectric materials. However, monolayer TMD materials are not regarded as suitable for actual piezoelectric devices due to their insufficient mechanical durability for sustained operation while Bernal‐stacked bilayer TMD materials lose noncentrosymmetry and consequently piezoelectricity. Here, it is shown that WSe₂ bilayers fabricated via turbostratic stacking have reliable piezoelectric properties that cannot be obtained from a mechanically exfoliated WSe₂ bilayer with Bernal stacking. Turbostratic stacking refers to the transfer of each chemical vapor deposition (CVD)‐grown WSe₂ monolayer to allow for an increase in degrees of freedom in the bilayer symmetry, leading to noncentrosymmetry in the bilayers. In contrast, CVD‐grown WSe₂ bilayers exhibit very weak piezoelectricity because of the energetics and crystallographic orientation. The flexible piezoelectric WSe₂ bilayers exhibit a prominent mechanical durability of up to 0.95% of strain as well as reliable energy harvesting performance, which is adequate to drive a small liquid crystal display without external energy sources, in contrast to monolayer WSe₂ for which the device performance becomes degraded above a strain of 0.63%.     

Printable and Rewritable Full Block Copolymer Structural Color

Structural colors (SCs) of photonic crystals (PCs) arise from selective constructive interference of incident light. Here, an ink‐jet printable and rewritable block copolymer (BCP) SC display is demonstrated, which can be quickly written and erased over 50 times with resolution nearly equivalent to that obtained with a commercial office ink‐jet printer. Moreover, the writing process employs an easily modified printer for position‐ and concentration‐controlled deposition of a single, colorless, water‐based ink containing a reversible crosslinking agent, ammonium persulfate. Deposition of the ink onto a self‐assembled BCP PC film comprising a 1D stack of alternating layers enables differential swelling of the written BCP film and produces a full‐colored SC display of characters and images. Furthermore, the information can be readily erased and the system can be reset by application of hydrogen bromide. Subsequently, new information can be rewritten, resulting in a chemically rewritable BCP SC display.     

Nanomaterials for radiotherapeutics-based multimodal synergistic cancer therapy

Over the past decade, numerous studies have attempted to enhance the effectiveness of radiotherapy (external beam radiotherapy and internal radioisotope therapy) for cancer treatment. However, the low radiation absorption coefficient and radiation resistance of tumors remain major critical challenges for radiotherapy in the clinic. With the development of nanomedicine, nanomaterials in combination with radiotherapy offer the possibility to improve the efficiency of radiotherapy in tumors. Nanomaterials act not only as radiosensitizers to enhance radiation energy, but also as nanocarriers to deliver therapeutic units in combating radiation resistance. In this review, we discuss opportunities for a synergistic cancer therapy by combining radiotherapy based on nanomaterials designed for chemotherapy, photodynamic therapy, photothermal therapy, gas therapy, genetic therapy, and immunotherapy. We highlight how nanomaterials can be utilized to amplify antitumor radiation responses and describe cooperative enhancement interactions among these synergistic therapies. Moreover, the potential challenges and future prospects of radio-based nanomedicine to maximize their synergistic efficiency for cancer treatment are identified.