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Atomically thin two-dimensional transition metal dichalcogenides (TMDCs) have been regarded as ideal and promising nanomaterials that bring broad application prospects in extensive fields due to their ultrathin layered structure, unique electronic band structure, and multiple spatial phase configurations. TMDCs with different phase structures exhibit great diversities in physical and chemical properties. By regulating the phase structure, their properties would be modified to broaden the application fields. In this mini review, focusing on the most widely concerned molybdenum dichalcogenides (MoX2: X = S, Se, Te), we summarized their phase structures and corresponding electronic properties. Particularly, the mechanisms of phase transformation are explained, and the common methods of phase regulation or phase stabilization strategies are systematically reviewed and discussed. We hope the review could provide guidance for the phase regulation of molybdenum dichalcogenides nanomaterials, and further promote their real industrial applications. [ABSTRACT FROM AUTHOR]

As an emerging zero-dimensional nano crystalline porous material, porous organic cages (POCs) with soluble properties in organic solvents, are promising candidates as molecular fillers in mixed matrix membranes (MMMs). The pore structure of POCs should be adjusted to trigger efficient gas separation performance, and the interaction between filler and matrix should be optimized. In this work, ionic liquid (IL) was introduced into the molecular fillers of CC3, to construct the IL@CC3/PIM-1 membrane to effectively separate CO2 from CH4. The advantages of doping IL include: (1) narrowing the cavity size of POCs from 4.4 to 3.9 Å to enhance the diffusion selectivity, (2) strengthening the CO2 solubility to heighten the gas permeability, and (3) improving the compatibility between filler and matrix to upgrade membrane stability. After the optimization of the membrane composite, the IL@CC3/PIM-1-10% membrane possesses the CO2 permeability of 7868 Barrer and the CO2/CH4 selectivity of 73.4, which compared to the CC3/PIM-1-10% membrane, improved by 15.9% and 106.2%, respectively. Furthermore, the membrane has maintained a stable separation performance at varied temperatures and pressures during the long-term test. The proposed method offers an efficient way to improve the performance of POCs-based MMMs in gas separation. [ABSTRACT FROM AUTHOR]

We introduce a “solution‐processing‐transformation” strategy, deploying solvent vapor as scaffolds, to fabricate high‐quality hydrogen‐bonded organic framework (HOF) membranes. This strategy can overcome the mismatch in processing conditions and crystal growth thermodynamics faced during the facile solution processing of the membrane. The procedure includes the vapor‐trigged in situ transformation of dense amorphous supramolecules to crystalline HOF‐16, with HOF‐11 as the transient state. The mechanism involves a vapor‐activated dissolution‐precipitation equilibrium shifting and hydrogen bonding‐guided molecule rearrangement, elucidated through combined experimental and theoretical analysis. Upon removal of the molecular scaffolds, the resulting HOF‐16 membranes showcase significant improvement in hydrogen separation performance over their amorphous counterparts and previously reported HOF membranes. The method's broad applicability is evidenced by successfully extending it to other substrates and HOF structures. This study provides a fundamental understanding of guest‐induced ordered supramolecular assembly and paves the way for the advanced manufacture of high‐performance HOF membranes for gas separation processes. [ABSTRACT FROM AUTHOR]

Interface strain significantly affects the band structure and electronic states of metal‐nanocrystal‐2D‐semiconductor heterostructures, impacting system performance. While transmission electron microscopy (TEM) is a powerful tool for studying interface strain, its accuracy may be compromised by sample overlap in high‐resolution images due to the unique nature of the metal‐nanocrystals‐2D‐semiconductors heterostructure. Utilizing digital dark‐field technology, the substrate influence on metal atomic column contrasts is eliminated, improving the accuracy of quantitative analysis in high‐resolution TEM images. Applying this method to investigate Pt on MoS2 surfaces reveals that the heterostructure introduces a tensile strain of ≈3% in Pt nanocrystal. The x‐directional linear strain in Pt nanocrystals has a periodic distribution that matches the semi‐coherent interface between Pt nanocrystals and MoS2, while the remaining strain components localize mainly on edge atomic steps. These results demonstrate an accurate and efficient method for studying interface strain and provide a theoretical foundation for precise heterostructure fabrication. [ABSTRACT FROM AUTHOR]

Two-dimensional (2D) semiconducting transition metal dichalcogenides (TMDCs) are extensively employed as channel materials in advanced electronic devices. The electrical contacts between electrodes and 2D semiconductors play a crucial role in the development of high-performance transistors. While numerous strategies for electrode interface engineering have been proposed to enhance the performance of n-type 2D transistors, upgrading p-type ones in a similar manner remains a challenge. In this work, significant improvements in a p-type WSe 2 transistor are demonstrated by utilizing metallic MoO 2 nanosheets as the electrode contact, which are controllably fabricated through physical vapor deposition and subsequent annealing. The MoO 2 nanosheets exhibit an exceptional electrical conductivity of 8.4 × 10 4 S m ‒1 and a breakdown current density of 3.3 × 10 6 A cm ‒2 . The work function of MoO 2 nanosheets is determined to be ≈5.1 eV, making them suitable for contacting p-type 2D semiconductors. Employing MoO 2 nanosheets as the electrode contact in WSe 2 transistors results in a notable increase in the field-effect mobility to 92.0 cm 2 V ‒1 s ‒1 , which is one order of magnitude higher than the counterpart devices with conventional electrodes. This study not only introduces an intriguing 2D metal oxide to improve the electrical contact in p-type 2D transistors, but also offers an effective approach to fabricating all-2D devices., (© 2024 Wiley‐VCH GmbH.)

Purpose: Few studies have reported the integrated characteristics of hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) after long-term antiviral therapy. This study aimed to investigate the HBV integration features in HBV-HCC patients who had undergone long-term antiviral therapy, evaluate their impact on clinical indicators, and analyze the potential mechanisms involved., Patients and Methods: We utilized genome-wide association study (GWAS) to analyze liver cancer tissues and detect the presence of HBV integration. Seventeen patients with HBV integration were included in the integration (Int) group, while the remaining five patients were included in the non-integration (N-int) group. Clinical indicators were regularly monitored and compared between the two groups. The characteristics of HBV integration patterns were analyzed, and differences between the groups were explored at the chromosome and genomic levels., Results: After long-term antiviral therapy, although the frequency of HBV integration in HBV-HCC was reduced, residual HBV integration still accelerated the development of HCC. It affected the diagnosis, treatment, and prognosis of patients. HBV integration events led to changes in chromosome structure, which were closely related to HCC. Novel fusion genes were detected at a high frequency and had the potential to be specific detection sites for HBV-HCC., Conclusion: HBV integration events are synergistically involved in the human genome and HBV, which can lead to chromosome structural instability, gene rearrangement events closely related to HCC production, and the formation of new specific fusion genes., Competing Interests: The authors report no conflicts of interest in this work., (© 2024 Wang et al.)