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Nonvolatile memory is an indispensable component of electronic devices. However, the current technology makes it difficult to satisfy the emerging big data demand. To circumvent the existing problems, herein, a first attempt is made to achieve multifunctional nonvolatile memory based on all 2D heterostructures, consisting of histidine‐doped molybdenum disulfide quantum disks mixed with graphene oxide and a graphene macroscopic heterojunction. The designed device possesses intriguing hybrid electrically and optically controllable nonvolatile memory functionalities. By harnessing the unique properties of these materials, memory devices demonstrate long‐term stability and nonvolatile characteristics under both optical and electrical control signals. These devices possess outstanding features, such as multiple read‐write cycles, multi levels, and fast switching speeds, overcoming the limitations of traditional components. To explore the underlying physical mechanism, the Fermi level of graphene is measured and it is confirmed that the charge transfer and trapping across the heterojunctions are the major factors responsible for the observed behavior. This study demonstrates that 2D heterostructures for hybrid optically and electrically controllable nonvolatile memory pave an alternative route for the next‐generation information technology. [ABSTRACT FROM AUTHOR]

Poly(lactic acid) (PLA) is a biodegradable polymer with limited application because of its intrinsic brittleness, low toughness, and low elongation at break. Melt blends were prepared by mixing a natural rubber (NR, poly(1,4‐cis‐isoprene) in the form of liquid NR (LNR), liquid‐epoxidized NR (LENR), and polypropylene (PP) in the PLA matrix. Four blend systems were designed and prepared, i.e., PLA–PP, PLA–PP–LNR, and PLA–LNR or PLA–LENR. The composition of PP in the blend was fixed at 10 % PLAPP (90/10). Results showed that PLA–PP mixed with LNR improved impact and elongation at break. The binary blend of PLA–LNR (90/10) significantly enhanced impact strength and elongation at break properties. In contrast, the binary blends of PLA–LENR (90/10) showed a lower value of elongation at break (9.5 % vs. 37.3%) and impact strength (4.56 kJ m−2 vs. 6.44 kJ m−2). The melting temperature (Tm) and the glass transition temperature (Tg) were measured by differential scanning calorimetry, which recorded slight changes in the glass temperatures and melting temperatures. Scanning electron microscopy images of the tensile fracture of the PLA–LNR (90/10) blend showed the presence of large fibrils associated with the ductile failure related to neat PLA. Finally, the fracture toughness (KIC) of PLA–LNR (90/10) showed an increase of 39 % over neat PLA (2.94 MPa.m1/2 vs. 4.08 MPa.m1/2). [ABSTRACT FROM AUTHOR]

Fluoroquinolone antibiotics have been encountered in aquatic environments in quantities giving rise to significant concern recently. To cope with this problem, it is necessary to design a semiconductor photocatalyst having excellent photocatalytic efficiency to eliminate the antibiotics. The heterojunction is a likely situate where the efficiency of relevant photocatalyst can be strengthened. In this study, the performance of MnNb 2 O 6 /g-C 3 N 4 (MNO/g-CN) composites in the photocatalytic degradation of ciprofloxacin (CIP) and tetracycline-HCl (TCH) antibiotics was explored. Enhanced photocatalytic activity of MNO/g-CN was found to be owing to electron's shifting between the MNO, and g-CN sheets, which promotes the formation of photo-generated e⁻/h⁺ pairs. This shows a low-waste, high-performance material exists to eradicate CIP and TCH from wastewater. Further, the structural, photochemical and light interacted properties of the MNO/g-CN photocatalyst, prepared by solvothermal method and sonication, were described using photochemical, physiochemical and electrochemical approaches. The synthesized photocatalyst owes its particular efficiency to its methodical photo-degradation of CIP and TC using visible light. The optimum composite 15% MNO/g-CN evinced the greatest photocatalytic efficiency with CIP and TCH photo-degradation of 94.10%, and 98.50%, respectively, and degradation mechanism were investigated using LC-MS spectroscopy. The suitable photocatalytic activity is ascribed to lower the recombination's rate of e⁻/h⁺ pairs. The scavenging evaluations proved that the h + and • O 2 - were two major photoactive species accomplishing the CIP and TCH photodegradation over MNO/g-CN under visible region. Our findings pave the way for the construction of efficient binary photocatalysts for antibiotic restitution., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

The further development of an efficient and sustainable water treatment requires the development of a very active and controllable photocatalyst. The heterojunction is a promising site where the activity of such a photocatalyst can be enhanced. Organic dyes have become a severe concern in recent years owing to their significant presence in wastewater. Hexavalent Chromium (Cr (VI)) is a potential carcinogen also exhibiting great persistence in wastewater. So, a low-waste, high-performance materials is required to eliminate organic dyes and Cr (VI) from wastewater. In this study, CNO/g-CN (CuNb 2 O 6 /g-C 3 N 4 ) photocatalyst synthesized via co-precipitation, followed by calcination which were characterized using physiochemical and photo-electrochemical approaches to identify their structural, photochemical and optical traits. The uniqueness of the synthesized photocatalyst is due to both its efficient photo-reduction of Cr (VI) and photo-degradation of Rhodamine B (RhB), Methylene Blue (MB) and Methyl Orange (MO) under visible light. The CNO/g-CN composite with 30% CNO heterojunctions exhibited the highest photocatalytic activity with Cr (VI) 92.80% photoreduction and efficiency degradation for RhB, MB, MO of 99.6%, 98.50%, 99.0%, respectively, with constant rate (k). This efficient photocatalytic activity is attributed to the lower recombination rate of electron-hole pairs. Free radical trapping experiments showed that • O 2 - and h + play an important role in the photodegradation. The study, therefore, opens an alternative route in the synthesis of very efficient binary photocatalysts for application in environmental remediation., (Copyright © 2022 Elsevier Ltd. All rights reserved.)