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The oriental tobacco budworm Helicoverpa assulta (Lepidoptera: Noctuidae) is a specialist pest that may cause serious damages to important crops such as chili pepper and tobacco. Various man-made insecticides have been applied to control the infestation of this pest. To understand how this pest copes with insecticides, it is required to identify key players involved in insecticide transformation. In this study, a P450 gene of CYP6B subfamily was identified in the oriental tobacco budworm, and its expression pattern was revealed. Moreover, the activities of HassCYP6B6 against 12 insecticides were explored using recombinant enzymes produced in the facile Escherichia coli. Data from metabolic experiments showed that HassCYP6B6 was able to metabolize conventional insecticides including organophosporates (diazinon, malathion, phoxim), carbamate propoxur, and pyrethroid esfenvalerate, while no significant metabolism was observed towards new-type pesticides such as neonicotinoids (acetamiprid, imidacloprid), diamides (chlorantraniliprole, cyantraniliprole), macrocyclic lactone (emamectin benzoate, ivermectin), and metaflumizone. Structures of metabolites were proposed based on mass spectrometry analyses. The results demonstrate that HassCYP6B6 plays important roles in the transformation of multiple insecticides via substrate-dependent catalytic mechanisms including dehydrogenation, hydroxylation and oxidative desulfurization. The findings have important applied implications for the usage of insecticides., Competing Interests: Declaration of competing interest The authors declare no competing interests., (Copyright © 2024 Elsevier Inc. All rights reserved.)

The lack of stable p-type van der Waals (vdW) semiconductors with high hole mobility severely impedes the step of low-dimensional materials entering the industrial circle. Although p-type black phosphorus (bP) and tellurium (Te) have shown promising hole mobilities, the instability under ambient conditions of bP and relatively low hole mobility of Te remain as daunting issues. Here we report the growth of high-quality Te nanobelts on atomically flat hexagonal boron nitride (h-BN) for high-performance p-type field-effect transistors (FETs). Importantly, the Te-based FET exhibits an ultrahigh hole mobility up to 1370 cm 2  V -1  s -1 at room temperature, that may lay the foundation for the future high-performance p-type 2D FET and metal-oxide-semiconductor (p-MOS) inverter. The vdW h-BN dielectric substrate not only provides an ultra-flat surface without dangling bonds for growth of high-quality Te nanobelts, but also reduces the scattering centers at the interface between the channel material and the dielectric layer, thus resulting in the ultrahigh hole mobility ., (© 2022. The Author(s).)

Layered 2D materials, such as graphene, transition metal dichalcogenides, transition metal oxides, black phosphorus, graphitic carbon nitride, hexagonal boron nitride, and MXenes, have attracted intensive attention over the past decades owing to their unique properties and wide applications in electronics, catalysis, energy storage, biomedicine, etc. Further reducing the lateral size of layered 2D materials down to less than 10 nm allows for preparing a new class of nanostructures, namely, nanodots derived from layered materials. Nanodots derived from layered materials not only can exhibit the intriguing properties of nanodots due to the size confinement originating from the ultrasmall size, but also can inherit some unique properties of ultrathin layered 2D materials, making them promising candidates in a wide range of applications, especially in biomedicine and catalysis. Here, a comprehensive summary on the materials categories, advantages, synthesis methods, and potential applications of these nanodots derived from layered materials is provided. Finally, personal insights about the challenges and future directions in this promising research field are also given., (© 2021 Wiley-VCH GmbH.)

A rechargeable aqueous zinc-ion battery (ZIB) is one of the attractive candidates for large-scale energy storage. Its further application relies on the exploitation of a high-capacity cathode and the understanding of an intrinsic energy storage mechanism. Herein, we report a novel layered K 2 V 3 O 8 cathode material for the ZIB, adopting a strategy of charging first to extract part of K-ions from vanadate in initial few cycles, which creates more electrochemically active sites and lowers charge-transfer resistance of the ZIB system. As a result, a considerable specific capacity of 302.8 mA h g -1 at 0.1 A g -1 , as well as a remarkable cycling stability (92.3% capacity retention at 4 A g -1 for 2000 cycles) and good rate capability, are achieved. Besides, the energy storage mechanism was studied by in situ X-ray diffraction, in situ Raman spectroscopy, X-ray photoelectron spectroscopy, and inductively coupled plasma mass spectroscopy. An irreversible K-ion deintercalation in the first charge process is proved. It is believed that this novel cathode material for the rechargeable aqueous ZIB and the optimizing strategy will shed light on developing next-generation large-scale energy storage devices.

Li-rich layered oxides have been in focus because of their high specific capacity. However, they usually suffer from poor kinetics, severe voltage decay, and capacity fading. Herein, a long-neglected Li-deficient method is demonstrated to address these problems by simply reducing the lithium content. Appropriate lithium vacancies can improve dynamics features and induce in situ surface spinel coating and nickel doping in the bulk. Therefore, the elaborately designed Li 1.098 Mn 0.533 Ni 0.113 Co 0.138 O 2 cathode possesses improved initial Coulombic efficiency, excellent rate capability, largely suppressed voltage decay, and outstanding long-term cycling stability. Specifically, it shows a superior capacity retention of 93.1% after 500 cycles at 1 C (250 mA g -1 ) with respect to the initial discharge capacity (193.9 mA h g -1 ), and the average voltage still exceeds 3.1 V. In addition, the discharge capacity at 10 C can be as high as 132.9 mA h g -1 . More importantly, a Li-deficient cathode can also serve as a prototype for further performance enhancement, as there are plenty of vacancies.

Two-dimensional (2D) nanostructure engineering and surface modification with functional groups are of great importance to anode materials for rechargeable lithium-ion batteries. Herein, stacked NiO nanosheets@carbon (denoted as NiO@C) and 3 nm-ultrathin NiO nanosheets@functionalized carbon with surface functional groups NO3-, CO32-, OH-, and COOH- (denoted as NiO@FC) were prepared via a facile one-pot reaction and topotactic conversion. Specifically, NiO@FC exhibits excellent lithium storage performance: the capacity of NiO@FC is 489.2 mA h g-1, higher than that of NiO@C (1018.7 mA h g-1 at 0.2 A g-1), and maintains a capacity of 1133 mA h g-1 after 800 cycles, which exceed that of all previously reported NiO anodes. The enhanced lithium storage performance is attributed to the sufficient void space, which offers buffer space for volume change and speeds up the diffusion of Li+ ions. In addition, the surface functional groups were proved to not only hinder the agglomeration of nanosheets but also further donate active sites and improve storage capacity. These advantageous features achieved by designing such a stacked structure with functionalized carbon modification provide a promising strategy for the preparation of high-performance anode materials and other 2D functional materials.

As a novel and potential transition metal dichalcogenide (TMDC), NbSe 2 has low ion diffusion barrier when applied in energy-storage systems, such as traditional lithium-ion batteries and novel magnesium-ion batteries (MIBs). In this work, we have developed a novel hexagonal NbSe 2 material with a nanosized surface via a facile microwave-hydrothermal method. The Li + -storage mechanism of NbSe 2 with surface conversion and internal intercalation is thoroughly revealed by in situ X-ray diffraction (XRD), ex situ high-resolution transmission electron microscopy, and ex situ scanning electron microscopy. Besides, Mg 2+ intercalation mechanism is confirmed via ex situ XRD and ex situ X-ray photoelectron spectroscopy for the first time. In addition, as the cathode for MIBs, NbSe 2 with a nanosized surface exhibits a high rate capacity of 101 mA h g -1 at 200 mA g -1 with a high discharge plateau at 1.30 V. Our work builds a deep understanding of ion-storage mechanisms in TMDCs and provides guidance for designing new electrode materials with high electrochemical performances.

The development of manganese dioxide as the cathode for aqueous Zn-ion battery (ZIB) is limited by the rapid capacity fading and material dissolution. Here, a highly reversible aqueous ZIB using graphene scroll-coated α-MnO 2 as the cathode is proposed. The graphene scroll is uniformly coated on the MnO 2 nanowire with an average width of 5 nm, which increases the electrical conductivity of the MnO 2 nanowire and relieves the dissolution of the cathode material during cycling. An energy density of 406.6 Wh kg -1 (382.2 mA h g -1 ) at 0.3 A g -1 can be reached, which is the highest specific energy value among all the cathode materials for aqueous Zn-ion battery so far, and good long-term cycling stability with 94% capacity retention after 3000 cycles at 3 A g -1 are achieved. Meanwhile, a two-step intercalation mechanism that Zn ions first insert into the layers and then the tunnels of MnO 2 framework is proved by in situ X-ray diffraction, galvanostatic intermittent titration technique, and X-ray photoelectron spectroscopy characterizations. The graphene scroll-coated metallic oxide strategy can also bring intensive interests for other energy storage systems., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)