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Ultra-thin 2D materials have great potential as electrodes for micro-supercapacitors (MSCs) because of their facile ion transport channels. Here, a high-precision controllable photonic-synthesis strategy that provided 1 inch wafer-scale ultra-thin film arrays of alloyed W x Mo 2x S y with sulfur vacancies and expanded interlayer (13.2 Å, twice of 2H MoS 2 ) is reported. This strategy regulates the nucleation and growth of transition metal dichalcogenides (TMDs) on the picosecond or even femtosecond scale, which induces Mo-W alloying, interlayer expansion, and sulfur loss. Therefore, the diffusion barrier of W x Mo 2x S y is reduced, with charge transfer and ion diffusion enhancing. The as-prepared symmetric MSCs with the size of 100 × 100 µm 2 achieve ultrahigh specific capacitance (242.57 mF cm -2 and 242567.83 F cm -3 ), and energy density (21.56 Wh cm -3 with power density of 485.13 W cm 3 ). The established synthesis strategy fits numerous materials, which provides a universal method for the flexible synthesis of electrodes in microenergy devices., (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

Temperature is one of the governing factors affecting friction of solids. Undesired high friction state has been generally reported at cryogenic temperatures due to the prohibition of thermally activated processes, following conventional Arrhenius equation. This has brought huge difficulties to lubrication at extremely low temperatures in industry. Here, the study uncovers a hydrogen-correlated sub-Arrhenius friction behavior in hydrogenated amorphous carbon (a-C:H) film at cryogenic temperatures, and a stable ultralow-friction over a wide temperature range (103-348 K) is achieved. This is attributed to hydrogen-transfer-induced mild structural ordering transformation, confirmed by machine-learning-based molecular dynamics simulations. The anomalous sub-Arrhenius temperature dependence of structural ordering transformation rate is well-described by a quantum mechanical tunneling (QMT) modified Arrhenius model, which is correlated with quantum delocalization of hydrogen in tribochemical reactions. This work reveals a hydrogen-correlated friction mechanism overcoming the Arrhenius temperature dependence and provides a new pathway for achieving ultralow friction under cryogenic conditions., (© 2024 Wiley‐VCH GmbH.)

Understanding and controlling the wear process of heterogeneous interfaces between soft and hard phases is crucial for designing and fabricating materials, such as improving the wear resistance of particle reinforced metal matrix composites and the accuracy and efficiency of chemical mechanical polishing. However, the wear process can be hardly observed, as interfaces are buried under the surface. Here, we proposed a nanowear test method by combining focused ion beam cutting to expose interfaces, atomic force microscopy to rub against interfaces, and scanning electron microscope to characterize the interface damage. Using this method, three typical wear forms had been observed in Al/SiC composite, i.e., merely matrix wear, particle fracture, and particle pullout. A theoretical model was proposed that revealed that the increasing interfacial friction would induce particle fracture or pullout, depending on the particle edge angle and tip edge angle. This work sheds light on wear control in composites and nanofabrication.

Background: Owing to the long penetration depth of gamma (γ)-rays, individuals working in ionizing radiation environments are chronically exposed to low-dose γ-radiation, resulting in cognitive changes. Dose rate significantly affects radiation-induced biological effects; however, its role in chronic low-dose γ-irradiation-induced cognitive impairment remains unclear. We aimed to investigate whether chronic low-dose γ-irradiation at low-dose-rate (LDR) could induce cognitive impairment and to compare the cognitive alteration caused by chronic low-dose γ-irradiation at LDR and high-dose-rate (HDR)., Methods: The rats were exposed to γ-irradiation at a LDR of 6 mGy/h and a HDR of 20 mGy/h for 30 days (5 h/day). Functional imaging was performed to assess the brain inflammation and blood-brain barrier (BBB) destruction of rats. Histological and immunofluorescence analyses were used to reveal the neuron damage and the activation of microglia and astrocytes in the hippocampus. RNA sequencing was conducted to investigate changes in gene expression in hippocampus., Results: The rats in the LDR group exhibited more persistent cognitive impairment than those in the HDR group. Furthermore, irradiated rats showed brain inflammation and a compromised BBB. Histologically, the number of hippocampal neurons were comparable in the LDR group but were markedly decreased in the HDR. Additionally, activated M1-like microglia and A1-like astrocytes were observed in the hippocampus of rats in the LDR group; however, only M1-like microglia were activated in the HDR group. Mechanistically, the PI3K-Akt signaling pathway contributed to the different cognitive function change between the LDR group and HDR group., Conclusion: Compared with chronic low-dose γ-irradiation at HDR, LDR induced more severe cognitive impairment which might involve PI3K/Akt signaling pathway., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 Ma, Li, Sang, Liu, Luo, Peng, Wang, Luo, Fang, Wang, Wang and Zuo.)

Purposes: Radiotherapy can induce tumor cell autophagy, which might impair the antitumoral effect. This study aims to investigate the effect of autophagy inhibition on the targeted radionuclide therapy (TRT) efficacy of 131 I-FAP-2286 in pancreatic cancer., Methods: Human pancreatic cancer PANC-1 cells were exposed to 131 I-FAP-2286 radiotherapy alone or with the autophagy inhibitor 3-MA. The autophagy level and proliferative activity of PANC-1 cells were analyzed. The pancreatic cancer xenograft-bearing nude mice were established by the co-injection of PANC-1 cells and pancreatic cancer-associated fibroblasts (CAFs), and then were randomly divided into four groups and treated with saline (control group), 3-MA, 131 I-FAP-2286 and 131 I-FAP-2286 + 3-MA, respectively. SPECT/CT imaging was performed to evaluate the bio-distribution of 131 I-FAP-2286 in pancreatic cancer-bearing mice. The therapeutic effect of tumor was evaluated by 18 F-FDG PET/CT imaging, tumor volume measurements, and the hematoxylin and eosin (H&E) staining, and immunohistochemical staining assay of tumor tissues., Results: 131 I-FAP-2286 inhibited proliferation and increased the autophagy level of PANC-1 cells in a dose-dependent manner. 3-MA promoted 131 I-FAP-2286-induced apoptosis of PANC-1 cells via suppressing autophagy. SPECT/CT imaging of pancreatic cancer xenograft-bearing nude mice showed that 131 I-FAP-2286 can target the tumor effectively. According to 18 F-FDG PET/CT imaging, the tumor growth curves and immunohistochemical analysis, 131 I-FAP-2286 TRT was capable of suppressing the growth of pancreatic tumor accompanying with autophagy induction, but the addition of 3-MA enabled 131 I-FAP-2286 to achieve a better therapeutic effect along with the autophagy inhibition. In addition, 3-MA alone did not inhibit tumor growth., Conclusions: 131 I-FAP-2286 exposure induces the protective autophagy of pancreatic cancer cells, and the application of autophagy inhibitor is capable of enhancing the TRT therapeutic effect., (© 2024. The Author(s).)

Lubrication of polymeric materials generally involves processes of atomic-scale chemical bond forming/breaking at the interface and mesoscale chain reorientation, disentanglement, and so forth. However, it is difficult to describe the important aspects of tribochemical reactions by conventional coarse-grained molecular dynamics (CGMD) simulations. Here, reactive CGMD simulations were conducted based on the ReaxFF force field to study the tribochemical interactions between polytetrafluoroethylene (PTFE) and iron. The chemical bond forming/breaking between the molecular chain and countersurface was fitted through the bond dissociation energies of specific reaction sites from all-atom ReaxFF-MD simulations. This enabled a quantitative description of tribochemical reactions in a macromolecule system. First, the number of anchoring bonds between PTFE molecules and the countersurface showed a strong correlation with the friction coefficient. The shearing process induced breaking of the interfacial anchoring bonds as well as chain disentanglement in the matrix, which consequently led to ordering reorientation of molecular chains toward sliding direction and hence decrease of friction. Second, two competitive factors were clarified to affect polymer friction with varying temperatures. The decrease of interfacial anchoring reactivity and molecular chain mobility at low temperature prohibited reorientation of molecular chains and increased the friction coefficient. On the other hand, the hardening of PTFE and the reduction in effective contact area at low temperatures decreased the friction coefficient. This led to a turning point with a maximum friction coefficient around 100 K. These results shed light on the essential role of tribochemical reactions on polymer lubrication, especially under low temperatures, which provides design guidance of polymeric lubrication systems for engineering applications.

Using atomic force microscopy, we have shown that friction on graphene/h-BN superlattice structures may exhibit unusual moiré-scale stick slip in addition to the regular ones observed at the atomic scale. Such dual-scale slip instability will lead to unique length-scale dependent energy dissipation when the different slip mechanisms are sequentially activated. Assisted by an improved theoretical model and comparative experiments, we find that accumulation and unstable release of the in-plane strain of the graphene layer is the key mechanism underlying the moiré-scale behavior. This work highlights the distinct role of the internal state of the van der Waals interfaces in determining the rich dynamics and energy dissipation of layer-structured materials.

Atomic reconstruction has been widely observed in two-dimensional van der Waals structures with small twist angles 1-7 . This unusual behaviour leads to many novel phenomena, including strong electronic correlation, spontaneous ferromagnetism and topologically protected states 1,5,8-14 . Nevertheless, atomic reconstruction typically occurs spontaneously, exhibiting only one single stable state. Using conductive atomic force microscopy, here we show that, for small-angle twisted monolayer-multilayer graphene, there exist two metastable reconstruction states with distinct stacking orders and strain soliton structures. More importantly, we demonstrate that these two reconstruction states can be reversibly switched, and the switching can propagate spontaneously in an unusual domino-like fashion. Assisted by lattice-resolved conductive atomic force microscopy imaging and atomistic simulations, the detailed structure of the strain soliton networks has been identified and the associated propagation mechanism is attributed to the strong mechanical coupling among solitons. The fine structure of the bistable states is critical for understanding the unique properties of van der Waals structures with tiny twists, and the switching mechanism offers a viable means for manipulating their stacking states., (© 2022. The Author(s), under exclusive licence to Springer Nature Limited.)

A fundamental cryogenic study in tribology from 20 to 300 K revealed that a kind of disulfide film could exhibit a superlubricity state. Inspired by this, we designed a more delicate experiment and reported an extremely low friction coefficient for a multilayered MoS 2 -Ag film in a cryogenic environment against a bare steel ball under a high load. The results showed that the multilayered MoS 2 -Ag film could undergo a pressure exceeding 2 GPa to maintain a superlow friction coefficient of below 0.001 at 170 K. The film material was transferred to the sliding contacts to form an antifriction tribofilm. The superlubricity mechanism was attributed to the formation of MoS 2 -wrapped Ag nanoparticles accumulated at the sliding interface through nanoparticle movement and layered-structure sliding. This new kind of multilayered MoS 2 -Ag film provides a novel design for a solid lubricant and broadens the application of solid lubrication films under harsh working conditions for mechanical engineering.

For atomically thin two-dimensional materials, interfacial effects may dominate the entire response of devices, because most of the atoms are in the interface/surface. Graphene/sapphire has great application in electronic devices and semiconductor thin-film growth, but the nature of this interface is largely unknown. Here we find that the sapphire surface has a strong interaction with some of the carbon atoms in graphene to form a C-O-Al configuration, indicating that the interface interaction is no longer a simple van der Waals interaction. In addition, the structural relaxation of sapphire near the interface is significantly suppressed and very different from that of a bare sapphire surface. Such an interfacial C-O-Al bond is formed during graphene growth at high temperature. Our study provides valuable insights into understanding the electronic structures of graphene on sapphire and remote control of epitaxy growth of thin films by using a graphene-sapphire substrate.

Natural vascular plants leaves rely on differences in osmotic pressure, transpiration and guttation to produce tons of clean water, powered by sunlight. Inspired by this, we report a sunlight-driven purifier for high-efficiency water purification and production. This sunlight-driven purifier is characterized by a negative temperature response poly(N-isopropylacrylamide) hydrogel (PN) anchored onto a superhydrophilic melamine foam skeleton, and a layer of PNIPAm modified graphene (PG) filter membrane coated outside. Molecular dynamics simulation and experimental results show that the superhydrophilicity of the relatively rigid melamine skeleton significantly accelerates the swelling/deswelling rate of the PNPG-F purifier. Under one sun, this rational engineered structure offers a collection of 4.2 kg m -2  h -1 and an ionic rejection of > 99% for a single PNPG-F from brine feed via the cooperation of transpiration and guttation. We envision that such a high-efficiency sunlight driven system could have great potential applications in diverse water treatments.

Defect/active site control is crucial for tuning the chemical, optical, and electronic properties of MoS2, which can adjust the performance of MoS2 in application areas such as electronics, optics, catalysis, and molecular sensing. This study presents an effective method of inducing defect/active sites, including micro/nanofractured structures and S atomic vacancies, on monolayer MoS2 flakes by using femtosecond laser pulses, through which physical-chemical adsorption and charge transfer between foreign molecules (O2 or R6G molecules) and MoS2 are enhanced. The enhanced charge transfer between foreign molecules (O2 or R6G) and femtosecond laser-treated MoS2 can enhance the electronic doping effect between them, hence resulting in a photoluminescence photon energy shift (reaching 0.05 eV) of MoS2 and Raman enhancement (reaching 6.4 times) on MoS2 flakes for R6G molecule detection. Finally, photoluminescence control and micropatterns on MoS2 and surface-enhanced-Raman-scattering (SERS) enhancement of MoS2 for organic molecule detection are achieved. The proposed method, which can control the photoluminescence properties and arbitrary micropatterns on MoS2 and enhance its chemicobiological sensing performance for organic/biological molecules, has advantages of simplicity, maskless processing, strong controllability, high precision, and high flexibility, highlighting the superior ability of femtosecond laser pulses to achieve the property control and functionalization of two-dimensional materials.

Graphene and other two-dimensional materials have been proved to be able to offer low friction. Here we assembled van der Waals heterostructures with graphene and molybdenum disulphide monolayers. The Raman spectrum together with a modified linear chain model indicate a two-orders-of-magnitude decrease in the interlayer lateral force constant, as compared with their homogeneous bilayers, indicating a possible routine to achieve superlubricity. The decrease in the interlayer lateral force constant is consistent with the ultrasmall potential energy corrugation during sliding, which is derived from density functional theory calculations. The potential energy corrugation is found to be determined by the sliding-induced interfacial charge density fluctuation, suggesting a new perspective to understand the physical origin of the atomic scale friction of two-dimensional materials.

Edge-active site control of MoS 2 is crucial for applications such as chemical catalysis, synthesis of functional composites, and biochemical sensing. This work presents a novel nonthermal method to simultaneously tune surface chemical (edge-active sites) and physical (surface periodic micro/nano structures) properties of MoS 2 using temporally shaped femtosecond pulses, through which shape-controlled gold nanoparticles are in situ and self-assembly grown on MoS 2 surfaces to form Au-MoS 2 hybrids. The edge-active sites with unbound sulfurs of laser-treated MoS 2 drive the reduction of gold nanoparticles, while the surface periodic structures of laser-treated MoS 2 assist the shape-controllable growth of gold nanoparticles. The proposed novel method highlights the broad application potential of MoS 2 ; for example, these Au-MoS 2 hybrids exhibit tunable and highly sensitive SERS activity with an enhancement factor up to 1.2 × 10 7 , indicating the marked potential of MoS 2 in future chemical and biological sensing applications.