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Nano-sized crystalline silicon particles, prepared by a laser-induced vapour deposition method, were coated onto the surface of particles of a modified natural graphite (SSG) by sonicated dispersion and a subsequent heat-treatment process. The microstructure of the Si-coated SSG was characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). It was found that the nanometer-scale Si particles were uniformly and completely coated on the surface of SSG particles, and both the Si and SSG particles existed in the crystalline state. The Si-coated SSG exhibits a much higher reversible capacity than pristine SSG, while keeping the good cycling performance of SSG material. The higher capacity can be ascribed to the alloying of Si with lithium. Because of the heat-treatment at 600 °C, used to achieve a good combination of Si with the SSG base, the cycling of the composites is very satisfactory. As a result, Si-coated SSG is a promising anode material for lithium ion batteries. [ABSTRACT FROM AUTHOR]

Using temperature modulation, two distinct hydrogen bond organic frameworks HOF-C and HOF-K with different pore sizes were synthesized from the same ligands, tris(4-(4 H -1,2,4-triazole-4-yl)phenyl)amine. The pore size difference prevents TRZ from entering HOF-K, while allowing TRZ to selectively insert into the larger-pored HOF-C to form HOF-C-TRZ. The donor-acceptor (D-A) structure formed in HOF-C-TRZ enhances its photoelectric response and exhibits exceptional uranium reduction under visible light irradiation. This study provides an effective strategy for pore size regulation of HOFs and opens up new ideas for the development of advanced uranium photocatalysts.

A benzofuran-[ b ]-fused BODIPY trimer has been efficiently synthesized, featuring a unique structural design that harmoniously integrates TBET (through bond energy transfer) and PET (photo-induced electron transfer) mechanisms. This trimer boasts exceptional optical properties, including a large pseudo-Stokes shift of 100 nm, an impressive fluorescence quantum yield ( Φ FL = 0.931), an outstandingly high extinction coefficient (182 100 M -1 cm -1 ), a remarkable FEF (fluorescence enhancement factors, 22.4-fold) values as well as exhibiting AIE (aggregation-induced emission) activity, and has been successfully utilized in two-photon fluorescence imaging of live-cell lipid droplets.

Based on the enrichment potential of living plants for nanoparticles, this paper develops a new strategy to utilize Murray's law in plants to remove various shapes of gold nanoparticles and, in situ , convert them into Murray porous carbon. The inherent Murray network serves as an optimized hierarchical design and ensures the mechanical stability of the material, and Murray's law is employed to achieve uniform dispersion of nanoparticles in vivo , facilitating the preparation of metal nanoparticle-supported carbon materials.

Targeted at organic dye pollutants, a stable HOF was combined with an alginate (SA) hydrogel to enhance the affinity for cationic dyes. The as-obtained HOF@SA membrane (weight ratio: 1/1) shows a high adsorption capacity (729.21 mg g -1 ), adsorption selectivity and good recycling performance towards methylene blue.

Substituent-modulation induced electronic perturbations can fine-tune the charge cloud distribution around carbon defects. The transfer of electrons from electron-donating substituents to carbon defects will lead to lower p z band center of carbon atoms, stronger C-O bonds, narrower band gaps, and asymmetric orbital distribution, consequently enhancing the ORR thermodynamic activity and kinetic efficiency.

When microwave hyperthermia (MWH) array antenna technology is used to treat breast cancer, how to effectively target and heat deep tumors and reduce thermal damage to healthy tissues is still a challenge in clinical applications. In this study, the synergistic MWH effect of conformal-array antennas (CAA) and a novel microwave-thermal-sensitive nanomaterial (MTSN) was investigated for the treatment of subcutaneous deep in situ breast cancer. At the beginning of the study, the thermal damage score was used to evaluate the therapeutic efficacy of the CAA. It was found that although array antenna technology can achieve effective heating of deep tumors, its damage to healthy tissues is unacceptable. Consequently, we developed a novel MTSN, ZIF-8@HA, whose unique structure significantly enhanced the absorption of MW energy and MW thermal conversion efficiency in the local tumor region. The MW thermal conversion efficiency of ZIF-8@HA achieved was as high as 46.46% in in vivo MW heating experiments. In the phantom that simulates the electromagnetic environment of the human body, the microwave-thermal sensitization (MTS) effect is also significant, and the reduction in the average thermal damage score of healthy tissues by more than 10% was verified through measurements using the coaxial probe method and COMSOL simulations. Cellular experiments confirmed that the combination of ZIF-8@HA and MW irradiation could significantly reduce the survival rate of tumor cells. In addition, cross-tissue MW heating experiments revealed the advantages of ZIF-8@HA combined with the CAA. Finally, phantom experiments confirmed that the synergistic use of the CAA with ZIF-8@HA significantly accelerated the local heating rate of deep tumors, reduced the time required for the tumor region to achieve 100% thermal damage, and effectively minimized the thermal damage to healthy tissues.

Osteogenesis imperfecta (OI) is a hereditary skeletal disorder characterized by bone fragility and deformities, primarily attributed to defects in type I collagen, the most abundant structural protein in humans. Multiple phosphorylation sites have been detected within collagen, suggesting that phosphorylation may influence mineralization processes, thereby impacting the development of OI. In this study, we investigated the modulation of biomineralization morphology by phosphorylated collagen peptides mimicking Gly-Ser mutations in osteogenesis imperfecta. A series of collagen peptide sequences, including GPO 13 S, GPO 13 pS, GPO 12 S, GPO 12 pS, GPO 11 S, and GPO 11 pS, were synthesized to explore the role of phosphorylation in peptide stability and its templating effect on biomineralization. The CD results indicated that the phosphorylation of Gly-pSer mutants reduces the stability of collagen peptides. SEM images revealed that phosphorylated peptides acted as templates, guiding the morphology of calcium carbonate into either olive-like or spherical structures, depending on their conformational state of the peptides. Non-phosphorylated peptides maintained a calcite crystal structure. The XRD patterns predominantly exhibited peaks associated with calcite and vaterite for GPO 13 pS-CaCO 3 , GPO 12 pS-CaCO 3 , and GPO 11 pS-CaCO 3 , and peaks associated with calcite for GPO 13 S-CaCO 3 , GPO 12 S-CaCO 3 , and GPO 11 S-CaCO 3 , indicating a transformation of mesocrystals influenced by peptide phosphorylation. Our findings elucidate the crucial role of phosphorylated collagen peptides in mediating biomineralization morphology and polymorph selection, offering insights into the complex pathophysiology of OI.

Thrombosis and intimal hyperplasia (IH) are the main factors affecting the long-term patency of small-diameter vascular grafts (SDVGs). Fabricating a confluent endothelial cell (EC) layer on surfaces with physiological elasticity to mimic vascular endothelium should be an effective strategy to prevent restenosis that is caused by thrombosis and IH. However, the vascular endothelialization process is time-consuming and always constrained by hemocompatibility of the vascular grafts, since excellent hemocompatibility could guarantee a sufficient time window for the endothelialization process. Tetramethylpyrazine (TMP)-derived polyurethane (PU) with improved hemocompatibility and accelerated endothelialization ability is synthesized by incorporating TMP moieties into PU backbones. Results show that TMP-contained PU films possess improved hemocompatibility by down-regulating platelet adhesion/activation and increasing the clotting time. Furthermore, the in vitro human umbilical vein endothelial cell (HUVEC) test demonstrates that the introduction of TMP can significantly promote HUVEC adhesion and proliferation, and thus accelerate luminal endothelialization of vascular grafts. Moreover, the TMP-containing PU films exhibit excellent biocompatibility especially for HUVECs, and their excellent, adjustable elasticity (1123%) guarantees compliance accommodation of vascular grafts. This newly synthesized TMP-containing material with multiple biological functions is expected to make up for the shortcomings of available SDVGs in clinical practice, and has significant potential in improving the long-term patency of SDVGs.

Excess free radicals can have some negative effects on human health. In this paper, a nanozyme was successfully constructed by the coordination of copper ions and tannic acid, and its structure and elemental distribution were determined by Fourier transform infrared spectroscopy, scanning electron microscopy and X-ray photoelectron spectroscopy. Free radical scavenging experiments confirmed that it possessed superoxide dismutase-like activity, catalase-like activity, and hydroxyl radical scavenging ability. The results of thermogravimetric analysis experiments demonstrated that it possessed good thermal stability. A polyacrylonitrile hybrid nanofibrous membrane loaded with Cu/TA nanozyme was successfully constructed by electrospinning technology, and the maximum scavenging rate of DPPH and ABTS radicals can reach 64.22% and 58.44%, respectively. The nanofiber membrane also exhibited the ability to protect cells from oxidative stress damage. Therefore, the hybrid nanofibrous membrane has a broad application prospect in fields such as food preservation and biomedicine., Competing Interests: The authors declare that they have no conflict of interest., (This journal is © The Royal Society of Chemistry.)

Polymer-based ultralong room temperature phosphorescence (RTP) is more attractive than that of organic small molecules. However, the intrinsic contradictions between the motion of the chain and the stability of phosphors' triplet excitons make achieving ultralong lifetime in polymeric systems a big challenge. Herein, we have achieved ultralong RTP emission in a polymeric viscous flow state with free chain motion through a facile B-O click reaction among boric acid, polyvinyl alcohol, and hydroxyl silicone oil. The yielded RTP putties (RTPPs) exhibited long lifetimes under ambient conditions (up to 2.39 s), surpassing those of all reported elastic RTP polymers and most glassy RTP polymers. Furthermore, multi-color afterglow can be achieved in RTPPs using the triplet-to-singlet Förster resonance energy transfer strategy. Impressively, utilizing viscous liquid features combined with RTP performance, RTPPs can be easily applied in complex models, handiwork, and anti-counterfeiting. Therefore, this progress, achieving a long phosphorescence lifetime in a viscous flow state, greatly expands the application scope of polymeric RTP materials and further compels a conceptual advance of polymeric RTP.

Salt-free reductants have been extensively studied in the plutonium uranium reduction extraction (PUREX) process for Np(VI) reduction. Hydroxylamine derivatives as a class of promising salt-free reductants can reduce Np(VI) to Np(V) in nitric acid solution. The reduction reaction and kinetic behavior of Np(VI) to Np(V) by diethylhydroxylamine (DEHA) were studied experimentally. Herein, we explored the reduction mechanism of Np(VI) by DEHA in aqueous solution using scalar-relativistic density functional theory. Four stages are included in the process of Np(VI) reduction to Np(V) by DEHA. The intermediate C 2 H 5 N(O)C 2 H 4 is hydrolyzed to C 2 H 5 NHOH. The third and fourth stages of Np(VI) reduction are via two pathways due to different H atoms participating successively in the reduction process. The largest energy barrier for the four Np(VI) reduction processes is 12.3 kcal mol -1 for the third stage of Pathway I, consistent with the experimental observations. The Np-O yl bond distances and spin density on Np elucidate the reduction essence including outer-sphere electron transfer or hydrogen atom transfer. The analyses of bonding nature reveal the bonding evolution during the reduction process. This work elucidates the reduction mechanism of Np(VI) by DEHA and provides new insights into the reduction of Np(VI) by hydroxylamine derivatives.

Enantioenriched small carbocycles are key structures in numerous natural products and pharmaceutically important molecules as well as vital intermediates in organic synthesis. Although various catalytic approaches for the construction of such molecules from acyclic precursors have been developed, direct enantioselective functionalization of preformed three-membered and four-membered rings represents the most straightforward and modular strategy, enabling rapid and diversified synthesis of enantioenriched cyclopropanes and cyclobutanes from a single set of starting materials without the need for the incorporation of specific functional groups. In this Feature Article, we have summarized the recent advances in catalytic enantioselective functionalization of cyclopropenes and cyclobutenes through carbometallation. The plausible mechanisms of such reactions and future of this field are also discussed.

Titanium dioxide (TiO 2 ) is an exceptional compound with unique optical properties, which have been intensively used for applications in photocatalysis. Recent studies show that Cu 5 atomic quantum clusters (AQCs) could facilitate visible light absorption and enhance the photocatalytic properties of rutile TiO 2 by creating mid-gap states. In this work, to move the theory of these catalysts closer to the experiment, we investigate the electronic structures of Cu 5 adsorbed on a perfect and reduced rutile TiO 2 surface in the absence and presence of silicate SiO 3 2- ions, which are introduced for the purification of Cu 5 AQCs. Encouragingly, our DFT simulations predict that the presence of SiO 3 2- does not reduce the gap states of the Cu 5 @TiO 2 composite and could even enhance them by shifting more states into the band gap. Our results also demonstrate that the polarons created by oxygen vacancies (O v ) and Cu 5 coexist within the band gap of TiO 2 . Indeed an O v behaves like a negative gate on the electronic states located on the AQCs, thereby shifting states out of the valence band into the band gap, which could lead to enhanced photocatalytic performance.

A fluorescence method has been successfully constructed to accurately measure the D/L-Arb configuration content in optical isomers, and its application in ion detection has been expanded, which has greater sensitivity and universality than the circular dichroism (CD) method. It also promotes the study of the emission mechanism of nonconventional luminogens.

The processes of apoptosis and inflammatory responses, which are defensive strategies used by cells to confront external substances, can give rise to diverse diseases when prolonged or disrupted, such as cancer, Alzheimer's disease, and Parkinson's disease. Here we engineered a live-cell imaging fluorescent probe for nitric oxide (NO) based on naphthalimide and o -phenylenediamine, enabling the sensitive detection of NO in cancer cells and thereby live-monitoring of the doxorubicin-induced apoptosis and lipopolysaccharide-triggered inflammation reactions. Importantly, we found that the level of released NO can sensitively indicate the early stages of both cellular inflammatory responses and apoptotic processes. This suggested that cellular NO in fact behaves as a new class of signaling molecule for inflammatory responses and apoptosis processes, providing a potent tool for live-monitoring cellular physiological reactions.

Luteolin (LUT), a natural flavonoid known for its hypoglycemic properties, is primarily sourced from vegetables such as celery and broccoli. However, its poor stability and low bioavailability in the upper digestive tract hinder its application in the functional food industry. To address these challenges, this study employed porous starch (PS) as a carrier to develop PS microspheres loaded with luteolin (PSLUT), simulating its release in vitro . The research assessed the hypoglycemic effects of LUT in type 2 diabetes mellitus (T2DM) mice both before and after PS treatment. In vitro findings demonstrated that PS improved LUT's stability in simulated gastric fluids and enhanced its in vivo bioavailability, aligning with experimental outcomes. PSLUT administration significantly improved body weight, fasting blood glucose (FBG), oral glucose tolerance test (OGTT), pancreatic islet function, and other relevant indicators in T2DM mice. Moreover, PSLUT alleviated abnormal liver biochemical indicators and liver tissue injury caused by T2DM. The underlying hypoglycemic mechanism of PSLUT is thought to involve the regulation of protein kinase B (AKT-1) and glucose transporter 2 (GLUT-2). After four weeks of intervention, various PSLUT doses significantly reduced the Firmicutes to Bacteroidetes ratio at the phylum level and decreased the relative abundance of harmful bacteria at the genus level, including Acetatifactor , Candidatus-Arthromitus , and Turicibacter . This microbial shift was associated with improvements in hyperglycemia-related indicators such as FBG, the area under the curve (AUC) of OGTT, and homeostasis model assessment of insulin resistance (HOMA-IR), which are closely linked to these bacterial genera. Additionally, Lachnoclostridium , Parasutterella , Turicibacter , and Papillibacter were identified as key intestinal marker genera involved in T2DM progression through Spearman correlation analysis. In conclusion, PS enhanced LUT's hypoglycemic efficacy by modulating the transcription and protein expression levels of AKT-1 and GLUT-2, as well as the relative abundance of potential gut pathogens in T2DM mice. These results provide a theoretical foundation for advancing luteolin's application in the functional food industry and further investigating its hypoglycemic potential.

Herein, MoS 2 quantum dots (QDs) are constructed to serve as electrolyte additives for lithium-sulfur batteries, which can 'solidify' soluble polysulfides by chemisorption and promote sulfur conversion chemistry by electrocatalysis. The Li-S cell with MoS 2 QDs shows high retained capacity and high-rate capability, much better than the counterpart without MoS 2 QDs.

The development of novel narrow-band emitting phosphors with high efficiency and stability is of great significance for WLED backlights. In recent years, the research on Bi 3+ -activated narrow-band emitting phosphors has gained significant attention for developing novel phosphors for WLED backlight applications. This Frontiers article presents recent advances in Bi 3+ -activated narrow-band emitting phosphors, encompassing their coordination environment and photoluminescence properties. The latest advancements in Bi 3+ -activated narrow-band emitting phosphors are categorized into four types based on host materials: germanate, silicate, borate, and other hosts. Additionally, detailed discussions are provided on the challenges associated with developing novel Bi 3+ -activated narrow-band emitting phosphors and potential research directions for future work. Overall, the Bi 3+ -activated narrow-band emitting phosphors have demonstrated great potential for WLED backlights; however, significant efforts are still required to enhance their comprehensive performance in order to meet practical application requirements.

Quinones represent a class of crude organic compounds ubiquitously distributed in nature. Their distinctive quinone-type structure confers upon them unique properties and applications. Quinones demonstrate significant biological activities, including antioxidant, antimicrobial, and antitumor properties. Additionally, they demonstrate noteworthy physicochemical characteristics, including excellent dyeing properties and stability. Given their diverse qualities, quinones hold significant promise for applications in industrial manufacturing, healthcare, and food production, thus garnering considerable attention in recent years. While there is a growing body of research on quinones, the existing literature falls short of providing a comprehensive review encompassing recent advancements in this field along with established knowledge. This paper offers a comprehensive review of research progress for quinones, encompassing structural classification, source synthesis, extraction methods, properties, functions, and specific applications. It serves as a reference and theoretical foundation for the further development and utilization of quinones.

Formation of bacterial films on structural surfaces often leads to severe contamination of medical devices, hospital equipment, implant materials, etc. , and antimicrobial resistance of microorganisms has indeed become a global health issue. Therefore, effective therapies for controlling infectious and pathogenic bacteria are urgently needed. Being a promising active method for this purpose, surface acoustic waves (SAWs) have merits such as nanoscale earthquake-like vibration/agitation/radiation, acoustic streaming induced circulations, and localised acoustic heating effect in liquids. However, only a few studies have explored controlling bacterial growth and inactivation behaviour using SAWs. In this study, we proposed utilising piezoelectric thin film-based SAW devices on a silicon substrate for controlling bacterial growth and inactivation with and without using ZnO micro/nanostructures. Effects of SAW powers on bacterial growth for two types of bacteria, i.e. , E. coli and S. aureus , were evaluated. Varied concentrations of ZnO tetrapods were also added into the bacterial culture to study their effects and the combined antimicrobial effects along with SAW agitation. Our results showed that when the SAW power was below a threshold ( e.g. , about 2.55 W in this study), the bacterial growth was apparently enhanced, whereas the further increase of SAW power to a high power caused inactivation of bacteria. Combination of thin film SAWs with ZnO tetrapods led to significantly decreased growth or inactivation for both E. coli and S. aureus , revealing their effectiveness for antimicrobial treatment. Mechanisms and effects of SAW interactions with bacterial solutions and ZnO tetrapods have been systematically discussed.

The twist fusion of a benzothiophene group and the introduction of a 4-methyloxystyryl donor group to the BODIPY core resulted in large spin-orbit coupling values and smaller singlet-triplet energy gaps for the novel infrared absorbed photosensitizers named BSBDP. They show a high reactive oxygen species efficiency exceeding 69% and a fluorescence quantum yield of 23% and are successfully applied in imaging-guided photodynamic therapy in vitro and in vivo .

The discovery and designed synthesis of multifunctional materials is a leading pursuit in materials science. Herein, we report a novel hydro-isocyanurate, N 2 H 4 Zn(HC 3 N 3 O 3 ), which combines strong second harmonic generation (SHG) and ultra-long room-temperature phosphorescence (RTP). The SHG intensity is the highest within the cyanurate system (13 × KDP), and RTP lifetime extends up to 448 ms, accompanied by a long-lasting afterglow visible to the naked eye for 1.2 s, surpassing most of the current metal-organic complexes. This advancement holds promise for the development of multifunctional optoelectronic devices, particularly leveraging second-harmonic generation (SHG) processes., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The pancreatic tumor microenvironment presents multiple obstacles for polymer-based drug delivery systems, limiting tumor penetration and treatment efficacy. Here, we engineer a hyaluronidase/reactive oxygen species cascade-responsive size/charge bidirectional-tunable nanodelivery (btND, G/R@TKP/HA) for co-delivery of gemcitabine and KRAS siRNA, capable of navigating through tumor barriers and augmenting anticancer efficiency. When penetrating the tumor stroma barrier, the hyaluronic acid shell of the nanodelivery undergoes degradation by hyaluronidase in an extracellular matrix, triggering size tuning from large to small and charge tuning from negative to positive, thereby facilitating deeper penetration and cellular internalization. After endocytosis, the nanodelivery protonizes in the endo/lysosome, prompting rapid endo/lysosomal escape, effectively overcoming the lysosome barrier. Intracellular ROS further disrupt the nanodelivery, inducing its size tuning again from small to large and a positive charge decrease for high tumor retention and controlled drug release. The btND shows remarkable antitumor activity in pancreatic cancer mouse models, highlighting the efficacy of this approach in penetrating tumor barriers and enhancing anticancer outcomes., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

Two-dimensional (2D) materials have drawn tremendous interest as promising materials for photoelectric devices due to their extraordinary properties. As an outstanding 2D photoelectric material, Bi 2 O 2 Se (BOS) has exhibited good performance and great potential in photoelectric applications. In this report, we have constructed a photoelectric heterojunction based on BOS and CuInP 2 S 6 (CIPS) nanosheets to achieve enhanced photoelectric performance. With modulation of the ferroelectric-polarization-induced built-in electric field in CIPS, the photogenerated carriers in BOS are effectively separated to form a stable current that is independent of the applied voltage, so that the photoelectric performance of the heterojunction is significantly improved. The photoresponsivity ( R ), external quantum efficiency (EQE), and normalized detectivity ( D *) are calculated and analyzed to evaluate the photodetection performance of the heterojunction. Results demonstrate excellent photoelectric performance of BOS/CIPS heterojunction under irradiation of light from ultraviolet (365 nm), visible (405/550/650 nm) to near-infrared (980 nm). R , EQE, and D * are up to 338.94 A W -1 , 7.65 × 10 4 %, and 3.99 × 10 10 Jones, respectively, under the condition of 550 nm and 0.24 W m -2 . Meanwhile, the measured rise and fall times of the heterojunction reach 2.74 and 4.82 ms, respectively, indicating its fast photoelectric response. This work provides an effective approach to enhance the photoelectric response and stability of BOS via the ferroelectric-polarization-induced built-in electric field of CIPS.

This work deals with the fabrication of lignin containing cellulose nanofiber (LCNF)/Ag 2 Se films for thermoelectric applications. Ag 2 Se nanoparticles were synthesized within the LCNF network through in situ methods, employing Na 2 SeO 3 and AgNO 3 along with microwave energy treatment. LCNF/Ag 2 Se films fabricated with two LCNF : Ag 2 Se weight percent ratios ( i.e. , 50 : 50 and 30 : 70) were used to construct a flexible thermoelectric module. The obtained Ag 2 Se nanoparticles displayed a uniform size distribution in the LCNF network with smaller dimensions from the microwave energy treated group. The microstructure of LCNF/Ag 2 Se films was improved by hot-pressing, leading to enhanced film density thermoelectric properties. At a differential temperature of 50 K, films with 50% and 70% of Ag 2 Se exhibited output voltages of 18 and 21 mV; and Seebeck coefficients of -60 and -70 μV K -1 at 350 K, respectively. When microwave energy was applied, the films at 50% and 70% Ag 2 Se showed highest output voltages of 19 and 33 mV, respectively, and Seebeck coefficients of -63.3 and -110 μV K -1 at 350 K. The low-cost fabrication process associated with this module opens a pathway for applications such as energy harvesting., Competing Interests: No conflicts require declaration., (This journal is © The Royal Society of Chemistry.)

Walnut peptide, a low molecular weight peptide separated from walnuts by enzymatic hydrolysis, is considered as a potential nutraceutical with a variety of biological activities. In this study, we characterized the walnut peptide prepared by alkaline protease hydrolysis and evaluated its neuroprotective effect in zebrafish and rat models of memory disorders. Series of concentrations of the walnut peptide were orally administered to zebrafish and rats to examine its impact on the behavior and biochemical indicators. The results showed that the oral administration of walnut peptide significantly ameliorated the behavioral performance in zebrafish exposed to bisphenol AF (1 μg mL -1 ) and rats exposed to alcohol (30% ethanol, 10 mL kg -1 ). Furthermore, the walnut peptide upregulated the expression of neurotrophic-related molecules in zebrafish, such as the brain-derived neurotrophic factor (BDNF) and the glial cell-derived neurotrophic factor (GDNF). In the rat brain, the walnut peptide increased the activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px), while dramatically reduced malondialdehyde (MDA) level. Together, these findings elucidated that the walnut peptide might partially offset the declarative memory deficits via regulation of neurotrophic-related molecule expression and promotion of the antioxidant defense ability. Therefore, walnut peptide holds the potential for development into functional foods as a nutritional supplement for the management of certain neurodegenerative disorders.

Electrocatalytic water splitting is a promising production method for green hydrogen; however, its practical application is limited by the lack of robust catalysts for the cathode hydrogen evolution reaction (HER). Recently, the use of Ru in electrocatalytic HER has become a research hotspot because Ru has a metal-hydrogen bond strength similar to that of Pt - known for its excellent HER activity - but has a lower cost than Pt. Numerous modification strategies are available to further improve the HER activity of metal Ru such as vulcanisation, phosphating and atomisation. The atomisation strategy has attracted much attention owing to its extremely high Ru atomic utilisation efficiency and tunable electronic structures. However, isolated studies could not effectively address the bottlenecks. Therefore, to promote the effective exploration of Ru-based single-atom catalysts and clarify the research status in this field, studies on related topics ( e.g. Ru single-atom catalysts, Ru dual-atom catalysts, composite catalysts containing single-atom Ru and Ru nanoparticles) have been systematically and briefly summarised herein. Finally, the research challenges and prospects of Ru-based single-atom catalysts in the HER field have been discussed, which may provide valuable insights for further research.

Uranium is considered as a very important nuclear energy material because of the huge amount of energy it releases. As the main product of the spontaneous decay of uranium, it is difficult for helium to react with uranium because of its chemical inertness. Therefore, bubbles will be formed inside uranium, which could greatly reduce the performance of uranium or cause safety problems. Additionally, nuclear materials are usually operated in an environment of high-temperature and high-pressure, so it is necessary to figure out the exact state of helium inside uranium under extreme conditions. Here, we explored the structural stability of the U-He system under high pressure and high temperature by using density functional theory calculations. Two metastable phases are found between 50 and 400 GPa: U 4 He with space group Fmmm and U 6 He with space group P 1̄. Both are metallic and adopt layered structures. Electron localization function calculation combined with charge density difference analysis indicates that there are covalent bonds between U and U atoms in both Fmmm -U 4 He and P 1̄-U 6 He. Regarding the elastic modulus of α-U, the addition of helium has certain influence on the mechanical properties of uranium. Besides, first-principles molecular dynamics simulations were carried out to study the dynamical behavior of Fmmm -U 4 He and P 1̄-U 6 He at high-temperature. It was found that Fmmm -U 4 He and P 1̄-U 6 He undergo one-dimensional superionic phase transitions at 150 GPa. Our study revealed the exotic structure of U-He compounds beyond the formation of bubbles under high-pressure and high-temperature, which might be relevant to the performance and safety issues of nuclear materials under extreme conditions.

We report an ionogel with thermo-switchable conductivity and high processability based on physical self-assembly of poly(styrene- b -ethylene oxide- b -styrene) (PS-PEO-PS) in mixed ionic liquids composed of thermo-responsive 1,3-dimethylimidazolium bis(trifluoromethanesulfonyl)imide and polymerizable 1-(4-vinylbenzyl)-3-butylimidazolium bis(trifluoromethylsulfonyl)imide, and subsequent chemical crosslinking of the polymerizable component.

The advancement of anode materials for achieving high energy storage is a crucial topic for high-performance Li-ion batteries (LIBs). Here, first-principles calculations were used to conduct a thorough and systematic investigation into lithium storage properties of MXenes with new S functional groups as LIB anode materials. Density of states, diffusion energy barriers, open circuit voltages and storage capacities were calculated to comprehensively evaluate the lithium storage properties of S-functionalized MXenes. Based on the computational results, Ti 2 CS 2 and V 2 CS 2 were selected as excellent candidates from ten M 2 CS 2 MXenes. The diffusion energy barriers of M 2 CS 2 within the range of 0.26-0.32 eV are lower than those of M 2 CO 2 and M 2 CF 2 , indicating that M 2 CS 2 anodes exhibit faster charge/discharge rates. By examining the stable crystal structures and comparing atomic positions before and after Li adsorptions, structural phase transitions during Li-ion adsorptions could happen for nearly all M 2 CS 2 MXenes. The phase transitions predicted were directly observed using ab initio molecular dynamic simulations. The cycle stability, storage capacity and other lithium storage properties were enhanced by the reversible structural phase transition.

Solution plasma-Co(OH) 2 interaction significantly boosts nitrogen fixation and achieves a high concentration of NO x - at 9.42 mmol L -1 . This surpasses the nitrogen content requirement of 7.67 mmol L -1 for commercial nutrient solutions, offering a sustainable approach for nitrogen fixation from nitrogen, water and electricity.

With the widespread use of electronic goods, solving electromagnetic pollution has become one of the new challenges. Higher requirements for microwave-absorbing materials (MAM) have emerged to address this issue. The composite of carbon nanofiber (CNF) and magnetic nanoparticles is the material that effectively absorbs microwaves. This paper fabricated Ni/C nanofibers using a combination of electrospinning and high-temperature carbonization. With 50 wt% paraffin wax, Ni/C nanofibers demonstrated optimal microwave absorption capabilities. With a thickness of 3 mm, the minimum RL value can reach -30.6 dB, and the effective absorption bandwidth is 5.96 GHz. By encapsulating Ni nanoparticles in carbon nanofibers, the synergic interaction of dielectric and magnetic losses effectively meets the need for constant attenuation and impedance matching, and effectively improves microwave-absorbing properties. Hence, Ni/C nanofibers are promising for MAM application with excellent MA performance., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Several major roadblocks, including the "shuttle effect" caused by the dissolved higher-order sodium polysulfides (NaPSs), extremely poor conductivity of sulfur cathodes, and sluggish conversion kinetics of charging-discharging reactions, have hindered the commercialization of sodium-sulfur batteries (NaSBs). In our study, representative C 2 N-based single-atom catalysts (SACs), TM@C 2 N (TM = Fe, Ni and V), are proposed to improve the comprehensive performance of NaSBs. Based on first-principles calculations, we first discuss in detail the anchoring behavior of all adsorption systems, TM@C 2 N/(S 8 and NaPSs). The results indicate that compared to pristine C 2 N, TM@C 2 N substrates exhibit a stronger capability to capture S 8 /NaPSs clusters through physical/chemical binding, with V@C 2 N showing the most outstanding capability ranging from -2.37 to -5.03 eV. The density of states analysis reveals that metallic properties can be well maintained before and after adsorption of polysulfides. More importantly, TM@C 2 N configurations can greatly reduce the energy barriers of charging and discharging reactions, thereby accelerating the conversion efficiency of NaSBs. It is worth mentioning that V@C 2 N has lower charge-discharge energy barriers and Na ion migration rates, since the embedded TM atom weakens the strong binding of Na + in the N 6 cavity of C 2 N. The intrinsic mechanism analysis reveals that the interaction between the d orbitals of V and the p orbitals of S leads to the weakening of Na-S bonds, which can not only effectively inhibit the shuttle effect, but also promote the dissociation of Na 2 S. Overall, this work not only offers excellent catalytic materials, but also provides vital guidance for designing SACs in NaSBs.

Three new distinct NIR α,α-NH-bridged BODIPY dimers were prepared by a direct nucleophilic substitution reaction. The synergistic effects of the nitrogen bridges and strong excitonic coupling between each BODIPY unit play major roles in enhancing the delocalization of an electron spin over the entire BODIPY dimers. The in situ formed aminyl radical dimer showed an absorption maximum at 1040 nm.

Hydrogel-based flexible electronic devices serve as a next-generation bridge for human-machine interaction and find extensive applications in clinical therapy, military equipment, and wearable devices. However, the mechanical mismatch between hydrogels and human tissues, coupled with the failure of conformal interfaces, hinders the transmission of information between living organisms and flexible devices, which resulted in the instability and low fidelity of signals, especially in the acquisition of electromyographic (EMG) and electrocardiographic (ECG) signals. In this study, we designed an ion-conductive hydrogel (ICHgel) utilizing multiple physical interactions, successfully applied for human motion monitoring and the collection of epidermal physiological signals. By incorporating fumed silica (F-SiO 2 ) nanoparticles and calcium chloride into an interpenetrating network (IPN) composed of polyvinyl alcohol (PVA) and polyacrylamide (AAm)/acrylic acid (AA) chains, the ICHgel exhibited exceptional tunable stretchability (>1450% strain) and conductivity (10.58 ± 0.85 S m -1 ). Additionally, the outstanding adhesion of the ICHgel proved to be a critical factor for effective communication between epidermal tissues and flexible devices. Demonstrating its capability to acquire stable electromechanical signals, the ICHgel was attached to different parts of the human body. More importantly, as a flexible electrode, the ICHgel outperformed commercial Ag/AgCl electrodes in the collection of ECG and EMG signals. In summary, the synthesized ICHgel with its outstanding conformal interface capabilities and mechanical adaptability paves the way for enhanced human-machine interaction, fostering the development of flexible electronic devices.

The ocean ecological environments are seriously affected by oil spilling and plastic-debris, preventing and significantly reducing marine pollution via using biocomposite production from natural fiber reinforcement is a more friendly way to deal with marine oil pollution. Herein, we upcycled coir-coconut into lignin and coconut shell into spherical TENG by a combination of dip-dry and chemical treatment and used the SiO 2 nanoparticles together with cellulose nanofibrils to prepare serial sugar-templated, anisotropic and hybrid foams. The as-prepared lignin/SiO 2 porous sponge (LSPS) with a hierarchical porous morphology and uniformly dispersed nanoparticles structure benefits from the advantages of biomass-based additives, which presents reversible large-strain deformation (50%) and high compressive strength (11.42 kpa). Notably, the LSPS was significantly more hydrophobic (WCA ≈150°) than pure silicone-based foams, and its selective absorbability can separate oil from water under continuous pumping. Meanwhile, the coconut husk was also upcycled as a spherical TENG shell by a combination of the nanofiber-enhanced polymer spherical oscillator (CESO), which possessed high triboelectric properties ( U oc = 272 V, I sc = 14.5 μA, Q = 70 nC) and was comparable to the plastic shell TENG at low frequency (1.6 Hz). The monolithic foam structure developed using this clean synthetic strategy holds considerable promise for new applications in sustainable petroleum contamination remediation., Competing Interests: The authors declare no competing financial interest., (This journal is © The Royal Society of Chemistry.)

Copper oxides are promising photocathode materials for solar hydrogen production due to their narrow optical band gap energy allowing broad visible light absorption. However, they suffer from severe photocorrosion upon illumination, mainly due to copper reduction. Nanostructuring has been proven to enhance the photoresponse of CuO photocathodes; however, there is a lack of precise structural control on the nanoscale upon sol-gel synthesis and calcination for achieving optically transparent CuO thin film photoabsorbers. In this study, nanoporous and nanocrystalline CuO networks were prepared by a soft-templating and dip-coating method utilizing poly(ethylene oxide)- block -poly(propylene oxide)- block -poly(ethylene oxide) (Pluronic® F-127) as a structure-directing agent, resulting for the first-time in uniformly structured, crack-free, and optically transparent CuO thin films. The photoelectrochemical properties of the nanoporous CuO frameworks were investigated as a function of the calcination temperature and film thickness, revealing important information about the photocurrent, photostability, and photovoltage. Based on surface photovoltage spectroscopy (SPV), the films are p-type and generate up to 60 mV photovoltage at 2.0 eV (0.050 mW cm -2 ) irradiation for the film annealed at 750 °C. For these high annealing temperatures, the nanocrystalline domains in the thin film structure are more developed, resulting in improved electronic quality. In aqueous electrolytes with or without methyl viologen (as a fast electron acceptor), CuO films show cathodic photocurrents of up to -2.4 mA cm -2 at 0.32 V vs. RHE (air mass (AM) 1.5). However, the photocurrents were found to be entirely due to photocorrosion of the films and decay to near zero over the course of 20 min under AM 1.5 illumination. These fundamental results on the structural and morphological development upon calcination provide a direction and show the necessity for further (surface) treatment of sol-gel derived CuO photocathodes for photoelectrochemical applications. The study demonstrates how to control the size of nanopores starting from mesopore formation at 400 °C to the evolution of macroporous frameworks at 750 °C., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

A photochemical synthesis of enol ethers and furan-3(2 H )-ones from 1,3-dicarbonyl compounds and aryl diazoacetates has been developed. Significantly, 1,4-dioxane promoted O -alkylation of various 1,3-dicarbonyl compounds beyond previous carbene insertion into C-H and C-C bonds has been disclosed.

A concise and collective synthetic route to hypocretenolides was developed for the first time. This route features one-pot addition-alkylation and intramolecular 1,3-dipolar cycloaddition to efficiently assemble the 5/7/6 ring system. Our syntheses enabled multigram preparation of hypocretenolide which facilitated further biological evaluation. Preliminary CCK-8 cytotoxic results of hypocretenolide indicated its IC 50 values within 1 μM against 4 colon cancer cell lines. Wound healing and transwell assays suggested the promising inhibitory activities of hypocretenolide toward the migratory capabilities of colon cancer cells in vitro . The animal results confirmed that hypocretenolide can inhibit metastasis of colon cancer cells., Competing Interests: The authors declare no competing financial interest., (This journal is © The Royal Society of Chemistry.)

A DMP-initiated metal-free effective β,γ-asymmetric spirocyclopropanation of propanols strategy using oxidative iminium activation is described. This process has been realized by a synergistic amine-catalyzed one-pot cascade oxidation-Michael addition cyclopropanation for "one-pot" access to various spirocyclopropyl propionaldehydes/propanols from diverse 3-arylpropanols and α-brominated active methylene compounds under mild conditions and with high enantioselectivity (ee up to >99%).

Selective electrooxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) is of great significance in the manufacture of fine chemicals, liquid fuels, pharmaceuticals, plastics, etc. , but still suffers from the high potential input, resulting in high electricity consumption. Developing active, low-cost and stable electrocatalysts is crucial for this electrochemical reaction at low working potentials. Herein, a three-dimensional (3D) hierarchical Cu(OH) 2 @Ni 3 Co 1 -layered double hydroxide architecture with abundant oxygen vacancies (Vo) was synthesized by facile electrodeposition of Ni 3 Co 1 -LDH nanosheets on copper foam (CF) supported-Cu(OH) 2 nanorods (CF/Cu(OH) 2 @Ni 3 Co 1 -LDH) for the selective electrooxidation of HMF to FDCA. The 3D hierarchical architecture of the Cu(OH) 2 nanorod core loaded with Ni 3 Co 1 -LDH nanosheet shell facilitates the rapid transfer of charges and exposes more active sites. The synergistic effect of the core-shell nanoarray structure, atomic level dispersion of Ni and Co on LDH laminates, and rich Vo gives 98.12% conversion of HMF, 98.64% yield and 91.71% selectivity for FDCA at a low working potential of 1.0 V vs. RHE. In addition, CF/Cu(OH) 2 @Ni 3 Co 1 -LDH exhibits superior stability by maintaining 93.26% conversion of HMF, 93.65% yield and 91.57% selectivity of FDCA after eight successive cycles, showing the immense potential of utilizing electrochemical conversion for biomass., Competing Interests: The authors declare no conflict of interest., (This journal is © The Royal Society of Chemistry.)

The electrochemical performance of lithium-ion batteries (LIBs) is plagued by sluggish interfacial kinetics. Fortunately, the Li + solvation structure bridges the bulk electrolyte and interfacial chemistry, providing a pathway for promoting electrochemical kinetics in LIBs. Herein, we improve the interfacial kinetics by tuning the Li + coordination chemistry based on solvent molecular engineering. Specifically, 4-fluorobenzyl cyanide (FBCN), featuring steric hindrance and a weak Lewis basic center, is designed to construct a bulky coordination structure with Li + , weakening ion-dipole interaction (Li + -solvents) but promoting coulombic attraction (Li + -anions) at a normal Li salt concentration. This sterically-controlled solvation chemistry reduces the interfacial barrier and thus contributes to improved rate performance, as demonstrated practically in LiFePO 4 //graphite pouch cells. This study provides fresh insights into solvent steric control and coordination chemistry engineering, opening a new avenue for enhancing electrochemical kinetics in LIBs., Competing Interests: The authors declare no competing financial interests., (This journal is © The Royal Society of Chemistry.)

To bring about a revolution in energy storage through Li-ion batteries, it is crucial to develop a scalable preparation method for Si-based composite anodes. However, the severe volume expansion and poor ionic transport properties of Si-based composites present significant challenges. Previous research focused on SiO and nano Si/C composites to address these issues. In this study, mechanical milling was used to introduce a SiO x layer onto the surface of Si by mixing Si and SiO 2 in a 1 : 1 mass ratio. The resulting Si+SiO 2 composites (denoted as SS50) exhibited an initial coulombic efficiency (ICE) of 73.5% and high rate performance. To further stabilize the overall structure, kerosene was introduced as a carbon source precursor to generate a coating layer. The resulting multiphase composite structure (SiO x +SiO 2 +C), designated as SS50-900C, demonstrated a capacity retention of 79.5% over 280 cycles at its capacity of 487 mA h g -1 . These results suggest that a cost-effective mechanical ball milling refinement of Si+SiO 2 and a gas-phase encapsulation process can significantly improve the electrochemical performance of Si-based composites.

Despite extensive research on the photoluminescence properties of Bi 3+ ions, the origins of their emission and excitation bands remain elusive. Herein, we present a comprehensive analysis of the photoluminescence properties of Bi 3+ -activated LuXnGaO 4 (Xn = Mg, Zn), elucidating the underlying factors governing the intra-ionic and extra-ionic electronic transitions. By integrating crystal structure data and spectroscopic data analyses with semi-empirical formula calculations, the origins of excitation and emission states were elucidated. Moreover, the impact of alterations in chemical surroundings on the luminescence of Bi 3+ was investigated. Both LuXnGaO 4 :Bi 3+ phosphors exhibit three excitation peaks in the near ultraviolet region and display a broadband yellow emission. However, the luminous behavior of LuMgGaO 4 :Bi 3+ and LuZnGaO 4 :Bi 3+ differs due to variations in the band gap, bond length and neighboring atoms. It is anticipated that the investigation of Bi 3+ -activated gallates presents a promising avenue for advancing wide-band and long-wavelength emitting phosphors.

Supramolecular polymers are usually thermomechanically unstable, as their mechanical strength decreases drastically upon heating, which is a fatal shortcoming for their application. Herein, inspired by heat shock proteins (HSPs) which enable living organisms to tolerate lethal high temperatures, we design an HSP-like response to impart a supramolecular elastomer with high thermomechanical stability. The HSP-like response relies on the reversible hydrolysis of boronic acid and the tunable association strength of boron dative bonds. As the temperature increases, the boronic acid dehydrates and transforms into boroxane. The boroxane, acting as a heat shock chemical, prevents the disintegration of the supramolecular network through formation of multiple and stronger dative bonds with imidazole-containing polymers, thereby enabling the material to retain its mechanical strength at high temperatures. Such chemical transformation and network change induced by the HSP-like response are fully reversible during the heating and cooling processes. Moreover, due to the dynamic nature of the supramolecular network, the elastomer possesses recycling and self-healing abilities.

Enantiopure α-substituted phosphonic acids are widely utilized as drugs, pesticides, and ligands. Despite numerous synthetic approaches having been investigated, precise construction of P -adjacent chiral tertiary carbon centres by the employment of recoverable chiral auxiliaries is traditional and still one of the most reliable and practical synthetic methodologies so far. Herein, we present a highly diastereoselective synthesis of α-substituted phosphonates via the unique CAMDOL-derived P-substrates by an efficient sequential deprotonation with LiHMDS and alkylation/arylation with RI. A wide range of 30 structurally diverse α-substituted phosphonate products, including the well-known P-analogues of naproxen and ibuprofen, were thus afforded conveniently in up to 92% yields and 99 : 1 diastereomeric ratios. The related chiral phosphonic acid could be easily obtained by simple acidic hydrolysis with fully recovered auxiliary. This CAMDOL-enabled asymmetric synthetic protocol exhibits comparative advantages over known chiral-induction methods with easy accessibility and compatibility of furnishing a variety of C-stereogenic centres in the proximity of the phosphorus atom, including some rare examples.

The porous structure of composite nanofibers plays a key role in improving their electrochemical performance. However, the dynamic evolution of pore structures and their action during ion intercalation/extraction processes for negative electrodes are not clear. Herein, porous carbon composite nanofibers (Fe@Fe 2 O 3 /PCNFs) were prepared as negative electrode materials for potassium-ion batteries. Electrochemical test findings revealed that the composites had good electrochemical characteristics, and the porous structure endowed composite electrodes with pseudo-capacitive behaviors. After 1500 discharge/charge cycles at a current density of 1000 mA g -1 , the specific capacity of the potassium-ion batteries was 144.8 mAh g -1 . We innovatively used synchrotron small-angle X-ray scattering (SAXS) technique to systematically investigate the kinetic process of potassium formation in composites and showed that the kinetic process of potassium reaction in composites can be divided into four stages, and the pores with smaller average diameter distribution are more sensitive to changes in the reaction process. This work paves a new way to study the deposition kinetics of potassium in porous materials, which facilitates the design of porous structures and realizes the development of alkali metal ion-anode materials with high energies.

Recent advances in bioelectronics in mechanical and electrophysiological signal detection are remarkable, but there are still limitations because they are inevitably affected by environmental noise and motion artifacts. Thus, we develop a gel damper-integrated crack sensor inspired by the vibration response of the viscoelastic cuticular pad and slit organs in a spider. Benefitting from the specific crack structure design, the sensor possesses excellent sensing behaviors, including a low detection limit (0.05% strain), ultrafast response ability (3.4 ms) and superior durability (>300 000 cycles). Such typical low-amplitude fast response properties allow the ability to accurately perceive vibration frequency and waveform. In addition, the gel damper exhibits frequency-dependent dynamic mechanical behavior that results in improved stability and reliability of signal acquisition by providing shock resistance and isolating external factors. They effectively attenuate external motion artifacts and low-frequency mechanical noise, resulting in cleaner and more reliable signal acquisition. When the gel damper is combined with the crack-based vibration sensor, the integrated sensor exhibits superior anti-interference capability and frequency selectivity, demonstrating its effectiveness in extracting genuine vocal vibration signals from raw voice recordings. The integration of damping materials with sensors offers an efficient approach to improving signal acquisition and signal quality in various applications.