Search

Nanozymes, as an emerging class of enzyme mimics, have attracted much attention due to their adjustable catalytic activity, low cost, easy modification, and good stability. Researchers have made great efforts in developing and applying high-performance nanozymes. Recently, transition-metal-based nanozymes have been designed and widely developed because they possess unique photoelectric properties and high enzyme-like catalytic activities. To highlight these achievements and help researchers to understand the research status of transition-metal-based nanozymes, the development of transition-metal-based nanozymes from material characteristics to biological applications is summarized. Herein, we focus on introducing six categories of transition-metal-based nanozymes and highlight their progress in biomarker sensing and catalytic therapy for tumors. We hope that this review can guide the further development of transition-metal-based nanozymes and promote their practical applications in cancer diagnosis and treatment. [ABSTRACT FROM AUTHOR]

Transition-metal-catalyzed asymmetric allylic substitution reactions represent a hot research topic in the field of asymmetric synthesis, with significant progress having been made. Among diverse catalysis systems, relay catalysis enables sequential activation of multiple steps in one pot and the rapid construction of multiple chiral centers, providing a simple and powerful platform for organic synthesis. Recently, relay catalysis has been successfully applied to asymmetric allylic substitution reactions, and a variety of challenging transformations have been realized. This Short Review summarizes the related progress on asymmetric allylic substitution reactions based on relay catalysis over the last decade. 1 Introduction 2 The General Transformation Model 3 Allylation Relays Further Reaction 4 Initial Reaction Relays Allylation 5 Conclusion and Outlook [ABSTRACT FROM AUTHOR]

Transition metal compounds (TMCs) are potentially fruitful substitutes for noble metals for electrocatalytic splitting of water due to their intrinsic electrocatalytic activity, modifiable morphology, tunable electronic structure and their earth‐abundance. The combination of TMCs with graphene improves the dispersion of loaded catalysts, providing more catalytic active sites, enhancing the conductivity of hybrids, affording accelerated charge‐transfer kinetics, and minimizing catalyst bleaching, aggregation, and sintering under harsh reaction conditions. Additionally, graphene incorporation into TMCs modulates the electronic structure of active centers because of the synergistic interaction between them, thereby improving their catalytic performance. This review paper focuses on the recent progress made in designing different graphene‐transition metal‐based materials that can be used in the hydrogen evolution reaction (HER), the oxygen evolution reaction (OER), and overall water splitting (OWS). In‐situ characterization methodologies and DFT calculations that facilitate catalyst development are discussed elaborately. Finally, the advancements made in the development of graphene‐supported transition metal compounds for use in a functional water electrolyzer have been explored. In conclusion, a few specific recommendations have been made about the current challenges related to the widespread production of effective HER/OER electrocatalysts for water electrolysis. [ABSTRACT FROM AUTHOR]

Platinum‐based halide perovskites exhibit promising optoelectronic properties along with merits of low‐temperature processing and stability. Current research on Pt halide perovskites is limited to 0D A2BX6 structure as the ABX3 3D structure is thermodynamically unstable. Herein, the study reports the stabilization of the ABX3 structure into a 2D layered phase, CsPtI3(DMSO), that is stable up to 181.5 °C. The 2D phase shows an excitonic peak at the absorption edge of 600 nm, indicating quantum confinement. It also exhibits a large Stokes shift due to intersystem crossing (ISC), with a quenched singlet excitonic fluorescence at 610 nm and strong triplet emission at 852 nm. Pt(II) co‐ordinates with dimethyl sulfoxide (DMSO) via σ‐donation of S lone‐pair electrons and π‐ back donation from Pt to S, stabilizing CsPtI3(DMSO) layered structure. The strong electronic interaction between DMSO and Pt(II) and orbital mixing lead to spin‐orbit‐coupling, facilitating ISC and singlet‐to‐triplet exciton energy transfer. The interaction of Pt and DMSO is further confirmed by addition of thioacetamide (TAA), a strong S‐donor, which retards the formation of 2D layered structure, and directly results in Cs2PtI6 and Pt. [ABSTRACT FROM AUTHOR]

Electrochemical water splitting, including the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), is a promising hydrogen production technology. However, in practice, the high overpotentials and sluggish reaction kinetics associated with the anode OER process are the major obstacles to the smooth progress of electrocatalytic water splitting. Amorphous electrocatalysts, a crucial family of functional materials, exhibit unexpected performance due to their special short‐range ordered and long‐range disordered atom arrangement, abundant defect sites and adjustable composition. To date, while numerous recent publications showcase promising results for transition metal‐based amorphous electrocatalysts, including amorphous metal phosphide and metal hydroxide electrocatalysts with remarkable HER and OER properties respectively, the utilization of single‐function HER or OER catalysts tends to augment system complexity for water electrolysis, thereby escalating the cost of hydrogen production. In this regard, amorphous HER/OER bifunctional electrocatalysts are desired. In this review, we summarize the recent development on transition metal‐based amorphous catalysts for electrochemical water splitting. The design strategies for constructing HER/OER bifunctional transition‐metal‐based amorphous electrocatalysts are highlighted here, also including the exploration of relationship between catalyst structures and their remarkably improved performance. Finally, the possibilities of amorphous bifunctional catalysts for practical industrial applications are evaluated and future research direction are suggested. [ABSTRACT FROM AUTHOR]

8‐Methylquinoline is regarded as an ideal substrate to participate in diversely C(sp3)−H functionalization reactions. The presence of the chelating nitrogen atom enables 8‐methylquinoline to easily form cyclometallated complexes with various transition metals, leading to the selective synthesis of functionalized quinolines. Considering the great importance of quinoline cores in medicinal chemistry, in this review article, we have covered the publications related to the C−H activation and functionalization of 8‐methylquinoline under transition metal catalysis during the last decade. [ABSTRACT FROM AUTHOR]

The design of 2D metal–organic frameworks (2D MOFs) takes advantage of the combination of the diverse electronic properties of simple organic ligands with different transition metal (TM) centers. The strong directional nature of the coordinative bonds is the basis for the structural stability and the periodic arrangement of the TM cores in these architectures. Here, direct and clear evidence that 2D MOFs exhibit intriguing energy‐dispersive electronic bands with a hybrid character and distinct magnetic properties in the metal cores, resulting from the interactions between the TM electronic levels and the organic ligand π‐molecular orbitals, is reported. Importantly, a method to effectively tune both the electronic structure of 2D MOFs and the magnetic properties of the metal cores by exploiting the electronic structure of distinct TMs is presented. Consequently, the ionization potential characteristic of selected TMs, particularly the relative energy position and symmetry of the 3d states, can be used to strategically engineer bands within specific metal–organic frameworks. These findings not only provide a rationale for band structure engineering in 2D MOFs but also offer promising opportunities for advanced material design. [ABSTRACT FROM AUTHOR]

The present work describes the synthesis of graphitic carbon nitride (GCN) via simple two‐step thermal decomposition of urea at a moderate temperature of 550 °C. The as‐synthesized GCN is further doped with transition metals like nickel, and both the pure and doped GCN are characterized by X‐ray diffraction (XRD), field emission scanning electron microscope (FESEM), X‐ray photoelectron spectroscopy (XPS), and Fourier transformed infrared (FTIR) spectroscopy. XRD shows the perfect phase formation in the pure GCN, which also remains in the doped sample but with much lesser crystallinity. FESEM shows that after doping, the small chips‐like structure of GCN gets transformed to an elongated one. XPS confirms the successful doping by keeping the signature of both nickel 2P1/2 and 2P3/2 oxidation states in the spectra, whereas FTIR gave an idea about different bonding present in the sample. The pure sample, when irradiated with an excitation wavelength of 350 nm, gives an intense peak at 457 nm, which gets considerably quenched in the case of the doped sample. However, a new peak appears in the photoluminescence (PL) spectra of the doped sample at 624 nm. The quenching of PL intensity in the doped sample is assumed to be due to the fact that the dopant‐induced state traps the electron, hindering them from immediate recombination. This quenching of PL intensity generates the possibilities of sensing the presence of different metals and thus taking measurable steps for removing them. The CIE chromaticity diagrams for the doped and undoped samples confirm that the emission color changes from blue to cyan region after the doping. [ABSTRACT FROM AUTHOR]

5-(4-pyridyl) phenyl substituted functionalized nitronyl nitroxide biradical ligand holds MnII ions and TbIII / HoIII ions together to yield 3d-4f-biradical heterospin clusters, namely, [Ln2 Mn2 (hfac)10 (NITPhPybis)2] [Ln = Tb 1, Ho 2], wherein, two NITPhPybis radicals ligate two MnII ions via two NO groups and two nitrogen-atoms from pyridine rings. At the same time, each NITPhPybis encapsulates one LnIII ion through chelating mode with adjacent NO groups, generating an annular centrosymmetric heterometallic tetranuclear system. In addition, the direct current and alternating current magnetic properties and luminescent behavior were systematically studied. Magnetodynamic studies uncover that the cluster 1-TbMn exhibits slow magnetic relaxation. The fluorescence of two polynuclear clusters show the characteristic fluorescence of TbIII or HoIII ions. [ABSTRACT FROM AUTHOR]

The development of bifunctional electrocatalysts coupled with HER and OER activities in the same electrolyte to achieve overall water decomposition is more attractive and challenging for practical applications. Here, we prepared a CoFe‐LDH catalyst via a hydrothermal method, and grew highly dispersed Pt−CoFe@CC bifunctional catalyst on a carbon cloth via the ethylene glycol thermal reduction method. The low content of Pt was limited to CoFe‐LDH to balance the catalytic performance and cost, to achieve effective water decomposition. Surprisingly, the overall decomposition of water can be achieved with a voltage of only 1.6 V and good stability for up to 20 hours. This work provides a design idea and method for combining HER and OER bifunctional electrocatalysts. [ABSTRACT FROM AUTHOR]

ABSTRACT Imidazole moiety when fused with other heterocyclic system form numerous compounds with different types of pharmacological and biological activities. In this review, we discussed a comprehensive analysis of the synthetic methodologies and reaction mechanisms for imidazo‐fused heterocyclic molecules. These molecules represent a crucial class of compounds due to their significant applications and versatile chemical reactivity. This article meticulously examined various synthetic routes for the construction of imidazo‐fused heterocycles, ranging from traditional methods to modern approaches such as microwave‐assisted reactions, NPs‐catalyzed reactions, light‐mediated synthesis, electrochemical reactions, and transition metal‐free synthesis routes. By consolidating the current knowledge and highlighting future directions, this review aims to serve as a treasure for research community in the fields of organic chemistry, medicinal chemistry, and material science. [ABSTRACT FROM AUTHOR]

MoS 2 modification by doping transition metals is an effective way to change the Mo–S bond energy by taking advantage of the electronic variability of the d orbitals of transition metals. Herein, this study investigates the doping effect of different transition metals onto MoS 2 edge sites through DFT calculations. To screen out the metal additive effect, different transition metals were doped to the MoS 2 edge sites to see the effect on generating S vacancies that were generally regarded as the active sites. DFT simulation results proved that the ability of the valence electrons to populate the orbitals with the greatest overlap with the orientation of the edge Mo–S bond was a major factor in how simple it was to create S vacancies at the Mo-edge and S-edge sites. For the transition metals, the vacancy formation energy increases with the increase of periodic number for the same group, while decreases with the increase of the atomic weight for the same period. This implied that the upper right corner transition metals in the Periodic Table could be selected to modify MoS 2 to obtain the minimum vacancy formation energy. Therefore, nickel and cobalt are the best choice as the doping element for modifying MoS 2. [Display omitted] • The correlation between transition metal-doped MoS 2 edge sites and vacancy formation energy is unveiled. • Co and Ni doping modified MoS 2 were found to promote the generation of S-edge sites. • The correlation between electron filling in d orbitals and S vacancy formation energy is revealed. [ABSTRACT FROM AUTHOR]

Efficient hydrogen production relies on cost-effective and durable non-noble metal electrocatalysts for the hydrogen evolution reaction (HER). In this work, a liquid metal-assisted solid-flame combustion synthesis (SF-CS) method was used to create transition metal carbide TMC) nanocrystals with exposed facets. The TMCs include TiC, VC, NbC, TaC, Ta 2 C, WC, and Mo 2 C. In acidic solutions, the TMC nanocrystals show enhanced conductivity and superior HER performance, as evidenced by their lower Tafel slope, higher current density, and decreased overpotential. In particular, Mo 2 C nanocrystals exhibit an overpotential of 95 mV and a Tafel slope of 26 mV dec−1. These findings highlight a noteworthy improvement over previously reported nanostructures in recent years in terms of the HER properties of Mo 2 C with particular facets. This improvement is attributed to the unique surface characteristics, such as energy and active sites, which are impacted by various factors and require more investigation to meet the intended goals. [Display omitted] [ABSTRACT FROM AUTHOR]

A mixed transition metal borate Co5–xVxCoy[B12O26–z(OH)z] was synthesized in a Walker-type module using the high-pressure/high-temperature approach at 12 GPa and 1,300 °C. The product crystallizes in the space group I41/acd. It is isotypic to other 3d metal cation borates of the M5[B12O25(OH)]–M5M[B12O22(OH)4] solid solution series. The title compound features three different metal cation positions; one octahedral site contains a mixture of V and Co, another octahedral site is fully occupied with Co, and a cuboctahedral position that is partially occupied with Co. It is the first compound within this structure type to contain Co, increasing the range of elements that can be incorporated and thus illustrating the adaptability and structural diversity of this anionic borate network. [ABSTRACT FROM AUTHOR]

Currently, intercalation has become an effective way to modify the fundamental properties of two-dimensional (2D) van der Waals (vdW) materials. Using density functional theory, we systematically investigated the structures and electronic and magnetic properties of bilayer transition metal dichalcogenides (TMDs) intercalated with 3d TM atoms (TM = Sc–Ni), TM@BL_MS2 (M = Mo, V). Our results demonstrate that all the studied TM@BL_MS2s are of high stability, with large binding energies and high diffusion barriers of TM atoms. Interestingly, most TM@BL_MoS2s and TM@BL_VS2s are found to be stable ferromagnets. Among them, TM@BL_MoS2s (TM = Sc, Ti, Fe, Co) are ferromagnetic metals, TM@BL_MoS2 (TM = V, Cr) and TM@BL_VS2 (TM = Sc, V) are ferromagnetic half-metals, and the remaining systems are found to be ferromagnetic semiconductors. Exceptions are found for Ni@BL_MoS2 and Cr@BL_VS2, which are nonmagnetic semiconductors and ferrimagnetic half-metals, respectively. Further investigations reveal that the electromagnetic properties of TM@BL_MoS2 are significantly influenced by the concentration of intercalated TM atoms. Our study demonstrates that TM atom intercalation is an effective approach for manipulating the electromagnetic properties of two-dimensional materials, facilitating their potential applications in spintronic devices. [ABSTRACT FROM AUTHOR]

Inspired by the natural thermal charring capacity of lacquer tree bark, a novel halogen-free, bio-based and two-component synergistic flame retardant system has been constructed by introducing transition metal (Fe3+)-modified tannic acid (TA) as char source and ammonium polyphosphate (APP) as acid source, which was employed for overcoming the severe flammability problem for silicone rubber (SR). By systematically investigating the effect of APP/TA@Fe system on the flame retardancy of SR composites, it has been found that when 40 mass% APP and TA@Fe in a ratio of 3:1 are added, the limited oxygen index (LOI) and vertical combustion tests of SR composites can reach 30% and UL-94 V-0 rating with a rapid self-extinguishing capacity. Through the comprehensive analysis of the residues of SR composites after complete burning, a gas/condensed flame retardant mechanism is primarily proposed in detail. Among these, the ammonia and water vapor released by the decomposition of APP and TA@Fe during combustion can dilute the combustible gases and tannic acid will act via the free radicals scavenging ability. Besides, the continuous, intumescent and dense charring residues from the thermal interaction between APP and TA will exert a prominent role in restricting the heat/mass exchange process and inhibiting the SR matrix from further flame attacking. Surprisingly, the mechanical strength of SR system is attained even if the combination of APP and TA@Fe is blended. Consequently, this article has developed a bionic, eco-friendly and effective approach to settle the flammability problem of SR and broaden their applications in the fields of construction and decoration materials. [ABSTRACT FROM AUTHOR]

[Display omitted] • The intrinsic mechanism of the external electric field effects on the N 2 adsorption and NN* dissociation performances of three-atom transition metal clusters (TATMCs) is investigated. • Electric fields regulate the charge transfer between TATMCs and NN*, thus affecting the N−N bond activation. • The ICOHP values of two N atoms and E N are not limited by the linear relationship under different electric fields. Three-atom transition metal clusters (TATMCs) with remarkable catalytic activities, especially Nb 3 , Zr 3 , and Y 3 , are proven to be suitable candidates for efficient ammonia production. The pursuit of effective strategies to further promote the ammonia synthesis performance of TATMCs is necessary. In this study, we systematically investigate the effect of external electric fields on tuning the N 2 adsorption and NN* activation performances of Nb 3 , Zr 3 , and Y 3. Our findings demonstrate that the medium and low positive fields promote the N 2 adsorption performance of Nb 3 , while both positive and negative fields enhance nitrogen adsorption on Zr 3. Additionally, electric fields may impede N 2 fixation on Y 3 , yet the N 2 adsorption performance of Y 3 remains considerable. Negative electric fields enhance the NN* activation performance of Nb 3 and Y 3. But only high negative fields weaken the N N bond on Zr 3 , which is attributed to the promotion of the charge accumulation around two N atoms. Notably, Nb 3 and Zr 3 are identified as two TATMCs with the potential for simultaneous optimization of their E N and ICOHP values. This work sheds light on the field effects on the N 2 adsorption and NN* activation performances of TATMCs and guides the design of catalysts for achieving more sustainable ammonia synthesis. [ABSTRACT FROM AUTHOR]

This investigation aimed to study the effects of adding TiO 2 on many aspects of 1393-B3 glasses, including their physio-chemical, mechanical parameters, crystallization behaviour, in-vitro bioactivity, hemocompatibility, and cellular viability. Here, we replaced 1393 glass silica with boric oxide to determine a more effective alternative. 1393-B3 bioactive glasses having the general weight % composition (53-X) B 2 O 3 , 6 Na 2 O, 5 MgO, 20 CaO, 12 K 2 O, 4 P 2 O 5 , X TiO 2 (where X = 0, 1.0, 1.5, 2.0, and 2.5 %) were prepared using solid-state melt quenching method in platinum crucible at 1100 °C for 2 h in an electric furnace with air as furnace atmosphere. This research aimed to investigate the complete substitution of 1393 glass silica with boric oxide in order to get a reduced melting temperature forming 1393-B3. The objective was to develop a more energy-efficient and economical bioactive glass. Thermal analysis of the samples was obtained up to 700 °C. To evaluate the in-vitro bioactivity, the samples were immersed in simulated body fluid (SBF). These materials undergo XRD, FTIR, and SEM/EDAX analysis both before and after soaking in SBF. These characterization results show the presence of a hydroxyapatite (HA) layer forming on the samples of the bioactive glass surface. The haemolysis process performed on human blood shows its haemocompatibility result. To test these results for the human body. We performed cell proliferation and cell compatibility on the MG-63 cell line to see its effect on osteosarcoma patients. Density (2.31–2.48 gm/cm3), pH value (7.4–8.86), and mechanical parameters such as compressive strength (98–125 MPa), flexural strength (33–54), and elasticity are measured. As a result, physio-chemical, mechanical, biological properties and in-vitro bioactivity of these samples were obtained with increasing concentration of TiO 2 in 1393-B3 borate bioactive glass and found to increase with increasing concentration of TiO 2. [ABSTRACT FROM AUTHOR]

A mixed transition metal borate Co5–xVxCoy[B12O26–z(OH)z] was synthesized in a Walker-type module using the high-pressure/high-temperature approach at 12 GPa and 1,300 °C. The product crystallizes in the space group I41/acd. It is isotypic to other 3d metal cation borates of the M5[B12O25(OH)]–M5M[B12O22(OH)4] solid solution series. The title compound features three different metal cation positions; one octahedral site contains a mixture of V and Co, another octahedral site is fully occupied with Co, and a cuboctahedral position that is partially occupied with Co. It is the first compound within this structure type to contain Co, increasing the range of elements that can be incorporated and thus illustrating the adaptability and structural diversity of this anionic borate network. [ABSTRACT FROM AUTHOR]

Abstract Cell death is one of the most important mechanisms of maintaining homeostasis in our body. Ferroptosis and pyroptosis are forms of necrosis-like cell death. These cell death modalities play key roles in the pathophysiology of cancer, cardiovascular, neurological diseases, and other pathologies. Transition metals are abundant group of elements in all living organisms. This paper presents a summary of ferroptosis and pyroptosis pathways and their connection to significant transition metals, namely zinc (Zn), copper (Cu), molybdenum (Mo), lead (Pb), cobalt (Co), iron (Fe), cadmium (Cd), nickel (Ni), mercury (Hg), uranium (U), platinum (Pt), and one crucial element, selenium (Se). Authors aim to summarize the up-to-date knowledge of this topic. In this review, there are categorized and highlighted the most common patterns in the alterations of ferroptosis and pyroptosis by transition metals. Special attention is given to zinc since collected data support its dual nature of action in both ferroptosis and pyroptosis. All findings are presented together with a brief description of major biochemical pathways involving mentioned metals and are visualized in attached comprehensive figures. This work concludes that the majority of disruptions in the studied metals’ homeostasis impacts cell fate, influencing both death and survival of cells in the complex system of altered pathways. Therefore, this summary opens up the space for further research. Graphical abstract

With the increasingly serious environmental problems and the rising energy crisis， it is urgent to use electrocatalysis technology to develop sustainable green new energy. Transition metal low-dimensional nanomaterials have large active surface， high electron transfer rate and abundant surface vacancies， which can effectively improve the efficiency and stability of electrocatalytic reactions. In this paper， the transition metal low-dimensional nanomaterials are classified based on the material dimension， and their advantages are clarified respectively. The research achievements of zero-dimensional， one-dimensional and two-dimensional nanomaterials in the field of electrocatalysis are mainly reviewed. The relationship between the structure of low-dimensional nanostructure and the activity， as well as stability of electrocatalysis， is revealed， and it is clear that low-dimensional nanomaterials are an effective method to improve the performance of electrocatalysis. Finally， it is pointed out that the structure of transition metal low-dimensional nanocatalysts should be rationally designed and optimized according to demand. The future development direction of low-dimensional nanocatalysts should be the combination of basic research and computational research， guide the design with theory， combine with machine learning to pre-select the appropriate structural model and further development towards improving existing materials and combining more and more efficient composite materials.

Transition metal compounds (TMCs) provide the benefits of vast reserves, affordability, non-toxicity, and environmental friendliness, making them highly sought-after in recent times. Integrating transition metal salts into polymers may result in substantial enhancements in optical and electrical characteristics, making them appealing for many applications. Transition metal ions may display a range of electronic transitions, which enables the adjustment of absorption and emission spectra. This characteristic has significant value in applications such as light-emitting devices (LEDs) and sensors. The photoluminescence of polymers may be improved by the addition of transition metal salts, which results in light emission that is both more brilliant and more efficient. On the other hand, this is advantageous for screens and optoelectronic devices. The presence of transition metal salts in polymers may help to improve their optical stability, hence lowering the probability that the polymers will degrade or change color over time. When it comes to the performance of optical devices over the long run, this is quite essential. Elevating the electrical conductivity of polymers is possible via the use of transition metal salts. This is very helpful in the process of developing conductive polymers for use in applications such as electronic fabrics, organic solar cells, and flexible electronic devices. Transition metal salts can affect the electrical band structure of polymers, which enables the band gap of the material to be tuned. This is very necessary in order to maximize the amount of light that is absorbed by photovoltaic devices. Through having all these benefits, we conducted a review to find out the effects on polymeric materials. [ABSTRACT FROM AUTHOR]

AbstractTitanium dioxide (TiO2) nanoparticles possess intriguing properties and have been extensively utilized in medical applications due to their exceptional antimicrobial characteristics. The antimicrobial efficacy can be heightened by altering the structural morphology, size, and optical properties through the introduction of transition metal ions (M: Fe, Co, Ni, Cu, and Zn) with a concentration of x = 0.02 into TiO2, thereby producing Ti1-xMxO2 powder via the sol-gel method at a sintering temperature ranging from 500 °C to 600 °C. The morphological characteristics of Ti1-xMxO2 were analyzed using FT-IR, UV-DRS, XRD, TGA, BET, and SEM-EDAX techniques. Substituting M-doped TiO2 at a sintering temperature of 500 °C results in all doping ions yielding the Ti1-xMxO2 anatase phase. Conversely, at 600 °C, the doping ions M: Cu, Co, Zn exhibit a tendency to substitute the TiO2 structure, destabilizing the anatase phase and leading to the formation of an anatase-rutile dual phase with larger crystal size. At elevated temperatures, ions with larger radii than Ti (0.61), namely Cu (0.73), Co (0.75), and Zn (0.74), tend to be substituted, thereby altering the structure of TiO2. The antimicrobial efficacy, evaluated based on the inhibition zone, demonstrates that Ti1-xMxO2 effectively inhibits the cellular activity of Salmonella typhimurium (Gram -) and Staphylococcus aureus (Gram +) bacteria compared to TiO2. [ABSTRACT FROM AUTHOR]

The development of low‐cost transition metal compounds with high‐performance for efficient oxygen evolution reaction (OER) is of great significance in promoting the development of electrocatalysis. In this study, a Ce‐doped Ni3S4 catalyst (Ce0.2−Ni3S4) was synthesized through a one‐step solvothermal method, where the doped rare earth element Ce induced the transformation of NiS to Ni3S4. The Ce0.2−Ni3S4 catalyst exhibited excellent OER performance in 1 M KOH. At a current density of 10 mA cm−2, it showed a low overpotential of 230 mV and a low Tafel slope of 52.39 mV dec−1. Long‐term OER tests at the same potential lasted for 24 h without significant loss of current density. This work introduces a novel method of Ce element doping for modifying transition metal sulfides, providing new insights into the effective utilization of rare earth elements in the field of electrochemistry. It creates more chances for the progress of highly efficient catalysts for efficient OER, contributing to the advancement of electrocatalysis. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) receive wide attention owing to their high specific surface area, porosity, and structural designability. In this paper, ZC-Ru and ZC-Cu electrodes loaded with monatomic Ru and Cu doped with nitrogen were prepared by pyrolysis, ion impregnation, and carbonization process using ZIF-8 synthesized by static precipitation as a precursor. ZC-Cu has a high specific surface area of 859.78 m2 g−1 and abundant heteroatoms O (10.04%) and N (13.9%), showing the specific capacitance of 222.21 F g−1 at 0.1 A g−1 in three-electrode system, and low equivalent series resistance (Rct: 0.13 Ω), indicating excellent energy storage capacity and electrical conductivity. After 10,000 cycles at 1 A g−1 in 6 M KOH electrolyte, it still has an outstanding capacitance retention of 99.42%. Notably, symmetric supercapacitors ZC-Cu//ZC-Cu achieved the maximum power density and energy density of 485.12 W·kg−1 and 1.61 Wh·kg−1, respectively, positioning ZC-Cu among the forefront of previously known MOF-based electrode materials. This work demonstrates the enormous potential of ZC-Cu in the supercapacitor industry and provides a facile approach to the treatment of transition metal. [ABSTRACT FROM AUTHOR]

By using density functional theory (DFT), the adsorption behavior of gas molecules on defective graphene doped with manganese and nitrogen were investigated. The geometric structure, electronic structure, and magnetic properties of two substrates were calculated and the sensing mechanism was also analyzed. The results indicate that the MnSV-GP and MnN3-GP have stronger structural stability, in which Mn atoms and their coordination atoms will become the adsorption point for five gas molecules (CH2O, CO, N2O, SO2, and NH3), respectively. Moreover, at room temperature (298 K), the recovery time of the MnSV-GP sensor for N2O gas molecules is approximately 1.1 s. Therefore, it can be concluded that the MnSV-GP matrix as a magnetic gas sensor has a promising potential for detecting N2O. These results also provide a new pathway for the potential application of Mn-doped graphene in the field of gas sensors. [ABSTRACT FROM AUTHOR]

[Display omitted] Researchers are interested in single-atom catalysts with atomically scattered metals relishing the enhanced electrocatalytic activity for nitrogen reduction and 100 % metal atom utilization. In this paper, we investigated 18 transition metals (TM) spanning 3d to 5d series as efficient nitrogen reduction reaction (NRR) catalysts on defective 2D SiP V layered structures through first-principles calculation. A systematic screening identified Mo@SiP V , Nb@SiP V , Ta@SiP V and W@SiP V as superior, demonstrating enhanced ammonia synthesis with significantly lower limiting potentials (−0.25, −0.45, −0.49 and −0.15 V, respectively), compared to the benchmark −0.87 eV for the defective SiP. In addition, the descriptor Δ G *N was introduced to establish the relationship between the different NRR intermediates, and the volcano plot of the limiting potentials were determined for their potential-determining steps (PDS). Remarkably, the limiting voltage of the NRR possesses a good linear relationship with the active center TM atom Ɛ d , which is a reliable descriptor for predicting the limiting voltage. Furthermore, we verified the stability (using Ab Initio Molecular Dynamics − AIMD) and high selectivity (U L (NRR)- U L (HER) > -0.5 V) of these four catalysts in vacuum and solvent environments. This study systematically demonstrates the strong catalytic potential of 2D TM@SiP V (TM = Mo, Nb, Ta, W) single-atom catalysts for nitrogen reduction electrocatalysis. [ABSTRACT FROM AUTHOR]

Monolithic catalyst is very important for the further industrial application of hydrogen production via NaBH 4 hydrolysis. Nowadays, the structural stability and catalytic performance of aerogel based monolithic catalysts still need to be further improved. Herein, the amorphous Ru–Co(OH) x @GO particles are synthesized by in-situ growth and transformation of ZIF-67 on the surface of GO, the hydrogen generation rate and activation energy via catalytic NaBH 4 hydrolysis can reach 11,062 mL min−1 g−1 and 36.2 kJ mol−1, respectively. Meanwhile, the composite aerogel of Ru–Co(OH) x @GO, chitosan and carbonylated cellulose nanofiber is prepared by solution blending and freeze drying, and the hydrogen generation rate has 7680 mL min−1 g−1 (retained 69.4%) under the same amount of Ru–Co(OH) x @GO. Furthermore, after high speed catalytic hydrogen generation, the aerogel can still maintain its structural integrity, thus facilitating recovery and reuse, which is attributed to the co-structural coupling of carbonylated cellulose nanofiber and chitosan macromolecule to the skeleton. This work provides a convenient and controllable strategy for the development of monolithic catalysts. • ZIF-67 nanocrystalline was in-situ grown on GO. • Amorphous RuCo(OH) x was transformed by etching. • Composite aerogel displayed lamellar skeleton and porous channel. • The hydrogen generation rate of the aerogel had 7680 mL min−1 g−1. • The aerogel had a complete structure after catalytic hydrogen production. [ABSTRACT FROM AUTHOR]

Comprehensive Summary Recent advances in transition metal‐catalyzed o‐carborane B—H activation have led to the rapid development of various methodologies for cage boron functionalization. For catalytic cage B—H acyloxylation, intermolecular oxygenation gave products with different regioselectivities (B(3)‐, B(4)‐, and B(8,9)‐selectivities). Herein, an efficient palladium‐catalyzed direct cage B(4)–H oxygenation of o‐carboranylacetic acids has been achieved, where the carboxylic group serves as not only a directing group, but also a coupling partner. A wide range of substituted o‐carboranylacetic acids have been cyclized via the formation of B(4)−O bond to give the corresponding γ‐lactones in modest to excellent yields. A Pd(IV) intermediate is proposed to be involved in the catalytic cycle. This work offers valuable references for the BH/OH dehydrocoupling reactions under mild conditions to produce carborane‐featuring functional molecules. [ABSTRACT FROM AUTHOR]

In this work, in situ-generated cobalt oxide was infused into g-BCN to fabricate a heterocomposite (CoBCN) with multiple active sites. The electronic structure of CoBCN was further modified via the introduction of n- (Ni) and p-(Fe) type metals to investigate the activities of CoBCN-type materials with loosely bound electrons for electrocatalytic hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR) which symbolize the reduction/oxidation of water and reduction of fuel gas oxygen that goes on in concurrent electrocatalytic and fuel cell. Experimental results indicated that not only the electronic nature of the surface but also the binding energy between the involved metals and intermediates varied accordingly for the association/dissociation steps, resulting in the superiority of p-doped materials in HER and the n-doped material in the OER and ORR. The HER activity was governed by Fe–CoBCN with an overpotential of 97 mV (@ 10 mA cm−2), whereas Ni–CoBCN showed superior performance for the OER and ORR with an overpotential and E 1/2 of 130 mV (@ 10 mA cm−2) and 0.79 V, respectively. p-/n-effect on CoBCN material for its multifunctional electrocatalytic activity for HER, OER and ORR. [Display omitted] • Fe and Ni oxide were doped individually to observe the p-/n-effect. • Fe–CoBCN dominated HER with a low overpotential due to facile Cat-H interaction. • Ni–CoBCN outperformed for OER and ORR with a low overpotential and E 1/2. [ABSTRACT FROM AUTHOR]

Density functional theory (DFT) analyses were carried out to study electronic structures and magnetic properties of Mn- and Cu-doped GaNNS. To investigate the influence of transition metal atoms (TM) on magnetic properties, we substituted Ga atoms with Mn and Cu atoms in different concentrations. Investigation shows that TM leads to electronic structural reconstruction which changes their properties in this way, and plays a significant role in spin polarization. Although the pure nanosheet is a nonmagnetic semiconductor, the doped atoms induce magnetism in the structure. The band gap changes monotonically depending on the concentration of TM atoms. The observed good half-metal ferromagnetism GaNNS:Mn, allows them to be a potential candidate for use in spintronics. The local magnetic moment calculated from Mulliken analyses for the Mn atom is approximately 4.05 μ B. By choosing the appropriate concentration of impurity atoms one can obtain a magnetic semiconductor and is half-metal. Thus, Mn-atoms may induce half-metallic ferromagnetism in GaN nanosheet, which makes it a potential candidate for spintronics device applications. Also observed, was weak ferromagnetism in Cu-doped GaNNS is not suitable for use in spintronics. [ABSTRACT FROM AUTHOR]

In the twenty-first century, we are witnessed of a large number of infectious ailments which spread very quickly worldwide and effect the public health significantly. Thus, in the current research, with the aim of a suitable malaria and oxidant controlling agent, micro-assay, DPPH and ABTS protocols were conducted against previously synthesized and well-characterized (mass spectrometry, NMR (1H and 13C), powder XRD, IR, electronic spectra, TGA magnetic moment, molar conductivity and SEM) hydrazone ligands (1–2) and their Co(II), Ni(II), Cu(II), Ni(II) metal complexes (3–10) of benzaldehyde derivatives and 3,5-dichlorobenzohydrazide. The biological assessment revealed that the (8), (9), (10) complexes were more potent to inhibit the malarial and oxidant infections although the complex (10) has highest ability (0.42 ± 0.05 µM for antimalaria and 1.98 ± 0.09–99 ± 0.08 µM for antioxidant) to control these diseases with comparable IC50 value to quinine and ascorbic acid. Moreover, molecular docking (against 8E1Z and 1U5A proteins), DFT and ADMET investigations were examined against the highly potent HL2 ligand and its (7–10) complexes to corroborate the acquired biological findings. The theoretical investigations also advocate the more potency of complex (10) through significant binding affinity, binding modes, hardness, softness, etc. [ABSTRACT FROM AUTHOR]

Cell death is one of the most important mechanisms of maintaining homeostasis in our body. Ferroptosis and pyroptosis are forms of necrosis-like cell death. These cell death modalities play key roles in the pathophysiology of cancer, cardiovascular, neurological diseases, and other pathologies. Transition metals are abundant group of elements in all living organisms. This paper presents a summary of ferroptosis and pyroptosis pathways and their connection to significant transition metals, namely zinc (Zn), copper (Cu), molybdenum (Mo), lead (Pb), cobalt (Co), iron (Fe), cadmium (Cd), nickel (Ni), mercury (Hg), uranium (U), platinum (Pt), and one crucial element, selenium (Se). Authors aim to summarize the up-to-date knowledge of this topic. In this review, there are categorized and highlighted the most common patterns in the alterations of ferroptosis and pyroptosis by transition metals. Special attention is given to zinc since collected data support its dual nature of action in both ferroptosis and pyroptosis. All findings are presented together with a brief description of major biochemical pathways involving mentioned metals and are visualized in attached comprehensive figures. This work concludes that the majority of disruptions in the studied metals' homeostasis impacts cell fate, influencing both death and survival of cells in the complex system of altered pathways. Therefore, this summary opens up the space for further research. [ABSTRACT FROM AUTHOR]

Copyright of Asian Journals of Ecotoxicology is the property of Gai Kan Bian Wei Hui and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of China University of Petroleum is the property of China University of Petroleum and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Transition metal‐catalyzed synthesis of propargylic esters has been widely investigated, offering distinctive opportunities to build 1,3‐diene skeletons. Access to 1,2,3,4‐tetrasubstituted 1,3‐dienes has been a longstanding challenge in organic synthesis due to a great diversity of stereoisomers from four substituents and unpredictable regioselectivity. Given the synthetic challenges and the importance, inventing methods for the generation of this valuable architecture has gathered much more attention. Recently, several intriguing works concerning this topic have been achieved towards the high regio‐ and stereoselective elaborate 1,2,3,4‐tetrasubstituted 1,3‐dienes. Herein, this concept summarizes recent advances in transition metal‐catalyzed construction of 1,2,3,4‐tetrasubstituted 1,3‐dienes from propargylic esters and discusses the mechanism as well as their applications. [ABSTRACT FROM AUTHOR]

The denitrification efficiency of carbon‐based zero valent iron catalyst (C‐ZFe) for low‐temperature selective catalytic reduction (SCR) (<140°C) highly depends on the structural species of iron oxide (FexOy) and the physicochemical properties of the catalyst. In the study, we investigated the main factors affecting the low‐temperature denitrification efficiency of C‐ZFe such as temperature, iron content and O2. The results showed that the average NOX conversion was 72.6 % at 135°C when the space velocity was 459 h−1 and the mass ratio of carbon to iron was 15 % to 85 %. The surface morphology and structure of C‐ZFe were characterized by the surface area and pore size distribution measurements, X‐ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR) and X‐ray photoelectron spectroscopy (XPS). The results indicated that the iron on the catalyst surface was oxidized by O2 to Fe2O3, which could retain NO and then formed intermediate products. NO entered the mesoporous structure along C‐ZFe surface and proceeded a catalytic reduction reaction with the adjacent carbon. [ABSTRACT FROM AUTHOR]

Precise regulation of the active site structure is an important means to enhance the activity and selectivity of catalysts in CO2 electroreduction. Here, we creatively introduce anionic groups, which can not only stabilize metal sites with strong coordination ability but also have rich interactions with protons at active sites to modify the electronic structure and proton transfer process of catalysts. This strategy helps to convert CO2 into fuel chemicals at low overpotentials. As a typical example, a composite catalyst, CuO/Cu−NSO4/CN, with highly dispersed Cu(II)−SO4 sites has been reported, in which CO2 electroreduction to formate occurs at a low overpotential with a high Faradaic efficiency (−0.5 V vs. RHE, FEformate=87.4 %). Pure HCOOH is produced with an energy conversion efficiency of 44.3 % at a cell voltage of 2.8 V. Theoretical modeling demonstrates that sulfate promotes CO2 transformation into a carboxyl intermediate followed by HCOOH generation, whose mechanism is significantly different from that of the traditional process via a formate intermediate for HCOOH production. [ABSTRACT FROM AUTHOR]

Virgin and environmentally aged polypropylene (PP) micropowders (V-PP and E-PP, respectively) were used as reference microplastics (MPs) in comparative photo- and thermo-oxidative ageing experiments performed on their mixtures with a natural ferrous sand (NS) and with a metal-free silica sand (QS). The ferrous NS was found to catalyze the photo-oxidative degradation of V-PP after both UV and simulated solar light irradiation. The catalytic activity in the V-PP/NS mixture was highlighted by the comparatively higher fraction of photo-oxidized PP extracted in dichloromethane, and the higher carbonyl index of the bulk polymer extracted with boiling xylene, when compared with the V-PP/QS mixture. Similarly, NS showed a catalytic effect on the thermal degradation (at T = 60 °C) of E-PP. The results obtained indicate that, under suitable environmental conditions (in this case, an iron-containing sediment or soil matrix, combined with simulated solar irradiation), the degradation of some types of MPs could be much faster than anticipated. Given the widespread presence of iron minerals (including the magnetite and iron-rich serpentine found in NS) in both coastal and mainland soils and sediments, a higher than expected resilience of the environment to the contamination by this class of pollutants is anticipated, and possible routes to remediation of polluted natural environments by eco-compatible iron-based minerals are envisaged. [ABSTRACT FROM AUTHOR]

Using cobalt sulfate and nickel sulfate as main electrolytes, ammonium sulfate as an auxiliary electrolyte and buffer agent, and cheap iron pieces (FP) as the substrates, nickel and/or cobalt phosphide/metal heterogeneous catalytic electrode (M2P/M/FP) was grown on the substrate in situ by electrodeposition followed by low temperature phosphating. M2P/M/FP functioned as a good bifunctional electrode for HER and OER in 1 mol/L KOH, where Co2P/Co/FP needed an overpotential of 52 and 288 mV, and (NC)2P/(NC)/FP required that of 75 mV and 293 mV to afford 10 mA/cm2. Previous similar studies often ignored the role of metal and only considered the water electrolysis catalysis of metal phosphide. In this research, it was clarified that for water electrolysis, the essence of high catalysis activity of the M2P/M/FP electrode was the electronic interaction between metal and metal phosphide. [ABSTRACT FROM AUTHOR]

Recently, transition metal‐catalyzed ortho‐C−H bond activation/annulations involving two internal alkyne molecules have been extensively used to synthesize highly substituted polycyclic aromatic scaffolds. Such reactions have emerged as a powerful atom and step‐economical strategy for the assembly of multifunctional bioactive molecules. In this context, we focused on the recent achievements of dual C−H bond activation/annulations, as well as functionalization reactions involving diaryl/alkyl alkynes. [ABSTRACT FROM AUTHOR]

A porous carbon‐based monolithic chainmail electrode, namely Co2P@CSA, is fabricated via direct carbonization of Co2+‐cross‐linked‐starch aerogel (Co2+‐SA) followed by low‐temperature vapor phosphorization. During successive carbonization‐phosphorization, the SA framework is formulated into 3D hierarchically porous carbon membrane matrix comprising hollow open carbon microspheres while the cross‐linked Co species are converted into uniformly distributed carbon‐encapsulated Co2P nanoparticles on carbon microspheres. Thanks to the high porosity, excellent electrolyte wettability, unique chainmail structure, and good mechanical strength, the monolithic Co2P@CSA can be directly used as a binder‐free bifunctional electrocatalyst for alkaline water splitting, and it can afford a high current density of 100 mA cm−2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) at low overpotentials of 140.0 and 305.5 mV, respectively, with outstanding stability at 50 mA cm−2 for >30 h. More significantly, an alkaline electrolyzer assembled using Co2P@CSA achieves a current density of 100 mA cm−2 for overall water splitting (OWS) at a cell voltage of 1.94 V with unit Faradaic efficiency and provides a high solar‐to‐hydrogen (STH) conversion efficiency of 13.4 % when driven by a commercial silicon solar cell. This work offers an effective strategy towards cost‐effective fabrication of high‐performance carbon‐based monolithic chainmail electrocatalysts for energy conversion reactions. [ABSTRACT FROM AUTHOR]

The electrolysis of water to produce hydrogen is an important technique to replace traditional fossil fuel-based hydrogen production. This method efficiently converts electrical energy into chemical energy, it is ostensibly a promising candidate for addressing the energy crisis. Significant effort has been devoted to developing efficient electrocatalysts for water electrolysis. The exploration of suitable catalytic materials for the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and other bifunctional electrocatalytic reactions is crucial. Transition metal selenides (TMSes) have emerged as potential HER and OER electrocatalysts because of their unique electronic structures, which are beneficial for charge transfer, tuneable bandgaps, distinctive morphologies, and low-cost. This review discusses the mechanisms and performance comparisons of TMSes in overall water splitting under various pH conditions. From an industrial and commercial perspective, the catalytic performance of TMSes for the HER and OER is not ideal. Methods for preparing electrocatalytic materials and optimizing materials for overall water decomposition and modulation mechanisms have been introduced to improve electrocatalytic performance, such as element doping, carbon composites, bimetallic systems, morphology control, and heterogeneous interface engineering. Finally, the challenges and prospects of TMSes were discussed. [ABSTRACT FROM AUTHOR]

The urgent removal of Cd, Co, and Ni from nitrate and sulfate is essential to mitigate the potential risk of chemical pollution from large volumes of industrial wastewater. In this study, these metal ions were rapidly recovered through applying voltage on nitrate and sulfate, utilizing laser-induced graphene/polyimide (LIG/PI) film as the electrode. Following the application of external voltage, both the pH value and conductivity of the solution undergo changes. Compared to Co2+ and Ni2+, Cd2+ exhibits a lower standard electrode potential and stronger reducibility. Consequently, in both nitrate and sulfate solutions, the reaction sequence follows the order of Cd2+ > Co2+ > Ni2+, with the corresponding electrode adsorption quantities in the order of Cd2+ > Co2+ ~ Ni2+. Additionally, using the recovered Co(OH)2 as the raw material, a LiCoO2 composite was prepared. The assembled battery with this composite exhibited a specific capacity of 122.8 mAh g−1, meeting practical application requirements. This research has significance for fostering green development. [ABSTRACT FROM AUTHOR]

Copyright of Technology of Water Treatment is the property of Technology of Water Treatment Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Journal of Materials Engineering / Cailiao Gongcheng is the property of Journal of Materials Engineering Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Cellular responses to toxic metals depend on metal accessibility to intracellular targets, reaching interaction sites, and the intracellular metal concentration, which is mainly determined by uptake pathways, binding/sequestration and efflux pathways. ATP-binding cassette (ABC) transporters are ubiquitous in the human body—usually in epithelia—and are responsible for the transfer of indispensable physiological substrates (e.g. lipids and heme), protection against potentially toxic substances, maintenance of fluid composition, and excretion of metabolic waste products. Derailed regulation and gene variants of ABC transporters culminate in a wide array of pathophysiological disease states, such as oncogenic multidrug resistance or cystic fibrosis. Cadmium (Cd) has no known physiological role in mammalians and poses a health risk due to its release into the environment as a result of industrial activities, and eventually passes into the food chain. Epithelial cells, especially within the liver, lungs, gastrointestinal tract and kidneys, are particularly susceptible to the multifaceted effects of Cd because of the plethora of uptake pathways available. Pertinent to their broad substrate spectra, ABC transporters represent a major cellular efflux pathway for Cd and Cd complexes. In this review, we summarize current knowledge concerning transport of Cd and its complexes (mainly Cd bound to glutathione) by the ABC transporters ABCB1 (P-glycoprotein, MDR1), ABCB6, ABCC1 (multidrug resistance related protein 1, MRP1), ABCC7 (cystic fibrosis transmembrane regulator, CFTR), and ABCG2 (breast cancer related protein, BCRP). Potential detoxification strategies underlying ABC transporter-mediated efflux of Cd and Cd complexes are discussed. [ABSTRACT FROM AUTHOR]

Antimicrobial resistance has significantly increased over the last 30 years, prompting scientists to continuously look for novel, effective ways to combat drug-resistant bacteria and fungi. Due to their broad range of effectiveness, ease of synthesis, and ability to avoid resistance, antimicrobial peptides (AMPs) represent a potential approach. The direct investigation of metal effects on peptide activity has not received much attention. Divalent metal ions such as Zn(II), Cu(II), Ni(II), and Fe(II) do, in fact, influence some AMPs, producing an effect on their mode of action or function. Although the precise process by which metals are involved in microbial death is not well understood, this review goes into detail on several potential strategies to enhance AMPs activity through the synergy with metals. Important variables in these interactions include the individual peptide sequence, the type of metal ion, the capacity of metal to form chelates, and the softness of the ligand/metal complex. This article offers a thorough summary of the ways in which metal ions alter the structure of AMPs to boost their activity or sequester metal to impact on bacteria function.

Abstract The design of 2D metal–organic frameworks (2D MOFs) takes advantage of the combination of the diverse electronic properties of simple organic ligands with different transition metal (TM) centers. The strong directional nature of the coordinative bonds is the basis for the structural stability and the periodic arrangement of the TM cores in these architectures. Here, direct and clear evidence that 2D MOFs exhibit intriguing energy‐dispersive electronic bands with a hybrid character and distinct magnetic properties in the metal cores, resulting from the interactions between the TM electronic levels and the organic ligand π‐molecular orbitals, is reported. Importantly, a method to effectively tune both the electronic structure of 2D MOFs and the magnetic properties of the metal cores by exploiting the electronic structure of distinct TMs is presented. Consequently, the ionization potential characteristic of selected TMs, particularly the relative energy position and symmetry of the 3d states, can be used to strategically engineer bands within specific metal–organic frameworks. These findings not only provide a rationale for band structure engineering in 2D MOFs but also offer promising opportunities for advanced material design.

This study presents the synthesis and comprehensive characterization of undoped MoO3 and its cerium (Ce) and iron (Fe) doped counterparts via hydrothermal route, with a 5 % doping concentration. Structural analysis by X-ray diffraction confirmed the formation of MoO3 with successful doping. UV–vis spectroscopy demonstrated tunable optical properties, with band gap energies of 2.3 eV, 2.0 eV, and 2.8 eV for undoped, Ce-doped and Fe-doped MoO3 respectively. Morphological investigation using scanning electron microscopy revealed distinct nanostructures, including nanorods, agglomerated nanoparticles, and pebble-like structures, influenced by doping. Electrochemical characterization through cyclic voltammetry and potentio electrochemical impedance spectroscopy showcased superior charge storage capacity in Fe-doped MoO3, attributed to the largest area under the curve in cyclic voltammograms. Fe-doped MoO3 exhibited lowest resistance as compared to undoped and Ce doped MoO3, suggesting enhanced conductivity. The presence of a Warburg element in all samples indicated diffusion-limited electrochemical processes. The variation of log (scan rate) with log (current) revealed distinct charge transfer mechanisms, with near-unity slopes for doped samples and a slope near 0.5 for undoped MoO3. These findings provide insights into the tunable properties of doped MoO3, offering potential applications in various electrochemical devices.