Interlayer Ions Research Articles

Enhanced phosphorus adsorption performance of ZnAl-LDO by fluorine‑chlorine co-doping and synergistic mechanism exploration

Layered double hydroxides (LDHs) and their calcined products layered double oxides (LDOs) are widely used as adsorbents for pollutant removal. Their adsorption performance are significantly influenced by intercalated ions, while previous studies primarily focusing on the impact of individual ions. For the first time, this paper reports the mechanism of the synergistic enhancement of phosphate adsorption properties of LDO by bicomponent interlayer ions. The ZnAl-LDO by fluorine‑chlorine co-doping (F, Cl-ZnAl-LDO) exhibits excellent adsorption capacity of 158.9 mgP/g, surpassing that of single-component intercalation Cl-ZnAl-LDO and F-ZnAl-LDO, as well as most LDH-based adsorbents. Further research and density functional theory calculations indicate the differential adsorption enhancement mechanism of the interlayer ions. Chlorine functions as the exchanged anion, whereas fluorine facilitates the complete replacement of chloride ions and hydroxyl groups by phosphate. This finding highlights the potential of utilizing the synergistic effects between different interlayer ions to design and synthesize advanced phosphate adsorbent materials.

Covalent Organic Frameworks Interfacial Modification of Ceramic Electrolytes for Enhanced Electrochemical Performance

AbstractThe interface instability between inorganic ceramic electrolytes and lithium metal anodes seriously affects the cycling behavior of high‐performance lithium‐metal batteries. Herein, an in situ interfacial modification strategy is proposed to build the precise hybrid organic/inorganic lithium‐ion conducting layer where the Li1.3Al0.3Ti1.7(PO4)3 (LATP) particle surface is anchored by ion‐conducting covalent organic frameworks (COF) with affluent poly(ethylene glycol) (PEG) moieties. This interlayer features ion transport regulation to avoid high interfacial resistance and enhances interfacial stability by building a functional COF‐based shield against electrons. These as‐prepared particles are employed to fabricate flexible quasi‐solid electrolyte membranes interconnected by polytetrafluoroethylene binder based on the dry process. The obtained membranes perform two‐fold increase in ion conductivity at 30 °C of 2.55 × 10−3 S cm−1 and the prolonged lithium deposition up to 1000 h compared to the pristine, which are attributed to synergistic effects in the inorganic/organic phase. Moreover, an integrated cathode/electrolytes design is proposed and exhibits excellent cycling performance with capacity retention of 98.8% after 200 cycles at 1 C. The corresponding pouch cells can light up LED after bending and recovery. This research provides new insights into the great potential of fabricating soft ceramic‐based membranes in a low‐cost and green way for highly‐stable lithium‐metal batteries.

Biomass modified carbon nanofibers use for flexible supercapacitor electrodes with thermal conductive performances

The advancement of flexible electrode with excellent energy storage is essential for supercapacitors. Herein, a porous biomass-doped carbon nanofiber@bimetallic oxide composite (B-CNF@NiO/Co3O4) has been prepared as a binder-free flexible electrode. The heteroatoms form biomass not only offer pseudocapacitance but also a multitude of active sites for the grow of bimetallic oxides. The well-grown B-CNF@NiO/Co3O4 shows a high specific capacitance (629.5 F g−1) and the asymmetric flexible supercapacitor (ASC) has an energy density of 31.5 Wh kg−1 at a power density of 757.4 W kg−1. The properties of bimetallic oxides and 3D networks facilitate transportation of interlayer ion, providing a straightforward approach to fabricate non-adhesive flexible electrode with dual functionalities of energy storage. In addition, the thermal conductive experiment demonstrated a favorable thermal conductivity (TC) of 1.06 W m−1 K−1.

Insights into Adsorption Behavior and Mechanism of Br- onto Nickel-Aluminum Layered Double Hydroxides Intercalated with Different Inorganic Anions.

Layered double hydroxides (LDHs) have garnered significant attention from researchers in the field of adsorption due to their unique laminated structures and ion exchange properties. LDHs with various anion intercalation showed different adsorption effects on adsorbing ions, but the corresponding adsorption mechanisms are ambiguous. In this study, three types of NiAl-LDHs were synthesized, utilizing NO3-, CO32-, or Cl- as the interlayer anions. Batch tests were conducted to study their adsorption performances for Br-. Among them, the LDH with a NO3- intercalation layer exhibited the highest adsorption capacity for Br-, reaching up to 1.40 mmol g-1. The adsorption kinetics, mechanism, and renewability of these NiAl-LDHs were systematically compared. As a result, the type of Br- adsorption by all three materials was single molecular layer chemisorption. Moreover, the thermodynamic results of adsorption suggested that the adsorption of Br- was a spontaneous exothermic process. X-ray photoelectron spectroscopy, X-ray diffraction, and point of zero charge analysis collectively indicated that the adsorption of Br- by LDHs primarily occurred through interlayer ion exchange and electrostatic interactions. Structural characterizations of the adsorbents revealed that Br- entered the interlayers of the three LDHs, causing varying degrees of reduction in the interlayer spacing. Density functional theory calculations indicated that the interlayer binding energy of LDH with NO3- intercalation was the lowest, thereby making it more susceptible NO3- to be exchanged with Br-. Finally, the stability of the NiAl-LDHs was studied. The NiAl-LDHs retains a high removal efficiency of Br- even after 5 cycles of adsorption and desorption.

One-step synthesis of double-walled NiCo2O4 hollow nanotubes using hollow fiber templates created by airflow-coaxial electrospinning

Metal oxide electrode material NiCo2O4 has significant potential for application as an Electrode material due to its excellent electrochemical performance and environmentally friendly characteristics. This paper utilizes a unique airflow-coaxial electrospinning technique combined with a simple one-step solution reaction to prepare NiCo2O4 nanotubes with a complex double-walled hollow structure. The XPS and XRD results demonstrated the synthesis of the NiCo2O4 materials, while the SEM and TEM results verified the presence of a double-walled hollow structure in the NiCo2O4 nanotubes. The electrochemical performance of the NiCo2O4 double-walled hollow nanotubes is significantly improved compared to those single-layer hollow nanotubes. The maximum specific capacitance of those two kinds of nanotubes is 437.5 F/g and 336.7 F/g under the current density of 1 A/g, respectively. The origin of the electrochemical performance improvement can be attributed to the increased specific surface area and the presence of interlayer ion transport channels in the double-walled hollow structure. The study is very helpful in improving the application prospect of NiCo2O4 material as the electrode material of supercapacitors. Equally important, this study also presents an efficient method to fabricate double-walled hollow nanostructures based on special templates.

NiAl LDH nanosheets based on Ag nanoparticles-decoration and alkali etching strategies for high performance supercapacitors

Layered double hydroxides (LDHs) represent a category of two-dimensional layered intercalation materials, showing significant potential as electrode materials for the production of high-energy-density supercapacitors due to their tunable composition, ease of synthetic modification, and low cost. Here, we constructed alkali-etched NiAl LDH-OH nanosheets/Ag nanoparticles (NPs) composite material (Ag@NiAl LDH-OH) for high-performance supercapacitors through a simple solvent-thermal reaction. The alkali treatment is employed to selectively etch some Al3+ ions, generating cation vacancies as active sites for energy storage. Additionally, under the simultaneous influence of strong alkalis and vacancies, the interlayer spacing of LDHs expands, aiding in the promotion of interlayer ion mobility. Meanwhile, the decoration of silver nanoparticles ensures excellent electron conductivity in the NiAl-LDH-OH nanosheets, thereby facilitating improved utilization of the active substance and achieving outstanding rate performance. The Ag@NiAl LDH-OH electrode, when prepared, demonstrates a significant increase in specific capacitance, reaching 1790 F g−1 at a current density of 1 A g−1. This represents approximately 7 times the specific capacitance of the pristine NiAl LDH electrode, with a capacity retention of 79 % even under a high current density of 20 A g−1. Moreover, the assembled asymmetric supercapacitor (ASC) attains a maximum energy density of 138.25 Wh kg−1 at a power density of 700 W kg−1, maintaining 81 % of its initial specific capacitance after 20000 cycles. This research introduces novel pathways for advancing high-energy-density SCs.

Molecular dynamics study of temperature and defects on mechanical properties of Gr(GO)/C-S-H composites

In this paper, the effects of temperature and different defect types on the interfacial properties, kinetic properties and mechanical properties of Gr(GO)/C-S-H composites were investigated by molecular dynamics. It is shown that the incorporation of graphene (Gr) and graphene oxide (GO) improves the mechanical properties of the calcium silicate hydrate (C-S-H) model to varying degrees. The presence of defects at different temperatures affects the ordering of oxygen (Ow) in water in the proximal range of interlayer Ca ions and can effectively influence the spatial correlation between interlayer Ca ions and oxygen (Oc) in functional groups. The bond lengths of some Caw-Oc at different temperatures can be modulated by defects, thus affecting the interaction between calcium ions and graphene oxide. Compared with Gr/GO and C-S-H composites in perfect state, the incorporation of defects slows down the rate of C atoms, which can effectively enhance the interfacial connection. At temperatures of 100K-300 K, the effect of defect type on Gr/GO and C-S-H composites is small and the mobility of H atoms did not change significantly. Whereas, at high temperatures 400 K and 500 K, the presence of defects gives higher mobility of H atoms, which affects the properties of the composites. The tensile strength (compressive strength) and Young's modulus of Gr(GO)/C-S-H composites at perfect and different defect types basically show a decreasing trend with increasing temperature. The system structure changes during the relaxation process because of the different defect types and Gr (GO), which make the initial structure different, and thus the mechanical properties change.

Calcium-Pillar Boosting Smooth Phase Transition in Potassium Vanadate Nanobelts toward Superior Cycling Performance in Potassium-Ion Batteries.

The depletion of lithium resources has prompted exploration into alternative rechargeable energy storage systems, and potassium-ion batteries (PIBs) have emerged as promising candidates. As an active cathode material for PIBs, potassium vanadate (KxV2O5) usually suffers from structural damage during electrochemical K-ion insertion/extraction and hence leading to unsatisfactory cycling performance. Here, we introduce Ca2+ ions as pillars into the potassium vanadate to enhance its structural stability and smooth its phase transition behavior. The additional Ca2+ not only stabilizes the layered structure but also promotes the rearrangement of interlayer ions and leads to a smooth solid-solution phase transition. The optimal composition K0.36Ca0.05V2O5 (KCVO) exhibits outstanding cyclic stability, delivering a capacity of ∼90 mA h g-1 at 20 mA g-1 with negligible capacity decay even after 700 cycles at 500 mA g-1. Theoretical calculations indicate lower energy barriers for K+ diffusion, promoting rapid reaction kinetics. The excellent performances and detailed investigations offer insights into the structural regulation of layered vanadium cathodes.

Transition Metal Ions Synergistic Bilayer H2O Pillared MXene Directing In Situ Ordered Embedding Growth of Highly Efficient NiFe Alloy Catalysts

AbstractEfficient, stable, and inexpensive electrocatalysts are essential to overcome the high overpotential and slow kinetics of the oxygen evolution reaction (OER) process during water electrolysis applications. 2D transition metal carbides (MXene) show great potential in functional heterogeneous interface engineering for electrocatalytic OER. However, it is still a challenge to regulate the interlayer space and realize the heterogeneous layer‐by‐layer ordered embedding for MXene. Herein, a simple hydrothermal‐assisted strategy is proposed to prepare highly conductive Ti3C2Tx MXene supported by synergized Ni2+, Co2+, and Fe3+ with bilayer H2O, which significantly enlarges the interlayer distances and improves the interlayer ion concentrations. Benefiting from modulated interface chemistry, embedded metal ions undergo multi‐directional in situ growth on the MXene substrate, thereby forming a stable 0D/2D@2D nano‐hybrid material (NiFe/MX‐HT). Combining density functional theory calculations with experiments demonstrates that MXene offers a framework for electron transfer, enhances the exposure of active sites, modulates the electronic structure, and greatly reduces the energy barrier of the rate‐determining step in the process of OER. Thus, NiFe/MX‐HT requires only 230 mV to achieve 10 mA cm−2 and maintains stability even after operating at 100 mA cm−2 for 150 h. This work offers new insights into exploring various functional MXene‐based heterogeneous materials.

Removal of Cu(II) by sodium hexametaphosphate and nano zero-valent iron modified calcium bentonite: characteristic, adsorption performance and mechanism

Cu (II) is a toxic heavy metal commonly identified in groundwater contaminants. Bentonite-based cutoff wall is the most used method in isolating and adsorbing contaminants, while the bentonite in it easily to fail due to Cu(II) exchange. This study synthesized a novel material through the modification of calcium bentonite (CaB) utilizing sodium hexametaphosphate (SHMP) and nano zero-valent iron (NZVI). The characteristics, adsorption performance, and mechanism of the NZVI/SHMP-CaB were investigated comprehensively. The results showed that SHMP can disperse CaB and reduce flocculation, while NZVI can be further stabilized without agglomeration. The best adsorption performance of NZVI/SHMP-CaB could be obtained at the dosage of 2% SHMP and 4% NZVI. The NZVI/SHMP-CaB exhibited an outstanding removal efficiency of over 60% and 90% at a high Cu(II) concentration (pH = 6, Cu(II) = 300 mg/L) and acidic conditions (pH = 3–6, Cu(II) = 50 mg/L), respectively. The adsorption of Cu(II) by NZVI/SHMP-CaB followed a pseudo-second-order kinetic model, and fitting results from the Freundlich isothermal model suggested that the adsorption process occurred spontaneously. Besides the rapid surface adsorption on the NZVI/SHMP-CaB and ion exchange with interlayer ions in bentonite, the removal mechanism of Cu(II) also involved the chemical reduction to insoluble forms such as Cu0 and Cu2O. The generated FePO4 covered the surface of the homogenized NZVI particles, enhancing the resistance of NZVI/SHMP-CaB to acidic and oxidative environments. This study indicates that NZVI/SHMP-CaB is a promising alternative material which can be used for heavy metal removal from contaminated soil and water.

Built-in hybrid intercalation cations facilitated fast lithium-ion conduction of lamellar montmorillonite for safety lithium-metal batteries

Solid-state lithium-metal batteries have good prospects such as high theoretical energy density and excellent safety while available solid-state electrolytes cannot meet the electrochemical requirements. In this study, hybrid cations are built-in intercalated in lamellar montmorillonite to facilitate fast lithium-ion conduction, and a stable and safe lithium-metal battery is achieved. The hybrid intercalation cation of the large-size organic molecule cetyltrimethylammonium bromide (CTAB) broadens the insertion space as well as the Li+ insertion ensuring the concentration of interlayer conduction carriers. Based on hybrid intercalated montmorillonite, a 35 μm-thick high inorganic content solid-state electrolyte with excellent flexibility, superior hardness, and heat resistance has been prepared by the solution casting method. This electrolyte possesses high ionic conductivity (7.64 × 10−4 S·cm−1 at 25 °C), low ionic mobility energy (0.16 eV), and a wide window of electrochemical stabilization (4.92 V). With such a high-performance electrolyte, Li symmetric cells are stably cycled over 2000 h at 25 °C with a low overpotential of 30 mV. The Li||LiFePO4 solid-state battery exhibits excellent cycling stability with 94.1 % capacity retention for 200 cycles at 25 °C. This interface regulation and interlayer ion transfer strategy may provide a new method for high-performance solid-state batteries.

Layered Double Hydroxides: Recent Progress and Promising Perspectives Toward Biomedical Applications.

Layered double hydroxides (LDHs) have been widely studied for biomedical applications due to their excellent properties, such as good biocompatibility, degradability, interlayer ion exchangeability, high loading capacity, pH-responsive release, and large specific surface area. Furthermore, the flexibility in the structural composition and ease of surface modification of LDHs makes it possible to develop specifically functionalized LDHs to meet the needs of different applications. In this review, the recent advances of LDHs for biomedical applications, which include LDH-based drug delivery systems, LDHs for cancer diagnosis and therapy, tissue engineering, coatings, functional membranes, and biosensors, are comprehensively discussed. From these various biomedical research fields, it can be seen that there is great potential and possibility for the use of LDHs in biomedical applications. However, at the same time, it must be recognized that the actual clinical translation of LDHs is still very limited. Therefore, the current limitations of related research on LDHs are discussed by combining limited examples of actual clinical translation with requirements for clinical translation of biomaterials. Finally, an outlook on future research related to LDHs is provided.

Regulating core-shell interfacial interaction by oxygen bridging for enhancing electrochemical performance

It is crucial to design core-shell materials with interfacial interaction, which enhances their electrical conductivity, structural stability, and facilitates efficient charge transfer at the interface. In this study, two core-shell electrodes NC-O-PBA (NC: nickel cobalt layered double hydroxides, O-bridged core-shell materials) and LCCH@Ni(OH)2@PBA (LCCH: linear cobalt carbonate hydroxides, PBA: prussian blue analogs) were fabricated via interfacial contrast strategy to investigate the optimization function of oxygen at core-shell interface. Results show that as-prepared NC-O-PBA with high oxygen content creates an ideal condition for the formation of oxygen bridging. Moreover, the NC-O-PBA promotes a strong bond cooperation between core (NiCo-LDH) and shell (NiCo PBAs). The unit in PBAs can partly coordinate with the oxygen (from hydroxyl groups and interlayer ions in LDH), thus forming a strong interfacial coordination bonding between LDH and PBAs (Ni/Co(LDH)-O-CN(PBAs) or Ni/Co(LDH)-O-Ni/Co(PBAs)). Subsequently, NC-O-PBA electrode presents a high capacity of 1040.6 F g−1 at 1 A g−1 and a retention rate of 87.5% at 1500 cycles of 3 A g−1, much higher than LCCH@Ni(OH)2@PBA (462.4 F g−1 and 41.26%). Finally, in-situ Raman results demonstrated the enhanced Faraday redox reaction of NC-O-PBA. This interfacial contrast strategy and oxygen-bridged approach provide a novel idea for the development of high-performance core-shell electrode materials and facilitate deeper insights into mechanism.

Unraveling Interface-Driven and Loss Mechanism-Centric Phenomena in 3D/2D Halide Perovskites: Prospects for Optoelectronic Applications.

In recent years, organic-inorganic metal halide perovskite solar cells (PSCs) have attracted considerable interest due to their remarkable and rapidly advancing efficiencies. Over the past decade, PSC efficiencies have significantly approached those of state-of-the-art silicon-based photovoltaics, making them a promising material. Currently, the scientific community widely recognizes the performance of 3D-PSCs and 2D-PSCs individually. However, when both are combined to form a heterostructure, the lattice and charge dynamics at the interface undergo a multitude of mechanisms that affect their performance. The interface between heterostructures facilitates the degradation of PSCs. The degradation pathways can be attributed to lattice distortions, inhomogeneous energy landscapes, interlayer ion migration, nonradiative recombination, and charge accumulation. This Review is dedicated to examining the phenomena that arise at the interface of 3D/2D halide perovskites and their related photophysical properties and loss mechanism processes. We mainly focus on the impact of lattice mismatch, energy level alignment, anomalous carrier dynamics, and loss mechanisms. We propose a "cause-impact-identify-rectify" approach to gain a comprehensive understanding of the ultrafast processes occurring within the material. Finally, we highlight the importance of advanced spectroscopic and imaging techniques in unraveling these intricate mechanisms. This discussion delves into the future possibilities of fabricating 3D/2D heterostructure-based optoelectronic devices, pushing the boundaries of performance across diverse fields. It envisions the creation of devices with unparalleled capabilities, exceeding the limitations of current technologies.

3D self-assembled polar vs. non-polar NiO nanoparticles nanoengineered from turbostratic Ni3(OH)4(NO3)2 and ordered β-Ni(OH)2 intermediates.

A surfactant-free ammonia and carbamide precursor-modulated engineering of self-assembled flower-like 3D NiO nanostructures based on ordered β-Ni(OH)2 and turbostratic Ni3(OH)4(NO3)2 nanoplate-structured intermediates is reported. By employing complementary structural and spectroscopic techniques, fundamental insights into structural and chemical transformations from intermediates to NiO nanoparticles (NPs) are provided. FTIR, Raman and DSC analyses show that the transformation of intermediates to NiO NPs involves subsequent loss of NO3- and OH- species through a double-step phase transformation at 306 and 326 °C corresponding to the loss of free interlayer ions and H2O species, respectively, followed by the loss of chemically bonded OH- and NO3- ions. Transformation to NiO NPs via the ammonia route proceeds as single-phase transition, accompanied with a loss of OH- species at 298 °C. The full transformation to NiO NPs of both intermediates is achieved at 350 °C through annealing in the air atmosphere. Ammonia-derived NPs maintain nanoflower morphology by self-assembling into nanoplates, which is enabled by H2O-mediated adhesion on the NiO NPs' {100} neutral surfaces. Structural transformations of turbostratic Ni3(OH)4(NO3)2 nanoplates result in the formation of NiO NPs dominantly shaped by inert polar OH-terminated (111) atomic planes, leading to the loss of the initial self-assembled 3D structure. DFT calculations support these observations, confirming that H2O adsorbs dissociatively on polar {111} surfaces, while only physisorption is energetically feasible on {100} surfaces. NiO NPs obtained via two different routes have overall different properties: carbamide-derived NPs are 3 times larger (15.5 vs. 5.4 nm), possess a larger band gap (3.6 vs. 3.2 eV) and are more Ni deficient. The intensity ratio of surface optical (SO) modes to transversal and longitudinal optical modes is ∼40 times higher in the NiO NPs obtained from β-Ni(OH)2 compared to Ni3(OH)4(NO3)2-derived NPs. The SO phonon lifetime is an order of magnitude shorter in NiO obtained from β-Ni(OH)2, reflecting a much smaller NP size. The choice of a precursor defines the size, morphology, crystallographic surface orientations and band gap of the NiO NPs, with Ni deficiency providing pathways for utilizing them as p-type materials, allowing for the precise nanoengineering of polar and neutral surface-dominated NiO NPs, which is of exceptional importance for use in catalysis.

Clay based heterogeneous catalysts for carbon-nitrogen bond formation: a review.

Clay and modified clay-based catalysts are widely used in organic transformation. Owing to the interlayer ions and good ion exchange capacity of clay, replacement with another ion and incorporation of different nanomaterials can be done. Due to these significant properties of clay, it can be utilized in the synthesis of various organic compounds. Carbon-nitrogen bonded compounds possess diverse applications in different fields. These compounds are prepared using different solid acid heterogeneous catalysts. This review presents a detailed discussion on clay used for the carbon-nitrogen bond formation reaction, such as the Biginelli reaction and A3 and KA2 coupling reactions. Additionally, other C-N bond formation reactions using various clay-based catalysts such as bentonite, montmorillonite, hydrotalcite and halloysite clay with various metals, metal oxides, Kegging type heteropoly acid and various nanomaterial incorporated clay heterogeneous catalysts are discussed.

Adsorption of Polyetheramine-230 on Expansive Clay and Structure Properties Investigation.

Polyetheramine (PEA) is a swelling inhibitor used to address engineering challenges arising from the interaction between montmorillonite (Mt) and water. This study comprehensively investigates the adsorption characteristics of PEA on three representative expansive clay samples: Na-Mt, Ca-Mt, and engineered expansive soil. Additionally, the desorption of exchangeable ions is examined. The findings reveal that a two-stage adsorption kinetic model and a pseudo-second-order kinetic model can properly describe the adsorption kinetics of PEA on expansive clays. PEA exhibits a strong capacity for ion exchange with sodium ions, while the exchange capacity for calcium ions is limited. Both protonated and non-protonated PEA contribute to rapid adsorption processes. The adsorption isotherms are well-fitted by the Langmuir and Freundlich models, with the Langmuir model being reasonable. At lower equilibrium concentrations, a higher proportion of the adsorption amount is attributed to ion exchange compared to higher equilibrium concentrations. Ion exchange emerges as the primary factor contributing to the adsorption of PEA on Na-Mt, whereas the adsorption of PEA on Ca-Mt and expansive soil is primarily attributed to physical adsorption by non-protonated PEA. X-ray diffraction results reveal significant intercalation effects of PEA as they penetrate the interlayer space and hinder interlayer ion hydration. Fourier transform infrared spectrum results demonstrate that the adsorption of PEA minimally impacts the framework of Mt structural units but primarily reduces the adsorbed water content. Clay-PEA composites exhibit a decreased affinity for water. Zeta potential experiments indicate that the adsorption of PEA significantly diminishes the surface potential of clay-PEA composite particles, effectively inhibiting their hydration dispersion.

Progress of 2D MXene as an Electrode Architecture for Advanced Supercapacitors: A Comprehensive Review.

Supercapacitors, designed to store more energy and be proficient in accumulating more energy than conventional batteries with numerous charge-discharge cycles, have been developed in response to the growing demand for energy. Transition metal carbides/nitrides called MXenes have been the focus of researchers' cutting-edge research in energy storage. The 2D-layered MXenes are a hopeful contender for the electrode material due to their unique properties, such as high conductivity, hydrophilicity, tunable surface functional groups, better mechanical properties, and outstanding electrochemical performance. This newly developed pseudocapacitive substance benefits electrochemical energy storage because it is rich in interlayer ion diffusion pathways and ion storage sites. Making MXene involves etching the MAX phase precursor with suitable etchants, but different etching methods have distinct effects on the morphology and electrochemical properties. It is an overview of the recent progress of MXene and its structure, synthesis, and unique properties. There is a strong emphasis on the effects of shape, size, electrode design, electrolyte behavior, and other variables on the charge storage mechanism and electrochemical performance of MXene-based supercapacitors. The electrochemical application of MXene and the remarkable research achievements in MXene-based composites are an intense focus. Finally, in light of further research and potential applications, the challenges and future perspectives that MXenes face and the prospects that MXenes present have been highlighted.

Ultra-high Curie temperature transparent piezoelectric Bi doped Ca2Nb2O7 single crystals

Ca2Nb2O7 is a promising material for high-temperature piezoelectric applications due to its ultra-high Curie temperature, which makes it a suitable candidate for use in harsh environments. However, their piezoelectric performance needs improvement. Here, through chemical engineering methods, we have successfully grown Bi3+ doped Ca2Nb2O7 single crystals using the optical floating zone technique. The Ca1.94Bi0.06Nb2O7 single crystals achieved better high-temperature stability, transparency and a higher piezoelectric constant of 12.8 pC/N at 298 K and 20.0 pC/N at 660 K. In addition to the dopant effects, mechanisms for enhancing the piezoelectric properties of perovskite-like layer structure (PLS) materials have been identified, highlighting the significant contribution of the NbO6 octahedron and interlayer ions. These findings offers valuable insights into improving the performance of PLS materials, which is crucial for promoting their practical applications as high-temperature lead-free piezoelectric materials.

Molecular dynamics study on the structure and mechanical properties of tobermorite

The calcium silicate hydrate (C-S-H) structure has been indicated its atomic structure in the early stage of hydration resembles the geometry of tobermorite which is a natural calcium silicate hydrate. The mechanical properties of tobermorite crystals were investigated based on molecular dynamics (MD) method in this study. Uniaxial tension simulation in the z-direction was performed to the layered structure of tobermorite 9 Å, 11 Å and 14 Å at molecular level. The stress–strain relationships were obtained, and the structure analysis of tobermorite was carried out in terms of the relative concentration profile and mean square displacement. It has been found that tobermorite 9 Å has the greatest tensile strength compared with tobermorite 11 Å and 14 Å. It also shows that strong interaction between interlayer Ca ions and silicon-oxygen tetrahedra will increase the resistance of tensile loading. These findings may contribute to have a deep knowledge of the intrinsic property of C-S-H.