Transition Metal Dichalcogenide (TMD) monolayers are very widely studied due to their unique physical properties. Recently, Janus TMD monolayer MoSSe, with a sandwiched S-Mo-Se structure, has been ...synthesized by replacing the top S atomic layer in MoS
with Se atoms. In this work, we systematically investigate the phonon transport and lattice thermal conductivity (κ
) in MoSSe monolayers using first-principles calculations and the linearized phonon Boltzmann equation within the single-mode relaxation time approximation (RTA). The calculated results show that the κ
of MoSSe monolayers is much lower than that of MoS
monolayers, and higher than that of MoSe
monolayers. The corresponding thermal sheet conductance of MoSSe monolayers is 342.50 W K
at room temperature. This can be understood by studying the phonon group velocities and lifetimes. Compared to MoS
monolayers, the smaller group velocities and shorter phonon lifetimes of MoSSe monolayers give rise to a lower κ
. The larger group velocities of MoSSe compared to those of MoSe
monolayers are the main reason for the higher κ
. The elastic properties of MoS
, MoSSe and MoSe
monolayers are also calculated, and the order of the Young's modulus is identical to that of the κ
. The calculated results show that isotope scattering leads to a 5.8% reduction of the κ
. The size effects on the κ
are also considered, and are usually used in device implementation. When the characteristic length of the MoSSe monolayer is about 110 nm, the κ
reduces to half. These results may offer perspectives on thermal management of MoSSe monolayers, for applications in thermoelectrics, thermal circuits and nanoelectronics, and may motivate further theoretical or experimental efforts to investigate thermal transport in Janus TMD monolayers.
Considering the ever‐growing climatic degeneration, sustainable and renewable energy sources are needed to be effectively integrated into the grid through large‐scale electrochemical energy storage ...and conversion (EESC) technologies. With regard to their competent benefit in cost and sustainable supply of resource, room‐temperature sodium‐ion batteries (SIBs) have shown great promise in EESC, triumphing over other battery systems on the market. As one of the most fascinating cathode materials due to the simple synthesis process, large specific capacity, and high ionic conductivity, Na‐based layered transition metal oxide cathodes commonly suffer from the sluggish kinetics, multiphase evolution, poor air stability, and insufficient comprehensive performance, restricting their commercialization application. Here, this review summarizes the recent advances in layered oxide cathode materials for SIBs through different optimal structure modulation technologies, with an emphasis placed on strategies to boost Na+ kinetics and reduce the irreversible phase transition as well as enhance the store stability. Meanwhile, a thorough and in‐depth systematical investigation of the structure–function–property relationship is also discussed, and the challenges as well as opportunities for practical application electrode materials are sketched. The insights brought forward in this review can be considered as a guide for SIBs in next‐generation EESC.
The recent research progress of structure modulation technology on layered transition metal oxide cathodes for sodium‐ion batteries is summarized, concentrating especially on morphology design, coating technology, phase transition, ordering‐disordering, air stability, and composite structure to boost Na+ kinetics, suppress the irreversible phase transition, enhance the storage stability, improve the overall performance, and further realize sodium‐ion battery commercialization for market applications.
Two-dimensional materials provide extraordinary opportunities for exploring phenomena arising in atomically thin crystals. Beginning with the first isolation of graphene, mechanical exfoliation has ...been a key to provide high-quality two-dimensional materials, but despite improvements it is still limited in yield, lateral size and contamination. Here we introduce a contamination-free, one-step and universal Au-assisted mechanical exfoliation method and demonstrate its effectiveness by isolating 40 types of single-crystalline monolayers, including elemental two-dimensional crystals, metal-dichalcogenides, magnets and superconductors. Most of them are of millimeter-size and high-quality, as shown by transfer-free measurements of electron microscopy, photo spectroscopies and electrical transport. Large suspended two-dimensional crystals and heterojunctions were also prepared with high-yield. Enhanced adhesion between the crystals and the substrates enables such efficient exfoliation, for which we identify a gold-assisted exfoliation method that underpins a universal route for producing large-area monolayers and thus supports studies of fundamental properties and potential application of two-dimensional materials.
Host–guest complexation between calix5arene and aggregation‐induced emission luminogen (AIEgen) can significantly turn off both the energy dissipation pathways of intersystem crossing and thermal ...deactivation, enabling the absorbed excitation energy to mostly focus on fluorescence emission. The co‐assembly of calix5arene amphiphiles and AIEgens affords highly emissive supramolecular AIE nanodots thanks to their interaction severely restricting the intramolecular motion of AIEgens, which also show negligible generation of cytotoxic reactive oxygen species. In vivo studies with a peritoneal carcinomatosis‐bearing mouse model indicate that such supramolecular AIE dots have rather low in vivo side toxicity and can serve as a superior fluorescent bioprobe for ultrasensitive fluorescence image‐guided cancer surgery.
Calix5arene‐based supramolecular AIE nanodots were synthesized with high quantum yields in water by virtue of the host–guest complexation. The absorbed excitation energy was mostly focused on fluorescence emission, leading to an ultrahigh signal‐to‐background ratio in fluorescence‐image‐guided cancer surgery.
Making highly efficient catalysts for an overall water splitting reaction is vitally important to bring solar/electrical‐to‐hydrogen energy conversion processes into reality. Herein, the synthesis ...of ultrathin nanosheet‐based, hollow MoOx/Ni3S2 composite microsphere catalysts on nickel foam, using ammonium molybdate as a precursor and the triblock copolymer pluronic P123 as a structure‐directing agent is reported. It is also shown that the resulting materials can serve as bifunctional, non‐noble metal electrocatalysts with high activity and stability for the hydrogen evolution reaction (HER) as well as the oxygen evolution reaction (OER). Thanks to their unique structural features, the materials give an impressive water‐splitting current density of 10 mA cm−2 at ≈1.45 V with remarkable durability for >100 h when used as catalysts both at the cathode and the anode sides of an alkaline electrolyzer. This performance for an overall water splitting reaction is better than even those obtained with an electrolyzer consisting of noble metal‐based Pt/C and IrOx/C catalytic couple—the benchmark catalysts for HER and OER, respectively.
A novel, non‐noble metal‐based water splitting electrocatalyst comprising nickel foam‐supported, ultrathin nanosheet‐built, hollow MoOx/Ni3S2 microspheres has been synthesized. This material gives an impressive water‐splitting current density of 10 mA cm−2 at ≈1.45 V with remarkable durability for >100 h when used as electrocatalysts both at the cathode and the anode sides of an alkaline electrolyzer.
Calixarenes (CAs), representing the third generation of supramolecular hosts and one of the most widely studied macrocyclic scaffolds, offer (almost) unlimited structure and application possibilities ...due to their ease of modification, which allows one to establish a large molecular library as a material basis for diverse biomedical applications. Moreover, CAs and their derivatives engage in various noncovalent interactions for the facile recognition of guests including bioactive molecules and are also important building blocks for the fabrication of supramolecular architectures. In view of their molecular recognition and self‐assembly properties, CAs are extensively applied in biosensing, bioimaging, and drug/gene delivery. Additionally, some CA derivatives exhibit biological activities and can therefore be used as new therapeutic agents. Herein, we summarize the diverse biomedical applications of CAs including in vitro diagnosis (biosensing), in vivo diagnosis (bioimaging), and therapy.
Calixarenes (CAs) represent the third generation of supramolecular hosts and one of the most widely studied macrocyclic scaffolds. They offer almost unlimited structural possibilities due to their ease of modification, providing a tremendous molecular library as a material basis for diverse biomedical applications.
Poly(vinylidene fluoride) (PVDF) membranes have been extensively applied to scientific research and industrial process due to its outstanding properties such as high thermal stability, good chemical ...resistance and membrane forming properties. This article provides an overview of recent progress on the application and modification of PVDF membranes. The applications include water treatment, membrane distillation, gas separation, pollutants removal, bioethanol recovery, separator for lithium ion battery, support for preparing composite membranes, etc. Subsequently, on the basis of two major problems of PVDF membranes in applications, i.e., membrane fouling and membrane wetting, the hydrophilic modification and hydrophobic modification methods are comprehensively reviewed. Finally, the key issues associated with the modification of PVDF membranes for actual applications are discussed. This paper may provide an insight for the development of PVDF membranes in future.
•A broad overview of applications of PVDF membranes is presented.•Hydrophilic modification to reduce membrane fouling in water treatment.•Hydrophobic modification to improve wetting resistance in membrane contactor.•Improving membrane preparation process and modifying existing membranes.
Simultaneous realization of improved activity, enhanced stability, and reduced cost remains a desirable yet challenging goal in the search of oxygen evolution electrocatalysts in acid. Herein we ...report iridium‐containing strontium titanates (Ir‐STO) as active and stable, low‐iridium perovskite electrocatalysts for the oxygen evolution reaction (OER) in acid. The Ir‐STO contains 57 wt % less iridium relative to the benchmark catalyst IrO2, but it exhibits more than 10 times higher catalytic activity for OER. It is shown to be among the most efficient iridium‐based oxide electrocatalysts for OER in acid. Theoretical results reveal that the incorporation of iridium dopants in the STO matrix activates the intrinsically inert titanium sites, strengthening the surface oxygen adsorption on titanium sites and thereby giving nonprecious titanium catalytic sites that have activities close to or even better than iridium sites.
Iridium OER titanium: Iridium‐containing strontium titanate perovskites (Ir‐STO) are identified as active and stable, low‐iridium‐content electrocatalysts for the oxygen evolution reaction (OER) under acidic conditions. The iridium activates the previously inert titanium sites, making them nonprecious‐metal catalytic sites that have activities close to or even better than the Ir catalytic sites.
As one of the most promising cathodes for rechargeable sodium‐ion batteries (SIBs), O3‐type layered transition metal oxides commonly suffer from inevitably complicated phase transitions and sluggish ...kinetics. Here, a NaLi0.05Ni0.3Mn0.5Cu0.1Mg0.05O2 cathode material with the exposed {010} active facets by multiple‐layer oriented stacking nanosheets is presented. Owing to reasonable geometrical structure design and chemical substitution, the electrode delivers outstanding rate performance (71.8 mAh g−1 and 16.9 kW kg−1 at 50C), remarkable cycling stability (91.9% capacity retention after 600 cycles at 5C), and excellent compatibility with hard carbon anode. Based on the combined analyses of cyclic voltammograms, ex situ X‐ray absorption spectroscopy, and operando X‐ray diffraction, the reaction mechanisms behind the superior electrochemical performance are clearly articulated. Surprisingly, Ni2+/Ni3+ and Cu2+/Cu3+ redox couples are simultaneously involved in the charge compensation with a highly reversible O3–P3 phase transition during charge/discharge process and the Na+ storage is governed by a capacitive mechanism via quantitative kinetics analysis. This optimal bifunctional regulation strategy may offer new insights into the rational design of high‐performance cathode materials for SIBs.
An O3‐type NaLi0.05Ni0.3Mn0.5Cu0.1Mg0.05O2 cathode material with exposed {010} active facets by multiple‐layer oriented stacking nanosheets is successfully constructed via reasonable structure design and chemical substitution. An optimal bifunctional regulation is demonstrated to be an efficient strategy to restrain the unfavorable multiphase transformation and greatly improve Na+ transport kinetics resulting in excellent performance for sodium‐ion batteries.
Although a number of nonprecious materials can exhibit catalytic activity approaching (sometimes even outperforming) that of iridium oxide catalysts for the oxygen evolution reaction, their catalytic ...lifetimes rarely exceed more than several hundred hours under operating conditions. Here we develop an energy-efficient, cost-effective, scaled-up corrosion engineering method for transforming inexpensive iron substrates (e.g., iron plate and iron foam) into highly active and ultrastable electrodes for oxygen evolution reaction. This synthetic method is achieved via a desired corrosion reaction of iron substrates with oxygen in aqueous solutions containing divalent cations (e.g., nickel) at ambient temperature. This process results in the growth on iron substrates of thin film nanosheet arrays that consist of iron-containing layered double hydroxides, instead of rust. This inexpensive and simple manufacturing technique affords iron-substrate-derived electrodes possessing excellent catalytic activities and activity retention for over 6000 hours at 1000 mA cm
current densities.
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