Broadening the Voltage Window of 3D-Printed MXene Micro-Supercapacitors with a Hybridized Electrolyte.

The burgeoning demand for miniaturized energy storage devices compatible with the miniaturization trend of electronic technologies necessitates advancements in micro-supercapacitors (MSCs) that promise safety, cost efficiency, and high-speed charging capabilities. However, conventional aqueous MSCs face a significant limitation due to their inherently narrow electrochemical potential window, which restricts their operational voltage and energy density compared to their organic and ionic liquid counterparts. In this study, we introduce an innovative aqueous NaCl/H2O/EG hybrid gel electrolyte (comprising common salt (NaCl), H2O, ethylene glycol (EG), and SiO2) for Ti3C2Tx MXene MSCs that substantially widens the voltage window to 1.6 V, a notable improvement over traditional aqueous system. By integrating the hybrid electrolyte with 3D-printed MXene electrodes, we realized MSCs with remarkable areal capacitance (1.51 F cm-2) and energy density (675 µWh cm-2), significantly surpassing existing benchmarks for aqueous MSCs. The strategic formulation of the hybrid electrolyte-a low-concentration NaCl solution with EG-ensures both economic and environmental viability while enabling enhanced electrochemical performance. Furthermore, the MSCs fabricated via 3D printing technology exhibit exceptional flexibility and are suitable for modular device integration, offering a promising avenue for the development of high-performance, sustainable energy storage devices. This advancement not only provides a tangible solution to the challenge of limited voltage windows in aqueous MXene MSCs but also sets a new precedent for the design of next-generation MSCs that align with the needs of an increasingly microdevice-centric world.

Construction of MnO2-Mn3O4 heterostructures to facilitate high-performance aqueous magnesium ion energy storage.

MnO2-Mn3O4 heterostructure materials are applied in aqueous magnesium ion energy storage for the first time. The heterostructure yields an exceptionally high pseudocapacitance contribution, resulting in a specific capacitance of 313.5 F g-1 at 1 A g-1, which contrasts with that of MnO2 (108.8 F g-1) and Mn3O4 (123.5 F g-1). Additionally, it shows potential for practical applications as a cathode for magnesium ion hybrid supercapacitors (MHS).

K-birnessite-MnO2/hollow mulberry-like carbon complexes with stabilized and superior rate performance for aqueous magnesium ion storage.

Manganese oxides are commonly employed as a cathode for magnesium ion storage in aqueous magnesium ion hybrid supercapacitors (MHS). However, sluggish reaction kinetics still hinders their practical application. Herein, we designed K-birnessite-MnO2 and electrostatically spun mulberry-like carbon composites (K-MnO2/HMCs) via an in situ growth technique. Benefiting from the 3D conductive carbon network substrate, the in situ fabricated K-MnO2 exhibits more active sites and provides more interfacial contact area between the electrode material and the electrolyte. This improvement enhances its conductivity, facilitating the rapid transfer of electrons, diffusion of ions, and redox reactions. As a result, K-MnO2/HMC-based MHS achieves a specific capacity of 168 mA h g-1 at 0.5 A g-1, simultaneously exhibiting a superior energy density of 111.1 W h kg-1 at a power density of 505 W kg-1. Furthermore, it demonstrates excellent high rate performance and a long cycling life for aqueous magnesium ion storage, offering new insights for MHS applications.

Simultaneously realizing enhancement of sensitivity for freshness monitoring and multinomial properties of carrageenan/konjac glucomannan/blueberry anthocyanin-based intelligent film by diatomite.

Here, highly sensitive blueberry anthocyanin (BBA)-induced intelligent indicating films were fabricated by incorporating a novel composite ingredient, diatomite (DA), into a matrix of konjac glucomannan (KGM), carrageenan (CAR) and BBA. We systematically investigated the effects of introducing DA and BBA on the structure, physical properties, colorimetric response, and practical application of the KGM/CAR film. Our findings revealed that the DA particles and BBA were well-distributed in the KGM/CAR matrix through hydrogen bonding interactions. This distribution significantly improved tensile strength, surface hydrophobicity, thermal stability, and barrier properties of the KGM/CAR film. Notably, the KGM/CAR-based intelligent film loaded with 6 % DA exhibited the most optimal properties. Furthermore, DA exhibited a hierarchical porous structure, enabling the KGM/CAR film to detect volatile amines with heightened sensitivity. When applied to monitor shrimp spoilage in transparent plastic packaging, the color of the composite film underwent remarkable changes from bright pink to bluish violet. These color changes correlated well with the total volatile basic nitrogen (TVB-N) and pH changes in the shrimp, as determined by standard laboratory procedures. Our work presents a promising approach to the development of high-performance and intelligent food packaging materials. These materials hold great potential for practical applications in the field of food packaging.

Probabilistic Keyphrase Generation From Copy and Generating Spaces.

Keyphrase generation is one of the most fundamental tasks in natural language processing (NLP). Most existing works on keyphrase generation mainly focus on using holistic distribution to optimize the negative log-likelihood loss, but they do not directly manipulate the copy and generating spaces, which may reduce the generability of the decoder. Additionally, existing keyphrase models are either unable to determine the dynamic numbers of keyphrases or produce the number of keyphrases implicitly. In this article, we propose a probabilistic keyphrase generation model from copy and generating spaces. The proposed model is built upon the vanilla variational encoder-decoder (VED) framework. On top of VED, two separate latent variables are adopted to model the distribution of data within the latent copy and generating spaces, respectively. Specifically, we adopt a von Mises-Fisher (vMF) distribution to obtain a condensed variable for modifying the generating probability distribution over the predefined vocabulary. Meanwhile, we utilize a clustering module, which is designed to promote Gaussian Mixture learning and subsequently extract a latent variable for the copy probability distribution. Moreover, we utilize a natural property of the Gaussian mixture network and use the number of filtered components to determine the number of keyphrases. The approach is trained based on latent variable probabilistic modeling, neural variational inference, and self-supervised learning. Experiments on social media and scientific article datasets outperform the state-of-the-art baselines in generating accurate predictions and controllable keyphrase numbers.

Rumor detection driven by graph attention capsule network on dynamic propagation structures.

Rumor detection aims to judge the authenticity of posts on social media (such as Weibo and Twitter), which can effectively prevent the spread of rumors. While many recent rumor detection methods based on graph neural networks can be conducive to extracting the global features of rumors, each node of the rumor propagation structure learned from graph neural networks is considered to have multiple individual scalar features, which are insufficient for reflecting the deep-level rumor properties. To address the above challenge, we propose a novel model named graph attention capsule network on dynamic propagation structures (GACN) for rumor detection. Specifically, GACN consists of two components: a graph attention network enforced by capsule network that can encode static graphs into substructure classification capsules for mining the deep-level properties of rumor, and a dynamic network framework that can divide the rumor structure into multiple static graphs in chronological order for capturing the dynamic interactive features in the evolving process of the rumor propagation structure. Moreover, we use the capsule attention mechanism to combine the capsules generated from each substructure to focus more on informative substructures in rumor propagation. Extensive validation on two real-world datasets demonstrates the superiority of GACN over baselines.

Optimized mesopores enable enhanced capacitance of electrochemical capacitors using ultrahigh surface area carbon derived from waste feathers.

Porous carbons with high specific surface area are critical engineering materials for current electrochemical capacitors (ECs) technology. Controlling the pore size distribution of porous carbons remains a significant challenge as it is a key aspect in many applications. Herein, we synthesized porous carbon as the electrode material of ECs by means of a two-step synthesis procedure using abandoned feathers as carbon precursor and potassium hydroxide as activating agent. The optimal sample (AFHPC-800-1:3) exhibited an ultra-high specific surface area (SBET) of 3474 m2/g and a huge total pore volume (VT) of 1.82 m3 g-1 as well as abundant small mesopores ranging from 2 to 5 nm in size. The ECs based on the AFHPC-800-1:3 electrode exhibited an ultra-high specific capacitance (Csp) of up to 709F g-1 at 0.5 A g-1. More interestingly, a capacitance of 212F g-1 was retained even at 100 A g-1, demonstrating excellent high-rate capacitive performance. Furthermore, the symmetrical capacitor yielded an excellent energy density of 35.1 Wh kg-1 when the specific power density was 625 W kg-1, substantiating the potential of the small mesopores in promoting the overall capacitance and energy density of electrode materials.

Progress in the Study of Vortex Pinning Centers in High-Temperature Superconducting Films.

Since the discovery of high-temperature superconductors (HTSs), significant progress in the fabrication of HTS films has been achieved. In this review, we intend to provide an overview of recent progress in how and why superconductivity can be enhanced by introducing nanoscale vortex pinning centers. The comprehensive control of morphology, dimension, orientation and concentration of artificial pinning centers (APCs) and the principle of vortex pinning are the focus of this review. According to the existing literature, HTSs with the best superconductivity can be obtained when one-dimensional (1D) and three-dimensional (3D) nanoscale APCs are combined for vortex pinning.

A Review on Strain Study of Cuprate Superconductors.

Cuprate superconductors have attracted extensive attention due to their broad promising application prospects. Among the factors affecting superconductivity, the effect of strain cannot be ignored, which can significantly enhance or degrade superconductivity. In this review, we discuss and summarize the methods of applying strain to cuprate superconductors, strain measurement techniques, and the influence of strain on superconductivity. Among them, we pay special attention to the study of strain in high-temperature superconducting (HTS) films and coating. We expect this review can guide further research in the field of cuprate superconductors.

Polyaniline coated MOF-derived Mn2O3 nanorods for efficient hybrid capacitive deionization.

Mn-based oxides are efficient pseudocapacitive electrode materials and have been investigated for capacitive deionization (CDI). However, their poor conductivity seriously affects their desalination performance. In this work, polyaniline coated Mn2O3 nanorods (PANI/Mn2O3) are synthesized by oxidizing a Mn-based metal organic framework (MOF) and subsequent in-situ chemical polymerization. The polyaniline not only acts as a conductive network for faradaic reactions of Mn2O3, but also enhances the desalination rate. PANI/Mn2O3 has a specific capacitance of 87 F g-1 (at 1 A g-1), superior to that of Mn2O3 nanorod (52 F g-1 at 1 A g-1). The hybrid CDI cell constructed with a PANI/Mn2O3 cathode and an active carbon anode shows a high desalination capacity of 21.6 mg g-1, superior recyclability with only 11.3% desalination capacity decay after 30 desalination cycles and fast desalination rate of 2.2 mg g-1 min-1. PANI/Mn2O3 is a potential candidate for high performance CDI applications.

One-step production of N-O-P-S co-doped porous carbon from bean worms for supercapacitors with high performance.

In recent years, multi-heteroatom-doped hierarchical porous carbons (HPCs) derived from natural potential precursors and synthesized in a simple, efficient and environmentally friendly manner have received extensive attention in many critical technology applications. Herein, bean worms (BWs), a pest in bean fields, were innovatively employed as a precursor via a one-step method to prepare N-O-P-S co-doped porous carbon materials. The pore structure and surface elemental composition of carbon can be modified by adjusting KOH dosage, exhibiting a high surface area (S BET) of 1967.1 m2 g-1 together with many surface functional groups. The BW-based electrodes for supercapacitors were shown to have a good capacitance of up to 371.8 F g-1 in 6 M KOH electrolyte at 0.1 A g-1, and good rate properties with 190 F g-1 at a high current density of 10 A g-1. Furthermore, a symmetric supercapacitor based on the optimal carbon material (BWPC1/3) was also assembled with a wide voltage window of 2.0 V, demonstrating satisfactory energy density (27.5 W h kg-1 at 200 W kg-1) and electrochemical cycling stability (97.1% retention at 10 A g-1 over 10 000 charge/discharge cycles). The facile strategy proposed in this work provides an attractive way to achieve high-efficiency and scalable production of biomass-derived HPCs for energy storage.

A carbon-coated shuttle-like Fe2O3/Fe1-x S heterostructure derived from metal-organic frameworks with high pseudocapacitance for ultrafast lithium storage.

Pursuing active, low-cost, and stable electrode materials with superior rate capability and long-life cycling performances for lithium-ion batteries remains a big challenge. In this study, a carbon-coated shuttle-like Fe2O3/Fe1-x S heterostructure is synthesized by simply annealing Fe-based metal-organic frameworks (MIL-88(Fe)) as precursors and sublimed sulfur. Carbon-coated Fe2O3/Fe1-x S displays a unique structure with ultrafine Fe2O3/Fe1-x S nanoparticles distributed in the hollow and porous carbon matrix, which offers a large specific surface area and fast charge transfer ability, and alleviates the volume change upon cycling. When evaluated as an anode material for lithium-ion batteries, it exhibits an ultra-high specific capacity of 1200 mA h g-1 at 0.1 A g-1, and superior high rate capability with a capacity of 345 mA h g-1 at a very high current density of 5.0 A g-1 owing to its high electrical conductivity and enhanced pseudocapacitive contribution from surface effects. The current strategy is promising to synthesize the carbon-coated porous structure from metal-organic frameworks for next-generation energy-storage applications.

One-step preparation of N,O co-doped 3D hierarchically porous carbon derived from soybean dregs for high-performance supercapacitors.

Hierarchically porous carbon (HPC) material based on environmental friendliness biomass has spurred much attention, due to its high surface area and porous structure. Herein, three-dimensional (3D) N,O co-doped HPC (N-O-HPC) was prepared by using a one-step fabrication process of simultaneously carbonizing and activating soybean dregs and used as an electrode for supercapacitors (SCs). The obtained N-O-HPC with 4.8 at% N and 6.1 at% O exhibits a pretty small charge transfer resistance (0.05 Ω) and a large specific capacitance (408 F g-1 at 1 A g-1), due to its 3D hierarchically porous framework structure with extremely large specific surface area (1688 m2 g-1). Moreover, a symmetrical SC assembled with the HPC electrode exhibits an amazingly high energy density (22 W h kg-1 at 450 W kg-1) and a stable long cycling life with only 6% capacitance loss after 5000 cycles in 1 M Na2SO4 solution. This work provides a facile, green, and low-cost way to prepare electrode materials for SCs.

N, O and P co-doped honeycomb-like hierarchical porous carbon derived from Sophora japonica for high performance supercapacitors.

Novel N, O and P co-doped honeycomb-like hierarchically porous carbon (N-O-P-HHPC) materials with a large specific surface area from Sophora japonica were prepared via a one-step activation and carbonization method and used as an electrode for supercapacitors. The results indicate that as-prepared N-P-HHPC with a large specific surface area (2068.9 m2 g-1) and N (1.5 atomic%), O (8.4 atomic%) and P (0.4 atomic%) co-doping has a high specific capacitance of 386 F g-1 at 1 A g-1. Moreover, a 1.8 V symmetrical SC was assembled from the N-O-P-HHPC-3 electrode using 1 M Na2SO4 gel electrolyte, presenting a high energy density (28.4 W h kg-1 at 449.9 W kg-1) and a long life cycling stability with only 7.3% capacitance loss after 10 000 cycles. Furthermore, the coin-type symmetrical SC using EMIMBF4 as electrolyte presents an ultrahigh energy density (80.8 W h kg-1 at 1500 W kg-1). When the two coin-type symmetrical SCs are connected in series, eight red light-emitting diodes (LEDs) and a small display screen can be powered. These results demonstrate as-prepared N, O and P co-doped HHPC is a considerable candidate as a carbon electrode for energy storage devices.

Electronic and Steric Tuning of an Atropisomeric Disulfoxide Ligand Motif and Its Use in the Rh(I)-Catalyzed Addition Reactions of Boronic Acids to a Wide Range of Acceptors.

A novel chiral disulfoxide ligand pair bearing fluorine atoms at the 6 and 6' position of its atropisomeric backbone, ( M, S, S)- and ( P, S, S)- p-Tol-6F-BIPHESO, was synthesized. Complexation to a rhodium(I) precursor gave rise to µ-Cl- and µ-OH-bridged rhodium dimer complexes incorporating the new ( M, S, S)- p-Tol-6F-BIPHESO ligand, while its sibling ( P, S, S)- p-Tol-6F-BIPHESO was not complexed efficiently to the rhodium precursor. The performance of this disulfoxide ligand [( M, S, S)- p-Tol-6F-BIPHESO] in catalysis was tested in both 1,4- and 1,2-addition reactions of arylboronic acids. We show that addition to both cyclic and acyclic enones as well as N-tosylarylimines proceeds with high yields and high enantioselectivities to give the corresponding products. The synthesis of enantiomerically pure p-Tol-6F-BIPHESO is straightforward and inexpensive which, together with the high catalytic performance and wide substrate scope for these addition reactions, makes it a very attractive alternative to more classical chiral ligand entities.

New, potentially chelating NHC ligands; synthesis, complexation studies, and preliminary catalytic evaluation.

Two new N-heterocyclic carbene (NHC) ligands bearing 2-morpholino and 2-piperidinyl naphthyl wingtips were synthesised (2-SIMorNap and 2-SIPipNap). Nuclear magnetic resonance studies, in conjunction with crystal structures and derivatisation of the NHC salts using a chiral counteranion, revealed that the ligand wingtips are oriented anti with respect to each other. From the free carbene, palladium, ruthenium and iridium complexes were prepared. NHC-iridium dicarbonyl complexes were made in order to extract the TEP values for these ligands. The study showed that these NHC ligands are more electron-donating than normal, aryl-substituted NHCs. The palladium complexes were tested in representative Suzuki-Miyaura cross-coupling reactions and compared to the state of the art systems. Ruthenium-catalysed ring-closing metathesis with these ligands was also performed. It was found that Grubbs' 2nd generation catalyst incorporating 2-SIPipNap did not initiate at room temperature and required heating for RCM to occur.

Smart stimuli-responsive spherical nanostructures constructed from supramolecular metallodendrimers via hierarchical self-assembly.

In this article, we present the design and construction of a series of supramolecular poly(benzyl ether) metallodendrimers featuring a well-defined hexagonal metallacycle at their cores via coordination-driven self-assembly. It was found that the second generation metallodendrimer 3c was able to hierarchically self-assemble into the regular vesicle-like structures. These nanoscale vesicles were monodisperse in shape and relatively monodisperse in size as detected in SEM, TEM, AFM, and DLS experiments. Notably, this kind of hierarchically formed vesicle-like nanostructure adopted a discrete metallacycle as the main skeleton, which is obviously different from many previous reports of nanoscale spherical architectures. Moreover, such supramolecular vesicle-like structures could encapsulate some fluorescent molecules, like BODIPY and SRB, etc. By taking advantage of the dynamic nature of metal-ligand bonds, the disassembly and reassembly of the hexagonal cavity core could be reversibly controlled by the addition and removal of bromide ions, resulting in the transition from the vesicles to micelles. Thus, the controlled release of fluorescence dye was successfully realized by the halide-induced vesicles-micelles transition. These findings not only enrich the library of supramolecular metallodenrimers but also provide a new avenue to the construction of novel "smart" nanomaterials, which have potential application in functional molecules delivery and release.

Stimuli-responsive supramolecular gels through hierarchical self-assembly of discrete rhomboidal metallacycles.

A new class of supramolecular organometallic gels with a discrete rhomboidal metallacycle as the main skeleton was fabricated through hierarchical self-assembly (see figure). More importantly, by taking advantage of the dynamic nature of metal-ligand bonds, the stimuli-responsive gel-sol transition of the obtained gels was realized by disassembly and reassembly of the rhomboidal scaffold as controlled by bromide anions.

Synthesis of triangular metallodendrimers via coordination-driven self-assembly.

A new family of 60° dendritic di-Pt(II) acceptor tectons have been successfully designed and synthesized, from which a series of novel "three-component" triangular metallodendrimers were prepared via [3 + 3] coordination-driven self-assembly. The structures of newly designed triangular metallodendrimers are characterized by multinuclear NMR ((1)H and (31)P), (1)H DOSY NMR, mass spectrometry (CSI-TOF-MS), and elemental analysis. The shape and size of all supramolecular dendritic triangles were investigated with PM6 semiempirical molecular orbital methods.

Suppression of continuous lasing in a carbon nanotube polyimide film mode-locked erbium-doped fiber laser.

We demonstrated an erbium-doped mode-locked fiber laser using a single-walled carbon nanotube-dispersed polyimide (SWNT-PI) film. Different mode-locking operations were compared and analyzed utilizing SWNT-PI films with different concentrations (2, 1, and 0.25 wt.%, respectively). It was found that the continuous single-pulse mode-locking operation was often accompanied by a continuous wave oscillation part for the 1 and 0.25 wt.% SWNT-PI films, whereas the 2 wt.% SWNT-PI film presented the most excellent mode-locking performance, thanks to sufficient modulation depth. Using the 2 wt.% SWNT-PI film, a stable pulse train with a pulse width of 840 fs and a repetition rate of 15.3 MHz was achieved. The average output power was 0.33 mW at the pump power of 155 mW under an output coupling ratio of 10%. Operational performance of the laser cavity when employing the 2 wt.% SWNT-PI film was also demonstrated.