EBMGC-GNF: Efficient Balanced Multi-view Graph Clustering via Good Neighbor Fusion.

Exploiting consistent structure from multiple graphs is vital for multi-view graph clustering. To achieve this goal, we propose an Efficient Balanced Multi-view Graph Clustering via Good Neighbor Fusion (EBMGC-GNF) model which comprehensively extracts credible consistent neighbor information from multiple views by designing a Cross-view Good Neighbors Voting module. Moreover, a novel balanced regularization term based on p-power function is introduced to adjust the balance property of clusters, which helps the model adapt to data with different distributions. To solve the optimization problem of EBMGC-GNF, we transform EBMGC-GNF into an efficient form with graph coarsening method and optimize it based on accelareted coordinate descent algorithm. In experiments, extensive results demonstrate that, in the majority of scenarios, our proposals outperform state-of-the-art methods in terms of both effectiveness and efficiency.

A Luminescent Cd-MOF Used as a Chemosensor for High-Efficiency Sensing of Fe3+, Cr(IV), Trinitrophenol, and Colchicine.

A Cd-MOF was constructed based on 3,5-bis(4-carboxyphenyl) pyridine under solvothermal conditions. Its structure and phase purity were verified by single-crystal X-ray diffraction. Thereafter, some studies on the morphology, structure, and luminescent properties of the compound were carried out. The compound exhibited a highly sensitive response to Fe3+, Cr(IV), trinitrophenol (TNP), and colchicine based on the fluorescence-quenching mechanism. The possible mechanism of luminescence quenching was discussed in detail.

Sufficient driving force for quinoidal isoindigo-based diradicaloids with tunable diradical characters.

Stable organic π-conjugated diradcialoids with tunable diradical characters can profoundly affect emerging technology. Over the past years, great efforts have been devoted to studying the structure-diradical character relationship in diradicaloids. Herein, a series of quinoidal isoindigo (IID) compounds with different attached terminal end groups were designed. Detailed analysis focuses on elucidating the driving force for evoking and enhancing the diradical character in the quinoidal IID systems. The arylene units of the IID core and the bridged aromatic units determine the contribution of the open-shell diradical form in the ground state. Diradical character y0 correlates well with bond length alternation (BLA), the total HOMA, and the total NICS(1)zz, and it is tuned by bridged aromatic units and terminal end groups in symmetric systems. The zwitterionic character weakens the diradical character in asymmetric systems to different extents. This work contributes to the deep understanding of evoking and enhancing the diradical character in quinoidal IID-based diradcialoids, providing useful guidelines to produce new molecules with desirable properties.

Fast Multiview Clustering by Optimal Graph Mining.

Multiview clustering (MVC) aims to exploit heterogeneous information from different sources and was extensively investigated in the past decade. However, far less attention has been paid to handling large-scale multiview data. In this brief, we fill this gap and propose a fast multiview clustering by an optimal graph mining model to handle large-scale data. We mine a consistent clustering structure from landmark-based graphs of different views, from which the optimal graph based on the one-hot encoding of cluster labels is recovered. Our model is parameter-free, so intractable hyperparameter tuning is avoided. An efficient algorithm of linear complexity to the number of samples is developed to solve the optimization problems. Extensive experiments on real-world datasets of various scales demonstrate the superiority of our proposal.

Dealloying fabrication of hierarchical porous Nickel-Iron foams for efficient oxygen evolution reaction.

Designing and preparing highly active oxygen evolution reaction (OER) electrodes are essential for improving the overall efficiency of water splitting. Increasing the number of active sites is the simplest way to enhance OER performance. Herein, we present a dealloy-etched Ni-Fe foam with a hierarchical nanoporous structure as integrated electrodes with excellent performance for OER. Using the dealloying method on the Ni-Fe foam framework, a nanoporous structure is produced, which is named nanoporous Ni-Fe@Ni-Fe foam (NP-NF@NFF). Because of the peculiarities of the dealloying method, the NP-NF@NFF produced contains oxygen vacancies and heterojunctions. As a result, NP-NF@NFF electrode outperforms state-of-the-art noble metal catalysts with an extremely low overpotential of 210 and 285 mV at current densities of 10 and 100 mA cm-2, respectively. Additionally, the NP-NF@NFF electrode shows a 60-h stability period. Therefore, NP-NF@NFF provides new insights into the investigation of high-performance transition metal foam electrodes with effective active sites for efficient oxygen evolution at high current densities.

Luminescence of Mn4+ in a Zero-Dimensional Organic-Inorganic Hybrid Phosphor [N(CH3)4]2ZrF6 for Dual-Mode Temperature Sensing.

Searching for new low-dimensional organic-inorganic hybrid phosphors is of great significance due to their unique optical properties and wide applications in the optoelectronic field. In this work, we report a Mn4+ doped zero-dimensional organic-inorganic hybrid phosphor [N(CH3)4]2ZrF6, which was synthesized by a wet chemical method. The crystal structure, thermal stability, and optical properties were systemically investigated by means of XRD, SEM, TG-DTA, FTIR, DRS, emission spectra, excitation spectra, as well as decay curves. Narrow red emission with high color purity can be observed from [N(CH3)4]2ZrF6:Mn4+ phosphor, which maintains effective emission intensity even at room temperature, indicating its potential practical application in WLEDs. In the temperature range of 13-295 K, anti-Stokes and Stokes sidebands of Mn4+ ions exhibit different temperature responses. By applying the emission intensity ratio of anti-Stokes vs. Stokes sidebands as temperature readout, an optical thermometer with a maximum absolute sensitivity of 2.13% K-1 and relative sensitivity of 2.47% K-1 can be obtained. Meanwhile, the lifetime Mn4+ ions can also be used for temperature sensing with a maximum relative sensitivity of 0.41% K-1, demonstrating its potential application in optical thermometry.

A Water-Stable Zn-MOF Used as Multiresponsive Luminescent Probe for Sensing Fe3+/Cu2+, Trinitrophenol and Colchicine in Aqueous Medium.

A water-stable Zn-MOF was constructed based on H2PBA and 1, 10-phenanthroline under solvothermal conditions. The compound exhibited a 3D (2,3,8)-connected (43)2(46.66.815.12)(8) topology framework. The crystal structure and phase purity of the compound was verified by single crystal X-ray diffraction. Subsequently, some studies on the morphology, structure, and luminescent properties were carried out. The results showed that this compound could be used as a versatile chemosensor for Fe3+/Cu2+, trinitrophenol and colchicine via a luminescence quenching effect in an aqueous medium.

Wideband, high spectral resolution UV convex grating imaging spectrometer based on an Offner structure.

Ultraviolet is an effective electromagnetic spectrum in material detection, which has wide application prospects in aerospace and environmental monitoring. A conventional imaging spectrometer has a narrow UV band and low spectral resolution. To solve this problem, a convex grating imaging spectrometer based on an Offner structure with F#2.5 and a 13 mm long slit was designed and developed. The working wavelength ranges from 200 to 433 nm, and the spectral resolution is greater than 0.5 nm. A hyperspectral data cube with both high spatial and spectral resolutions of external scenes can be obtained by the push-broom imaging mode. Fine Fraunhofer lines can be distinguished in the spectrum. The ultraviolet hyperspectral imager can be used for marine oil spills, trace gas monitoring, and other applications that require high signal-to-noise ratios, wide bands, and high spectral resolutions.

Hierarchical Co(OH)2 Dendrite Enriched with Oxygen Vacancies for Promoted Electrocatalytic Oxygen Evolution Reaction.

It is critical to develop efficient oxygen evolution reaction (OER) catalysts with high catalytic properties for overall water splitting. Electrocatalysts with enriched vacancies are crucial for enhancing the catalytic activity of OER through defect engineering. We demonstrated the dealloying method in a reducing alkaline solution using the Co5Al95 alloy foil as a precursor to produce a new oxygen-vacancy-rich cobalt hydroxide (OV-Co(OH)2) hierarchical dendrite. The as-synthesised OV-Co(OH)2 showed superior electrocatalytic activities toward OER when compared to pristine cobalt hydroxide (p-Co(OH)2), which had a low onset overpotential of only 242 mV and a small Tafel slope of 64.9 mV dec-1. Additionally, for the high surface area provided by the hierarchical dendrite, both p-Co(OH)2 and OV-Co(OH)2 showed a superior activity as compared to commercial catalysts. Furthermore, they retained good catalytic properties without remarkably decaying at an overpotential of 350 mV for 12 h. The as-made OV-Co(OH)2 has prospective applications as an anode electrocatalyst in electrochemical water-splitting technologies with the advantages of superior OER performances, large surface area and ease of preparation.

Discrete and Parameter-Free Multiple Kernel k-Means.

The multiple kernel k -means (MKKM) and its variants utilize complementary information from different sources, achieving better performance than kernel k -means (KKM). However, the optimization procedures of most previous works comprise two stages, learning the continuous relaxation matrix and obtaining the discrete one by extra discretization procedures. Such a two-stage strategy gives rise to a mismatched problem and severe information loss. Even worse, most existing MKKM methods overlook the correlation among prespecified kernels, which leads to the fusion of mutually redundant kernels and bad effects on the diversity of information sources, finally resulting in unsatisfying results. To address these issues, we elaborate a novel Discrete and Parameter-free Multiple Kernel k -means (DPMKKM) model solved by an alternative optimization method, which can directly obtain the cluster assignment results without subsequent discretization procedure. Moreover, DPMKKM can measure the correlation among kernels by implicitly introducing a regularization term, which is able to enhance kernel fusion by reducing redundancy and improving diversity. Noteworthily, the time complexity of optimization algorithm is successfully reduced, through masterly utilizing of coordinate descent technique, which contributes to higher algorithm efficiency and broader applications. What's more, our proposed model is parameter-free avoiding intractable hyperparameter tuning, which makes it feasible in practical applications. Lastly, extensive experiments conducted on a number of real-world datasets illustrated the effectiveness and superiority of the proposed DPMKKM model.

Design of a confocal micro-Raman spectroscopy system and research on microplastics detection.

Traditional micro-Raman spectroscopy technology has the disadvantages of a weak signal and low signal-to-noise ratio. To fix these issues, a cost-effective and rigorous design method is proposed in this paper, whereby a confocal micro-Raman spectroscopy system is designed and built, and a low-cost reflector and high-pass filter are introduced into the Raman signal-receiving module. The Raman light incident is fully perpendicular to the coupling lens by adjusting the reflection angle of the mirror, making the focus of the coupling lens highly conjugate with the focus of the microscope objective, to enhance the intensity of the Raman signal and improve the signal-to-noise ratio. In order to better apply this technology to the detection and study of microplastics in offshore sediments, a reflective illumination light path is used to avoid the visual interference caused by the capillary structure and opacity of the glass cellulose filter membrane. The detection and analysis of the microplastics on the glass cellulose filter membrane have been carried out by the confocal micro-Raman system designed, which is low cost and capable of obtaining good detection results and meeting the requirements of microplastics detection. The system designed in this paper is expected to be applied to the research and development of Raman detection equipment for microplastics in marine sediments, which is beneficial to promote the development of marine microplastic monitoring technology in the world.

A Multifunctional 3D Supermolecular Co Coordination Polymer With Potential for CO2 Adsorption, Antibacterial Activity, and Selective Sensing of Fe3+/Cr3+ Ions and TNP.

A 3D supermolecular structure [Co3(L)2 (2,2'-bipy)2](DMF)3(H2O)3 1) (H3L = 4,4',4″-nitrilotribenzoic acid) has been constructed based on H3L, and 2,2'-bipy ligands under solvothermal conditions. Compound 1 can be described as a (3, 6)-connected kgd topology with a Schläfli symbol (43)2(46.66.83) formed by [Co3(CO2)6] secondary building units. The adsorption properties of the activated sample 1a has been studied; the result shows that 1a has a high adsorption ability: the CO2 uptakes were 74 cm3·g-1 at 273 K, 50 cm3·g-1 at 298 K, the isosteric heat of adsorption (Qst) is 25.5 kJ mol-1 at zero loading, and the N2 adsorption at 77 K, 1 bar is 307 cm3 g-1. Magnetic measurements showed the existence of an antiferromagnetic exchange interaction in compound 1, besides compound 1 exhibits effective luminescent performance for Fe3+/Cr3+ and TNP.

Evaluation of Fused Aromatic-Substituted Diketopyrrolopyrrole Derivatives for Singlet Fission Sensitizers.

Singlet fission (SF) is a spin-allowed carrier multiplication process that has potential to overcome the Shockley-Queisser limit of solar energy conversion efficiency for single-junction solar cells. It is of importance to prescreen appropriate SF candidates for both basic research and practical applications of SF. Besides common polycyclic aromatic hydrocarbons (PAHs), diketopyrrolopyrrole (DPP) derivatives also undergo efficient SF. A series of DPP derivatives with fused aromatic substituents were investigated considering their conjugation length, constitution, and the introduction of terminal substituents. A comparison of SF properties between nonfused and fused aromatic-substituted DPP derivatives was carried out. Detailed analysis focused on elucidating the relationship between the frontier molecular orbital energies, multiple diradical characters, and SF-relevant excited-state energy levels. Compared to nonfused aromatic-substituted DPP derivatives, fused aromatic-substituted DPP derivatives which contain three aromatic units (thiophene or furan) still share more appropriate energy levels for SF sensitizers. Changing the five-membered aromatic units with benzene ring and introducing -F, -OMe, and -COOH as terminal substituents are both effective ways to improve their performance as SF sensitizers. The results of this research help us to understand the SF properties of DPP derivatives deeply and are beneficial for the design of new DPP-based SF sensitizers.

Oxygen-Vacancy-Enhanced Peroxidase-like Activity of Reduced Co3O4 Nanocomposites for the Colorimetric Detection of H2O2 and Glucose.

Colorimetric assays have drawn increasing research interest with respect to the quantitative detection of hydrogen peroxide (H2O2) based on artificial enzymes because of their advantages with respect to natural enzymes, including design flexibility, low cost, and high stability. Regardless, the majority of the artificial enzymes exhibit low affinity to H2O2 with large Michaelis-Menten constants (Km). This indicates that the catalytic oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) to blue-colored oxTMB requires a high H2O2 concentration, hindering the sensitivity of the colorimetric assay. To address this problem, novel reduced Co3O4 nanoparticles (R-Co3O4) have been synthesized in this study via a step-by-step procedure using ZIF-67 as the precursor. R-Co3O4 exhibits a considerably enhanced peroxidase-like activity when compared with that exhibited by pristine Co3O4 (P-Co3O4). The catalytic process in the case of R-Co3O4 occurs in accordance with the typical Michaelis-Menten equation, and the affinity of R-Co3O4 to H2O2 is apparently higher than that of P-Co3O4. Furthermore, the density functional theory calculations revealed that the introduction of oxygen vacancies to R-Co3O4 enhances its H2O2 adsorption ability and facilitates the decomposition of H2O2 to produce ·OH radicals, resulting in improved peroxidase-like activity. A simple and convenient colorimetric assay has been established based on the excellent peroxidase-like activity of R-Co3O4 for detecting H2O2 in concentrations of 1-30 µM with a detection limit of 4.3 × 10-7 mol/L (S/N = 3). Furthermore, the R-Co3O4-based colorimetric method was successfully applied to glucose detection in human serum samples, demonstrating its potential for application in complex biological systems.

Cobalt Nanoparticles Embedded into N-Doped Carbon from Metal Organic Frameworks as Highly Active Electrocatalyst for Oxygen Evolution Reaction.

Cystosepiment-like cobalt nanoparticles@N-doped carbon composite named Co-NPs@NC with highly efficient electrocatalytic performance for oxygen evolution reaction was prepared from carbonization of N-doped Co-MOFs. The optimized Co-NPs@NC-600 shows overpotentials of 315 mV to afford a current density of 10 mA·cm-2. Meanwhile, the electrocatalys presents excellent long-term durability. The outstanding electrocatalytic performance can be attributed to the unique cystosepiment-like architecture with high specific surface area (214 m2/g), high conductivity of N-doped carbon and well-distributed active sites.

A Porous Cobalt (II) Metal⁻Organic Framework with Highly Efficient Electrocatalytic Activity for the Oxygen Evolution Reaction.

A 3D porous framework ([Co1.5(tib)(dcpna)]·6H2O) (1) with a Wei topology has been synthesized by solvothermal reaction of 1,3,5-tris(1-imidazolyl)-benzene (tib), 5-(3',5'-dicarboxylphenyl)nicotinic acid (H3dcpna) and cobalt nitrate. The electrocatalytic activity for water oxidation of 1 has been investigated in alkaline solution. Compound 1 exhibits good oxygen evolution reaction (OER) activities in alkaline solution, exhibiting 10 mA·cm-2 at η = 360 mV with a Tafel slope of 89 mV·dec-1. The high OER activity can be ascribe to 1D open channels along b axis of 1, which expose more activity sites and facilitate the electrolyte penetration.

Design, synthesis, and self-assembly of optically active perylenetetracarboxylic diimide bearing two peripheral chiral binaphthyl moieties.

An optically active perylenetetracarboxylic diimide (PTCDI) bearing two optically active binaphthyl moieties has been designed and synthesized. The self-assembly properties of these novel PTCDI derivatives in DMF/H2O were systematically investigated by electronic absorption, circular dichroism (CD) spectra, IR spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and X-ray diffraction (XRD) technique. Observation of CD signal in the whole absorption region of PTCDI chromophore, indicates effective chiral information transfer from the chiral binaphthyl units to the central PTCDI chromophore at molecular level. The intermolecular π-π interaction between PTCDI rings together with the additionally formed hydrogen bonds between the crown ether moieties of (S)-1 and additional water molecules and the chiral discrimination of periphery chiral side chains induces further intensified asymmetrical perturbation of the chiral binaphthyl units to the central PTCDI chromophore during the self-assembly process, resulting in the formation of right-handed helical arrangement of corresponding molecules in a stack of PTCDI chromophores in aggregates. In addition, the formed nanostructures were revealed to show good semiconducting properties.

Sandwich-type (phthalocyaninato)(porphyrinato) europium triple-decker nanotubes. Effects of the phthalocyanine peripheral substituents on the molecular packing.

Three sandwich-type (phthalocyaninato)(porphyrinato) europium triple-decker complexes, namely Eu(2)(Pc)(2)(TClPP) (1), Eu(2)[Pc(ß-OC(4)H(9))(8)](2)(TClPP) (2), and Eu(2)[Pc(ß-OC(8)H(17))(8)](2)(TClPP) (3), have been designed, synthesized, and fabricated into nanotubes using nanoporous anodized aluminium oxide (AAO) membrane as the template. In particular, the effects of peripheral-substituents at the two phthalocyanine ligands in the triple-decker molecule on the molecular stacking relative to the alumina surface and the molecular packing mode in the nanotubes were clarified on the basis of the scanning electron microscopy (SEM), spectroscopic, and X-ray diffraction results. High-resolution TEM (HRTEM) images, in combination with the electronic absorption and XRD results, indicate that the discotic molecules of 1 without peripheral substituent on the phthalocyanine ligands form columnar structures on the alumina surface with homeotropic molecular stacking depending on the intermolecular π-π interactions in a head-to-tail manner. In good contrast, introduction of eight long octyloxy substituents at the peripheral-positions of the phthalocyanine ligands of 3 induces an increase in the interaction of the triple-decker molecules with the alumina surface, resulting in the formation of nanotubes with discotic molecules of 3 parallel stacking relative to the alumina surface depending on the intermolecular π-π interactions in a face-to-face manner. Most interestingly, introduction of eight shorter length butyloxy substituents at the peripheral-positions of the phthalocyanine ligands of 2 leads to the formation of nanotubes with discotic molecules of 2 parallel stacking relative to the alumina surface but depending on the intermolecular π-π interactions in a head-to-tail manner. X-Ray diffraction (XRD) data confirm the above-mentioned results.

Optically active mixed (phthalocyaninato)(porphyrinato) rare earth triple-decker complexes. Synthesis, spectroscopy, and effective chiral information transfer.

With the view to creating novel sandwich-type tetrapyrrole rare earth complexes toward potential applications in material science and chiral catalysis, two new optically active mixed (phthalocyaninato)(porphyrinato) rare earth triple-decker complexes with both (R)- and (S)-enantiomers [M(2)(Pc)(2)(TCBP)] {TCBP = Meso-tetrakis [3,4-(11,12:13,14-di(1',2'-naphtho)-1,4,7,10,15,18-hexaoxacycloeicosa-2,11,13-triene)-phenyl] porphyrinate; M = Eu (1), Y (2)} have been designed and prepared by treating optically active metal free porphyrin (R)-/(S)-H(2)TCBP with M(Pc)(2) in the presence of corresponding M(acac)(3)·nH(2)O (acac = acetylacetonate) in refluxing 1,2,4-trichlorobenzene (TCB). These novel mixed ring rare earth triple-decker compounds were characterized by a wide range of spectroscopic methods including MS, (1)H NMR, IR, electronic absorption, and magnetic circular-dichroism (MCD) spectroscopic measurements in addition to elemental analysis. Perfect mirror image relationship was observed in the Soret and Q absorption regions in the circular-dichroism (CD) spectra of the (R)- and (S)-enantiomers, indicating the optically active nature of these two mixed (phthalocyaninato)(porphyrinato) rare earth triple-decker complexes. This result reveals the effective chiral information transfer from the peripheral chiral binaphthyl units to the porphyrin and phthalocyanine chromophores in the triple-decker molecule because of the intense π-π interaction between porphyrin and phthalocyanine rings. In addition, their electrochemical properties have also been investigated by cyclic voltammetry (CV).

Helical nanostructures self-assembled from optically active phthalocyanine derivatives bearing four optically active binaphthyl moieties: effect of metal-ligand coordination on the morphology, dimension, and helical pitch of self-assembled nanostructures.

(R)- and (S)-enantiomers of optically active metal free tetrakis[11,12:13,14-di(1',2'-naphtho)-1,4,7,10,15,18-hexaoxacycloeicosa-2,11,13-trieno]-phthalocyanine and their zinc complexes, (R)- and (S)-H(2)Pc (1) and (R)- and (S)-ZnPc (2), were prepared from the tetramerization of corresponding phthalonitriles, (R)- and (S)-2,3-(4',5'-dicyanobenzo)-11,12:13,14-di(1',2'-naphtho)-1,4,7,10,15,18-hexaoxacycloeicosa-2,11,13-triene, in the absence and presence of Zn(OAc)(2).2H(2)O template, respectively, promoted by organic base 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Their self-assembly behavior in the absence and presence of 4,4'-bipyridine has been comparatively investigated by electronic absorption and circular dichroism (CD) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD) technique, and X-ray photoelectron spectroscopy (XPS). The metal free phthalocyanine self-assembles into highly ordered fibrous nanostructures (ca. 3 microm length, 70 nm width, and 125 nm helical pitch) with left-handed and right-handed helicity for (R)-1 and (S)-1, respectively, through the hierarchical manner via one-dimensional helices with chirality determined by the optically active binaphthyl side chains. In contrast, self-assembly of the phthalocyaninato zinc analogue leads to the formation of nanoparticles. However, in the presence of 4,4'-bipyridine, additionally formed metal-ligand Zn-N(4,4'-bipyridine) coordination bonds between the nitrogen atoms of additive 4,4'-bipyridine molecule and the zinc center of (R)- and (S)-2 molecules together with pi-pi interaction and chiral discrimination of chiral side chains induce a right-handed and left-handed helical arrangement in a stack of (R)- and (S)-2 molecules, respectively, which further hierarchically packs into highly ordered fibrous nanostructures of average tens of micrometers in length, 30 nm width, and 106 nm helical pitch with the same helicity to the stack, revealing the effect of metal-ligand coordination bonding interaction on the morphology, dimension, handedness, and helical pitch of self-assembled nanostructures.