Hierarchical chiral MOFs with the induced chirality of AIE ligands exhibiting non-reciprocal CPL.

Two pairs of chiral MOFs with hierarchical chiral structures were constructed through assembly of achiral AIE-type multidentate linkers and chiral camphoric acid. Non-reciprocal circularly polarized luminescence (CPL) can be observed on the macroscopic due to the coexistence of optical anisotropic and chiroptical nature. This study provides a new perspective to recognize and construct chiral crystalline materials.

Transition-Metal Porphyrin-Based MOFs In Situ-Derived Hybrid Catalysts for Electrocatalytic CO2 Reduction.

Excellent electrocatalytic CO2 reduction reaction activity has been demonstrated by transition metals and nitrogen-codoped carbon (M-N-C) catalysts, especially for transition-metal porphyrin (MTPP)-based catalysts. In this work, we propose to use one-step low-temperature pyrolysis of the isostructural MTPP-based metal-organic frameworks (MOFs) and electrochemical in situ reduction strategies to obtain a series of hybrid catalysts of Co nanoparticles (Co NPs) and MTPP, named Co NPs/MTPP (M = Fe, Co, and Ni). The in situ introduction of Co NPs can efficiently enhance the electrocatalytic ability of MTPP (M = Fe, Co, and Ni) to convert CO2 to CO, particularly for FeTPP. Co NPs/FeTPP endowed a high CO faradaic efficiency (FECOmax = 95.5%) in the H cell, and the FECO > 90.0% is in the broad potential range of -0.72 to -1.22 VRHE. In addition, the Co NPs/FeTPP achieved 145.4 mA cm-2 at a lower potential of -0.70 VRHE with an FECO of 94.7%, and the CO partial currents increased quickly to reach 202.2 mA cm-2 at -0.80 VRHE with an FECO of 91.6% in the flow cell. It is confirmed that Co NPs are necessary for hybrid catalysts to get superior electrocatalytic activity; Co NPs also can accelerate H2O dissociation and boost the proton supply capacity to hasten the proton-coupled electron-transfer process, effectively adjusting the adsorption strength of the reaction intermediates.

Ultrafast Response in Nonenzymatic Electrochemical Glucose Sensing with Ni(II)-MOFs by Dimensional Manipulation.

Metal-organic frameworks (MOFs) are emerging as promising candidates for electrochemical glucose sensing owing to their ordered channels, tunable chemistry, and atom-precision metal sites. Herein, the efficient nonenzymatic electrochemical glucose sensing is achieved by taking advantage of Ni(II)-based metal-organic frameworks (Ni(II)-MOFs) and acquiring the ever-reported fastest response time. Three Ni(II)-MOFs ({[Ni6L2(H2O)26]4H2O}n (CTGU-33), {Ni(bib)1/2(H2L)1/2(H2O)3}n (CTGU-34), {Ni(phen)(H2L)1/2(H2O)2}n (CTGU-35)) have been synthesized for the first time, which use benzene-1,2,3,4,5,6-hexacarboxylic acid (H6L) as an organic ligand and introduce 1,4-bis(1-imidazoly)benzene (bib) or 1,10-phenanthroline (phen) as spatially auxiliary ligands. Bib and phen convert the coordination mode of CTGU-33, affording structural dimensions from 2D of CTGU-33 to 3D of CTGU-34 or 1D of CTGU-35. By tuning the dimension of the skeleton, CTGU-34 with 3D interconnected channels exhibits an ultrafast response of less than 0.4 s, which is superior to the existing nonenzymatic electrochemical sensors. Additionally, a low detection limit of 0.12 µM (S/N = 3) and a high sensitivity of 1705 µA mM-1 cm-2 are simultaneously achieved. CTGU-34 further showcases desirable anti-interference and cycling stability, which demonstrates a promising application prospect in the real-time detection of glucose.

Seaweed-like phosphates/MOF heterostructures as a synergistic electrocatalyst for alcohol oxidation.

A series of seaweed-like heterogeneous Co3(PO4)2/Ni3(PO4)2/MOF-74-x electrocatalysts were synthesized via a hydrothermal method. The optimal composite exhibits excellent catalytic performance toward methanol/ethanol oxidation reactions (MOR/EOR) with peak current densities reaching 27.5 and 32.6 mA cm-2, respectively. This work heralds the advent of more efficient heterogeneous electrocatalysts for DAFCs and other energy conversion systems.

Nonenzymatic Electrochemical Sensing Platform Based on 2D Isomorphic Co/Ni-Metal-Organic Frameworks for Glucose Detection.

Two-dimensional metal-organic framework (MOF) crystalline materials possess promising potential in the electrochemical sensing process owing to their tunable structures, high specific surface area, and abundant metal active sites; however, developing MOF-based nonenzymatic glucose (Glu) sensors which combine electrochemical activity and environmental stability remains a challenge. Herein, utilizing the tripodic nitrogen-bridged 1,3,5-tris(1-imidazolyl) benzene (TIB) linker, Co2+ and Ni2+, two 2D isomorphic crystalline materials, including Co/Ni-MOF {[Co (TIB)]·2BF4} (CTGU-31) and {[Ni(TIB)]·2NO3} (CTGU-32), with a binodal (3, 6)-connected kgd topological net were firstly synthesized and fabricated with conducting acetylene black (AB). When modified on a glassy carbon electrode, the optimized AB/CTGU-32 (1:1) electrocatalyst demonstrated a higher sensitivity of 2.198 µA µM-1 cm-2, a wider linear range from 10 to 4000 µM, and a lower detection limit (LOD) value (0.09 µM, S/N = 3) compared to previously MOF-based Glu sensors. Moreover, AB/CTGU-32 (1:1) exhibited desirable stability for at least 2000 s during the electrochemical process. The work indicates that MOF-based electrocatalysts are a promising candidate for monitoring Glu and demonstrate their potential for preliminary screening for diabetes.

Ar plasma assists in enhanced oxygen evolution kinetics of MOG-derived multicomponent transition metal sulfides.

Transition metal sulfides are low-cost oxygen evolution reaction (OER) electrocatalysts that can potentially substitute noble metal catalysts. However, the adsorption process of their OER is impeded by their intrinsic poor catalytic activity. Constructing heterojunction and vacancy defects in transition metal sulfides is an efficient method to promote the process of oxygen evolution. Herein, a facile approach based on in situ sulfurization of metal-organic gels (MOGs) and a short-time plasma treatment was developed to fabricate vacancy-modified polymetallic sulfides heterojunction. The synergistic effect of the multi-component heterojunction and sulfur vacancy contributed greatly to improving the electron migration efficiency and OER ability of the electrocatalyst. As a result, the optimum oxygen evolution activity was achieved with appropriate surface vacancy concentrations by regulating the plasma radio frequency powers. The plasma-treated catalyst under 400 W showed the best OER performance (lower overpotential of 235 mV in 1 M KOH solution with the Tafel slope of 31 mV dec-1) and good durability over 11 h of chronopotentiometry testing. This work sheds new light on constructing multimetal-based heterojunction electrocatalysts with rich vacancy defects for oxygen evolution reactions.

Multicolor-tunable room-temperature afterglow and circularly polarized luminescence in chirality-induced coordination assemblies.

Dynamic long-lived multicolor room temperature afterglow and circularly polarized luminescence (CPL) are promising for optoelectronic applications, but integration of these functions into a single-phase chiroptical material is still a difficult and meaningful challenge. Here, a nitrogen-doped benzimidazole molecule 1H-1,2,3-triazolopyridine (Trzpy) showing pure organic room-temperature phosphorescence (RTP) acted as a linker, and then, we propose a chirality-induced coordination assembly strategy to prepare homochiral crystal materials. Two homochiral coordination polymers DCF-10 and LCF-10 not only exhibit multicolor-tunable RTP, the color changed from green to orange under various excitation wavelengths, but also show remarkable excitation-dependent circularly polarized luminescence (CPL), and the dissymmetry factors of CPL in DCF-10 and LCF-10 are 1.8 × 10-3 and 2.4 × 10-3, respectively. Experimental and theoretical studies demonstrated that molecular atmospheres with different aggregation degrees give rise to multiple emission centers for the generation of multicolor-tunable emission. The multicolor-tunable photophysical properties endowed LCF-10 with a huge advantage for multi-level anti-counterfeiting. This work opens up new perspectives for the development and application of color-tunable RTP and CPL.

Facile in Situ Transformation of NiOOH into MOF-74(Ni)/NiO OH Heterogeneous Composite for Enchancing Electrocatalytic Methanol Oxidation.

A new MOF-74(Ni)/NiOOH heterogeneous composite was synthesized via NiOOH microsphere precursor. The electrocatalytic methanol oxidation reactions' (MOR) performance was assessed. The as-prepared MOF-74(Ni)/NiOOH exhibited excellent activity with high peak current density (27.62 mA·cm-2) and high mass activity (243.8 mA·mg-1). The enhanced activity could be a result of the synergistic effect of the MOF-74(Ni)/NiOOH heterocomposite providing more exposed active sites, a beneficial diffusion path between the catalyst surface and electrolyte, and improved conductivity, favorable for improving MOR performance.

Thermal treatment for promoting interfacial interaction in Co-BDC/Ti3C2Tx hybrid nanosheets for hybrid supercapacitors.

The design and synthesis of high-performance metal-organic frameworks (MOFs)-based electrodes are important for hybrid supercapacitors (HSC). Herein, enhanced interfacial interaction in Co-BDC/Ti3C2Tx (denoted as CoTC) hybrid nanosheets is achieved through thermal treatment, giving remarkably improved capacity performance compared with CoTC. The low temperature annealing treatment enables modulation of the bridging bonds content of CoTC and thus regulates the interfacial coupling effect between Co-BDC and Ti3C2Tx. Moreover, both the detailed XPS and XANES analysis reveal that the strong interfacial interactions between the two components promote a partial electron transfer from Ti3C2Tx to Co-BDC through the Ti-O-Co interfacial bonds. Consequently, it endows the Co-BDC with enhanced conductivity as well as the higher valence of Ti species in Ti3C2Tx, hence contributes a remarkable enhanced specific capacity. This work will provide a pathway to design advanced MOF/MXene materials for HSC.

In Situ Synthesis of Surface-Mounted Novel Nickel(II) Trimer-Based MOF on Nickel Oxide Hydroxide Heterostructures for Enhanced Methanol Electro-Oxidation.

Engineering the heterogeneous interface fusing MOFs and inorganic active component is an effective strategy to improve the electrochemical performance. Herein, we report a new Ni3-based MOF (denoted as CTGU-24) with an infrequent two-fold interpenetrating 3D (3,8)-connected network constructed from Ni(II) trimer and mixed tripodal tectonics for the electrocatalytic methanol oxidation reaction (MOR). In order to improve its stability and activities, the heterogeneous hybrid CTGU-24@NiOOH has been fabricated successfully via the first preparation of the NiOOH nanosphere and then in situ formation of CTGU-24 decorated on the NiOOH surface. Moreover, the integration of CTGU-24@NiOOH and different additives [acetylene black (AB) and ketjen black (KB)], resulting in the optimized hybrid sample AB&CTGU-24@NiOOH (4:4). It attains better MOR performance with an area-specific peak current density of 34.53 mA·cm-2 than pure CTGU-24 (14.99 mA·cm-2) and improved durability in an alkali medium. The new findings indicate that the CTGU-24@NiOOH heterostructure formed in situ and the integration of moderate additives are critical to optimizing and improving electrocatalytic activity of pure MOF crystalline material.

Common Strategy: Mounting the Rod-like Ni-Based MOF on Hydrangea-Shaped Nickel Hydroxide for Superior Electrocatalytic Methanol Oxidation Reaction.

Developing efficient metal-organic framework (MOF)-based electrocatalysts with improvable activity and persistence toward the methanol oxidation reaction (MOR) is attracting great research attention but still remains an enormous challenge. Herein, a facile strategy, hydrangea-shaped nickel hydroxide template-directed synthesis of the hierarchically structured Ni-MOF on the Ni(OH)2 heterocomposite (denoted as Ni-Ni) for efficient MOR, is developed. The unique hierarchical structure and synergistic effect of the heterocomposite afford more exposed active sites, a facile ion diffusion path, and improved conductivity, favorable for improving MOR catalytic performance. Remarkably, the optimized Ni-Ni-2 material delivers an excellent activity with a high peak current density (24.6 mA cm-2). Furthermore, to prove the universality of this strategy, NixCu1-x(OH)2 isometallic hydroxide was used as the precursor, and a series of MOF-74/CuxNi1-x(OH)2 (denoted as Ni-NiCu) heterogeneous materials have been prepared and could be used as an effective electrocatalyst to catalyze MOR. The results indicate that this strategy can be used in the synthesis of other new composite materials with specific hierarchical structures for a more efficient electrocatalytic system.

In situ synthesis of hierarchical NiCo-MOF@Ni1-xCox(OH)2 heterostructures for enhanced pseudocapacitor and oxygen evolution reaction performances.

Integrating the merits of different components to construct heterostructures for energy storage and conversion has attracted intensive attention. Herein, taking advantage of bimetallic MOFs and transition bimetal hydroxide, we have successfully used nanoflower-like Ni1-xCox(OH)2 as both the precursor and template to in situ construct three dimensional (3D) NiCo-MOF@Ni1-xCox(OH)2 (denoted as MOF@TMH) hierarchical heterostructures. Benefiting from the optimized composition with hierarchical heterostructures assembled by ultrathin nanosheets, MOF@TMH-2 possesses rich effective active sites and high electrochemical reactivity, delivering superior pseudocapacitor performance with a specific capacitance of 1855.3 F g-1 at 2 A g-1 and good rate performance. Besides, MOF@TMH-2 also exhibits excellent OER activity with small overpotentials of 193 mV and 310 mV at 10 and 100 mA cm-2, respectively.

The highly selective detecting of antibiotics and support of noble metal catalysts by a multifunctional Eu-MOF.

Designing novel multifunctional rare-earth metal-organic frameworks (MOFs) has attracted intensive attention. In particular, employing such materials for sensing or catalytic reactions is still very challenging. Here, a new 3D porous Eu(iii)-MOF, [Eu(cppa)(OH)]·xS (denoted as CTGU-19, S = solvent molecule, CTGU = China Three Gorges University), was synthesized by using 5-(4-carboxyphenyl)picolinic acid (H2cppa) as an organic ligand, and it shows a 3D (3,12)-connected topological net with the point symbol (420·628·818)(43)4, constructed from cubane-shaped tetranuclear europium building units. Interestingly, CTGU-19 can be used as a highly sensitive luminescent sensor to identify ornidazole (ODZ) and nitrofurantoin (NFT) at different excitation wavelengths. This result represents the first example of a lanthanide-metal-organic-framework (Eu-MOF) that can be employed as a discriminating fluorescent probe to recognize ODZ and NFT at different excitation wavelengths. Furthermore, after loading CTGU-19 with Ag and/or Au nanoparticles, the composites exhibit efficient catalytic performance for reducing 2-/3-/4-nitrophenols (2-/3-/4-NP), in which the unit mass reduction rate constants of Ag0.8Au0.2@CTGU-19 for 2-NP, 3-NP, and 4-NP reach 68.8, 53.80, and 52.34 s-1 g-1, respectively.

Synthesis of Semiconducting 2H-Phase WTe2 Nanosheets with Large Positive Magnetoresistance.

Tungsten ditelluride (WTe2) is provoking immense interest because of its unique electronic properties, but studies about its semiconducting hexagonal (2H) phase are quite rare. Herein, we report the synthesis of semiconducting 2H WTe2 nanosheets with large positive magnetoresistance, for the first time, by a simple lithium-intercalation-assisted exfoliation strategy. Systematic characterizations including high-resolution transmission electron microscopy, X-ray diffraction, and Raman and X-ray photoelectron spectroscopies provide clear evidence to distinguish the structure of 2H WTe2 nanosheets from the orthorhombic (Td) phase bulk counterpart. The corresponding electronic phase transition from metal to semiconductor is also confirmed by density of states calculation, optical absorption, and electrical transport property measurements. Besides, the 2H WTe2 nanosheets exhibit large positive magnetoresistance with values of up to 29.5% (10 K) and 16.2% (300 K) at 9 T. Overall, these findings open up a promising avenue into the exploration of WTe2-based materials in the semiconductor field.

Investigation on the Component Evolution of a Tetranuclear Nickel-Cluster-Based Metal-Organic Framework in an Electrochemical Oxidation Reaction.

Understanding the active species derived from metal-organic frameworks (MOFs) plays a vital role in the fabrication of highly efficient and stable oxygen evolution reaction (OER) electrocatalysts. Herein, a new alkaline-stable 3D nickel metal-organic framework (Ni-MOF), containing a 1D rod-packing chain structure fused with a tetranuclear nickel cluster [Ni4(µ3-OH)2], is used as a target material to explore its OER properties. The electrocatalytic activities of pure Ni-MOF and hybrid materials made from Ni-MOF with different acetylene black loaded electrodes, such as glassy carbon, fluorine-doped tin oxide, and nickel foam, have been evaluated. Further analysis unravels that the enhanced OER performance might be attributed to the synergistic interactions of two catalytic active species between in situ formed ß-Ni(OH)2 and a tetranuclear Ni4(µ3-OH)2 cluster in Ni-MOF. The findings will shed fresh light on the fabrication of MOF-derived catalysts for efficient electrochemical energy conversion.

Stable Bimetal-MOF Ultrathin Nanosheets for Pseudocapacitors with Enhanced Performance.

Exploring high-performance metal-organic frameworks (MOFs) for pseudocapacitors is quite meaningful for energy storage. Herein a bimetal NiCo-MOF with ultrathin thickness was prepared via a simple hydrothermal method, which shows excellent electrochemical performance with specific capacitances of 1945.83 and 1700.40 F/g at current densities of 0.5 and 1 A/g, respectively, while maintaining good stability. X-ray photoelectron spectroscopy and X-ray absorption near-edge spectroscopy spectra unravel that the strong coupling between Ni and Co species enhances the valence state of Ni2+ in the ultrathin nanosheets, which facilitates the charge transfer during the electrochemical reaction and results in greatly improved pseudocapacitive reactivity. This work provides guidance on the promising prospect of MOF materials for pseudocapacitor applications.

Bi-Microporous Metal-Organic Frameworks with Cubane [M4 (OH)4 ] (M=Ni, Co) Clusters and Pore-Space Partition for Electrocatalytic Methanol Oxidation Reaction.

Embedding cubane [M4 (OH)4 ] (M=Ni, Co) clusters within the matrix of metal-organic frameworks (MOFs) is a strategy to develop materials with unprecedented synergistic properties. Herein, a new material type based on the pore-space partition of the cubic primitive minimal-surface net (MOF-14-type) has been realized. CTGU-15 made from the [Ni4 (OH)4 ] cluster not only has very high BET surface area (3537 m2 g-1 ), but also exhibits bi-microporous features with well-defined micropores at 0.86 nm and 1.51 nm. Furthermore, CTGU-15 is stable even under high pH (0.1 m KOH), making it well suited for methanol oxidation in basic medium. The optimal hybrid catalyst KB&CTGU-15 (1:2) made from ketjen black (KB) and CTGU-15 exhibits an outstanding performance with a high mass specific peak current of 527 mA mg-1 and excellent peak current density (29.8 mA cm-2 ) at low potential (0.6 V). The isostructural cobalt structure (CTGU-16) has also been synthesized, further expanding the application potential of this material type.

A Water-Stable Terbium(III)-Organic Framework as a Chemosensor for Inorganic Ions, Nitro-Containing Compounds and Antibiotics in Aqueous Solutions.

Effective detection of organic/inorganic pollutants, such as antibiotics, nitro-compounds, excessive Fe3+ and MnO4 - , is crucial for human health and environmental protection. Here, a new terbium(III)-organic framework, namely [Tb(TATAB)(H2 O)]⋅2H2 O (Tb-MOF, H3 TATAB=4,4',4''-s-triazine-1,3,5-triyltri-m-aminobenzoic acid), was assembled and characterized. The Tb-MOF exhibits a water-stable 3D bnn framework. Due to the existence of competitive absorption, Tb-MOF has a high selectivity for detecting Fe3+ , MnO4 - , 4-nirophenol and nitroimidazole (ronidazole, metronidazole, dimetridazole, ornidazole) in aqueous through luminescent quenching. The results suggest that Tb-MOF is a simple and reliable reagent with multiple sensor responses in practical applications. To the best of our knowledge, this work represents the first TbIII -based MOF as an efficient fluorescent sensor for detecting metal ions, inorganic anions, nitro-compounds, and antibiotics simultaneously.

Integration of Semiconductor Oxide and a Microporous (3,10)-Connected Co6-Based Metal-Organic Framework for Enhanced Oxygen Evolution Reaction.

Developing high-efficiency and cost-effective electrocatalytic oxygen evolution reaction (OER) catalysts would determine the future distributions of energy conversion technologies. Metal-organic frameworks (MOFs), with unsaturated active metal sites, functionalized organic linkers, and large surface areas, are emerging heterogeneous electrocatalysts for the water oxidation process. Herein, we report an oxygen-evolving microporous (3,10)-connected Co6-based MOF (denoted as CTGU-14) for the electrocatalytic OER. Moreover, the integration of Co-MOF and SnO2, SnO2 (15%) & CTGU-14 composite attains remarkable electrochemical OER performance with a small Tafel slope of 68 mV·dec-1, a positive overpotential of 388 mV at 10 mA·cm-2, and overall durability in an alkali medium. The superior OER activities might be ascribed to more convenient electron transfer from the SnO2 additive to the electrode medium, effective surface area and unsaturated active cobalt centers, and more beneficial delivery for hydroxy radicals in the microporous Co-MOF skeleton in the process of the OER.

In situ synthesis of a Fe3S4/MIL-53(Fe) hybrid catalyst for an efficient electrocatalytic hydrogen evolution reaction.

The development of efficient MOF-based electrocatalysts with good stability to produce hydrogen is a great challenge in the field of sustainable energy conversion. Herein, we introduced a controlled in-situ sulfurization strategy to generate a highly active and stable hybrid catalyst containing good conductive Fe3S4 ultrasmall nanosheets attached on the surface of 3D MIL-53(Fe) for the hydrogen evolution reaction in acidic solutions.