Tremendous Enhancement Research Articles

Chloride-salt separation type nanofiltration membranes for efficient crude salt refinement

Application of unrefined crude salt not only leads to a serious equipment scaling and a low product quality, but also increases operational risks and poses health hazards. Therefore, it is essential to refine crude salt prior to its use. However, traditional methods of crude salt refinement are energy-intensive and probably produce additional chemical by-products. In this work, membrane technology was used to accomplish the refinement of crude salt due to its unique characteristics, such as environmentally friendly and lower energy consumption. To improve the separation performance, the membranes were fabricated by simply adjusting the aqueous monomer concentration. For single-salt feed, the membrane (M10) prepared with a high ratio of 10 exhibited excellent salt rejection due to the formation of a thicker and denser PA layer. And it owned a superior MgCl2/NaCl selectivity of ∼22.0, demonstrating that the membrane can achieve outstanding selectivity for mono-/divalent ions. The selectivity of Mg2+/Na+ increased to ∼23.5 for bi-salt feed and further improved to 66.2 for multi-salt feed due to the stronger charge shielding effect. Most importantly, the membrane was also successfully applied in the refinement of crude salt. When using crude salt (NaCl 30 g/L, purity 0.90) as feed, the M10 exhibited both excellent retention of bivalent ions and permeation of univalent ions, resulting in the corresponding Mg2+/Na+ selectivity up to ∼251.6 and the tremendous enhancement in the Na + purity of ∼0.997. This work offers a feasible strategy for crude salt refinement, and could expand to some other potential applications such as resource utilization in the salinization industry and zero-liquid discharge of industrial wastewater.

UV activated formaldehyde gas sensing based on gold decorated ZnO@ In2O3 hollow nanospheres at room temperature

Using uniform carbon nanospheres as sacrificial templates, gold nanoparticle-modified ZnO@ In2O3 hollow nanospheres with controlled dimensions and porous architectures were successfully synthesized through water bath, hydrothermal and chemical reduction methods. Gas sensing evaluation revealed that the Au-decorated ZnO@ In2O3 hollow nanostructures exhibited a dramatically amplified response up to 14.8 when exposed to 10 ppm formaldehyde analyte at room temperature. Furthermore, multifaceted performance benefits of Au-decorated ZnO@ In2O3 over single-phase ZnO, Au-ZnO, ZnO@ In2O3 heterojunction-based composites were observed, including excellent selectivity towards formaldehyde even in complex gas mixtures; tremendous sensitivity enhancement stemming from synergies between efficient gas diffusion through hollow heterojunction nanospheres and accelerated surface reactions at catalytically-active Au sites; and rapid, fully-reversible response/recovery time of 32 s and 42 s, respectively. In-depth investigations were conducted into the fundamental sensing mechanisms enabling formaldehyde detection using AC impedance spectroscopy, in situ diffuse reflectance Fourier transform infrared spectroscopy (DRIFTS), and density functional theory (DFT) computational modeling analyses.

Novel Nonthermal Atmospheric Plasma Irradiation of Titanium Implants Promotes Osteogenic Effect in Osteoporotic Conditions.

Osteoporosis is a metabolic disease characterized by bone density and trabecular bone loss. Bone loss may affect dental implant osseointegration in patients with osteoporosis. To promote implant osseointegration in osteoporotic patients, we further used a nonthermal atmospheric plasma (NTAP) treatment device previously developed by our research group. After the titanium implant (Ti) is placed into the device, the working gas flow and the electrode switches are turned on, and the treatment is completed in 30 s. Previous studies showed that this NTAP device can remove carbon contamination from the implant surface, increase the hydroxyl groups, and improve its wettability to promote osseointegration in normal conditions. In this study, we demonstrated the tremendous osteogenic enhancement effect of NTAP-Ti in osteoporotic conditions in rats for the first time. Compared to Ti, the proliferative potential of osteoporotic bone marrow mesenchymal stem cells on NTAP-Ti increased by 180% at 1 day (P = 0.004), while their osteogenic differentiation increased by 149% at 14 days (P < 0.001). In addition, the results indicated that NTAP-Ti significantly improved osseointegration in osteoporotic rats in vivo. Compared to the Ti, the bone volume fraction (BV/TV) and trabecular number (Tb.N) values of NTAP-Ti in osteoporotic rats, respectively, increased by 18% (P < 0.001) and 25% (P = 0.007) at 6 weeks and the trabecular separation (Tb.Sp) value decreased by 26% (P = 0.02) at 6 weeks. In conclusion, this study proved a novel NTAP irradiation titanium implant that can significantly promote osseointegration in osteoporotic conditions.

Tremendous enhancement of green emission from Er3+/In3+ co-doped β-Ga2O3 ultrawide bandgap semiconductors

Er3+ singly doped and Er3+/In3+ co-doped gallium oxide ceramics with intense green emission were prepared using the conventional solid-state reaction method. The Ga2-x-yErxInyO3 ceramics exhibit green and red emission at 555 and 673 nm, and follow the two-photon absorption process under the excitation of 980 nm. Systematic measurements of the upconversion luminescence spectra of Ga2-x-yErxInyO3 show that the optimal doping concentrations, sintering temperature and time are x = 0.015, y = 0.035, 1250 °C, and 8 h, respectively. For a fixed Er3+ doping concentration of x = 0.015, the green emission intensity at 555 nm can be enhanced by 60 folds through 3.5 mol% In3+ doping, which is attributed to reduced non-radiative decay, enhanced energy transfer from In3+ ions to Er3+ ions via defect states, and increased photon absorption. The introduction of 3.5 mol% In3+ also increases the fluorescence lifetime by 235–272%. These observations provide compelling evidence for the presence of effective energy transfer between In3+ and Er3+ ions.

Greatly Intensified Guest Exchange Strategy for Highly-Efficient Activation of Metal-Organic Frameworks.

The preservation and accessibility of pores are prerequisites to the application of metal-organic frameworks (MOFs). Activation is a key step to eliciting rich features of pores, but it needs a repeated solvent-exchange process which is tedious and time/cost-consuming. Herein, a facile strategy for highly-efficient activation of MOFs utilizing rotating packed bedis proposed. With the tremendous enhancement of molecular mixing and mass transfer in high-gravity and strong-shearing surrounding, nine representative MOFs are completely activated within 2h without structural change. Compared with conventional process, this activation displays surprising efficiency by accelerating the diffusion of solvents and redissolution of residual reactants in the pores. The complete activation time can be significantly shortened by over 90%. As a proof-of-concept, the methane storage of as-activated UiO-66 is five times that of as-synthesized UiO-66. This strategy provides a potential platform with industrial worth for the activation of MOF materials with ultra-high efficiency and versatility.

Serum-Based Detection of Liver Pathology Using a Fluorogenic Alkaline Phosphatase Probe.

Development of "ultrahigh contrast" fluorogenic probes for trapping alkaline phosphatase (ALP) activities in human serum is highly desirable for clinical auxiliary diagnosis for hepatobiliary diseases. However, the intrinsic dilemma of incomplete ionization of intramolecular charge transfer (ICT)-based ALP fluorophores and autofluorescence interference of serum result in low sensitivity and accuracy. Given that unique halogen effects could lead to a drastic decrease in the pKa value and a significant enhancement in the fluorescence quantum yield, herein we report an enzyme-activatable near-infrared probe based on a difluoro-substituted dicyanomethylene-4H-chromenep for achieving fluorescent quantification of human serum ALP. Rational design strategy is demonstrated by altering the substituted halogen groups to well regulate the pKa for meeting the physiological precondition. Owing to the complete ionization at pH 7.4 with tremendous fluorescence enhancement, the difluoro-substituted DCM-2F-HP manifests a linear relationship between the emission intensity and ALP concentration in both solution and serum samples. Along with measuring 77 human serum samples, the DCM-2F-HP based fluorescence method not only exhibits significant correlations with clinical colorimetry, but also distinguishes ALP patients from healthy volunteers, as well as assessing the progress of liver disease, thus providing a potential toolbox for quantitatively detecting ALP and warning the stage of hepatopathy.

Non-amplification on-spot identifying the sex of dioecious kiwi plants by a portable Raman device.

The kiwi plant is dioecious, and its sex is generally identified from flower morphology at blossoming, which takes several years. It is quite necessary but challenging to on-spot identify the plant sex in juvenile stage. Here the target DNA was obtained by screening the Friendly boy (FrBy) gene which is sex-related for different kiwi plant species. Its complementary sequence was divided into two parts as primer DNA and further attached to different gold nanoparticles (GNPs). The connection between target DNA and primer DNA will promote the formation of plasmonic dimers. Dark field microscopy (DFM) can distinguish particles in different aggregation states. Various conditions were optimized based on the standard of increasing the proportion of dimers while reducing that of large aggregates. Furthermore, two Raman reporters (RR) are separately labeled on the nanoprobes, and the plasmonic dimers lead to a tremendous Raman enhancement of two reporters located at the dimer nanogap. Double-blind tests proved the feasibility of this method on the actual samples of kiwi plant leaves. Our SERS method is sensitive, specific, and reliable for rapid sex identification analysis at the kiwi seeding stage, with great promise for decision-making in field management.

A nonlinear scaling-based normalized metal artifact reduction to reduce low-frequency artifacts in energy-integrating and photon-counting CT.

Metal within the scan plane can cause severe artifacts when reconstructing X-ray computed tomography (CT) scans. Both in clinical use and recent research, normalized metal artifact reduction (NMAR) has established as the reference method for correcting metal artifacts, but NMAR introduces inconsistencies within the sinogram, which can cause additional low-frequency artifacts after image reconstruction. This paper introduces an extension to NMAR by applying a nonlinear scaling function (NLS-NMAR) to reduce low-frequency artifacts, which get introduced by the reconstruction of interpolation-edge-related sinogram inconsistencies in the normalized sinogram domain. After linear interpolation of the metal trace, an NLS function is applied in the prior-normalized sinogram domain to reduce the impact of the interpolation edges during filtered backprojection. After sinogram denormalization and image reconstruction, the low frequencies of the NLS image are combined with different high frequencies to restore anatomic details. An anthropomorphic dental phantom with removable metal inserts was utilized on two different CT systems to quantitatively assess the artifact reduction performance in terms of HU deviations and the root-mean-square-error within relevant regions of interest. Clinical dental examples were assessed to qualitatively demonstrate the problem of the interpolation-related blooming as well as to demonstrate the performance of the NLS function to reduce respective artifacts. To quantitatively prove HU consistency, HU values were assessed in central ROIs in the clinical cases. In addition, single clinical cases of a hip replacement and pedicle screws in the spine are shown to demonstrate the method's results in other body regions. The NLS-NMAR can minimize the effect of interpolation-related sinogram inconsistencies and thus reduce resulting hyperdense blooming artifacts. In the phantom results, the reconstructions with the NLS-NMAR-corrected low frequencies demonstrate the lowest error. In the qualitative assessment of the clinical data, the NLS-NMAR shows a tremendous enhancement in image quality, also performing best within all assessed images series. The NLS-NMAR provides a small yet effective extension to conventional NMAR by reducing low-frequency hyperdense metal trace-interpolation-related artifacts in computed tomography.

Hierarchical Hollow-TiO2@CdS/ZnS Hybrid for Solar-Driven CO2-Selective Conversion.

Light-driven valorization conversion of CO2 is an encouraging carbon-negative pathway that shifts energy-reliance from fossil fuels to renewables. Herein, a hierarchical urchin-like hollow-TiO2@CdS/ZnS (HTO@CdS/ZnS) Z-scheme hybrid synthesized by an in situ self-assembly strategy presents superior photocatalytic CO2-to-CO activity with nearly 100% selectivity. Specifically, benefitting from the reasonable architectural and interface design, as well as surface modification, this benchmarked visible-light-driven photocatalyst achieves a CO output of 62.2 μmol·h-1 and a record apparent quantum yield of 6.54% with the Co(bpy)32+ (bpy = 2,2'-bipyridine) cocatalyst. It rivals all the incumbent selective photocatalytic conversion of CO2 to CO in the CH3CN/H2O/TEOA reaction systems. Specifically, the addition of HTO and stabilized ZnS enables the photocatalyst to effectively upgrade optical and electrical performances, contributing to efficient light-harvesting and photogenerated carrier separation, as well as interfacial charge transfer. The tremendous enhancement of photocatalytic performance reveals the superiority of the Z-scheme heterojunction assembled from HTO and CdS/ZnS, featuring the inner electric field derived from the band bending of HTO@CdS/ZnS make CdS resistant to photocorrosion. This study allows access to inspire studies on rationally modeling and constructing diverse heterostructures for the storage and conversion of renewables and chemicals.

Temporal patterns of childhood cancer survival 1991 to 2016: A nationwide register-study based on data from the German Childhood Cancer Registry.

Childhood cancer is the leading disease-related cause of death among under 15 year olds in Europe. Since primary preventive measures are lacking, improving survival probabilities and long-term well-being remain primary goals. With this report, we provide the first long-term assessment and interpretation of patterns in childhood cancer survival in Germany, covering a period of 30 years. Using data from the German Childhood Cancer Registry, we assessed temporal patterns of cancer survival among children (0-14 years) diagnosed in Germany from 1991 to 2016, by cancer type, age at diagnosis and sex. We calculated overall survival (OS) and average annual percentage changes of the respective 5-year OS estimates. OS improved across all cancer types, age groups as well as for boys and girls over time. Five-year OS for all childhood cancers combined increased from 77.8% in 1991-1995 to 86.5% in 2011-2016, with stronger improvements during the early 1990s. The most pronounced survival improvement was seen for acute myeloid leukaemia, at 2% annually and 5-year OS recently reaching 81.5%. Survival improvements for some diagnoses such as neuroblastoma, renal tumours and bone tumours have flattened out. Tremendous enhancements in diagnostics, treatment and supportive care have affected average survival improvements for most cancer types. Recently, survival improvements have decelerated overall and for some cancer types, it plateaued at an unsatisfactory level. As not all children benefited equally from the survival improvements, personal factors (eg, socioeconomic circumstances, health literacy, access to care) likely affect individual prognosis and warrant further investigation.

Giant Out-of-Plane Exciton Emission Enhancement in Two-Dimensional Indium Selenide via a Plasmonic Nanocavity

Out-of-plane (OP) exciton-based emitters in two-dimensional semiconductor materials are attractive candidates for novel photonic applications, such as radially polarized sources, integrated photonic chips, and quantum communications. However, their low quantum efficiency resulting from forbidden transitions limits their practicality. In this work, we achieve a giant enhancement of up to 34000 for OP exciton emission in indium selenide (InSe) via a designed Ag nanocube-over-Au film plasmonic nanocavity. The large photoluminescence enhancement factor (PLEF) is attributed to the induced OP local electric field (Ez) within the nanocavity, which facilitates effective OP exciton-plasmon interaction and subsequent tremendous enhancement. Moreover, the nanoantenna effect resulting from the effective interaction improves the directivity of spontaneous radiation. Our results not only reveal an effective photoluminescence enhancement approach for OP excitons but also present an avenue for designing on-chip photonic devices with an OP dipole orientation.

Designing of phenothiazine-based hole-transport materials with excellent photovoltaic properties for high-efficiency perovskite solar cells (PSCs)

In this study, a series of highly efficient organic hole-transporting materials (HTMs) were designed using Schiff base chemistry by modifying a phenothiazine-based core with triphenylamine through end-capped acceptor engineering via thiophene linkers. The designed HTMs (AZO1-AZO5) exhibited superior planarity and greater attractive forces, making them ideal for accelerated hole mobility. They also showed deeper HOMO energy levels (−5.41 eV to −5.28 eV) and smaller energy band gaps (2.22 eV to 2.72 eV), which improved charge transport behavior, open-circuit current, fill factor, and power conversion efficiency of perovskite solar cells (PSCs). The dipole moments and solvation energies of the HTMs revealed their high solubility, making them suitable for the fabrication of multilayered films. The designed HTMs showed tremendous enhancements in power conversion efficiency (26.19 % to 28.76 %) and open-circuit voltage (1.43 V to 1.56 V), with higher absorption wavelength than the reference molecule (14.43 %). Overall, the Schiff base chemistry-driven design of thiophene-bridged end-capped acceptor HTMs is highly effective in enhancing the optical and electronic properties of perovskite solar cells.

Pyrene based Schiff base ligand: A highly selective fluorescence chemosensor for the detection of Cu2+ ions

A Schiff base ligand L has been designed and synthesized by the condensation of 1′-Hydroxy-2′-acetonaphthonehydrazide with pyrene aldehyde for the detection of Cu2+ ions. The ligand was spectroscopically characterized by all possible techniques. Among different metal ions, Cu2+ ions give a tremendous enhancement of fluorescence intensity in 20% water with THF. The “Turn-On” fluorescence for Cu2+ ions utilizes the Photo-induced Electron Transfer (PET) mechanism. It has been observed that the presence of relevant cations and anions did not affect the probe's fluorescence intensity. The stoichiometric binding mode of the complex is confirmed using Job's method. The low detection limit and reversibility make it cost-effective.

Effect of B addition on microstructures and properties of Cu-15Ni-8Sn alloy

The effect of B addition on microstructures and properties of as-cast, solution-treated and aged Cu-15Ni-8Sn alloy was systematically investigated in the present study. It is found that the micron-scale Ni6.67SnB2 phase is identified in as-cast microstructure for B-containing Cu-15Ni-8Sn-xB alloys. Moreover, it is suggested the segregation of Sn element at grain boundary could be alleviated to a certain degree with B addition. After being solution-treated at 850 °C for 4 h, the Ni6.67SnB2 phase is still existed in the matrix, thereby resulting in a significant influence on the microstructures and properties during subsequent aging process. Results demonstrate that, during aging treatment at 400 °C, the transformation of DO22 ordered phase into L12 ordered phase can be increasingly inhibited with increase of B content and completely prevented for 0.3 and 0.5 wt% B addition. Additionally, the appropriate B addition (0.04, 0.08, 0.1 wt%) could remarkably suppress the formation and growth of the discontinuous precipitation. Nevertheless, with excess B addition (0.3, 0.5 wt%), the discontinuous precipitation is instead promoted. More importantly, alloys with appropriate B addition (0.04, 0.08, 0.1 wt%) could also maintain the peak hardness without deterioration as long as 18 h during the aging process, which suggests the tremendous enhancement of softening resistance. It is believed that the suppression of discontinuous precipitation by Ni6.67SnB2 phase should be responsible for such enhancement of softening resistance. It is anticipated that the current work could provide guidance for the multi-component design of high-performance Cu-Ni-Sn alloy.

Bismuth concentration influenced competition between electrochemical reactions in the all-vanadium redox flow battery

The current obstacles for all-vanadium redox flow batteries (VRFBs) include the sluggish reaction kinetics of electrode materials and the overlapping potential range of the hydrogen evolution reaction (HER) with the negative redox couple. Bismuth (Bi) additives have exhibited tremendous enhancement of battery performance; however, the performance plateaus with concentration of Bi and the catalytic mechanism remains inconclusive and controversial. Quantified kinetic values from three electrochemical methodologies, including modelling, show that the performance plateau with Bi concentration was related to the kinetics of the vanadium redox reaction (VRR) instead of dissolution of Bi, and VRR reaction rate was improved three orders of magnitude with the addition of Bi, with the highest VRR reaction rate observed for electrolyte with 750 ppm Bi additive. Additionally, a competing relationship between VRR and the HER was explored via electrochemical methodologies. It was further confirmed that Bi effectively selectively catalysed VRR over HER via in-situ mass spectrometry measurements during battery cycling, which allows for a higher battery charging cut-off potential of 1.7 V without electrolyte imbalance caused by water electrolysis, achieving 86% of the theoretical electrolyte capacity at 110 mA cm−2 with 750 ppm Bi. The full battery performance with 750 ppm Bi additive is among the best in the literature to date.

Giant enhancement of the initial SERS activity for plasmonic nanostructures via pyroelectric PMN-PT.

Herein, a simply-prepared and highly sensitive electric field-induced surface-enhanced Raman spectroscopy (E-SERS) substrate is proposed by combining a pyroelectric material (PMN-PT) with the plasmonic silver nanoparticles (Ag NP). The intensity of SERS signals is further enhanced by more than 100 times after the application of positive or negative pyroelectric potentials. Theoretical calculations and experimental characterizations demonstrate that the chemical mechanism (CM) as induced by the charge transfer (CT) is mainly responsible for enhanced E-SERS. In addition, a novel nanocavity structure with PMN-PT/Ag/Al2O3/silver nanocubes (Ag NCs) was also introduced, which could effectively convert light energy into heat energy and realize a tremendous enhancement of SERS signals. These findings are expected to further accelerate the application of plasmonic metal nanoparticle-based pyroelectric materials in the fields of energy conversion, optical-sensors and photocatalysts.

Design of an alternating distributed large and small amounts of CNT/polyether amine coating on carbon fiber to derive enhancement in interfacial adhesion

In this paper, an innovative concept of alternating distributed large and small amounts of CNT/polyether amine coating is proposed to be wrapped around the carbon fiber via vacuum filtration. This coating feature is similar to “concave-convex” interval structure, which significantly distinguishes it from widely reported CNT coating with uniform encapsulation. The modified fiber reinforced epoxy composite presents a tremendous enhancement in interfacial bond strength reaching up to 81.8% relative to de-sized fiber composite. This increase comes from the synergistic effects of alternating distribution of strong-weak interactions that effectively dissipating energy, improved wettability, increased mechanical interlocking, as well as pinning and crack suppression effects of CNTs. The concept of interval distribution of large and small levels of coating has more possibilities for optimization. Thus, this unique coating structure, simple and flexible approach provides an attracting candidate for enhancing interphase performance of composites, also with the potential of practical and scalable.

A highly sensitive and selective artificial nanochannel for in situ detection of hydroxyl radicals in single living cell

As the most aggressive reactive oxygen species (ROS), hydroxyl radical (•OH) can directly modulate the biological ion channel and interfere with the progression of diseases. Inspired by biological •OH-activated ion channel, we reported a novel •OH-regulated glass nanopore functionalized with protoporphyrin Ⅸ (PP) film. This system showed outstanding •OH selective response owing to the ultra-fast reaction between •OH and thiol derivatives. In this case, the PP film is responsible for the changing not only of wettability but also of the inner surface charge. The synergetic effect of the dual transitions can regulate the ion transportation within the nanochannels and enabled tremendous enhancement of responsive efficiency. The detection limit could be achieved down to 1.58 nM. Taking advantage of the excellent analytical performance and mechanical qualities of this glass nanopore, the changes of •OH in single living cells were in situ monitored. Together, this study is beneficial for exploring the role of •OH in pathological events and shows promising potential for biomedical research.

Mechanics of shape-locking-governed R2G adhesion with shape memory polymers

Shape memory polymers (SMPs), with unique properties such as tunable elastic modulus, temporary shape locking and shape recovery upon external stimulation, are emerging as a new class of smart materials with switchable adhesion capabilities. A prominent feature of the adhesion between SMP and a spherical indenter is the so-called R2G adhesion, defined as making contact in the rubbery state to a certain indentation depth followed by detachment in the glassy state. While it has been demonstrated that the R2G adhesion with SMPs can achieve orders of magnitude higher adhesive strength compared to conventional elastic adhesive systems with similar geometrical and adhesion parameters, the fundamental mechanics of R2G adhesion and why it leads to such tremendous adhesion enhancement remain largely mysterious at this point. Here, combined experimental testing, theoretical analysis, and finite element analysis (FEA) based on a thermomechanical constitutive model of SMP are performed to investigate the mechanics of R2G adhesion with a rigid spherical indenter. It is shown that the orders of magnitude enhancement of R2G adhesion over conventional elastic adhesion systems is mostly governed by the shape locking effect during the transition from the rubbery to glassy states. The shape locking effect freezes the deformed configuration of the SMP substrate, resulting in nearly conformal contact between the spherical indenter and the glassy-state SMP substrate, thus greatly increases the effective radius of curvature of the contact surface. Our experimental measurements and FEA simulations demonstrate that the net effect of shape locking leads to a pull-off force of a sphere nearly the same as that of a flat punch on an elastic half-space with the same contact radius. An explicit expression of the pull-off force for R2G adhesion is proposed based on flat-punch adhesion. Our results from combined experimentation, modeling and simulations reveal the fundamental mechanics of R2G adhesion. Such understanding provides guidance for the design of SMP smart adhesives.

Facile monomer interlayered MOF based thin film nanocomposite for efficient arsenic separation

The thin film nanocomposites (TFN) based membranes are sensitive to the synergy between the polymer and nanoparticles. TFN incorporating metal-organic frameworks (MOFs) have shown tremendous enhancement in permeability. This study investigates alternate MOF positioning during TFC fabrication for a highly selective membrane. Co–Zn-based mixed metal-organic framework (mMOF) was interlayered between m-phenylenediamine (MPD) and trimesoyl chloride (TMC) to form a polyamide (PA) selective layer. The practiced method conveniently allowed exact loading of mMOF and thus prevented the loss. Owing to the mMOF's placement between MPD and TMC, an increase in PA cross-linking was observed. The mMOF-MPD monomer compatibility allowed homogeneous distribution and formation of a defect-free PA layer. The surface morphology showed a more pronounced formation of leaves-like features due to interfacial degassing. Neutral solute-based filtration tests determined mean pore size, probability distribution, and MWCO. The incorporation of mMOF led to formation of additional nanochannels in the membrane surface. The perm-selectivity studies performed on a dead-end filtration unit resulted in 94% As5+ retention with 2.5 times higher permeance than the control. The current study pronounced the viability of the monomer interlayer method to form a highly selective TFN for water separation and related applications.