3D Mesh Structure Research Articles

Evaluation of mechanical and tribological properties of Cu-based friction materials reinforced by 3D mesh structure

Cu-based friction materials (CBFMs) are widely used in brake system such as High-Speed Trains and Wind Power Generation, its mechanical and tribological properties are of vital importance for the stable and safe operation. In this study, CBFMs holding 3D mesh structure were designed and fabricated by wet granulation and particle coating technology. Stress and temperature fields were obtained by finite element simulation. After that, the mechanical and tribological properties were investigated. The results showed that 3D mesh structure can enhance the compressive strength of CBFMs to 34.56 % and reduce wear rate to a large extent. This study was expected to open up a new direction in enhancing comprehensive performances of CBFMs without changing its composition.

3-aminopropyltriethoxysilane modified MXene on three-dimensional nonwoven fiber substrates for low-cost, stable, and efficient solar-driven interfacial evaporation desalination

Recently, the solar-driven interfacial evaporation desalination has attracted more and more attentions due to the advantages of low cost, zero energy consumption, and high water purification rate, etc. One of the bottlenecks of this emerging technique lies in a lack of simple and low-cost ways to construct three-dimensional (3D) hierarchical microstructures for photothermal membranes. To this end, a two-step strategy is carried out by combining surface functionalization with substrate engineering. Firstly, a silane coupling agent 3-aminopropyltriethoxysilane (APTES) is grafted onto an ideal photothermal material of Ti3C2Tx MXene, to improve the nanochannel sizes and hydrophilicity, which are attributed to enlarged interspaces of MXene and introduced hydrophilic group e.g., –NH2 and –OH, respectively. Secondly, a low-cost and robust nonwoven fiber (NWF) substrate, which has a 3D micron-sized mesh structure with interlaced fiber stacks, is employed as the skeleton to load enough APTES-grafted MXene by a simple soaking method. Benefited from above design, the Ti3C2Tx-APTES/NWF composite membrane with a 3D hierarchical structure shows enhanced light scattering and utilization, water transport and vapor escape. A remarkable evaporation rate of 1.457 kg m−2 h−1 and an evaporation efficiency of 91.48 % are attained for a large-area (5 × 5 cm2) evaporator, and the evaporation rate is further increased to 1.672 kg m−2 h−1 for a small-area (2 × 2 cm2) device. The rejection rates of salt ions and heavy metal ions are higher than 99 % and 99.99 %, respectively, and the removal rates of organic dye molecules are nearly to 100 %. Besides, the composite photothermal membrane exhibits great stabilities in harsh conditions such as high salinities, long cycling, large light intensities, strong acid/alkali environments, and mechanical bending. Most importantly, the photothermal membrane shows a considerable cost-effectiveness of 89.4 g h−1/$. Hence, this study might promote the commercialization of solar-driven interfacial evaporation desalination by collaboratively considering surface modification and substrate engineering for MXene.

3D porous NiCo2(CO3)3/reduced graphene oxide aerogel with heterogeneous interfaces for high-efficiency microwave absorption

Advanced electromagnetic absorbing materials (EAMs) with strong absorption and a wide effective absorption bandwidth (EAB), using innovative microstructural design and suitable multicomponents remain a persistent challenge. Here, we report the production of a material by the hydrothermal reduction of a mixture of graphene oxide (GO), Ni(NO3)2·6H2O, and Co(NO3)2·6H2O, resulting in reduced GO (RGO) with a self-assembled 3D mesh structure filled with NiCo2(CO3)3. The unique microstructure of this assembly not only solves the problem of NiCo2(CO3)3 particles agglomerating but also changes the electromagnetic parameters, thereby improving the impedance matching and attenuation ability. High electromagnetic wave absorption (EMA) was achieved by combining the 3D interconnected mesh structure and the various interfaces between NiCo2(CO3)3 and RGO. The minimal reflection loss (RLmin) was −58.5 dB at 2.3 mm, and the EAB was 6.5 GHz. The excellent EMA performance of the aerogel can be attributed to the multiple reflection, scattering, and relaxation process of the porous 3D structure as well as the strong polarization of the interfacial matrix.

A rapid one-step preparation method of the repairable three-dimensional antifouling superhydrophobic 2.5EPZF coating on magnesium alloys

Although three-dimensional (3D) superhydrophobic coating has been gradually prepared on the surface of metal substrate for anticorrosion and antifouling, their complex preparation steps and equipment requirements limit their practical application. Herein, by a rapid one-step spray preparation method the fabricating 3D superhydrophobic 2.5EPZF (2.5 g epoxy resin/polycaprolactone (PCL)/zinc oxide/perfluorodecyltriethoxysilane) coating is prepared. This method utilizes a certain degree of directional arrangement of macromolecular long chain polymers (PCL) as solvent evaporation during the spraying process to form a filamentous structure to construct the 3D coating. This preparation mechanism provides us a novel theoretical guidance method for preparing 3D coating. Further, the silk thickness and mesh density of the 3D mesh structure is controlled by adding epoxy resin. When the amount of epoxy resin is 2.5 g, the surface of 2.5EPZF coating is with about 1–3 μm thick branch frame and 0.1–0.4 μm thin treetop. And the water-contact angle (CA) of 2.5EPZF is 156.6 ± 1.5° and the sliding angle (SA) is < 10° . The 2.5EPZF coating exhibits durable antifouling, strong mechanical&chemical durability, and corrosion resistance. The corrosion current of the 2.5EPZF coating for 0 day's immersion and 35 days’ immersion in NaCl solution is 1.043 × 10−12 A•cm−2 and 1.1703 × 10−11 A•cm−2, respectively. Under solar irradiation and at 50 °C for 30 min, the 2.5EPZF coating is with scratching recovering. Additionally, the composite coating can be prepared by a large area. It is expected that this method is readily used and shows great application potentials.

An intrinsic polymer electrolyte via in situ cross-linked for solid lithium-based batteries with high performance.

Since the introduction of poly(ethylene oxide) (PEO)-based polymer electrolytes more than 50 years, few other real polymer electrolytes with commercial application have emerged. Due to the low ion conductivity at room temperature, the PEO-based electrolytes cannot meet the application requirements. Most of the polymer electrolytes reported in recent years are in fact colloidal/composite electrolytes with plasticizers and fillers, not genuine electrolytes. Herein, we designed and synthesized a cross-linked polymer with a three-dimensional (3D) mesh structure which can dissolve the Li bis(trifluoromethylsulfonyl)imide (LiTFSI) salt better than PEO due to its unique 3D structure and rich oxygen-containing chain segments, thus forming an intrinsic polymer electrolyte (IPE) with ionic conductivity of 0.49 mS cm-1 at room temperature. And it can hinder the migration of large anions (e.g. TFSI-) in the electrolyte and increase the energy barrier to their migration, achieving Li+ migration numbers (tLi+) of up to 0.85. At the same time, IPE has good compatibility with lithium metal cathode and LiFePO4 (LFP) cathode, with stable cycles of more than 2,000 and 700 h in Li//Li symmetric batteries at 0.2 and 0.5 mAh cm-2 current densities, respectively. In addition, the Li/IPE/LFP batteries show the capacity retention >90% after 300 cycles at 0.5 C current density. This polymer electrolyte will be a pragmatic way to achieve commercializing all-solid-state, lithium-based batteries.

Effect of nano TiO2 and SiO2 on gelation performance of HPAM/PEI gels for high-temperature reservoir conformance improvement

Nanoparticles have been widely used in polymer gel systems in recent years to improve gelation performance under high-temperature reservoir conditions. However, different types of nanoparticles have different effects on their gelation performance, which has been little researched. In this study, the high-temperature gelation performance, chemical structure, and microstructure of polymer gels prepared from two nanomaterials (i.e., nano-SiO2 and nano-TiO2) were measured. The conventional HPAM/PEI polymer gel system was employed as the control sample. Results showed that the addition of nano-TiO2 could significantly enhance the gel strength of HPAM/PEI gel at 80 °C. The gel strength of the enhanced HPAM/PEI gel with 0.1 wt% nano-TiO2 could reach grade I. The system also had excellent high-temperature stability at 150 °C. The enhanced HPAM/PEI gel with 0.02 wt% nano-TiO2 reached the maximum gel strength at 150 °C with a storage modulus (G′) of 15 Pa, which can meet the need for efficient plugging. However, the nano-SiO2 enhanced HPAM/PEI polymer gel system showed weaker gel strength than that with nano-TiO2 at both 80 and 150 °C with G′ lower than 5 Pa. Microstructures showed that the nano-TiO2 enhanced HPAM/PEI gel had denser three-dimensional (3D) mesh structures, which makes the nano-TiO2 enhanced HPAM/PEI gel more firmly bound to water. The FT-IR results also confirmed that the chemical structure of the nano-TiO2 enhanced HPAM/PEI gel was more thermally stable than nano-SiO2 since there was a large amount of –OH groups on the structure surface. Therefore, nano-TiO2 was more suitable as the reinforcing material for HPAM/PEI gels for high-temperature petroleum reservoir conformance improvement.

Fast ion diffusion alloy layer facilitating 3D mesh substrate for dendrite-free zinc-ion hybrid capacitors

Although aqueous zinc ion hybrid capacitors have advantageous integration of batteries and supercapacitors, they still suffer from the inherent problems of dendrite growth and interfacial side reactions on Zn anodes. Herein, a universal fast zinc-ion diffusion layer on a three-dimensional (3D) mesh structure model is demonstrated to effectively improve Zn plating/stripping reversibility. The fast ion diffusion alloy layer accelerates the Zn2+ migration in an orderly manner to homogenize Zn2+ flux and overcomes the defects of the commercial mesh substrate, effectively avoiding dendrite growth and side reactions. Consequently, the proof-of-concept silver-zinc alloy modified stainless steel mesh delivers superb reversibility with the high coulombic efficiency over 99.4% at 4 mA cm−2 after 1600 cycles and excellent reliability of over 830 h at 1 mA cm−2, Its feasibility is also evidenced in commercial zinc ion hybrid capacitors with activated carbon as the cathode. This work enriches the fundamental comprehension of fast zinc-ion diffusion layer combined with a 3D substrate on the Zn deposition and opens a universal approach to design advanced host for Zn electrodes in zinc ion hybrid capacitors.

Mesh Ti6Al4V Material Manufactured by Selective Laser Melting (SLM) as a Promising Intervertebral Fusion Cage.

Intervertebral cages made of Ti6Al4V alloy show excellent osteoconductivity, but also higher stiffness, compared to commonly used polyether-ether-ketone (PEEK) materials, that may lead to a stress-shielding effect and implant subsidence. In this study, a metallic intervertebral fusion cage, with improved mechanical behavior, was manufactured by the introduction of a three-dimensional (3D) mesh structure to Ti6Al4V material, using an additive manufacturing method. Then, the mechanical and biological properties of the following were compared: (1) PEEK, with a solid structure, (2) 3D-printed Ti6Al4V, with a solid structure, and (3) 3D-printed Ti6Al4V, with a mesh structure. A load-induced subsidence test demonstrated that the 3D-printed mesh Ti6Al4V cage had significantly lower tendency (by 15%) to subside compared to the PEEK implant. Biological assessment of the samples proved that all tested materials were biocompatible. However, both titanium samples (solid and mesh) were characterized by significantly higher bioactivity, osteoconductivity, and mineralization ability, compared to PEEK. Moreover, osteoblasts revealed stronger adhesion to the surface of the Ti6Al4V samples compared to PEEK material. Thus, it was clearly shown that the 3D-printed mesh Ti6Al4V cage possesses all the features for optimal spinal implant, since it carries low risk of implant subsidence and provides good osseointegration at the bone-implant interface.

A Stabilized Polyacrylonitrile-Encapsulated Matrix on a Nanolayered Vanadium-Based Cathode Material Facilitating the K-Storage Performance.

Layered vanadium-based metal oxides were regarded as promising cathode materials accounting for suitable K+ transport channels as well as high work potential in K-ion batteries. Nevertheless, because of the large radius of K+ and the rigid structure of inorganic materials, the typical K0.486V2O5 suffers from volume expansion seriously in the repeated charging and discharging processes along with poor ionic and electronic conductivity, consequently determining inevitably poor electrochemical properties. Herein, we proposed a stabilized polymer (PAN) matrix on K0.486V2O5 nanobelts by a liquid-assisted methodology and further electrospinning technology. As a result, a nanocomposite containing a 3D conductive and interconnected mesh structure was thus constructed. By avoiding the full carbonization of polyacrylonitrile (PAN) with appropriate thermal treatment, the elastic properties of the PAN precursor can be retained, effectively inhibiting the volume effect, and the stabilized PAN-encapsulated matrix can also greatly accelerate transport rates of K+ and electrons at a high rate as well as restrict the decomposition of organic electrolytes and side reactions. This work can supply significant basic scientific value of the polymer surface coating methodology for the far-reaching development of inorganic cathode materials in K-ion batteries.

A Method for Determining the Shape Similarity of Complex Three-Dimensional Structures to Aid Decay Restoration and Digitization Error Correction

This paper introduces a new method for determining the shape similarity of complex three-dimensional (3D) mesh structures based on extracting a vector of important vertices, ordered according to a matrix of their most important geometrical and topological features. The correlation of ordered matrix vectors is combined with perceptual definition of salient regions in order to aid detection, distinguishing, measurement and restoration of real degradation and digitization errors. The case study is the digital 3D structure of the Camino Degli Angeli, in the Urbino’s Ducal Palace, acquired by the structure from motion (SfM) technique. In order to obtain an accurate, featured representation of the matching shape, the strong mesh processing computations are performed over the mesh surface while preserving real shape and geometric structure. In addition to perceptually based feature ranking, the new theoretical approach for ranking the evaluation criteria by employing neural networks (NNs) has been proposed to reduce the probability of deleting shape points, subject to optimization. Numerical analysis and simulations in combination with the developed virtual reality (VR) application serve as an assurance to restoration specialists providing visual and feature-based comparison of damaged parts with correct similar examples. The procedure also distinguishes mesh irregularities resulting from the photogrammetry process.

Self-transforming stainless-steel into the next generation anode material for lithium ion batteries

Here, an extremely cost-effective and simple method is proposed in order to morphologically self-transform stainless steel from a completely inactive material to a fully operational, nanowire-structured, 3D anode material for lithium ion batteries. The reagentless process of a single heating step of the plain stainless steel in a partially reducing atmosphere, converts the stainless steel into an active anode via metal-selective oxidation, creating vast spinel-structured nanowires directly from the electrochemically inactive surface. The simple process allows the complete utilization of the 3D mesh structure as the electrochemically-active spinel nanowires greatly enhance the active surface area. The novel material and architecture exhibits high capacities (~1000 mAh/g after ~400 cycles), long cycle life (>1100 cycles) and fast rate performance (>2C). Simple modulation of the substrate can result in very high areal and volumetric capacities. Thus, areal capacities greater than 10 mAh/cm2 and volumetric capacities greater than 1400 mAh/cm3 can be achieved. Using the proposed method, the potential reduction in cost from the use of battery-grade graphite is at least an order of magnitude, with considerable better results achieved in terms of capacity and intrinsic structural benefits of the substrate, which include direct contact of the active material with the current collector, lack of delamination and binder-free performance. This work provides a new paradigm and a key step in the long route to replace the commercial graphite anode as the next-generation anode material.

Biomass porous carbon-based composite for high performance supercapacitor

Biomass porous carbons with abundant pore structure, surface functional groups, and excellent electrical conductivity, are widely used for electrode materials. In this work, biomass carbon with 3D mesh structure was loaded with metal sulfide to synthesize porous carbon-based ultrathin Ni3S2 layered nanosheet structure supercapacitor composite material electrode. C/Ni3S2-16 showed 600 F g−1 of high specific capacitance with 20 A g−1 current density. After 5,000 charge and discharge cycles, 88.8% of the maximum (imital) specific capacitance was maintained at 10 A g−1. The assembled C/Ni3S2-16//C asymmetric supercapacitor achieved an energy density of up to 35.7 Wh Kg−1, which was remained at 27.9 Wh Kg−1 with a high power density at 1500 W kg−1. Developed pore structure of biomass porous carbon provide sufficient space for the electrolyte in and out of the electrode, therefore the potentially high electrochemical activity and energy density of the transition metal sulfide were fully exhibited.

Bone-derived dECM/alginate bioink for fabricating a 3D cell-laden mesh structure for bone tissue engineering

Alginate bioink has been widely employed to fabricate 3D cell-laden structures because of its low toxicity, appropriate biocompatibility, and easy/fast cross-linking ability. However, the low bioactivity of the hydrogel is a main shortcoming, so that physical or chemical modification with bioactive components is a promising strategy to efficiently increase the biological activity of alginate hydrogel. The present study proposes a new method to obtain bioactive alginate-based bioink by supplementing it with methacrylated (Ma)-decellularized extracellular matrix (dECM) derived from bone tissues. We demonstrate that the appropriate processing conditions and concentration of Ma-dECM in the bioink offer not only reasonable printability for fabricating 3D cell-laden structures, but also meaningful cell viability of the printed cell-laden construct. Moreover, the biologically improved microenvironment of alginate-based cell-laden structures formed using our method demonstrated a substantial effect on the osteogenic differentiation of the human adipose derived stem cells that were laden in the bioink.

A large area mesh-like MoS2 with an expanded interlayer distance synthesized by one-pot method and lithium storage performance

Abstract Nowadays, molybdenum disulfide is gaining increasing attention due to its unique properties and diverse areas of application. In this study, a mesh with a large area and a structure similar to that of MoS2 were synthesized using a simple one-pot synthesis method. The results revealed that irregular MoS2 nanoparticles with layer spacing (⁓0.92 nm) larger than that of the bulk MoS2 were stacked on a 3D mesh structure similar to that of MoS2 with submicron-sized macropores. And in lithium ion battery applications, the MoS2 nanoparticles obtained in this study significantly improved the electrochemical performance of an anode material. As a result of this improvement, the problems of substantial volume changes and low utilization efficiency of active materials during the charge/discharge cycle could be solved. The reversible cycle capacity of the active material gradually increased till it stabilized, and after 100 cycles, with reversible capacities of 877 and 665 mAh g−1 at 0.1 and 0.5 A g−1 were maintained and the rate performance was found to be excellent.

Ultraviolet sensor with fast response characteristics based on an AgNW/ZnO bi-layer

We demonstrate an ultraviolet (UV) sensor with fast response characteristics based on an AgNW/ZnO bi-layer. This UV sensor is a surface acoustic wave (SAW)-based sensor fabricated using a 128°YX black lithium niobate substrate, which is a piezoelectric in nature. This sensor, which is a two-port SAW resonator, was manufactured by fabricating interdigitated electrodes with a wavelength of 16.4 μm and depositing UV sensing layers such as ZnO, Sn/ZnO, and AgNW/ZnO. Among these sensing layers, the frequency response characteristics were found to be improved in the bi-layer structure. In addition, the AgNW/ZnO-based sensor showed a significant improvement in response and recovery times. These results contributed to rapid oxygen adsorption on the ZnO surface due to the large oxygen contact area that can attributed to the AgNW’s 3D mesh structure and the compensation of the internal electron trap center due to the contact of the metal-semiconductor. The proposed sensor with the metal-semiconductor bi-layer structure based on AgNW nanomaterials showed the fastest response characteristics compared to previous SAW UV sensors.

Direct Write of 3D Nanoscale Mesh Objects with Platinum Precursor via Focused Helium Ion Beam Induced Deposition.

The next generation optical, electronic, biological, and sensing devices as well as platforms will inevitably extend their architecture into the 3rd dimension to enhance functionality. In focused ion beam induced deposition (FIBID), a helium gas field ion source can be used with an organometallic precursor gas to fabricate nanoscale structures in 3D with high-precision and smaller critical dimensions than focused electron beam induced deposition (FEBID), traditional liquid metal source FIBID, or other additive manufacturing technology. In this work, we report the effect of beam current, dwell time, and pixel pitch on the resultant segment and angle growth for nanoscale 3D mesh objects. We note subtle beam heating effects, which impact the segment angle and the feature size. Additionally, we investigate the competition of material deposition and sputtering during the 3D FIBID process, with helium ion microscopy experiments and Monte Carlo simulations. Our results show complex 3D mesh structures measuring ~300 nm in the largest dimension, with individual features as small as 16 nm at full width half maximum (FWHM). These assemblies can be completed in minutes, with the underlying fabrication technology compatible with existing lithographic techniques, suggesting a higher-throughput pathway to integrating FIBID with established nanofabrication techniques.

Na+-induced in situ reconstitution of metal phosphate enabling efficient electrochemical water oxidation in neutral and alkaline media

Exploring highly activity and stable electrocatalysts for oxygen evolution reaction (OER) is of vital importance for sustainable energy conversion processes. Herein, a facile strategy is developed to synthesize Ni-doped CoOOH nanosheets with poor crystallinity and 3D mesh structure, which is in situ derived from the Na+-induced spontaneous reconstitution of polymetallic phosphate precursors during OER process. The resulted Ni-CoOOH/NF with a large number of active sites exhibits a highly efficient OER catalytic activity outperforming the commercial RuO2 catalysts, indicated by low overpotentials of only 265 and 410 mV at a current density of 10 mA cm−2 in alkaline and neutral media, respectively. This Na+-induced in situ conversion strategy opens up a new way for the design and synthesis of electrocatalysis towards various energy systems.

Heteroatom-doped hierarchical porous carbon aerogels from chitosan for high performance supercapacitors

Carbon aerogel with various morphology and structural characteristics were prepared from chitosan by freeze drying-carbonization/activation process. The carbon aerogel obtained without activation (CNS-800) exhibited sheet structure and disordered micropores, N mostly existing in the forms of N-5 and N-6 groups. After phosphoric acid activation (CNSP-800), a 3D-honeycomb structure with long-range ordered pore channels was presented, with N-X being the main nitrogen-containing groups, some P-O/P=O and PC groups were also detected. KOH activation of CNS (CNSK-800) led to the formation of incomplete 3D-mesh structure and some graphite-like structure, which is the most unordered structure attributed to the high intense of KOH activation. All the samples showed micro-mesoporous structure, the specific surface area of CNS-800, CNSk-800 and CNSP-800 were 421, 1215 and 1475 m2/g, respectively. When used as electrode in the three-electrode supercapacitor, the capacitance values of 171, 318 and 416 F/g were obtained at 1 A/g in 1 M H2SO4 electrolyte for CNS-800, CNSK-800 and CNSP-800, with the pseudo capacitance contribution rates of 25.4%, 31.6% and 37.6% respectively. Additionally, the capacitance values were 98, 126 and 168 F/g in the two-electrode system respectively, and their energy densities reached 3.35, 4.69 and 6.36 Wh/kg at a power density of 25 W/kg accordingly.

Development and Evaluation of Fall Impact Protection Pads Using Additive Manufacturing.

This paper presents the development and evaluation of fall-impact protection pants for elderly women using additive manufacturing. The protective pants were designed incorporating a protective pad in the hip area to reduce the impact of falls on the human body. The protective pad is a 3D mesh structure with a curved surface to fit the human body. Pads printed with flexible thermoplastic polyurethane were combined with foam to create the final pad. The impact-absorbing performance of the pad was verified through physical impact experiments. When dropping a bowling ball onto the protective pad from heights of 15, 20, and 25 cm, the protective pad was found to reduce the impact force by more than 82% in all cases. The impact force was less than the average fracture threshold of 3472 N. A subject group and an expert group evaluated the appearance, pad characteristics, motion functionality, and the wearability of the protection pants. Despite the insertion of a pad, the pants appeared natural and had a good fit. The pads were evaluated as being well-designed in terms of their position, shape, area, thickness, weight, flexibility, ease of insertion, and ease of use. Users were comfortable performing various motions when wearing the designed protective clothing. Therefore, this work can be considered to have developed protective clothing that provides satisfactory impact-protection performance and comfort thereby advancing the possibility of applying additive manufacturing to the creation of functional garments.

Highly sensitive three-dimensional interdigitated microelectrode biosensors embedded with porosity tunable hydrogel for detecting proteins

This study focused on fabricating a target-specific electrical biosensor with high sensitivity and dynamic range by embedding a hydrogel, that incorporated a much larger number of antibodies in the reaction region of the sensor, allowing all biomolecules except the target molecules to be filtered off. The biosensor is comprised of a three-dimensional interdigitated microelectrode (3D IMEs) with much higher aspect ratios than conventional IMEs and a hydrogel with a 3D mesh structure. The hydrogel increases the number of antibodies in the reaction region of the 3D IMEs by approximately 1,000-fold and enhances the impedance change induced by the specific binding of biomolecules. The hydrogel density is altered according to the target biomolecules. The impedance change by Aβ42 binding was maximized to approximately 12.135 ± 0.903% in the 3D IMEs with a ‘dense’ hydrogel. The change by prostate-specific antigen (PSA) binding was maximized in the 3D IMEs with a ‘loose’ hydrogel. Thus, the dynamic range and sensitivity for detecting Aβ42 were enhanced by a maximum of two orders and by approximately 2.58-fold compared to planar IMEs. These results demonstrate the high performance of the hydrogel-embedded 3D IMEs and its applicability for biological fluid-based diagnosis.