Nanoporous Structure Research Articles

A robust polyaniline hydrogel electrode enables superior rate capability at ultrahigh mass loadings

Simultaneously achieving high mass loading and superior rate capability in electrodes is challenging due to their often mutually constrained nature, especially for pseudocapacitors for high-power density applications. Here, we report a robust porous polyaniline hydrogel (PPH) prepared using a facile ice-templated in situ polymerization approach. Owing to the conductive, robust, and porous nanostructures suitable for ultrafast electron and ion transport, the self-supporting pure polyaniline hydrogel electrode exhibits superior areal capacitance without sacrificing rate capability and gravimetric capacitance at an ultrahigh mass loading and notable current density. It achieves a high areal capacitance (15.2 F·cm−2 at 500 mA·cm−2) and excellent rate capability (~92.7% retention from 20 to 500 mA·cm−2) with an ultrahigh mass loading of 43.2 mg cm−2. Our polyaniline hydrogel highlights the potential of designing porous nanostructures to boost the performance of electrode materials and inspires the development of other ultrafast pseudocapacitive electrodes with ultrahigh loadings and fast charge/discharge capabilities.

Understanding protein adsorption on silica mesoporous materials through thermodynamic simulations

This work presents a molecular thermodynamic theory to study protein interactions within a charge-regulating silica-like nanopore structure. The theory accounts for electrostatic interactions, steric repulsions, finite-size entropic effects, and protonation equilibrium of silanol groups on silica and protein residue side-chains. Coarse-grained representations of proteins based on their 3D crystallographic structures are employed. We evaluate the influence of pH, salt concentration, and pore size on the adsorption of selected proteins (cytochrome c, lysozyme, and myoglobin) in both single- and binary-protein solutions. The surface charge density on the nanopore walls is less negative than on the adjacent planar surface, primarily influenced by pH and salt concentration. Adsorption within the nanopore from single protein solutions exhibits a non-monotonic behavior with pH, increasing with decreasing salt concentration and diminishing pore size. Analysis of the effective interactions between proteins and silica surfaces indicates that adsorption is enhanced when the protein size matches that of the nanopore. Evaluation of various adsorption pathways indicates minimized free energy when the protein enters the nanopore through its edge and contacts its cylindrical walls. In binary solutions, the presence of another protein significantly alters the affinity of a protein for the silica surfaces, potentially preventing its adsorption, and affects its organization on these surfaces upon adsorption.

Cyclodextrin Nanosponges: A Revolutionary Drug Delivery Strategy.

Nanosponges are porous solid cross-linked polymeric nanostructures. This study focuses on cyclodextrin-based nanosponges. Nanosponges based on cyclodextrin can form interactions with various lipophilic or hydrophilic compounds. The release of the entrapped molecules can be altered by altering the structure to obtain either a longer or faster release kinetics. The nanosponges might increase the aqueous solubility of weakly water-soluble compounds, develop long-lasting delivery systems, or construct novel drug carriers for nanomedicine. CD-NS (cyclodextrin-based nanosponges) are evolving as flexible and promising nanomaterials for medication administration, sensing, and environmental cleanup. CD-NS are three-dimensional porous structures of cyclodextrin molecules cross-linked by a suitable polymeric network, resulting in a large surface area. This overview covers CD-NS synthesis methods and applications.

Nanoporous, Ultrastiff, and Transparent Plastic-like Polymer Hydrogels Enabled by Hydrogen Bonding-Induced Self-Assembly.

Most natural supporting tissues possess both exceptional mechanical strength, a significant amount of water, and the anisotropic structure, as well as nanoscale assembly. These properties are essential for biological processes, but have been challenging to emulate in synthetic materials. In an effort to achieve simultaneous improvement of these trade-off features, a hydrogen bonding-induced self-assembly strategy was introduced to create nanoporous plastic-like polymer hydrogels. Multiple hydrogen bonding-mediated networks and nanoporous orientation structures endow transparent hydrogels with remarkable mechanical robustness. They exhibit Young's modulus of up to 223.7 MPa and a breaking strength of up to 10.3 MPa, which are superior to those of most common polymer hydrogels. The uniform porous nanostructures of hydrogen-bonded hydrogels contribute to a significantly larger specific surface area compared to conventional hydrogels. This allows for the retention of high mechanical properties in environments with a high water content of 70 wt %. A rubbery stage is observed during the heating process, which can reverse and reshape the manufacture of objects with various desired 2D or 3D shapes using techniques such as origami and kirigami. Finally, as a proof-of-concept, the outstanding mechanical properties of poly(MAA-co-AA-co-NVCL) hydrogel, combined with its high water content, make it suitable for applications such as smart temperature monitors, multilevel information anticounterfeiting, and artificial muscles.

Influence of Ni-doping on CuCo2O4 electrode for enhanced supercapacitor performance and sustainable energy storage

This work provides a revolutionary strategy for creating high-performance supercapacitors by designing and fabricating a unique nanostructured bimetallic oxide electrode. The proposed electrode leveraged the synergistic effects of metal oxides to enhance both energy density and charge-discharge kinetics. Ni-doped CuCo2O4 nanostructures (Cu1-xNixCo2O4) were synthesized in incremental order (x = 0.0, 0.05, 0.10, and 0.15) by facile sol-gel auto-combustion route. The nanostructures analyzed through x-ray diffraction, FTIR spectroscopy, Micro-Raman spectroscopy, x-ray photoelectron spectroscopy (XPS) and Scanning electron microscopy revealed the single phase and polycrystalline nature of CuCo2O4, with some impurity phases of CuO. The surface morphology studies showed numerous pores among the grains of Cu1-xNixCo2O4. Cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy (EIS) were used to investigate the electrochemical performance of synthesized Cu1-xNixCo2O4 samples. In a 3 M KOH electrolyte solution, the Cu1-xNixCo2O4 electrodes with x = 0.05 exhibited 2340 Fg−1 specific capacitance at 5 mVs−1, demonstrating superior electrochemical performance with excellent rate capability. Furthermore, it exhibited 35.88 Whkg−1 energy density, an exceptional 2484.74 Wkg−1 power density, and retained 99.9 % capacitance after 5000 cycles, demonstrating good stability. The results suggest that porous bimetallic oxide nanostructures can be promising candidates for the development of high-performance, environmentally friendly supercapacitors.

Improvement of rate capability and cycle life of Na-NiCl2 battery via designing a graphene anchoring porous nickel nanostructures as cathode

The integration of renewable energy with advanced energy storage technologies is essential. The sodium-based batteries, particularly sodium-nickel chloride (Na-NiCl2) batteries, show promise due to the abundance and low redox potential of sodium (−2.7 V vs. SHE). Despite their advantages in terms of cost, safety, and high efficiency, the improvement of rate and cycling performance of Na-NiCl2 batteries remains a challenge. To address this issue, a Ni nanostructure-supported reduced graphene oxide (RGO) composite is synthesized and combined with NaCl to serve as the cathode material for Na-NiCl2 batteries. Benefiting from the strong anchoring function of RGO, the growth of Ni is inhibited. As a result, the obtained cathode exhibits a notable specific capacity of 132.7 mAh/g at a high rate of 0.6C, along with excellent Coulombic efficiency of 100 % over 500 cycles and high energy efficiency (95.8 %). In addition, the outstanding conductivity, high specific surface area and abundant pore distribution of Ni@RGO contribute to enhanced conversion reaction and ion diffusion, and thus promoting rate capability. In contrast, the pure Ni nanosheets-based (Ni NSs) cathode is subjected to serious grain growth, which leads to poor rate performance and rapid capacity fading. By introducing conductive framework of RGO and constructing porous Ni nanostructure, the rapid electrons transport and diffusion of ions is achieved, and thus presenting the exceptional electrochemical properties.

Biotemplate synthesis of SnO2 hollow porous structures for enhanced isopropanol sensing performance

Researchers are showing significant interest in the development of nanostructures with hierarchical porosity. This study introduces an eco-friendly, cost-effective, and straightforward method to create SnO2 hollow porous nanostructures using the peony as a biotemplate. A comprehensive analysis of the gas sensing characteristics of these hierarchical SnO2 hollow porous nanostructures is conducted. The results show that the gas sensor based on SnO2 showcases relatively high response values measuring 18.3 and exhibits rapid response speed of 1 s to 100 ppm isopropanol, even at a comparably low operating temperature of 180 °C. Additionally, the sensor displays good repeatability and long-term stability, which can be attributed to the inherent advantages stemming from its distinct structure. Therefore, this study provides experimental and theoretical foundations for the potential application of hollow porous SnO2 structures in sensor technology.

Extreme mixing in nanoporous high-entropy oxides for highly durable energy storage

The ability to mix many different metal cations in a single-phase nanoscale oxide is critical for property adjusting and new material discovery. However, synthesizing multicomponent high-entropy oxides (HEOs) consisting of over ten metal cations remains a challenge due to dissimilarity and immiscibility among these elements. Herein, we explore the accommodation ability of Al3Ni-type and Al3Ti-type intermetallic phases and find that the Al3Ni-type phase is powerful to accommodate many different kinds metal elements. By chemically dealloying the Al from the multicomponent Al3Ni-type intermetallic phase, multicomponent spinel oxides such as 7-component (AlNiCoRuMoCrFe)3O4, 8-component (AlNiCoRuMoCrFeTi)3O4, 13-component (AlNiCoCrFeCuMoVTaNbHfZrTi)3O4, 16-component (AlNiCoCrFeCuMoTaNbHfZrTiRuVPdY)3O4 et al., with nanoporous structure and poor crystallity are obtained. As a case study, we find that when applied in Li-ion battery anode, our 16-component nanoporous HEO exhibits a high capacity of ∼1141.2 mAh g−1 after 290 cycles at 0.1 A g−1 and excellent cycling stability. This study greatly expands the composition space of nanoscale HEOs and provides an interesting route for new materials discovery.

Liquid Metal-Enabled Tunable Synthesis of Nanoporous Polycrystalline Copper for Selective CO2-to-Formate Electrochemical Conversion.

Copper-based catalysts exhibit high activity in electrochemical CO2 conversion to value-added chemicals. However, achieving precise control over catalysts design to generate narrowly distributed products remains challenging. Herein, a gallium (Ga) liquid metal-based approach is employed to synthesize hierarchical nanoporous copper (HNP Cu) catalysts with tailored ligament/pore and crystallite sizes. The nanoporosity and polycrystallinity are generated by dealloying intermetallic CuGa2 formed after immersing pristine Cu foil in liquid Ga in a basic or acidic solution. The liquid metal-based approach allows for the transformation of monocrystalline Cu to the polycrystalline HNP Cu with enhanced CO2 reduction reaction (CO2RR) performance. The dealloyed HNP Cu catalyst with suitable crystallite size (22.8nm) and nanoporous structure (ligament/pore size of 45nm) exhibits a high Faradaic efficiency of 91% toward formate production under an applied potential as low as -0.3 VRHE. The superior CO2RR performance can be ascribed to the enlarged electrochemical catalytic surface area, the generation of preferred Cu facets, and the rich grain boundaries by polycrystallinity. This work demonstrates the potential of liquid metal-based synthesis for improving catalysts performance based on structural design, without increasing compositional complexity.

In-situ SANS study on spatial evolution of coal nanoporosity during pyrolysis at elevated temperatures

The nanopore evolution in coal during pyrolysis is vital for optimizing heat and mass transfer in coal conversion processes. Therefore, small-angle neutron scattering (SANS) was utilized to examine the in-situ changes in the nanopore structures of two subbituminous Chinese coal samples during pyrolysis. The nanopore structures were examined in terms of average pore size, pore volume distribution, fractal dimension by SANS at elevated temperatures. Throughout the pyrolysis process, a consistent enlargement of the average size of nanoscale pores was noted as temperatures escalated, with an expansion ranging from 5.3 to 8.2 nm. Particularly during the devolatilization phase (300–500 °C), there was a marked surge in the volume of large pores, exhibiting a growth rate of about 88.1–150.5%. High-temperature (600–800 °C) conditions facilitated the formation of new and smaller pores. While the surface roughness of nanopores experienced a slight reduction throughout the pyrolysis, the directional growth of the pores maintained an isotropic distribution.

Application prospects of graphene in environmental science

Nanomaterials and graphene, as cutting-edge materials, have play a crucial role in environmental governance. The introduction of nanomaterials brings new hope to environmental governance. Graphene not only improves the efficiency and cost-effectiveness of water treatment but also drives innovation and development in environmental technologies. This article provides a summary and analysis review starting from the characteristics of nanomaterials and Graphene, comprehensively reviewing Graphenes advantage in environmental technologies and discovered its application in this area. The research summarized the conclusion that Graphenes characteristics make it suitable for addressing environmental issues such as water pollution, its composites can play an important role in water treatment process including water purification, heavy metal adsorption, organic compound adsorption and removal through different preparation and reaction mechanisms. By introducing Nanopore structures and artificially designed stacking structures on graphene membranes, the permeation performance could be modulated and improved. By the way of physical and chemical adsorption, ion exchange, electrochemical and photocatalysis, Graphene and its oxide could be applied to remove heavy metal ion and organic substances from polluted water. The article also introduced the main preparation methods of Graphene and its potential secondary pollution problem. This article provides valuable insights for scientific research and engineering practices in environmental protection and sustainable development.

Dynamic Bubbling Balanced Proactive CO2 Capture and Reduction on a Triple-Phase Interface Nanoporous Electrocatalyst.

The formation and preservation of the active phase of the catalysts at the triple-phase interface during CO2 capture and reduction is essential for improving the conversion efficiency of CO2 electroreduction toward value-added chemicals and fuels under operational conditions. Designing such ideal catalysts that can mitigate parasitic hydrogen generation and prevent active phase degradation during the CO2 reduction reaction (CO2RR), however, remains a significant challenge. Herein, we developed an interfacial engineering strategy to build a new SnOx catalyst by invoking multiscale approaches. This catalyst features a hierarchically nanoporous structure coated with an organic F-monolayer that modifies the triple-phase interface in aqueous electrolytes, substantially reducing competing hydrogen generation (less than 5%) and enhancing CO2RR selectivity (∼90%). This rationally designed triple-phase interface overcomes the issue of limited CO2 solubility in aqueous electrolytes via proactive CO2 capture and reduction. Concurrently, we utilized pulsed square-wave potentials to dynamically recover the active phase for the CO2RR to regulate the production of C1 products such as formate and carbon monoxide (CO). This protocol ensures profoundly enhanced CO2RR selectivity (∼90%) compared with constant potential (∼70%) applied at -0.8 V (V vs RHE). We further achieved a mechanistic understanding of the CO2 capture and reduction processes under pulsed square-wave potentials via in situ Raman spectroscopy, thereby observing the potential-dependent intensity of Raman vibrational modes of the active phase and CO2RR intermediates. This work will inspire material design strategies by leveraging triple-phase interface engineering for emerging electrochemical processes, as technology moves toward electrification and decarbonization.

Multi-Component and Nanoporous Design toward RuO2-Based Electrocatalyst with Enhanced Performance for Acidic Water Splitting.

Developing electrocatalysts with excellent activity and stability for water splitting in acidic media remains a formidable challenge due to the sluggish kinetics and severe dissolution. As a solution, a multi-component doped RuO2 prepared through a process of dealloying-annealing is presented. The resulting multi-doped RuO2 possesses a nanoporous structure, ensuring a high utilization efficiency of Ru. Furthermore, the dopants can regulate the electronic structure, causing electron aggregation around unsaturated Ru sites, which mitigates Ru dissolution and significantly enhances the catalytic stability/activity. The representative catalyst (FeCoNiCrTi-RuO2) shows an overpotential of 167 mV at 10 mAcm-2 for oxygen evolution reaction (OER) in 0.5 m H2SO4 solution with a Tafel slope of 53.1mVdec-1, which is among the highest performance reported. Moreover, it remains stable for over 200 h at a current density of 10mAcm-2. This work presents a promising approach for improving RuO2-based electrocatalysts, offering a crucial advancement for electrochemical water splitting.

NiCo2V2O8@NC Spheres with Mesoporous Yolk- Bilayer Hierarchical Structure for Enhanced Lithium Storage.

Metal vanadates as negative electrode materials for lithium-ion batteries have attracted widespread attention, attributed to their substantial capacity, broad availability, and exceptional safety. In this study, NiCo2V2O8@NC microspheres featuring a yolk-double shell structure were successfully synthesized via ion exchange reactions and surface deposition techniques, employing metal glycerolate as a template. Owing to the bimetallic cobalt-nickel synergistic effect and the N-doped carbon network, this configuration not only optimizes the pore structure but also enhances conductivity, thereby augmenting the stability of the overall structure. The unique yolk-double shell design significantly enhances the utilization of active components and reduces the ion transport distance, thereby achieving high capacity. Thanks to the synergistic effects of this bimetallic and intricate structure, the material demonstrates exceptional capacity and cycle stability in lithium storage. The initial discharge capacity possesses 1522 mAh g-1 at a current density of 0.2 A g-1, with the reversible capacity still maintained at 1197 mAh g-1 after 100 cycles. In addition, at a high current density of 0.5 A g-1, the initial discharge capacity is 1487 mAh g-1, with a reversible capacity of 747 mAh g-1 maintained after 500 cycles. This study offers a perspective and methodology for the design and fabrication of complex porous double shell nanostructures.

Novel three-dimensional architectured ZnMgAl ternary layered double hydroxide@reduced graphene oxide nanocomposites as electrode material for high-performance supercapacitor

Ternary layered double hydroxides (LDH) have recently attracted immense attention owing to their stupendous features, such as fine compositional tuning, multiple valence states, and superior electrochemical activity. Moreover, their intriguing structures and distinctive physiochemical properties delineate them as an exemplary material to serve as electrodes for high-performance supercapacitors (SCs). The present work reports the in-situ synthesis of Zinc Magnesium Aluminium LDH (ZMA) integrated with reduced graphene oxide (rGO) through a single-step hydrothermal approach. The resulting novel ternary ZMA@rGO nanocomposite (ZMAG) possesses a unique architecture incorporating hierarchical 3D nanoflowers of ZMA embedded on graphene nanosheets. The porous morphology of LDH improves interfacial charge transport, which results in more faradaic reactions at the electrochemically active sites. In addition, the conductive graphene nanosheets render a high specific surface area, endowing excellent capacitive behavior. The amalgamated electrochemical properties of ZMA and rGO develop a competent electrode material (ZMAG) for SCs. The ZMAG2 nanocomposite having ZMA and rGO in 1:1, evinces a specific capacitance (Cs) of 656.7 F/g at a current density (Id) of 1 A/g. Furthermore, the asymmetric supercapacitor (ASC) features admirable cycle stability (retains 89% of initial capacitance after 15,000 charge/discharge cycles). Herein, the real-time application of ZMA@rGO//AC ASC has also been demonstrated. Therefore, hierarchical porous nanostructure proclaims new prospects for fabricating proficient electrode materials for energy storage devices.

The Influence of SC-CO2 on the Nanopore Structures of Different Types of Shales Based on Small-Angle Neutron Scattering and Multifractal Methods

The Influence of SC-CO₂ on the Nanopore Structures of Different Types of Shales Based on Small-Angle Neutron Scattering and Multifractal Methods

Conformal TiO2 Aerogel-Like Films by Plasma Deposition: from Omniphobic Antireflective Coatings to Perovskite Solar Cell Photoelectrodes.

The ability to control the porosity of thin oxide films is a key factor determining their properties. Despite the abundance of dry processes for synthesizing oxide porous layers, a high porosity range is typically achieved by spin-coating-based wet chemical methods. Besides, special techniques such as supercritical drying are required to replace the pore liquid with air while maintaining the porous network. In this study, we propose a new method for the fabrication of ultraporous titanium dioxide thin films at room or mild temperatures (T ≤ 120 °C) by a sequential process involving plasma deposition and etching. These films are conformal to the substrate topography even for high-aspect-ratio substrates and show percolated porosity values above 85% that are comparable to those of advanced aerogels. The films deposited at room temperature are amorphous. However, they become partly crystalline at slightly higher temperatures, presenting a distribution of anatase clusters embedded in the sponge-like open porous structure. Surprisingly, the porous structure remains after annealing the films at 450 °C in air, which increases the fraction of embedded anatase nanocrystals. The films are antireflective, omniphobic, and photoactive, becoming superhydrophilic when subjected to ultraviolet light irradiation. The supported, percolated, and nanoporous structure can be used as an electron-conducting electrode in perovskite solar cells. The properties of the cells depend on the aerogel-like film thickness, which reaches efficiencies close to those of commercial mesoporous anatase electrodes. This generic solvent-free synthesis is scalable and applicable to ultrahigh porous conformal oxides of different compositions, with potential applications in photonics, optoelectronics, energy storage, and controlled wetting.

Enhancing electrochemical properties of bacterial cellulose-derived carbon nanofibers through physical CO2 activation

Carbon nanofiber (CNF) derived from carbonization of bacterial cellulose (BC), with a unique three-dimensional porous nanostructure, has received significant interest in electrochemical applications. In this study, CNF samples were physically activated in CO2 at different temperatures and durations. Raman spectroscopy and FTIR analysis showed that CO2 activation caused hexagonal lattice defects, disorder, and oxygen-related functional groups in an amorphous carbon structure. CNF surface morphology changed after physical activation, reducing fiber diameter to 55 nm and introducing mesopores. Through activation temperature and time adjustments, surface area (870.1 m2/g) and micropore surface area (535.6 m2/g) and pore volume (0.2148 cm3/g) increased. EDX elemental analysis showed that activated CNF had a carbon concentration of > 90 %, while XPS analysis showed surface functional groups like C-C (sp2) and C-C (sp3) hybridization, which could improve electrolyte ion adsorption and accessibility. Electrochemical properties improved owing to CO2 activation. The optimal activation condition of 800 ℃ for 60 min resulted in the highest specific area capacitance of 552 mF cm−2 at 1 mA cm−2. This activated CNF electrode retained capacitance nearly unchanged up to 3,000 cycles. It also achieved the highest energy density of 76.7 mWh cm−2 at 500 mW cm−2. This study demonstrates the efficacy of CO2 physical activation for enhancing the electrochemical properties of CNF electrodes. The findings also highlight the importance of tailoring activation conditions, providing valuable insights for the design of advanced energy storage materials.

Vapor-Tailored Nanojunctions in Ultraporous ZnO Nanoparticle Networks for Superior UV Photodetection.

High quality nanojunctions are known to effectively improve the conductivity and structural robustness of ultraporous nanoparticle networks, surpassing the performance of natural van der Waals interfaces. Nevertheless, the traditional approach of forming these junctions by thermal annealing is incompatible with thermolabile polymers and slender metal electrodes found in modern wearable technologies. Herein, we present a low temperature, solvent vapor-based method to rapidly elicit high-quality metal-oxide nanojunctions in a fast, effortless, inexpensive, and easily scalable process; capable of generating necked interparticle interfaces in a matter of minutes. When applied to ultraporous-based ZnO Ultraviolet (UV) photodetectors, the vapor-tailoring process produces an incredible 128,000-fold improvement in responsivity (6.6 A.W-1) over untreated structures (51.2µA.W-1), and a 5300-fold improvement in responsivity over thermally annealed structures; all while maintaining exceptionally low dark currents of 140 pA at a low bias voltage of 1V. Most importantly, the exceptional performance enabled by room temperature synthesis suggests high potential adaptability of this process toward wearable UV sensors, shedding lights on the strategy of modifying weakly bonded porous nanostructures for improved physical properties.

Enhancing the performance of porous silicon biosensors: the interplay of nanostructure design and microfluidic integration

This work presents the development and design of aptasensor employing porous silicon (PSi) Fabry‒Pérot thin films that are suitable for use as optical transducers for the detection of lactoferrin (LF), which is a protein biomarker secreted at elevated levels during gastrointestinal (GI) inflammatory disorders such as inflammatory bowel disease and chronic pancreatitis. To overcome the primary limitation associated with PSi biosensors—namely, their relatively poor sensitivity due to issues related to complex mass transfer phenomena and reaction kinetics—we employed two strategic approaches: First, we sought to optimize the porous nanostructure with respect to factors including layer thickness, pore diameter, and capture probe density. Second, we leveraged convection properties by integrating the resulting biosensor into a 3D-printed microfluidic system that also had one of two different micromixer architectures (i.e., staggered herringbone micromixers or microimpellers) embedded. We demonstrated that tailoring the PSi aptasensor significantly improved its performance, achieving a limit of detection (LOD) of 50 nM—which is >1 order of magnitude lower than that achieved using previously-developed biosensors of this type. Moreover, integration into microfluidic systems that incorporated passive and active micromixers further enhanced the aptasensor’s sensitivity, achieving an additional reduction in the LOD by yet another order of magnitude. These advancements demonstrate the potential of combining PSi-based optical transducers with microfluidic technology to create sensitive label-free biosensing platforms for the detection of GI inflammatory biomarkers.