Mesoporous Carbon Research Articles

Integrated Two-in-one Strategy for Efficient Neutral Hydrogen Peroxide Electrosynthesis via Phosphorous Doping in 2D Mesoporous Carbon Carriers.

Herein, we demonstrate a two-in-one strategy for efficient neutral electrosynthesis of H2O2 via two-electron oxygen reduction reaction (2e-ORR), achieved by synergistically fine-modulating both the local microenvironment and electronic structure of indium (In) single atom (SA) sites. Through a series of finite elemental simulations and experimental analysis, we highlight the significant impact of phosphorous (P) doping on an optimized 2D mesoporous carbon carrier, which fosters a favorable microenvironment by improving the mass transfer and O2 enrichment, subsequently leading to an increased local pH levels. Consequently, an outstanding 2e-ORR performance is observed in neutral electrolytes, achieving over 95% selectivity for H2O2 across a broad voltage range of 0.1 to 0.5 V vs RHE. In a flow cell, the production rate of H2O2 exceeds 22.54 mol gcat-1 h-1 while maintaining high stability at industrial-level current densities. These results are comparable to, if not better than, those achieved under alkaline conditions. Further analysis, both experimental and theoretical, indicates that the P dopant occupies the second coordination sphere of the In SA, which shows optimized OOH* binding strength for an enhanced 2e- ORR kinetic.

Nanoconfinement-Driven Energy-Efficient CO2 Capture and Release at High Pressures on a Unique Large-Pore Mesoporous Carbon.

Although microporous carbons can perform well for CO2 separations under high pressure conditions, their energy-demanding regeneration may render them a less attractive material option. Here, we developed a large-pore mesoporous carbon with pore sizes centered around 20-30 nm using a templated technical lignin. During the soft-templating process, unique cylindrical supramolecular assemblies form from the copolymer template. This peculiar nanostructuring takes place due to the presence of polyethylene glycol (PEG) segments on both the Pluronic® template and the PEG-grafted lignin derivative (glycol lignin). A large increase in CO2 uptake occurs on the resulting large-pore mesoporous carbon at 270 K close to the saturation pressure (3.2 MPa), owing to capillary condensation. This phenomenon enables a CO2/CH4 selectivity(SCO2/CH4,mol/mol) of 3.7 at 270 K and 3.1 MPa absolute pressure, and a swift pressure swing regeneration process with desorbed CO2 per unit pressure far outperforming a benchmark activated carbon (i.e., notably rapid decrease in the amount of adsorbed CO2 with decreasing pressure). We propose large-pore mesoporous carbons as a novel family of CO2 capture adsorbents, based on the phase-transition behavior shift of CO2 in the nanoconfined environment. This novel material concept may open new horizons for physisorptive CO2 separations with energy-efficient regeneration options.

Probing Impact of Support Pore Diameter on Three-phase Interfaces of Pt/C Catalysts by Molecular Dynamic Simulation.

Investigating how the size of carbon support pores influences the three-phase interface of platinum (Pt) particles in fuel cells is essential for enhancing catalyst utilization. This study employed molecular dynamics simulations and density functional theory calculation to examine the effects of mesoporous carbon support size, specifically its pore diameter, on Nafion ionomer distribution, as well as on proton and gas/liquid transport channels, and the utilization of Pt active sites. The findings show that when Pt particles are located within the pores of carbon support (Pt/PC), there is a significant enhancement in the spatial distribution of Nafion ionomer, along with a reduction in encapsulation around the Pt particles, compared to when Pt particles are positioned on the surface or in excessively large pores of the carbon support. While increasing pore diameter improves the construction of proton transport channels formed by sulfonate groups of Nafion ionomer and water molecules, it also raises the risk of obstructing oxygen diffusion. To achieve maximum Pt utilization and exchange current density, it is essential to balance the proton and gas/liquid transport channels. Among the models investigated, the Pt/PC-8 nm system demonstrates the highest Pt utilization. This work offers valuable insights for designing carbon support materials to optimize three-phase interfaces in the catalytic layer of fuel cells.

Coptis Root-Derived Hierarchical Carbon-Supported Ag Nanoparticles for Efficient and Recyclable Alkyne Halogenation

The advancement of green chemistry and sustainable chemical processes has been significantly facilitated by catalytic systems derived from plant roots, which also present substantial application prospects in the realm of chemical synthesis. This study utilized the roots of Rhizoma Coptidis as a support to successfully fabricate a silver-based nanocatalyst. By depositing silver nanoparticles onto the root material of Coptis chinensis and subjecting it to carbonization, a silver/carbon composite was synthesized, featuring monodisperse silver nanoparticles and a hierarchical mesoporous carbon framework. This composite exhibits robust surface activity, a well-defined pore structure, and superior mechanical properties. The catalyst achieves a catalytic yield nearing 90%, showcasing remarkable activity in terminal alkyne halogenation reactions. Its stability and recyclability are markedly enhanced; it retains 95% of its mass and remains unaltered in the reaction solvent for over 160 h after five cycles. This method simplifies the synthesis of terminal alkynes and their derivatives, rendering the process more environmentally benign and efficacious. Furthermore, it broadens the potential applications of Rhizoma Coptidis in synthetic chemistry and pioneers a novel approach for the synthesis of precious metal catalysts from renewable resources.

Review—Meeting Fuel Cell Catalyst Requirements for Heavy-Duty Vehicle Applications

Abstract Catalyst requirements for proton exchange membrane (PEM) fuel cells differ by applications. Commercial heavy-duty vehicle (HDV) applications consume more H2 fuel and demand higher durability than many others and the total cost of ownership (TCO) of the vehicle is largely related to the performance and durability of catalysts. This article is written to bridge the gap between the industrial requirements and academic activity for advanced cathode catalysts with an emphasis on durability. From a materials perspective, the underlying nature of the carbon support, Pt-alloy crystal structure, stability of the alloying element, cathode ionomer volume fraction, and catalyst-ionomer interface play a critical role in improving performance and durability. We provide our perspective on four major approaches, namely, mesoporous carbon supports, ordered PtCo intermetallic alloys, thrifting ionomer volume fraction, and shell-protection strategies that are currently being pursued. While each approach has its merits and demerits, their key developmental needs for future are highlighted.

Nano-Metal-Organic Frameworks Isolated in Mesoporous Structures.

As an alternative to bulk counterparts, metal-organic framework (MOF) nanoparticles isolated within conductive mesoporous carbon matrices are of increasing interest for electrochemical applications. Although promising, a "clean" carbon surface is generally associated with poor compatibility and weak interactions with metal/ligand precursors, which leads to the growth of MOFs with inhomogeneous particle sizes on outer pore walls. Here, a general methodology for in situ synthesis of eight nanoMOF composites within mesochannels with high dispersity and stability are reported. Mesoporous polydopamine (mesoPDA)-F127 nanospheres with unique surface chemistry, e.g., nanoconfined spaces, catechol functional groups, pyrrolic N doping, and hydrophilic PEO blocks, are found to be a suitable molecular platform. Sliced cross-sectional TEM, HAADF-STEM, and corresponding EDS elemental mapping, as well as nitrogen adsorption characterizations, are utilized to visualize the in situ growth process of ZIF-8 nanoparticles. These careful analyses provides direct evidence that the highly dispersed ZIF-8 is exclusively located inside the internal mesochannels. After moderate carbonization of the mesoPDA-F127/ZIF-8 nanocomposites, a prototype for a mesoporous carbon-isolated ZIF-8 nanostructure is achieved, which can regulate Zn2+ plating electrochemistry toward stable aqueous Zn batteries. This is the first report of the complete impregnation and even dispersion of nanoscale MOFs within the interior channels of mesoporous carbons.

Refining the Distinct Cu-N4 Coordination in Mesoporous N-Doped Carbon to Boost Selective Deuteration under Mild Conditions.

Deuterated compounds have broad applications across various fields, with dehalogenative deuteration serving as an efficient method to obtain these molecules. However, the diverse electronic structures of active sites in the heterogeneous system and the limited recyclability in the homogeneous system significantly hinder the advancement of dehalogenative deuteration. In this study, we present a catalyst composed of copper single-atom sites anchored within an ordered mesoporous nitrogen-doped carbon matrix, synthesized via a mesopore confinement method. The Cu1/OMNC-1100 catalyst, characterized by Cu-N4 sites, demonstrates exceptional performance, high functional group tolerance, and remarkable durability in the deuteration of 2-bromo-6-methoxynaphthalene under relatively mild conditions (80 °C, 2 MPa of CO). Experimental results combined with X-ray absorption fine structure analysis reveal that Cu-N3 sites can be converted into more stable Cu-N4 counterparts at higher pyrolysis temperatures, resulting in enhanced catalytic activity. This work demonstrates a strategy for designing single-atom site catalysts with tunable coordination environments, providing a promising approach to improving catalytic performance in selective dehalogenative reactions under relatively mild conditions.

Mesoporous Nitrogen-Doped Carbon Support from ZIF-8 for Pt Catalysts in Oxygen Reduction Reaction.

Zeolitic imidazolate framework-8 (ZIF-8) has been extensively studied as a precursor for nitrogen-doped carbon (NC) materials due to its high surface area, tunable porosity, and adjustable nitrogen content. However, the intrinsic microporous structure of the ZIF-8 limits mass transport and accessibility of reactants to active sites, reducing its effectiveness in electrochemical applications. In this study, a soft templating approach using a triblock copolymer was used to prepare mesoporous ZIF-8-derived NC (Meso-ZIF-NC) samples. The hierarchical porous structure was investigated by varying the ratios of Pluronic F-127, NaClO4, and toluene. The resulting Meso-ZIF-NC exhibited widespread pore size distribution with an enhanced mesopore (2-50 nm) volume according to the composition of the reaction mixtures. Pt nanoparticles were uniformly dispersed on the Meso-ZIF-NC to form Pt/Meso-ZIF-NC catalysts, which presented a high electrochemical surface area and improved oxygen reduction reaction activity. The study highlights the important role of mesopore structure and nitrogen doping in enhancing catalytic performance, providing a pathway for advanced fuel cell catalyst design.

Applications of Nanomaterial Coatings in Solid-Phase Microextraction (SPME)

This review explores the advances in developing adsorbent materials for solid-phase microextraction (SPME), focusing on nanoparticles, nanocomposites, and nanoporous structures. Nanoparticles, including those of metals (e.g., gold, silver), metal oxides (e.g., TiO2, ZnO), and carbon-based materials (e.g., carbon nanotubes, graphene), offer enhanced surface area, improved extraction efficiency, and increased selectivity compared to traditional coatings. Nanocomposites, such as those combining metal oxides with polymers or carbon-based materials, exhibit synergistic properties, further improving extraction performance. Nanoporous materials, including metal–organic frameworks (MOFs) and ordered mesoporous carbons, provide high surface area and tunable pore structures, enabling selective adsorption of analytes. These advanced materials have been successfully applied to various analytes, including volatile organic compounds (VOCs), polycyclic aromatic hydrocarbons (PAHs), pesticides, and heavy metals, demonstrating improved sensitivity, selectivity, and reproducibility compared to conventional SPME fibers. The incorporation of nanomaterials has significantly expanded the scope and applicability of SPME, enabling the analysis of trace-level analytes in complex matrices. This review highlights the significant potential of nanomaterials in revolutionizing SPME technology, offering new possibilities for sensitive and selective analysis in environmental monitoring, food safety, and other critical applications.

Atomically Dispersed Fe-Mo Catalysts Mediate Fenton-Like Reaction to Efficiently Degrade Chlorophenol Pollutants Through Synergistic Oxidation and Dechlorination Reactions.

Chlorophenols are difficult to degrade and mineralize by traditional advanced oxidation processes due to the strong electronegativity of chlorine. Here, a dual-site atomically dispersed catalyst (FeMoNC) is reported, which Fe/Mo supported on mesoporous nitrogen-doped carbon is prepared through high-temperature migration. The FeMoNC exhibits a high dechlorination rate of 93.3% within 1 min. Theoretical calculation suggested that the doping of high-valence Mo6+ as the electron reservoir, promoted electronic delocalization at Fe sites, thereby enhancing the adsorption and dissociation of peroxymonosulfate (PMS), subsequent generation of Fe (IV) = O and singlet oxygen (1O2) species. An interesting finding is that Mo sites can adsorb chlorine sites in 4-chlorophenol (4-CP) and induce C─Cl bond fracture. Thus, the FeMoNC/PMS system has high catalytic performance due to the synergistic effects of Mo-induced dechlorination and non-radical species (Fe(IV) = O and 1O2) as the degradation pathways, the degradation efficiency of 99.1% of 4-CP within 5 min without significant performance decline after 168h ≈15,120-bed volumes. These findings can advance mechanistic understanding of PMS activation at the molecular level and guide the rational design of efficient eco-friendly single-atom catalysts (SACs) catalysts with bimetallic atomic sites.

Mesoporous Boron-Doped Carbon with Curved B4C Active Sites for Highly Efficient H2O2 Electrosynthesis in Neutral Media and Air-Supplied Environments.

Hydrogen peroxide (H2O2) electrosynthesis via the 2e- oxygen reduction reaction (ORR) is considered as a cost-effective and safe alternative to the energy-intensive anthraquinone process. However, in more practical environments, namely, the use of neutral media and air-fed cathode environments, slow ORR kinetics and insufficient oxygen supply pose significant challenges to efficient H2O2 production at high current densities. In this work, mesoporous B-doped carbons with novel curved B4C active sites, synthesized via a carbon dioxide (CO2) reduction using a pore-former agent, to simultaneously achieve excellent 2e- ORR activity and improved mass transfer properties are introduced. Through a combination of experimental analysis and theoretical calculations, it is confirmed that the curved B4C configuration, formed by mesopores in the carbon, demonstrates superior selectivity and activity for 2e- ORR due to its weaker interaction with *OOH intermediates compared to planar B4C in neutral media. Moreover, the mesopores facilitate oxygen supply and suppress the hydrogen evolution reaction, achieving a Faradaic efficiency of 86.2% at 150mA cm-2 under air-supplied conditions, along with an impressive O2 utilization efficiency of 93.6%. This approach will provide a route to catalyst design for efficient H2O2 electrosynthesis in a practical environment.

Electrochemical aptasensor based on zirconium/copper oxides embedded in mesoporous carbon derived from bimetallic metal-organic framework for ultrasensitive detection of miR-21.

A novel electrochemical aptasensor based on bimetallic zirconium and copper oxides embedded within mesoporous carbon (denoted as ZrO2CuOx@mC) was constructed to detect miRNA. The porous ZrO2CuOx@mC was created through the pyrolysis of bimetallic zirconium/copper-based metal-organic framework (ZrCu-MOF). The substantial surface area and high porosity of ZrO2CuOx@mC nanocomposite along with its robust affinity toward aptamer strands, facilitated the effective anchoring of aptamer strands on the ZrO2CuOx@mC-modified electrode surface. This, coupled with the remarkable electrochemical performance arising from the presence of metal oxides and mesoporous carbon, resulted in the exceptional sensitivity of the ZrO2CuOx@mC-based aptasensor for the detection of miR-21. The prepared aptasensor not only demonstrated a broad detection range from 10 zM to 100 pM, featuring an exceptionally low detection limit of 0.52 zM, but also exhibited notable selectivity against interferences. Moreover, it displayed good stability, reproducibility, and acceptable applicability for miR-21 detection in human serum. The fabricated aptasensor offers a promising platform for ultrasensitive miR-21 detection, with potential applications in accurate and early diagnosis of diseases related to miRNA.

Enhanced Performance and Durability of Proton Exchange Membrane Fuel Cell Catalyst Supports via Nanodrilling-Induced Selective Mesoporous Carbon Structures

Enhanced Performance and Durability of Proton Exchange Membrane Fuel Cell Catalyst Supports via Nanodrilling-Induced Selective Mesoporous Carbon Structures

Synergistic Integration of Mesocarbon Microbeads, Graphitic Nanofibers, and Mesoporous Carbon for Advanced Supercapacitor Electrodes

In this study, a novel multiscale carbon architecture was developed by integrating mesocarbon microbeads (MCMBs), graphitic nanofibers (GNFs), and mesoporous carbon, aimed at enhancing the performance of symmetric supercapacitors. The unique combination of spherical MCMB particles, conductive GNF nanofibers, and mesoporous carbon sheets resulted in a highly effective electrode material, offering improved conductivity, increased active sites for charge storage, and enhanced structural stability. The fabricated MCMB/GNF/MC architecture demonstrated a remarkable specific capacitance of 393 F g−1 at 1 A g−1 in a three-electrode system, significantly surpassing the performance of individual MCMBs and MCMB/GNF electrodes. Furthermore, the architecture was incorporated into a symmetric supercapacitor (SSC) device, where it achieved a capacitance of 86 F g−1 at 1 A g−1. The device exhibited excellent cycling stability, retaining 92% of its initial capacitance after 10,000 charge–discharge cycles, with an outstanding coulombic efficiency of 99%. At optimal operating conditions, the SSC device delivered an energy density of 11 Wh kg−1 at a power density of 500 W kg−1, making it a promising candidate for high-performance energy-storage applications. This multiscale carbon architecture represents a significant advancement in the design of electrode materials for symmetric supercapacitors, offering a balance of high energy and power density, long-term stability, and excellent scalability for practical applications. This work not only contributes to the development of high-performance electrode materials but also paves the way for scalable, long-lasting supercapacitors for future energy-storage technologies.

Role of Mesoporosity in Hard Carbon Anodes for High-Energy and Stable Potassium-Ion Storage.

Herein, NaCl-templated mesoporous hard carbons (NMCs) have been designed and engineered with tunable surface properties as anode materials for potassium-ion batteries (KIBs) and hybrid capacitors (KICs). By utilizing "water-in-oil" emulsions, the size of NaCl templates is precisely modified, leading to smaller particles that enable the formation of primary carbon structures with reduced particle size and secondary structures with 3D interconnected mesoporosity. These features significantly enhance electrode density, reduce particle-to-particle resistance, and improve electrolyte wettability. The resulting NMC delivers high gravimetric and volumetric capacities of 323.5 mAh g-1 and 142.3 mAh cm-3, respectively, with outstanding cycling stability, retaining 292.7 mAh g-1 after 620 cycles. Full-cell evaluations demonstrate the potential of NMC-based anodes paired with KIB (Prussian blue cathode) and KIC (activated carbon-cathode), achieving a capacity of 109.4 mAh g-1 and capacitance of 254.6 F g-1, respectively. As a KIB, the cell delivers a high average voltage of 3.4V, resulting in a specific energy of 256Wh kg-1, while KIC reaches 141.4Wh kg-1 and high specific power of 58.6kW kg-1. These results underscore the importance of morphological features and porosity in enhancing the electrochemical performance of materials, providing insights for future energy storage solutions.

Ordered mesoporous silica and carbon as controlled release systems for cephalexin: Influence of surface modification and porosity

This study compares two in vitro loading and release systems for the antibiotic cephalexin (CFX), based on ordered mesoporous silica (SBA-15) and carbon (CMK-5) materials, both pure and modified with 3-aminopropyltriethoxysilane. Drug loading was performed using the adsorption method under constant conditions (pH: 6, T: 30°C, and t: 8 h), and the release mechanisms were investigated at gastric and intestinal pH to understand the phenomena involved in the oral delivery of CFX studied. The results revealed a higher adsorption capacity of CMK-5 due to its microporosity and π-π stacking interactions compared to SBA-15. Furthermore, the presence of functional groups prevented the formation of crystalline phases by adsorption on the external surface. A reduction in the release rate of CFX was observed with both carriers, governed by a Fickian diffusion mechanism. Notably, CMK-5 exhibited a higher release rate at gastric pH compared to SBA-15, while the opposite was true at intestinal pH. These findings provide deeper insights into the behavior of carriers with different chemical compositions in antibiotic release, suggesting their potential as an alternative to address issues associated with the dosing frequency of these drugs.

A Ti3C2Tx MXene/alginic acid-derived mesoporous carbon nanocomposite as a potential electrode material for coin-cell asymmetric supercapacitors.

In this study, we demonstrate MXene (Ti3C2Tx)-based coin-cell asymmetric supercapacitor (coin-cell ASC) exhibiting high energy density and high power density along with good capacitance. We synthesized mesoporous carbon (MC) by annealing alginic acid at varying temperatures (900 °C, 1000 °C and 1100 °C). Among the prepared samples, MC-1000 exhibited a highly porous structure and a higher surface area. We then developed a Ti3C2Tx/MC (MC-1000) nanocomposite using a simple and efficient solvothermal method. The synthesized nanocomposite displayed the layered morphology of MXene alongside the amorphous characteristics of carbon, indicating a strong interaction between the two materials. Notably, the Ti3C2Tx/MC-9 nanocomposite features a higher number of pores and a larger surface area than either MXene or MC-1000, significantly enhancing its capacitive performance. We evaluated the performance using a three-electrode system, revealing an impressive specific capacitance (Csp) of 1629 F g-1 at 1 A g-1, with a retention of 99.9% even after 35 000 cycles. Furthermore, the fabricated coin-cell ASC using (MC-1000//Ti3C2Tx/MC-9) electrodes demonstrated a Csp of 80.3 F g-1 at 1 A g-1 and a high energy density of 56 W h kg-1, corresponding to a maximum power density of 10 423 W kg-1 at 5 A g-1. The key factors contributing to the enhanced electrochemical performance include the strong connection between MXene and MC-1000, along with the large specific surface area and high porosity of the electrode materials.

Enhanced supercapacitor performance of hierarchical mesoporous sulfur-doped carbon particles from biomass waste for energy storage

Enhanced supercapacitor performance of hierarchical mesoporous sulfur-doped carbon particles from biomass waste for energy storage

Effect of pre-treatment conditions on the electrochemical performance of hard carbon derived from bio-waste.

Sodium-ion batteries (SIBs) offer several advantages over traditional lithium-ion batteries, including a more uniform sodium distribution, lower-cost materials, and safer transportation options. A promising development in SIBs is the use of hard carbons as anode materials due to their low insertion voltage and larger interlayer spacing, which improve sodium-ion insertion. Traditionally, hard carbons are made from costly carbon sources, but recent advancements have focussed on using abundant bio-waste, like coffee grounds. This approach reduces costs and helps manage global waste. This research investigates the electrochemical performance of bio-waste-derived hard carbons, which is significantly impacted by various pre-treatment methods. Techniques such as BET, XRD, TEM, and XPS are employed to examine the effects of pre-treatment variables, including washing solvents (organic, acidic, or distilled water), pre-oxidation temperatures, and post-heating processes. These factors influence the structural properties and purity of the hard carbon, impacting its effectiveness as an anode material in SIBs. A significant finding is a mesoporous hard carbon produced from coffee grounds that, after washing with distilled water, pre-oxidation at 150 °C, and thermal treatment at 1300 °C in argon, shows a 23% yield, a reversible capacity of 304 mA h g-1, and Initial coulombic efficiency of 78%. This study underscores the importance of pre-treatments in removing impurities and enhancing the material's sodium storage capabilities.

Single Zn Atoms Anchored in Mesoporous N-Doped Carbon Rods Derived from Metal-Organic Frameworks for Enhanced Electrocatalytic Oxygen Reduction Reaction

Nitrogen-carbon (N-C) materials have been recently explored to activate Fenton-reaction-inactive Zn single atoms as active sites for electrocatalytic oxygen reduction reaction (ORR). However, achieving Zn-N-C electrocatalysts with high activity and...