High Specific Surface Area Research Articles

Recent Progress of Electrospun Nanofiber Dressing in the Promotion of Wound Healing.

The nanofiber materials of three-dimensional spatial structure synthesized by electrospun have the characteristics of high porosity, high specific surface area, and high similarity to the natural extracellular matrix (ECM) of the human body. These are beneficial for absorbing wound exudate, effectively blocking the invasion of external bacteria, and promoting cell respiration and proliferation, which provides an ideal microenvironment for wound healing. Moreover, electrospun nanofiber dressings can flexibly load drugs according to the condition of the wound, further promoting wound healing. Recently, electrospun nanofiber materials have shown promising application prospects as medical dressings in clinical. Based on current research, this article reviewed the development history of wound dressings and the principles of electrospun technology. Subsequently, based on the types of base material, polymer-based electrospun nanofiber dressing and electrospun nanofiber dressing containing drug-releasing factors were discussed. Furthermore, the application of electrospun nanofiber dressing on skin tissue is highlighted. This review aims to provide a detailed overview of the current research on electrospun nanomaterials for wound healing, addressing challenges and suggesting future research directions to advance the field of electrospun dressings in wound healing.

Bimetallic PdCu anchored to 3D flower-like carbon material for portable and efficient detection of glyphosate

Glyphosate (Gly), as a widely used broad-spectrum herbicide, may lead to soil and water pollution due to its persistence in the environment. Herein, the co-reduction method was employed to anchor bimetallic PdCu onto the Ni and nitrogen-doped 3D Flower-like Carbon Materials (Ni@NC), creating a composite material (PdCu/Ni@NC) with high specific surface area and good catalytic performance. This composite was used to modify screen-printed electrodes (SPE) to develop a portable and efficient Gly detection platform. In the presence of Cl⁻, the copper active sites convert to CuCl, achieving signal amplification. Upon the addition of Gly, a competitive reaction between Cu and Gly converts CuCl into a Cu-Gly complex, resulting in a sharp decrease in the electrochemical signal. This signal drop is used to detect Gly. The bimetallic PdCu nanoparticles (NPs) endowed the sensing platform with better stability and electrochemical performance due to their synergistic effect, and their stability was simply verified by Density functional theory (DFT). The sensor demonstrates a linear detection range spanning from 1 × 10⁻¹ ³ to 1 × 10⁻⁵ M, with a limit of detection (LOD) of 3.72 × 10⁻¹ ⁴ M. The sensor demonstrated a recovery rate of 95.9 % to 104.5 % in actual samples such as water and soil, indicating its potential for practical application.

Self-sulfur doped mesoporous novel carbon electrodes derived from poly-anthraquinone sulfide for high-performance supercapacitors! A comparative study

Carbon materials are suitable electrode candidates in supercapacitors (SCs) because of their availability, well-defined microstructures, and ultrahigh surface areas. Herein, a universal chemical activation method was utilized to obtain activated carbon (C-KOH) from poly-anthraquinone sulfide (PAQS) at 850 °C and reduced activated carbon (C-KOH-H) from C-KOH via a mild hydrogen reduction process at low temperature. The electrochemical performances of the PAQS derived activated carbon electrodes were investigated by assembling electric double-layer capacitors (EDLCs). Electrodes fabricated from C-KOH and C-KOH-H showed 174 and 182.3 F g−1 specific capacitances at 0.5 A g−1 current density, respectively. Whereas their energy densities were 44 and 46 Wh kg−1 at 350 and 423 W kg−1 power densities, respectively. SCs assembled from C-KOH-H showed excellent rate performance, that retained 140 F g−1 even at high current density (20 A g−1), while the one assembled with C-KOH stored 54 F g−1. Furthermore, the C-KOH-H electrode retained 98 % of the initial capacitance at 1 A g−1 over 20,000 continuous cycles. The experimental results revealed that C-KOH-H showed the best electrochemical performance in SCs, which is attributed to the presence of less sulfur and oxygen than C-KOH after the mild reduction. These results prove that PAQS show excellent activation with KOH to produce well-organized porous activated carbons having high specific surface areas, which can be utilized as high-performance electrode materials in SCs.

Antimony removal using zero-valent iron-manganese bimetallic nanomaterial: Adsorption behavior and mechanism

Although the effectiveness of zero-valent iron (ZVI) and zero-valent manganese (ZVMn) in heavy metal removal is well-established, their combined synergistic potential for antimony (Sb) remediation from wastewater has remained largely unexplored. Addressing this gap, this study introduced a magnetic zero-valent iron-manganese bimetallic material (ZVIM), synthesized via the borohydride reduction method, to investigate its capabilities and underlying mechanisms for Sb reduction and adsorption. The ZVIM, characterized by a high specific surface area of 220 m²/g, exhibited a high adsorption capacity (614.6 mg/g for Sb(III) and 241.7 mg/g for Sb(V)), facilitating over 96.7 % removal for both Sb(III) and Sb(V). The adsorption conformed to the pseudo-second-order kinetic model, and the isotherm data aligned with the Freundlich model, indicative of a heterogeneous adsorption process. The removal of Sb(III) predominantly occurred via surface complexation and electrostatic adsorption to the positively charged ZVIM surface, accompanied by a partial oxidation of Sb(III) to Sb(V). In contrast, the elimination of Sb(V) was primarily facilitated through surface complexation mechanism, encompassing both reduction and electrostatic adsorption. The outcomes of this study shed light on the intricate interactions between Sb species and the ZVIM, revealing the material as a promising candidate for the efficacious removal of Sb from wastewater.

Facile synthesis of MWCNT hexagonal needles grown on interconnected honeycombs like MnCo2O4/MnO2 nanoporous electrode for high-performance asymmetric supercapacitor

The construction of a honeycomb-like structure composed of MnCo2O4/MnO2was effectively achieved using a combination of hydrothermal processing and heat treatment. The whole surface of the MnCo2O4/MnO2 honeycomb is coated with neatly arranged hexagonal nano needles made of MWCNT, leading to a substantial enhancement in the specific surface area. At 1 A/g, the supercapacitor electrode composed of MnCo2O4/MnO2@MWCNT composite exhibited an exceptional specific capacitance of around 1539 F/g. Furthermore, it maintained approximately 95.5 % of its capacity even after undergoing 10,000 cycles. The asymmetric capacitor device, with MnCo2O4/MnO2@MWCNT and AC electrode, has a power density of 1537.8 W kg−1 and an energy density of 48.78 Wh kg−1. The MnCo2O4/MnO2composite exhibits exceptional rate performance, significant capacitance, and excellent cycle performance due to the synergistic effect between MnCo2O4/MnO2 and MWCNT, as well as the high specific surface area and unique structure. Consequently, it presents a viable option for the advancement of high-efficiency electrochemical super capacitors in the next generation.

Superconductivity in Monolayer Carbon Allotropes with High Thermal Stability.

Intrinsic superconductivity is rarely discovered in sp2-hybridized monolayer carbon allotropes. Here we design a carbon monolayer configured of pentagon, heptagon, and hexagon rings with p2 plane group symmetry. Full-sp2 hybridization is proposed to favor thermal metastability on a low Gibbs free energy. The extremely small thermal expansion coefficient is predicted to the turn negative value to positive with elevating temperature. Carbon polygon structures remain intact at a high thermal temperature of 3,000 K. The high specific surface area is found to approach 2,700 m2/g, with O2-adsorption being advantageous over pristine graphene. We reveal electronic Fermi surfaces mediated by phonon modes of carbon out-of-plane vibrations. By calculating the Eliashberg equation, we evaluate intrinsic superconductivity with a large electron-phonon coupling coefficient. The superconducting transition temperature is estimated to reach 20 K under a high logarithmic average frequency. These first-principles calculations shall stimulate experimentalists' interest in exploring low-dimensional carbon superconductors with gas sensitivity.

Soil diversity at Jezero crater and Comparison to Gale crater, Mars

The martian soil is of particular interest as it can help us understand the different processes that have occurred on Mars by studying the chemistry and mineralogy of its constituents as a function of grain size. The fine-grained martian soil is thought to be homogeneous across the planet and thus to represent a global component. In this study we report on the soil targets analysed by the SuperCam instrument aboard the Perseverance rover, which is currently exploring Jezero crater. A total of 343 targets were analysed. Their grain size distribution confirms the sparsity of 250–900 Âμm particles in the martian soil, although both smaller and larger grains are present. We found that the local components, due to erosion of the local bedrock, are present not only in the very coarse grains or larger gravels of the soil, but also in the very fine ones (¡250 Âμm). We detected some very coarse grains enriched in olivine, pyroxene and carbonate in both the crater floor and the delta front locations, whereas phyllosilicate-rich grains have been encountered only in the delta front. We have compared the Jezero fine-grained soil targets with those of Gale crater using ChemCam data. We found that those at Jezero show no evidence of Mg sulfates, in contrast to the observation at Gale. In addition, the fine-grained soil at Jezero is more hydrated than that at Gale, probably due to its higher specific surface area.

Adsorption, photocatalysis, and sonocatalytic activities of LaFeO3/methylcellulose/multi-walled carbon nanotubes-NiCu2O4/Zn for removal of organic pollutant: preparation, main factor, and mechanism

The primary objective of this study was to create and analyze a new type of LaFeO3/methylcellulose/multi-walled carbon nanotubes-NiCu2O4/Zn nanocomposite, called LFO/MC/MWCNT-NCO/Z, which has multiple functions. Structural investigation using field emission scanning electron microscopy showed that the nanoparticles (40–50 nm) were evenly distributed throughout the nanocomposite, suggesting that they were successfully incorporated without any clumping. FTIR research verified the existence of functional groups that facilitate electrostatic interactions with contaminants, hence strengthening catalytic performance and improving adsorption efficiency. The BET analysis revealed a significantly high specific surface area of 72.61 m2/g, which greatly enhances its ability to adsorb substances. The nanocomposite demonstrated high removal efficiency in adsorption (74.55%), photocatalysis (68.19%), and sonocatalysis (91.22%) procedures, highlighting its potential for effectively removing bisphenol A as organic pollutants. The synthesized LFO/MC/MWCNT-NCO/Z nanocomposite shows great potential in effectively eliminating organic contaminants from water solutions. This offers a sustainable way to address water pollution and protect human health and the environment.

Synthesis and enhanced H2S gas sensing performances of Co-doped NiO@g-C3N4 heterocomposites

Metal doping is an efficient approach to improve H2S gas sensing performances, but the metal-doped NiO is still faced poor recovery capability at low working temperature. Herein, Co-doped NiO@g-C3N4 heterocomposites were constructed firstly via a simple solid phase reaction. Texture characterizations indicate that Co-doped NiO@g-C3N4 heterocomposites with the architecture of hierarchical microspheres show high specific surface areas and rich surface oxygen vacancies. The gas-sensitive measurements exhibit that the response value of the heterocomposites with g-C3N4 content of 30 wt% (Co-NiO@g-C3N4-3) increases to 45 toward 20 ppm H2S gas at 172 °C, which is about 1.8 times of Co-NiO (23), as well as response/recovery times decreased to ca. 100/130 s. Besides, excellent repeatability, stability and selectivity of Co-NiO@g-C3N4-3 sensors are obtained. The improved H2S gas sensing performances of Co-NiO@g-C3N4 heterocomposites is mainly contributed to the formation of nano-heterojunctions, which promotes electron accumulation at nano-heterojunctions near Co-NiO, facilitates O2 molecules adsorption on the material surface and accelerates the resistance change of the sensors, resulting the enhanced gas sensing performances.

Synthesis of N/O Atoms Co-doped Biochar with 3D Porous Structure for Effective Electromagnetic Wave Absorption.

Developing biochar with large specific surface area (SSA), heteroatom doping, and porous structure is attracting substantial attention to absorb electromagnetic wave (EMW) in recent. Herein, a novel method of ethanol and KOH co-treatment is used to produce the biomass carbon deriving from pitaya peels. The obtained carbon possesses the high SSA of 1580 m2/g, successful N/O atoms co-doping, and massive pores with different size. The results of EMW absorption measurement show that the prepared biochar could achieve over 99% absorpition to EMW, which the highest reflection loss is of ca. -45.25 dB at 7.54 GHz with an effective absorption bandwidth (EAB) of ca. 4.87 GHz. The execellent microwave absorption property is caused by the surface defects, dipole and interface polarizations of the synthesized biochar owning unique microstructure and N/O atoms co-doping. Hence, this avenue provides a new reference for fabricating low-cost and eco-friendly biochar as a microwave absorber.

“Partner” cellulose gel with “dialysis” function: Achieve the integration of filtration-enrichment-SERS detection

Hydrogel and aerogel materials have garnered significant attention in constructing effective surface-enhanced Raman spectroscopy (SERS) substrates due to their excellent adsorption capabilities, high specific surface area, and abundant chemical groups. However, in liquids with complex compositions, non-specific adsorption of macromolecules can lead to surface scaling and pore clogging of the substrate material, limiting the selective enrichment and SERS detection of target molecules. To address this, an innovative aerogel-chimeric hydrogel material (CH@S-CNF/SA/Ag NPs) was developed. The aerogel component, with its high specific surface area and electronegative properties, functions as a SERS “chip” for adsorption and detection of target molecules. Simultaneously, the mesoporous structure of the hydrogel “shell” effectively filters macromolecules from the solution. These CH@S-CNF/SA/Ag NPs were utilized as SERS substrate materials for detecting urine from healthy individuals and patients with chronic kidney disease stage 5 (CKD5). When combined with machine learning algorithms, the detection accuracy reached 99.50%. This work represents a significant advancement in the specific adsorption and SERS detection of small molecules in complex biological samples such as urine and blood.

Graphene with suitable-size nitrogen-doped cavity being an excellent photocatalyst for proton-coupled electron transfer in water splitting

Aiming to attain porous carbon nitride photocatalysts with high specific surface area, abundant active sites, broad absorption range and effective electron-hole separation, we remove carbon rings from graphene and replace all the edge carbon atoms of the cavity with nitrogen atoms. The accurate electronic structures and exciton properties of the proposed materials are revealed by the ab initio many-body Green's function theory. Computational results show that the absorption of the designed materials can cover both the visible and the near-infrared light region. The exciton binding energies of the materials are one order of magnitude lower than those of the typical two-dimensional photocatalyst graphitic carbon nitride. Due to the formation of hydrogen bonds between pyridinic nitrogen atoms and water molecules during water splitting, the key excited-state proton-coupled electron transfer reactions are barrierless. These findings could serve as guidelines for the realization of high-performance metal-free two-dimensional photocatalysts.

Hierarchically porous MgO/biochar composites for efficient CO2 capture: Structure, performance and mechanism

For enhancing the CO2 uptake performance of MgO-based materials, hierarchically porous MgO/biochar composites were prepared using a microwave-assisted hydrothermal method. The CO2 adsorption properties was investigated in detail and the adsorption mechanism was revealed by considering structure − function relationships and performing density functional theory calculations. The MgO/biochar-1 had hierarchical pore structure and high specific surface area (1453 m2·g−1) with abundant narrow micropores (<1.0 nm), facilitating the adsorption of CO2. The results demonstrated that MgO/biochar-1 exhibited the highest CO2 capture capacity of 6.65 mol⋅kg−1 (273 K, 1 bar) and excellent selectivity for CO2/N2 (96.70 at CO2/N2 = 15:85, v/v). After 3 cycles, the adsorption capacity of MgO/biochar-1 still remained at 5.70 mol⋅kg−1 (273 K, 1 bar), suggesting the well cycling performance. The results of density functional theory calculation indicated that the oxygen-containing functional groups and MgO particles substantially enhanced the CO2 capture performance due to the enhanced interactions between MgO/biochar and CO2. This study provides novel insights for the construction of efficient and cheap solid adsorbents for CO2 capture.

Sensitive detection of NH3 at room temperature at ppb level via facile ZIF calcination

This study introduces an innovative approach for preparing gas sensors involving the formation of metal oxides from metal–organic framework materials via a two-step calcination process. A gas-sensitive material capable of detecting NH3 at a concentration of 11 ppb at room temperature was developed using a simple and facile experimental method. Compared with materials produced in previous studies by one-step calcination, the C-doped ZnO developed in this study had a dispersed cubic porous morphology with a higher specific surface area and smaller pore size. During two-step calcination, urea acts as a structure-directing agent and increases the gas adsorption capacity of the final material. Additionally, the incorporation of urea slightly reduced the material's band gap. Further examinations confirmed the material's exceptional selectivity and long-term stability in detecting NH3, and response tests at 59 %, 75 %, and 85 % relative humidity indicated its tolerance to high-humidity environments. These outstanding characteristics suggest that the proposed fabrication method can produce metal-oxide materials with substantially enhanced gas-sensing performance.

Ultralight M5 aerogels with superior thermal stability and inherent flame retardancy.

Ultra-lightweight materials often face the formidable challenge of balancing their low density, high porosity, high mechanical stiffness, high thermal and environmental stability, and low thermal conductivity. This study introduces an innovative method for synthesizing high-performance polymer aerogels to address the challenge. Specifically, we detail the production of poly (2,5-dihydroxy-1,4-phenylene pyridine diimidazole) (PIPD or M5) aerogels. This process involves chemically stripping M5 "super" fibers into nanofibers, undergoing a Sol-Gel transition, followed by freeze-drying and subsequent thermal annealing. The M5 aerogels excel beyond existing polymer aerogels, boasting an ultralight density of 6.03 mg cm-3, superior thermal insulation with thermal conductivity at 32 mW m-1 K-1, inherent flame retardancy (LOI = 50.3%), 80% compression resilience, a high specific surface area of 462.1 m2 g-1, and outstanding thermal stability up to 463 °C. These multi-faceted properties position the M5 aerogel as a front-runner in lightweight insulation materials, demonstrating the strategic use of high-performance polymer assembly units in aerogel design.

CFs-supported La-BiOIO3/Bi2O3 heterostructures via in situ growth strategies for efficiently removing diclofenac: Fermi level modulation, intermediates identification and radical mechanism

The charge transfer efficiency and the recyclability were still the potential factors limiting the widespread application of photocatalysts for pollutant removal. Herein, a novel design perspective for BiOIO3-based S-scheme heterojunction (La-BiOIO3/Bi2O3) with modulated Fermi level and enhanced internal electric field was proposed by in situ liquid-phase growth strategy. Meanwhile, the CFs@La-BiOIO3/Bi2O3 catalysts with high stability and easy recyclability were assembled based on industrial carbon fiber cloths, which can achieve efficiently photocatalytic removal of diclofenac (DCF, 95.5 %, 20 min) and bisphenol A (BPA, 100 %, 30 min) under simulated sunlight irradiation. The photocatalytic degradation rates of DCF were 52.8 and 12.4 times that of pure BiOIO3 and Bi2O3, respectively. The high specific surface area (39.74 m2·g−1) and suitable bandgap structure (2.74 eV) also demonstrated the excellence of the CFs@La-BiOIO3/Bi2O3 degradation system. Verification of heteroatom-driven electron rearrangement and charge migration route in heterostructure was performed through XPS analysis and Mott-Schottky experiments. Gaussian calculations, LC-MS, and toxicity assessments demonstrated that reactive oxygen species (ROS) such as ·O2− and ·OH selectively attacked the electronic groups of DCF and its intermediates, which combined with holes (h+) retained in the valence bands of Bi2O3 to synergistically achieve efficient degradation and detoxification of DCF. Finally, the charge migration mechanism for the photocatalytic elimination of DCF over CFs@La-BiOIO3/Bi2O3 photocatalyst was proposed. Similar studies can be extended to other structures capable of achieving rational Fermi level modulation and synchronous carrier introduction for the remediation of polluted waters, providing novel perspectives for improving photocatalytic driving capacity.

Self-powered strain sensing devices with wireless transmission: DIW-printed conductive hydrogel electrodes featuring stretchable and self-healing properties

With rapid advancements in health and human–computer interaction, wearable electronic skins (e-skins) designed for application on the human body provide a platform for real-time detection of physiological signals. Wearable strain sensors, integral functional units within e-skins, can be integrated with Internet of Things (IoT) technology to broaden the applications for human body monitoring. A significant challenge lies in the reliance of most existing wearable strain sensors on rigid external power supplies, limiting their practical flexibility. In this study, we present an innovative strategy to fabricate glutaraldehyde (GA)-poly(vinyl alcohol) (PVA)/cellulose nanocrystals (CNC)/Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) conductive hydrogels through multiple hydrogen bonding systems. Combining the advantageous rheological properties of the precursor solution and the high specific surface area after freeze–thaw cycling, we have created a self-powered sensing system prepared by large-area printing using direct ink writing (DIW) printing. The resulting conductive hydrogel exhibits commendable mechanical properties (411 KPa), impressive stretchability (580 %), and robust self-healing capabilities (>98.3 %). The strain sensor, derived from the conductive hydrogel, demonstrates a gauge factor (GF) of 2.5 within a stretching range of 0–580 %. Additionally, the resultant supercapacitor displays a peak energy density of 0.131 mWh/cm3 at a power density of 3.6 mW/cm3. Benefiting from its elevated strain response and remarkable power density features, this self-powered strain sensing system enables the real-time monitoring of human joint motion. The incorporation of a 5G transmission module enhances its capabilities for remote data monitoring, thereby contributing to the progress of wireless tracking technologies for self-powered electronic skin.

Selective electrosorption of heavy metal ions from wastewater with S-doped hierarchical porous carbon derived from waste Camellia oleifera shell

Capacitive deionization (CDI) has garnered significant attention in desalination and the removal of heavy metal ions. The quest for cost-effective and high-performance electrode materials is crucial to advance CDI applications. Herein, we report a sulfur-doped hierarchical porous carbon (SPC) derived from waste camellia oleifera shells via a sustainable hydrothermal carbonization process followed by KOH/ammonium salt activation. The optimized SPC-0.2 exhibits exceptional characteristics, featuring a high specific surface area of 1875 m2 g−1 and substantial sulfur doping at 8.65 %, leading to enhanced specific capacitance (161.3 F g−1) in a 1 M NaCl solution. Under optimal operating conditions (1.2 V, 10 mL min−1, 500 mg L−1 NaCl), the SPC-0.2 electrode achieves a notable desalination capacity of 26.64 mg g−1. In particular, the electrode can selectively remove >99 % of Cr3+ and Cu2+ ions (each 10 mg L−1) in a 100 mg L−1 NaCl solution. This high selectivity is attributed to the formation of sulfides via low adsorption energies between the doped sulfur atoms and the targeted heavy metal ions. Furthermore, the SPC-0.2 electrode demonstrates robust reusability and high efficiency in the actual water body. Collectively, our findings underscore the significant potential of the synthesized SPC as an electrode material for CDI, particularly in the selective capacitive removal of heavy metal ions from wastewater. This work not only contributes to the circular economy by using waste biomass, but also offers a viable solution for environmental remediation.

Phase change material composites based on 3D lignin-derived porous carbon prepared by in-situ activation for efficient solar-driven energy conversion and storage

Utilization of three-dimensional biomass-derived porous carbons can effectively address issues of easy leakage, low thermal conductivity, and weak photothermal conversion of phase change materials (PCMs). This enables the production of high-performance composites for solar-induced energy collection, conversion, and storage. In this study, hierarchical lignin-derived porous carbon (HLPC), microporous lignin-derived porous carbon (MILPC) and mesoporous lignin-derived porous carbon (MELPC) were prepared through high-temperature in-situ activation using lignosulphonate (LS) as a carbon precursor and CaCO3, KOH and ZnCO3 as activators. Carbon-based PCM composites with high performance were obtained by encapsulating paraffin wax (PW) in porous carbon supports. Results demonstrated that PW/HLPC exhibited comprehensive performance superior to other tested PW composites owing to its higher specific surface area (2,358 m2/g), larger pore volume (1.1 cm3/g) and well-interconnected framework structure. Additionally, PW/HLPC displayed relatively high latent heat (123.4 kJ/kg), photothermal conversion and storage efficiency (95 %), and photoelectric conversion performance (174.5 mV). Moreover, PW/HLPC also showed better leak-proof properties at 90 °C. The cycling stability and photothermal conversion performance of PW/HLPC were superior to those of the selected crude biochar-based PW composites. This study highlights the advantages of the prepared PW/HLPC for both the high-value utilization of lignin and its practical applications in solar-induced energy harvest, conversion, and storage.

Scalable fabrication of high surface area g-C3N4 nanotubes for efficient photocatalytic hydrogen production

In this research, we present a novel facile, scalable, and template-free technique of synthesizing graphitic carbon nitride (g-C3N4) nanotubes for generating hydrogen through photocatalysis. The hybrid technique involves a two-fold mixing of the precursor materials melamine (M) and cyanuric acid (CA), involving ball milling followed by solution mixing. By varying the M:CA molar ratios, different compositions of g-C3N4 nanotubes were fabricated. The study focused on examining the surface characteristics and the photocatalytic hydrogen evolution performance of these nanotubes. Nanotubes with high specific surface area of 206 m2 g−1 for M:CA molar ratio of 1:3 and 178 m2 g−1 for M:CA molar ratio of 1:5 were produced, with H2 evolution rates of 543 μmol h−1 g−1 and 740 μmol h−1 g−1 respectively, which were an increase of 4 and 5-fold, respectively, in comparison to the pristine sample. The enhanced efficiency of hydrogen production through photocatalysis by nanotubes, when contrasted with pristine material, can be ascribed to their high crystallinity, superior specific surface areas, decreased recombination rates of electron-hole pairs generated during light exposure, and improved dynamics of charge carriers. This hybrid technique provides a new pathway for cost-effective fabrication of g-C3N4 nanotubes with substantial surface areas and high yield photocatalysts on an industrial scale, without the use of templates and hydrothermal processes for efficient hydrogen generation.