Search Results (142)

The transformation of waste plastics into hydrogen and functional carbon (C) materials represents a promising pathway for achieving both resource recycling and the production of value-added products. Owing to their tunable physicochemical properties, plastic-derived carbons have attracted significant attention in electrochemical energy storage applications. Various C nanostructures, including graphene, porous C, hard C, and C nanotubes (CNTs), can be generated from discarded plastics through thermochemical processes. The electrochemical performance of these materials is closely governed by their structural characteristics, such as pore architecture, specific surface area, heteroatom doping, surface functionalities, and dimensional morphology. This review aims to provide a comprehensive and systematic overview of the conversion of waste plastics into functional C nanomaterials via thermochemical routes, particularly catalytic pyrolysis and carbonization. The resulting C nanostructures are systematically categorized based on their dimensional architectures (0D, 1D, 2D, and 3D) and comparatively analyzed in terms of their structural features and electrochemical performance. Emphasis is placed on the transformation of diverse plastic feedstocks into high-value C materials with tailored dimensional architectures, including graphene, CNTs, C nanospheres, C nanosheets, porous carbons, and their composites. Furthermore, recent progress and critical challenges in utilizing these materials for electrochemical energy storage systems, such as supercapacitors and rechargeable batteries (Li-ion, Na-ion, K-ion, Li-S, and Zn-air), are discussed. Distinct from previous reports, this review highlights the correlation between thermochemical processing strategies, resulting structural features, and electrochemical performance, providing new insights into the rational design of high-performance C materials. These findings are expected to facilitate the advancement of sustainable energy storage technologies while contributing to effective plastic waste valorization. Full article

Developing free-standing electrodes without the need of metal current collectors, binders, and conductive additives are essential for promoting the development of sodium-ion batteries (SIBs) to attain higher energy density. In this study, we developed and effectively synthesized a novel three-dimensional free-standing sodium-ion battery anode material with the composition of Bi@MoS₂@C carbon nanofibers by cleverly utilizing the energy storage advantages of each material. By growing MoS₂ nanospheres on Bi carbon nanofibers and coating them with a carbon layer, this free-standing system achieves both structural optimization and synergistic performance enhancement. Experimental results show that this composite electrode has a remarkably high initial specific capacity of 275.31 mA h g⁻¹ at a current density of 0.5 A g⁻¹, significantly exceeding that of Bi carbon nanofibers (150.6 mA h g⁻¹). Furthermore, it retains a capacity retention of 96.07% after 800 cycles, which significantly exceeds that of pristine MoS₂ (72.33 mA h g⁻¹) as a sodium-ion battery anode. The significant performance improvement originates from the free-standing structural design and synergistic effects of Bi carbon nanofibers, MoS₂ nanospheres and carbon layer, which not only provide 3D electron transport pathways and improved conductivity but also effectively accommodate volume changes during the charging and discharging processes. This work offers a promising and practical strategy for designing high-performance free-standing energy storage electrodes through hybrid mechanisms and synergistic effects. Full article

The rapid advancement of flexible electronics has propelled the development of lightweight, wearable piezoresistive sensors that integrate high sensitivity, excellent mechanical properties, and multifunctionality, making them a research hotspot. This work presents a flexible and lightweight multifunctional polyvinyl alcohol (PVA) composite hydrogel film, which is constructed based on a synergistic conductive network of cuttlefish ink-derived carbon nanospheres (CNPs) and polypyrrole (PPy). Within this composite, the CNPs and PPy form an interpenetrating conductive network throughout the PVA matrix, where PPy effectively suppresses the agglomeration of CNPs, thereby significantly enhancing the electron transport efficiency. This unique structure endows the material with improved flame retardancy and hydrophobicity while maintaining its lightweight characteristic. Consequently, the sensor demonstrates fast response (64 ms) and recovery times (66 ms) and a high sensitivity factor of 4.34 kPa⁻¹ within a pressure range of 11.2–16.8 kPa. Excellent stability is retained after nearly 6000 loading–unloading cycles, primarily attributed to the efficient response of the contact points and conductive pathways within the synergistic network under stress. Furthermore, this flexible sensor can not only reliably monitor human physiological activities (such as finger joint bending and facial expression changes) but also generate distinct current responses to subtle mouse-clicking actions, enabling tactile handwriting input. This study provides a novel strategy for constructing high-performance sensing materials by utilizing natural biomass-derived carbon materials and conductive polymers, highlighting the significant application potential of such lightweight, multifunctional hydrogel films in next-generation flexible electronic devices. Full article

The solar-driven water splitting for the production of renewable green hydrogen fundamentally relies on the exploration of efficient photocatalysts. Nanostructured TiO₂ is widely recognized as a promising material for photocatalysis, yet it remains hindered by inadequate light harvesting and fast photogenerated carrier recombination. Herein, calcined C/TiO₂ xerogels with yolk–shell and core–shell nanostructures (denoted as YS-C/TiO₂ and CS-C/TiO₂) were designed and fabricated via a typical sol–gel–calcination assisted approach. Thanks to the encapsulation of carbon nanospheres into TiO₂, it effectively enhances light absorption, improves carrier separation, and lessens carrier recombination, making the well-designed YS-C/TiO₂ composite display a remarkable hydrogen evolution rate of 975 µmol g⁻¹ h⁻¹ under simulated solar light irradiation and without the use of any co-catalyst, which is approximately 21.7 times that of the commercial TiO₂. The work provides an efficacious design concept in developing nanostructured TiO₂-based photocatalysts and in boosting broad photocatalytic applications. Full article

This study aimed to develop an industrially scalable coating route for enhancing the oxidation resistance of carbon fiber fabrics, a critical requirement for next-generation aerospace and high-temperature composite structures. To achieve this goal, synthesis of hexagonal boron nitride (h-BN) layers was achieved via a single wet step in which the fabric was impregnated with an ammonia–borane/THF solution and subsequently nitrided for 2 h at 1000–1500 °C in flowing nitrogen. Thermogravimetric analysis coupled with X-ray diffraction revealed that amorphous BN formed below ≈1200 °C and crystallized completely into (002)-textured h-BN (with lattice parameters a ≈ 2.50 Å and c ≈ 6.7 Å) once the dwell temperature reached ≥1300 °C. Complementary XPS, FTIR and Raman spectroscopy confirmed a near-stoichiometric B:N ≈ 1:1 composition and the elimination of O–H/N–H residues as crystallinity improved. Low-magnification SEM (100×) confirmed the uniform and large-area coverage of the BN layer on the carbon fiber tows, while high-magnification SEM revealed a progressive densification of the coating from discrete nanospheres to a continuous nanosheet barrier on the fibers. Oxidation tests in flowing air shifted the onset of mass loss from 685 °C for uncoated fibers to 828 °C for the coating produced at 1400 °C; concurrently, the peak oxidation rate moved ≈200 °C higher and declined by ~40%. Treatment at 1500 °C conferred no additional benefit, indicating that 1400 °C provides the optimal balance between full crystallinity and limited grain coarsening. The resulting dense h-BN film, aided by an in situ self-healing B₂O₃ glaze above ~800 °C, delayed carbon fiber oxidation by ≈140 °C. Overall, the process offers a cost-effective, large-area alternative to vapor-phase deposition techniques, positioning BN-coated carbon fiber fabrics for robust service in extreme oxidative environments. Full article

Addressing the urgent need for robust and sustainable catalysts to detoxify nitroaromatic pollutants, this study introduces a novel approach for synthesizing cobalt oxide nanocomposites via pyrolysis of cobalt benzene-1,3,5-tricarboxylate. By integrating porous carbon (PC) and nano silica (NS) supports with Co₃O₄ to form (Co₃O₄/PC) and (Co₃O₄/NS), we achieved precise morphological control, as evidenced by SEM and TEM analysis. SEM revealed 80–500 nm Co₃O₄ microspheres, 300 nm Co₃O₄/PC microfibers, and 2–5 µm Co₃O₄/NS spheres composed of 100 nm nanospheres. TEM further confirmed the presence of ~15 nm nanoparticles. Additionally, FTIR spectra exhibited characteristic Co–O bands at 550 and 650 cm⁻¹, while UV–Vis absorption bands appeared in the range of 450–550 nm, confirming the formation of cobalt oxide structures. Catalytic assays toward p-nitrophenol reduction revealed exceptional kinetics (k = 0.459, 0.405, and 0.384 min⁻¹) and high turnover numbers (TON = 5.1, 6.7, and 6.3 mg 4-NP reduced per mg of catalyst), outperforming most of the recently reported systems. Notably, both supported catalysts retained over 95% activity after two regeneration cycles. These findings not only fill a gap in the development of efficient, regenerable cobalt-based catalysts, but also pave the way for practical applications in environmental remediation. Full article

Public health concerns related to food contaminants, including biotoxins, pesticide and veterinary drug residues, illegal additives, foodborne pathogens, and heavy metals, have garnered significant public attention in recent years. Consequently, there is an urgent need to develop rapid and accurate technologies to detect these harmful substances. Surface-enhanced Raman spectroscopy (SERS), due to its characteristics of high sensitivity and specificity enabling the detection of food contaminants within complex matrices, has attracted widespread interest. This review focuses on the application of noble metal-based nanocomposites as SERS-active substrates for food contaminant detection. It particularly highlights the structure–performance relationships of metallic nanomaterials, including gold and silver nanoparticles (e.g., nanospheres, nanostars, nanorods), bimetallic structures (e.g., Au@Ag core–shell), as well as metal–nonmetal composite nanomaterials such as semiconductor-based, carbon-based, and porous framework-based materials. All of which play a crucial role in achieving effective Raman signal enhancement. Furthermore, the significant applications in detecting various contaminants and distinct advantages in terms of the sensitivity and selectivity of noble metal-based nanomaterials are also discussed. Finally, this review addresses current challenges associated with SERS technology based on noble metal-based nanomaterials and proposes corresponding strategies alongside future perspectives. Full article

The development of multifunctional conductive hydrogels with rapid self-healing capabilities and powerful sensing functions is crucial for advancing wearable electronics. This study designed and prepared a polyvinyl alcohol (PVA)–borax hydrogel incorporating carbon nanotubes (CNTs) and biomass carbon nanospheres (CNPs) as dual-carbon fillers. This hydrogel exhibits excellent conductivity, mechanical flexibility, and self-recovery properties. Serving as a highly sensitive piezoresistive sensor, it efficiently converts mechanical stimuli into reliable electrical signals. Sensing tests demonstrate that the CNT/CNP/PVA–borax hydrogel sensor possesses an extremely fast response time (88 ms) and rapid recovery time (88 ms), enabling the detection of subtle and rapid human motions. Furthermore, the hydrogel sensor also exhibits outstanding cyclic stability, maintaining stable signal output throughout continuous loading–unloading cycles exceeding 3200 repetitions. The hydrogel sensor’s characteristics, including rapid self-healing, fast-sensing response/recovery, and high fatigue resistance, make the CNT/CNP/PVA–borax conductive hydrogel an ideal choice for multifunctional wearable sensors. It successfully monitored various human motions. This study provides a promising strategy for high-performance self-healing sensing devices, suitable for next-generation wearable health monitoring and human–machine interaction systems. Full article

Photodynamic therapy (PDT) is a non-invasive therapeutic method with over a century of medical use, especially in dermatology, ophthalmology, dentistry, and, notably, cancer treatment. With an increasing number of clinical trials, there is growing demand for innovation in PDT. Despite being a promising treatment for cancer and bacterial infections, PDT faces limitations such as poor water solubility of many photosensitizers (PS), limited light penetration, off-target accumulation, and tumor hypoxia. This review focuses on chlorins—well-established macrocyclic PSs known for their strong activity and clinical relevance. We discuss how nanotechnology addresses PDT’s limitations and enhances therapeutic outcomes. Nanocarriers like lipid-based (liposomes, micelles), polymer-based (cellulose, chitosan, silk fibroin, polyethyleneimine, PLGA), and carbon-based ones (graphene oxide, quantum dots, MOFs), and nanospheres are promising platforms that improve chlorin performance and reduce side effects. This review also explores their use in Antimicrobial Photodynamic Therapy (aPDT) against multidrug-resistant bacteria and in oncology. Recent in vivo studies demonstrate encouraging results in preclinical models using nanocarrier-enhanced chlorins, though clinical application remains limited. Full article

The extensive use of sodium-ion batteries has made it important to develop high-performance anode materials. Owing to their good sustainability, low cost, and excellent electrochemical properties, hard carbon materials are expected to be a good choice, especially biomass-derived hard carbon. In this study, we successfully synthesized a coir-based carbon nanosphere as an anode material. The hard carbon has a low degree of structural ordering, small particle size, and multiple pore networks for easy sulfur doping compared to the conventional direct high-temperature sulfur doping. The material has a high reversible capacity of 536 mAh g⁻¹ and an initial Coulombic efficiency of 53%, maintaining a reversible capacity of 308 mAh g⁻¹ at a high current density of 5 A g⁻¹, achieving a capacity retention of 90.3% after 1000 cycles. The performance enhancement stems from a combination of enlarged layer spacing, an increased specific surface area, enhanced porosity, and doped sulfur atoms. This study provides an effective strategy for the conversion of biomass waste into high-performance sodium-ion anode material batteries. Full article

This review explores the structural and electrochemical characteristics of carbon materials derived from polybenzoxazines, emphasizing their potential in supercapacitors. A detailed analysis of thermal degradation by-products during carbonization reveals distinct competing mechanisms, underscoring the exceptional thermal stability of benzoxazines. These materials exhibit significant pseudocapacitive behavior and excellent charge retention, making them strong candidates for energy storage applications. The versatility of polybenzoxazine-based carbons enables the formation of diverse morphologies—nanospheres, foams, films, nanofibers, and aerogels—each tailored for specific functionalities. Advanced synthesis techniques allow for precise control over porosity at the nanoscale, optimizing performance for supercapacitors and beyond. Their exceptional thermal stability, electrical conductivity, and tunable porosity extend their utility to gas adsorption, catalysis, and electromagnetic shielding. Additionally, their intumescent properties (unique ability to expand when exposed to high heat) make them promising candidates for flame-retardant coatings. The combination of customizable architecture, superior electrochemical performance, and high thermal resistance highlights their transformative potential in sustainable energy solutions and advanced protective applications. Full article

The Earth abounds in water resources; however, only 0.4% of the freshwater resources are suitable for drinking. The scarcity of freshwater resources has a severe impact on the sustainable development of human society. Desalination is regarded as one of the most effective solutions. In this study, a research approach integrating materials and devices was utilized to synthesize manganese oxide-coated carbon nanospheres (CS@MnO₂). Experimental results demonstrated that the system, by combining the distinctive performance merits of the CS@MnO₂ material and the balanced desalination features, exhibited outstanding desalination performance. In the EDS elemental mapping analysis, the relatively feeble signal of carbon was ascribed to the encapsulation of MnO₂ on the outer surface of CS. Through computational TGA analysis, the mass fraction of carbon in CS@MnO₂-2 was determined to be approximately 51.2%. The excellent hydrophilicity of the material facilitated the permeation of the salt solution throughout the electrode, thereby enhancing the capacitance. CS@MnO₂-2 manifested a high salt adsorption capacity of 27.42 mg g⁻¹ and the fastest electrosorption rate of 7.81 mg g⁻¹ min⁻¹. During 50 adsorption desorption cycles, the adsorption capacity showed good results. The adsorption kinetics and adsorption isotherm fitting indicated that the desalination process involved electrostatic and multilayer adsorption. This study holds great significance for reducing the cost of desalinated water and guaranteeing a sustainable supply of freshwater resources. Full article

Wellbore instability caused by the invasion of drilling fluids into formations remains a significant challenge in the application of oil-based drilling fluids (ODFs). In this study, carbon nanospheres (CNSs) were synthesized using glucose as the carbon source through a microwave-assisted method. The effects of the reaction temperature, carbon source concentration, and reaction time on the particle size of CNSs were systematically investigated. The results revealed that under optimal conditions, CNSs with an average particle size of 670 nm were successfully synthesized, exhibiting high sphericity and excellent dispersibility. CNSs demonstrated stable dispersion in mineral oil when lecithin was used as a dispersant. The plugging performance of CNSs in ODFs was evaluated through low-pressure filtration and high-temperature, high-pressure (HTHP) filtration tests. After aging at 180 °C for 16 h, the addition of 2% CNSs reduced the filtration volume from 10.6 mL to 2.5 mL on standard filter paper (average pore size: 3 μm) and from 8.5 mL to 1.6 mL on microporous membranes (average pore size: 0.5 μm). Additionally, the HTHP filtration volume decreased from 73 mL to 18 mL, and the permeability of the filter cake formed during HTHP filtration was reduced from 26.5 × 10⁻³ mD to 1.2 × 10⁻³ mD. Furthermore, CNSs improved the rheological properties and emulsion stability of ODFs. With excellent compatibility and applicability, CNSs offer a promising solution for enhancing the performance of oil-based drilling fluids. Full article

Inverse opals (IOs) are intensively researched in the field of photocatalysis, since their optical properties can be fine-tuned by the initial nanosphere size and material. Another possible route for photonic crystal programming is to stack IOs with different pore sizes. Accordingly, single and double IOs were synthesized using vertical deposition and atomic layer deposition. In the case of the double IOs, the alternating use of the two preparation methods was successfully performed. Hydrothermally synthesized 326 and 458 nm carbon nanospheres were utilized to manufacture two different IOs; hence the name 326 nm and 458 nm IOs. Heat treatment removed the sacrificial template carbon nanospheres, and the as-deposited TiO₂ crystallized upon annealing into nanocrystalline anatase form. Reflectance mode UV–visible spectroscopy showed that most IOs had photonic properties, i.e., a photonic band gap, and by the “slow” photon effect enhanced absorbance, except the 326 nm IO, even though it also had an increase in absorbance. The IOs were tested by photocatalytic degradation of Rhodamine 6-G under visible light. Photocatalytic experiments showed that the 458 nm IO was more active and the double IOs showed higher efficiency compared to monolayers, even if the less effective 326 nm IO was the top layer. Full article

Converting carbon dioxide (CO₂) into solar fuels through photocatalysis represents an appealing approach to tackling the escalating energy crisis and mitigating the greenhouse effect. In this study, using melamine–formaldehyde (MF) nanospheres as a nitrogen source, a N element was simultaneously doped into the TiO₂ nanoparticle structure supported by carbon hollow spheres using a one-step carbonization method to form a heterojunction N-CHS@N-TiO₂ (marked as (N-(CHS@TiO₂)). The composite showed superior photocatalytic activity in reducing CO₂ compared with TiO₂ and N-CHS: after 6 h of visible light irradiation, the CO yield was 4.3 times that of N-CHS and TiO₂; 6 h of UV irradiation later, the CO yield reached 2.6 times that of TiO₂ and 7 times that of N-CHS. The substantial enhancement in photocatalytic activity was attributed to the nitrogen simultaneously doped carbon hollow spheres and TiO₂, mesoporous structure, small average TiO₂ crystal size, large surface areas, and the heterostructure formed by N-CHS and N-TiO₂. The UV-vis diffuse reflectance spectra (DRS) exhibit a significant improvement in light absorption, attributed to the visible-light-active carbon hollow sphere and the N element doping, thereby enhancing solar energy utilization. Full article