Morphology Of Nanomaterials Research Articles

Nanostructure-dependent colouration efficiency of electrochromic coatings using 0D, 1D, and 2D WO3 for smart windows

Towards the development of highly efficient electrochromic coatings, the crystallinity, morphology (e.g. size and shape) of electrochromic nanomaterials, and their charge insertion capacities play a significant role. Herein, we report the structure-dependent colouration effciency in electrochromic coatings based on the use of 0D, 1D and 2D tungsten trioxide (WO3) nanostructures. A series of WO3 with different nanostructures were prepared and used as working electrodes to fabricate electrochromic devices for smart windows applications. Facile spray coating was applied on fluorine-doped tin oxide (FTO) substrate to make ∼70 ​% transparent working electrodes to investigate their charge insertion capacities, electrochromic active surface area, and colouration efficiency. Results showed that the 2D WO3 nanoflakes displayed the highest diffusion coefficient for the intercalation of 1.52 ​× ​10 −10 ​cm2/s with an increased electrochemical active surface area of 25.10 ​mF/cm2, a large modulation of optical reflectance (42.63 ​%) with 3.79 ​s shorter response time for bleaching and a greater colouration efficiency (CE) value (89.29 ​cm2/C) at 700 ​nm compared to the CE value for 1D WO3 (of 22 ​cm2/C) and 0D WO3 (8 ​cm2/C). The outcome of this study provides a new insight and valuable contribution to design an efficient electrochromic coating by controlling and optimising the nanostructures of selective electrochromic materials.

State of the Art Synthesis of Ag-ZnO-Based Nanomaterials by Atmospheric Pressure Microplasma Techniques

Atmospheric pressure microplasma is a simple, cost-effective, efficient, and eco-friendly procedure, which is superior to the traditional nanomaterials synthesis techniques. It generates high yields and allows for a controlled growth rate and morphology of nanomaterials. The silver (Ag) nanomaterials, with their unique physical and chemical properties, exhibit outstanding antibacterial and antifungal properties. Similarly, zinc oxide (ZnO) nanomaterials, known for their low toxicity and relatively lower cost, find wide applications in wound repair, bone healing, and antibacterial and anticancer applications. The use of core–shell nanomaterials in certain situations where some nanoparticles can cause serious harm to host tissues or organs is a testament to their potential. A benign material is coated over the core to reduce toxicity in these cases. This review compares the numerous configurations of microplasma systems used for synthesizing nanomaterials and their use in producing Ag, ZnO, and their core–shell (Ag-ZnO) nanomaterials for biomedical applications. The summary also includes the effect of control parameters, including cathode diameter, gas flow rate, precursor concentration, voltage, and current, on the nanomaterial’s characteristics and applications. In addition, it provides a research gap in the synthesis of Ag, ZnO, and core–shell nanomaterials by this technique, as well as the development and limitations of this technique and the use of these nanoparticles for biomedical applications.

Different temperature-dependent fluorescence properties of CsPbBr3 nanorods and nanowires

Abstract The morphology of totally inorganic metal halide perovskites has a certain influence on their optoelectronic properties. In this study, one-dimensional CsPbBr3 nanorods (NRs) and nanowires (NWs) were arranged utilizing a boiling injection strategy. By controlling the processing time, NRs with a length of roughly 63 nm and NWs with a length of 300 nm were obtained, and it was found that the nanowires were grown from the nanorods. Temperature-dependent photoluminescence (PL) measurements were conducted on CsPbBr3 NRs and NWs, and NRs exhibit a more stable excitonic state at high temperatures (>240 K). This study provides a method to change the morphology of one-dimensional metal halide perovskite nanomaterials without doping, further promoting the application of one-dimensional all-inorganic perovskite materials in the field of optoelectronics.

Design and Preparation of One-Dimensional Cathode By Electrophoretic Deposition Method for Flexible Knitted Batteries

Rechargeable batteries are highly promising energy storage systems that can convert and store electrical energy. Effective energy storage systems should have high energy density, high power, safety, environmentally friendliness, and long cycle life. To meet the aforementioned objectives, researchers have attempted to use different morphologies of nanomaterials as electrodes to improve the electrochemical performance of batteries. Among the materials available, one-dimensional structures have unique properties over traditional ones and extensive applications in wearable devices due to their flexibility [1]. Flexible batteries have several advantages such as mechanical flexibility, good energy storage capabilities, affordability, and environmental safety [2]. They knitted or sewed into textiles, folded into random forms, and wrapped around body parts like the neck or wrist [3]. However, there is little research that covers Li-ion batteries that have a one-dimensional flexible structure.Achieving simultaneous high electronic/ionic conductivity and electrochemical stability is difficult in a homogeneous single-component electrode material. Consequently, the development of precisely defined functional one-dimensional (1D) hetero-nanostructures that effectively integrate the advantages and address the limitations of various electrochemically active materials becomes critical [1].The proposed methodology involves the electrophoretic deposition of lithium iron phosphate on conductive nickel wire, providing a one-dimensional cathode structure. As an anode, nickel-tin is deposited on nickel wire by electrochemical deposition. The deposition method allows greater precision and control over the deposition of active material on the current collector and also has possible applications on different structures such as 1D and 3D. Also, the electrolyte was obtained by layer-by-layer method, by dipping the cathode and anode, separately, in polymers to coat the cathode material as an electrolyte-separator film. The full cell was assembled and the better results will be presented in the meeting. Acknowledgments This research was funded by the Science Committee of the Ministry of Education and Science of the Republic of Kazakhstan (Grant No. АР19679855).

Enhancing Electrochemical Sensor Performance: Studies of Electrodes Tailored with ZnO/ZnFe2O4 Nanoparticles

Spinel metal oxides possess excellent magnetic, electrical, and optical properties. They take AB2O4 (face centered cubic) form with oxygen anions providing tetrahedral (Td) and octahedral (Oh) sites for A+2 and B+3 cations. Spinel can have a normal, inverse, or mixed form based on the occupancy of different cations in Td and Oh sites. The peculiarity of the spinel crystal structure is that its composition can be easily modified without affecting the crystal structure based on the type of cation. The type of cation in the composition defines if the spinel has a normal or inverse form [1]. Based on these premises, we have already synthesized ZnxNi1-xFe2O4 (x =0, 0.2, 0.4, 0.6, 0.8, 1) nanomaterials achieving a clear gradual transition from inverse (x=0) to normal (x=1) spinel. Synthesized nanomaterials were employed as mediators in electron transfer between the screen-printed carbon working electrode and paracetamol to understand the effect of chemical composition and crystal structure on the electron transfer at the electrochemical interface [1]. Normal spinel ZnFe2O4 was found to be the best nanomaterial in terms of sensitivity and kinetic rate constant. In further works, with the aim to understand the effect of ionic radii on sensitivity and electron transfer rate constant in electrochemical sensing of paracetamol, we have focused on the normal spinel structure and modified the composition by varying the concentration of Fe3+ with Cr3+ and Bi3+ [2,3]. This study also proved that the normal spinel ZnFe2O4 has the highest sensitivity and electron transfer rate constant towards paracetamol sensing.In this work, we will present the synergic effect that can be obtained by interfacing ZnFe2O4 with ZnO nanomaterials by tuning the band gap of the heterogeneous structure. The aim is to understand the effect of band gap on sensitivity and electron transfer rate constant in electrochemical sensing. ZnFe2O4, ZnO, and ZnO/ZnFe2O4 nanomaterials are synthesized by a simple, single step auto combustion technique using the respective metal nitrates as precursors. Nanomaterial morphology and particles size are investigated by scanning electron microscopy. X-ray diffraction technique is employed to analyze the crystal structure and identify different phases in the newly synthesized materials. Then, commercially available screen-printed carbon electrodes with carbon working electrode and carbon counter electrodes are used for the electrochemical measurements in combination with an external double junction Ag/AgCl as a reference electrode. The synthesized nanomaterials are mixed with 1-butanol and a 5 μL solution is used to modify the surface of the carbon working electrode to mediate the redox reactions between the carbon surface and the molecule of interest. Primarily the sensors are characterized using cyclic voltammetry with ferri/ferrocyanide redox couple as a probe molecule. Improvement in sensitivity is observed for ZnFe2O4 (8.85 ± 0.50 μA/mM), ZnO (8.50 ± 0.30 μA/mM), and ZnO/ZnFe2O4 (8.22 ± 0.16 μA/mM) sensors compared to the bare carbon one (6.30 ± 0.40 μA/mM). By performing cyclic voltammetry at different scan rates (ν) from 25 to 125 mV/s, a good linearity of redox currents with respect to v0.5 is observed and redox peak positions are varying linearly with ln(ν). Peak-to-peak separation (ΔEp) is reduced for ZnO/ZnFe2O4 sensors compared to the carbon one. All these results suggest a faster electron transfer at the interface when the modified electrodes are used. Laviron model is employed to calculate the electron transfer rate coefficient and constant. The rate constant for ZnFe2O4 (41.8 ± 2.6 ms-1), ZnO (46.0 ± 4.0 ms-1), and ZnO/ZnFe2O4 (33.1 ± 4.5 ms-1) sensors is 3 to 5 times higher as compared to the bare carbon one (9.97 ± 0.78 ms-1). We are currently studying the potential application of ZnO/ZnFe2O4 nanomaterials in electrochemical sensing of small molecules relevant in biomedical field (dissolved oxygen, pH) and pharmaceutical drugs (paracetamol) to assess the potential for their use in different clinical settings.

(Invited) Near Field Photocatalysis for Site-Selective Reactions By Using ZnO Nanoplates

Nanofabrication is a technology for control of the morphology, orientation, and configuration of nanomaterials. When ordinary, propagating light is employed as a processing tool, subwavelength fabrication is difficult due to the diffraction limit. However, if optical near field, which is localized in a subwavelength region is used, nanofabrication beyond the diffraction limit is possible.We have demonstrated that subwavelength nanofabrication is possible by taking advantage of the optical near field. Since hot electron-hole pairs are generated at around the plasmonic resonance sites, the energetic carriers can be used to drive oxidative dissolution of Ag,1,2 oxidative deposition of PbO2,3,4 and reductive deposition of Ag,5 in a site-selective manner. These techniques have been applied to subwavelength photochromic data storage,1,2 fabrication of chiral nanoparticles,4-7 and site-selective modification of a plasmonic photocatalyst with a co-catalyst.8 Generation of optical near field is possible even at non-plasmonic, semiconducting or dielectric nanostructures. Here we employed In-doped ZnO (In:ZnO) as a semiconductor photocatalyst. Hexagonal In:ZnO nanoplates were synthesized and adsorbed onto a glass substrate, and irradiated with linearly polarized UV light in the presence of Ag ions for reductive deposition of Ag. The optical near field generated under polarized UV light gave rise to site-selective Ag deposition. Also, the sample exhibited linear dichroism (LD) signals, indicating that the nanoparticles have optical anisotropy. On the other hand, unpolarized UV light gave no optical anisotropy. Electromagnetic simulations successfully reproduced the LD spectra. We have also performed site-selective oxidation reactions by using the hexagonal In:ZnO nanoplates. Tanabe, I.; Tatsuma, T. Nano Lett. 2012, 12, 5418–5421. Saito, K.; Tanabe, I.; Tatsuma, T. J. Phys. Chem. Lett. 2016, 7, 4363–4368.Nishi, H.; Sakamoto, M.; Tatsuma, T. Chem. Commun. 2018, 54, 11741–11744.Saito, K.; Tatsuma, T. Nano Lett. 2018, 18, 3209–3212.Ishida, T.; Isawa, A.; Kuroki, S.; Kameoka, Y.; Tatsuma, T. Appl. Phys. Lett. 2023, 123, 061111.Morisawa, K.; Ishida, T.; Tatsuma, T. ACS Nano 2020, 14, 3603–3609.Shimomura, K.; Nakane, Y.; Ishida, T.; Tatsuma, T. Appl. Phys. Lett. 2023, 122, 151109.Kim, K.; Nishi, H.; Tatsuma, T. J. Chem. Phys. 2022, 157, 111101.

Green synthesis of magnetite iron oxide nanoparticles using Azadirachta indica leaf extract loaded on reduced graphene oxide and degradation of methylene blue

In the current arena, new-generation functional nanomaterials are the key players for smart solutions and applications including environmental decontamination of pollutants. Among the plethora of new-generation nanomaterials, graphene-based nanomaterials and nanocomposites are in the driving seat surpassing their counterparts due to their unique physicochemical characteristics and superior surface chemistry. The purpose of the present research was to synthesize and characterize magnetite iron oxide/reduced graphene oxide nanocomposites (FeNPs/rGO) via a green approach and test its application in the degradation of methylene blue. The modified Hummer's protocol was adopted to synthesize graphene oxide (GO) through a chemical exfoliation approach using a graphitic route. Leaf extract of Azadirachta indica was used as a green reducing agent to reduce GO into reduced graphene oxide (rGO). Then, using the green deposition approach and Azadirachta indica leaf extract, a nanocomposite comprising magnetite iron oxides and reduced graphene oxide i.e., FeNPs/rGO was synthesized. During the synthesis of functionalized FeNPs/rGO, Azadirachta indica leaf extract acted as a reducing, capping, and stabilizing agent. The final synthesized materials were characterized and analyzed using an array of techniques such as scanning electron microscopy (SEM)-energy dispersive X-ray microanalysis (EDX), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction analysis, and UV–visible spectrophotometry. The UV–visible spectrum was used to evaluate the optical characteristics and band gap. Using the FT-IR spectrum, functional groupings were identified in the synthesized graphene-based nanomaterials and nanocomposites. The morphology and elemental analysis of nanomaterials and nanocomposites synthesized via the green deposition process were investigated using SEM–EDX. The GO, rGO, FeNPs, and FeNPs/rGO showed maximum absorption at 232, 265, 395, and 405 nm, respectively. FTIR spectrum showed different functional groups (OH, COOH, C=O), C–O–C) modifying material surfaces. Based on Debye Sherrer's equation, the mean calculated particle size of all synthesized materials was < 100 nm (GO = 60–80, rGO = 90–95, FeNPs = 70–90, Fe/GO = 40–60, and Fe/rGO = 80–85 nm). Graphene-based nanomaterials displayed rough surfaces with clustered and spherical shapes and EDX analysis confirmed the presence of both iron and oxygen in all the nanocomposites. The final nanocomposites produced via the synthetic process degraded approximately 74% of methylene blue. Based on the results, it is plausible to conclude that synthesized FeNPs/rGO nanocomposites can also be used as a potential photocatalyst degrader for other different dye pollutants due to their lower band gap.

Revealing into the formation mechanism of various nanostructures self-assembled from a bipyridine containing homopolymer

The control of the morphology and nanostructure of soft nanomaterials self-assembled from amphiphilic polymers has attracted significant attention. In this study, various nanostructures including bowl-shaped nanoparticles with controlled openings, round Yuanbao-shaped assemblies, nanowires and butterfly shaped twin nanosheets are formed by manipulating the self-assembly pathway of an amphiphilic homopolymer. The amphiphilic (poly(N-(2,2′-bipyridyl-4-acrylamide), PBPyAA) with bipyridine pendants is designed and synthesized by reversible addition fragmentation chain transfer (RAFT) polymerization, which can self-assemble into bowl-shaped nanoparticles with controlled openings by solvent switch method at different initial concentrations. In addition, core–shell nanostructures are obtained taking advantage of the coordination between bipyridine and Fe2+. Upon annealing in ethanol, butterfly shaped twin nanosheets with thickness of about 10 nm are formed by controlling the cooling rate, while round Yuanbao-shaped assemblies are formed by naturally cooling. Revealing into the formation mechanism of the butterfly shaped twin nanosheets, a fusion induced assembly process of nanowires is observed. Overall, various nanostructures are obtained by manipulating the self-assembly pathways of a bipyridine containing amphiphilic homopolymer.

Using multi-scale interaction mechanisms in yolk-shell structured C/Co composite materials for electromagnetic wave absorption

Advanced chemical engineering for simultaneous modulation of nanomaterial morphology, defects, interfaces, and structure to enhance electromagnetic and microwave absorption (MA) performance. However, accurately distinguishing the MA contributions of different scale factors and tuning the optimal combined effects remains a formidable challenge. This study employs a synergistic approach combining template protection etching and vacuum annealing to construct a controlled system of micrometer-sized cavities and amorphous carbon matrices in metal-organic framework (MOF) derivatives. The results demonstrate that the spatial effects introduced by the hollow structure enhance dielectric loss but significantly weaken impedance matching. By increasing the proportion of amorphous carbon, the balance between electromagnetic loss and impedance matching can be effectively maintained. Importantly, in a suitable graphitization environment, the presence of oxygen vacancies in amorphous carbon can induce significant polarization to compensate for the reduced conductivity loss due to the absence of sp2 carbon. Through the synergistic effects of morphology and composition, the samples exhibit a broader absorption bandwidth (6.28 GHz) and stronger reflection loss (−61.64 dB) compared to the original MOF. In conclusion, this study aims to elucidate the multiscale impacts of macroscopic micro-nano structure and microscopic defect engineering, providing valuable insights for future research in this field.

Decoding the Effect of Synthesis Factors on Morphology of Nanomaterials: A Case Study to Identify and Optimize Experimental Conditions for Silver Nanowires

Silver nanowires (AgNWs) are one kind of nanomaterials for various applications such as solar panel cells and biosensors. However, the morphology of AgNWs, particularly their length and diameter, plays a critical role in determining the efficiency of energy storage systems and the transmittance of biosensors. Thus, it is imperative to study synthesis strategy for morphology control. This study focuses on synthesizing AgNWs through the solvothermal approach and aims to understand the individual and combined effects of three nucleants, NaCl, Fe(NO3)3 and NaBr, on the morphology of AgNWs. Using a modified successive multistep growth (SMG) approach and fine-tuning the nucleant concentrations, this study synthesized AgNWs with controllable aspect ratios, while minimizing the presence of undesirable byproducts like nanoparticles. Our results demonstrated the successful synthesis of AgNWs with favorable morphologies, including lengths of approximately 180 µm and diameters of 40 nm, thus resulting in aspect ratios of 4500. In addition, to assess the quality of the synthesized AgNWs, this work developed computational tools that uses MATLAB to automate the analysis of scanning electron microscope (SEM) images for detecting silver nanoparticles. This automated approach provides a quantitative analysis tool for material characterization and holds the promise for long-term evaluation of diverse AgNW samples, thereby paving the way for advancements in their synthesis and application. Overall, this study demonstrates the significance of morphology control in AgNW synthesis and presents a robust framework for material characterization and quality analysis.

Alleviative effects of C60 fullerene nanoparticles on arsenate transformation and toxicity to Danio rerio

Widely-used C60 fullerene nanoparticles (C60) result in their release into the aquatic environment, which may affect the distribution and toxicity of pollutants such as arsenic (As), to aquatic organism. In this study, arsenate (As(V)) accumulation, speciation and subcellular distribution was determined in Danio rerio (zebrafish) intestine, head and muscle tissues in the presence of C60. Meanwhile we compared how single-walled carbon nanotubes (SWCNTs), multi-walled carbon nanotubes (MWCNTs), graphene oxide (GO) and graphene (GN) nanoparticles alter the behaviors of As(V). Results showed that C60 significantly inhibited As accumulation and toxicity in D. rerio, due to a decrease in total As and monomethylarsonic acid (MMA) and As(V) species concentrations, a lower relative distribution in the metal-sensitive fraction (MSF). It was attributed that C60 may coat As(V) ion channels and consequently, affect the secretion of digestive enzymes in the gut, favoring As excretion and inhibiting As methylation. Similarly, MWCNTs reduced the species concentration of MMA and As(V) in the intestines, low GSH (glutathione) contents in the intestine. Due to the disparity of other carbon-based nanomaterial morphologies, SWCNTs, GO and GN exhibited the various effects on the toxicity of As(V). In addition, the possible pathway of arsenobetaine (AsB) biosynthesis included migration from the intestine to muscle in D. rerio, with the precursor of AsB likely to be 2-dimethylarsinylacetic acid (DMAA). The results of this study suggest that C60 is beneficial for controlling As(V) pollution and reducing the impact of As(V) biogeochemical cycles throughout the ecosystem.

Effect of different MoS2 morphologies on the formation and performance of adsorptive-catalytic nanocomposite membranes

This study synthesized three MoS₂ morphologies—nanospheres, nanoplatelets, and nanosheets—under varied conditions and incorporated them into chitosan membranes. TEM confirmed unique morphologies and crystallinity. Clean water flux showed that the nanoplatelet (P-CM) membrane had the highest flux due to higher porosity. The P-CM membrane excelled in removing Mn²⁺ and Zn²⁺ ions, achieving 93.0 ± 0.5% and 90.4 ± 1.5% removal, outperforming membranes with nanospheres (S-CM) and nanosheets (T-CM). Its superior performance is attributed to thicker nanoplatelets forming more water channels. The MoS₂‘s tri-layered structure generated reactive oxygen species (ROS) via H₂O₂ catalysis, contributing to enhanced heavy metal removal. These adsorptive-catalytic membranes combine adsorption with catalytic decomposition of heavy metals, highlighting the work’s novelty and superior performance. The membranes demonstrated excellent flux recovery and reusability (96.0 ± 0.5% for P-CM) after chemical cleaning. The findings emphasize the impact of nanomaterial morphologies on membrane performance in water treatment and environmental remediation.

Precursor engineering for soft selective synthesis of phase pure metal-rich digenite (Cu9S5) and djurleite (Cu31S16) nanocrystals and investigation of their photo-switching characteristics.

Copper sulfide nanostructures have evolved as one of the most technologically important materials for energy conversion and storage owing to their economic and non-toxic nature and superior performances. This paper presents a direct, scalable synthetic route aided by a single source molecular precursor (SSP) approach to access copper sulfide nanomaterials. Two SSPs, CuX(dmpymSH)(PPh3)2 (where X = Cl or I), were synthesized in quantitative yields and thermolyzed under appropriate conditions to afford the nanostructures. The analysis of the nanostructures through pXRD, EDS and XPS suggested that phase pure digenite (Cu9S5) and djurleite (Cu31S16) nanostructures were isolated from -Cl and -I substituted SSPs, respectively. The morphologies of the as-synthesized nanomaterials were investigated using electron microscopy techniques (SEM and TEM). DRS studies on pristine materials revealed blue shifted optical band gaps, which were found to be optimum for photoelectrochemical application. A prototype photoelectrochemical cell fabricated using the pristine nanostructures exhibited a stable photo-switching property, which presents these materials as suitable economic and environmentally friendly photon absorber materials.

A sensitive gold nanoflower-based lateral flow assay coupled with gold staining technique for the detection of SARS-CoV-2 antigen.

Anenhanced lateral flow assay (LFA) is presentedfor rapid and highly sensitive detection of acute respiratory syndrome coronavirus-2 (SARS-CoV-2) antigens with gold nanoflowers (Au NFs) as signaling markers and gold enhancement to amplify the signal intensities. First, the effect of the morphology of gold nanomaterials on the sensitivity of LFA detection was investigated. The results showed that Au NFs prepared by the seed growth method showed a 5-fold higher detection sensitivity than gold nanoparticles (Au NPs) of the same particle size, which may benefit from the higher extinction coefficient and larger specific surface area of Au NFs. Under the optimized experimental conditions, the Au NFs-based LFA exhibited a detection limit (LOD) of 25 pg mL-1 for N protein using 135nm Au NFs as the signaling probes. Thesignal was further amplified by using a gold enhancement strategy, and the LOD for the detection of N protein achieved was5 pg mL-1. The established LFA also exhibited good repeatability and stability and showed applicability in the diagnosis of SARS-CoV-2 infection.

Sandwich-like tribofilm induced highly effective lubrication for MoDTP coupled with hydroxy-magnesium silicate (MSH)

In the field of lubrication enhancement, nanomaterials are becoming increasingly important. However, the issue of their stable dispersion in lubrication oil remains a persistent challenge. To address this issue, we synthesized two distinct morphologies of MSH nanomaterials, subsequently modifying them with alkylsilane (OTMS) to enhance their dispersion stability. Particularly, the 1.0 wt% of OTMS-modified laminar MSH (LMSH@OTMS) combined with 0.3 wt% molybdenum dialkyldithiophosphate (MoDTP) exhibited remarkable lubricating performance in PAO10. The result indicate there is a synergistic effect between two components, resulting in the formation of a main sandwich-like tribofilm. The tribofilm is comprised of two distinct layers: a lubricating layer derived from MoDTP and an anti-wear layer stemming from LMSH@OTMS. These findings offer significant potential for enhancing durability of mechanical systems.

Experimental study and process evaluation of coproduction graphene, acetylene and hydrogen from methane pyrolysis by thermal plasma

This paper developed a process for the coproduction of graphene, acetylene and hydrogen from methane pyrolysis by thermal plasma. Bench-scale tests under three specific energy input (SEI) were carried out to investigate the morphology of carbon nanomaterials and the product selectivity. The process was evaluated by exergy and exergoeconomic analyses. Results indicated that a higher SEI improved the selectivity of graphene nanoflakes (GNFs) and reduced their defects. The product selectivity of GNFs played a critical role in the decrease of total fuel exergy per unit of GNFs as the SEI increased. The plasma reactor exhibited the highest exergy loss ratio in the entire process due to heat dissipation. The quenching device exhibited the second-highest exergy loss ratio in the process, stemming from irreversible entropy increase causing exergy loss. Improving the design of the plasma reactor to enhance thermal efficiency and implementing a feasible waste heat recovery system were identified as effective strategies to enhance exergy efficiency. Excluding consideration of co-products, GNFs with high SEI had the lowest cost of 199.41 CNY/kg, when co-products were considered, the lowest cost decreases by 30%, and the low SEI had the lowest GNFs cost at 140.71 CNY/kg. This indicated that there was enough investment potential to tailor the properties of GNFs produced by such processes for application scenarios. The unit exergy cost of GNFs decreased from 0.89 CNY/MJ to 0.80 CNY/MJ as the SEI of the plasma reactor increased. Subsequently, it rose to 1.16 CNY/MJ. Prioritizing the increase in investment costs for the plasma reactor to reduce exergy loss costs should be considered first, and optimizing the waste heat recovery process was also a key direction to minimize exergy loss costs.

The tune of shell numbers of multi-shell hollow mesoporous carbon microspheres for enhanced microwave absorption

The morphology of carbon nanomaterials plays significant effect on the complex permittivity and microwave absorption (MA) capability. Elaborate morphology design would bring about efficient MA performance. In this work, we develop a hollow mesoporous carbon microspheres with different shells (from single to quadruple shells) through a facile template method and layer-by-layer etching process. This multi-shell hollow mesoporous carbon microspheres (MS-HMCMs) can be regarded as a complex composite morphology consisting of hollow, mesoporous and yolk-shell structure, which presents the tunable number of shells for optimal impedance matching, multiple interfacial polarization and the extended microwave transmission path from internal spaces. Thus, the MS-HMCMs demonstrates wide effective absorption bandwidth (EAB) of 6.4 GHz and 5.96 GHz at the thicknesses of 2.5 mm and 3.0 mm. Besides, the complex permittivity and MA properties can be effectively tuned via regulating the shell numbers. This MS-HMCMs with controllable shells may be a promising wideband and lightweight microwave absorber.

The impact of hollow core-shell nanozymes in biosensing: A case study of p-Fe3O4@PDA@ZIF-67

BackgroundNanozymes, a new class of nanomaterials, have emerged as promising substitutes for enzymes in biosensor design due to their exceptional stability, affordability, and ready availability. While nanozymes address many limitations of natural enzymes, they still face challenges, particularly in achieving the catalytic activity levels of their natural counterparts. This indicates the need for enhancing the sensitivity of biosensors based on nanozymes. The catalytic activity of nanozyme can be significantly improved by regulating its size, morphology, and surface composition of nanomaterial. ResultsIn this work, a kind of hollow core-shell structure was designed to enhance the catalytic activity of nanozymes. The hollow core-shell structure material consists of a nanozymes core layer, a hollow layer, and a MOF shell layer. Taking the classic peroxidase like Fe3O4 as an example, the development of a novel nanozyme@MOF, specifically p-Fe3O4@PDA@ZIF-67, is detailed, showcasing its application in enhancing the sensitivity of sensors based on Fe3O4 nanozymes. This innovative nanocomposite, featuring that MOF layer was designed to adsorb the signal molecules of the sensor to improve the utilization rate of reactive oxygen species generated by the nanozymes catalyzed reactions and the hollow layer was designed to prevent the active sites of nanozymes from being cover by the MOF layer. The manuscript emphasizes the nanocomposite's remarkable sensitivity in detecting hydrogen peroxide (H2O2), coupled with high specificity and reproducibility, even in complex environments like milk samples. Significance and noveltyThis work firstly proposed and proved that Fe3O4 nanozyme@MOF with hollow layer structure was designed to improve the catalytic activity of the Fe3O4 nanozyme and the sensitivity of the sensors based on Fe3O4 nanozyme. This research marks a significant advancement in nanozyme technology, demonstrating the potential of structural innovation in creating high-performance, sensitive, and stable biosensors for various applications.

Efficient green combustion production of pure nickel oxide (NiO) and silver-doped NiO nanoparticles using Aloe Vera gel extract: Its supercapacitors applications

This study employs the synthesis of pure NiO and Ag-doped NiO with varying concentrations (1, 3, 5, 7 and 9 mol%) of Ag2O nanoparticles by solution combustion method. The Structural and morphology of nanomaterials were elucidated by analytical spectroscopic methods. XRD revealed alterations in physical properties, such as crystallite size and lattice parameters, of NiO nanoparticles due to the presence of Ag2O. UV-Vis spectroscopy demonstrated a reduction in the bandgap from 3.41 eV (pure NiO) to 3.21 eV for 1, 3, 5, 7 and 9 mol% Ag2O-doped NiONPs. To assess their viability as active electrode materials in supercapacitors, the synthesized samples were subjected to analysis in a 0.1 M HCl electrolyte. Electrochemical studies done through various tests, including Electrochemical-Impedance, Cyclic-Voltammetry and Galvanic Charge-Discharge. Remarkably, the 5 mol% Ag2O-doped NiO in a 3-electrode system exhibited a notable capacitance value of 248 Fg−1 at a scan rate of 5 Ag−1. Additionally, it demonstrated robust cycling stability, maintaining over 90% of the original capacitance after 2000 cycles in GCD studies. The potential chemical interaction between nanoscale Ag2O and NiO could be responsible for the enhanced capacitance. These findings offer valuable insights for researchers exploring the development of novel electrode materials for energy-storage devices.

Freestanding Penta-Twinned Palladium Nanosheets.

Control over the morphology of nanomaterials to have a 2D structure and manipulating the surface strain of nanostructures through defect control have proved to be promising for developing efficient catalysts for sustainable chemical and energy conversion. Here a one-pot aqueous synthesis route of freestanding Pd nanosheets with a penta-twinned structure (PdPT NSs) is presented. The generation of the penta-twinned nanosheet structure can be succeeded by directing the anisotropic growth of Pd under the controlled reduction kinetics of Pd precursors. Experimental and computational investigations showed that the surface atoms of the PdPT NSs are effectively under a compressive environment due to the strain imposed by their twin boundary defects. Due to the twin boundary-induced surface strain as well as the 2D structure of the PdPT NSs, they exhibited highly enhanced electrocatalytic activity for oxygen reduction reaction compared to Pd nanosheets without a twin boundary, 3D Pd nanocrystals, and commercial Pd/C and Pt/C catalysts.