Sustainable synthesis of spongy-like porous carbon for supercapacitive energy storage systems towards pollution control.

In this study, the fruit of Terminalia chebula, commonly known as chebulic myrobalan, is used as the precursor for carbon for its application in supercapacitors. The Terminalia chebula biomass-derived sponge-like porous carbon (TC-SPC) is synthesized using a facile and economical method of pyrolysis. TC-SPC thus obtained is subjected to XRD, FESEM, TEM, HRTEM, XPS, Raman spectroscopy, ATR-FTIR, and nitrogen adsorption-desorption analyses for their structural and chemical composition. The examination revealed that TC-SPC has a crystalline nature and a mesoporous and microporous structure accompanied by a disordered carbon framework that is doped with heteroatoms such as nitrogen and sulfur. Electrochemical studies are performed on TC-SPC using cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. TC-SPC contributed a maximum specific capacitance of 145 F g-1 obtained at 1 A g-1. The cyclic stability of TC-SPC is significant with 10,000 cycles, maintaining the capacitance retention value of 96%. The results demonstrated that by turning the fruit of Terminalia chebula into an opulent product, a supercapacitor, TC-SPC generated from biomass has proven to be a potential candidate for energy storage application.

Narrative of hazardous chemicals in water: Its potential removal approach and health effects.

H2O is essential for life to exist on earth; it is important to guarantee both the quality and supply of water to satisfy world demand. However, it became contaminated by a number of hazardous, inorganic industrial pollutants, which caused a number of issues like irrigation activities and unsafe human ingestion. Long-term exposure to harmful substances can result in respiratory, immunological, and neurological illnesses, cancer, and problems during pregnancy. Therefore, removing hazardous substances from wastewater and natural water sources is crucial. It is necessary to develop an alternate method that can effectively remove these toxins from water bodies, as conventional methods have several drawbacks. This review primarily aims to achieve the following goals: 1) to discuss the distribution of harmful chemicals: 2) to give specifics on numerous possible strategies for getting rid of hazardous chemicals, and 3) its effects on the environment and consequences for human health have been examined.

Recent Advanced Synthesis Strategies for the Nanomaterial-Modified Proton Exchange Membrane in Fuel Cells.

Hydrogen energy is converted to electricity through fuel cells, aided by nanostructured materials. Fuel cell technology is a promising method for utilizing energy sources, ensuring sustainability, and protecting the environment. However, it still faces drawbacks such as high cost, operability, and durability issues. Nanomaterials can address these drawbacks by enhancing catalysts, electrodes, and fuel cell membranes, which play a crucial role in separating hydrogen into protons and electrons. Proton exchange membrane fuel cells (PEMFCs) have gained significant attention in scientific research. The primary objectives are to reduce greenhouse gas emissions, particularly in the automotive industry, and develop cost-effective methods and materials to enhance PEMFC efficiency. We provide a typical yet inclusive review of various types of proton-conducting membranes. In this review article, special focus is given to the distinctive nature of nanomaterial-filled proton-conducting membranes and their essential characteristics, including their structural, dielectric, proton transport, and thermal properties. We provide an overview of the various reported nanomaterials, such as metal oxide, carbon, and polymeric nanomaterials. Additionally, the synthesis methods in situ polymerization, solution casting, electrospinning, and layer-by-layer assembly for proton-conducting membrane preparation were analyzed. In conclusion, the way to implement the desired energy conversion application, such as a fuel cell, using a nanostructured proton-conducting membrane has been demonstrated.

Facile Synthesis of Functionalized Porous Carbon by Direct Pyrolysis of Anacardium occidentale Nut-Skin Waste and Its Utilization towards Supercapacitors.

Preparing electrode materials plays an essential role in the fabrication of high-performance supercapacitors. In general, heteroatom doping in carbon-based electrode materials enhances the electrochemical properties. Herein, nitrogen, oxygen, and sulfur co-doped porous carbon (PC) materials were prepared by direct pyrolysis of Anacardium occidentale (AO) nut-skin waste for high-performance supercapacitor applications. The as-prepared AO-PC material possessed interconnected micropore/mesopore structures and exhibited a high specific surface area of 615 m2 g-1. The Raman spectrum revealed a moderate degree of graphitization of AO-PC materials. These superior properties of the as-prepared AO-PC material help to deliver high specific capacitance. After fabricating the working electrode, the electrochemical performances including cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy measurements were conducted in 1 M H2SO4 aqueous solution using a three-electrode configuration for supercapacitor applications. The AO-PC material delivered a high specific capacitance of 193 F g-1 at a current density of 0.5 A g-1. The AO-PC material demonstrated <97% capacitance retention even after 10,000 cycles of charge-discharge at the current density of 5 A g-1. All the above outcomes confirmed that the as-prepared AO-PC from AO nut-skin waste via simple pyrolysis is an ideal electrode material for fabricating high-performance supercapacitors. Moreover, this work provides a cost-effective and environmentally friendly strategy for adding value to biomass waste by a simple pyrolysis route.

Water Soluble PMPC-Derived Bright Fluorescent Nitrogen/Phosphorous-Doped Carbon Dots for Fluorescent Ink (Anti-Counterfeiting) and Cellular Multicolor Imaging.

Here, a simple one-step hydrothermal-assisted carbonization process was adopted for the preparation of nitrogen/phosphorous-doped carbon dots from a water-soluble polymer, poly 2-(methacryloyloxy)ethyl phosphorylcholine (PMPC). By the free-radical polymerization method, PMPC was synthesized using 2-(methacryloyloxy)ethyl phosphorylcholine (MPC) and 4,4'-azobis (4-cyanovaleric acid). The water-soluble polymers, PMPC, that have nitrogen/phosphorus moieties are used to prepare carbon dots (P-CDs). The resulting P-CDs were thoroughly characterized by various analytical techniques such as field emission-scanning electron microscopy (FESEM) with energy-dispersive X-ray spectroscopy (EDS), high-resolution transmittance electron microscopy (HRTEM), X-ray diffraction (XRD), Raman spectroscopy, attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), Ultraviolet-visible (UV-vis) spectroscopy and fluorescence spectroscopy to determine their structural and optical properties. The synthesized P-CDs displayed bright/durable fluorescence, were stable for long periods, and confirmed the enrichment of functionalities including oxygen, phosphorus, and nitrogen heteroatoms in the carbon matrix. Since the synthesized P-CDs showed bright fluorescence with excellent photostability, excitation-dependent fluorescence emission, and excellent quantum yield (23%), it has been explored as a fluorescent (security) ink for drawing and writing (anti-counterfeiting). Further, cytotoxicity study results advised for biocompatibility and thus were used for cellular multicolor imaging in nematodes. This work not only demonstrated the preparation of CDs from polymers that can be used as advanced fluorescence ink, a bioimaging agent for anti-counterfeiting, and cellular multicolor imaging candidate, but additionally prominently opened a new perspective on the bulk preparation of CDs simply and efficiently for various applications.

Natural Nitrogen-Doped Carbon Dots Obtained from Hydrothermal Carbonization of Chebulic Myrobalan and Their Sensing Ability toward Heavy Metal Ions.

Chebulic Myrobalan is the main ingredient in the Ayurvedic formulation Triphala, which is used for kidney and liver dysfunctions. Herein, natural nitrogen-doped carbon dots (NN-CDs) were prepared from the hydrothermal carbonization of Chebulic Myrobalan and were demonstrated to sense heavy metal ions in an aqueous medium. Briefly, the NN-CDs were developed from Chebulic Myrobalan by a single-step hydrothermal carbonization approach under a mild temperature (200 °C) without any capping and passivation agents. They were then thoroughly characterized to confirm their structural and optical properties. The resulting NN-CDs had small particles (average diameter: 2.5 ± 0.5 nm) with a narrow size distribution (1-4 nm) and a relatable degree of graphitization. They possessed bright and durable fluorescence with excitation-dependent emission behaviors. Further, the as-synthesized NN-CDs were a good fluorometric sensor for the detection of heavy metal ions in an aqueous medium. The NN-CDs showed sensitive and selective sensing platforms for Fe3+ ions; the detection limit was calculated to be 0.86 µM in the dynamic range of 5-25 µM of the ferric (Fe3+) ion concentration. Moreover, these NN-CDs could expand their application as a potential candidate for biomedical applications and offer a new method of hydrothermally carbonizing waste biomass.

Silver nanoparticles loaded graphene-poly-vinylpyrrolidone composites as an effective recyclable antimicrobial agent.

Silver nanoparticles (AgNPs) are often used as antibacterial agents. Here, graphene-silver nanoparticles (G-Ag) and graphene-silver nanoparticles poly-vinylpyrrolidone (G-AgPVPy) were prepared by chemical reduction and in-situ polymerization of vinylpyrrolidone (VPy). The prepared G-Ag and G-AgPVPy composites were characterized using various techniques. The size of the AgNPs on the graphene surface in the prepared G-Ag and G-AgPVPy composites was measured as ∼20 nm. The graphene sheets size in the G-Ag and G-AgPVPy composites were measured as 6.0-2.0 µm and 4.0-0.10 µm, respectively, which are much smaller than graphene sheets in graphite powder (GP) (10.0-3.0 µm). The physicochemical analysis confirmed the formation of G-Ag and G-AgPVPy composites and even the distribution of AgNPs and PVPy on the graphene sheets. The synthesized composites (G-AgPVPy, G-Ag) exhibited a broad-spectrum antibacterial potential against both Gram-negative and Gram-positive bacteria. The lowest minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values were calculated as >40 µg/mL using G-Ag and GP, while G-AgPVPy showed as 10 µg/mL against Staphylococcus aureus. Among GP, G-Ag, and G-AgPVPy, G-AgPVPy disturbs the cell permeability, damages the cell walls, and causes cell death efficiently. Also, G-AgPVPy was delivered as a significant reusable antibacterial potential candidate. The MIC value (10 µg/mL) did not change up to six subsequent MIC analysis cycles.

Polymer Nanoparticles: Synthesis and Applications.

Polymer nanoparticles (PNPs) are generally formed by the spontaneous self-assembly of polymers that vary size from 1 to 1000 nm [...].

Sustainable Synthesis of Bright Fluorescent Nitrogen-Doped Carbon Dots from Terminalia chebula for In Vitro Imaging.

In this study, sustainable, low-cost, and environmentally friendly biomass (Terminalia chebula) was employed as a precursor for the formation of nitrogen-doped carbon dots (N-CDs). The hydrothermally assisted Terminalia chebula fruit-derived N-CDs (TC-CDs) emitted different bright fluorescent colors under various excitation wavelengths. The prepared TC-CDs showed a spherical morphology with a narrow size distribution and excellent water dispensability due to their abundant functionalities, such as oxygen- and nitrogen-bearing molecules on the surfaces of the TC-CDs. Additionally, these TC-CDs exhibited high photostability, good biocompatibility, very low toxicity, and excellent cell permeability against HCT-116 human colon carcinoma cells. The cell viability of HCT-116 human colon carcinoma cells in the presence of TC-CDs aqueous solution was calculated by MTT assay, and cell viability was higher than 95%, even at a higher concentration of 200 µg mL-1 after 24 h incubation time. Finally, the uptake of TC-CDs by HCT-116 human colon carcinoma cells displayed distinguished blue, green, and red colors during in vitro imaging when excited by three filters with different wavelengths under a laser scanning confocal microscope. Thus, TC-CDs could be used as a potential candidate for various biomedical applications. Moreover, the conversion of low-cost/waste natural biomass into products of value promotes the sustainable development of the economy and human society.

Synthesis of Water-Dispersed Sulfobetaine Methacrylate-Iron Oxide Nanoparticle-Coated Graphene Composite by Free Radical Polymerization.

Research on the synthesis of water-soluble polymers has accelerated in recent years, as they are employed in many bio-applications. Herein, the synthesis of poly[2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (PSB) by free radical polymerization in a sonication bath is described. PSB and iron oxide nanoparticles (IONPs) were simultaneously stabilized on the graphene surface. Graphene surfaces with PSB (GPSB) and graphene surfaces with PSB and IONPs (GPSBI) were prepared. Since PSB is a water-soluble polymer, the hydrophobic nature of graphene surfaces converts to hydrophilic nature. Subsequently, the prepared graphene composites, GPSB and GPSBI, were well-dispersed in water. The preparation of GPSB and GPSBI was confirmed by X-ray diffraction, Raman spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis. The impacts of PSB and IONPs on the graphene surfaces were studied systematically.

A review on bismuth-based materials for the removal of organic and inorganic pollutants.

Modernized lifestyle and increased industrialization threaten living organisms because of the pollutants released from industries and household wastes. The presence of even small amounts of pollutants (organic pollutants (OPs) and inorganic pollutants-heavy metals (HMs)) shows significant effects. Thus wastewater treatment is urgently needed before being subjected to use. Many methods and materials have been developed and reported for the removal of pollutants from wastewater. This review focused on the removal of both OPs and HMs using bismuth-based (Bi-based) materials because of their low toxicity and excellent properties compared to other metals. Bi-based materials as a photocatalyst for photodegradation of OPs are discussed in detail with synthesis methods. Further, since few reviews are available on the Bi-based material for the removal and sensing of HMs, this topic was intentionally summarized. About 200 published articles and reviews have been reviewed here. Additionally, the key point that needs to be focused on the development of Bi-based photocatalysts for the removal of OPs and for upgrading the Bi-based materials as adsorbents for HMs are conferred in the outlook. This will help many researchers in their upcoming work.

Synthesis and Characterization of Monodispersed Spherical Calcium Oxide and Calcium Carbonate Nanoparticles via Simple Pyrolysis.

In this study, calcium carbonate nanoparticles (CCNPs) and calcium oxide nanoparticles (CONPs) are synthesized by the carbonization/calcination of calcium oleate. CONPs are an essential inorganic material, and they are used as catalysts and as effective chemisorbents for toxic gases. CCNPs are widely used in plastics, printing ink, and medicines. Here, calcium oleate is used as a starting material for the preparation of CCNPs and CONPs. This calcium oleate is prepared from calcium hydroxide and oleic acid in ethanol under mild reflux conditions. The effect of the calcination temperature of calcium oleate is examined during the synthesis of CCNPs and CONPs. By simple carbonization/calcination, calcite-type CCNPs and CONPs are prepared at <550 °C and >600 °C, respectively. The synthesized nanomaterials are analyzed by various physicochemical characterization techniques such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy, thermogravimetric analysis (TGA) with derivative thermogravimetry (DTG), and scanning electron microscopy (SEM) with energy dispersive X-ray analysis. An X-ray diffractometer and the Scherrer formula are used to analyze the crystalline phase and crystallite size of prepared nanoparticles. TGA techniques confirm the thermal stability of the calcium oleate, CCNPs, and CONPs. The SEM analysis illustrates the dispersive behavior and cubic/spherical morphologies of CCNPs/CONPs. Furthermore, the obtained results are compared to the CCNP and CONP samples prepared using calcium hydroxide. As a result, the carbonization/calcination of calcium oleate produces monodispersed CONPs, which are then compared to the CONPs from calcium hydroxide. Additionally, from calcium oleate, CONPs can be prepared on a large scale in a cheap, convenient way, using simple equipment which can be applied in various applications.

Controlled Synthesis of Platinum and Silver Nanoparticles Using Multivalent Ligands.

Here, the controlled formation of platinum nanoparticles (PtNPs) and silver nanoparticles (AgNPs) using amine-functionalized multivalent ligands are reported. The effects of reaction temperature and ligand multivalency on the growth kinetics, size, and shape of PtNPs and AgNPs were systematically studied by performing a stepwise and a one-step process. PtNPs and AgNPs were prepared in the presence of amine ligands using platinum (II) acetylacetonate and silver (I) acetylacetonate, respectively. The effects of ligands and temperature on the formation of PtNPs were studied using a transmission electron microscope (TEM). For the characterization of AgNPs, additionally, ultraviolet-visible (UV-Vis) absorption was employed. The TEM measurements revealed that PtNPs prepared at different temperatures (160-200 °C, in a stepwise process) are monodispersed and of spherical shape regardless of the ligand multivalency or reaction temperature. In the preparation of PtNPs by the one-step process, ligands affect the shape of the PtNPs, which can be explained by the affinity of the ligands. The TEM and UV-Vis absorption studies on the formation of AgNPs with mono-, di-, and trivalent ligands showed narrower size distributions, while increasing the temperature from 80 °C to 120 °C and with a trivalent ligand in a one-step process.

Lotus-biowaste derived sulfur/nitrogen-codoped porous carbon as an eco-friendly electrocatalyst for clean energy harvesting.

Recent research is focused on biomass-derived porous carbon materials for energy harvesting (hydrogen evolution reaction) because of their cost-effective synthesis, enriched with heteroatoms, lightweight, and stable properties. Here, the synthesis of porous carbon (PC) materials from lotus seedpod (LP) and lotus stem (LS) is reported by the pyrolysis method. The porous and graphitic structure of the prepared LP-PC and LS-PC materials were confirmed by field emission scanning electron microscopy, transmission electron microscopy with selected area electron diffraction, X-ray diffraction, and nitrogen adsorption-desorption measurements. Heteroatoms in LP-PC and LS-PC materials were investigated by attenuated total reflection-Fourier transform infrared and X-ray photoelectron spectroscopy. The specific surface area of LP-PC and LS-PC were calculated as 457 and 313 m2 g-1, respectively. Nitrogen and sulfur enriched LP-PC and LS-PC materials were found to be effective electrocatalysts for hydrogen evolution reactions. LP-PC catalyst showed a very low overpotential of 111 mV with the Tafel slope of 69 mV dec-1, and LS-PC catalyst achieved a Tafel slope of 85 mV dec-1 with a low overpotential of 135 mV. This work is expected to be extended for the development of biomass as a sustainable porous carbon electrocatalyst with a tunable structure, elements, and electronic properties. Furthermore, preparing carbon materials from the biowaste and applying clean energy harvesting might reduce environmental pollution.

Facile synthesis of novel molybdenum disulfide decorated banana peel porous carbon electrode for hydrogen evolution reaction.

Hydrogen is one of the cleanest renewable and environmentally friendly energy resource that can be generated through water splitting. However, hydrogen evolution occurs at high overpotential, and efficient hydrogen evolution catalysts are desired to replace state-of-the-art catalysts such as platinum. In the present work, a novel molybdenum disulfide decorated banana peel porous carbon (MoS2@BPPC) catalyst has been developed using banana peel carbon and molybdenum disulfide (MoS2) for hydrogen evolution reaction (HER). Banana peel porous carbon (BPPC) was initially synthesized from the banana peel (biowaste) by a simple carbonization method. Subsequently, 20 wt% of bare MoS2 was distributed on the pristine BPPC matrix using the dry-impregnation method. The resulting MoS2@BPPC composites were systematically investigated to determine the morphology and structure. Finally, using a three-electrode cell system, pristine BPPC, bare MoS2, and MoS2@BPPC composite were used as HER electrocatalysts. The developed MoS2@BPPC composite showed greater HER activity and possessed excellent stability in the acid solution, including an overpotential of 150 mV at a current density of -10 mA cm-2, and a Tafel slope of 51 mV dec-1. This Tafel study suggests that the HER takes place by Volmer-Heyrovsky mechanism with a rate-determining Heyrovsky step. The excellent electrochemical performance of MoS2@BPPC composite for HER can be ascribed to its unique porous nanoarchitecture. Further, due to the synergetic effect between MoS2 and porous carbon. The HER activity using the MoS2@BPPC electrode advises that the prepared catalyst may hold great promise for practical applications.

A Review of Polymeric Micelles and Their Applications.

Self-assembly of amphiphilic polymers with hydrophilic and hydrophobic units results in micelles (polymeric nanoparticles), where polymer concentrations are above critical micelle concentrations (CMCs). Recently, micelles with metal nanoparticles (MNPs) have been utilized in many bio-applications because of their excellent biocompatibility, pharmacokinetics, adhesion to biosurfaces, targetability, and longevity. The size of the micelles is in the range of 10 to 100 nm, and different shapes of micelles have been developed for applications. Micelles have been focused recently on bio-applications because of their unique properties, size, shape, and biocompatibility, which enhance drug loading and target release in a controlled manner. This review focused on how CMC has been calculated using various techniques. Further, micelle importance is explained briefly, different types and shapes of micelles are discussed, and further extensions for the application of micelles are addressed. In the summary and outlook, points that need focus in future research on micelles are discussed. This will help researchers in the development of micelles for different applications.

Simultaneous removal of heavy metal ions using carbon dots-doped hydrogel particles.

Heavy metal ions (HMI) have attracted worldwide concern due to their serious environmental pollution which led to the risk of health conditions. From Red Malus floribunda fruits, nitrogen-doped carbon dots (N-CDs) were prepared, followed by hybrid-spherical shaped hydrogel particles (CGCDs) were prepared. The prepared CGCDs were utilized as adsorbents for HMI-(Hg(II), Cd(II), Pb(II), and Cr(III)) from water. N-CDs with about 4.0 nm in diameter were characterized by various techniques such as field emission-scanning electron microscopy (FE-SEM) and attenuated total reflection-fourier transform infrared spectroscopy (ATR-FTIR) that confirm the presence of nitrogen, oxygen, and carbon functionalities. The prepared spherical CGCDs were characterized very well before it was used as HMI adsorbents. The sizes of the CGCDs were ranges between 20 and 300 µm and the degree of swelling was calculated as 1320 %. ATR-FTIR and X-ray diffraction analyses reveal the presence of N-CDs in CGCDs. Further, FE-SEM confirms the spherical shape morphology of CGCDs. Three different concentrations of HMI solutions were 500 mg/L, 1000 mg/L, and 1500 mg/L. Hg(II) adsorbed proficiently by CGCDs in single metal ion systems with ~72 % and almost complete removal of Hg(II) ions (99 %) in multiple metal ion systems was observed. Moreover, all metal ions Hg(II), Cd(II), Pb(II), and Cr(III) were efficiently (>70 %) removed in multiple systems by CGCDs. After HMI adsorption experiments, the elemental mapping from FE-SEM and X-ray photoelectron spectroscopy studies conveys the presence of HMI on CGCDs. This suggests that CGCDs would be a suitable adsorbent for the simultaneous removal of multiple HMI from wastewater.

Utilization of waste biomass of Poa pratensis for green synthesis of n-doped carbon dots and its application in detection of Mn2+ and Fe3.

In this study, a novel and sustainable approach was used to synthesize nitrogen-doped carbon dots (NCDs) from the waste biomass of Poa Pratensis (Kentucky bluegrass (KB)) by a facile hydrothermal method. The prepared KBNCDs were subjected to various characterization techniques, including X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, and Fourier-transform infrared spectroscopy to verify the formation of carbon dots and their surface functional groups. The KBNCDs exhibited good hydrophilic fluorescence (FLU) properties with an acceptable quantum yield (7%). The synthesized KBNCDs showed excitation wavelength-dependent FLU emission behavior with strong cyan-blue FLU upon irradiation with 365 nm UV-light. The hydrophilic optical properties of the as-synthesized KBNCDs were used to detect Fe3+ and Mn2+ ions in an aqueous medium with good selectivity and sensitivity. It was found that the FLU of the KBNCDs is quenched in the presence of Fe3+ and Mn2+ ions, and the quenching rate was linear with the concentration of Fe3+ and Mn2+ ions. The limit of detection (LOD) of KBNCDs with metal ions was calculated using the Stern-Volmer relationship. The LOD values for Fe3+ or Mn2+ ions were calculated as 1.4 and 1.2 µM, respectively with the detection range from 5.0 to 25 µM. Based on these results, this study provides an underpinning for the development of KBNCD as FLU sensors that can be used in aqueous media.

Tunable fluorescent carbon dots from biowaste as fluorescence ink and imaging human normal and cancer cells.

Growing global biowaste and its environmental issues challenge the need for converting biowastes into a beneficial product. Among the biowaste, here kiwi fruit (Actinidia Deliciosa) peels are considered for the preparation of carbon dots (CDs). Using a green one-pot hydrothermal-carbonization method, kiwi fruit peels were effectively converted into valuable kiwi fruit peel carbon dots (KFP-CDs). The morphology, physio-chemical and optical properties of as-synthesized KFP-CDs were analyzed using various analytical techniques such as X-ray powder diffraction, Raman spectroscopy, attenuated total reflection-Fourier transform infrared spectroscopy, field emission scanning electron microscopy, high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy, Ultraviolet-visible, and fluorescence spectroscopy. The KFP-CDs revealed a homogeneous spherical shape, monodispersed with an average size of 5 nm. The characterization confirms that KFP-CDs have functional groups such as -CN, -COOH, and -OH which are responsible for the easy dispersion of KFP-CDs in aqueous media. Without any preprocessing, KFP-CDs exhibit strong fluorescence upon exposure to UV light. Further, KFP-CDs displayed excitation-dependent fluorescence emission with a good quantum yield of about 18%. Thus by considering the excellent properties of KFP-CDs, KFP-CDs were used as fluorescent ink for drawing and writing without any capping/passivation agent. The pictures and words were instantaneously viewed when exposed to UV light. In addition, KFP-CDs tested for cell imaging in four human cell lines (normal and cancer cells) bestowed excellent biocompatibility and low cytotoxicity, which is important for the safe and long-term development of cellular imaging. The findings imply that KFP-CDs can be utilized as a cell labeling agent for mesenchymal stem cells, breast cancer, and thyroid cancer cells in vitro imaging. Thus, these observations revealed that investigating sustainable resource-based CDs can open up new avenues for tackling environmental issues.

Facile synthesis of nitrogen-doped porous carbon materials using waste biomass for energy storage applications.

A simple, low-cost, and green route for the preparation of lotus carbon (LC) materials using lotus parts including leaves, flowers, fruits (seed pods), and stems as a renewable precursor is reported. Different porous carbons, leaf-carbon (LF-carbon), flower-carbon (FL-carbon), fruit-carbon (FR-carbon), and stem-carbon (ST-carbon) were synthesized from different parts of the lotus plant by simple carbonization method. The as-synthesized LC materials were well-characterized by many techniques such as electron microscopy and spectroscopy techniques, X-ray diffraction, and BET-surface area analysis. These techniques confirmed the porous structure of LC materials and the existence of heteroatoms in the prepared LC materials. The mesoporous structure of LC materials suggested employing it for the supercapacitor applications. The obtained FR-Carbon exhibits a high specific capacitance of 160 F/g in a three-electrode system in an aqueous 1 M H2SO4 electrolyte with a high rate performance of 52% retention from 0.5 to 5.0 A/g with good cycling stability of 95%. These results indicate that the porous carbon derived from lotus fruits is a potential electrode material for high-performance supercapacitors.