Good Water Dispersibility Research Articles

A facile surface modification strategy for fabrication of fluorescent silica nanoparticles with the aggregation-induced emission dye through surface-initiated cationic ring opening polymerization

Fluorescent silica nanoparticles (FSNPs) have attracted great interest for potential applications in biological and biomedical fields because they possess higher fluorescence quantum yield and better fluorescence stability as comparison with small organic fluorescent molecules. The encapsulation of covalent linkage with fluorescent organic dyes or fluorescent metal complexes has demonstrated to be the commonly adopted strategies for fabrication of FSNPs previously. However, it is still challengeable to obtain FSNPs based polymer composites with intensive fluorescence and good water dispersibility through a one-pot surface modification strategy. In this paper, we developed a facile method to fabricate novel FSNPs based polymer composites (PhE@MSNs-PEtOx) through introducing the aggregation-induced emission (AIE) dye (PhE-OH) and poly(2-ethyl-2-oxazoline) (PEtOx) onto mesoporous silica nanoparticles (MSNs) based on cationic ring opening polymerization (CROP). The resulting PhE@MSNs-PEtOx composites possess strong fluorescence emission, excellent hydrophilicity and biocompatibility. These features make the final FSNPs based polymer composites great potential for biomedical applications. Taken together, we have developed for the first time that FSNPs based polymer composites can be facilely prepared through the one-pot introduction of AIE dyes and hydrophilic PEtOx on MSNs. Moreover, the novel FSNPs based composites could also be utilized for other biomedical applications considered their properties.

Enhanced response of tamoxifen toward the cancer cells using a combination of chemotherapy and photothermal ablation induced by lentinan-functionalized multi-walled carbon nanotubes

A lentinan (LEN) functionalized multi-walled carbon nanotubes (MWCNTs) drug delivery system, using tamoxifen (TAM) as a model anticancer agent, was developed by a simple non-covalent approach. This developed system (MWCNTs-TAM-LEN) possessed good stability, water dispersibility and extraordinary photothermal properties. It was demonstrated by the in vitro experiments that MWCNTs-TAM-LEN had enhanced cellular uptake, antitumor activity and cell apoptosis on Mcf-7 cells in comparison with TAM and MWCNTs-TAM. The cell inhibition rate and apoptosis rate of Mcf-7 cells treated by MWCNTs-TAM-LEN with near-infrared (NIR) were 67.1% and 66.5% higher than that of equivalent concentration of TAM with NIR irradiation treatment, respectively. The enhanced antitumor efficacy of MWCNTs-TAM-LEN was realized via the synergistic function of chemotherapy and photothermal ablation under NIR laser irradiation.

Development of High-Functionality and -Quality Lipids with RGD Peptide Ligands: Application for PEGylated Liposomes and Analysis of Intratumoral Distribution in a Murine Colon Cancer Model.

High-functionality and -quality (HFQ) lipids have a discrete molecular weight and good water dispersibility and can be produced by solid-phase peptide synthesis. Therefore, HFQ lipids are a promising material for the preparation of ligand-grafted PEGylated liposomes. Recently, we have reported serine-glycine repeated peptides ((SG) n) as a spacer of HFQ lipids and to substitute a conventional PEG spacer. We demonstrated the advantage of using (SG) n spacers for peptide ligand presentation on the liposomal surface in vitro; however, the use of (SG) n spacers in ligand-grafted PEGylated liposomes in vivo has not been validated. The aim of this study was to validate the in vivo targeting ability of HFQ lipid-grafted PEGylated liposomes. We synthesized lipids containing GRGDS (RGD-(SG) n-lipid) to target integrin αvβ3 and prepared RGD-(SG) n/PEGylated liposomes. Subsequently, their cellular uptake characteristics in murine colon carcinoma (Colon-26) cells were evaluated. Two-color imaging of liposomes and tumor blood vessels following tissue clearing was performed to examine the spatial intratumoral distribution of liposomes. RGD-(SG)5/PEGylated liposomes were selectively associated with the cells in vitro. In vivo analysis of intratumoral distribution following tissue clearing revealed the superior targeting ability of RGD-(SG)5/PEGylated liposomes compared with that of conventional RGD-PEG2000/PEGylated liposomes for both tumor tissues and tumor blood vessels. We successfully synthesized RGD-HFQ lipids to prepare RGD-grafted PEGylated liposomes for the efficient targeting of integrin αvβ3-expressing cells. To the best of our knowledge, this is the first report of the intratumoral distribution of ligand-grafted PEGylated liposomes by two-color imaging following tissue clearing.

Light-responsive nanocomposites combining graphene oxide with POSS based on host-guest chemistry

Based on the reversible host-guest inclusion/exclusion of cyclodextrin-functionalized graphene oxide (GO-CD) and azobenzene-terminated polyhedral oligomeric silsesquioxane (Azo-POSS), a novel kind of light-responsive nanocomposites GO-POSS was developed under mild condition. 1H NMR, FT-IR, TG, TEM and UV–vis spectroscopy were conducted to characterize the chemical composition and photo-responsive performance of obtained GO-POSS nanocomposites. The results demonstrated that nanocage-structured POSS and nanosheet GO components in GO-POSS exhibited pronounced supramolecular assembly/disassembly behavior upon UV/vis irradiation. Moreover, GO-POSS nanocomposites showed good water dispersity and had remarkable impact on oxygen permeability of conventional PVA-coated films under varied light irradiation conditions, which would be valuable for developing smart gas barrier materials in packaging.

Water-dispersible and recyclable magnetic TiO2/graphene nanocomposites in wastewater treatment

The water-dispersible and recyclable magnetic TiO2/graphene nanocomposites (TiO2/Fe3O4/GN-SO3H) were fabricated and applied as efficient photocatalyst for removal of methylene blue (MB) from water. The nanocomposites displayed good water-dispersibility, high photocatalytic activity and convenient magnetic separation. Furthermore, the novel photocatalyst could be recovered and recycled for 10 consecutive trials without significant loss of its activity.

Ultrasensitive biosensor based on long period grating coated with polycarbonate-graphene oxide multilayer

In this work, we report about an ultrasensitive fiber optic biosensor realized using a single-ended Long Period Grating (LPG). The LPG working point is tuned in the highest sensitivity region of mode transition, through a multilayer system consisting of Polycarbonate (PC) film and much thinner layer of Graphene Oxide (GO). Due to the coexistence of hydrophobic domain from pristine graphite structure and hydrophilic oxygen containing functional groups, GO exhibits good water dispersibility, biocompatibility, and high affinity for specific biomolecules. These properties of GO provide many opportunities for the development of novel biological sensing platforms. The so prepared LPG performance level has been evaluated using the highly stable streptavidin-biotin binding. By means of a careful design of the mode transition layers, as well as the bio-functionalization protocol, the detection of biotinylated BSA (Bovine Serum Albumin) concentrations in range 0.1–1000 aM was demonstrated, with a limit of detection below 0.2 aM, which is one of the lowest reached so far with this sensing technology. Functionalized LPG is therefore proven a powerful tool for the detection of biological species even down to attomolar detection limit, providing real-time detection, small size, and simple fabrication. Finally, a plain procedure for taking into account the effects of fabrication tolerances on the sensor characteristics is successfully proposed and applied.

Bimodal Phosphorescence-Magnetic Resonance Imaging Nanoprobes for Glutathione Based on MnO2 Nanosheet-Ru(II) Complex Nanoarchitecture.

Bimodal fluorescence-magnetic resonance imaging (MRI) technique has shown great utilities in bioassays because it combines the advantages of both optical imaging and MRI to provide more sufficient information over any modality alone. In this work, on the basis of a MnO2 nanosheet-Ru(II) complex nanoarchitecture, a bimodal phosphorescence-MRI nanoprobe for glutathione (GSH) has been constructed. The nanoprobe, Ru(BPY)3@MnO2, was constructed by integrating MnO2 nanosheets with a phosphorescent Ru(II) complex [Ru(BPY)3](PF6)2 (BPY = 2,2'-bipyridine), which resulted in complete phosphorescence quenching of the Ru(II) complex, accompanied by very low longitudinal and transverse relaxivity. Upon exposure to GSH, the reduction of MnO2 nanosheets by GSH triggers a recovery of phosphorescence and simultaneously produces a number of Mn2+ ions, a perfect MRI contrast agent. The as-prepared nanoprobe showed good water dispersion and biocompatibility and a rapid, selective, and sensitive response toward GSH in the phosphorescence and MR detection modes. The practicability of the nanoprobe was proved by time-gated luminescence assay of GSH in human serum, phosphorescent imaging of endogenous GSH in living cells, zebrafish, and tumor-bearing mice, as well as the MRI of GSH in tumor-bearing mice. The research outcomes suggested the potential of Ru(BPY)3@MnO2 for the bimodal phosphorescence-MRI sensing of GSH in vitro and in vivo.

Biocompatible semiconducting polymer nanoparticles as robust photoacoustic and photothermal agents revealing the effects of chemical structure on high photothermal conversion efficiency

Understanding the relationship between polymer chemical structure and its performance of photoacoustic imaging (PAI) and photothermal therapy (PTT) is important for developing ideal PAI/PTT agents. In this report, four semiconducting polymer nanoparticles (SPNs) with different donor-acceptor architectures are self-assembled for highly effective PAI-guided PTT. In particular, SPN1 with the longest π-conjugation length and the highest mass extinction coefficient which are beneficial for intramolecular charge transfer as well as light harvesting, exhibits the highest photothermal conversion efficiency up to 52.6%. Moreover, the as-prepared SPN1 possess good water-dispersibility, robust size-stability and excellent photothermal properties. Furthermore, the SPN1 not only exhibits a remarkable cancer cell-killing ability but also shows a prominent tumor inhibition capacity. Finally, the as-prepared water-dispersible SPN1 displays good biocompatibility and biosafety, making it a promising candidate for future biomedical applications. Considering the plenty of near-infrared absorbing semiconducting polymer available, our work provides fundamental insights for rational design and preparation of highly efficient SPN-based PAI/PTT agents for cancer theranostics.

Preparation of Carbon Dots by PyrolyzingCarboxylate Ammonium Salt and its Application in Probing Ferric Ions

In this paper, we have reported a novel and facile synthesis approach of fluorescent carbon dots (C-Dots) through a one-step pyrolytic route of carboxylate ammonium salt(formed between citric acid (CA) and N- (β-aminoethyl-γ-aminopropyl) methyl dimethoxysilane (AEAPMS)) without further passivation. The as-synthesized C-Dots possess excitation dependent fluorescence behaviors, strong blue photoluminescence (PL) emission with a quantum yield of 20.5% and pH stability. The morphology and structure of prepared C-Dots have been characterized by transmission electron microscope (TEM), X-ray diffraction (XRD) and Fourier transformed infrared spectroscopy (FTIR),TEMspectra reveal that the C-Dots arespherical nanoparticles with the size about 6.5 nm; FTIR indicate that there are lots of hydrophilic functional groups on C-Dots’ surface, which contribute to good water dispersibility. In addition, the obtained C-Dots exhibit a highly sensitive and selective fluorescence quenching effect toward Fe3+ ions in aqueous solution with a linear range of 0.05-0.20mM and a detection limit of 19.3 nM, which has great potential in environmental applications for Fe3+ detection.

Magnetic nanoparticles modified by citrate groups for magnetically responsive photonic crystals

Induced by appropriate magnetic field, Fe3O4 nanoparticles self-assemble into magnetically responsive photonic crystals (MRPC), showing the potential applications in color display, bioimaging agents and sensors. We report a kind of Fe3O4 clusters synthesized by one-pot hydrothermal reaction with the attachment of a small molecule (citrate groups) on the surface, which increases negative charge density and demonstrates the characteristics of good water-dispersity and stability. The characteristics of the nanoparticles are measured by TEM, SEM, FT-IR, XRD, XPS, TG and VSM. The variation of Fe3O4 nanoparticles size is determined by the amount of citrate. The MRPC show tunable photonic performance under a magnetic field ranging from 80 to 374 G, which could be controlled by the size, concentration, washing method and washing cycles.

Facile Fabrication of Highly Active Magnetic Aminoclay Supported Palladium Nanoparticles for the Room Temperature Catalytic Reduction of Nitrophenol and Nitroanilines

Magnetically recyclable nanocatalysts with excellent performance are urgent need in heterogeneous catalysis, due to their magnetic nature, which allows for convenient and efficient separation with the help of an external magnetic field. In this research, we developed a simple and rapid method to fabricate a magnetic aminoclay (AC) based an AC@Fe3O4@Pd nanocatalyst by depositing palladium nanoparticles (Pd NPs) on the surface of the magnetic aminoclay nanocomposite. The microstructure and the magnetic properties of as-prepared AC@Fe3O4@Pd were tested using transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and vibrating sample magnetometry (VSM) analyses. The resultant AC@Fe3O4@Pd nanocatalyst with the magnetic Fe-based inner shell, catalytically activate the outer noble metal shell, which when combined with ultrafine Pd NPs, synergistically enhanced the catalytic activity and recyclability in organocatalysis. As the aminoclay displayed good water dispersibility, the nanocatalyst indicated satisfactory catalytic performance in the reaction of reducing nitrophenol and nitroanilines to the corresponding aminobenzene derivatives. Meanwhile, the AC@Fe3O4@Pd nanocatalyst exhibited excellent reusability, while still maintaining good activity after several catalytic cycles.

The tribological behaviors of polyacrylate/graphene oxide and polyacrylate/surfactant-modified reduced graphene oxide composite coatings on flexible leather substrates

An anionic surfactant, linear alkylbenzene sulfonate (LAS), was used to modify reduced graphene oxide by in-situ reduction process to enhance its compatibility in polyacrylate latex. Polyacrylate/graphene oxide (PA/GO) and polyacrylate/surfactant-modified reduced graphene oxide (PA/LAS-rGO) were prepared to investigate their tribological behaviors on flexible leather substrates. The structure and morphologies of GO and LAS-rGO were investigated by XRD, FT-IR, Raman spectroscopy, SEM and TEM. The tribological behaviors of polyacrylate composite coatings were studied by mechanical properties, wear loss of coated leather and ESEM. The results of XRD, FT-IR and Raman spectroscopy confirmed that LAS-rGO was modified by LAS and had good dispersity in water. SEM and TEM images implied the layered structure of GO and LAS-rGO. The mechanical and tribological properties of polyacrylate/LAS-rGO are better than that of polyacrylate/GO. The analysis of ESEM show that LAS-rGO can form self-lubrication and barrier layer owing to its amphiphilicity and π-π stacking with water evaporating.

Correction to "Fluorescent Carbon Quantum Dots with Intrinsic Nucleolus-Targeting Capability for Nucleolus Imaging and Enhanced Cytosolic and Nuclear Drug Delivery".

Nucleolus tracking and nucleus-targeted photodynamic therapy are attracting increasing attention due to the importance of nucleolus and the sensitivity of nucleus to various therapeutic stimuli. Herein, a new class of multifunctional fluorescent carbon quantum dots (or carbon dots, CDs) synthesized via the one-pot hydrothermal reaction of m-phenylenediamine and l-cysteine was reported to effectively target nucleolus. The as-prepared CDs possess superior properties, such as low-cost and facile synthesis, good water dispersibility, various surface groups for further modifications, prominent photostability, excellent compatibility, and rapid/convenient/wash-free staining procedures. Besides, as compared with SYTO RNASelect (a commonly used commercial dye for nucleolus imaging) that can only image nucleolus in fixed cells, the CDs can realize high-quality nucleolus imaging in not only fixed cells but also living cells, allowing the real-time tracking of nucleolus-related biological behaviors. Furthermore, aft...

Simultaneous Surface Modification and Chemical Reduction of Graphene Oxide Using Glucose.

In this paper, we develop a simple and facile approach to prepare graphene nanosheets through chemical reduction with glucose as reducing agent and modification agent. The reduced and modified graphene by glucose (denoted as g-rGO) was characterized with techniques of Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectra, scanning electron microscopy (SEM) and transmission electron microscopy (TEM), etc. It is found that, besides the desired reduction capability to graphene oxide (denoted as GO), glucose plays an important role as a modifying reagent in stabilizing the as-prepared graphene nanosheets simultaneously and the g-rGO exhibits good dispersibility and stability in water and waterborne polyurethane matrix (denoted as WPU). Moreover, the g-rGO can improve evidently the mechanical properties, weather ability and water resistance of WPU.

Adsorption of bis(2-hydroxy-3-chloropropyl) dodecylamine on quartz surface and its implication on flotation

Abstract In order to clarify the effect of polar group modification on flotation performance of amine collector, flotation properties of quartz and hematite using bis(2-hydroxy-3-chloropropyl) dodecylamine (N23) as a collector were investigated. And the adsorption mechanism of N23 on quartz surface was established by zeta potential measurements, SEM/EDS measurements, and molecular structure analysis. Single mineral flotation results indicated that N23 showed stronger collecting ability on quartz and hematite than DDA-CH 3 COOH. However, starch could depress the flotation of hematite. Flotation recovery of 98.10% for quartz could be achieved, when N23 concentration was 43.33 mg/L and starch concentration was 16.67 mg/L at natural slurry pH. Separation of artificially mixed minerals of hematite and quartz was achieved effectively using N23 as the collector. The optimized separation result with 66.29% iron grade and 90.06% iron recovery in concentrate was obtained when slurry pH was 7.34 with 43.33 mg/L N23 and 23.33 mg/L starch. The interaction energies of N23 with mineral surface also showed well consistency with flotation results. SEM/EDS analyses and zeta potential measurements revealed that N23 could absorb on quartz surface in the forms of strong electrostatic and hydrogen bonding interaction. Compared with DDA, N23 had a higher HLB value and better water-solubility, which resulted in better dispersion in water and stronger adsorption on mineral surface.

Functionalized Hydrophilic Superparamagnetic Iron Oxide Nanoparticles for Magnetic Fluid Hyperthermia Application in Liver Cancer Treatment.

In this work, we report the synthesis of hydrophilic and surface-functionalized superparamagnetic iron oxide nanoparticles (SPIOs) to utilize them as nanomedicines for treating liver cancer via magnetic fluid hyperthermia (MFH)-based thermotherapy. For this purpose, initially, we have synthesized the SPIOs through co-precipitation/thermolysis methods, followed by in situ surface functionalization with short-chained molecules, such as 1,4-diaminobenzene (14DAB), 4-aminobenzoic acid (4ABA) and 3,4-diaminobenzoic acid (34DABA) and their combination with terephthalic acid (TA)/2-aminoterephthalic acid (ATA)/trimesic acid (TMA)/pyromellitic acid (PMA) molecules. The as-prepared SPIOs are investigated for their structure, morphology, water dispersibility, and magnetic properties. The heating efficacies of the SPIOs are studied in calorimetric MFH (C-MFH) with respect to their concentrations, surface coatings, dispersion medium, and applied alternating magnetic fields (AMFs). Although all of the as-prepared SPIOs have exhibited superparamagnetic behavior, only 14DAB-, 4ABA-, 34DABA-, and 4ABA-TA-coated SPIOs have shown higher magnetization values (Ms = 55–71 emu g–1) and good water dispersibility. In C-MFH studies, 34DABA-coated SPIO-based aqueous ferrofluid (AFF) has revealed faster thermal response to the applied AMF and reached therapeutic temperature even at the lowest concentration (0.5 mg mL–1) compared with 14DAB-, 4ABA-, and 4ABA-TA-coated SPIO-based AFFs. Moreover, 34DABA-coated SPIO-based AFF has exhibited high heating efficacies (i.e., specific absorption rate/intrinsic loss power values of 432.1 W gFe–1/5.2 nHm2 kg–1 at 0.5 mg mL–1), which could be mainly due to (i) enhanced π–π conjugation paths of surface-attached 34DABA coating molecules because of intrafunctional group attractions and (ii) improved anisotropy from the formation of clusters/linear chains of the SPIOs in ferrofluid suspensions, owing to interfunctional group attractions/interparticle interactions. Moreover, the 34DABA-coated SPIOs have demonstrated (i) very good cytocompatibility for 24/48 h incubation periods and (ii) higher killing efficiency of 61–88% (via MFH) in HepG2 liver cancer cells as compared to their treatment with only AMF/water-bath-based thermotherapy. In summary, the 34DABA-coated SPIOs are very promising heat-inducing agents for MFH-based thermotherapy and thus could be used as effective nanomedicines for cancer treatments.

Radiotherapy-Sensitized Tumor Photothermal Ablation Using γ-Polyglutamic Acid Nanogels Loaded with Polypyrrole.

Development of versatile nanoscale platforms for cancer diagnosis and therapy is of great importance for applications in translational medicine. In this work, we present the use of γ-polyglutamic acid (γ-PGA) nanogels (NGs) to load polypyrrole (PPy) for thermal/photoacoustic (PA) imaging and radiotherapy (RT)-sensitized tumor photothermal therapy (PTT). First, a double emulsion approach was used to prepare the cystamine dihydrochloride (Cys)-cross-linked γ-PGA NGs. Next, the cross-linked NGs served as a reactor to be filled with pyrrole monomers that were subjected to in situ oxidation polymerization in the existence of Fe(III) ions. The formed uniform PPy-loaded NGs having an average diameter of 38.9 ± 8.6 nm exhibited good water-dispersibility and colloid stability. The prominent near-infrared (NIR) absorbance feature due to the loaded PPy endowed the NGs with contrast enhancement in PA imaging. The hybrid NGs possessed excellent photothermal conversion efficiency (64.7%) and stability against laser irradiation, and could be adopted for PA imaging and PTT of cancerous cells and tumor xenografts. Importantly, we also explored the cooperative PTT and X-ray radiation-mediated RT for enhanced tumor therapy. We show that PTT of tumors can be more significantly sensitized by RT using the sequence of laser irradiation followed by X-ray radiation as compared to using the reverse sequence. Our study suggests a promising theranostic platform of hybrid NGs that may be potentially utilized for PA imaging and combination therapy of different types of tumors.

Fluorescent Carbon Quantum Dots with Intrinsic Nucleolus-Targeting Capability for Nucleolus Imaging and Enhanced Cytosolic and Nuclear Drug Delivery.

Nucleolus tracking and nucleus-targeted photodynamic therapy are attracting increasing attention due to the importance of nucleolus and the sensitivity of nucleus to various therapeutic stimuli. Herein, a new class of multifunctional fluorescent carbon quantum dots (or carbon dots, CDs) synthesized via the one-pot hydrothermal reaction of m-phenylenediamine and l-cysteine was reported to effectively target nucleolus. The as-prepared CDs possess superior properties, such as low-cost and facile synthesis, good water dispersibility, various surface groups for further modifications, prominent photostability, excellent compatibility, and rapid/convenient/wash-free staining procedures. Besides, as compared with SYTO RNASelect (a commonly used commercial dye for nucleolus imaging) that can only image nucleolus in fixed cells, the CDs can realize high-quality nucleolus imaging in not only fixed cells but also living cells, allowing the real-time tracking of nucleolus-related biological behaviors. Furthermore, after conjugating with protoporphyrin IX (PpIX), a commonly used photosensitizer, the resultant CD-PpIX nanomissiles showed remarkably increased cellular uptake and nucleus-targeting properties and achieved greatly enhanced phototherapeutic efficiency because the nuclei show poor tolerance to reactive oxygen species produced during the photodynamic therapy. The in vivo experiments revealed that the negatively charged CD-PpIX nanomissiles could rapidly and specifically target a tumor site after intravenous injection and cause efficient tumor ablation with no toxic side effects after laser irradiation. It is believed that the present CD-based nanosystem will hold great potential in nucleolus imaging and nucleus-targeted drug delivery and cancer therapy.

Mechanically improved polyvinyl alcohol-composite films using modified cellulose nanowhiskers as nano-reinforcement

Cellulose nanowhiskers (CWs) extracted from cotton fibers were successfully modified with distinct anhydrides structures and used as additives in poly(vinyl alcohol) (PVA) nanocomposite films. The surface modification of CWs was performed with maleic, succinic, acetic or phthalic anhydride to compare the interaction and action the carboxylic groups into PVA films and how these groups influence in mechanical properties of the nanocomposites. CWs presented a high degree of crystallinity and good dispersion in water, with average length at the nanoscale. The addition of specific amounts (3, 6 and 9 wt.%) of modified-CWs increased up to 4.4 times the storage modulus (PVA88-CWSA 9 wt.%), as observed from dynamic mechanical analysis (DMA), compared to the bare PVA films. A significant increase in mechanical properties such as tensile strength, elastic modulus, and elongation at break showed a close relationship to the amount and chemical surface characteristics of CWs added, suggesting that these modified-CWs could be explored as reinforcement additives in PVA films.

Facile approach to synthesis the curly leaf-like Nano-sheets of g-C3N4 with enhanced photocatalytic ability

Exfoliation of porous g-C3N4 has been proved a very effective way to prepare g-C3N4 nanosheets (2D layered materials). Here, we present an environment-friendly, high-efficiency and easy scale-up preparation method of curly leaf-like g-C3N4 nanosheets (CL-CN) by liquid-phase exfoliation of honeycomb-like porous g-C3N4 (HP-CN). Two-dimensional curly nanosheets have induced excellent physicochemical properties, i.e. large surface area, high fluorescence quantum efficiency, wide band gap and good water-dispersibility. The photocatalytic performance of CL-CN in degradation of RhB under visible light is much better than that of honeycomb-like porous g-C3N4 and bulk g-C3N4. The improved photocatalytic performance of CL-CN is well explained by the improved physicochemical properties and photocatalytic mechanism. In addition, CL-CN being a 2D layered material with excellent photoluminescence characteristic and non-toxic behavior can be widely applied in bio-medicine, bio-imaging and biosensors field.