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Aggregation‐induced emission (AIE) carbon dot (CDs) in solid state with tunable multicolor emissions have sparked significant interest in multidimensional anti‐counterfeiting. However, the realization of solid‐state fluorescence (SSF) by AIE effect and the regulation of fluorescence wavelength in solid state is a great challenge. In order to solve this dilemma, the AIE method to prepare multi‐color solid‐state CDs with fluorescence wavelengths ranging from bright blue to red emission is employed. Specifically, by using thiosalicylic acid and carbonyl hydrazine as precursors, the fluorescence wavelength can be accurately adjusted by varying the reaction temperature from 150 to 230 °C or changing the molar ratio of the precursors from 1:1 to 1:2. Structural analysis and theoretical calculations consistently indicate that increasing the sp2 domains or doping with graphite nitrogen both cause a redshift in the fluorescence wavelength of CDs in the solid state. Moreover, with the multi‐dimensional and adjustable fluorescence wavelength, the application of AIE CDs in the fields of multi‐anti‐counterfeiting encryption, ink printing, and screen printing is demonstrated. All in all, this work opens up a new way for preparing solid‐state multi‐color CDs using AIE effect, and further proposes an innovative strategy for controlling fluorescence wavelengths. Herein, they proposed an efficient and precise wavelength tuning mechanism for the Aggregation‐induced emission (AIE) carbon dots (CDs). Specifically, by using thiosalicylic acid and carbonyl hydrazine as precursors, they can accurately adjust the fluorescence wavelength by varying the reaction temperature or changing the molar ratio of the precursors. Moreover, the application of AIE CDs in the fields of multi anti‐counterfeiting encryption has been demonstrated.

Since the 21st century, with the popularization of computers and mobile phones to the upgrading of various kinds of electronic products, human needs are also changing, among which the flexible touch screen has received wide attention. To achieve a wide application of flexible touch screens, this paper needs to make more materials innovations, and graphene’s unique and excellent performance has attracted wide attention. Among them, the metal doping, non-metallic doping, metallic and non-metallic co-doping of graphite phase carbon nitride has broad development prospects, widely used, or may be widely used in the production and production of flexible touch screen. This paper briefly analyzes and compares three nitrogen-containing graphene materials’ properties and preparation methods (metal doping, non-metal doping, metal, and non-metal co-doping) in 2D nanomaterials, and discusses the possible applications in the field of flexible touch screens. Urea-reduced GO graphene, Fe-P co-doped graphite phase nitride carbon and potassium ion-doped graphite phase nitride carbon all have easy raw materials, simple production mode, electrical, and excellent optical properties; meanwhile, different doping methods and dosage change the performance of graphene in different directions. Therefore, nitrogen-containing graphene materials have a lot for development in the part of flexible touch screens.

Owing to the difficulty in controlling the dopant or defect types and their homogeneity in carbon materials, it is still a controversial issue to identify the active sites of carbon-based metal-free catalysts. Here we report a proof-of-concept study on the active-site evaluation for a highly oriented pyrolytic graphite catalyst with specific pentagon carbon defective patterns (D-HOPG). It is demonstrated that specific carbon defect types (an edged pentagon in this work) could be selectively created via controllable nitrogen doping. Work-function analyses coupled with macro and micro-electrochemical performance measurements suggest that the pentagon defects in D-HOPG served as major active sites for the acidic oxygen reduction reaction, even much superior to the pyridinic nitrogen sites in nitrogen-doped highly oriented pyrolytic graphite. This work enables us to elucidate the relative importance of the specific carbon defects versus nitrogen-dopant species and their respective contributions to the observed overall acidic oxygen reduction reaction activity. The active sites of metal-free carbon catalysts for the oxygen reduction reaction remain still elusive. Now, Yao, Dai and co-workers combine work-function analyses with macro/micro-electrochemical measurements on highly oriented pyrolytic graphite and conclude that pentagon defects are the main active sites for acidic oxygen reduction.

Cancer poses a global challenge, affecting millions of people and placing a significant burden on families and healthcare systems. Chemotherapy, radiotherapy, hormone therapy, and immunotherapy are commonly used for cancer treatment; their side effects can be severe. Photothermal therapy (PTT) has emerged as a promising alternative due to its minimal invasiveness and high efficiency. In this study, graphene oxide (GO) was synthesized and functionalized to obtain nitrogen-doped graphene oxide (NGO) and boron-doped graphene oxide (BGO) via a hydrothermal process, aiming to use them as photoactive agents (PAs) in PTT. Atomic force microscopy (AFM) analysis revealed that GO, BGO, and NGO exhibit monolayer atomic structures. Spectroscopic analyses confirmed the presence of oxygen and carbon in all samples, along with successful boron and nitrogen doping in BGO and NGO, respectively. Cytotoxicity assays yielded half-maximal inhibitory concentrations (IC50) of 1025.26 μg/mL for GO, 2695.03 μg/mL for BGO, and 1319.81 μg/mL for NGO. Photothermal experiments were conducted using a 635 nm light source with an intensity of 65.5 mW/cm2, resulting in temperature thresholds of 44.87 °C for GO, 48.36 °C for NGO, and 55.91 °C for BGO. Anticancer assays were performed using the T-47D breast cancer cell line, demonstrating tumor cell elimination rates of 97.93% for GO, 98.54% for BGO, and 97.98% for NGO, underscoring their efficacy as PAs. Density functional theory (DFT) simulations were carried out to determine the absorbance coefficient as a function of doping percentage. The results revealed that increased doping enhances light absorbance and, consequently, the photothermal response, as higher absorbance at the irradiation wavelength leads to greater energy absorption and temperature elevation.

Highlights Single-atom Fe–N 4 sites embedded into graphene were successfully synthesized to exert the dielectric properties of graphene. The absorption mechanisms of metal-nitrogen doping reduced graphene oxide mainly include enhanced dipole polarization, interface polarization, conduction loss and defect-induced polarization. Excellent reflection loss of − 74.05 dB (2.0 mm) and broad effective absorption bandwidth of 7.05 GHz (1.89 mm, with filler loading only 1 wt%) were obtained. Developing effective strategies to regulate graphene's conduction loss and polarization has become a key to expanding its application in the electromagnetic wave absorption (EMWA) field. Based on the unique energy band structure of graphene, regulating its bandgap and electrical properties by introducing heteroatoms is considered a feasible solution. Herein, metal-nitrogen doping reduced graphene oxide (M–N-RGO) was prepared by embedding a series of single metal atoms M–N 4 sites (M = Mn, Fe, Co, Ni, Cu, Zn, Nb, Cd, and Sn) in RGO using an N-coordination atom-assisted strategy. These composites had adjustable conductivity and polarization to optimize dielectric loss and impedance matching for efficient EMWA performance. The results showed that the minimum reflection loss ( RL min ) of Fe–N-RGO reaches − 74.05 dB (2.0 mm) and the maximum effective absorption bandwidth (EAB max ) is 7.05 GHz (1.89 mm) even with a low filler loading of only 1 wt%. Combined with X-ray absorption spectra (XAFS), atomic force microscopy, and density functional theory calculation analysis, the Fe–N 4 can be used as the polarization center to increase dipole polarization, interface polarization and defect-induced polarization due to d-p orbital hybridization and structural distortion. Moreover, electron migration within the Fe further leads to conduction loss, thereby synergistically promoting energy attenuation. This study demonstrates the effectiveness of metal-nitrogen doping in regulating the graphene′s dielectric properties, which provides an important basis for further investigation of the loss mechanism.

Nitrogen doped graphene quantum dots (NGQDs) were successfully prepared via a hydrothermal method using citric acid and urea as the carbon and nitrogen precursors, respectively. Due to different post-treatment processes, the obtained NGQDs with different surface modifications exhibited blue light emission, while their visible-light absorption was obviously different. To further understand the roles of nitrogen dopants and N-containing surface groups of NGQDs in the photocatalytic performance, their corresponding composites with TiO2 were utilized to degrade RhB solutions under visible-light irradiation. A series of characterization and photocatalytic performance tests were carried out, which demonstrated that NGQDs play a significant role in enhancing visible-light driven photocatalytic activity and the carrier separation process. The enhanced photocatalytic activity of the NGQDs/TiO2 composites can possibly be attributed to an enhanced visible light absorption ability, and an improved separation and transfer rate of photogenerated carriers.

To improve the adsorption efficiency of pollutants by biochar, preparing graphene-like biochar (GBC) or nitrogen-doped biochar are two commonly used methods. However, the difference in the nitrogen doping (N-doping) effects upon the adsorption of pollutants by pristine biochar (PBC) and GBC, as well as the underlying mechanisms, are still unclear. Take the tetracycline (TC) as an example, the present study analyzed the characteristics of the adsorption of TCs on biochars (PBC, GBC, N-PBC, N-GBC), and significant differences in the effects of N-doping on the adsorption of TCs by PBC and GBC were consistently observed at different solution properties. Specifically, N-doping had varied effects on the adsorption performance of PBC, whereas it uniformly improved the adsorption performance of GBC. To interpret the phenomenon, the N-doping upon the adsorption was revealed by the QSAR model, which indicated that the pore filling (VM) and the interactions between TCs with biochars (Ead-v) were found to be the most important two factors. Furthermore, the density functional theory (DFT) results demonstrated that N-doping slightly affects biochar’s chemical reactivity. The van der Waals (vdWs) and electrostatic interactions are the main forces for TCs-biochars interactions. Moreover, N-doping mostly strengthened the electrostatic interactions of TCs-biochars, but the vdWs interactions of most samples remained largely unaffected. Overall, the revealed mechanism of N-doping on TCs adsorption by biochars will enhance our knowledge of antibiotic pollution remediation.

Highlights Nitrogen and phosphorus dual-doped multilayer graphene (NPG) was prepared by arc discharge process. NPG exhibits good rate capability and stable cycling performance in both lithium and potassium ion batteries. Full carbon-based lithium/potassium ion capacitors are assembled and show excellent electrochemical performance. Lithium/potassium ion capacitors (LICs/PICs) have been proposed to bridge the performance gap between high-energy batteries and high-power capacitors. However, their development is hindered by the choice, electrochemical performance, and preparation technique of the battery-type anode materials. Herein, a nitrogen and phosphorus dual-doped multilayer graphene (NPG) material is designed and synthesized through an arc discharge process, using low-cost graphite and solid nitrogen and phosphorus sources. When employed as the anode material, NPG exhibits high capacity, remarkable rate capability, and stable cycling performance in both lithium and potassium ion batteries. This excellent electrochemical performance is ascribed to the synergistic effect of nitrogen and phosphorus doping, which enhances the electrochemical conductivity, provides a higher number of ion storage sites, and leads to increased interlayer spacing. Full carbon-based NPG‖LiPF 6 ‖active carbon (AC) LICs and NPG‖KPF 6 ‖AC PICs are assembled and show excellent electrochemical performance, with competitive energy and power densities. This work provides a route for the large-scale production of dual-doped graphene as a universal anode material for high-performance alkali ion batteries and capacitors.

To investigate the alternatives to lithium-ion batteries, potassium-ion batteries have attracted considerable interest due to the cost-efficiency of potassium resources and the relatively lower standard redox potential of K+/K. Among various alternative anode materials, hard carbon has the advantages of extensive resources, low cost, and environmental protection. In the present study, we synthesize a nitrogen-doping hard-carbon-microsphere (N-SHC) material as an anode for potassium-ion batteries. N-SHC delivers a high reversible capacity of 248 mAh g−1 and a promoted rate performance (93 mAh g−1 at 2 A g−1). Additionally, the nitrogen-doping N-SHC material also exhibits superior cycling long-term stability, where the N-SHC electrode maintains a high reversible capacity at 200 mAh g−1 with a capacity retention of 81% after 600 cycles. DFT calculations assess the change in K ions’ absorption energy and diffusion barriers at different N-doping effects. Compared with an original hard-carbon material, pyridinic-N and pyrrolic-N defects introduced by N-doping display a positive effect on both K ions’ absorption and diffusion.

Graphene quantum dots (GQDs) represent a class of promising nanomaterials characterized by adjustable optical properties, making them well suited for applications in biosensing and chemical detection. However, challenges persist in achieving scalable, cost-effective synthesis and enhancing detection sensitivity. In this study, we have developed a simple and environmentally friendly method to prepare blue graphene quantum dots, c-GQDs, using nitronaphthalene as a precursor, and yellow graphene quantum dots, y-GQDs, using nitronaphthalene doped acid. The quantum yield is 29.75%, and the average thickness is 2.08 nm and 3.95 nm, respectively. The synthesized c-GQDs exhibit a prominent cyan fluorescence at a wavelength of 490 nm under excitation at 380 nm, while the y-GQDs show a distinct yellow fluorescence at a wavelength of 540 nm under excitation at 494 nm. The introduction of p-aminobenzoic acid (PABA) introduced a marked red shift in fluorescence, attributed to the electron-withdrawing effect of the carboxyl groups on PABA. This key finding significantly enhanced the sensitivity of GQDs for detecting trace copper(II) ions (Cu2+), a heavy metal contaminant posing serious environmental risks. The fluorescence of the GQDs was selectively quenched in the presence of Cu2+, facilitating accurate and sensitive detection even in complex ion matrices. Mechanistic studies revealed that the quenching effect is driven by strong static quenching interactions, which inhibit non-radiative transitions. This work not only introduces a scalable method for producing high-performance GQDs but also highlights their potential as effective fluorescent probes for environmental monitoring and heavy metal ion detection.