MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Chao Li,Juan Lu,Yanjia Guo,Jing Wang,Yujia Song,Ruidan Li,Li Tian,Xuwen Li
In this study, a solid-state electrochemiluminescence (ECL) sensor was developed for ultrasensitive and specific detection of sulfapyridine (SPY) using graphitic carbon nitride (g-C 3 N 4 ) as a luminescent reagent. The sensor was fabricated by sequentially coating composite material g-C 3 N 4 @ZIF-8 and Nafion onto the electrode surface. The g-C 3 N 4 , synthesized through high-temperature pyrolysis of melamine, generated a sensitive ECL signal in K 2 S 2 O 8 solution. And g-C 3 N 4 served as a carrier for ZIF-8, with the latter acting as a co-reaction promoter within the g-C 3 N 4 -K 2 S 2 O 8 system, leading to a significant enhancement of the ECL signal. Additionally, molecularly imprinted polymers (MIPs) with SPY were introduced to further enhance the performance of the sensor by specifically recognizing SPY. Under optimal conditions, the prepared ECL sensor showed sensitive measurement of SPY in the linear range of 5.0 × 10 −13 ∼ 5.0 × 10 −8 mol/L, with a detection limit (LOD) of 1.67 × 10 −13 (S/N = 3). The developed MIP-ECL sensor demonstrated good stability, high sensitivity, and reliable reproducibility, thus making it suitable for detecting SPY in real samples.
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高影响因子
COMPOSITES PART B-ENGINEERING
·
2024
·
IF 12.7
Shasha Wang,Yuli Wei,Rongzhe Wang,Qing Liu,Qing Wang,Shaohua Luo,Yahui Zhang,Shengxue Yan,Pengqing Hou,Xin Liu,Jing Guo,Wenning Mu
Nitrogen-doped carbon is regarded as a promising anode for potassium ion batteries (PIBs) because nitrogen atoms can regulate the structures of carbon and generate abundant active sites. How to improve the nitrogen content in carbon through simple and effective methods remains to be further addressed. In this paper, a carbon material (60NC) with ultrahigh nitrogen content (16 %) was prepared from graphite phase carbon nitride (g-C 3 N 4 ) by a convenient freeze-drying and high-temperature pyrolysis method, assisted by citric acid. When used as an anode for PIBs, 60NC exhibited a superior reversible capacity of 318.1 mAh g −1 after 200 cycles at 0.1 A g −1 . Even at the high current density of 1A g −1 , 60NC maintained a specific capacity of 261.8 mAh g −1 after 1000 cycles. The excellent electrochemical performance of 60NC mainly stems from its abundant K + storage active sites caused by nitrogen doping, large layer spacing, and hierarchical porous structure.
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高影响因子
PHYSICA B-CONDENSED MATTER
·
2024
·
IF 2.8
Yongyi Li,Huixing Yang,Wei Li,Zhigang Shao,Yongzhuo Yu,Huixiang Yan,Shichao Jiao,Di Lin,Wenxu Zhang,Chaoyu Lv,Yuxin Huang
In this work, ultrathin lamellar g-C 3 N 4 /In 2 S 3 S-scheme heterojunctions doped with P were synthesized by urea recrystallization and investigated to see which ratio was more favorable for photocatalysis. The P doping formed a new Fermi energy level and reduced the forbidden bandwidth. The ultrathin lamellar structure facilitated rapid charge transfer, and the formation of S-scheme heterojunction, the presence of the interfacial electric field, and band bending effectively separated strong redox-capable electron-hole pairs, thus significantly improving the photocatalytic performance. Among the prepared materials, the 50UP-C 3 N 4 /In 2 S 3 photocatalyst with 50 % UP-C 3 N 4 mass fraction showed optimal photocatalytic H 2 production performance, with a hydrogen production rate of 12,387 μmol h −1 g −1 . Moreover, it showed good performance in photocatalytic degradation, with a degradation efficiency of up to 90.2 % of ofloxacin after 120 min of light exposure. This article provided a new perspective on the synthesis of other photocatalysts with carbazide-based S-scheme heterojunction structures.
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高影响因子
ACS Applied Energy Materials
·
2025
·
IF 5.5
Liru Yan,Shishuai Sun,Shuangting Ruan,Xiaocheng Liu,Huanqi Cao,Shougen Yin
Design of the photosensitive electrode material provides an effective strategy to improve the capacity and stability of supercapacitors. In this study, the photothermal-driven cobalt–zinc-doped Ni(OH)2/g-C3N4@NF nanoflower electrode materials were prepared base on the in situ chemical etching strategy. The electrochemical performance indicated that the optimized CZNC2.18 (cobalt–zinc codoped β-Ni(OH)2@g-C3N4) electrode material with exceptional stability (103.74% capacitance retention after 5000 cycles at 20 mA/cm2) exhibited an ultrahigh capacitance of 19.10 F/cm2 at a current density of 10 mA/cm2 under illumination, compared to 12.8 F/cm2 under dark conditions, achieving a light gain of 149%. The assembled asymmetric photothermal-assisted supercapacitor device delivers energy densities of 3.55 mWh/cm2 (1.23 mWh/cm2) at corresponding power densities of 8.39 mW/cm2 (37.03 mW/cm2) under illumination, surpassing performance metrics observed under dark conditions. The synergistic effects of photogenerated carriers (holes oxidizing Ni(OH)2 to NiOOH and electrons enhancing conductivity), Zn/Co codoping-induced conductivity improvement, and photothermal-assisted ion transport collectively enable CZNC2.18 exceptional photoelectrochemical performance, establishing a paradigm for light-responsive energy storage material design.
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Bioactive Materials
·
2025
·
IF 20.3
Yuyun Ye,Yan Liu,Shengchao Ma,Xipeng Li,Wei Wang,Xu Chen,Judun Zheng,Zhijin Fan,Yideng Jiang,Yuhui Liao
Infectious wound healing remains a significant medical challenge due to chronic inflammation and bacterial colonization. Effective antimicrobial and anti-inflammatory therapies are essential to facilitate wound recovery. Herein, we introduce a highly biocompatible, ROS-responsive DNA hydrogel (LGAH), modified with aggregation-induced emission luminogens (AIEgen) and incorporating ginseng-derived exosomes (G-Exos) and nitric oxide (NO) donor-L-arginine (L-Arg) to promote healing of infected wounds. The hydrogel degrades in response to elevated ROS levels, releasing therapeutic agents. Upon laser irradiation, AIEgen generates 1 O 2 , which activates L-Arg to produce NO, leading to a synergistic antimicrobial effect. NO is particularly effective at inhibiting bacterial growth and promoting angiogenesis, supporting wound healing. G-Exos modulate immune responses, reduce inflammation, and promote the transition from the inflammatory to the proliferative phase. They also enhance cell proliferation, migration, and collagen production, which are key to tissue regeneration. In vivo experiments demonstrated that LGAH significantly accelerates S. aureus -infected wound healing by modulating the wound microenvironment and promoting tissue regeneration. Transcriptomic analysis revealed that LGAH down-regulates gene expression in inflammation and immune response signaling pathways while up-regulating genes related to energy metabolism. Biosafety evaluations at cellular and animal levels have demonstrated that LGAH possesses excellent biocompatibility and biodegradability, making it ideal for tissue repair and regeneration. This multifunctional DNA hydrogel system offers a safe and promising strategy for the clinical treatment of infected wounds.
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PubMed
高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2024
·Vol. 59
·期 8
·3573-3584
·
IF 3.5
Xu Man,Luo Yongping,Zeng Linsheng,Huang Ping,Xu Shunjian,Liu Yike,Wang Yongya,Li Xianchang,xie Yu
In consideration of the increased activity of Pt-based catalysts for methanol oxidation in direct methanol fuel cells, it is necessary to apply an ideal support in the construction of Pt-based catalyst for methanol oxidation. In this study, Ag/g-C 3 N 4 nanosheets (Ag/GCNN) nanocomposites with different Ag contents were synthesized and used as the progressive support to construct Pt/Ag/GCNN catalyst. As a nitrogen-rich polymeric semiconductor, GCNN is easily coordinated with various metals. The introduction of Ag nanoparticles can improve the electrical conductivity of the catalyst and cooperate with Pt for optimizing the performance of electrocatalytic oxidation of methanol. The electrochemical experiment results demonstrated that Pt/Ag/GCNN has higher electrocatalytic activity and stability for methanol oxidation than Pt/GC and Pt/GCNN. The mass activity of Pt/Ag/GCNN-0.6 (18.66 mA mg Pt −1 ) is 7.07, 4.60 and 1.26 times that of Pt/GCNN (4.06 mA mg Pt −1 ), Pt/Ag/GCNN-0.4 (4.06 mA mg Pt −1 ) and Pt/Ag/GCNN-0.8 (14.76 mA mg Pt −1 ) at the forward peak potential. The J f / J b ratio of Pt/Ag/GCNN-0.6 is 3.31, which is bigger than that of Pt/GCCN (2.62), Pt/Ag/GCNN-0.4 (2.69), and Pt/Ag/GCNN-0.8 (2.56). A suitable mechanism was proposed to explain that Ag/GCNN supported Pt catalyst can improve the CO toxicity resistance and electrocatalytic performance. Based on the coordination of GCNN, Ag was first modified to form a support, and then the remaining coordination sites were used to support Pt. It provided a new strategy for the design of catalysts for methanol electrooxidation. Graphical abstract
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高影响因子
Catalysts
·
2024
·Vol. 14
·期 9
·579
·
IF 3.8
Qingbao Gan,Jianwei Zhang,Jinglin Wang,Yuntian Wei,Shikun Chen,Shuguang Cai,Xueqing Xiao,Chan Zheng
The excessive discharge of antibiotics into aquatic systems is a major issue in many countries worldwide and poses a threat to human health and the sustainable development of society. Hence, developing efficient treatment methods and purification technologies to degrade antibiotics is essential. Herein, we present the synthesis of low-cost, self-propelled tubular Fe3+-incorporated graphitic carbon nitride (g-C3N4-Fe@KF) micromotors using kapok fibers (KFs) as templates and their application as photo-catalysts for the photo-Fenton degradation of tetracycline (TC) under visible-light irradiation. The g-C3N4-Fe@KF micromotors moved rapidly when being propelled by oxygen bubbles generated in a hydrogen peroxide (H2O2) solution as a result of a photo-assisted Fenton reaction. The motion behavior of the g-C3N4-Fe@KF micromotors was dependent on the concentration of H2O2and the length of the micromotors. The propulsion mechanism was discussed in detail. The micromotors efficiently degraded antibiotics via the photo-Fenton process. Photo-Fenton degradation efficiency was attributed to the synergistic effects of the doped Fe3+and g-C3N4under visible-light irradiation and self-propulsion of the micromotors. In addition, the micromotors possessed good reusability, thereby efficiently realizing multiple cycles of degradation. The current work offers an avenue for the design of micromotors, using inexpensive approaches, for various potential environmental applications.
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高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2015
·
IF 7.435
Wangyang Lu,Tiefeng Xu,Yu Wang,Hongguang Hu,Nan Li,Xuemei Jiang,Wenxing Chen
Visible light-responsive photocatalysis has shown great potential for effluent treatment as an environmentally friendly method. Herein, the photocatalyst of graphitic carbon nitride (g-C 3 N 4 ) coupled with zinc phthalocyanine (g-C 3 N 4 /ZnTcPc) was prepared by immobilizing zinc tetracarboxyphthalocyanine (ZnTcPc) onto g-C 3 N 4 covalently. The spectral response region of g-C 3 N 4 has been extended from 450 nm to more than 800 nm sensitized by ZnTcPc, which is well known for the red/near-IR (Q band) light absorption. Compared with pure g-C 3 N 4 and ZnTcPc, g-C 3 N 4 /ZnTcPc presented a significantly enhanced photocatalytic activity for the degradation of rhodamine B (RhB) and 4-chlorophenol (4-CP) under visible irradiation. The photocatalytic activity of g-C 3 N 4 has been improved by the coupled interaction with ZnTcPc over a wide pH range. Moreover, besides photogenerated hole, the presence of singlet oxygen ( 1 O 2 ), superoxide radical ( O 2 − ) and hydroxyl radical ( OH) has been evidenced in the visible light-responsive catalytic system with g-C 3 N 4 /ZnTcPc, especially in alkaline condition. The possible photocatalytic degradation pathway of RhB has been proposed according to the results of ultra-performance liquid chromatography and high-definition mass spectrometry (UPLC Synapt G2-S HDMS). This synergistic photocatalytic process will provide useful insights to make full use of solar light for future application to eliminate recalcitrant organic pollutants .
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高影响因子
Journal of Environmental Chemical Engineering
·
2026
·
IF 7.5
Haize Jin,Yuwang Chen,Kaiqiang Hong,Ziyuan Wang,Xiaoxia Huang,Qikun Wang
SDS-modified geopolymer/Ag 9 (SiO 4 ) 2 NO 3 /g-C 3 N 4 (SGC) unites adsorption, photocatalysis and PDS activation • SGC powder removes 94.12% of pymetrozine at 2 min under simulated sunlight with 3 mM PDS. • 3D-printed SGC monolithic device achieves 96.97% removal at 60 min and stays stable over 5 dynamic cycles. • The h⁺, ·OH, ·O₂⁻, ·SO₄⁻, and ¹O₂ all contribute to PYM degradation by SGC. Photocatalysis combined with peroxydisulfate (PDS) offers a promising route for degrading organic pesticides, but rational design of adsorption and catalytic sites at the nanoscale remains challenging. Here, an innovative sodium dodecyl sulfate (SDS)-modified geopolymer/Ag 9 (SiO 4 ) 2 NO 3 /g-C 3 N 4 (SGC) adsorbent-photocatalyst was reported, which integrated rapid pollutant capture, photocatalysis and PDS activation into a synergistic system for pymetrozine (PYM) degradation. The SDS promoted the uniform intergrowth of GP nanoclusters and ASN nanocrystals on g-C 3 N 4 , and also endowed the SGC with a relatively high surface negative charge density over a wide pH range and could quickly capture cationic or zwitterionic PYM molecules via electrostatic attraction. And the SDS also enhanced the visible-light response capability and narrowed the energy band gaps of SGC, contributing to improving photogenerated charge separation and more efficient PDS activation. The SGC powder achieved a PYM removal efficiency of 94.12% within 2 min, while the 3D-printed SGC fabricated by direct ink writing exhibited a removal efficiency of 96.97% at 60 min under simulated sunlight. Mechanistic investigations revealed that photogenerated electrons were primarily responsible for PDS activation, while h + , ·OH, ·O 2 - , ·SO 4 - , and 1 O 2 all contributed to PYM oxidation. Toxicity assessment of intermediate products and seed germination tests demonstrated a marked reduction in biotoxicity following degradation treatment. Moreover, the 3D-printed SGC maintained high stability over five dynamic cycles, and the in-situ photoreduction of Ag 0 during the cyclic process helped sustain radical generation. This work provides a new design strategy for high-performance adsorption-photocatalysis-PDS synergy systems and demonstrates a practical route for sustainable pesticide wastewater treatment. Download: Download high-res image (274KB) Download: Download full-size image
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高影响因子
DESALINATION
·
2026
·
IF 9.9
Zhouxiao Zhai,Jingce Bi,Linshan Wang,Ningning Liu,Yi Wang,Xia Zhang,Zhuopeng Wang,Yide Han
A g-C 3 N 4 /Bi 2 MoO 6 /Bi 2 WO 6 ternary heterojunction was constructed via simple mechanical grinding and thermal treatment. • GBMW follows a dual Z -scheme charge-transfer pathway, preserving strong redox capability for enhanced photocatalysis. • U(VI) acts as an electron acceptor to promote charge separation and improve photocatalytic performance. Due to the difficulty of conventional photocatalytic systems in simultaneously achieving strong oxidation and reduction processes, the treatment of wastewater containing coexisting uranium and organic pollutants remains a critical challenge in the field of photocatalysis. Herein, a novel g-C 3 N 4 /Bi 2 MoO 6 /Bi 2 WO 6 (GBMW) ternary photocatalyst with a dual Z -scheme heterojunction architecture was rationally constructed for the removal of U(VI) and tetracycline (TC) under visible-light irradiation. The dual Z-scheme heterojunction extends the visible-light response range and accelerates interfacial charge transfer, while preserving strong redox potentials. Within 100 min, GBMW achieves a U(VI) reduction efficiency of 91.6% and a TC degradation efficiency of 97.6%, with corresponding k obs values of 0.02332 and 0.03664 min −1 , respectively, which are significantly superior to those of BiMO, BiWO, GCN and GBW. Notably, U(VI) can act as an efficient electron acceptor to promote the separation of electrons and holes in GBMW, which significantly facilitates the degradation of TC. Moreover, GBMW demonstrates excellent stability and anti-interference performance in various real water matrices. This work not only provides a feasible strategy for constructing high-efficiency dual Z -scheme heterojunctions photocatalysts, but also offers an effective solution for treating complex wastewater containing coexisting organic pollutants and radioactive contaminants. Download: Download high-res image (264KB) Download: Download full-size image
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高影响因子
DIAMOND AND RELATED MATERIALS
·
2026
·
IF 5.2
Lu Sun,Jie Wei,Qing Hu,Xiuquan Xu,Jing Wu,Yaoyao Cao,Yao Zhang,Haoyan Wu
A Fe/V-CN nanozyme with synergistically enhanced POD-like activity was rationally designed. • A sensitive cascade colorimetric platform for detecting gastric cancer-related D-amino acids was successfully constructed. • The assay supports reliable quantification of D-amino acids in complex human saliva matrices. The development of a practical and reliable cascade colorimetric method for detecting D-amino acids (DAAs) provides a promising tool for the prevention and preliminary diagnosis of gastric cancer. Herein, a bimetallic Fe V supported on graphitic carbon nitride (Fe/V-CN) nanozyme was rationally designed and synthesized via a simple annealing strategy. The atomic dispersion of Fe and V species, along with their coexisting multivalent states (Fe 2+ / 3+ , V 4+ / 5+ ) synergistically boosted the intrinsic peroxidase-like (POD) activity to Fe/V-CN, which were characterized by a high substrate affinity ( K m of 0.078 and 0.083 mM for TMB and H 2 O 2 ) and an accelerated catalytic turnover ( V max of 4.94 × 10 −7 and 7.76 × 10 −7 M·s −1 , respectively). Leveraging this improved activity, a cascade colorimetric sensing system was developed by integrating Fe/V-CN with D-amino acid oxidase (DAAO) for the specific detection of DAAs. The platform exhibited favorable analytical performance for D-proline (D-Pro) and D-alanine (D-Ala), offering wide linear ranges of 0–200 μM and 0–160 μM and low detection limits of 0.93 μM and 1.45 μM, respectively, combined with acceptable selectivity against common interferents. For real-sample analysis, the platform was successfully implemented in determine DAAs in human saliva, delivering satisfactory recoveries (95.8–105.7%) and good precision (RSD < 3.5%). This work presented a synergistic Fe/V bimetallic nanozyme and a practical sensing strategy, demonstrating the feasibility of DAAs detection in complex biological matrices. Download: Download high-res image (70KB) Download: Download full-size image
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高影响因子
Biosensors-Basel
·
2026
·Vol. 16
·期 7
·376
·
IF 6.2
Mengli Wang,Yuanyuan Xia,Yulei Li,Lifen Chen,Kunyan Wang,Shuangshuang Wu,Yuelan Zhang
In this work, we developed a novel, ultrasensitive fluorescence sensing platform for determination of organophosphorus pesticides (OPs), using chlorpyrifos as a representative model analyte. The sensing strategy was constructed upon the key inner filter effect (IFE) between graphitic carbon nitride (g-C3N4) nanosheets and silver-coated gold core–shell nanoparticles (Au@Ag NPs). Initially, gold nanoparticles (Au NPs), silver nanoparticles (Ag NPs), and Au@Ag NPs were successfully synthesized, and their fluorescence quenching efficiencies toward g-C3N4were systematically evaluated. Owing to the superior spectral overlap with the fluorescence emission of g-C3N4, Au@Ag NPs exhibited the most obvious quenching effect and were thereby selected as the optimal quencher for sensor fabrication. Then, acetylcholinesterase (AChE) catalyzed the hydrolysis of acetylthiocholine (ATCH) into thiocholine. The generated thiocholine then induced aggregation of Au@Ag NPs via electrostatic and Ag-S interactions, which reduced the IFE efficiency and ultimately restored the fluorescence of g-C3N4. In contrast, the presence of chlorpyrifos effectively inhibits AChE activity, thereby suppressing ATCH hydrolysis and the subsequent aggregation of Au@Ag NPs. The fluorescence intensity of g-C3N4was quenched by Au@Ag NPs and the signal was low. Under optimal experimental conditions, the response signal was found to be proportional to chlorpyrifos (CPF). This work presents a rapid, cost-effective, and highly sensitive approach for CPF residue analysis, holding great potential for applications in food safety monitoring and environmental surveillance.
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PubMed
高影响因子