Yanan Niu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Yanan Niu has a total of 20 co-authors. Here are the top co-authors by number of shared publications:
- Xi Cao
School of Information Science and Technology, Beijing University of Chemical Technology, Beijing 100029, China
4 shared publications - Yuguang Lv
College of Materials Science and Engineering, Jiamusi University, Jiamusi 154007, China
4 shared publications - Yan Zhao
School of Civil Engineering and Architecture, Wuyi University, Wuyishan 354300, China
2 shared publications - Chang Feng
School of Chemistry and Chemical Engineering, Mudanjiang Normal University, Mudanjiang 157000, China
1 shared publication - Chaoyu Song
College of Pharmacy, Jiamusi University, Jiamusi 154007, China
1 shared publication - Huachao Ma
College of Materials Science and Engineering, Jiamusi University, Jiamusi 154007, China
1 shared publication
Latest Publications
- Open Access
- 1 June 2026
- Published by MDPI AG in Chemosensors
- Vol. 14 (6) , 126
Fluorogenic Probe-Coupled Single-Molecule Fluorescence Imaging for Photocatalytic Mechanism Research
Elucidating structure–activity relationships in semiconductor photocatalysis has been significantly impeded by the inherent limitations of ensemble-averaged characterization techniques, which obscure the spatiotemporal heterogeneity intrinsic to catalytic surfaces. Single-molecule fluorescence microscopy (SMFM) surmounts this bottleneck by offering nanometer-scale spatial resolution coupled with the capacity to resolve single-turnover events. Herein, we provide a comprehensive overview of the State-of-the-Art applications of fluorogenic probe-coupled SMFM in deciphering the microscopic mechanisms governing photocatalysis. We begin by delineating the operational principles of total internal reflection fluorescence (TIRF) microscopy and categorizing the response mechanisms of three distinct classes of fluorogenic probes: oxidative (e.g., Amplex Red, APF), reductive (e.g., Resazurin, DN-BODIPY), and acidic (e.g., furfuryl alcohol, thiophene) reporters. Subsequently, we highlight seminal studies wherein SMFM has been leveraged to visualize facet-dependent charge separation on model photocatalysts—including TiO2, BiOBr, and InSe—to map the dynamic activity associated with surface defects and to precisely locate active sites during photoelectrochemical water splitting. Finally, we critically assess the prevailing technical challenges, such as limitations in probe specificity and background interference, while offering a perspective on prospective avenues for methodological refinement. This review is intended to serve as a methodological cornerstone for advancing mechanistic understanding in photocatalysis and for guiding the rational design of high-performance catalysts.
- 1 June 2026
- Published by MDPI AG in Chemosensors
- Vol. 14 (6) , 126
Open AccessFluorogenic Probe-Coupled Single-Molecule Fluorescence Imaging for Photocatalytic Mechanism Research
Elucidating structure–activity relationships in semiconductor photocatalysis has been significantly impeded by the inherent limitations of ensemble-averaged characterization techniques, which obscure the spatiotemporal heterogeneity intrinsic to catalytic surfaces. Single-molecule fluorescence microscopy (SMFM) surmounts this bottleneck by offering nanometer-scale spatial resolution coupled with the capacity to resolve single-turnover events. Herein, we provide a comprehensive overview of the State-of-the-Art applications of fluorogenic probe-coupled SMFM in deciphering the microscopic mechanisms governing photocatalysis. We begin by delineating the operational principles of total internal reflection fluorescence (TIRF) microscopy and categorizing the response mechanisms of three distinct classes of fluorogenic probes: oxidative (e.g., Amplex Red, APF), reductive (e.g., Resazurin, DN-BODIPY), and acidic (e.g., furfuryl alcohol, thiophene) reporters. Subsequently, we highlight seminal studies wherein SMFM has been leveraged to visualize facet-dependent charge separation on model photocatalysts—including TiO2, BiOBr, and InSe—to map the dynamic activity associated with surface defects and to precisely locate active sites during photoelectrochemical water splitting. Finally, we critically assess the prevailing technical challenges, such as limitations in probe specificity and background interference, while offering a perspective on prospective avenues for methodological refinement. This review is intended to serve as a methodological cornerstone for advancing mechanistic understanding in photocatalysis and for guiding the rational design of high-performance catalysts.
- Open Access
- 18 February 2026
- Published by MDPI AG in Nanomaterials
- Vol. 16 (4) , 267
Research Progress on Nanopolymer Composites in Civil Engineering
Civil engineering infrastructure suffers material degradation, shortened service life and high maintenance costs under harsh environments and natural aging, threatening public safety. Nanopolymer composites, featuring designable microstructures and excellent macroscopic properties, provide a revolutionary solution to improve the weather resistance and toughness of civil engineering materials. This paper systematically clarifies the modification mechanisms of nanocomposites, focusing on nanofiller–polymer matrix interfacial interactions (physical adsorption, chemical bonding) and their synergistic effects in enhancing environmental aging resistance (UV, corrosion, freeze–thaw) and mechanical performance (toughening, strengthening, dynamic load resistance). It summarizes the latest applications in nanomodified protective coatings, sealing/bonding materials and composite structural components, revealing the inherent “structure-property-application” relationships. Furthermore, this paper addresses core large-scale application challenges, including technical bottlenecks, performance evaluation limitations and economic/environmental barriers. Finally, future research directions are proposed, covering multifunctional intelligent materials, green development, interdisciplinary computational methods and standardized systems. This review offers an integrated perspective, providing theoretical guidance and practical references for advancing durable, resilient and sustainable civil engineering.
- 18 February 2026
- Published by MDPI AG in Nanomaterials
- Vol. 16 (4) , 267
Open AccessResearch Progress on Nanopolymer Composites in Civil Engineering
Civil engineering infrastructure suffers material degradation, shortened service life and high maintenance costs under harsh environments and natural aging, threatening public safety. Nanopolymer composites, featuring designable microstructures and excellent macroscopic properties, provide a revolutionary solution to improve the weather resistance and toughness of civil engineering materials. This paper systematically clarifies the modification mechanisms of nanocomposites, focusing on nanofiller–polymer matrix interfacial interactions (physical adsorption, chemical bonding) and their synergistic effects in enhancing environmental aging resistance (UV, corrosion, freeze–thaw) and mechanical performance (toughening, strengthening, dynamic load resistance). It summarizes the latest applications in nanomodified protective coatings, sealing/bonding materials and composite structural components, revealing the inherent “structure-property-application” relationships. Furthermore, this paper addresses core large-scale application challenges, including technical bottlenecks, performance evaluation limitations and economic/environmental barriers. Finally, future research directions are proposed, covering multifunctional intelligent materials, green development, interdisciplinary computational methods and standardized systems. This review offers an integrated perspective, providing theoretical guidance and practical references for advancing durable, resilient and sustainable civil engineering.
- Open Access
- 12 September 2025
- Published by MDPI AG in Inorganics
- Vol. 13 (9) , 305
Advances in the Mechanism and Application of Nanoparticles in Concrete Property Modification
Nanoparticles leverage their unique nanoscale effects to optimize concrete performance through synergistic multi-mechanism interactions. Core mechanisms include micro-filling effects (graded pore filling, optimized pore structure), nucleation (promoting crystallization of hydration products, refining microstructure), chemical reactivity (e.g., pozzolanic reaction of nano-SiO2, enhancing interfacial transition zones), and interfacial strengthening (improving ITZ structure and stress transfer). Common nanomaterials (e.g., nano-SiO2, Al2O3, carbon nanotubes) significantly enhance concrete’s mechanical properties, durability, and functionalities (e.g., self-sensing, electromagnetic shielding). However, nano-modified concrete still faces challenges such as poor dispersion, high cost, and environmental/health risks. Future efforts should focus on multi-scale mechanism research, green low-cost synthesis processes, and intelligent composite systems development to advance the engineering applications pf nano-modified concrete.
- 12 September 2025
- Published by MDPI AG in Inorganics
- Vol. 13 (9) , 305
Open AccessAdvances in the Mechanism and Application of Nanoparticles in Concrete Property Modification
Nanoparticles leverage their unique nanoscale effects to optimize concrete performance through synergistic multi-mechanism interactions. Core mechanisms include micro-filling effects (graded pore filling, optimized pore structure), nucleation (promoting crystallization of hydration products, refining microstructure), chemical reactivity (e.g., pozzolanic reaction of nano-SiO2, enhancing interfacial transition zones), and interfacial strengthening (improving ITZ structure and stress transfer). Common nanomaterials (e.g., nano-SiO2, Al2O3, carbon nanotubes) significantly enhance concrete’s mechanical properties, durability, and functionalities (e.g., self-sensing, electromagnetic shielding). However, nano-modified concrete still faces challenges such as poor dispersion, high cost, and environmental/health risks. Future efforts should focus on multi-scale mechanism research, green low-cost synthesis processes, and intelligent composite systems development to advance the engineering applications pf nano-modified concrete.
- Open Access
- 16 May 2025
- Published by MDPI AG in Nanomaterials
- Vol. 15 (10) , 752
Preparation of g-C3N4/Co3O4/NS-CQDs Composite Materials and Their Application in the Detection of Hydrogen Peroxide and Glucose
G-C3N4, a biocompatible material, has prominent applications in biology and is ideal for nano-enzyme studies. Though reported as a peroxidase mimic, its activity remains low. This group combined N,S-doped carbon quantum dots (NS-CQDs) with g-C3N4 (7NSC-g), verifying its peroxidase-like activity. Based on this, a ternary composite of Co3O4 in different forms and 7NSC-g was developed to enhance peroxidase activity, to design a g-C3N4-based composite enzyme. Characterizations determined the composition and morphology. Colorimetry evaluated peroxidase activity, where the simulated enzyme catalyzes blue product formation from the TMB substrate in the presence of H2O2. UV-Vis spectrophotometry measured absorbance changes to determine target concentrations. The results show Co3O4 doping improves catalytic activity, with larger specific surface area providing more activation sites. The highest activity of g-C3N4/NS-CQDs/Co3O4 was at 5% floral Co3O4, being efficient due to Co3O4’s electron-transfer acceleration and hydroxyl-radical mechanism. Under optimal conditions, the composite detected H2O2 (10.0–230.0 μM, detection limit of 0.031 μM) and glucose (10.0–650.0 μM, detection limit of 1.024 μM).
- 16 May 2025
- Published by MDPI AG in Nanomaterials
- Vol. 15 (10) , 752
Open AccessPreparation of g-C3N4/Co3O4/NS-CQDs Composite Materials and Their Application in the Detection of Hydrogen Peroxide and Glucose
G-C3N4, a biocompatible material, has prominent applications in biology and is ideal for nano-enzyme studies. Though reported as a peroxidase mimic, its activity remains low. This group combined N,S-doped carbon quantum dots (NS-CQDs) with g-C3N4 (7NSC-g), verifying its peroxidase-like activity. Based on this, a ternary composite of Co3O4 in different forms and 7NSC-g was developed to enhance peroxidase activity, to design a g-C3N4-based composite enzyme. Characterizations determined the composition and morphology. Colorimetry evaluated peroxidase activity, where the simulated enzyme catalyzes blue product formation from the TMB substrate in the presence of H2O2. UV-Vis spectrophotometry measured absorbance changes to determine target concentrations. The results show Co3O4 doping improves catalytic activity, with larger specific surface area providing more activation sites. The highest activity of g-C3N4/NS-CQDs/Co3O4 was at 5% floral Co3O4, being efficient due to Co3O4’s electron-transfer acceleration and hydroxyl-radical mechanism. Under optimal conditions, the composite detected H2O2 (10.0–230.0 μM, detection limit of 0.031 μM) and glucose (10.0–650.0 μM, detection limit of 1.024 μM).
- Open Access
- 17 April 2025
- Published by MDPI AG in Inorganics
- Vol. 13 (4) , 124
Application of Fluorescent Probes for the Detection of Zinc Ions in Cells and Oil Paintings
Zinc is an essential trace metal element in the human body, but it also constitutes a variety of proteins in the body of the important elements necessary; this element plays an important role in physiological metabolism. Disturbances in the metabolism of zinc ions in the body can significantly threaten human health, especially neurological diseases. Therefore, developing a rapid and straightforward method for determining zinc ions is important. Fluorescent probe technology has been widely used for detecting and labeling zinc ions. Among many fluorescent probes, the rhodamine derivative LPDQ fluorescent probe has unique application scenarios, for example, it plays an important role in the detection of zinc white in oil colors, and its advantages are simplicity, rapidity, and real-time operation. This paper introduces the types of fluorescent probes for zinc ions and the three main mechanisms of fluorescent probe detection. The characteristics, design strategies, and application effects of the three fluorescent probes for zinc ions, as well as their advantages and limitations, are reviewed and summarized, which are intended to provide valuable references for the development of new probes for zinc ions detection in the future and for the future direction of research in this field.
- 17 April 2025
- Published by MDPI AG in Inorganics
- Vol. 13 (4) , 124
Open AccessApplication of Fluorescent Probes for the Detection of Zinc Ions in Cells and Oil Paintings
Zinc is an essential trace metal element in the human body, but it also constitutes a variety of proteins in the body of the important elements necessary; this element plays an important role in physiological metabolism. Disturbances in the metabolism of zinc ions in the body can significantly threaten human health, especially neurological diseases. Therefore, developing a rapid and straightforward method for determining zinc ions is important. Fluorescent probe technology has been widely used for detecting and labeling zinc ions. Among many fluorescent probes, the rhodamine derivative LPDQ fluorescent probe has unique application scenarios, for example, it plays an important role in the detection of zinc white in oil colors, and its advantages are simplicity, rapidity, and real-time operation. This paper introduces the types of fluorescent probes for zinc ions and the three main mechanisms of fluorescent probe detection. The characteristics, design strategies, and application effects of the three fluorescent probes for zinc ions, as well as their advantages and limitations, are reviewed and summarized, which are intended to provide valuable references for the development of new probes for zinc ions detection in the future and for the future direction of research in this field.
- Open Access
Shell-like ZnO–Graphene/Epoxy Coating with Outstanding Anticorrosion Performance and Weather Resistance
Throughout millions of years of biological evolution, shell structures have developed a highly complex layered organic–inorganic structure that makes them effective against a wide range of external impacts, including mechanical stress and chemical corrosion. Therefore, shell-like biomimetic materials are considered to possess high strength and toughness. Nevertheless, although shell structures have exhibited superior performance across multiple domains, understanding of their structural complexities and corrosion protection mechanisms remains relatively limited within the scope of human knowledge. In this study, alternating ZnO–graphene/epoxy coatings featuring shell-like structures were synthesized, and their anticorrosion properties were evaluated through the incorporation of ZnO to enhance the dispersion of graphene. Electrochemical impedance spectroscopy (EIS) tests showed that with an increased number of ZnO–graphene layers, the coating resistance of the bionic composite coating also increased: from 8.21 × 107 Ω·cm2 of the pure epoxy coating to 7.64 × 108 Ω cm2. The composite coating, comprising three alternating layers of zinc oxide and four layers of epoxy resin, exhibited an electrochemical impedance two orders of magnitude greater than that of pure epoxy resin following immersion in a 3.5% sodium chloride solution, demonstrating excellent corrosion resistance. The results showed that with increased ZnO–graphene layers, ZnO–graphene disperses more uniformly in water and has greater rigidity.
Open AccessShell-like ZnO–Graphene/Epoxy Coating with Outstanding Anticorrosion Performance and Weather Resistance
Throughout millions of years of biological evolution, shell structures have developed a highly complex layered organic–inorganic structure that makes them effective against a wide range of external impacts, including mechanical stress and chemical corrosion. Therefore, shell-like biomimetic materials are considered to possess high strength and toughness. Nevertheless, although shell structures have exhibited superior performance across multiple domains, understanding of their structural complexities and corrosion protection mechanisms remains relatively limited within the scope of human knowledge. In this study, alternating ZnO–graphene/epoxy coatings featuring shell-like structures were synthesized, and their anticorrosion properties were evaluated through the incorporation of ZnO to enhance the dispersion of graphene. Electrochemical impedance spectroscopy (EIS) tests showed that with an increased number of ZnO–graphene layers, the coating resistance of the bionic composite coating also increased: from 8.21 × 107 Ω·cm2 of the pure epoxy coating to 7.64 × 108 Ω cm2. The composite coating, comprising three alternating layers of zinc oxide and four layers of epoxy resin, exhibited an electrochemical impedance two orders of magnitude greater than that of pure epoxy resin following immersion in a 3.5% sodium chloride solution, demonstrating excellent corrosion resistance. The results showed that with increased ZnO–graphene layers, ZnO–graphene disperses more uniformly in water and has greater rigidity.