Jingjing Du
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Jingjing Du has a total of 36 co-authors. Here are the top co-authors by number of shared publications:
- Jinpu Xie
School of Packaging Engineering, Hunan University of Technology, Zhuzhou 412007, China
3 shared publications - Lijian Xu
School of Biological Science and Medical Engineering, Hunan University of Technology, Zhuzhou 412007, China
3 shared publications - Pingping Yang
School of Biological Science and Medical Engineering, Hunan University of Technology, Zhuzhou 412007, China
3 shared publications - Yukun Tang
School of Packaging Engineering, Hunan University of Technology, Zhuzhou 412007, China
3 shared publications - Tengfei Duan
School of Materials Science and Engineering, Hunan University of Technology, Zhuzhou 412007, China
2 shared publications - Yinchen Liu
College of Science and Technology, Hunan University of Technology, Zhuzhou 412007, China
2 shared publications
Latest Publications
- Open Access
A Novel Dopamine Electrochemical Sensor Based on Pt/CNTs-N-S/Electrode
Dopamine (DA) plays an extremely crucial role in the metabolic processes of the human body. Accurate detection of DA is of great significance for many major diseases. This study reports an innovative synthesis method for composite material in which sulfur (S) and nitrogen (N) are incorporated into multi-walled carbon nanotubes (MWCNTs), and platinum (Pt) nanoparticle sensors (Pt/CNTs-N-S) are loaded for the highly sensitive and selective electrochemical detection of DA. The linear range of this sensor is from 0.0078 to 2 mM, and the limit of detection (LOD) is 0.73 μM (S/N = 3) for DA detection. The outstanding detection performance exhibited by Pt/CNTs-N-S is mainly attributed to the co-doping of N and S, which improves the surface properties of MWCNTs, and the dispersion of Pt nanoparticles (5.22 nm), which significantly increases the electrochemically active surface area (ESCA). In addition, the Pt/CNTs-N-S sensor also exhibits excellent stability and anti-interference performance. Overall, this study provides a simple and practical strategy for the potential application of Pt-based sensors in the detection of DA.
Open AccessA Novel Dopamine Electrochemical Sensor Based on Pt/CNTs-N-S/Electrode
Dopamine (DA) plays an extremely crucial role in the metabolic processes of the human body. Accurate detection of DA is of great significance for many major diseases. This study reports an innovative synthesis method for composite material in which sulfur (S) and nitrogen (N) are incorporated into multi-walled carbon nanotubes (MWCNTs), and platinum (Pt) nanoparticle sensors (Pt/CNTs-N-S) are loaded for the highly sensitive and selective electrochemical detection of DA. The linear range of this sensor is from 0.0078 to 2 mM, and the limit of detection (LOD) is 0.73 μM (S/N = 3) for DA detection. The outstanding detection performance exhibited by Pt/CNTs-N-S is mainly attributed to the co-doping of N and S, which improves the surface properties of MWCNTs, and the dispersion of Pt nanoparticles (5.22 nm), which significantly increases the electrochemically active surface area (ESCA). In addition, the Pt/CNTs-N-S sensor also exhibits excellent stability and anti-interference performance. Overall, this study provides a simple and practical strategy for the potential application of Pt-based sensors in the detection of DA.
- Open Access
An Ultrasensitive Electrochemical Sensor Pd/MWCNTs-N-S for Detection of Dopamine
Dopamine (DA) is an important catecholamine neurotransmitter in human metabolism that is associated with various critical diseases. Accurate detection of DA is of great significance for the diagnosis of these diseases. Here, we constructed a sensitive electrochemical sensor, S, N co-doped multi-walled carbon nanotubes (MWCNTs-N-S) loaded with Pd nanoparticles (Pd/MWCNTs-N-S). The linear range of the Pd/MWCNTs-N-S sensor is from 0.0001 to 2.0 mM, and the limit of detection (LOD) is 4.37 nM (S/N = 3) for DA detection. The improved detection performance of this sensor is attributed to the optimization of MWCNTs carrier structure and surface properties by N, S co-doping, as well as the significant improvement of electrochemical surface area (ECSA) for the commendable dispersion of Pd nanoparticles (3.79 nm). What is more, the Pd/MWCNTs-N-S sensor also exhibits good reproducibility, stability, and anti-interference ability. Overall, this study presents a straightforward strategy for the potential applications of Pd-based double co-doped MWCNTs sensors.
Open AccessAn Ultrasensitive Electrochemical Sensor Pd/MWCNTs-N-S for Detection of Dopamine
Dopamine (DA) is an important catecholamine neurotransmitter in human metabolism that is associated with various critical diseases. Accurate detection of DA is of great significance for the diagnosis of these diseases. Here, we constructed a sensitive electrochemical sensor, S, N co-doped multi-walled carbon nanotubes (MWCNTs-N-S) loaded with Pd nanoparticles (Pd/MWCNTs-N-S). The linear range of the Pd/MWCNTs-N-S sensor is from 0.0001 to 2.0 mM, and the limit of detection (LOD) is 4.37 nM (S/N = 3) for DA detection. The improved detection performance of this sensor is attributed to the optimization of MWCNTs carrier structure and surface properties by N, S co-doping, as well as the significant improvement of electrochemical surface area (ECSA) for the commendable dispersion of Pd nanoparticles (3.79 nm). What is more, the Pd/MWCNTs-N-S sensor also exhibits good reproducibility, stability, and anti-interference ability. Overall, this study presents a straightforward strategy for the potential applications of Pd-based double co-doped MWCNTs sensors.
- Open Access
Unique Four-Layer Core–Shell NaYF4:Yb3+,Er3+@NaYF4@CdS@Au Nanocomposites for Enhanced Full-Spectrum Photocatalytic Degradation of Rhodamine B
In recent years, cadmium sulfide (CdS) has been widely investigated due to its excellent photocatalytic performance. However, its practical application in pollutant treatment is limited by its narrow photoresponse range and susceptibility to photocorrosion. Herein, we design a unique four-layer core–shell structure NaYF4:Yb3+,Er3+@NaYF4@CdS@Au (CSNPs@CdS@Au), with an inert NaYF4 shell coating on NaYF4:Yb3+,Er3+ (CNPs) to form NaYF4:Yb3+,Er3+@NaYF4 (CSNPs) and CdS depositing on CSNPs (CSNPs@CdS); Au nanoparticles are loaded on CdS (CSNPs@CdS@Au). Compared with CdS (9.81%), CSNPs (5.0%), CSNPs/CdS (6.9%), and CSNPs@CdS (81.0%), CSNPs@CdS@Au degrades 97.7% Rhodamine B (RhB) within 15 min, exhibiting superior photocatalytic performance, attributable to two key factors: (1) the NaYF4 inert shell encapsulation amplifies upconversion (UC) luminescence intensity by suppressing surface quenching; and (2) the electron transfer between Au nanoparticles and CdS effectively promotes spatial separation of photogenerated charge carriers and increases reactive active sites. Additionally, after five degradation cycles, CSNPs@CdS@Au still maintains a 93.25% degradation rate for RhB, confirming its excellent stability. This remarkable stability is attributed to the uniquely designed multilayer core–shell architecture, which significantly enhances structural integrity through physical isolation effects. This study establishes a material preparation strategy for efficient photocatalytic pollutant degradation.
Open AccessUnique Four-Layer Core–Shell NaYF4:Yb3+,Er3+@NaYF4@CdS@Au Nanocomposites for Enhanced Full-Spectrum Photocatalytic Degradation of Rhodamine B
In recent years, cadmium sulfide (CdS) has been widely investigated due to its excellent photocatalytic performance. However, its practical application in pollutant treatment is limited by its narrow photoresponse range and susceptibility to photocorrosion. Herein, we design a unique four-layer core–shell structure NaYF4:Yb3+,Er3+@NaYF4@CdS@Au (CSNPs@CdS@Au), with an inert NaYF4 shell coating on NaYF4:Yb3+,Er3+ (CNPs) to form NaYF4:Yb3+,Er3+@NaYF4 (CSNPs) and CdS depositing on CSNPs (CSNPs@CdS); Au nanoparticles are loaded on CdS (CSNPs@CdS@Au). Compared with CdS (9.81%), CSNPs (5.0%), CSNPs/CdS (6.9%), and CSNPs@CdS (81.0%), CSNPs@CdS@Au degrades 97.7% Rhodamine B (RhB) within 15 min, exhibiting superior photocatalytic performance, attributable to two key factors: (1) the NaYF4 inert shell encapsulation amplifies upconversion (UC) luminescence intensity by suppressing surface quenching; and (2) the electron transfer between Au nanoparticles and CdS effectively promotes spatial separation of photogenerated charge carriers and increases reactive active sites. Additionally, after five degradation cycles, CSNPs@CdS@Au still maintains a 93.25% degradation rate for RhB, confirming its excellent stability. This remarkable stability is attributed to the uniquely designed multilayer core–shell architecture, which significantly enhances structural integrity through physical isolation effects. This study establishes a material preparation strategy for efficient photocatalytic pollutant degradation.
- Open Access
- 17 December 2019
- Published by MDPI AG in Nanomaterials
- Vol. 9 (12) , 1795
Electrodeposition of Ti-Doped Hierarchically Mesoporous Silica Microspheres/Tungsten Oxide Nanocrystallines Hybrid Films and Their Electrochromic Performance
In this paper, a novel Ti-doped hierarchically mesoporous silica microspheres/tungsten oxide (THMS/WO3) hybrid film was prepared by simultaneous electrodeposition of Ti-doped hierarchically mesoporous silica microspheres (THMSs) and WO3 nanocrystallines onto the fluoride doped tin dioxide (FTO) coated glass substrate. It is demonstrated that the incorporation of THMSs resulted in the hybrid film with improved electrochromic property. Besides, the content of THMSs plays an important role on the electrochromic property of the hybrid film. An excellent electrochromic THMS/WO3 hybrid film with good optical modulation (52.00% at 700 nm), high coloration efficiency (88.84 cm2 C−1 at 700 nm), and superior cycling stability can be prepared by keeping the weight ratio of Na2WO4·2H2O (precursor of WO3):THMSs at 15:1. The outstanding electrochromic performances of the THMS/WO3 hybrid film were mainly attributed to the porous structure, which facilitates the charge-transfer, promotes the electrolyte infiltration and alleviates the expansion of the film during Li+ insertion. This kind of porous THMS/WO3 hybrid film is promising for a wide range of applications in smart homes, green buildings, airplanes, and automobiles.
- 17 December 2019
- Published by MDPI AG in Nanomaterials
- Vol. 9 (12) , 1795
Open AccessElectrodeposition of Ti-Doped Hierarchically Mesoporous Silica Microspheres/Tungsten Oxide Nanocrystallines Hybrid Films and Their Electrochromic Performance
In this paper, a novel Ti-doped hierarchically mesoporous silica microspheres/tungsten oxide (THMS/WO3) hybrid film was prepared by simultaneous electrodeposition of Ti-doped hierarchically mesoporous silica microspheres (THMSs) and WO3 nanocrystallines onto the fluoride doped tin dioxide (FTO) coated glass substrate. It is demonstrated that the incorporation of THMSs resulted in the hybrid film with improved electrochromic property. Besides, the content of THMSs plays an important role on the electrochromic property of the hybrid film. An excellent electrochromic THMS/WO3 hybrid film with good optical modulation (52.00% at 700 nm), high coloration efficiency (88.84 cm2 C−1 at 700 nm), and superior cycling stability can be prepared by keeping the weight ratio of Na2WO4·2H2O (precursor of WO3):THMSs at 15:1. The outstanding electrochromic performances of the THMS/WO3 hybrid film were mainly attributed to the porous structure, which facilitates the charge-transfer, promotes the electrolyte infiltration and alleviates the expansion of the film during Li+ insertion. This kind of porous THMS/WO3 hybrid film is promising for a wide range of applications in smart homes, green buildings, airplanes, and automobiles.