Query：
学者姓名：池毓务
Refining：
Year
Type
Indexed by
Source
Complex
Former Name
Co-
Language
Clean All
Abstract ：
Tris(2,2 '-bipyridine)ruthenium(II) ([Ru(bpy)3]2+), as a versatile molecule, has been widely applied in various fields, such as photocatalysis, electrochemiluminescence and fluorescence probes, solar cell and LED due to its excellent optical and electrical properties, good water solubility, high chemical stability. In this work, we prepared electrostatic nanoaggregates from [Ru(bpy)3]2+ and silver nanoparticles (AgNPs@[Ru(bpy)3]2+ ENAs) as a new type of SERS nanotags. Each [Ru(bpy)3]2+ ion carries two positive charges with strong affinity to negative surfaces, which enables a strong electrostatic interaction between [Ru(bpy)3]2+ and negatively charged silver nanoparticles (AgNPs) and fast (within 10 min) formation of AgNPs@[Ru(bpy)3]2+ ENAs. The prepared AgNPs@ [Ru(bpy)3]2+ ENAs had a very strong and stable SERS activity due to abundant bipyridine molecules in [Ru (bpy)3]2+ and the location of many [Ru(bpy)3]2+ SERS reporters at the electromagnetic "hot spots" (i.e. the junction of two adjacent AgNPs), and thus could act as novel and excellent SERS nanotags. Further conjugated with antibodies, AgNPs@[Ru(bpy)3]2+ nanotags were used to develop new SERS-based immunochromatography test strips (SERS-ICTSs), showing excellent sensing performances. The AgNPs@[Ru(bpy)3]2+ ENAs based SERSICTSs not only inherit the merit of fast and visualize quantitative analysis from traditional ICTSs, but also realize much more sensitive biosensing (with detection limit of 25 pg/mL HCG) using the SERS technology.
Keyword ：
Electrostatic aggregation Electrostatic aggregation Immunoassay Immunoassay Raman spectroscopy Raman spectroscopy SERS SERS Silver nanoparticles Silver nanoparticles Tris(2,2 '-bipyridine)ruthenium(II) Tris(2,2 '-bipyridine)ruthenium(II)
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Zheng, Danmin , Hu, Doudou , Shao, Jiwei et al. Tris(2,2′-bipyridine)ruthenium(II)-silver nanoparticle electrostatic nanoaggregates (AgNPs@[Ru(bpy)3]2+ENAs) as novel SERS nanotags for rapid, sensitive and selective immunosensing [J]. | TALANTA , 2025 , 285 . |
| MLA | Zheng, Danmin et al. "Tris(2,2′-bipyridine)ruthenium(II)-silver nanoparticle electrostatic nanoaggregates (AgNPs@[Ru(bpy)3]2+ENAs) as novel SERS nanotags for rapid, sensitive and selective immunosensing" . | TALANTA 285 (2025) . |
| APA | Zheng, Danmin , Hu, Doudou , Shao, Jiwei , Chi, Yuwu . Tris(2,2′-bipyridine)ruthenium(II)-silver nanoparticle electrostatic nanoaggregates (AgNPs@[Ru(bpy)3]2+ENAs) as novel SERS nanotags for rapid, sensitive and selective immunosensing . | TALANTA , 2025 , 285 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
The sensitive detection of glutathione (GSH) level is of great significance to disease diagnosis. However, commonly used fluorometry method usually suffers from limited sensitivity, potential interferences and inefficient detection. In this work, a smartphone-assisted and perovskite-based sensing platform for dual-readout detection of GSH was developed: the silica coated perovskite quantum dots (PQD@SiO2) with a single particle level and high fluorescence efficiency were employed as fluorophore, which greatly avoids aggregation-caused quenching effect caused by multi-particles embedded in one SiO2 shell, and the manganese dioxide (MnO2) nanosheets were used as quencher. With the addition of GSH, the fluorescence intensity of PQD@SiO2-MnO2 composites gradually enhances, while the color of solution turns from dark brown to light yellow under sunlight, which enables the dual-signal (fluorescence and colorimetric) and reliable detection of GSH level. In addition, the introduction of smartphones integrated image recording and data processing, further promotes the simple, visualized, cost-effective and real-time determination of GSH. The synthesis of PQD@SiO2 at a single particle level, as well as the strategies of dual-mode and smartphone-assisted detection, holds the promising prospect in biosensing and chemical sensing.
Keyword ：
Dual-mode detection Dual-mode detection Glutathione Glutathione Silica coated perovskite quantum dots Silica coated perovskite quantum dots Single particle level Single particle level Smartphone-assisted sensing platform Smartphone-assisted sensing platform
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Chen, Jie , Wu, Haishan , Zhang, Weiwei et al. Silica coated perovskite quantum dots with single-particle level for dual-mode and smartphone-assisted detection of glutathione [J]. | SENSORS AND ACTUATORS B-CHEMICAL , 2025 , 432 . |
| MLA | Chen, Jie et al. "Silica coated perovskite quantum dots with single-particle level for dual-mode and smartphone-assisted detection of glutathione" . | SENSORS AND ACTUATORS B-CHEMICAL 432 (2025) . |
| APA | Chen, Jie , Wu, Haishan , Zhang, Weiwei , Huang, Yun , Zheng, Jingcheng , Shao, Jiwei et al. Silica coated perovskite quantum dots with single-particle level for dual-mode and smartphone-assisted detection of glutathione . | SENSORS AND ACTUATORS B-CHEMICAL , 2025 , 432 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Dichloromethane (DCM), which is a widely used organic solvent in industrial production, is currently classified as a Class 2A carcinogen. Considering its potential harm to human health, it is necessary to design a convenient and economical method to monitor the concentration of DCM in the environment in real time. Here, we present a visualized fluorescence sensor for DCM utilizing photochromic CsPbBr3 perovskite nanocrystals (PNCs). By measuring the amount of chloride ions dissociated from DCM under 365 nm UV light catalysis, the resulting ion exchange products of CsPbBr3-xClx exhibit distinct fluorescence colors based on the halogen ratio, enabling visual detection. In addition, we have observed a linear relationship between the concentration of DCM and the wavelength shift difference of PNCs after a 30 min 365 nm UV exposure, within the DCM concentration range of 1-20% (0.16-3.11 mM). And the limit of detection was calculated to be 0.29%. We have successfully utilized this sensor to detect the concentration of DCM in laboratory waste liquid, achieving a high recovery rate. This application is beneficial for long-term laboratory personnel to promptly identify the source of harmful gases, thereby significantly contributing to the maintenance of laboratory safety and physical health.
Keyword ：
dichloromethane dichloromethane fluorescent sensor fluorescent sensor perovskite perovskite photochromism photochromism visualized detection visualized detection
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Zheng, Jingcheng , He, Hao , Chen, Jie et al. Visualized Fluorescence Sensor for Dichloromethane Based on Photochromic Perovskite Nanocrystals [J]. | ACS APPLIED NANO MATERIALS , 2024 , 7 (18) : 21463-21470 . |
| MLA | Zheng, Jingcheng et al. "Visualized Fluorescence Sensor for Dichloromethane Based on Photochromic Perovskite Nanocrystals" . | ACS APPLIED NANO MATERIALS 7 . 18 (2024) : 21463-21470 . |
| APA | Zheng, Jingcheng , He, Hao , Chen, Jie , Sun, Ruifen , Zhang, Weiwei , Huang, Yun et al. Visualized Fluorescence Sensor for Dichloromethane Based on Photochromic Perovskite Nanocrystals . | ACS APPLIED NANO MATERIALS , 2024 , 7 (18) , 21463-21470 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Acute myocardial infarction (AMI) is one of the leading causes of human mortality worldwide. In the early stages of AMI, the patient's electrocardiogram (ECG) may not change, so the fast, sensitive, and accurate detection of the specific biomarker of cardiac troponin I (cTnI) is of great importance in the early diagnosis of AMI. In this work, for the first time, electrostatic nanoaggregates of negatively charged Au nanoparticles and positively charged trisbipyridine ruthenium(II) ions (i.e., (-)AuNPs|[Ru(bpy)(3)](2+) ENAs) as novel and signal-amplifying surface-enhanced Raman scattering (SERS) tags were synthesized in an easy and rapid (<3 min) way and applied in the highly sensitive, rapid detection of cTnI in human serum by being combined with an immunochromatographic test strip (ICTS). The synthesized (-)AuNPs|[Ru(bpy)(3)](2+) ENAs exhibited strong SERS activity due to the multiple Raman-active units (three bpy ligands) carried by each [Ru(bpy)(3)](2+) complex ion and abundant hotspots in each SERS tag. The developed (-)AuNPs|[Ru(bpy)(3)](2+) ENAs-based SERS-ICTS has been validated to be applicable in detection of cTnI in human serum with excellent sensing performances, such as fast testing (5 min) and a low detection limit (60 pg/mL). It is envisioned that the developed (-)AuNPs|[Ru(bpy)(3)](2+) ENAs-based SERS-ICTS sensor may have promising applications in point of care testing of various biomarkers in clinic. Additionally, this work may inspire the finding and the application of new types of Raman reporter molecules based on high valent metal-multi ligand coordination compounds like [Ru(bpy)(3)](2+).
Keyword ：
Cardiac troponin I Cardiac troponin I Electrostatic interaction Electrostatic interaction Gold nanoparticle Gold nanoparticle Immunoassay Immunoassay Nanoaggregate Nanoaggregate Raman Raman Test strip Test strip Trisbipyridine ruthenium(II) Trisbipyridine ruthenium(II)
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Shao, Jiwei , Zhang, Weiwei , Huang, Yun et al. Au Nanoparticles-Trisbipyridine Ruthenium(II) Nanoaggregates as Signal-Amplifying SERS Tags for Immunoassay of cTnI [J]. | ACS APPLIED MATERIALS & INTERFACES , 2024 , 16 (45) : 61703-61713 . |
| MLA | Shao, Jiwei et al. "Au Nanoparticles-Trisbipyridine Ruthenium(II) Nanoaggregates as Signal-Amplifying SERS Tags for Immunoassay of cTnI" . | ACS APPLIED MATERIALS & INTERFACES 16 . 45 (2024) : 61703-61713 . |
| APA | Shao, Jiwei , Zhang, Weiwei , Huang, Yun , Zheng, Jingcheng , Chi, Yuwu . Au Nanoparticles-Trisbipyridine Ruthenium(II) Nanoaggregates as Signal-Amplifying SERS Tags for Immunoassay of cTnI . | ACS APPLIED MATERIALS & INTERFACES , 2024 , 16 (45) , 61703-61713 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Self-enhanced electrochemiluminescence (ECL) probes have attracted more and more attention in analytical chemistry for their significant simplification of the ECL sensing operation while improving the ECL sensing sensitivity. However, the development and applications of self-enhanced ECL probes are still in their infancy and mainly suffer from the requirement of a complicated synthesis strategy and relatively low self-enhanced ECL activity. In this work, we took advantage of the recently emerged perovskite quantum dots (PQDs) with high optical quantum yields and easy surface engineering to develop a new type of PQD-based self-enhanced ECL system. The long alkyl chain (C-18) diethanolamine (i.e., N-octadecyldiethanolamine (ODA)) with high ECL coreactant activity was selected as a capping ligand to synthesize an ODA-capped PQD self-enhanced ECL probe. The preparation of the coreactant-capped PQDs is as simple as for the ordinary oleylamine (OAm)-capped PQDs, and the obtained ODA-capped PQDs exhibit very strong self-enhanced ECL activity, 82.5 times higher than that of traditional OAm-capped PQDs. Furthermore, the prepared ODA-PQDs have a unique nanostructure (ODA-CsPbBr3@CsPb2Br5), with the highly emissive 3D CsPbBr3 PQD as the core and the water-stable 2D CsPb2Br5 as the shell, which allows ODA-PQDs to be very stable in aqueous media. It is envisioned that the prepared ODA-3D@2D PQDs with the easy preparation method, strong self-enhanced ECL, and excellent water stability have promising applications in ECL sensing.
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Sun, Ruifen , Xiong, Shuyun , Zhang, Weiwei et al. Highly Active Coreactant-Capped and Water-Stable 3D@2D Core-Shell Perovskite Quantum Dots as a Novel and Strong Self-Enhanced Electrochemiluminescence Probe [J]. | ANALYTICAL CHEMISTRY , 2024 , 96 (14) : 5711-5718 . |
| MLA | Sun, Ruifen et al. "Highly Active Coreactant-Capped and Water-Stable 3D@2D Core-Shell Perovskite Quantum Dots as a Novel and Strong Self-Enhanced Electrochemiluminescence Probe" . | ANALYTICAL CHEMISTRY 96 . 14 (2024) : 5711-5718 . |
| APA | Sun, Ruifen , Xiong, Shuyun , Zhang, Weiwei , Huang, Yun , Zheng, Jingcheng , Shao, Jiwei et al. Highly Active Coreactant-Capped and Water-Stable 3D@2D Core-Shell Perovskite Quantum Dots as a Novel and Strong Self-Enhanced Electrochemiluminescence Probe . | ANALYTICAL CHEMISTRY , 2024 , 96 (14) , 5711-5718 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Fluorescent immunochromatographic test (FICT) strips have received extensive attention due to their virtue of simple operation, low cost, and a point-of-care (POC) assay. In recent years, people are constantly seeking new labels to improve the sensitivity of immunosensors. Perovskite nanocrystals (PNCs) possess strong fluorescence and a narrow emission peak, making them an excellent choice as a new fluorescent signal label. Herein, we have developed a simple, fast, and environmentally friendly method to synthesize CsPbBr 3 /CsPb 2 Br 5 @SiO 2 with the good water stability and high biocompatibility. These CsPbBr 3 /CsPb 2 Br 5 @SiO 2 have been applied to construct FICT strips. To achieve the quantitative determination of human chorionic gonadotropin (HCG), a lab-made FICT strips detection system was established. The FICT strips had a good linear relationship to HCG in the range of 5 -500 ng/mL, and the detection limit was 2.09 ng/mL. In addition, the recovery results of HCG detection in human urine samples also proved the feasibility of this FICT strips. CsPbBr 3 /CsPb 2 Br 5 @SiO 2 can also be modified with different biomarkers for functionalization, which exhibits a promising application in the development of sensing platform of FICT strips.
Keyword ：
Fluorescent immunochromatographic test Fluorescent immunochromatographic test HCG detection HCG detection Perovskite Perovskite Sensor Sensor strips strips
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Zheng, Jingcheng , Chen, Jie , Sun, Ruifen et al. A fluorescent immunochromatographic strip based on CsPbBr 3 / CsPb 2 Br 5 @SiO 2 facile encapsulation in pure water for the detection of human chorionic gonadotropin (HCG) antigen [J]. | SENSORS AND ACTUATORS B-CHEMICAL , 2024 , 410 . |
| MLA | Zheng, Jingcheng et al. "A fluorescent immunochromatographic strip based on CsPbBr 3 / CsPb 2 Br 5 @SiO 2 facile encapsulation in pure water for the detection of human chorionic gonadotropin (HCG) antigen" . | SENSORS AND ACTUATORS B-CHEMICAL 410 (2024) . |
| APA | Zheng, Jingcheng , Chen, Jie , Sun, Ruifen , Zhang, Weiwei , Huang, Yun , Shao, Jiwei et al. A fluorescent immunochromatographic strip based on CsPbBr 3 / CsPb 2 Br 5 @SiO 2 facile encapsulation in pure water for the detection of human chorionic gonadotropin (HCG) antigen . | SENSORS AND ACTUATORS B-CHEMICAL , 2024 , 410 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Recently emerging perovskite nanocrystals (PNCs) are very attractive fluorescence nanomaterials due to their very narrow emission peak, tunable wavelength, and extremely high quantum yield, but their chemosensing, biosensing and bioimaging applications suffer from the poor stability of ordinary PNCs in aqueous media, especially in biological matrices. Recently developed water-stable 2D CsPb2Br5-encapsulated 3D CsPbBr3 PNCs (i.e., CsPbBr3/CsPb2Br5 PNCs) show extremely stable light emission in pure water, but their fluorescence is seriously quenched in aqueous media containing biological molecules due to their chemical reactions. In this work, we used a facile method to encapsulate pure water-stable CsPbBr3/CsPb2Br5 PNCs in water with SiO2 and polyethylene glycol hexadecyl ether (Brij58) into a new kind of biological environment-stable PNCs (CsPbBr3/CsPb2Br5@SiO2-Brij58). The synthesis of the target PNCs can be accomplished in a fast, easy, and green way. The obtained CsPbBr3/CsPb2Br5@SiO2-Brij58 PNCs maintain strong fluorescence emission for a long time, all in pH 7.4 PBS, BSA, and minimum essential medium, exhibiting excellent biological environment stability. Moreover, the developed biological environment-stable PNCs show good biocompatibility and have been successfully used in cell imaging. Overall, the work provides an easy, low-cost, and efficient application of PNCs in bioimaging.
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Zheng, Jingcheng , Zhang, Weiwei , Huang, Yun et al. Encapsulation of Pure Water-Stable Perovskite Nanocrystals (PNCs) into Biological Environment-Stable PNCs for Cell Imaging [J]. | INORGANIC CHEMISTRY , 2024 , 63 (12) : 5623-5633 . |
| MLA | Zheng, Jingcheng et al. "Encapsulation of Pure Water-Stable Perovskite Nanocrystals (PNCs) into Biological Environment-Stable PNCs for Cell Imaging" . | INORGANIC CHEMISTRY 63 . 12 (2024) : 5623-5633 . |
| APA | Zheng, Jingcheng , Zhang, Weiwei , Huang, Yun , Shao, Jiwei , Khan, Malik Saddam , Chi, Yuwu . Encapsulation of Pure Water-Stable Perovskite Nanocrystals (PNCs) into Biological Environment-Stable PNCs for Cell Imaging . | INORGANIC CHEMISTRY , 2024 , 63 (12) , 5623-5633 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Excessive ultraviolet (UV) radiation has serious damage to human's health, therefore the development of visible, portable, and wearable sensor for monitoring UV radiation, especially the cumulative UV dosage, is highly desired but full of challenges. Herein, a wearable and flexible UV dosimeter based on photochromic perovskite nanocrystals (PNCs) is designed. The obtained CsPbCl3 PNCs dispersed in dibromomethane (PNCs-DBM) undergo continuous, vivid, and multiple (from very weak purple to blue, cyan, and finally strong green) color change in response to UV radiation. It is demonstrated that the UV-induced degradation of DBM and subsequent anion-exchange reaction between CsPbCl3 and Br-, play a crucial role in the color change of PNCs-DBM. The properties of continuous fluorescence color change and enhanced fluorescence intensity enable the construction of sensitive and visible UV dosimeter. Furthermore, by integrated photochromic PNCs with flexible bracelet or PDMS substrate, a wearable UV sensor or a multi-indicator array for the detection of solar UV dosage is developed. This work may advance the fundamental understanding about photochromic perovskite, and show promising application of perovskite nanomaterials in easily fabricated, low-cost, visualized, and wearable solar UV dosimeter. Traditional photochromic materials may be used to detect UV intensity rather than UV dose due to single color transformation upon sustained UV exposure. The photochromic perovskite-dibromomethane system can undergo continuous, real-time, very wide range and sensitive color change with increasing UV dose, which shows a very promising application of PNCs in developing wearable sensor for detection of solar UV dose. image
Keyword ：
anion-exchange anion-exchange flexible multi-indicator array flexible multi-indicator array photochromic perovskite nanocrystals photochromic perovskite nanocrystals UV dosage UV dosage wearable UV sensor wearable UV sensor
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Chen, Jie , Sun, Ruifen , Zheng, Jingcheng et al. Photochromic Perovskite Nanocrystals for Ultraviolet Dosimetry [J]. | SMALL , 2024 , 20 (29) . |
| MLA | Chen, Jie et al. "Photochromic Perovskite Nanocrystals for Ultraviolet Dosimetry" . | SMALL 20 . 29 (2024) . |
| APA | Chen, Jie , Sun, Ruifen , Zheng, Jingcheng , Zhang, Weiwei , Huang, Yun , Shao, Jiwei et al. Photochromic Perovskite Nanocrystals for Ultraviolet Dosimetry . | SMALL , 2024 , 20 (29) . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
The intrinsic instability of halide perovskites toward to external stimulus, has created a competitive advantage for designing stimuli-responsive materials. However, the external environment tuning reversibly fluorescence emission of perovskite system is still limited. In this work, humidity is verified to act as a new option to modulate the emission properties of mixed-halide perovskite. The perovskite nanocrystals (PNCs) photoirradiated in dichloromethane are easily and stably redispersed in water, and emit bright fluorescence which is quite different from the original. Moreover, the perovskites confined on glass slide can reversibly switch their fluorescence between blue and green colors under moisture. It is demonstrated that the factors of different solubilities of CsCl and CsBr in water, the structural transformation of perovskites and the confine of glass matrix play key roles in the reversible transformation. Finally, the combination of hydrochromic CsPb(BrxCly)(3) and water-resistant CsPb(BrxCly)(3)-polymethyl methacrylate have been applied in advanced anti-counterfeiting, which greatly improves the information security. This work not only give an insight into the effects of humidity on fluorescence and structures of PNCs, but also offer a new class of hydrochromic PNCs materials based on reversible emission transformation for potential application in sensors, anti-counterfeiting and information encryption.
Keyword ：
anti-counterfeiting anti-counterfeiting hydrochromic hydrochromic ion migration ion migration mixed-halide perovskite mixed-halide perovskite photoirradiated perovskite-dichloromethane photoirradiated perovskite-dichloromethane
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Chen, Jie , Zeng, Yiwen , Sun, Ruifen et al. Hydrochromic Perovskite System with Reversible Blue-Green Color for Advanced Anti-Counterfeiting [J]. | SMALL , 2023 , 19 (33) . |
| MLA | Chen, Jie et al. "Hydrochromic Perovskite System with Reversible Blue-Green Color for Advanced Anti-Counterfeiting" . | SMALL 19 . 33 (2023) . |
| APA | Chen, Jie , Zeng, Yiwen , Sun, Ruifen , Zhang, Weiwei , Huang, Yun , Zheng, Jingcheng et al. Hydrochromic Perovskite System with Reversible Blue-Green Color for Advanced Anti-Counterfeiting . | SMALL , 2023 , 19 (33) . |
| Export to | NoteExpress RIS BibTex |
Version ：
Abstract ：
Recently,the newly emerging lead halide perovskite nanocrystals(PNCs) have been intensely researched in many fields, such as light-emittingdiodes (LEDs), solar cells, lasers, and display devices. The extremelyhigh fluorescence quantum yield (near 100%) of PNCs over classic fluorescentmaterials would enable good applications of PNCs in sensing. However,the study on PNCs for bio- and chemical sensing, especially for detectingtargets that exist in aqueous medium, faces great challenges due tothe well-known instability of PNCs in polar solvents, especially water.Although the encapsulation of polymers or inorganic materials canefficiently protect PNCs from decomposition in aqueous solution, thesensing based on the interaction between PNCs and targets is severelyhindered by the compact protection coating at the surfaces of PNCs.In this work, novel water-dispersed PNCs (W-PNCs), i.e., CsPbBr3@CsPb2Br5 PNCs, with strong fluorescenceand excellent water stability were synthesized from OAm-capped CsPbBr3 PNCs by a simple "oil-solid-water"phase transition. The W-PNCs without being encapsulated with compactpolymers or inorganic materials can sensitively and stably sense targetsin the pure water phase via direct chemical reactions. For the firsttime, ion exchanges between PNCs and halide ions and their effectson the fluorescence wavelength of PNCs were investigated in the purewater phase, on the basis of which a new, visualized, selective, andsensitive smartphone-based sensing platform for halide ions has beenestablished by the integration of the conveniently prepared W-PNCnanoprobe and the portable mobile phone. It is envisioned that theuncoated but extremely water-stable and highly fluorescent W-PNCshave promising applications in chemical sensing, biosensing, and bioimagingof targets in aqueous medium.
Cite：
Copy from the list or Export to your reference management。
| GB/T 7714 | Chen, Jie , Shao, Jiwei , Sun, Ruifen et al. Anion Exchanges of Water-Stable Perovskite Nanocrystals in the Pure Water Phase and Applications in Detecting Halide Ions via a Smartphone-Based Sensing Platform [J]. | ANALYTICAL CHEMISTRY , 2023 , 95 (31) : 11839-11848 . |
| MLA | Chen, Jie et al. "Anion Exchanges of Water-Stable Perovskite Nanocrystals in the Pure Water Phase and Applications in Detecting Halide Ions via a Smartphone-Based Sensing Platform" . | ANALYTICAL CHEMISTRY 95 . 31 (2023) : 11839-11848 . |
| APA | Chen, Jie , Shao, Jiwei , Sun, Ruifen , Zhang, Weiwei , Huang, Yun , Zheng, Jingcheng et al. Anion Exchanges of Water-Stable Perovskite Nanocrystals in the Pure Water Phase and Applications in Detecting Halide Ions via a Smartphone-Based Sensing Platform . | ANALYTICAL CHEMISTRY , 2023 , 95 (31) , 11839-11848 . |
| Export to | NoteExpress RIS BibTex |
Version ：
Export
| Results： |
Selected to |
| Format： |
