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Institution

Nanjing Tech University

EducationNanjing, China
About: Nanjing Tech University is a education organization based out in Nanjing, China. It is known for research contribution in the topics: Catalysis & Membrane. The organization has 21827 authors who have published 21794 publications receiving 364050 citations. The organization is also known as: Nangongda & Nánjīng Gōngyè Dàxúe.


Papers
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Journal ArticleDOI
TL;DR: The designed phototheranostics could completely inhibit the tumor growth with the help of laser and provides a paradigm to develop highly efficient photosensitizers with photodynamic and photothermal capability for personalized cancer therapy.
Abstract: Continuous irradiation during photodynamic therapy (PDT) inevitably induces tumor hypoxia, thereby weakening the PDT effect. In PDT-induced hypoxia, providing singlet oxygen from stored chemical energy may enhance the cell-killing effect and boost the therapeutic effect. Herein, we present a phototheranostic (DPPTPE@PEG-Py NPs) prepared by using a 2-pyridone-based diblock polymer (PEG-Py) to encapsulate a semiconducting, heavy-atom-free pyrrolopyrrolidone-tetraphenylethylene (DPPTPE) with high singlet-oxygen-generation ability both in dichloromethane and water. The PEG-Py can trap the 1 O2 generated from DPPTPE under laser irradiation and form a stable intermediate of endoperoxide, which can then release 1 O2 in the dark, hypoxic tumor microenvironment. Furthermore, fluorescence-imaging-guided phototherapy demonstrates that this phototheranostic could completely inhibit tumor growth with the help of laser irradiation.

128 citations

Journal ArticleDOI
TL;DR: In this study, an efficient poly(vinylpyrrolidone) (PVP)-assisted hydrothermal method for the in situ growth of WS2 nanosheets with layer-controllability on reduced graphene oxide (rGO) is reported.
Abstract: In this study, an efficient poly(vinylpyrrolidone) (PVP)-assisted hydrothermal method for the in situ growth of WS2 nanosheets with layer-controllability on reduced graphene oxide (rGO) is reported. The number of layers (from a monolayer to ∼25 layers) of the exfoliated WS2 can be accurately controlled by adjusting the amount of PVP. The layer structure and the morphology of the as-prepared hybrids are confirmed by field emission scanning electron microscopy and high-resolution transmission microscopy. The X-ray diffraction, Raman, and X-ray photoemission spectroscopy of the obtained WS2–rGO hybrid nanosheets indicate highly crystallized structures, a clear Raman shift and a stoichiometry, which is dependent on the number of layers. Furthermore, these highly active and durable catalysts exhibit an electrocatalytic current density of 10 mA cm−2 at a small hydrogen evolution reaction (HER) overpotential (−170 mV) and a Tafel slope of 52 mV dec−1 with an excellent electrocatalytic stability (after 6 months storage).

128 citations

Journal ArticleDOI
TL;DR: In this article, the authors proposed a structure with high symmetry and extraordinary electrochemical performance for Bi0.5Sr 0.5FeO3-δ, which is capable of competing effectively with the current Co-based cathode benchmark with additional advantages of lower thermal expansion and cost.
Abstract: Bi doping of SrFeO3−δ results in the formation of a structure with high symmetry and extraordinary electrochemical performance for Bi0.5Sr0.5FeO3-δ, which is capable of competing effectively with the current Co-based cathode benchmark with additional advantages of lower thermal expansion and cost.

128 citations

Journal ArticleDOI
TL;DR: In this article, the behavior of a packed bed latent heat thermal energy storage system with phase change material (PCM) capsules as filler is analyzed using enthalpy method, and the results indicated that decreasing the size of capsule and fluid inlet velocity, or increasing the storage height, results in an increase in the charge efficiency.

127 citations

Journal ArticleDOI
TL;DR: The upconversion luminescence of β-NaYF4:Yb3+/Er3+ was greatly enhanced by increasing the molar ratio of KF to RE3+ (RE = Y, Yb, Er), which is attributed to the distortion of local crystal field symmetry around lanthanide ions through K+ ions doping.
Abstract: A strategy has been adopted for simultaneous morphology manipulation and upconversion luminescence enhancement of β-NaYF4:Yb(3+)/Er(3+) microcrystals by simply tuning the KF dosage. X-ray power diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and photoluminescence spectra (PL) were used to characterize the samples. The influence of molar ratio of KF to Y(3+) on the crystal phase and morphology has been systematically investigated and discussed. It is found that the molar ratio of KF to Y(3+) can strongly control the morphology of the as-synthesized β-NaYF4 samples because of the different capping effect of F(-) ions on the different crystal faces. The possible formation mechanism has been proposed on the basis of a series of time-dependent experiments. More importantly, the upconversion luminescence of β-NaYF4:Yb(3+)/Er(3+) was greatly enhanced by increasing the molar ratio of KF to RE(3+) (RE = Y, Yb, Er), which is attributed to the distortion of local crystal field symmetry around lanthanide ions through K(+) ions doping. This synthetic methodology is expected to provide a new strategy for simultaneous morphology control and remarkable upconversion luminescence enhancement of yttrium fluorides, which may be applicable for other rare earth fluorides.

127 citations


Authors

Showing all 22047 results

NameH-indexPapersCitations
Yi Chen2174342293080
Richard H. Friend1691182140032
Hua Zhang1631503116769
Wei Huang139241793522
Jian Zhou128300791402
Haiyan Wang119167486091
Jian Liu117209073156
Lain-Jong Li11362758035
Hong Wang110163351811
Jun-Jie Zhu10375441655
Stefan Kaskel10170536201
Hong Liu100190557561
Dirk De Vos9664233214
Peng Li95154845198
Feng Liu95106738478
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023125
2022502
20212,924
20202,572
20192,340
20181,967