In recent years, the increasing demand of various fields of radiation detection materials has led to intensive researches in scintillation materials 1-2]. The scintillators can absorb high-energy X-ray photons and the...In recent years, the increasing demand of various fields of radiation detection materials has led to intensive researches in scintillation materials 1-2]. The scintillators can absorb high-energy X-ray photons and then convert them into low-energy visible photons, which are widely applied in radiation monitoring, security detection, X-ray astronomy and medical radiology 3"l].展开更多
Nanosized cerium-doped lutetium aluminum garnet (LuAG:Ce) phosphors were prepared by nitrate-citrate solgel combustion process using 1:1 ratio of the citrate:nitrate. The prepared LuAG:Ce phosphors were characte...Nanosized cerium-doped lutetium aluminum garnet (LuAG:Ce) phosphors were prepared by nitrate-citrate solgel combustion process using 1:1 ratio of the citrate:nitrate. The prepared LuAG:Ce phosphors were characterized by XRD, TEM, photoluminescence and radioluminescence spectra excited by UV and X-ray, respectively. The purified crystalline phase of LuAG:Ce was obtained at 900 ℃ by directly crystallizing from amorphous materials. The resultant Lu- AG:Ce phosphors were uniform and had good dispersivity with an average particle size of about 30 urn. Both photoluminescence and radioluminescence were well-known Ce^3+ emissions located in the range of 470 -600 nm consisting of two emission bands because of the transition from the lowest 5d excited state (2D) to the 4f ground state of Ce^3+, which matched well with the sensitivity curve of the Si-photodiode. There was a little red shift for the emission components from the UV-excited emission spectrum to the X-ray-excited emission spectrum. The fast scintillation decay component of 26 ns satisfies the requirements of fast scintillators.展开更多
This review article highlights the exploration of inorganic nanoscintillators for various scientific and technological applications in the fields of radiation detection,bioimaging,and medical theranostics.Various aspe...This review article highlights the exploration of inorganic nanoscintillators for various scientific and technological applications in the fields of radiation detection,bioimaging,and medical theranostics.Various aspects of nanoscintillators pertaining to their fundamental principles,mechanism,structure,applications are briefly discussed.The mechanisms of inorganic nanoscintillators are explained based on the fundamental principles,instrumentation involved,and associated physical and chemical phenomena,etc.Subsequently,the promise of nanoscintillators over the existing single-crystal scintillators and other types of scintillators is presented,enabling their development for multifunctional applications.The processes governing the scintillation mechanisms in nanodomains,such as surface,structure,quantum,and dielectric confinement,are explained to reveal the underlying nanoscale scintillation phenomena.Additionally,suitable examples are provided to explain these processes based on the published data.Furthermore,we attempt to explain the different types of inorganic nanoscintillators in terms of the powder nanoparticles,thin films,nanoceramics,and glasses to ensure that the effect of nanoscience in different nanoscintillator domains can be appreciated.The limitations of nanoscintillators arc also highlighted in this review article.The advantages of nanostructured scintillators,including their property-driven applications,are also explained.This review article presents the considerable application potential of nanostructured scintillators with respect to important aspects as well as their physical and application significance in a concise manner.展开更多
Organic and inorganic clusteroluminescence have attracted great attention while the underlying mechanisms is still not well understood.Here,we employed a series of ancient inorganic complexes platinocyanides with aggr...Organic and inorganic clusteroluminescence have attracted great attention while the underlying mechanisms is still not well understood.Here,we employed a series of ancient inorganic complexes platinocyanides with aggregation-induced emission property to elucidate the mechanism of clusteroluminescence including how does the chromophore form and how does the solid structures influence the luminescence behaviors.The results indicate that the isolated platinocyanide cannot work as a chromophore to emit visible light,while their clusterization at aggregate state can trigger the d-orbitals coupling of the platinum atoms to facilitate the electron exchange and delocalization to form a new chromophore to emit visible light.Furthermore,the counter ions and H2O ligands help to rigidify the three-dimensional network structure of the platinocyanides to suppress the excited state nonradiative decay,resulting in the high quantum yield of up to 96%.This work fundamentally helps understanding both the organic and inorganic clusteroluminescence phenomenon.展开更多
Materials that exhibit visible luminescence upon X-ray irradiation show great potential in the medical and industrial fields.Pure organic materials have recently emerged as promising scintillators for X-ray detection ...Materials that exhibit visible luminescence upon X-ray irradiation show great potential in the medical and industrial fields.Pure organic materials have recently emerged as promising scintillators for X-ray detection and radiography,due to their diversified design,low cost,and facile preparation.However,recent progress in efficient radioluminescence has mainly focused on small molecules,which are inevitably associated with processability and repeatability issues.Here,a concise strategy is proposed to prepare radioluminescent polymers that exhibit multiple emission colors from blue to yellow with high brightness in an amorphous state by the radical copolymerization of negatively charged polyacrylic acid and different positively charged quaternary phosphonium salts.One of the obtained polymers exhibits excellent photostability under a high X-ray irradiation dosage of 27.35 Gy and has a detection limit of 149 nGy s^(−1).This performance is superior to that of conventional anthracene-based scintillators.Furthermore,by simply drop-casting a polymer methanol solution on a quartz plate,a transparent scintillator screen was successfully fabricated for X-ray imaging with a resolution of 8.7 line pairs mm^(−1).The pure organic phosphorescent polymers with a highly efficient radioluminescence were demonstrated for the first time,and the strategy reported herein offers a promising pathway to expand the application range of amorphous organic scintillators.展开更多
文摘In recent years, the increasing demand of various fields of radiation detection materials has led to intensive researches in scintillation materials 1-2]. The scintillators can absorb high-energy X-ray photons and then convert them into low-energy visible photons, which are widely applied in radiation monitoring, security detection, X-ray astronomy and medical radiology 3"l].
基金Project supported by the National Defence Fundamental Research Project of China
文摘Nanosized cerium-doped lutetium aluminum garnet (LuAG:Ce) phosphors were prepared by nitrate-citrate solgel combustion process using 1:1 ratio of the citrate:nitrate. The prepared LuAG:Ce phosphors were characterized by XRD, TEM, photoluminescence and radioluminescence spectra excited by UV and X-ray, respectively. The purified crystalline phase of LuAG:Ce was obtained at 900 ℃ by directly crystallizing from amorphous materials. The resultant Lu- AG:Ce phosphors were uniform and had good dispersivity with an average particle size of about 30 urn. Both photoluminescence and radioluminescence were well-known Ce^3+ emissions located in the range of 470 -600 nm consisting of two emission bands because of the transition from the lowest 5d excited state (2D) to the 4f ground state of Ce^3+, which matched well with the sensitivity curve of the Si-photodiode. There was a little red shift for the emission components from the UV-excited emission spectrum to the X-ray-excited emission spectrum. The fast scintillation decay component of 26 ns satisfies the requirements of fast scintillators.
基金supported by the National Natural Science Foundation of China(22171105 and 12004384)Shandong Provincial Natural Science Foundation(ZR2020KB012,ZR2021MB001,and ZR2022YQ14)+1 种基金the Fund of State Key Laboratory of Structural Chemistry(20210015)the Special Foundation of Taishan Scholar Project.
基金the United States-India Education Foundation(USIEF,India)the Institute of International Education(HE,USA)for his Fulbright Nehru Postdoctoral Fellowship(Award#2268/FNPDR72017)the financial support provided by the IIT startup funds.
文摘This review article highlights the exploration of inorganic nanoscintillators for various scientific and technological applications in the fields of radiation detection,bioimaging,and medical theranostics.Various aspects of nanoscintillators pertaining to their fundamental principles,mechanism,structure,applications are briefly discussed.The mechanisms of inorganic nanoscintillators are explained based on the fundamental principles,instrumentation involved,and associated physical and chemical phenomena,etc.Subsequently,the promise of nanoscintillators over the existing single-crystal scintillators and other types of scintillators is presented,enabling their development for multifunctional applications.The processes governing the scintillation mechanisms in nanodomains,such as surface,structure,quantum,and dielectric confinement,are explained to reveal the underlying nanoscale scintillation phenomena.Additionally,suitable examples are provided to explain these processes based on the published data.Furthermore,we attempt to explain the different types of inorganic nanoscintillators in terms of the powder nanoparticles,thin films,nanoceramics,and glasses to ensure that the effect of nanoscience in different nanoscintillator domains can be appreciated.The limitations of nanoscintillators arc also highlighted in this review article.The advantages of nanostructured scintillators,including their property-driven applications,are also explained.This review article presents the considerable application potential of nanostructured scintillators with respect to important aspects as well as their physical and application significance in a concise manner.
基金National Natural Science Foundation of China,Grant/Award Numbers:21788102,52003228Science and Technology Plan of Shenzhen,Grant/Award Number:JCYJ20180306174910791+2 种基金Natural Science Foundation of Guangdong Province,Grant/Award Number:2019B121205002Research Grants Council of Hong Kong,Grant/Award Numbers:N_HKUT609/19,16305518,A-HKUST605/16,C6009-17GInnovation and Technology Commission,Grant/Award Numbers:ITC-CNERC14SC01,ITCPD/17-9。
文摘Organic and inorganic clusteroluminescence have attracted great attention while the underlying mechanisms is still not well understood.Here,we employed a series of ancient inorganic complexes platinocyanides with aggregation-induced emission property to elucidate the mechanism of clusteroluminescence including how does the chromophore form and how does the solid structures influence the luminescence behaviors.The results indicate that the isolated platinocyanide cannot work as a chromophore to emit visible light,while their clusterization at aggregate state can trigger the d-orbitals coupling of the platinum atoms to facilitate the electron exchange and delocalization to form a new chromophore to emit visible light.Furthermore,the counter ions and H2O ligands help to rigidify the three-dimensional network structure of the platinocyanides to suppress the excited state nonradiative decay,resulting in the high quantum yield of up to 96%.This work fundamentally helps understanding both the organic and inorganic clusteroluminescence phenomenon.
基金the financial support from the National Funds for Distinguished Young Scientists(61825503)the National Natural Science Foundation of China(62075101,61775101,and 61775103)the Natural Science Foundation of Jiangsu Province of China(BK20200095).
文摘Materials that exhibit visible luminescence upon X-ray irradiation show great potential in the medical and industrial fields.Pure organic materials have recently emerged as promising scintillators for X-ray detection and radiography,due to their diversified design,low cost,and facile preparation.However,recent progress in efficient radioluminescence has mainly focused on small molecules,which are inevitably associated with processability and repeatability issues.Here,a concise strategy is proposed to prepare radioluminescent polymers that exhibit multiple emission colors from blue to yellow with high brightness in an amorphous state by the radical copolymerization of negatively charged polyacrylic acid and different positively charged quaternary phosphonium salts.One of the obtained polymers exhibits excellent photostability under a high X-ray irradiation dosage of 27.35 Gy and has a detection limit of 149 nGy s^(−1).This performance is superior to that of conventional anthracene-based scintillators.Furthermore,by simply drop-casting a polymer methanol solution on a quartz plate,a transparent scintillator screen was successfully fabricated for X-ray imaging with a resolution of 8.7 line pairs mm^(−1).The pure organic phosphorescent polymers with a highly efficient radioluminescence were demonstrated for the first time,and the strategy reported herein offers a promising pathway to expand the application range of amorphous organic scintillators.