As a burgeoning research field, ultrasound-responsive materials have attracted intense interest in healthcare research. However, the basic mechanism of sonochemical effect in the quasi-solid state is far from being we...As a burgeoning research field, ultrasound-responsive materials have attracted intense interest in healthcare research. However, the basic mechanism of sonochemical effect in the quasi-solid state is far from being well understood than those in the solution. Herein, we showcase mechanochemical transformations of europium(Ⅲ) complexes in a supramolecular hydrogel matrix. With the combination of labile terpyridine-europium complexes(TPY-Eu^(3+)) as mechanochromic moieties and an ultrasound-responsive fluorogen(URF) as a molecular tweezer, the hydrogel produces a notable fluorescence change in response to ultrasound. The mechanochemical transformation was elucidated by molecular dynamics(MD) simulations, and fully probed and evidenced by electrochemical experiments, X-ray photoelectron spectroscopy(XPS), and attenuated total reflectance-Fourier transform infrared(ATR-FTIR) spectroscopy.展开更多
Ultralong organic room temperature phosphorescence(RTP)is attracting increas-ing attention due to its fascinating optical phenomena and wide applications.Among various RTP,excimer phosphorescence is of fundamental sig...Ultralong organic room temperature phosphorescence(RTP)is attracting increas-ing attention due to its fascinating optical phenomena and wide applications.Among various RTP,excimer phosphorescence is of fundamental significance,but it remains a considerable challenge to achieveflexible,multicolor and large-area excimer RTP materials,which should greatly advance the understanding and devel-opment of organic light-emitting devices.Herein,we present ultralong excimer RTPfilms by the self-assembly and confinement of terpyridine(Tpy)derivatives in polymeric matrices.Strikingly,the self-assembly of Tpy derivatives induces the formation of excimer complexes,thus immensely minimizing singlet-triplet split-ting energy(ΔEST)to promote the intersystem crossing process.Furthermore,the confinement by multiple hydrogen bonding interactions as well as the compact aggregation of phosphors jointly suppresses the nonradiative transitions,leading to long-lived excimer RTP(τ543.9 ms,19,000-fold improvements over the pow-=der).On account of the outstanding afterglow performance and color-tunability of RTP materials,flexible and large-areafilms were fabricated for intelligent display,anticounterfeiting,and time-resolved information encryption.展开更多
In order to clarify the solvent extraction and separation behaviors of rare earths and impurity of Al during the extraction and enrichment of low-concentration leach solution of ion-adsorption rare earth ore,the extra...In order to clarify the solvent extraction and separation behaviors of rare earths and impurity of Al during the extraction and enrichment of low-concentration leach solution of ion-adsorption rare earth ore,the extraction mechanism and separation behaviors of Nd^(3+)and Al^(3+)in the Nd_(2)(SO_(4))_(3)-AI_(2)(SO_(4))_(3) mixed solution using P507 were studied in this work.The extraction of Nd^(3+)and Al^(3+)follows the cation exchange mechanism.With the increase of the equilibrium pH,β_(Nd/Al) in the extraction of the Nd_(2)(SO_(4))_(3)-Al_(2)(SO_(4))_(3) mixed solution using P507 is always higher than that in the extraction of single Nd_(2)(SO_(4))_(3) and Al_(2)(SO_(4))_(3) solutions.It can be attributed to the fact that the extraction of Nd^(3+)using P507 is much faster than that of Al^(3+),and Al^(3+)is more prone to be hydrolyzed at lower pH.β_(Nd/Al) in the extraction of the Nd_(2)(SO_(4))_(3)-Al_(2)(SO_(4))_(3) mixed solution decreases gradually with the increase of mixing time within the equilibrium pH range of 1.5-1.9.The extraction of Nd^(3+)using P507 is much faster than that of Al^(3+),but the stability of Al^(3+)-Ioaded organic phase is better than that of Nd^(3+)-loaded organic phase,thus Nd^(3+)in the Nd^(3+)-loaded organic phase is gradually replaced by Al^(3+)in the aqueous phase with the increase of mixing time.展开更多
基金supported by the National Key R&D Program of China(No.2018YFC0114900)National Natural Science Foundation of China(No.52103246,U1967217)+9 种基金Zhejiang Provincial Natural Science Foundation of China(Nos.LD22E050008,LD22A020002)China Postdoctoral Science Foundation(No.2021TQ0341,2020M671828)Ningbo Natural Science Foundation(No.2021J203,202003N4361)Youth Innovation Promotion Association of Chinese Academy of Sciences(No.2019297)Key Research Program of Frontier Science,Chinese Academy of Sciences(No.QYZDB-SSW-SLH036)the Sino-German Mobility Program(No.M-0424)K.C.Wong Education Foundation(No.GJTD-2019–13)National Independent Innovation Demonstration Zone Shanghai Zhangjiang Major Projects(No.ZJZX2020014)the Starry Night Science Fund of Zhejiang University Shanghai Institute for Advanced Study(No.SN-ZJU-SIAS-003)Director Foundation of Ningbo Institute of Materials Technology and Engineering。
文摘As a burgeoning research field, ultrasound-responsive materials have attracted intense interest in healthcare research. However, the basic mechanism of sonochemical effect in the quasi-solid state is far from being well understood than those in the solution. Herein, we showcase mechanochemical transformations of europium(Ⅲ) complexes in a supramolecular hydrogel matrix. With the combination of labile terpyridine-europium complexes(TPY-Eu^(3+)) as mechanochromic moieties and an ultrasound-responsive fluorogen(URF) as a molecular tweezer, the hydrogel produces a notable fluorescence change in response to ultrasound. The mechanochemical transformation was elucidated by molecular dynamics(MD) simulations, and fully probed and evidenced by electrochemical experiments, X-ray photoelectron spectroscopy(XPS), and attenuated total reflectance-Fourier transform infrared(ATR-FTIR) spectroscopy.
基金National Key Research and Development Program of China,Grant/Award Numbers:2022YFB3204301,2021YFA1201201National Natural Science Foundation of China,Grant/Award Numbers:22205249,U1967217+3 种基金China Postdoctoral Science Foundation,Grant/Award Numbers:2021TQ0341,2022M723252Zhejiang Provincial Natural Science Foundation of China,Grant/Award Number:LQ23B040002Natural Science Foundation of Ningbo,Grant/Award Number:2021J203Foundation of the Director of NIMTE,Grant/Award Number:2021SZKY0305。
文摘Ultralong organic room temperature phosphorescence(RTP)is attracting increas-ing attention due to its fascinating optical phenomena and wide applications.Among various RTP,excimer phosphorescence is of fundamental significance,but it remains a considerable challenge to achieveflexible,multicolor and large-area excimer RTP materials,which should greatly advance the understanding and devel-opment of organic light-emitting devices.Herein,we present ultralong excimer RTPfilms by the self-assembly and confinement of terpyridine(Tpy)derivatives in polymeric matrices.Strikingly,the self-assembly of Tpy derivatives induces the formation of excimer complexes,thus immensely minimizing singlet-triplet split-ting energy(ΔEST)to promote the intersystem crossing process.Furthermore,the confinement by multiple hydrogen bonding interactions as well as the compact aggregation of phosphors jointly suppresses the nonradiative transitions,leading to long-lived excimer RTP(τ543.9 ms,19,000-fold improvements over the pow-=der).On account of the outstanding afterglow performance and color-tunability of RTP materials,flexible and large-areafilms were fabricated for intelligent display,anticounterfeiting,and time-resolved information encryption.
基金Project supported by the Major Research Plan of the National Natural Science Foundation of China(91962211)National Key Research and Development Program of China(2018YFC1801803)+1 种基金National Natural Science Foundation of China(51804273)Major Project of Guangxi Science and Technology(Guike-AA18242022)。
文摘In order to clarify the solvent extraction and separation behaviors of rare earths and impurity of Al during the extraction and enrichment of low-concentration leach solution of ion-adsorption rare earth ore,the extraction mechanism and separation behaviors of Nd^(3+)and Al^(3+)in the Nd_(2)(SO_(4))_(3)-AI_(2)(SO_(4))_(3) mixed solution using P507 were studied in this work.The extraction of Nd^(3+)and Al^(3+)follows the cation exchange mechanism.With the increase of the equilibrium pH,β_(Nd/Al) in the extraction of the Nd_(2)(SO_(4))_(3)-Al_(2)(SO_(4))_(3) mixed solution using P507 is always higher than that in the extraction of single Nd_(2)(SO_(4))_(3) and Al_(2)(SO_(4))_(3) solutions.It can be attributed to the fact that the extraction of Nd^(3+)using P507 is much faster than that of Al^(3+),and Al^(3+)is more prone to be hydrolyzed at lower pH.β_(Nd/Al) in the extraction of the Nd_(2)(SO_(4))_(3)-Al_(2)(SO_(4))_(3) mixed solution decreases gradually with the increase of mixing time within the equilibrium pH range of 1.5-1.9.The extraction of Nd^(3+)using P507 is much faster than that of Al^(3+),but the stability of Al^(3+)-Ioaded organic phase is better than that of Nd^(3+)-loaded organic phase,thus Nd^(3+)in the Nd^(3+)-loaded organic phase is gradually replaced by Al^(3+)in the aqueous phase with the increase of mixing time.
