All-inorganic 3D lead-free vacancy-ordered double perovskites(DPs)in the A_(2)MX_(6)phase have garnered significant attention in the fields of photovoltaics and light-emitting diodes(LED)due to their exceptional optoe...All-inorganic 3D lead-free vacancy-ordered double perovskites(DPs)in the A_(2)MX_(6)phase have garnered significant attention in the fields of photovoltaics and light-emitting diodes(LED)due to their exceptional optoelectronic properties[1].These properties encompass a high optical absorption coefficient,tunable bandgap,and long carrier diffusion dis-tance.展开更多
Organic electrode materials(OEMs),withmerits of structural diversity,molecular-level controllability,resource abundance,and environmental friendliness,have become a promising electrode candidate for low-carbon renewab...Organic electrode materials(OEMs),withmerits of structural diversity,molecular-level controllability,resource abundance,and environmental friendliness,have become a promising electrode candidate for low-carbon renewable batteries.Safer,environmentally benign,and sustainable aqueous rechargeable batteries are particularly appealing for large-scale energy storage applications.This review aims to provide an insightful discussion of OEMs in nonmetallic charge carrier-based batteries,especially for the application in aqueous rechargeable systems.The emerging application of OEMs in versatile aqueous batteries will be analyzed emphatically,including aqueous proton batteries,aqueous ammonium-ion batteries,and air self-charging batteries.We expect that this review can serve as a guide for the future development of OEMs in nonmetallic charge carrier-based batteries and provide inspiration for unmet challenges.展开更多
Inorganic luminescent nanocrystals(NCs)doped with main-group ns^(2)-metal ions have evoked tremendous interest in many technological fields owing to their superior optical properties.Herein,we report a new class of lu...Inorganic luminescent nanocrystals(NCs)doped with main-group ns^(2)-metal ions have evoked tremendous interest in many technological fields owing to their superior optical properties.Herein,we report a new class of luminescent nanoprobes based on 5s2-metal Sb3+-doped CaS NCs that are excitable by using a near ultraviolet light-emitting diode.The optical properties and excited-state dynamics of Sb3+in CaS NCs are comprehensively surveyed through temperature-dependent steady-state and transient photoluminescence(PL)spectroscopies.Owing to the strong electron-phonon coupling of Sb^(3+)in CaS NCs,Sb3+ions experience a dynamic Jahn-Taller distortion on the excited state,which results in bright green PL of Sb3+with a broad emission band,a large Stokes shift,and a high PL quantum yield up to 17.3%.By taking advantage of the intense PL of Sb^(3+),we show in proof-of-concept experiments the application of biotinylated CaS:Sb^(3+)NCs as sensitive luminescent nanoprobes for biotin receptor-targeted cancer cell imaging and zebrafish imaging with a high imaging contrast.These findings provide fundamental insights into the excited-state dynamics of Sb^(3+)in CaS NCs,thus laying a foundation for future design of novel and versatile luminescent nanoprobes via main-group ns2-metal doping.展开更多
Luminescent metal halides doped with ns^(2-)metal ions such as 6s^(2-)metal Bi^(3+)have aroused reviving interest owing to their outstanding optical properties;however,the origin of the photoluminescence(PL)remains co...Luminescent metal halides doped with ns^(2-)metal ions such as 6s^(2-)metal Bi^(3+)have aroused reviving interest owing to their outstanding optical properties;however,the origin of the photoluminescence(PL)remains controversial and unclear.Herein,we report a strategy for the controlled synthesis of Bi^(3+)-doped vacancy-ordered double perovskite Cs_(2)SnCl_(6)nanocrystals(NCs)and unravel the triplet excited-state dynamics of Bi^(3+)through temperature-dependent PL and ultrafast femtosecond transient absorption spectroscopies.Owing to the aliovalent Bi^(3+)doping in the spatially confined zero-dimensional(0D)structure of Cs2SnCl6,Bi^(3+)ions experience an enhancive Jahn-Teller distortion in the excited state,which results in intense broadband blue PL originating from the inter-configurational 3P0,1→1S0 transitions of Bi^(3+)at 450 nm,with a large Stokes shift and a quantum yield of 35.2%.Specifically,an unusual thermal-enhanced Jahn-Teller splitting of the excitation band and a remarkable transition of the PL lifetime from ms at 10 K toμs at 300 K were observed,as solid evidence for the isolated Bi^(3+)emission.These findings clarify the controversy about the PL origin in ns^(2-)metal ion-doped lead-free luminescent metal halides,thereby paving the way for exploring their optoelectronic applications.展开更多
基金supported by Senior Talent Fund of Jiangsu University(No.5501310021)China Postdoctoral Science Foundation(No.2023M741419)the Young Elite Scientist Sponsorship Program by ZJAST(No.G301310002).
文摘All-inorganic 3D lead-free vacancy-ordered double perovskites(DPs)in the A_(2)MX_(6)phase have garnered significant attention in the fields of photovoltaics and light-emitting diodes(LED)due to their exceptional optoelectronic properties[1].These properties encompass a high optical absorption coefficient,tunable bandgap,and long carrier diffusion dis-tance.
基金All authors would like to acknowledge the support from the National Natural Science Foundation of China(NSFC no.51872128)the Ministry of Science and Technology of China(grant nos.G2021014005L and G2022014098L)+1 种基金the Natural Science Foundation of Jiangsu Province(grant no.BK20210744)the Young Talent Support Fund from Jiangsu University(grant no.5501310023).
文摘Organic electrode materials(OEMs),withmerits of structural diversity,molecular-level controllability,resource abundance,and environmental friendliness,have become a promising electrode candidate for low-carbon renewable batteries.Safer,environmentally benign,and sustainable aqueous rechargeable batteries are particularly appealing for large-scale energy storage applications.This review aims to provide an insightful discussion of OEMs in nonmetallic charge carrier-based batteries,especially for the application in aqueous rechargeable systems.The emerging application of OEMs in versatile aqueous batteries will be analyzed emphatically,including aqueous proton batteries,aqueous ammonium-ion batteries,and air self-charging batteries.We expect that this review can serve as a guide for the future development of OEMs in nonmetallic charge carrier-based batteries and provide inspiration for unmet challenges.
基金supported by the Science and Technology Cooperation Fund between Chinese and Australian Governments(No.2017YFE0132300)the Strategic Priority Research Program of the CAS(No.XDB20000000)+2 种基金the National Natural Science Foundation of China(Nos.11774345,12074379,21771185,21875250,and 11904365)the CAS/SAFEA International Partnership Program for Creative Research Teams,Natural Science Foundation of Fujian Province(No.202010037)Fujian Science&Technology Innovation Laboratory for Optoelectronic Information of China(No.2021ZR125).
文摘Inorganic luminescent nanocrystals(NCs)doped with main-group ns^(2)-metal ions have evoked tremendous interest in many technological fields owing to their superior optical properties.Herein,we report a new class of luminescent nanoprobes based on 5s2-metal Sb3+-doped CaS NCs that are excitable by using a near ultraviolet light-emitting diode.The optical properties and excited-state dynamics of Sb3+in CaS NCs are comprehensively surveyed through temperature-dependent steady-state and transient photoluminescence(PL)spectroscopies.Owing to the strong electron-phonon coupling of Sb^(3+)in CaS NCs,Sb3+ions experience a dynamic Jahn-Taller distortion on the excited state,which results in bright green PL of Sb3+with a broad emission band,a large Stokes shift,and a high PL quantum yield up to 17.3%.By taking advantage of the intense PL of Sb^(3+),we show in proof-of-concept experiments the application of biotinylated CaS:Sb^(3+)NCs as sensitive luminescent nanoprobes for biotin receptor-targeted cancer cell imaging and zebrafish imaging with a high imaging contrast.These findings provide fundamental insights into the excited-state dynamics of Sb^(3+)in CaS NCs,thus laying a foundation for future design of novel and versatile luminescent nanoprobes via main-group ns2-metal doping.
基金supported by the National Natural Science Foundation of China(NSFC,Nos.12074379,U1805252,21875250,12074380,11904365,and 12004384)the Chinese Academy of Sciences/State Administration of Foreign Experts Affairs(CAS/SAFEA)International Partnership Program for Creative Research Teams.
文摘Luminescent metal halides doped with ns^(2-)metal ions such as 6s^(2-)metal Bi^(3+)have aroused reviving interest owing to their outstanding optical properties;however,the origin of the photoluminescence(PL)remains controversial and unclear.Herein,we report a strategy for the controlled synthesis of Bi^(3+)-doped vacancy-ordered double perovskite Cs_(2)SnCl_(6)nanocrystals(NCs)and unravel the triplet excited-state dynamics of Bi^(3+)through temperature-dependent PL and ultrafast femtosecond transient absorption spectroscopies.Owing to the aliovalent Bi^(3+)doping in the spatially confined zero-dimensional(0D)structure of Cs2SnCl6,Bi^(3+)ions experience an enhancive Jahn-Teller distortion in the excited state,which results in intense broadband blue PL originating from the inter-configurational 3P0,1→1S0 transitions of Bi^(3+)at 450 nm,with a large Stokes shift and a quantum yield of 35.2%.Specifically,an unusual thermal-enhanced Jahn-Teller splitting of the excitation band and a remarkable transition of the PL lifetime from ms at 10 K toμs at 300 K were observed,as solid evidence for the isolated Bi^(3+)emission.These findings clarify the controversy about the PL origin in ns^(2-)metal ion-doped lead-free luminescent metal halides,thereby paving the way for exploring their optoelectronic applications.