The sodium-iodine(Na-I)battery exhibits significant potential as an alternative energy storage device to the lithium-ion battery.However,its development is hindered by inadequate electrical and thermal stability,as we...The sodium-iodine(Na-I)battery exhibits significant potential as an alternative energy storage device to the lithium-ion battery.However,its development is hindered by inadequate electrical and thermal stability,as well as the dissolution and shuttling of polyiodide.In this study,we report a preparation method for melamine carbon sponge(MC)via carbonizing a commercially available kitchen sponge.It was revealed that the as-prepared MC,composed of unique self-growing carbon nanotubes,could provide both physical and chemical adsorption capabilities for intermediate polyiodides to improve the electrochemical performance of NaI.Consequently,the NaI/MC electrode effectively minimized polyiodide dissolution and reduced the electrochemical impedance.The NaI/MC cathode demonstrated a high average discharge capacity of 92.75 mAh·g^(–1)over 200 cycles while maintaining a coulombic efficiency of 94%.The research findings from our study have promising applications in Na-I batteries.展开更多
The valorization of nitrous oxide(N_(2)O)as an oxygen atom donor presents an attractive opportunity for green chemistry applications,leveraging both its industrial abundance and thermodynamically favorable oxidation p...The valorization of nitrous oxide(N_(2)O)as an oxygen atom donor presents an attractive opportunity for green chemistry applications,leveraging both its industrial abundance and thermodynamically favorable oxidation potential.However,practical implementation has been constrained by the inherent kinetic inertness and poor coordinating ability of N_(2)O.While prior studies achieved N_(2)O-mediated conversion of aryl halides to phenols,such transformations necessitated stoichiometric chemical reductants and elevated pressure(2 atm),posing challenges in operational safety and process scalability.This study focuses on an electrochemical strategy that enables efficient oxygen atom transfer under ambient pressure through controlled current application.This methodology facilitates the selective transformation of aryl iodides to phenols without external reducing agents,establishing an environmentally benign synthetic pathway.By replacing traditional chemical reductants with electrons as the sole reducing equivalent,our approach addresses critical sustainability challenges in aromatic oxygenation chemistry while maintaining operational simplicity under mild conditions.展开更多
We herein present an efficient denitrative iodination method of(hetero)nitroarenes mediated by commercially available and cost-effective hydroiodic acid(HI).During the reaction process,HI plays its dual roles as both ...We herein present an efficient denitrative iodination method of(hetero)nitroarenes mediated by commercially available and cost-effective hydroiodic acid(HI).During the reaction process,HI plays its dual roles as both the sustainable reductant of nitro group and iodine source in the iodination step,which successfully integrates three steps into a one-pot procedure and significantly simplifies the reaction system.This approach enables a smooth metal-free conversion of nitroarenes to corresponding aryl iodides via one-pot process,exhibits a broad substrate scope and good reaction efficiency,and was conveniently applied in the concise synthesis of pharmaceuticals.展开更多
Perovskite solar cells(PSCs)based onα-phase FAPbI_(3)(α-FAPbI_(3))microcrystals precursor outperform those withδ-phase mi-crocrystals due to their superior crystallinity and fewer defects,makingα-phase microcrysta...Perovskite solar cells(PSCs)based onα-phase FAPbI_(3)(α-FAPbI_(3))microcrystals precursor outperform those withδ-phase mi-crocrystals due to their superior crystallinity and fewer defects,makingα-phase microcrystals precursor more advantageous for high-per-formance PSCs.However,most reported synthesis methods of perovskite microcrystals,especially for aqueous synthesis,fail to reach the energy threshold required forα-phase transformation and therefore exhibit theδphase.In this study,we introduce a novel aqueous syn-thesis method to fabricateα-FAPbI_(3) microcrystals.Our approach overcomes the energy barrier by properly heating the reaction system,enabling the direct formation ofα-FAPbI_(3) in water.This direct one-step aqueous synthesis route yieldsα-FAPbI_(3) microcrystals with su-perior phase purity,crystallinity,and minimal defect density.Combined with green anti-solvent,the high-qualityα-FAPbI_(3) microcrystals serving as exceptional precursors endow perovskite films with reduced nonradiative recombination.The PSC achieves a remarkable power conversion efficiency(PCE)of 24.43%,which is one of the highest PCE reports for using the green anti-solvent in ambient air condition.This aqueous synthesis approach shows a significant potential for scalable production of high-performance PSCs.展开更多
Poly(3-hexylthiophene)(P3HT)has been used in CsPbI_(3)per-ovskite solar cells(PSCs)as the hole transport layer(HTL),due to its excellent hydrophobic prop-erty and cheap cost.However,the inevitable defects in perovskit...Poly(3-hexylthiophene)(P3HT)has been used in CsPbI_(3)per-ovskite solar cells(PSCs)as the hole transport layer(HTL),due to its excellent hydrophobic prop-erty and cheap cost.However,the inevitable defects in perovskite lead to the limited photovoltaic performance of CsPbI_(3)PSCs.In this study,diethylammonium io-dide(DEAI)was doped as an ad-ditive to passivate the defects in P3HT based CsPbI_(3)perovskite.Considering the diethylamine cations can effectively form hydrogen bonds with halide ion,the DEAI doping method could not only reduce the defect density but also facilitate the extraction and transport of carriers in the device.The optimal power conversion efficiency of the device prepared with DEAI doping method increases from 14.68%to 16.75%.In addition,the stability of the device is also signifi-cantly upgraded due to the improvement of CsPbI_(3)perovskite film.This work can provide re-liable theoretical and experimental evidence for further PSCs research.展开更多
Antimony sulfide(Sb_(2)S_(3))is a promising material for photoelectrochemical(PEC)devices that generate green hydrogen from sunlight and water.In this study,we present a synthesis of high-performance Sb_(2)S_(3)photoa...Antimony sulfide(Sb_(2)S_(3))is a promising material for photoelectrochemical(PEC)devices that generate green hydrogen from sunlight and water.In this study,we present a synthesis of high-performance Sb_(2)S_(3)photoanodes via an interface-engineered hydrothermal growth followed by rapid thermal annealing(RTA).A TiO_(2)interfacial layer plays a crucial role in ensuring homogeneous precursor deposition,enhancing light absorption,and forming efficient heterojunctions with Sb_(2)S_(3),thereby significantly improving charge separation and transport.RTA further improves crystallinity and interfacial contact,resulting in dense and uniform Sb_(2)S_(3)films with enlarged grains and fewer defects.The optimized Sb_(2)S_(3)photoanode achieves a photocurrent density of 2.51 mA/cm^(2)at 1.23 V vs.the reversible hydrogen electrode(RHE),one of the highest reported for Sb_(2)S_(3)without additional catalysts or passivation layers.To overcome the limitations of oxygen evolution reaction(OER),we employ the iodide oxidation reaction(IOR)as an alternative,significantly lowering the overpotential and improving charge transfer kinetics.Consequently,it produces a record photocurrent density of 8.9 mA/cm^(2)at 0.54 V vs.RHE.This work highlights the synergy between TiO_(2)interfacial engineering,RTA-induced crystallization,and IOR-driven oxidation,offering a promising pathway for efficient and scalable PEC hydrogen production.展开更多
Tetrazole-l-acetic acid was found to serve as a superior ligand for Cul-catalyzed N-arylation of imidazoles with aryl iodides under a low catalyst loading （5 mol% of Cul）. A variety of aryl iodides could he aminated...Tetrazole-l-acetic acid was found to serve as a superior ligand for Cul-catalyzed N-arylation of imidazoles with aryl iodides under a low catalyst loading （5 mol% of Cul）. A variety of aryl iodides could he aminated to provide the N-arylated products in good to excellent yields without the need of an inert atmosphere.展开更多
Functionalized alkylzinc iodides will undergo 1,4-conjugation reaction with derivatives of β-nitrostyrene in the presence of Cu(OAc)2/LiCl to afford a polyfunctional nitro-compound in high yield.
In the presence of CrC13 /Fe bimetal couple,per(poly)fluoroalkyl iodides add to vinyl cyclopropane compounds giving addition-ring-opening products in good yields.
(CH_3OCH_2CH_2C_5H_4)_2LnI(Ln=La,Nd)complexes have been synthesized by the reaction between NaI and[(CH_3OCH_2CH_2C_5H_4)_2LnCl]2 in THF;A single crystal X-ray study has shown that the lanthanum complex is an unsolvat...(CH_3OCH_2CH_2C_5H_4)_2LnI(Ln=La,Nd)complexes have been synthesized by the reaction between NaI and[(CH_3OCH_2CH_2C_5H_4)_2LnCl]2 in THF;A single crystal X-ray study has shown that the lanthanum complex is an unsolvated monomer with lanthanum(Ⅲ)in a trigonal bipyramidal coordination geometry if the cyclopentadienyl ring is regarded as occupying a single polyhedral vertex.展开更多
Stereoselective transformation of Baylis-Hillman acetates I into corresponding （Z）-allyl iodides 2 has been achieved by treatment of I with samarium triiodide in THF. Remarkable rate acceleration of samarium triiodi...Stereoselective transformation of Baylis-Hillman acetates I into corresponding （Z）-allyl iodides 2 has been achieved by treatment of I with samarium triiodide in THF. Remarkable rate acceleration of samarium triiodide-mediated iodination of 1 was found when ionic liquid 1-n-butyl-3-methyl-imidazolium tetrafluroborate （[bmim]BF4） was used as reaction media in stead of THF. This novel approach proceeds readily at 50 ℃ within a few minutes to afford （Z）-allyl iodides 2 in excellent yields. A mechanism involving stereoselective iodination of the acetates of Baylis-Hillman adducts by samarium triiodide is described, in which a six-membered ring transition state played a key role in the stereoselective formation of 2.展开更多
An operationally simple and inexpensive catalyst system was developed for the cross coupling of potassium thiocyanate with aryl iodides by using CuI as catalyst, 1, 10-phenanthroline as ligand, and tetraethylammonium ...An operationally simple and inexpensive catalyst system was developed for the cross coupling of potassium thiocyanate with aryl iodides by using CuI as catalyst, 1, 10-phenanthroline as ligand, and tetraethylammonium iodide as activator. The procedure is applicable for the synthesis of diverse aryl thiocyanates without any exotic, poisonous reagents.展开更多
Reaction of polystyrene-supported lithium selenide with 3-acetoxy-2-methylene-alkanoates afforded the corresponding allyl selenide resins and subsequent cleavage from the polymer by treating with methyl iodide to furn...Reaction of polystyrene-supported lithium selenide with 3-acetoxy-2-methylene-alkanoates afforded the corresponding allyl selenide resins and subsequent cleavage from the polymer by treating with methyl iodide to furnish （Z）-allyl iodides in good yields and high purities. The polymeric selenium reagent can be regenerated and reused. So it is a environmentally benign reagent.展开更多
Initiated by CP_2TiCl_2/Fe redox system,2-halotetrafluoroethyl iodides readily reacted with alkynes or alkenes to give 1:1 adducts in good to excellent yields.
perfluoroalkyl iodides reacted with alkenes in acetonitrile solu- tion containing catalytic amount of organophosphine under mild condition to give the corresponding adducts in moderate to good yields.Reaction was show...perfluoroalkyl iodides reacted with alkenes in acetonitrile solu- tion containing catalytic amount of organophosphine under mild condition to give the corresponding adducts in moderate to good yields.Reaction was shown to involve a free radical mechanism.展开更多
Lead iodide(PbI2) is a vital raw material for preparing perovskite solar cells(PSCs),and it not only takes part in forming the light absorption layer but also remains in the grain boundary as a passivator.In other wor...Lead iodide(PbI2) is a vital raw material for preparing perovskite solar cells(PSCs),and it not only takes part in forming the light absorption layer but also remains in the grain boundary as a passivator.In other words,the PbI2 content in the precursor and as formed film will affect the efficiency and stability of the PSCs.With moderate residual PbI2,it passivates the bulk/surface defects of perovskite,reduces the interfacial recombination,promotes the perovskite stability,minimizes the device hysteresis,and so on.Deficient PbI2 residue will reduce the interfacial passivation effect and device performance.In addition to facilitating the non-radiative recombination,over PbI2 residue can also lead to electronic insulation in the grain boundary and deteriorate the device performance.However,the impact and regulation of PbI2 residue on the device performance and stability is still not fully understood.Herein,a comprehensive and detailed review is presented by discussing the PbI2 residue impact and its regulation strategies(i.e., elimination,facilitation and conversion of the residue PbI2) to manipulate the PbI2 content,distribution and forms.Finally,we also show future outlooks in this field,with an aim to help further the progression of high-efficiency and stable PSCs.展开更多
In recent years,copper iodide(CuI)is an emerging p-type wide bandgap semiconductor with high intrinsic Hall mobility,high optical absorption and large exciton binding energy.However,the spectral response and the photo...In recent years,copper iodide(CuI)is an emerging p-type wide bandgap semiconductor with high intrinsic Hall mobility,high optical absorption and large exciton binding energy.However,the spectral response and the photoelectric conversion efficiency are limited for CuI-based heterostructure devices,which is related to the difficulty in fabrication of high-quality CuI thin films on other semiconductors.In this study,a p-CuI/n-Si photodiode has been fabricated through a facile solid-phase iodination method.Although the CuI thin film is polycrystalline with obvious structural defects,the CuI/Si diode shows a high weak-light sensitivity and a high rectification ratio of 7.6×10^(4),indicating a good defect tolerance.This is because of the unilateral heterojunction behavior of the formation of the p^(+)n diode.In this work,the mechanism of photocurrent of the p^(+)n diode has been studied comprehensively.Different monochromatic lasers with wavelengths of 400,505,635 and 780 nm have been selected for testing the photoresponse.Under zero-bias voltage,the device is a unilateral heterojunction,and only visible light can be absorbed at the Si side.On the other hand,when a bias voltage of-3 V is applied,the photodiode is switched to a broader“UV-visible”band response mode.Therefore,the detection wavelength range can be switched between the“Visible”and“UV-visible”bands by adjusting the bias voltage.Moreover,the obtained CuI/Si diode was very sensitive to weak light illumination.A very high detectivity of 10^(13)-1014 Jones can be achieved with a power density as low as 0.5μW/cm^(2),which is significantly higher than that of other Cu-based diodes.These findings underscore the high application potential of CuI when integrated with the traditional Si industry.展开更多
Owing to uncontrolled and uneven electrodeposition and side reactions,Zn metal anodes inevitably suffer from issues such as dendrite growth,hydrogen evolution reactions,and surface passivation.This paper proposes an e...Owing to uncontrolled and uneven electrodeposition and side reactions,Zn metal anodes inevitably suffer from issues such as dendrite growth,hydrogen evolution reactions,and surface passivation.This paper proposes an efficient strategy to address these critical issues for realizing long-life and high-capacity aqueous zinc-ion hybrid supercapacitors(ZHSCs)by incorporating low-concentration(0.05 mol·L^(-1))redox RbI electrolyte additives.Specifically,rubidium cations have the ability to influence the negative Zn electrode surface via an electrostatic shielding mechanism,effectively protecting the electrode and minimizing undesired side reactions.In an aqueous solution,iodide anions actively solvate Zn^(2+)ions by stabilizing and modulating the solvation shell surrounding Zn^(2+).Moreover,the presence of iodide ions promotes the uniform deposition of Zn^(2+)species by selective adsorption onto the electrode surface.The synergistic effect of the electrostatic shielding and halogen ions enables the realization of aqueous symmetric Zn||Zn cells with a substantial cycle life of more than 2000 h Additionally,when applied to commercial activated carbon(AC),the proposed strategy facilitates the development of aqueous ZHSCs,exhibiting high specific capacitances(148.8 F·g^(-1)at 4 A·g^(-1))and ultra-long cycling stability.展开更多
We investigated dissolved iodine species in seawater from the northern South China Sea Shelf.Iodide concentrations were determined by cathodic stripping square wave voltammetry,and iodate was measured by spectrophotom...We investigated dissolved iodine species in seawater from the northern South China Sea Shelf.Iodide concentrations were determined by cathodic stripping square wave voltammetry,and iodate was measured by spectrophotometry.Dissolved organic iodine(DOI)was measured with reference to reduced iodide.R-TDI(R-X or rationalized-X is the concentration of X normalized to a salinity of 35,TDI represents total dissolved iodine)was in the range of 0.43–0.46μmol/L,showing a relatively conservative behavior,while iodate,iodide,and DOI showed non-conservative behaviors.Distribution characteristics in the surface waters showed R-iodate values in the 0.28–0.32μmol/L range and an offshore>inshore trend,while R-iodide was in the 0.11–0.19μmol/L range and R-DOI in the 0–0.07μmol/L range,reflecting an inshore>offshore trend for both.The vertical distribution showed the highest R-iodide concentrations in the surface waters and decreased values with depth,reaching less than0.01μmol/L at depths>200 m.R-iodate increased with depth with a measured peak value of 0.43μmol/L.Seawater with high iodate/iodide ratio(up to 2.9)was found in the central upwelling region and gradually decreased to 2.0 far from this center.The relationship between R-iodide and R-iodate among all samples followed the 1:1 relationship with a slope slightly less than 1,indicating that the conversion between iodate and iodide species could not account for the observed changes.This finding also suggests that DOI may be an important participant in the mass balance.A box model was applied to calculate the input and output of iodine species,and the result showed that approximately 8%of iodate(1.50×10~8 mol/a)imported to the shelf sea was reduced.Concomitantly,the amount of iodide and DOI produced in the shelf amounted to 1.07×10~8 mol/a,roughly 14%higher than the input iodide.展开更多
基金supported by Shenzhen Key Laboratory of Advanced Functional Carbon Materials Research and Comprehensive Application(Grant No.ZDSYS20220527171407017).
文摘The sodium-iodine(Na-I)battery exhibits significant potential as an alternative energy storage device to the lithium-ion battery.However,its development is hindered by inadequate electrical and thermal stability,as well as the dissolution and shuttling of polyiodide.In this study,we report a preparation method for melamine carbon sponge(MC)via carbonizing a commercially available kitchen sponge.It was revealed that the as-prepared MC,composed of unique self-growing carbon nanotubes,could provide both physical and chemical adsorption capabilities for intermediate polyiodides to improve the electrochemical performance of NaI.Consequently,the NaI/MC electrode effectively minimized polyiodide dissolution and reduced the electrochemical impedance.The NaI/MC cathode demonstrated a high average discharge capacity of 92.75 mAh·g^(–1)over 200 cycles while maintaining a coulombic efficiency of 94%.The research findings from our study have promising applications in Na-I batteries.
基金National Natural Science Foundation of China(Project No.:52320105003,Project No.:52303019)the CAS-ANSO Co-funding Research Project(Project No.:CAS-ANSO-CF-2024)+2 种基金the National Key R&D Program of China(Project No.:2023YFC3707201)the Fundamental Research Funds for the Central Universities(Project No.:E3ET1803)China Postdoctoral Science Foundation(Project No:2024T170904)。
文摘The valorization of nitrous oxide(N_(2)O)as an oxygen atom donor presents an attractive opportunity for green chemistry applications,leveraging both its industrial abundance and thermodynamically favorable oxidation potential.However,practical implementation has been constrained by the inherent kinetic inertness and poor coordinating ability of N_(2)O.While prior studies achieved N_(2)O-mediated conversion of aryl halides to phenols,such transformations necessitated stoichiometric chemical reductants and elevated pressure(2 atm),posing challenges in operational safety and process scalability.This study focuses on an electrochemical strategy that enables efficient oxygen atom transfer under ambient pressure through controlled current application.This methodology facilitates the selective transformation of aryl iodides to phenols without external reducing agents,establishing an environmentally benign synthetic pathway.By replacing traditional chemical reductants with electrons as the sole reducing equivalent,our approach addresses critical sustainability challenges in aromatic oxygenation chemistry while maintaining operational simplicity under mild conditions.
基金the National Key Research and Development Project(No.2023YFF1205103)the National Natural Science Foundation of China(No.22371007)the Peking University Medicine plus X Pilot Program-Key Technologies R&D Project(No.2024YXXLHGG001)for financial support。
文摘We herein present an efficient denitrative iodination method of(hetero)nitroarenes mediated by commercially available and cost-effective hydroiodic acid(HI).During the reaction process,HI plays its dual roles as both the sustainable reductant of nitro group and iodine source in the iodination step,which successfully integrates three steps into a one-pot procedure and significantly simplifies the reaction system.This approach enables a smooth metal-free conversion of nitroarenes to corresponding aryl iodides via one-pot process,exhibits a broad substrate scope and good reaction efficiency,and was conveniently applied in the concise synthesis of pharmaceuticals.
基金financially supported by the National Key Research and Development Program of China(No.2022YFB3803300)the Major Scientific and Technological Project in 2022 of Changsha,China(No.kq2301002).
文摘Perovskite solar cells(PSCs)based onα-phase FAPbI_(3)(α-FAPbI_(3))microcrystals precursor outperform those withδ-phase mi-crocrystals due to their superior crystallinity and fewer defects,makingα-phase microcrystals precursor more advantageous for high-per-formance PSCs.However,most reported synthesis methods of perovskite microcrystals,especially for aqueous synthesis,fail to reach the energy threshold required forα-phase transformation and therefore exhibit theδphase.In this study,we introduce a novel aqueous syn-thesis method to fabricateα-FAPbI_(3) microcrystals.Our approach overcomes the energy barrier by properly heating the reaction system,enabling the direct formation ofα-FAPbI_(3) in water.This direct one-step aqueous synthesis route yieldsα-FAPbI_(3) microcrystals with su-perior phase purity,crystallinity,and minimal defect density.Combined with green anti-solvent,the high-qualityα-FAPbI_(3) microcrystals serving as exceptional precursors endow perovskite films with reduced nonradiative recombination.The PSC achieves a remarkable power conversion efficiency(PCE)of 24.43%,which is one of the highest PCE reports for using the green anti-solvent in ambient air condition.This aqueous synthesis approach shows a significant potential for scalable production of high-performance PSCs.
基金supported by the National Natural Scientific Foundation of China(No.62305243)Fundamental Research Program of Shanxi Province(Nos.20210302124629,20210302124163,20210302124392,202203021212217)funded by China Scholarship Council。
文摘Poly(3-hexylthiophene)(P3HT)has been used in CsPbI_(3)per-ovskite solar cells(PSCs)as the hole transport layer(HTL),due to its excellent hydrophobic prop-erty and cheap cost.However,the inevitable defects in perovskite lead to the limited photovoltaic performance of CsPbI_(3)PSCs.In this study,diethylammonium io-dide(DEAI)was doped as an ad-ditive to passivate the defects in P3HT based CsPbI_(3)perovskite.Considering the diethylamine cations can effectively form hydrogen bonds with halide ion,the DEAI doping method could not only reduce the defect density but also facilitate the extraction and transport of carriers in the device.The optimal power conversion efficiency of the device prepared with DEAI doping method increases from 14.68%to 16.75%.In addition,the stability of the device is also signifi-cantly upgraded due to the improvement of CsPbI_(3)perovskite film.This work can provide re-liable theoretical and experimental evidence for further PSCs research.
基金supported by the National Research Foundation of Korea(NRF)grant fu nded by the Korean government(MSIT)(No.RS-2024-00335976)。
文摘Antimony sulfide(Sb_(2)S_(3))is a promising material for photoelectrochemical(PEC)devices that generate green hydrogen from sunlight and water.In this study,we present a synthesis of high-performance Sb_(2)S_(3)photoanodes via an interface-engineered hydrothermal growth followed by rapid thermal annealing(RTA).A TiO_(2)interfacial layer plays a crucial role in ensuring homogeneous precursor deposition,enhancing light absorption,and forming efficient heterojunctions with Sb_(2)S_(3),thereby significantly improving charge separation and transport.RTA further improves crystallinity and interfacial contact,resulting in dense and uniform Sb_(2)S_(3)films with enlarged grains and fewer defects.The optimized Sb_(2)S_(3)photoanode achieves a photocurrent density of 2.51 mA/cm^(2)at 1.23 V vs.the reversible hydrogen electrode(RHE),one of the highest reported for Sb_(2)S_(3)without additional catalysts or passivation layers.To overcome the limitations of oxygen evolution reaction(OER),we employ the iodide oxidation reaction(IOR)as an alternative,significantly lowering the overpotential and improving charge transfer kinetics.Consequently,it produces a record photocurrent density of 8.9 mA/cm^(2)at 0.54 V vs.RHE.This work highlights the synergy between TiO_(2)interfacial engineering,RTA-induced crystallization,and IOR-driven oxidation,offering a promising pathway for efficient and scalable PEC hydrogen production.
基金supported fnancially by the National Basic Research Program of China(973 Program,No.2012CB722603)the Start-Up Foundation for Young Scientists of Shihezi University(Nos.RCZX201012,RCZX201014,RCZX201015)
文摘Tetrazole-l-acetic acid was found to serve as a superior ligand for Cul-catalyzed N-arylation of imidazoles with aryl iodides under a low catalyst loading （5 mol% of Cul）. A variety of aryl iodides could he aminated to provide the N-arylated products in good to excellent yields without the need of an inert atmosphere.
文摘Functionalized alkylzinc iodides will undergo 1,4-conjugation reaction with derivatives of β-nitrostyrene in the presence of Cu(OAc)2/LiCl to afford a polyfunctional nitro-compound in high yield.
文摘In the presence of CrC13 /Fe bimetal couple,per(poly)fluoroalkyl iodides add to vinyl cyclopropane compounds giving addition-ring-opening products in good yields.
文摘(CH_3OCH_2CH_2C_5H_4)_2LnI(Ln=La,Nd)complexes have been synthesized by the reaction between NaI and[(CH_3OCH_2CH_2C_5H_4)_2LnCl]2 in THF;A single crystal X-ray study has shown that the lanthanum complex is an unsolvated monomer with lanthanum(Ⅲ)in a trigonal bipyramidal coordination geometry if the cyclopentadienyl ring is regarded as occupying a single polyhedral vertex.
基金Project (No. 2004C21032) supported by the Key Technology R & DProgram of Zhejiang Province, China
文摘Stereoselective transformation of Baylis-Hillman acetates I into corresponding （Z）-allyl iodides 2 has been achieved by treatment of I with samarium triiodide in THF. Remarkable rate acceleration of samarium triiodide-mediated iodination of 1 was found when ionic liquid 1-n-butyl-3-methyl-imidazolium tetrafluroborate （[bmim]BF4） was used as reaction media in stead of THF. This novel approach proceeds readily at 50 ℃ within a few minutes to afford （Z）-allyl iodides 2 in excellent yields. A mechanism involving stereoselective iodination of the acetates of Baylis-Hillman adducts by samarium triiodide is described, in which a six-membered ring transition state played a key role in the stereoselective formation of 2.
文摘An operationally simple and inexpensive catalyst system was developed for the cross coupling of potassium thiocyanate with aryl iodides by using CuI as catalyst, 1, 10-phenanthroline as ligand, and tetraethylammonium iodide as activator. The procedure is applicable for the synthesis of diverse aryl thiocyanates without any exotic, poisonous reagents.
基金the National Natural Science Foundation of China （No. 20562005） NSF of Jiangxi Province （No. 0620021） for financial support.
文摘Reaction of polystyrene-supported lithium selenide with 3-acetoxy-2-methylene-alkanoates afforded the corresponding allyl selenide resins and subsequent cleavage from the polymer by treating with methyl iodide to furnish （Z）-allyl iodides in good yields and high purities. The polymeric selenium reagent can be regenerated and reused. So it is a environmentally benign reagent.
文摘Initiated by CP_2TiCl_2/Fe redox system,2-halotetrafluoroethyl iodides readily reacted with alkynes or alkenes to give 1:1 adducts in good to excellent yields.
文摘perfluoroalkyl iodides reacted with alkenes in acetonitrile solu- tion containing catalytic amount of organophosphine under mild condition to give the corresponding adducts in moderate to good yields.Reaction was shown to involve a free radical mechanism.
基金financially supported by the National Natural Science Foundation of China(U21A2078,22179042,and 12104170)the Natural Science Foundation of Fujian Province(2020J06021 and 2020J01064)Scientific Research Funds of Huaqiao University(23BS109)。
文摘Lead iodide(PbI2) is a vital raw material for preparing perovskite solar cells(PSCs),and it not only takes part in forming the light absorption layer but also remains in the grain boundary as a passivator.In other words,the PbI2 content in the precursor and as formed film will affect the efficiency and stability of the PSCs.With moderate residual PbI2,it passivates the bulk/surface defects of perovskite,reduces the interfacial recombination,promotes the perovskite stability,minimizes the device hysteresis,and so on.Deficient PbI2 residue will reduce the interfacial passivation effect and device performance.In addition to facilitating the non-radiative recombination,over PbI2 residue can also lead to electronic insulation in the grain boundary and deteriorate the device performance.However,the impact and regulation of PbI2 residue on the device performance and stability is still not fully understood.Herein,a comprehensive and detailed review is presented by discussing the PbI2 residue impact and its regulation strategies(i.e., elimination,facilitation and conversion of the residue PbI2) to manipulate the PbI2 content,distribution and forms.Finally,we also show future outlooks in this field,with an aim to help further the progression of high-efficiency and stable PSCs.
基金National Natural Science Foundation of China(62074056)Fundamental Research Funds for the Central Universities。
文摘In recent years,copper iodide(CuI)is an emerging p-type wide bandgap semiconductor with high intrinsic Hall mobility,high optical absorption and large exciton binding energy.However,the spectral response and the photoelectric conversion efficiency are limited for CuI-based heterostructure devices,which is related to the difficulty in fabrication of high-quality CuI thin films on other semiconductors.In this study,a p-CuI/n-Si photodiode has been fabricated through a facile solid-phase iodination method.Although the CuI thin film is polycrystalline with obvious structural defects,the CuI/Si diode shows a high weak-light sensitivity and a high rectification ratio of 7.6×10^(4),indicating a good defect tolerance.This is because of the unilateral heterojunction behavior of the formation of the p^(+)n diode.In this work,the mechanism of photocurrent of the p^(+)n diode has been studied comprehensively.Different monochromatic lasers with wavelengths of 400,505,635 and 780 nm have been selected for testing the photoresponse.Under zero-bias voltage,the device is a unilateral heterojunction,and only visible light can be absorbed at the Si side.On the other hand,when a bias voltage of-3 V is applied,the photodiode is switched to a broader“UV-visible”band response mode.Therefore,the detection wavelength range can be switched between the“Visible”and“UV-visible”bands by adjusting the bias voltage.Moreover,the obtained CuI/Si diode was very sensitive to weak light illumination.A very high detectivity of 10^(13)-1014 Jones can be achieved with a power density as low as 0.5μW/cm^(2),which is significantly higher than that of other Cu-based diodes.These findings underscore the high application potential of CuI when integrated with the traditional Si industry.
基金financially supported by the National Natural Science Foundation of China(No.22209101)National Key R&D Program of China(No.2020YFA0710500)the Key Research and Development Program of Shaanxi(No.2022GXLH-01-23)for financial support。
文摘Owing to uncontrolled and uneven electrodeposition and side reactions,Zn metal anodes inevitably suffer from issues such as dendrite growth,hydrogen evolution reactions,and surface passivation.This paper proposes an efficient strategy to address these critical issues for realizing long-life and high-capacity aqueous zinc-ion hybrid supercapacitors(ZHSCs)by incorporating low-concentration(0.05 mol·L^(-1))redox RbI electrolyte additives.Specifically,rubidium cations have the ability to influence the negative Zn electrode surface via an electrostatic shielding mechanism,effectively protecting the electrode and minimizing undesired side reactions.In an aqueous solution,iodide anions actively solvate Zn^(2+)ions by stabilizing and modulating the solvation shell surrounding Zn^(2+).Moreover,the presence of iodide ions promotes the uniform deposition of Zn^(2+)species by selective adsorption onto the electrode surface.The synergistic effect of the electrostatic shielding and halogen ions enables the realization of aqueous symmetric Zn||Zn cells with a substantial cycle life of more than 2000 h Additionally,when applied to commercial activated carbon(AC),the proposed strategy facilitates the development of aqueous ZHSCs,exhibiting high specific capacitances(148.8 F·g^(-1)at 4 A·g^(-1))and ultra-long cycling stability.
基金The Zhangzhou National Science Foundation of Fujian under contract No.JJ2020J29。
文摘We investigated dissolved iodine species in seawater from the northern South China Sea Shelf.Iodide concentrations were determined by cathodic stripping square wave voltammetry,and iodate was measured by spectrophotometry.Dissolved organic iodine(DOI)was measured with reference to reduced iodide.R-TDI(R-X or rationalized-X is the concentration of X normalized to a salinity of 35,TDI represents total dissolved iodine)was in the range of 0.43–0.46μmol/L,showing a relatively conservative behavior,while iodate,iodide,and DOI showed non-conservative behaviors.Distribution characteristics in the surface waters showed R-iodate values in the 0.28–0.32μmol/L range and an offshore>inshore trend,while R-iodide was in the 0.11–0.19μmol/L range and R-DOI in the 0–0.07μmol/L range,reflecting an inshore>offshore trend for both.The vertical distribution showed the highest R-iodide concentrations in the surface waters and decreased values with depth,reaching less than0.01μmol/L at depths>200 m.R-iodate increased with depth with a measured peak value of 0.43μmol/L.Seawater with high iodate/iodide ratio(up to 2.9)was found in the central upwelling region and gradually decreased to 2.0 far from this center.The relationship between R-iodide and R-iodate among all samples followed the 1:1 relationship with a slope slightly less than 1,indicating that the conversion between iodate and iodide species could not account for the observed changes.This finding also suggests that DOI may be an important participant in the mass balance.A box model was applied to calculate the input and output of iodine species,and the result showed that approximately 8%of iodate(1.50×10~8 mol/a)imported to the shelf sea was reduced.Concomitantly,the amount of iodide and DOI produced in the shelf amounted to 1.07×10~8 mol/a,roughly 14%higher than the input iodide.
