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
Perovskite solar cells(PSCs)commonly exhibit significant performance degradation due to ion migration through the top charge transport layer and ultimately metal electrode corrosion.Here,we demonstrate an interfacial ...Perovskite solar cells(PSCs)commonly exhibit significant performance degradation due to ion migration through the top charge transport layer and ultimately metal electrode corrosion.Here,we demonstrate an interfacial management strategy using a boron chloride subphthalocyanine(Cl_(6)SubPc)/fullerene electron-transport layer,which not only passivates the interfacial defects in the perovskite,but also suppresses halide diffusion as evidenced by multiple techniques,including visual element mapping by electron energy loss spectroscopy.As a result,we obtain inverted PSCs with an efficiency of 22.0%(21.3%certified),shelf life of 7000 h,T_(80) of 816 h under damp heat stress(compared to less than 20 h without Cl_(6)SubPc),and initial performance retention of 98%after 2000 h at 80℃in inert environment,90%after 2034 h of illumination and maximum power point tracking in ambient for encapsulated devices and 95%after 1272 h outdoor testing ISOS-O-1.Our strategy and results pave a new way to move PSCs forward to their potential commercialization solidly.展开更多
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.
基金supported by the National Natural Science Foundation of China (61775091, and U2001216)the Shenzhen Key Laboratory Project (ZDSYS201602261933302)+2 种基金Natural Science Foundation of Shenzhen Innovation Committee (JCYJ20180504165851864)the support of Research Grants Council Collaborative Research Fund (RGC- CRF) grant C5037-18GSeed Funding for Strategic Interdisciplinary Research Scheme of the University of Hong Kong and Shenzhen Science and Technology Commission Projects (JCYJ20170818141216288)
文摘Perovskite solar cells(PSCs)commonly exhibit significant performance degradation due to ion migration through the top charge transport layer and ultimately metal electrode corrosion.Here,we demonstrate an interfacial management strategy using a boron chloride subphthalocyanine(Cl_(6)SubPc)/fullerene electron-transport layer,which not only passivates the interfacial defects in the perovskite,but also suppresses halide diffusion as evidenced by multiple techniques,including visual element mapping by electron energy loss spectroscopy.As a result,we obtain inverted PSCs with an efficiency of 22.0%(21.3%certified),shelf life of 7000 h,T_(80) of 816 h under damp heat stress(compared to less than 20 h without Cl_(6)SubPc),and initial performance retention of 98%after 2000 h at 80℃in inert environment,90%after 2034 h of illumination and maximum power point tracking in ambient for encapsulated devices and 95%after 1272 h outdoor testing ISOS-O-1.Our strategy and results pave a new way to move PSCs forward to their potential commercialization solidly.
