In this paper,we examine the tiny polarization rotation effect in total internal reflection due to the spin–orbit interaction of light.We find that the tiny polarization rotation rate will induce a geometric phase gr...In this paper,we examine the tiny polarization rotation effect in total internal reflection due to the spin–orbit interaction of light.We find that the tiny polarization rotation rate will induce a geometric phase gradient,which can be regarded as the physical origin of photonic spin Hall effect.We demonstrate that the spin-dependent splitting in position space is related to the polarization rotation in momentum space,while the spin-dependent splitting in momentum space is attributed to the polarization rotation in position space.Furthermore,we introduce a quantum weak measurement to determine the tiny polarization rotation rate.The rotation rate in momentum space is obtained with 118 nm,which manifests itself as a spatial shift,and the rotation rate in position space is achieved with 38 μrad∕λ,which manifests itself as an angular shift.The investigation of the polarization rotation characteristics will provide insights into the photonic spin Hall effect and will enable us to better understand the spin–orbit interaction of light.展开更多
As a small catalytic DNA molecule, 10-23 DNAzyme has cleavage ability against complementary RNA. Previous studies of chemical modification have shown that its catalytic core can be further optimized in order to obtain...As a small catalytic DNA molecule, 10-23 DNAzyme has cleavage ability against complementary RNA. Previous studies of chemical modification have shown that its catalytic core can be further optimized in order to obtain more powerful catalytic ability. The analogues of 2＇-deoxyadenosine （5） and 2＇-deoxyguanosine （6） could improve the cleavage ability of the DNAzyme when positioned at positions A9, （32 and G14 in the catalytic core, respectively. Moreover, their combinatorial incorporations were studied, the results implicated that the effect was position-dependent, and positive additive results could be achieved at some positions. The highly conserved G1, G2 and G14 could be optimized by single or combinatorial modification with 2＇-deoxyguanosine analogues. Chemical modifications on the functional groups of the core residues would be a feasible approach for the optimization of 10-23 DNAzyme.展开更多
基金National Natural Science Foundation of China(NSFC)(11274106,11474089)
文摘In this paper,we examine the tiny polarization rotation effect in total internal reflection due to the spin–orbit interaction of light.We find that the tiny polarization rotation rate will induce a geometric phase gradient,which can be regarded as the physical origin of photonic spin Hall effect.We demonstrate that the spin-dependent splitting in position space is related to the polarization rotation in momentum space,while the spin-dependent splitting in momentum space is attributed to the polarization rotation in position space.Furthermore,we introduce a quantum weak measurement to determine the tiny polarization rotation rate.The rotation rate in momentum space is obtained with 118 nm,which manifests itself as a spatial shift,and the rotation rate in position space is achieved with 38 μrad∕λ,which manifests itself as an angular shift.The investigation of the polarization rotation characteristics will provide insights into the photonic spin Hall effect and will enable us to better understand the spin–orbit interaction of light.
基金The National Natural Science Foundation of China(Grant No.21572268)
文摘As a small catalytic DNA molecule, 10-23 DNAzyme has cleavage ability against complementary RNA. Previous studies of chemical modification have shown that its catalytic core can be further optimized in order to obtain more powerful catalytic ability. The analogues of 2＇-deoxyadenosine （5） and 2＇-deoxyguanosine （6） could improve the cleavage ability of the DNAzyme when positioned at positions A9, （32 and G14 in the catalytic core, respectively. Moreover, their combinatorial incorporations were studied, the results implicated that the effect was position-dependent, and positive additive results could be achieved at some positions. The highly conserved G1, G2 and G14 could be optimized by single or combinatorial modification with 2＇-deoxyguanosine analogues. Chemical modifications on the functional groups of the core residues would be a feasible approach for the optimization of 10-23 DNAzyme.
