NORHA,a long non-coding RNA(lncRNA),serves as a key inducer of follicular atresia in sows by triggering granulosa cells(GCs)apoptosis.However,its regulation by N6-methyladenosine(m6A)-the most abundant RNA modificatio...NORHA,a long non-coding RNA(lncRNA),serves as a key inducer of follicular atresia in sows by triggering granulosa cells(GCs)apoptosis.However,its regulation by N6-methyladenosine(m6A)-the most abundant RNA modification-remains unresolved.This study identified NORHA as a functional target of the m6A reader HNRNPA2B1 in sow GCs(sGCs).Transcriptome-wide mapping of RNA modification sites revealed extensive m6A enrichment on NORHA,with HNRNPA2B1 binding directly to the transcript and enhancing its stability via modification of multiple m6A sites,including A261,A441,and A919.HNRNPA2B1 suppressed 17β-estradiol(E2)biosynthesis and promoted sGC apoptosis by activating the NORHA-FoxO1 axis.FoxO1 subsequently repressed expression of cytochrome P450 family 19 subfamily A member 1(CYP19A1),which encodes the enzyme essential for E2 biosynthesis.Additionally,HNRNPA2B1 functioned as a critical mediator of METTL3-dependent m6A modification,modulating NORHA expression and activity in sGCs.This study highlights an important m6Adependent regulatory mechanism governing NORHA expression in sGCs.展开更多
The NASICON-structured Na_(2)VTi(PO_(4))_(3)(NVTPO)has attracted significant attention due to its exceptional structural stability and rapid Na~+mobility.However,the development of this material has been hindered by p...The NASICON-structured Na_(2)VTi(PO_(4))_(3)(NVTPO)has attracted significant attention due to its exceptional structural stability and rapid Na~+mobility.However,the development of this material has been hindered by poor electronic conductivity and inadequate low-temperature performance.Herein,a feasible strategy of lattice regulation integrated with surface modification for NVTPO by nitrogen(N)deep doping is proposed.Systematic characterizations and theoretical calculations confirm that N is doped into both the inner crystal structure of NVTPO and the outer carbon layer.The blueshift of the P—O bonds and charge redistribution induced by the V/Ti—N bonds strengthen the local environment and narrow the bandgap,thereby enabling reversible structural evolution and improving electronic conductivity.As expected,the optimized NVTPO/N@CN material achieves an ultra-high capacity of 188.48 mA h g^(-1)at 10 mA g^(-1)and a long-term lifespan of 2000 cycles at 1 A g^(-1).More importantly,it exhibits competitive low-temperature performance(92.15%retention after 1000 cycles at 300 mA g^(-1)and-15℃)due to reduced charge transfer impedance and activation energy.This deep doping strategy modification is expected to broaden the applications of NASICON-type cathodes.展开更多
Sodium-ion batteries(SIBs)are the promising rechargeable batteries in large-scale energy storage systems for their low cost,high safety,wide temperature range adaptability,environmental friendliness and excellent fast...Sodium-ion batteries(SIBs)are the promising rechargeable batteries in large-scale energy storage systems for their low cost,high safety,wide temperature range adaptability,environmental friendliness and excellent fast-charging capabilities.Significant research endeavors in SIBs have focused on the exploration of high-performance electrode materials and thorough investigation of their mechanisms.Na_(2)FePO_(4)F(NFPF)is one of potential cathode materials because of low cost,minimal volume strain and extended cycle performance.This review summarizes the crystal structure,sodium ion migration pathways,and synthesis methods of NFPF and discusses the effect of various strategies including hybridization with carbon materials,ion doping,morphology control and electrolyte optimization on its electrochemical performance.Additionally,the application of the NFPF in different batteries is summarized.Finally,the challenges and future directions of NFPF are proposed.This review is both timely and important for promoting the applications of cost-effective NFPF.展开更多
To satisfy the demands of modern society for high-energy–density sulfide-based all-solid-state lithium batteries(ASSLBs),Ni-rich cathode materials have gained much attention for their high capacity and energy density...To satisfy the demands of modern society for high-energy–density sulfide-based all-solid-state lithium batteries(ASSLBs),Ni-rich cathode materials have gained much attention for their high capacity and energy density.However,their practical deployment is hindered by accelerated interface degradation and capacity decay originating from surface oxygen release and lattice oxygen activation during prolonged cycling.In this study,Ti_(x)NbB_((1−x))C_(2)was successfully coated on the surface of LiNi_(0.94)Co_(0.05)Mn_(0.01)O_(2).Density functional theory(DFT)calculations first elucidate a“point-to-point”anchoring mechanism where each surface oxygen atom coordinates with single species(Ti/Nb/B)offered by Ti_(x)NbB_((1−x))C_(2),which forms robust O–M bonds and sustain a stable interface structure.The electron energy loss spectroscopy(EELS)reveals the segregation of Ti/Nb toward subsurface layers during cycling,creating an optimized lattice oxygen coordination environment and suppressing oxygen activation.The dual oxygen stabilization mechanism dramatically improves the reversibility of phase transition and the structural stability of the Ni-rich cathode materials.Moreover,Ti_(x)NbB_((1−x))C_(2)as the protective layer decreases mechanical strain and suppresses the parasitic reactions.Consequently,the engineered cathode delivers 91%capacity retention after 1000 cycles at 0.3 C,suggesting excellent cycling stability.The research delivers a new design philosophy for the coating layer that can stabilize surface oxygen.Furthermore,the atomistic understanding of the structure–property relationship of the Ni-rich cathode materials provides valuable guidance for the future design of new cathode materials with superior structural stability in ASSLBs.展开更多
The modification effect of neodymium （Nd） on Mg2Si in the hypereutectic Mg-3%Si （mass fraction） alloy was investigated by optical microcopy, scanning electron microscopy and X-ray diffraction. The results indicate...The modification effect of neodymium （Nd） on Mg2Si in the hypereutectic Mg-3%Si （mass fraction） alloy was investigated by optical microcopy, scanning electron microscopy and X-ray diffraction. The results indicate that the morphology of the primary Mg2Si transforms from coarse dendrite into fine polygon with increasing Nd content. The average size of the primary Mg2Si significantly decreases to about 10 ~ma with increasing Nd content up to 1.0%, and then becomes coarser again. The modification and refinement of the primary Mg2Si are mainly attributed to the poisoning effect. The NdMg2 phase in the primary Mg2Si transforms into NdSi and NdSi2 compounds as the Nd content exceeds 3.0%. Therefore, it is reasonable to conclude that the proper Nd （1.0%） addition can effectively modify and refine the primary Mg2Si.展开更多
基金supported by the National Natural Science Foundation of China(32072693)Fundamental Research Funds for the Central Universities(KYLH2025010)Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX24-0994)。
文摘NORHA,a long non-coding RNA(lncRNA),serves as a key inducer of follicular atresia in sows by triggering granulosa cells(GCs)apoptosis.However,its regulation by N6-methyladenosine(m6A)-the most abundant RNA modification-remains unresolved.This study identified NORHA as a functional target of the m6A reader HNRNPA2B1 in sow GCs(sGCs).Transcriptome-wide mapping of RNA modification sites revealed extensive m6A enrichment on NORHA,with HNRNPA2B1 binding directly to the transcript and enhancing its stability via modification of multiple m6A sites,including A261,A441,and A919.HNRNPA2B1 suppressed 17β-estradiol(E2)biosynthesis and promoted sGC apoptosis by activating the NORHA-FoxO1 axis.FoxO1 subsequently repressed expression of cytochrome P450 family 19 subfamily A member 1(CYP19A1),which encodes the enzyme essential for E2 biosynthesis.Additionally,HNRNPA2B1 functioned as a critical mediator of METTL3-dependent m6A modification,modulating NORHA expression and activity in sGCs.This study highlights an important m6Adependent regulatory mechanism governing NORHA expression in sGCs.
基金supported by the National Natural Science Foundation of China(22272205 and 22178094)the Hunan Provincial Nature Science Foundation of China(2022JJ30685,2023JJ20059 and 2024JJ5292)+2 种基金the Hunan Provincial Science and Technology Plan Projects of China(2022RC3050 and 2017TP1001)the financial support from the Aid Program for Science and Technology Innovative Research Team in Higher Educational Institutions of Hunan Provincesupport from the Young Elite Scientists Sponsorship Program by CAST(YESS20220432)。
文摘The NASICON-structured Na_(2)VTi(PO_(4))_(3)(NVTPO)has attracted significant attention due to its exceptional structural stability and rapid Na~+mobility.However,the development of this material has been hindered by poor electronic conductivity and inadequate low-temperature performance.Herein,a feasible strategy of lattice regulation integrated with surface modification for NVTPO by nitrogen(N)deep doping is proposed.Systematic characterizations and theoretical calculations confirm that N is doped into both the inner crystal structure of NVTPO and the outer carbon layer.The blueshift of the P—O bonds and charge redistribution induced by the V/Ti—N bonds strengthen the local environment and narrow the bandgap,thereby enabling reversible structural evolution and improving electronic conductivity.As expected,the optimized NVTPO/N@CN material achieves an ultra-high capacity of 188.48 mA h g^(-1)at 10 mA g^(-1)and a long-term lifespan of 2000 cycles at 1 A g^(-1).More importantly,it exhibits competitive low-temperature performance(92.15%retention after 1000 cycles at 300 mA g^(-1)and-15℃)due to reduced charge transfer impedance and activation energy.This deep doping strategy modification is expected to broaden the applications of NASICON-type cathodes.
基金supported by National Natural Science Foundation of China(No.52064031)Natural Science Foundation of Yunnan Province(Nos.202301BE070001–014,202301AT070150,202402AB080001)the Analysis and Testing Foundation of Kunming University of Science and Technology(No.2022T20210182)。
文摘Sodium-ion batteries(SIBs)are the promising rechargeable batteries in large-scale energy storage systems for their low cost,high safety,wide temperature range adaptability,environmental friendliness and excellent fast-charging capabilities.Significant research endeavors in SIBs have focused on the exploration of high-performance electrode materials and thorough investigation of their mechanisms.Na_(2)FePO_(4)F(NFPF)is one of potential cathode materials because of low cost,minimal volume strain and extended cycle performance.This review summarizes the crystal structure,sodium ion migration pathways,and synthesis methods of NFPF and discusses the effect of various strategies including hybridization with carbon materials,ion doping,morphology control and electrolyte optimization on its electrochemical performance.Additionally,the application of the NFPF in different batteries is summarized.Finally,the challenges and future directions of NFPF are proposed.This review is both timely and important for promoting the applications of cost-effective NFPF.
基金supported by the National Natural Science Foundation of China(21203008,21975025,12274025,22372008,and 22179007)Hainan Province Science and Technology Special Fund(ZDYF2021SHFZ232 and ZDYF2023GXJS022)Hainan Province Postdoctoral Science Foundation(300333)。
文摘To satisfy the demands of modern society for high-energy–density sulfide-based all-solid-state lithium batteries(ASSLBs),Ni-rich cathode materials have gained much attention for their high capacity and energy density.However,their practical deployment is hindered by accelerated interface degradation and capacity decay originating from surface oxygen release and lattice oxygen activation during prolonged cycling.In this study,Ti_(x)NbB_((1−x))C_(2)was successfully coated on the surface of LiNi_(0.94)Co_(0.05)Mn_(0.01)O_(2).Density functional theory(DFT)calculations first elucidate a“point-to-point”anchoring mechanism where each surface oxygen atom coordinates with single species(Ti/Nb/B)offered by Ti_(x)NbB_((1−x))C_(2),which forms robust O–M bonds and sustain a stable interface structure.The electron energy loss spectroscopy(EELS)reveals the segregation of Ti/Nb toward subsurface layers during cycling,creating an optimized lattice oxygen coordination environment and suppressing oxygen activation.The dual oxygen stabilization mechanism dramatically improves the reversibility of phase transition and the structural stability of the Ni-rich cathode materials.Moreover,Ti_(x)NbB_((1−x))C_(2)as the protective layer decreases mechanical strain and suppresses the parasitic reactions.Consequently,the engineered cathode delivers 91%capacity retention after 1000 cycles at 0.3 C,suggesting excellent cycling stability.The research delivers a new design philosophy for the coating layer that can stabilize surface oxygen.Furthermore,the atomistic understanding of the structure–property relationship of the Ni-rich cathode materials provides valuable guidance for the future design of new cathode materials with superior structural stability in ASSLBs.
基金Project(A0420110401)supported by the National Security Basic Research,China
文摘The modification effect of neodymium （Nd） on Mg2Si in the hypereutectic Mg-3%Si （mass fraction） alloy was investigated by optical microcopy, scanning electron microscopy and X-ray diffraction. The results indicate that the morphology of the primary Mg2Si transforms from coarse dendrite into fine polygon with increasing Nd content. The average size of the primary Mg2Si significantly decreases to about 10 ~ma with increasing Nd content up to 1.0%, and then becomes coarser again. The modification and refinement of the primary Mg2Si are mainly attributed to the poisoning effect. The NdMg2 phase in the primary Mg2Si transforms into NdSi and NdSi2 compounds as the Nd content exceeds 3.0%. Therefore, it is reasonable to conclude that the proper Nd （1.0%） addition can effectively modify and refine the primary Mg2Si.
