Neurodegenerative diseases are characterized by a decline in brain structure and function.Their pathology involves multiple cell death pathways,including ferroptosis,cuproptosis,and pyroptosis.These pathways are intri...Neurodegenerative diseases are characterized by a decline in brain structure and function.Their pathology involves multiple cell death pathways,including ferroptosis,cuproptosis,and pyroptosis.These pathways are intricately linked to genes associated with metabolism,antioxidant defense,lipid metabolism,chronic inflammation,and nerve regeneration processes.Key regulators of atypical cell death pathways show aberrant N^(6)-methyladenosine modification levels under pathological conditions.As the most abundant and dynamic RNA modification in brain tissue,N^(6)-methyladenosine plays crucial functional roles.Notably,there exists an intricate interplay between N^(6)-methyladenosine modifications and these cell death pathways,both of which are robustly associated with the pathogenesis of neurodegenerative diseases.However,the molecular mechanisms underlying this association remain unclear.This paper reviews the correlation between N^(6)-methyladenosine and various cell death patterns in neurodegenerative diseases,with emphasis on the molecular mechanisms underlying the interaction between N^(6)-methyladenosine epigenetic regulation and ferroptosis,cuproptosis,and pyroptosis in cognitive impairment.N^(6)-methyladenosine-modified ferroptosis plays an important role in neurodegenerative diseases.There is also a close association between N^(6)-methyladenosine modification and key molecules related to cuproptosis,which may promote the deposition of copper in the brain.Chronic inflammation,a hallmark of neurodegenerative diseases,is related to pyroptosis and N^(6)-methyladenosine modification.It is widely thought that ferroptosis,cuproptosis,and pyroptosis are interconnected processes that may share a common pathway affecting the pathogenesis of neurodegenerative diseases,and are related to key molecules involved in N^(6)-methyladenosine epigenetic modification.This suggests a great potential for future neurodegenerative diseases treatment strategies regulated by N^(6)-methyladenosine modification.N^(6)-methyladenosine modification plays a dual role in nerve injury and regeneration by dynamically regulating processes such as ferroptosis,cuproptosis,and pyroptosis and their key molecules.It maintains the“death-regeneration”balance in oxidative stress and inflammation while selectively promoting axon regeneration through the modulation of methylases.This mechanism indicates a considerable therapeutic target for neurological disorders.展开更多
Lithium/potassium ion capacitors(LICs/PICs) have been proposed to bridge the performance gap between high-energy batteries and high-power capacitors.However,their development is hindered by the choice,electrochemical ...Lithium/potassium ion capacitors(LICs/PICs) have been proposed to bridge the performance gap between high-energy batteries and high-power capacitors.However,their development is hindered by the choice,electrochemical performance,and preparation technique of the battery-type anode materials.Herein,a nitrogen and phosphorus dual-doped multilayer graphene(NPG) material is designed and synthesized through an arc discharge process,using low-cost graphite and solid nitrogen and phosphorus sources.When employed as the anode material,NPG exhibits high capacity,remarkable rate capability,and stable cycling performance in both lithium and potassium ion batteries.This excellent electrochemical performance is ascribed to the synergistic effect of nitrogen and phosphorus doping,which enhances the electrochemical conductivity,provides a higher number of ion storage sites,and leads to increased interlayer spacing.Full carbon-based NPG‖LiPF6‖active carbon(AC) LICs and NPG‖KPF6‖AC PICs are assembled and show excellent electrochemical performance,with competitive energy and power densities.This work provides a route for the large-scale production of dual-doped graphene as a universal anode material for high-performance alkali ion batteries and capacitors.展开更多
It is highly desirable to design and synthesize two-dimensional nanostructured electrode materials with high electrical conductivity,large electrolyte-accessible surface area and more exposed active sites for energy s...It is highly desirable to design and synthesize two-dimensional nanostructured electrode materials with high electrical conductivity,large electrolyte-accessible surface area and more exposed active sites for energy storage applications.Herein,MXene/Co Al-LDH heterostructure has been prepared through electrostatic ordered hetero-assembly of monolayer MXene and edge-rich Co Al-LDH nanosheets in a faceto-face manner on molecular-scale for supercapacitor applications.Benefiting from the unique structure,strong interfacial interaction and synergistic effects between MXene and Co Al-LDH nanosheets,the electrical conductivity and exposed electrolyte-accessible active sites are significantly enhanced.The asprepared MXene/Co Al-LDH-80%(ML-80)film exhibits high volumetric capacity of 2472 C cm-3 in 3 M KOH electrolyte with high rate capability of 70.6%at 20 A g-1.Notably,to the best of our knowledge,the high volumetric capacity is the highest among other previously reported values for supercapacitors in aqueous electrolytes.Furthermore,our asymmetric supercapacitor device fabricated with ML-80 and MXene/graphene composite as cathode and anode,respectively,exhibits impressive volumetric energy density of 85.4 Wh L-1 with impressive cycling stability of 94.4%retention ratio after 30,000 continuous charge/discharge cycles.展开更多
Aqueous zinc energy storage devices,holding various merits such as high specific capacity and low costs,have attracted extensive attention in recent years.Nevertheless,Zn metal anodes still suffer from a short lifespa...Aqueous zinc energy storage devices,holding various merits such as high specific capacity and low costs,have attracted extensive attention in recent years.Nevertheless,Zn metal anodes still suffer from a short lifespan and low Coulombic efficiency due to corrosion and side reactions in aqueous electrolytes.In this paper,we construct an artificial Sn inorganic layer on Zn metal anode through a facile strategy of atom exchange.The Sn layer suppresses Zn dendrite growth by facilitating homogeneous Zn plating and stripping during charge and discharge processes.Meanwhile,the Sn protective layer also serves as a physical barrier to decrease Zn corrosion and hydrogen generation.As a result,The Sn-coated anode(Sn|Zn)exhibits a low polarization voltage(~34 mV at 0.5 mAh/cm^(2))after 800 testing hours and displays a smooth and an even surface without corrosion.Moreover,the zinc ion capacitor(Sn|Zn‖activated carbon)is assembled with an enhanced capacity of 42 mAh/g and a capacity retention of 95%after 10,000 cycles at 5 A/g.This work demonstrates a feasible approach for the commercialization of aqueous Zn-based energy storage devices.展开更多
Aqueous Zn-based energy storage devices possess tremendous advantages, such as low cost, high safety,and competitive energy density, due to employing a Zn metal anode and aqueous electrolyte. However,the cycling stabi...Aqueous Zn-based energy storage devices possess tremendous advantages, such as low cost, high safety,and competitive energy density, due to employing a Zn metal anode and aqueous electrolyte. However,the cycling stability and rate ability of a Zn anode are hindered by Zn dendrite growth and sluggish ion transfer in the electrode/electrolyte interface. Herein, the interfacial properties of Zn anodes are improved through the introduction of a silver(Ag) protective layer, which facilitates uniform Zn deposition and regulates Zn ion transport. As a result, Ag-coated Zn anodes display stable cycling performance(600 h at 1 m A cm^(-2)) and low overpotential(150 mV at 50 mA cm^(-2)after 2000 cycles). The Ag layer in situ electrochemically converts into an AgZn_(3) layer and promotes Zn ion desolvation and threedimensional diffusion processes. Moreover, a Zn-ion capacitor assembled with an Ag-coated Zn anode and active carbon cathode shows a capable cycling lifespan and rate performance. This study provides a feasible strategy for constructing a stabilized and dendrite-free Zn anode for the development of high-performance Zn-based energy storage devices.展开更多
A novel plastic/multi-walled carbon nanotube（MWNTs）-nickel（Ni）-platinum（Pt） electrode（PMNP） is prepared by chemical-reducing Pt onto the surface of Ni film covered plastic/MWNTs（PM） substrate. The MWNTs are ...A novel plastic/multi-walled carbon nanotube（MWNTs）-nickel（Ni）-platinum（Pt） electrode（PMNP） is prepared by chemical-reducing Pt onto the surface of Ni film covered plastic/MWNTs（PM） substrate. The MWNTs are adhered by a piece of commercial double faced adhesive tape on the surface of plastic paper and the Ni film is prepared by a simple electrodeposition method. The morphology and phase structure of the PMNP electrode are characterized by scanning electron microscopy,transmission electron microscope and X-ray diffractometer. The catalytic activity of the PMNP electrode for Na BH4 electrooxidation is investigated by means of cyclic voltammetry and chronoamperometry. The catalyst combines tightly with the plastic paper and exhibits a good stability. MWNTs serve as both conductive material and hydrogen storage material and the Ni film and Pt are employed as electrochemical catalysts. The PMNP electrode exhibits a high electrocatalytic performance and the oxidation current density reaches to 10.76 A/（mg·cm） in 0.1 mol/dm3 Na BH4at0 V,which is much higher than those in the previous reports. The using of waste plastic reduces the discarding of white pollution and consumption of metal resources.展开更多
Interface chemical modulation strategies are considered as promising method to prepare electrocatalysts for the urea oxidation reaction(UOR).However,conventional interface catalysts are generally limited by the inhere...Interface chemical modulation strategies are considered as promising method to prepare electrocatalysts for the urea oxidation reaction(UOR).However,conventional interface catalysts are generally limited by the inherent activity and incompatibility of the individual components themselves,and the irregular charge distribution and slow charge transfer ability between interfaces severely limit the activity of UOR.Therefore,we optimized and designed a Ni_(2)P/CoP interface with modulated surface charge distribution and directed charge transfer to promote UOR activity.Density functional theorycalculations first predict a regular charge transfer from CoP to Ni_(2)P,which creates a built-in electric field between Ni_(2)P and CoP interface.Optimization of the adsorption/desorption process of UOR/HER reaction intermediates leads to the improvement of catalytic activity.Electrochemical impedance spectroscopy and ex situ X-ray photoelectron spectroscopy characterization confirm the unique mechanism of facilitated reaction at the Ni_(2)P/CoP interface.Electrochemical tests further validated the prediction with excellent UOR/HER activities of 1.28 V and 19.7 mV vs.RHE,at 10 mA cm^(-2),respectively.Furthermore,Ni_(2)P/CoP achieves industrial-grade current densities(500 mA cm^(−2))at 1.75 V and 1.87 V in the overall urea electrolyzer(UOR||HER)and overall human urine electrolyzer(HUOR||HER),respectively,and demonstrates considerable durability.展开更多
N6-methyladenosine(m^(6)A), the most prevalent and conserved RNA modification in eukaryotic cells, profoundly influences virtually all aspects of mRNA metabolism. mRNA plays crucial roles in neural stem cell genesis a...N6-methyladenosine(m^(6)A), the most prevalent and conserved RNA modification in eukaryotic cells, profoundly influences virtually all aspects of mRNA metabolism. mRNA plays crucial roles in neural stem cell genesis and neural regeneration, where it is highly concentrated and actively involved in these processes. Changes in m^(6)A modification levels and the expression levels of related enzymatic proteins can lead to neurological dysfunction and contribute to the development of neurological diseases. Furthermore, the proliferation and differentiation of neural stem cells, as well as nerve regeneration, are intimately linked to memory function and neurodegenerative diseases. This paper presents a comprehensive review of the roles of m^(6)A in neural stem cell proliferation, differentiation, and self-renewal, as well as its implications in memory and neurodegenerative diseases. m^(6)A has demonstrated divergent effects on the proliferation and differentiation of neural stem cells. These observed contradictions may arise from the time-specific nature of m^(6)A and its differential impact on neural stem cells across various stages of development. Similarly, the diverse effects of m^(6)A on distinct types of memory could be attributed to the involvement of specific brain regions in memory formation and recall. Inconsistencies in m^(6)A levels across different models of neurodegenerative disease, particularly Alzheimer's disease and Parkinson's disease, suggest that these disparities are linked to variations in the affected brain regions. Notably, the opposing changes in m^(6)A levels observed in Parkinson's disease models exposed to manganese compared to normal Parkinson's disease models further underscore the complexity of m^(6)A's role in neurodegenerative processes. The roles of m^(6)A in neural stem cell proliferation, differentiation, and self-renewal, and its implications in memory and neurodegenerative diseases, appear contradictory. These inconsistencies may be attributed to the timespecific nature of m^(6)A and its varying effects on distinct brain regions and in different environments.展开更多
基金supported by The Youth Talent Support Program of China Association of Chinese Medicine(2024-2026),No.CACM-2024-QNRC2-B36(to QX)The Central High-level Hospital of Traditional Chinese Medicine:Beijing University of Traditional Chinese Medicine Dongzhimen Hospital Talent Training Program-Youth Reserve Talent Project,No.DZMG-QNHB0010(to QX)the Natural Science Foundation of Heilongjiang Province(Outstanding Youth Program),No.YQ2022H003(to DW).
文摘Neurodegenerative diseases are characterized by a decline in brain structure and function.Their pathology involves multiple cell death pathways,including ferroptosis,cuproptosis,and pyroptosis.These pathways are intricately linked to genes associated with metabolism,antioxidant defense,lipid metabolism,chronic inflammation,and nerve regeneration processes.Key regulators of atypical cell death pathways show aberrant N^(6)-methyladenosine modification levels under pathological conditions.As the most abundant and dynamic RNA modification in brain tissue,N^(6)-methyladenosine plays crucial functional roles.Notably,there exists an intricate interplay between N^(6)-methyladenosine modifications and these cell death pathways,both of which are robustly associated with the pathogenesis of neurodegenerative diseases.However,the molecular mechanisms underlying this association remain unclear.This paper reviews the correlation between N^(6)-methyladenosine and various cell death patterns in neurodegenerative diseases,with emphasis on the molecular mechanisms underlying the interaction between N^(6)-methyladenosine epigenetic regulation and ferroptosis,cuproptosis,and pyroptosis in cognitive impairment.N^(6)-methyladenosine-modified ferroptosis plays an important role in neurodegenerative diseases.There is also a close association between N^(6)-methyladenosine modification and key molecules related to cuproptosis,which may promote the deposition of copper in the brain.Chronic inflammation,a hallmark of neurodegenerative diseases,is related to pyroptosis and N^(6)-methyladenosine modification.It is widely thought that ferroptosis,cuproptosis,and pyroptosis are interconnected processes that may share a common pathway affecting the pathogenesis of neurodegenerative diseases,and are related to key molecules involved in N^(6)-methyladenosine epigenetic modification.This suggests a great potential for future neurodegenerative diseases treatment strategies regulated by N^(6)-methyladenosine modification.N^(6)-methyladenosine modification plays a dual role in nerve injury and regeneration by dynamically regulating processes such as ferroptosis,cuproptosis,and pyroptosis and their key molecules.It maintains the“death-regeneration”balance in oxidative stress and inflammation while selectively promoting axon regeneration through the modulation of methylases.This mechanism indicates a considerable therapeutic target for neurological disorders.
基金supported by National Natural Science Foundation of China(Nos.51672056 and 51702063)Natural Science Foundation of Heilongjiang(LC2018004)+1 种基金China Postdoctoral Science Foundation(2018M630340)the Fundamental Research Funds for the Central University(HEUCFD201732)
文摘Lithium/potassium ion capacitors(LICs/PICs) have been proposed to bridge the performance gap between high-energy batteries and high-power capacitors.However,their development is hindered by the choice,electrochemical performance,and preparation technique of the battery-type anode materials.Herein,a nitrogen and phosphorus dual-doped multilayer graphene(NPG) material is designed and synthesized through an arc discharge process,using low-cost graphite and solid nitrogen and phosphorus sources.When employed as the anode material,NPG exhibits high capacity,remarkable rate capability,and stable cycling performance in both lithium and potassium ion batteries.This excellent electrochemical performance is ascribed to the synergistic effect of nitrogen and phosphorus doping,which enhances the electrochemical conductivity,provides a higher number of ion storage sites,and leads to increased interlayer spacing.Full carbon-based NPG‖LiPF6‖active carbon(AC) LICs and NPG‖KPF6‖AC PICs are assembled and show excellent electrochemical performance,with competitive energy and power densities.This work provides a route for the large-scale production of dual-doped graphene as a universal anode material for high-performance alkali ion batteries and capacitors.
基金supported by the financial support from the National Natural Science Foundation of China(21571040)the Young Top-Notch Talent of National Ten Thousand Talent Program+1 种基金Heilongjiang Touyan Innovation Team ProgramFundamental Research Funds for the Central Universities。
文摘It is highly desirable to design and synthesize two-dimensional nanostructured electrode materials with high electrical conductivity,large electrolyte-accessible surface area and more exposed active sites for energy storage applications.Herein,MXene/Co Al-LDH heterostructure has been prepared through electrostatic ordered hetero-assembly of monolayer MXene and edge-rich Co Al-LDH nanosheets in a faceto-face manner on molecular-scale for supercapacitor applications.Benefiting from the unique structure,strong interfacial interaction and synergistic effects between MXene and Co Al-LDH nanosheets,the electrical conductivity and exposed electrolyte-accessible active sites are significantly enhanced.The asprepared MXene/Co Al-LDH-80%(ML-80)film exhibits high volumetric capacity of 2472 C cm-3 in 3 M KOH electrolyte with high rate capability of 70.6%at 20 A g-1.Notably,to the best of our knowledge,the high volumetric capacity is the highest among other previously reported values for supercapacitors in aqueous electrolytes.Furthermore,our asymmetric supercapacitor device fabricated with ML-80 and MXene/graphene composite as cathode and anode,respectively,exhibits impressive volumetric energy density of 85.4 Wh L-1 with impressive cycling stability of 94.4%retention ratio after 30,000 continuous charge/discharge cycles.
基金partially supported by Hong Kong Scholars Programs(No.XJ2019024)China Postdoctoral Science Foundation(Nos.2018M630340,2019T120254)Fundamental Research Funds for the Central Universities and National Natural Science Foundation of China(No.22075171)。
文摘Aqueous zinc energy storage devices,holding various merits such as high specific capacity and low costs,have attracted extensive attention in recent years.Nevertheless,Zn metal anodes still suffer from a short lifespan and low Coulombic efficiency due to corrosion and side reactions in aqueous electrolytes.In this paper,we construct an artificial Sn inorganic layer on Zn metal anode through a facile strategy of atom exchange.The Sn layer suppresses Zn dendrite growth by facilitating homogeneous Zn plating and stripping during charge and discharge processes.Meanwhile,the Sn protective layer also serves as a physical barrier to decrease Zn corrosion and hydrogen generation.As a result,The Sn-coated anode(Sn|Zn)exhibits a low polarization voltage(~34 mV at 0.5 mAh/cm^(2))after 800 testing hours and displays a smooth and an even surface without corrosion.Moreover,the zinc ion capacitor(Sn|Zn‖activated carbon)is assembled with an enhanced capacity of 42 mAh/g and a capacity retention of 95%after 10,000 cycles at 5 A/g.This work demonstrates a feasible approach for the commercialization of aqueous Zn-based energy storage devices.
基金supported by the Hong Kong Scholars Programs(XJ2019024)the National Natural Science Foundation of China(51702063,51672056)+1 种基金the China Postdoctoral Science Foundation(2018 M630340,2019 T120254)the Fundamental Research Funds for the Central University。
文摘Aqueous Zn-based energy storage devices possess tremendous advantages, such as low cost, high safety,and competitive energy density, due to employing a Zn metal anode and aqueous electrolyte. However,the cycling stability and rate ability of a Zn anode are hindered by Zn dendrite growth and sluggish ion transfer in the electrode/electrolyte interface. Herein, the interfacial properties of Zn anodes are improved through the introduction of a silver(Ag) protective layer, which facilitates uniform Zn deposition and regulates Zn ion transport. As a result, Ag-coated Zn anodes display stable cycling performance(600 h at 1 m A cm^(-2)) and low overpotential(150 mV at 50 mA cm^(-2)after 2000 cycles). The Ag layer in situ electrochemically converts into an AgZn_(3) layer and promotes Zn ion desolvation and threedimensional diffusion processes. Moreover, a Zn-ion capacitor assembled with an Ag-coated Zn anode and active carbon cathode shows a capable cycling lifespan and rate performance. This study provides a feasible strategy for constructing a stabilized and dendrite-free Zn anode for the development of high-performance Zn-based energy storage devices.
基金supported by the Fundamental Research Funds for the Central Universities (HEUCF201403018)the Heilongjiang Postdoctoral Fund (LBHZ13059)+1 种基金the China Postdoctoral Science Foundation (2014M561332)the National Natural Science Foundation of China (21403044)
文摘A novel plastic/multi-walled carbon nanotube（MWNTs）-nickel（Ni）-platinum（Pt） electrode（PMNP） is prepared by chemical-reducing Pt onto the surface of Ni film covered plastic/MWNTs（PM） substrate. The MWNTs are adhered by a piece of commercial double faced adhesive tape on the surface of plastic paper and the Ni film is prepared by a simple electrodeposition method. The morphology and phase structure of the PMNP electrode are characterized by scanning electron microscopy,transmission electron microscope and X-ray diffractometer. The catalytic activity of the PMNP electrode for Na BH4 electrooxidation is investigated by means of cyclic voltammetry and chronoamperometry. The catalyst combines tightly with the plastic paper and exhibits a good stability. MWNTs serve as both conductive material and hydrogen storage material and the Ni film and Pt are employed as electrochemical catalysts. The PMNP electrode exhibits a high electrocatalytic performance and the oxidation current density reaches to 10.76 A/（mg·cm） in 0.1 mol/dm3 Na BH4at0 V,which is much higher than those in the previous reports. The using of waste plastic reduces the discarding of white pollution and consumption of metal resources.
文摘Interface chemical modulation strategies are considered as promising method to prepare electrocatalysts for the urea oxidation reaction(UOR).However,conventional interface catalysts are generally limited by the inherent activity and incompatibility of the individual components themselves,and the irregular charge distribution and slow charge transfer ability between interfaces severely limit the activity of UOR.Therefore,we optimized and designed a Ni_(2)P/CoP interface with modulated surface charge distribution and directed charge transfer to promote UOR activity.Density functional theorycalculations first predict a regular charge transfer from CoP to Ni_(2)P,which creates a built-in electric field between Ni_(2)P and CoP interface.Optimization of the adsorption/desorption process of UOR/HER reaction intermediates leads to the improvement of catalytic activity.Electrochemical impedance spectroscopy and ex situ X-ray photoelectron spectroscopy characterization confirm the unique mechanism of facilitated reaction at the Ni_(2)P/CoP interface.Electrochemical tests further validated the prediction with excellent UOR/HER activities of 1.28 V and 19.7 mV vs.RHE,at 10 mA cm^(-2),respectively.Furthermore,Ni_(2)P/CoP achieves industrial-grade current densities(500 mA cm^(−2))at 1.75 V and 1.87 V in the overall urea electrolyzer(UOR||HER)and overall human urine electrolyzer(HUOR||HER),respectively,and demonstrates considerable durability.
基金supported by the Natural Science Foundation of Heilongjiang Province of China,Outstanding Youth Foundation,No.YQ2022H003 (to DW)。
文摘N6-methyladenosine(m^(6)A), the most prevalent and conserved RNA modification in eukaryotic cells, profoundly influences virtually all aspects of mRNA metabolism. mRNA plays crucial roles in neural stem cell genesis and neural regeneration, where it is highly concentrated and actively involved in these processes. Changes in m^(6)A modification levels and the expression levels of related enzymatic proteins can lead to neurological dysfunction and contribute to the development of neurological diseases. Furthermore, the proliferation and differentiation of neural stem cells, as well as nerve regeneration, are intimately linked to memory function and neurodegenerative diseases. This paper presents a comprehensive review of the roles of m^(6)A in neural stem cell proliferation, differentiation, and self-renewal, as well as its implications in memory and neurodegenerative diseases. m^(6)A has demonstrated divergent effects on the proliferation and differentiation of neural stem cells. These observed contradictions may arise from the time-specific nature of m^(6)A and its differential impact on neural stem cells across various stages of development. Similarly, the diverse effects of m^(6)A on distinct types of memory could be attributed to the involvement of specific brain regions in memory formation and recall. Inconsistencies in m^(6)A levels across different models of neurodegenerative disease, particularly Alzheimer's disease and Parkinson's disease, suggest that these disparities are linked to variations in the affected brain regions. Notably, the opposing changes in m^(6)A levels observed in Parkinson's disease models exposed to manganese compared to normal Parkinson's disease models further underscore the complexity of m^(6)A's role in neurodegenerative processes. The roles of m^(6)A in neural stem cell proliferation, differentiation, and self-renewal, and its implications in memory and neurodegenerative diseases, appear contradictory. These inconsistencies may be attributed to the timespecific nature of m^(6)A and its varying effects on distinct brain regions and in different environments.
