Al-Zn-Mg alloys with different Zn/Mg mass ratios were evaluated as sacrificial anodes for cathodic protection of carbon steel in 3.5 wt.%Na Cl solution.The anodes were fabricated from pure Al,Zn and Mg metals using ca...Al-Zn-Mg alloys with different Zn/Mg mass ratios were evaluated as sacrificial anodes for cathodic protection of carbon steel in 3.5 wt.%Na Cl solution.The anodes were fabricated from pure Al,Zn and Mg metals using casting technique.Optical microscopy,SEM-EDS,XRD and electrochemical techniques were used.The results indicated that with decreasing Zn/Mg mass ratio,the grain size ofα(Al)and the particle size of the precipitates decreased while the volume fraction of the precipitates increased.The anode with Zn/Mg mass ratio>4.0 exhibited the lowest corrosion rate,while the anode with Zn/Mg mass ratio<0.62 gave the highest corrosion rate and provided the highest cathodic protection efficiency for carbon steel(AISI 1018).Furthermore,the results showed that the anode with Zn/Mg mass ratio<0.62 exhibited a porous corrosion product compared to the other anodes.展开更多
Silicon （Si） has the highest known theoretical specific capacity （3,590 mAh/g for Li1.5Si4, and 4,200 mAh/g for Li22Si4） as a lithium-ion battery anode, and has attracted extensive interest in the past few years. ...Silicon （Si） has the highest known theoretical specific capacity （3,590 mAh/g for Li1.5Si4, and 4,200 mAh/g for Li22Si4） as a lithium-ion battery anode, and has attracted extensive interest in the past few years. However, its application is limited by poor cyclability and early capacity fading due to significant volume changes during lithiation and delithiation processes. In this work, we report a coaxial silicon/anodic titanium oxide/silicon （Si-ATO--Si） nanotube array structure grown on a titanium substrate demonstrating excellent electrochemical cyclability. The ATO nanotube scaffold used for Si deposition has many desirable features, such as a rough surface for enhanced Si adhesion, and direct contact with the Ti substrate working as current collector. More importantly, our ATO scaffold provides a rather unique advantage in that Si can be loaded on both the inner and outer surfaces, and an inner pore can be retained to provide room for Si volume expansion. This coaxial structure shows a capacity above 1,500 mAh/g after 100 cycles, with less than 0.05% decay per cycle. Simulations show that this improved performance can be attributed to the lower stress induced on Si layers upon lithiation/delithiation compared with some other recently reported Si-based nanostructures.展开更多
Low volumetric energy density is a bottleneck for the application of lithium-sulfur (Li-S)battery.The low- density sulfur cooperated with the light-weight carbon sub- strate realizes electrochemical cycle stability,bu...Low volumetric energy density is a bottleneck for the application of lithium-sulfur (Li-S)battery.The low- density sulfur cooperated with the light-weight carbon sub- strate realizes electrochemical cycle stability,but leads to worse volumetric energy density.Here,nickel ferrite (NiFe2O4)nanofibers as novel substrate for sulfur not only anchor lithium polysulfides to enhance the cycle stability of sulfur cathode,but also contribute to the high volumetric capacity of the S/nickel ferrite composite.Specifically,the S/ nickel ferrite composite presents an initial volumetric capacity of 1,281.7mA h cm^-3-composite at 0.1C rate,1.9times higher than that of S/carbon nanotubes,due to the high tap density of the S/nickel ferrite composite.展开更多
The inherently low electrical conductivity of TiO2-based electrodes as well as the high electrical resistance between an electrode and a current collector represents a major obstacle to their use as an anode for lithi...The inherently low electrical conductivity of TiO2-based electrodes as well as the high electrical resistance between an electrode and a current collector represents a major obstacle to their use as an anode for lithium ion batteries. In this study, we report on high-density TiO2 nanotubes （NTs） branched onto a carbon nanofiber （CNF） ＂tree＂ that provide a low resistance current path between the current collector and the TiO2 NTs. Compared to a TiO2 NT array grown directly on the current collector, the branched TiO2 NTs tree, coupled with the CNF electrode, exhibited -10 times higher areal energy density and excellent rate capability （discharge capacity of -150 mA.h.g-1 at a current density of 1,000 mA·g-1）. Based on the detailed experimental results and associated theoretical analysis, we demonstrate that the introduction of CNFs with direct electric contact with the current collector enables a significant increase in areal capacity （mA·h·cm-2） as well as excellent rate capability.展开更多
Constructing potential anodes for sodium-ion batteries(SIBs)with a wide temperature property has captured enormous interests in recent years.Fe1-xS,a zero-band gap material confirmed by density states calculation,is a...Constructing potential anodes for sodium-ion batteries(SIBs)with a wide temperature property has captured enormous interests in recent years.Fe1-xS,a zero-band gap material confirmed by density states calculation,is an ideal electrode for fast energy storage on account of its low cost and high theoretical capacity.Herein,Fe1-xS nanosheet wrapped by nitrogen-doped carbon(Fe1-xS@NC)is engineered through a post-sulfidation strategy using Fe-based metal-organic framework(Fe-MOF)as the precursor.The obtained Fe1-xS@NC agaric-like structure can well shorten the charge diffusion pathway,and significantly enhance the ionic/electronic conductivities and the reaction kinetics.As expected,the Fe1-xS@NC electrode,as a prospective SIB anode,delivers a desirable capacity up to 510.2 mA h g^-1 at a high rate of8000 mA g^-1.Additionally,even operated at low temperatures of 0 and-25°C,high reversible capacities of 387.1 and 223.4 mA h g^-1 can still be obtained at 2000 mA g^-1,respectively,indicating its huge potential use at harsh temperatures.More noticeably,the full battery made by the Fe1-xS@NC anode and Na3 V2(PO4)2 O2 F cathode achieves a remarkable rate capacity(186.8 mA h g^-1 at 2000 m A g^-1)and an impressive cycle performance(183.6 m A h g^-1 after 100 cycles at700 mA g^-1)between 0.3 and 3.8 V.Such excellent electrochemical performance is mainly contributed by its pseudocapacitive-dominated behavior,which brings fast electrode kinetics and robust structural stability to the whole electrode.展开更多
文摘Al-Zn-Mg alloys with different Zn/Mg mass ratios were evaluated as sacrificial anodes for cathodic protection of carbon steel in 3.5 wt.%Na Cl solution.The anodes were fabricated from pure Al,Zn and Mg metals using casting technique.Optical microscopy,SEM-EDS,XRD and electrochemical techniques were used.The results indicated that with decreasing Zn/Mg mass ratio,the grain size ofα(Al)and the particle size of the precipitates decreased while the volume fraction of the precipitates increased.The anode with Zn/Mg mass ratio>4.0 exhibited the lowest corrosion rate,while the anode with Zn/Mg mass ratio<0.62 gave the highest corrosion rate and provided the highest cathodic protection efficiency for carbon steel(AISI 1018).Furthermore,the results showed that the anode with Zn/Mg mass ratio<0.62 exhibited a porous corrosion product compared to the other anodes.
文摘Silicon （Si） has the highest known theoretical specific capacity （3,590 mAh/g for Li1.5Si4, and 4,200 mAh/g for Li22Si4） as a lithium-ion battery anode, and has attracted extensive interest in the past few years. However, its application is limited by poor cyclability and early capacity fading due to significant volume changes during lithiation and delithiation processes. In this work, we report a coaxial silicon/anodic titanium oxide/silicon （Si-ATO--Si） nanotube array structure grown on a titanium substrate demonstrating excellent electrochemical cyclability. The ATO nanotube scaffold used for Si deposition has many desirable features, such as a rough surface for enhanced Si adhesion, and direct contact with the Ti substrate working as current collector. More importantly, our ATO scaffold provides a rather unique advantage in that Si can be loaded on both the inner and outer surfaces, and an inner pore can be retained to provide room for Si volume expansion. This coaxial structure shows a capacity above 1,500 mAh/g after 100 cycles, with less than 0.05% decay per cycle. Simulations show that this improved performance can be attributed to the lower stress induced on Si layers upon lithiation/delithiation compared with some other recently reported Si-based nanostructures.
基金supported by the New Energy Project for Electric Vehicles in National Key Research and Development Program (2016YFB0100200)the National Natural Science Foundation of China (21573114 and 51502145)
文摘Low volumetric energy density is a bottleneck for the application of lithium-sulfur (Li-S)battery.The low- density sulfur cooperated with the light-weight carbon sub- strate realizes electrochemical cycle stability,but leads to worse volumetric energy density.Here,nickel ferrite (NiFe2O4)nanofibers as novel substrate for sulfur not only anchor lithium polysulfides to enhance the cycle stability of sulfur cathode,but also contribute to the high volumetric capacity of the S/nickel ferrite composite.Specifically,the S/ nickel ferrite composite presents an initial volumetric capacity of 1,281.7mA h cm^-3-composite at 0.1C rate,1.9times higher than that of S/carbon nanotubes,due to the high tap density of the S/nickel ferrite composite.
文摘The inherently low electrical conductivity of TiO2-based electrodes as well as the high electrical resistance between an electrode and a current collector represents a major obstacle to their use as an anode for lithium ion batteries. In this study, we report on high-density TiO2 nanotubes （NTs） branched onto a carbon nanofiber （CNF） ＂tree＂ that provide a low resistance current path between the current collector and the TiO2 NTs. Compared to a TiO2 NT array grown directly on the current collector, the branched TiO2 NTs tree, coupled with the CNF electrode, exhibited -10 times higher areal energy density and excellent rate capability （discharge capacity of -150 mA.h.g-1 at a current density of 1,000 mA·g-1）. Based on the detailed experimental results and associated theoretical analysis, we demonstrate that the introduction of CNFs with direct electric contact with the current collector enables a significant increase in areal capacity （mA·h·cm-2） as well as excellent rate capability.
基金financially supported by the National Natural Science Foundation of China (21873018, 21573036 and 21274017)the open project of Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis (130028655)
文摘Constructing potential anodes for sodium-ion batteries(SIBs)with a wide temperature property has captured enormous interests in recent years.Fe1-xS,a zero-band gap material confirmed by density states calculation,is an ideal electrode for fast energy storage on account of its low cost and high theoretical capacity.Herein,Fe1-xS nanosheet wrapped by nitrogen-doped carbon(Fe1-xS@NC)is engineered through a post-sulfidation strategy using Fe-based metal-organic framework(Fe-MOF)as the precursor.The obtained Fe1-xS@NC agaric-like structure can well shorten the charge diffusion pathway,and significantly enhance the ionic/electronic conductivities and the reaction kinetics.As expected,the Fe1-xS@NC electrode,as a prospective SIB anode,delivers a desirable capacity up to 510.2 mA h g^-1 at a high rate of8000 mA g^-1.Additionally,even operated at low temperatures of 0 and-25°C,high reversible capacities of 387.1 and 223.4 mA h g^-1 can still be obtained at 2000 mA g^-1,respectively,indicating its huge potential use at harsh temperatures.More noticeably,the full battery made by the Fe1-xS@NC anode and Na3 V2(PO4)2 O2 F cathode achieves a remarkable rate capacity(186.8 mA h g^-1 at 2000 m A g^-1)and an impressive cycle performance(183.6 m A h g^-1 after 100 cycles at700 mA g^-1)between 0.3 and 3.8 V.Such excellent electrochemical performance is mainly contributed by its pseudocapacitive-dominated behavior,which brings fast electrode kinetics and robust structural stability to the whole electrode.
