Graphite, used as a carbon source in a conventional magnesia-carbon(MgO-C) refractory, was modified with an acid reagent, resulting in a negative charge on the surface of graphite, to enhance the coating efficiency of...Graphite, used as a carbon source in a conventional magnesia-carbon(MgO-C) refractory, was modified with an acid reagent, resulting in a negative charge on the surface of graphite, to enhance the coating efficiency of aluminum(Al) phase, which was compared to the pristine graphite through its dispersibity and oxidation behavior. The graphite particles with and without surface modification were added, respecticely, in an Al(NO3)3 suspension used as a coating reagent, and then filtered at room temperature. The modified graphite shows better disperbility than the pristine graphite, indicating that the coating efficiency of Al precursor is enhanced in the modified graphite. With respect to oxidation behavior, the modified graphite without the coating layer is totally reacted with oxygen at heat treatment of 900 °C in air. However, the Al-coated graphite starts to react with oxygen at heat treatment of 900 °C and fully reacted with oxygen at heat treatment of 1000 °C, showing the gray and white colors, respectively. It is verified that the Al layer is individually and uniformly formed on the surface of graphite and the oxidation resistance of graphite is enhanced owing to the increased coating efficiency of Al precursor.展开更多
The corrosion inhibition of metallic substrates is a prime issue for many potential applications where corrosion plays a crucial role. The development of carbon based on functionalized coatings could increase the life...The corrosion inhibition of metallic substrates is a prime issue for many potential applications where corrosion plays a crucial role. The development of carbon based on functionalized coatings could increase the lifetime of metallic substrates by inhibiting the corrosion process. Present work is an effort to develop a corrosion inhibiting composite coating of graphene oxide and polypyrrole for AISI (American Iron and Steel Institute) type 304 stainless steel substrates. The electrochemical galvanostatic deposition process was applied for coating development. The coating morphology and ability to cover the substrate surface was analyzed with a high-resolution scanning electron microscope. The coating's structural and electronic properties were analyzed with Raman spectroscopy. The investigation of corrosion inhibition involved open circuit potential, Tafel, and voltammetry analysis. The standard salt test ASTM (American Society for Testing and Materials) G48A for stainless steel substrate has also been studied. Significant enhancement of corrosion potential as well as pitting potential for the composite coated substrates has been noted. Furthermore, corrosion and breakdown potential increased upon changing the material from graphene oxide to its composite coating. During the salt test analysis, the durability of the composite coating was noted up to 72 h, which is the standard time scale. Based on experimental analysis, this composite material can be used as an effective carbon based on functionalized corrosion inhibitor for stainless steel substrates to increase their lifetime.展开更多
Although graphite anodes operated with representative de/intercalation patterns at low potentials are considered highly desirable for K-ion batteries,the severe capacity fading caused by consecutive reduction reaction...Although graphite anodes operated with representative de/intercalation patterns at low potentials are considered highly desirable for K-ion batteries,the severe capacity fading caused by consecutive reduction reactions on the aggressively reactive surface is inevitable given the scarcity of effective protecting layers.Herein,by introducing a flame-retardant localized high-concentration electrolyte with retentive solvation configuration and relatively weakened anion-coordination and non-solvating fluorinated ether,the rational solid electrolyte interphase characterized by well-balanced inorganic/organic components is tailored in situ.This effectively prevented solvents from excessively decomposing and simultaneously improved the resistance against K-ion transport.Consequently,the graphite anode retained a prolonged cycling capability of up to 1400 cycles(245 mA h g,remaining above 12 mon)with an excellent capacity retention of as high as 92.4%.This is superior to those of conventional and high-concentration electrolytes.Thus,the optimized electrolyte with moderate salt concentration is perfectly compatible with graphite,providing a potential application prospect for K-storage evolution.展开更多
The orientation control of graphene overlayers on metal surface is an important issue which remains as a challenge in graphene growth on Ni surface. Here we have demonstrated that epitaxial graphene overlayers can be ...The orientation control of graphene overlayers on metal surface is an important issue which remains as a challenge in graphene growth on Ni surface. Here we have demonstrated that epitaxial graphene overlayers can be obtained by annealing a nickel carbide covered Ni(111) surface using in situ surface imaging techniques. Epitaxial graphene islands nucleate and grow via segregation of dissolved carbon atoms to the top surface at about 400 ℃. This is in contrast to a mixture of epitaxial and non-epi- taxial graphene domains grown directly on Ni(111) at 540 ℃. The different growth behaviors are related to the nucleation dynamics which is controlled by local carbon densities in the near surface region.展开更多
Surface functionalization of epitaxial graphene overlayers on 6H-SiC(0001) has been attempted through thermal reactions in NH3. X-ray photoelectron spectroscopy and micro-region low energy electron diffraction resul...Surface functionalization of epitaxial graphene overlayers on 6H-SiC(0001) has been attempted through thermal reactions in NH3. X-ray photoelectron spectroscopy and micro-region low energy electron diffraction results show that a significant amount of N is present at the NHB-treated graphene surface, which results in strong band bending at the SiC surface as well as decoupling of the graphene overlayers from the substrate. The majority of the surface N species can be removed by annealing in vacuum up to 850 ~C, weakening the surface band bending and resuming the strong coupling of graphene with the SiC surface. The desorbed N atoms can be attributed to the intercalated species between graphene and SiC. Low temperature scanning tunneling spectroscopy and density functional theory simulations confirm the presence of N dopants in the graphene lattice, which are in the form of graphitic substitution and can be stable above 850 ~C. This is the first report of simultaneous N intercalation and N doping of epitaxial graphene overlayers on SiC, and it may be employed to alter the surface physical and chemical properties of epitaxial graphene overlayers.展开更多
基金Project(2011-0030058) supported by the National Research Foundation of Korea(NRF)Project(20134030200220) supported by the Human Resources Development Program of the Korea Institute of Energy Technology Evaluation,Korea+1 种基金Project supported by the Planning (KETEP) Grant Funded by the Korea Government Ministry of Trade,Industry and Energy and POSCO 2012,KoreaProject(10043795) supported by the Technology Innovation Program of the Ministry of Knowledge Economy Korea
文摘Graphite, used as a carbon source in a conventional magnesia-carbon(MgO-C) refractory, was modified with an acid reagent, resulting in a negative charge on the surface of graphite, to enhance the coating efficiency of aluminum(Al) phase, which was compared to the pristine graphite through its dispersibity and oxidation behavior. The graphite particles with and without surface modification were added, respecticely, in an Al(NO3)3 suspension used as a coating reagent, and then filtered at room temperature. The modified graphite shows better disperbility than the pristine graphite, indicating that the coating efficiency of Al precursor is enhanced in the modified graphite. With respect to oxidation behavior, the modified graphite without the coating layer is totally reacted with oxygen at heat treatment of 900 °C in air. However, the Al-coated graphite starts to react with oxygen at heat treatment of 900 °C and fully reacted with oxygen at heat treatment of 1000 °C, showing the gray and white colors, respectively. It is verified that the Al layer is individually and uniformly formed on the surface of graphite and the oxidation resistance of graphite is enhanced owing to the increased coating efficiency of Al precursor.
文摘The corrosion inhibition of metallic substrates is a prime issue for many potential applications where corrosion plays a crucial role. The development of carbon based on functionalized coatings could increase the lifetime of metallic substrates by inhibiting the corrosion process. Present work is an effort to develop a corrosion inhibiting composite coating of graphene oxide and polypyrrole for AISI (American Iron and Steel Institute) type 304 stainless steel substrates. The electrochemical galvanostatic deposition process was applied for coating development. The coating morphology and ability to cover the substrate surface was analyzed with a high-resolution scanning electron microscope. The coating's structural and electronic properties were analyzed with Raman spectroscopy. The investigation of corrosion inhibition involved open circuit potential, Tafel, and voltammetry analysis. The standard salt test ASTM (American Society for Testing and Materials) G48A for stainless steel substrate has also been studied. Significant enhancement of corrosion potential as well as pitting potential for the composite coated substrates has been noted. Furthermore, corrosion and breakdown potential increased upon changing the material from graphene oxide to its composite coating. During the salt test analysis, the durability of the composite coating was noted up to 72 h, which is the standard time scale. Based on experimental analysis, this composite material can be used as an effective carbon based on functionalized corrosion inhibitor for stainless steel substrates to increase their lifetime.
基金supported by the National Natural Science Foundation of China(91963118 and 52173246)Science Technology Program of Jilin Province(20200201066JC)the 111 Project(B13013)。
文摘Although graphite anodes operated with representative de/intercalation patterns at low potentials are considered highly desirable for K-ion batteries,the severe capacity fading caused by consecutive reduction reactions on the aggressively reactive surface is inevitable given the scarcity of effective protecting layers.Herein,by introducing a flame-retardant localized high-concentration electrolyte with retentive solvation configuration and relatively weakened anion-coordination and non-solvating fluorinated ether,the rational solid electrolyte interphase characterized by well-balanced inorganic/organic components is tailored in situ.This effectively prevented solvents from excessively decomposing and simultaneously improved the resistance against K-ion transport.Consequently,the graphite anode retained a prolonged cycling capability of up to 1400 cycles(245 mA h g,remaining above 12 mon)with an excellent capacity retention of as high as 92.4%.This is superior to those of conventional and high-concentration electrolytes.Thus,the optimized electrolyte with moderate salt concentration is perfectly compatible with graphite,providing a potential application prospect for K-storage evolution.
基金Acknowledgments This work was supported by the National Natural Science Foundation of China (21373208, 91545204, and 21321002), the National Basic Research Program of China (2016YFA0200200, 2013CB834603, and 2013CB933100), and the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB 17020200). The authors are grateful for the support for Nano-X from Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences (SINANO).
文摘The orientation control of graphene overlayers on metal surface is an important issue which remains as a challenge in graphene growth on Ni surface. Here we have demonstrated that epitaxial graphene overlayers can be obtained by annealing a nickel carbide covered Ni(111) surface using in situ surface imaging techniques. Epitaxial graphene islands nucleate and grow via segregation of dissolved carbon atoms to the top surface at about 400 ℃. This is in contrast to a mixture of epitaxial and non-epi- taxial graphene domains grown directly on Ni(111) at 540 ℃. The different growth behaviors are related to the nucleation dynamics which is controlled by local carbon densities in the near surface region.
文摘Surface functionalization of epitaxial graphene overlayers on 6H-SiC(0001) has been attempted through thermal reactions in NH3. X-ray photoelectron spectroscopy and micro-region low energy electron diffraction results show that a significant amount of N is present at the NHB-treated graphene surface, which results in strong band bending at the SiC surface as well as decoupling of the graphene overlayers from the substrate. The majority of the surface N species can be removed by annealing in vacuum up to 850 ~C, weakening the surface band bending and resuming the strong coupling of graphene with the SiC surface. The desorbed N atoms can be attributed to the intercalated species between graphene and SiC. Low temperature scanning tunneling spectroscopy and density functional theory simulations confirm the presence of N dopants in the graphene lattice, which are in the form of graphitic substitution and can be stable above 850 ~C. This is the first report of simultaneous N intercalation and N doping of epitaxial graphene overlayers on SiC, and it may be employed to alter the surface physical and chemical properties of epitaxial graphene overlayers.