采用常规的固相反应法结合机械球磨制备了含碳质量分数23.7%的Li_(2)Ni_(2)(MoO_(4))3@C复合材料,并应用于锂离子电池负极。与纯Li_(2)Ni_(2)(MoO_(4))3相比,Li_(2)Ni_(2)(MoO_(4))3@C具有优异的电化学性能,在电流密度为200 mA ·g^...采用常规的固相反应法结合机械球磨制备了含碳质量分数23.7%的Li_(2)Ni_(2)(MoO_(4))3@C复合材料,并应用于锂离子电池负极。与纯Li_(2)Ni_(2)(MoO_(4))3相比,Li_(2)Ni_(2)(MoO_(4))3@C具有优异的电化学性能,在电流密度为200 mA ·g^(-1)时,50周循环后,可逆容量高达845 mAh·g^(-1)。值得注意的是,Li_(2)Ni_(2)(MoO_(4))3@C的首周库仑效率高达85%。此外,运用循环伏安法对Li_(2)Ni_(2)(MoO_(4))3@C复合物存储锂行为进行了初步探索。展开更多
The photocatalytic reduction of CO2 with H2O to fuels and chemicals using solar energy is one of the most attractive but highly difficult routes.Thus far,only a very limited number of photocatalysts has been reported ...The photocatalytic reduction of CO2 with H2O to fuels and chemicals using solar energy is one of the most attractive but highly difficult routes.Thus far,only a very limited number of photocatalysts has been reported to be capable of catalyzing the photocatalytic reduction of CO2 under visible light.The utilization of the localized surface plasmon resonance(LSPR)phenomenon is an attractive strategy for developing visible-light photocatalysts.Herein,we have succeeded in synthesizing plasmonic MoO3?x-TiO2 nanocomposites with tunable LSPR by a simple solvothermal method.The well-structured nanocomposite containing two-dimensional(2D)molybdenum oxide(MoO3?x)nanosheets and one-dimensional(1D)titanium oxide nanotubes(TiO2-NT)showed LSPR absorption band in the visible-light region,and the incorporation of TiO2-NT significantly enhanced the LSPR absorption band.The MoO3?x-TiO2-NT nanocomposite is promising for application in the photocatalytic reduction of CO2 with H2O under visible light irradiation.展开更多
Simultaneous generation of H_(2) fuel and value-added chemicals has attracted increasing attention since the photogenerated electrons and holes can be both employed to convert solar light into chemical energy.Herein,f...Simultaneous generation of H_(2) fuel and value-added chemicals has attracted increasing attention since the photogenerated electrons and holes can be both employed to convert solar light into chemical energy.Herein,for realizing UV-visible-NIR light driven dehydrogenation of benzyl alcohol(BA)into benzaldehydes(BAD)and H_(2),a novel localized surface plasmon resonance(LSPR)enhanced S-scheme heterojunction was designed by combining noble-metal-free plasmon MoO_(3-x) as oxidation semiconductor and Zn_(0.1)Cd_(0.9)S as reduction semiconductor.The photoredox system of Zn_(0.1)Cd_(0.9)S/MoO_(3-x) displayed an unconventional reaction model,in which the BA served as both electron donor and acceptor.The S-scheme charge transfer mechanism induced by the formed internal electric field enhanced the redox ability of charge carriers thermodynamically and boosted charge separation kinetically.Moreover,due to the LSPR effect of MoO_(3-x) nanosheets,Zn_(0.1)Cd_(0.9)S/MoO_(3-x) photocatalysts exhibited strong absorption in the region of full solar spectrum.Therefore,the Zn_(0.1)Cd_(0.9)S/MoO_(3-x) composite generated H_(2) and BAD simultaneously via selective oxidation of BA with high production(34.38 and 33.83 mmol×g^(–1) for H_(2) and BAD,respectively)upon full solar illumination.Even under NIR light irradiation,the H_(2) production rate could up to 94.5 mmol×g^(–1)×h^(–1).In addition,the Zn_(0.1)Cd_(0.9)S/MoO_(3-x) composite displayed effective photocatalytic H_(2) evolution rate up to 149.2 mmol×g^(–1)×h^(–1) from water,which was approximate 6 times that of pure Zn_(0.1)Cd_(0.9)S.This work provides a reference for rational design of plasmonic S-scheme heterojunction photocatalysts for coproduction of high-value chemicals and solar fuel production.展开更多
Two-dimensional(2D)transition metal carbide MXene-based materials hold great potentials applied for new electromagnetic wave(EMW)absorbers.However,the application of MXenes in the field of electromagnetic wave absorpt...Two-dimensional(2D)transition metal carbide MXene-based materials hold great potentials applied for new electromagnetic wave(EMW)absorbers.However,the application of MXenes in the field of electromagnetic wave absorption(EMA)is limited by the disadvantages of poor impedance matching,single loss mechanism,and easy oxidation.In this work,MoO_(3)/TiO_(2)/Mo_(2)TiC_(2)T_(x)hybrids were prepared by the annealing-treated Mo_(2)TiC_(2)T_(x)MXene and uniform MoO_(3)and TiO_(2)oxides in-situ grew on Mo_(2)TiC_(2)T_(x)layers.At the annealing temperature of 300℃,the minimum reflection loss(RLmin)value of MoO_(3)/TiO_(2)/Mo_(2)TiC_(2)T_(x)reaches-30.76 dB(2.3 mm)at 10.18 GHz with a significantly broadening effective absorption bandwidth(EAB)of 8.6 GHz(1.8 mm).The in-situ generated oxides creating numerous defects and heterogeneous interfaces enhance dipolar and interfacial polarizations and optimize the impedance matching of Mo_(2)TiC_(2)T_(x).Considering the excellent overall performance,the MoO_(3)/TiO_(2)/Mo_(2)TiC_(2)T_(x)hybrids can be a promising candidate for EMA.展开更多
文摘采用常规的固相反应法结合机械球磨制备了含碳质量分数23.7%的Li_(2)Ni_(2)(MoO_(4))3@C复合材料,并应用于锂离子电池负极。与纯Li_(2)Ni_(2)(MoO_(4))3相比,Li_(2)Ni_(2)(MoO_(4))3@C具有优异的电化学性能,在电流密度为200 mA ·g^(-1)时,50周循环后,可逆容量高达845 mAh·g^(-1)。值得注意的是,Li_(2)Ni_(2)(MoO_(4))3@C的首周库仑效率高达85%。此外,运用循环伏安法对Li_(2)Ni_(2)(MoO_(4))3@C复合物存储锂行为进行了初步探索。
文摘The photocatalytic reduction of CO2 with H2O to fuels and chemicals using solar energy is one of the most attractive but highly difficult routes.Thus far,only a very limited number of photocatalysts has been reported to be capable of catalyzing the photocatalytic reduction of CO2 under visible light.The utilization of the localized surface plasmon resonance(LSPR)phenomenon is an attractive strategy for developing visible-light photocatalysts.Herein,we have succeeded in synthesizing plasmonic MoO3?x-TiO2 nanocomposites with tunable LSPR by a simple solvothermal method.The well-structured nanocomposite containing two-dimensional(2D)molybdenum oxide(MoO3?x)nanosheets and one-dimensional(1D)titanium oxide nanotubes(TiO2-NT)showed LSPR absorption band in the visible-light region,and the incorporation of TiO2-NT significantly enhanced the LSPR absorption band.The MoO3?x-TiO2-NT nanocomposite is promising for application in the photocatalytic reduction of CO2 with H2O under visible light irradiation.
文摘Simultaneous generation of H_(2) fuel and value-added chemicals has attracted increasing attention since the photogenerated electrons and holes can be both employed to convert solar light into chemical energy.Herein,for realizing UV-visible-NIR light driven dehydrogenation of benzyl alcohol(BA)into benzaldehydes(BAD)and H_(2),a novel localized surface plasmon resonance(LSPR)enhanced S-scheme heterojunction was designed by combining noble-metal-free plasmon MoO_(3-x) as oxidation semiconductor and Zn_(0.1)Cd_(0.9)S as reduction semiconductor.The photoredox system of Zn_(0.1)Cd_(0.9)S/MoO_(3-x) displayed an unconventional reaction model,in which the BA served as both electron donor and acceptor.The S-scheme charge transfer mechanism induced by the formed internal electric field enhanced the redox ability of charge carriers thermodynamically and boosted charge separation kinetically.Moreover,due to the LSPR effect of MoO_(3-x) nanosheets,Zn_(0.1)Cd_(0.9)S/MoO_(3-x) photocatalysts exhibited strong absorption in the region of full solar spectrum.Therefore,the Zn_(0.1)Cd_(0.9)S/MoO_(3-x) composite generated H_(2) and BAD simultaneously via selective oxidation of BA with high production(34.38 and 33.83 mmol×g^(–1) for H_(2) and BAD,respectively)upon full solar illumination.Even under NIR light irradiation,the H_(2) production rate could up to 94.5 mmol×g^(–1)×h^(–1).In addition,the Zn_(0.1)Cd_(0.9)S/MoO_(3-x) composite displayed effective photocatalytic H_(2) evolution rate up to 149.2 mmol×g^(–1)×h^(–1) from water,which was approximate 6 times that of pure Zn_(0.1)Cd_(0.9)S.This work provides a reference for rational design of plasmonic S-scheme heterojunction photocatalysts for coproduction of high-value chemicals and solar fuel production.
基金This work was financially supported by the National Natural Science Foundation of China(Nos.U2004177 and U21A2064)Outstanding Youth Fund of Henan Province(No.212300410081)Support Plan for Scientific and Technological Innovation Talents in Colleges and Universities of Henan Province(No.22HASTIT001)。
文摘Two-dimensional(2D)transition metal carbide MXene-based materials hold great potentials applied for new electromagnetic wave(EMW)absorbers.However,the application of MXenes in the field of electromagnetic wave absorption(EMA)is limited by the disadvantages of poor impedance matching,single loss mechanism,and easy oxidation.In this work,MoO_(3)/TiO_(2)/Mo_(2)TiC_(2)T_(x)hybrids were prepared by the annealing-treated Mo_(2)TiC_(2)T_(x)MXene and uniform MoO_(3)and TiO_(2)oxides in-situ grew on Mo_(2)TiC_(2)T_(x)layers.At the annealing temperature of 300℃,the minimum reflection loss(RLmin)value of MoO_(3)/TiO_(2)/Mo_(2)TiC_(2)T_(x)reaches-30.76 dB(2.3 mm)at 10.18 GHz with a significantly broadening effective absorption bandwidth(EAB)of 8.6 GHz(1.8 mm).The in-situ generated oxides creating numerous defects and heterogeneous interfaces enhance dipolar and interfacial polarizations and optimize the impedance matching of Mo_(2)TiC_(2)T_(x).Considering the excellent overall performance,the MoO_(3)/TiO_(2)/Mo_(2)TiC_(2)T_(x)hybrids can be a promising candidate for EMA.
