The technology of photothermal catalytic degradation of acetone and conversion of nitrogen monoxide(NO)not only reduces energy consumption compared to traditional thermal catalytic oxidation technology but also improv...The technology of photothermal catalytic degradation of acetone and conversion of nitrogen monoxide(NO)not only reduces energy consumption compared to traditional thermal catalytic oxidation technology but also improves degradation efficiency,effectively overcoming the limitations of single photocatalytic or thermal catalytic technology.This paper aims to control the lattice oxygen activity and oxygen vacancy concentration of the catalyst by optimizing the manganese-cobalt(Mn-Co)molar ratio and modifying the catalyst with Ce doping,thereby enhancing its photocatalytic and thermal catalytic performance for the degradation of acetone and NO.At 240℃,when the Mn-Co molar ratio is 4:2,the CoO_(x)/MnO_(x)@Fe_(2)O_(3)-2 catalyst exhibits good catalytic activity for both acetone and NO,with conversion rates of 52%and 63.8%for acetone and NO,respectively.Based on the optimization of the Mn-Co molar ratio,Ce was doped into the CoO_(x)/MnO_(x)@Fe_(2)O_(3)-2 sample using the co-precipitation method to synthesize samples with different Ce doping amounts.The sample of CeO_(2)/CoO_(x)/MnO_(x)@Fe_(2)O_(3)-2-0.25(nMn-Co:nCe=1:0.25)shows the highest catalytic performance compared with the other samples,with the conversion of acetone and NO reaching 60%and 70%,respectively,at 240℃.Additionally,the intrinsic mechanism under photothermal synergy is based on the Mars-van Krevelen redox cycle theory.展开更多
Although metallic rhodium(Rh)is regarded as a promising platinum-alternative anode catalyst of direct methanol fuel cell(DMFC),the conventional"particle-to-face"contact model between Rh and matrix largely li...Although metallic rhodium(Rh)is regarded as a promising platinum-alternative anode catalyst of direct methanol fuel cell(DMFC),the conventional"particle-to-face"contact model between Rh and matrix largely limits the overall electrocatalytic performance due to their insufficient cooperative effects.Herein,we report a controllable and robust heterointerface engineering strategy for the bottom-up fabrication of rhombic Rh nanosheets in situ confined on Ti_3C_(2)T_x MXene nanolamellas(Rh NS/MXene)via a convenient stereoassembly process.This unique design concept gives the resulting 2D/2D Rh NS/MXene heterostructure intriguing textural features,including large accessible surface areas,strong"face-toface"interfacial interactions,homogeneous Rh nanosheet distribution,ameliorative electronic structure,and high electronic conductivity.As a consequence,the as-prepared Rh NS/MXene nanoarchitectures exhibit exceptional electrocatalytic methanol oxidation properties in terms of a large electrochemically active surface area of 126.2 m~2 g_(Rh)~(-1),a high mass activity of 1056.9 mA mg_(Rh)-~1,and a long service life,which significantly outperform those of conventional particle-shaped Rh catalysts supported by carbon black,carbon nanotubes,reduced graphene oxide,and MXene matrixes as well as the commercial Pt nanoparticle/carbon black and Pd nanoparticle/carbon black catalysts with the same noble metal loading amount.Density functional theory calculations further demonstrate that the direct electronic interaction at the well-contacted 2D/2D heterointerfaces effectively enhances the adsorption energy of Rh nanosheets and induces a left shift of the d-band center,thereby making the Rh NS/MXene configuration suffer less from CO poisoning.This work highlights the importance of rational heterointerface design in the construction of advanced noble metal/MXene electrocatalysts,which may provide new avenues for developing the next-generation DMFC devices.展开更多
In this paper,we report a facile strategy to synthesize Co-BDC-NH2 material,which is used as a precursor towards an excellent OER electrocatalyst by thermal annealing in nitrogen.Ultra-small Co/Co Oxnanoparticles were...In this paper,we report a facile strategy to synthesize Co-BDC-NH2 material,which is used as a precursor towards an excellent OER electrocatalyst by thermal annealing in nitrogen.Ultra-small Co/Co Oxnanoparticles were uniformly dispersed on the rhombus N-doped carbon(NC)nanoflakes.Transmission electron microscopic,X-ray diffraction spectrometric,and X-ray photoelectron spectroscopic analyses revealed the coexistence of metallic Co and Co oxides nanoparticles.It was found that Co/CoO_(x)@NC obtained at 500℃ annealing temperature exhibited the highest electrocatalytic OER activity,with 307 and375 m V overpotential to achieve 10 and 100 m A cm^(-2) current densities.Besides,thanks to the in-situ annealing process,Co/CoO_(x)@NC showed excellent catalytic stability with 97.4%current density retention after 24 h electrolysis at 1.66 V vs.RHE electrode potential.Further investigations revealed that the ultrasmall Co/Co Oxnanoparticles distributed on N-doped carbon template contribute significantly towards OER electrocatalysis through enlarging the activity surface areas and enhancing the intrinsic electrochemical activity due to the presence of metallic Co.展开更多
Wet chemistry methods,including hot-injection and precipitation methods,have emerged as major synthetic routes for high-quality perovskite nanocrystals in backlit display and scintillation applications.However,low che...Wet chemistry methods,including hot-injection and precipitation methods,have emerged as major synthetic routes for high-quality perovskite nanocrystals in backlit display and scintillation applications.However,low chemical yield hinders their upscale production for practical use.Meanwhile,the labile nature of halide-based perovskite poses a major challenge for long-term storage of perovskite nanocrystals.Herein,we report a green synthesis at room temperature for gram-scale production of CsPbBr3 nanosheets with minimum use of solvent,saving over 95% of the solvent for the unity mass nanocrystal production.The perovskite colloid exhibits record stability upon long-term storage for up to 8 months,preserving a photoluminescence quantum yield of 63% in solid state.Importantly,the colloidal nanosheets show self-assembly behavior upon slow solidification,generating a crack-free thin film in a large area.The uniform film was then demonstrated as an efficient scintillation screen for X-ray imaging.Our findings bring a scalable tool for synthesis of high-quality perovskite nanocrystals,which may inspire the industrial optoelectronic application of large-area perovskite film.展开更多
The development of negative permittivity materials in multifunctional applications requests expansion of their operating frequency and improvement of stability of negative permittivity.Low electron density is benefici...The development of negative permittivity materials in multifunctional applications requests expansion of their operating frequency and improvement of stability of negative permittivity.Low electron density is beneficial to reduce plasma frequency so that negative permittivity is achieved in kHz region.Negative permittivity achieved by percolating composites is restricted in practicality due to its instability nature at high temperatures.To achieve temperature-stable negative permittivity in kHz region,monophase La_(1-x)Ba_(x)CoO_(3)ceramics were prepared,and the transition from dielectric to metal was elaborated in the perspective of electrical conductivity and negative permittivity.The plasma-like negative permittivity is attained in kHz region,which is interpreted by the collective oscillation of low electron density.The temperature-stable negative permittivity is based on the fact that the plasmonic state will not be undermined at high temperatures.In addition,zero-crossing behavior of real permittivity is observed in La_(0.9)Ba_(0.1)CoO_(3)sample,which provides a promising alternative to designing epsilon-near-zero materials.This work makes the La_(1-x)Ba_(x)CoO_(3)system a source material for achieving effective negative permittivity.展开更多
Oxygen reduction reaction(ORR)catalysts play a critical role in energy storage and conversion devices and have been attracted enormous interests,and however,it remains challenging to develop highly active cheap cataly...Oxygen reduction reaction(ORR)catalysts play a critical role in energy storage and conversion devices and have been attracted enormous interests,and however,it remains challenging to develop highly active cheap catalysts in a simple and green route.Inspired by the heme-copper oxidases(HOCs),in which the ORR active center is originated from the incorporation of Fe-N_(4)with copper atom,we here developed a fine manganese oxide nanosheets(MnO_(x)NSs)integrated with iron phthalocyanine(FePc)anchored on highly conductive graphene(MnO_(x)/FePc-G)through a green route only involve ethanol as the reagent.The bio-inspired catalyst MnO_(x)/Fe Pc-G demonstrated high ORR activity with a half-wave potential(E_(1/2))of 0.887 V,about 57 mV more positive than that of Pt/C.And the current density(j)at 0.9 V is about 1.9 m A cm^(-2),which is three times of Pt/C and FePc-G.More importantly,the bio-inspired systems show superior stability in comparison to commercial Pt/C,showing a potential of 0.863 V to deliver a j of 3 mA cm^(-2)after 18000 s polarization,about 80 mV higher than that of 0.783 V for Pt/C.The high activity is contributed by the integration of the Fe Pc and MnO_(x)NSs that plays the role to assist the cleavage of the O_(2)bond.Our approach provides a new evidence to develop highly efficient ORR catalysts through imitate the naturally involved systems through a simple route.展开更多
To obtain environmentally friendly,integrated and miniaturized gas sensors for the increasing request for the Internet of Things industry and other relative areas,the ultra-thin CoO_(x)/Zn O heterogeneous film with ac...To obtain environmentally friendly,integrated and miniaturized gas sensors for the increasing request for the Internet of Things industry and other relative areas,the ultra-thin CoO_(x)/Zn O heterogeneous film with active interfacial sites was in-situ deposited on micro-electro-mechanical systems(MEMS)as H_(2)S sensor.Atomic layer deposition(ALD)was employed to in-situ fabricate the uniform Zn O thin film.ALD CoO_(x)was deposited on ZnO surface to obtain CoO_(x)/Zn O heterojunction and active interfacial sites.The ultra-thin film(20 nm)with 50 ALD Co O_(x)decorated on 250 ALD Zn O displays excellent sensing performance,including very high response(4.45@200×10^(-9))and selectivity to H_(2)S with a limit of detection(LOD)of 0.38×10^(-9),long-term sensing stability,high response/recovery performance(7.5 s/15.7 s)and mechanical strength at 230。C.Reasons for the high sensing performance of CoO_(x)/Zn O have been confirmed by series of characterizations and density functional theory(DFT)calculation.Heterojunction film thickness with Debye length,the oxygen vacancies and the synergistic effect of active interfacial sites are main reasons for the high sensing performance.The strategy by fabrication of CoO_(x)/Zn O heterogeneous film within Debye length and employing synergistic effect of active interfacial sites offers a promising route for the design of environmentally friendly gas sensors.Furthermore,the ALD technique offers a facile in-situ strategy and high-throughput fabrication of MEMS gas sensors.展开更多
In this study,TiO_(2) nanosheets(NSs)grown in situ on extremely conductive Ti_(3)C_(2)T_(x) MXene to form TiO_(2)/Ti_(3)C_(2)T_(x) MXene composites with abundant active sites are proposed to effectively achieve elec‐...In this study,TiO_(2) nanosheets(NSs)grown in situ on extremely conductive Ti_(3)C_(2)T_(x) MXene to form TiO_(2)/Ti_(3)C_(2)T_(x) MXene composites with abundant active sites are proposed to effectively achieve elec‐trocatalytic NH_(3) synthesis.Electron transfer can be promoted by Ti_(3)C_(2)T_(x) MXene with high conduc‐tivity.Meanwhile,the TiO_(2) NSs in‐situ formation can not only avoid Ti_(3)C_(2)T_(x) MXene microstacking but also enhance the surface specific area of Ti_(3)C_(2)T_(x) MXene.The TiO_(2)/Ti_(3)C_(2)T_(x) MXene catalyst reach‐es a high Faradaic efϐiciency(FE)of 44.68%at−0.75 V vs.RHE and a large NH3 yield of 44.17µg h^(-1) mg^(-1)cat.at−0.95 V,with strong electrochemical durability.15N isotopic labeling experiments imply that the N in the produced NH3 originated from the N2 of the electrolyte.DFT calculations were conducted to determine the possible NRR reaction pathways for TiO_(2)/Ti_(3)C_(2)T_(x) MXene composites.MXene catalysts combined with other materials have been rationally designed for efficient ammonia production under ambient conditions。展开更多
The utilization of perovskite oxide materials as catalysts for the photodegradation of organic pollutants in water is a promising and rapidly advancing field.In this study,a series of La_(1−x)Ba_(x)CoO_(3)(x=0.2,0.3,0...The utilization of perovskite oxide materials as catalysts for the photodegradation of organic pollutants in water is a promising and rapidly advancing field.In this study,a series of La_(1−x)Ba_(x)CoO_(3)(x=0.2,0.3,0.4,0.5,0.6)catalysts with varying Ba doping ratios were synthesized using the citric acid complexation-hydrothermal synthesis combined method for the degradation of phenol under visible light irradiation.Among the synthesized catalysts,La_(0.5)Ba_(0.5)CoO_(3) exhibited the highest photocatalytic activity.In addition,the photocatalytic mechanism for La_(0.5)Ba_(0.5)CoO_(3) perovskite degradation of phenol was also discussed.The synthesized catalysts were characterized using XRD,SEM,FT-IR,XPS,MPMS and other characterization techniques.The results revealed that the diffraction peak intensity of La_(1−x)Ba_(x)CoO_(3) increased with higher Ba doping ratios,and the La_(0.4)Ba_(0.6)CoO_(3) exhibited the strongest diffraction peaks.The catalyst particle sizes ranged from 10 to 50 nm,and the specific surface area decreased with increasing Ba content.Additionally,the paramagnetic properties of La_(0.5)Ba_(0.5)CoO_(3) were similar to that of La_(0.4)Ba_(0.6)CoO_(3).The experimental results suggested that the incorporation of Ba could significantly improve the catalytic performance of La_(1−x)Ba_(x)CoO_(3) perovskites,promote electron transfer and favor to the generation of hydroxyl radicals(•OH),leading to the efficiently degradation of phenol.展开更多
基金supported by the Foundation of Guangxi Science and Technology of Base&Talent Special Program(AD20159067)Central Guiding Local Development of Science and Technology Plan Project in Guigang City(2023 No.2)。
文摘The technology of photothermal catalytic degradation of acetone and conversion of nitrogen monoxide(NO)not only reduces energy consumption compared to traditional thermal catalytic oxidation technology but also improves degradation efficiency,effectively overcoming the limitations of single photocatalytic or thermal catalytic technology.This paper aims to control the lattice oxygen activity and oxygen vacancy concentration of the catalyst by optimizing the manganese-cobalt(Mn-Co)molar ratio and modifying the catalyst with Ce doping,thereby enhancing its photocatalytic and thermal catalytic performance for the degradation of acetone and NO.At 240℃,when the Mn-Co molar ratio is 4:2,the CoO_(x)/MnO_(x)@Fe_(2)O_(3)-2 catalyst exhibits good catalytic activity for both acetone and NO,with conversion rates of 52%and 63.8%for acetone and NO,respectively.Based on the optimization of the Mn-Co molar ratio,Ce was doped into the CoO_(x)/MnO_(x)@Fe_(2)O_(3)-2 sample using the co-precipitation method to synthesize samples with different Ce doping amounts.The sample of CeO_(2)/CoO_(x)/MnO_(x)@Fe_(2)O_(3)-2-0.25(nMn-Co:nCe=1:0.25)shows the highest catalytic performance compared with the other samples,with the conversion of acetone and NO reaching 60%and 70%,respectively,at 240℃.Additionally,the intrinsic mechanism under photothermal synergy is based on the Mars-van Krevelen redox cycle theory.
基金supported by the National Natural Science Foundation of China(11872171 and 22209037)the Project on Excellent Post-graduate Dissertation of Hohai University。
文摘Although metallic rhodium(Rh)is regarded as a promising platinum-alternative anode catalyst of direct methanol fuel cell(DMFC),the conventional"particle-to-face"contact model between Rh and matrix largely limits the overall electrocatalytic performance due to their insufficient cooperative effects.Herein,we report a controllable and robust heterointerface engineering strategy for the bottom-up fabrication of rhombic Rh nanosheets in situ confined on Ti_3C_(2)T_x MXene nanolamellas(Rh NS/MXene)via a convenient stereoassembly process.This unique design concept gives the resulting 2D/2D Rh NS/MXene heterostructure intriguing textural features,including large accessible surface areas,strong"face-toface"interfacial interactions,homogeneous Rh nanosheet distribution,ameliorative electronic structure,and high electronic conductivity.As a consequence,the as-prepared Rh NS/MXene nanoarchitectures exhibit exceptional electrocatalytic methanol oxidation properties in terms of a large electrochemically active surface area of 126.2 m~2 g_(Rh)~(-1),a high mass activity of 1056.9 mA mg_(Rh)-~1,and a long service life,which significantly outperform those of conventional particle-shaped Rh catalysts supported by carbon black,carbon nanotubes,reduced graphene oxide,and MXene matrixes as well as the commercial Pt nanoparticle/carbon black and Pd nanoparticle/carbon black catalysts with the same noble metal loading amount.Density functional theory calculations further demonstrate that the direct electronic interaction at the well-contacted 2D/2D heterointerfaces effectively enhances the adsorption energy of Rh nanosheets and induces a left shift of the d-band center,thereby making the Rh NS/MXene configuration suffer less from CO poisoning.This work highlights the importance of rational heterointerface design in the construction of advanced noble metal/MXene electrocatalysts,which may provide new avenues for developing the next-generation DMFC devices.
基金partially supported by the National Natural Science Foundation of China(No.21805308)the Taishan Scholar Project of Shandong province,the Key Research and Development Program of Shandong Province(No.2019GSF109075)the Fundamental Research Funds for the Central Universities(No.18CX06065A,No.19CX05001A)。
文摘In this paper,we report a facile strategy to synthesize Co-BDC-NH2 material,which is used as a precursor towards an excellent OER electrocatalyst by thermal annealing in nitrogen.Ultra-small Co/Co Oxnanoparticles were uniformly dispersed on the rhombus N-doped carbon(NC)nanoflakes.Transmission electron microscopic,X-ray diffraction spectrometric,and X-ray photoelectron spectroscopic analyses revealed the coexistence of metallic Co and Co oxides nanoparticles.It was found that Co/CoO_(x)@NC obtained at 500℃ annealing temperature exhibited the highest electrocatalytic OER activity,with 307 and375 m V overpotential to achieve 10 and 100 m A cm^(-2) current densities.Besides,thanks to the in-situ annealing process,Co/CoO_(x)@NC showed excellent catalytic stability with 97.4%current density retention after 24 h electrolysis at 1.66 V vs.RHE electrode potential.Further investigations revealed that the ultrasmall Co/Co Oxnanoparticles distributed on N-doped carbon template contribute significantly towards OER electrocatalysis through enlarging the activity surface areas and enhancing the intrinsic electrochemical activity due to the presence of metallic Co.
基金supported by National Natural Science Foundation of China (Nos. 21805111 and 11405073)Taishan Scholar Fund
文摘Wet chemistry methods,including hot-injection and precipitation methods,have emerged as major synthetic routes for high-quality perovskite nanocrystals in backlit display and scintillation applications.However,low chemical yield hinders their upscale production for practical use.Meanwhile,the labile nature of halide-based perovskite poses a major challenge for long-term storage of perovskite nanocrystals.Herein,we report a green synthesis at room temperature for gram-scale production of CsPbBr3 nanosheets with minimum use of solvent,saving over 95% of the solvent for the unity mass nanocrystal production.The perovskite colloid exhibits record stability upon long-term storage for up to 8 months,preserving a photoluminescence quantum yield of 63% in solid state.Importantly,the colloidal nanosheets show self-assembly behavior upon slow solidification,generating a crack-free thin film in a large area.The uniform film was then demonstrated as an efficient scintillation screen for X-ray imaging.Our findings bring a scalable tool for synthesis of high-quality perovskite nanocrystals,which may inspire the industrial optoelectronic application of large-area perovskite film.
基金supported by the National Natural Science Foundation of China(Nos.51771104,51871146,51971119)the Natural Science Foundation of Shandong Province(No.ZR2020YQ32)the Innovation Program of Shanghai Municipal Education Commission(No.2019-01-07-00-10-E00053)。
文摘The development of negative permittivity materials in multifunctional applications requests expansion of their operating frequency and improvement of stability of negative permittivity.Low electron density is beneficial to reduce plasma frequency so that negative permittivity is achieved in kHz region.Negative permittivity achieved by percolating composites is restricted in practicality due to its instability nature at high temperatures.To achieve temperature-stable negative permittivity in kHz region,monophase La_(1-x)Ba_(x)CoO_(3)ceramics were prepared,and the transition from dielectric to metal was elaborated in the perspective of electrical conductivity and negative permittivity.The plasma-like negative permittivity is attained in kHz region,which is interpreted by the collective oscillation of low electron density.The temperature-stable negative permittivity is based on the fact that the plasmonic state will not be undermined at high temperatures.In addition,zero-crossing behavior of real permittivity is observed in La_(0.9)Ba_(0.1)CoO_(3)sample,which provides a promising alternative to designing epsilon-near-zero materials.This work makes the La_(1-x)Ba_(x)CoO_(3)system a source material for achieving effective negative permittivity.
基金funded by an Australian Research Council LIEF grant(LE120100026)supported by the National Natural Science Foundation of China(U19A2017)
文摘Oxygen reduction reaction(ORR)catalysts play a critical role in energy storage and conversion devices and have been attracted enormous interests,and however,it remains challenging to develop highly active cheap catalysts in a simple and green route.Inspired by the heme-copper oxidases(HOCs),in which the ORR active center is originated from the incorporation of Fe-N_(4)with copper atom,we here developed a fine manganese oxide nanosheets(MnO_(x)NSs)integrated with iron phthalocyanine(FePc)anchored on highly conductive graphene(MnO_(x)/FePc-G)through a green route only involve ethanol as the reagent.The bio-inspired catalyst MnO_(x)/Fe Pc-G demonstrated high ORR activity with a half-wave potential(E_(1/2))of 0.887 V,about 57 mV more positive than that of Pt/C.And the current density(j)at 0.9 V is about 1.9 m A cm^(-2),which is three times of Pt/C and FePc-G.More importantly,the bio-inspired systems show superior stability in comparison to commercial Pt/C,showing a potential of 0.863 V to deliver a j of 3 mA cm^(-2)after 18000 s polarization,about 80 mV higher than that of 0.783 V for Pt/C.The high activity is contributed by the integration of the Fe Pc and MnO_(x)NSs that plays the role to assist the cleavage of the O_(2)bond.Our approach provides a new evidence to develop highly efficient ORR catalysts through imitate the naturally involved systems through a simple route.
基金financially supported by the National Key Research and Development Program of China(No.2020YFB2008600)the financial support from China Scholarship Council(CSC)。
文摘To obtain environmentally friendly,integrated and miniaturized gas sensors for the increasing request for the Internet of Things industry and other relative areas,the ultra-thin CoO_(x)/Zn O heterogeneous film with active interfacial sites was in-situ deposited on micro-electro-mechanical systems(MEMS)as H_(2)S sensor.Atomic layer deposition(ALD)was employed to in-situ fabricate the uniform Zn O thin film.ALD CoO_(x)was deposited on ZnO surface to obtain CoO_(x)/Zn O heterojunction and active interfacial sites.The ultra-thin film(20 nm)with 50 ALD Co O_(x)decorated on 250 ALD Zn O displays excellent sensing performance,including very high response(4.45@200×10^(-9))and selectivity to H_(2)S with a limit of detection(LOD)of 0.38×10^(-9),long-term sensing stability,high response/recovery performance(7.5 s/15.7 s)and mechanical strength at 230。C.Reasons for the high sensing performance of CoO_(x)/Zn O have been confirmed by series of characterizations and density functional theory(DFT)calculation.Heterojunction film thickness with Debye length,the oxygen vacancies and the synergistic effect of active interfacial sites are main reasons for the high sensing performance.The strategy by fabrication of CoO_(x)/Zn O heterogeneous film within Debye length and employing synergistic effect of active interfacial sites offers a promising route for the design of environmentally friendly gas sensors.Furthermore,the ALD technique offers a facile in-situ strategy and high-throughput fabrication of MEMS gas sensors.
文摘In this study,TiO_(2) nanosheets(NSs)grown in situ on extremely conductive Ti_(3)C_(2)T_(x) MXene to form TiO_(2)/Ti_(3)C_(2)T_(x) MXene composites with abundant active sites are proposed to effectively achieve elec‐trocatalytic NH_(3) synthesis.Electron transfer can be promoted by Ti_(3)C_(2)T_(x) MXene with high conduc‐tivity.Meanwhile,the TiO_(2) NSs in‐situ formation can not only avoid Ti_(3)C_(2)T_(x) MXene microstacking but also enhance the surface specific area of Ti_(3)C_(2)T_(x) MXene.The TiO_(2)/Ti_(3)C_(2)T_(x) MXene catalyst reach‐es a high Faradaic efϐiciency(FE)of 44.68%at−0.75 V vs.RHE and a large NH3 yield of 44.17µg h^(-1) mg^(-1)cat.at−0.95 V,with strong electrochemical durability.15N isotopic labeling experiments imply that the N in the produced NH3 originated from the N2 of the electrolyte.DFT calculations were conducted to determine the possible NRR reaction pathways for TiO_(2)/Ti_(3)C_(2)T_(x) MXene composites.MXene catalysts combined with other materials have been rationally designed for efficient ammonia production under ambient conditions。
基金The Fundamental Research Program for Young Scientists of Shanxi Province(Project No.202103021223294)The Fundamental Research Program of Shanxi Province(Project No.202203021211203)+1 种基金The Start-up Fund for Doctorate Scientific Research Project of Taiyuan University of Science and Technology(Project No.20232124)The Innovation and Entrepreneurship Training Program for Undergraduate,Taiyuan University of Science and Technology(Project No.DCX2024162).
文摘The utilization of perovskite oxide materials as catalysts for the photodegradation of organic pollutants in water is a promising and rapidly advancing field.In this study,a series of La_(1−x)Ba_(x)CoO_(3)(x=0.2,0.3,0.4,0.5,0.6)catalysts with varying Ba doping ratios were synthesized using the citric acid complexation-hydrothermal synthesis combined method for the degradation of phenol under visible light irradiation.Among the synthesized catalysts,La_(0.5)Ba_(0.5)CoO_(3) exhibited the highest photocatalytic activity.In addition,the photocatalytic mechanism for La_(0.5)Ba_(0.5)CoO_(3) perovskite degradation of phenol was also discussed.The synthesized catalysts were characterized using XRD,SEM,FT-IR,XPS,MPMS and other characterization techniques.The results revealed that the diffraction peak intensity of La_(1−x)Ba_(x)CoO_(3) increased with higher Ba doping ratios,and the La_(0.4)Ba_(0.6)CoO_(3) exhibited the strongest diffraction peaks.The catalyst particle sizes ranged from 10 to 50 nm,and the specific surface area decreased with increasing Ba content.Additionally,the paramagnetic properties of La_(0.5)Ba_(0.5)CoO_(3) were similar to that of La_(0.4)Ba_(0.6)CoO_(3).The experimental results suggested that the incorporation of Ba could significantly improve the catalytic performance of La_(1−x)Ba_(x)CoO_(3) perovskites,promote electron transfer and favor to the generation of hydroxyl radicals(•OH),leading to the efficiently degradation of phenol.
