The dynamics of calcium(Ca)and magnesium(Mg)in the forest floor and topsoil caused by anthropogenic and natural processes continue to be a concern in temperate forests.However,the impacts of abiotic and biotic variabl...The dynamics of calcium(Ca)and magnesium(Mg)in the forest floor and topsoil caused by anthropogenic and natural processes continue to be a concern in temperate forests.However,the impacts of abiotic and biotic variables as well as their interactions remain unclear,especially in areas undergoing long-term forest restoration.In this study,Ca and Mg concentrations in the forest floor and topsoil from 239 forest plots across the Loess Plateau were measured,and the effects of forest types,climate,soil properties,stand characteristics and nitrogen deposition were explored.The results showed significantly higher Ca concentrations in the forest floor(20.68±8.04 mg/g)than in the topsoil(13.28±12.83 mg/g),whereas Mg exhibited the inverse pattern(3.64±1.09 and 10.11±2.51 mg/g,respectively).The effect of forest types was only significant on forest floor Ca,and Ca concentrations were higher in broadleaf and mixed forests than in coniferous forests.Overall,Ca and Mg concentrations in forest floor and topsoil increased with latitudes while decreased with elevations,and the significance of the trends varied among forest types.Forest floor Ca and Mg were mainly influenced by environmental variables aboveground,i.e.,basal area(BA)and mean annual precipitation(MAP),respectively;topsoil Ca and Mg were more affected by soil properties(soil C/N and pH,respectively).Those suggested a depletion of Ca belowground was associated with forest growth and enriched soil nitrogen,and the leaching of mobile Mg was correlated with rainfall and soil acidification.Besides,the impact of environmental variables on Ca-Mg balance(Ca/Mg ratio)belowground was primarily through the regulation of Ca.Elucidating the influence of environmental variables will improve our ability to predict future changes in base cations and thus forest soil health in the greening vegetated Loess Plateau.展开更多
In this study,sawdust served as a carbon source and urea as a nitrogen source to synthesize carbonsupported,nitrogen-doped TiO_(2)composites via a one-pot solvothermal method.The composites were characterized using FT...In this study,sawdust served as a carbon source and urea as a nitrogen source to synthesize carbonsupported,nitrogen-doped TiO_(2)composites via a one-pot solvothermal method.The composites were characterized using FTIR,powder X-ray diffraction,X-ray photoelectron spectroscopy,ultraviolet-visible diffuse reflectance spectroscopy,thermogravimetry-derivative thermogravimetry,scanning electron microscopy-energy dispersive spectroscopy,and transmission electron microscopy.Results indicated that all synthesized composites exhibit the anatase phase,with those calcined at 800℃ demonstrating enhanced crystallinity.Nitrogen is incorporated into the TiO_(2)lattice,while carbon is predominantly located on the surface.Photodegradation experiments showed that 20 mg of composite N-TiO_(2)/C-800 achieved degradation rates of 93.4% for methylene blue(20 mg·L^(-1),50 mL)and 99.4% for oxytetracycline(20 mg·L^(-1),50 mL)within 30 min.Free radical capture experiments indicated that h+was the primary active species in the photocatalytic degradation process.展开更多
Conventional electrocatalytic urea synthesis via CO_(2)+N_(2) or CO_(2)+NO_(3)^(-)coelectrolysis generally suffers from poor reactants coactivation,low C-N coupling efficiency,and serious competing reactions.To overco...Conventional electrocatalytic urea synthesis via CO_(2)+N_(2) or CO_(2)+NO_(3)^(-)coelectrolysis generally suffers from poor reactants coactivation,low C-N coupling efficiency,and serious competing reactions.To overcome these limitations,we implement HCOOH+NO_(3)^(-)coelectrolysis to urea using a Fe-Pd dual-atom catalyst(Fe_(1)Pd_(1)-DAC).Operando spectroscopic measurements and theoretical computations collectively reveal that Pd_(1) selectively dehydrogenates HCOOH to^(*)COOH,while Fe_(1) selectively activates NO_(3)^(-)to^(*)NH_(2).Specifically,the spatial proximity and electrophilic-nucleophilic synergy of^(*)COOH and^(*)NH_(2) enable the high C-N coupling efficiency and well-suppressed competing reactions.Consequently,Fe_(1)Pd_(1)-DAC assembled in a flow cell delivers the unprecedented urea yield rate up to 448.1 mmol h^(-1) g^(-1) and Faradaic efficiency of 78.3%at an industrial-level current density of-215 mA cm^(-2),far outperforming those obtained from CO_(2)+N_(2) or CO_(2)+NO_(3) coelectrolysis.Further techno-economic analysis demonstrates Fe_(1)Pd_(1)-DAC as a promising catalyst for economically feasible urea production via HCOOH+NO_(3)^(-)coelectrolysis.展开更多
Graphite and hexagonal boron nitride(h-BN),despite their structural similarity,exhibit opposing electronic properties,namely,metallic conductivity and wide-bandgap insulation,respectively.In recent years,graphene-h-BN...Graphite and hexagonal boron nitride(h-BN),despite their structural similarity,exhibit opposing electronic properties,namely,metallic conductivity and wide-bandgap insulation,respectively.In recent years,graphene-h-BN heterostructures have attracted significant research interest,with the resulting hybrid B-C-N atomic-layer systems exhibiting distinctive electronic properties.Notably,interface effects play a decisive role in governing the performance of these heterostructures.Nevertheless,owing to the lack of high-quality composites,the interfacial structure in B-C-N materials and the correlation with critical properties such as charge transport and band structure modulation are not fully clear.Here,we report the direct synthesis of a millimeter-sized hexagonal B-C-N composite via a solvent method under high-pressure and high-temperature conditions.Structural characterization reveals that the synthesized B-C-N composite contains isolated graphite and h-BN.Compared with pure h-BN,the B-C-N composite has a narrower bandgap and shows a pronounced photoelectric response in the visible light region.More interestingly,we find a graphite-like B-C compound with a thickness of about 30 nm at the graphite-h-BN interface,which forms Schottky junctions with graphite,thus realizing rectification properties.Our findings provide a method for synthesizing highquality B-C-N composites and offer new insights into the structure of the graphite-h-BN interface.展开更多
基金supported by the National Natural Science Foundation of China(42401054)Natural Science Foundation of Hebei Province(D2024205019)Science and Technology Project of Hebei Education Department(BJ2025014).
文摘The dynamics of calcium(Ca)and magnesium(Mg)in the forest floor and topsoil caused by anthropogenic and natural processes continue to be a concern in temperate forests.However,the impacts of abiotic and biotic variables as well as their interactions remain unclear,especially in areas undergoing long-term forest restoration.In this study,Ca and Mg concentrations in the forest floor and topsoil from 239 forest plots across the Loess Plateau were measured,and the effects of forest types,climate,soil properties,stand characteristics and nitrogen deposition were explored.The results showed significantly higher Ca concentrations in the forest floor(20.68±8.04 mg/g)than in the topsoil(13.28±12.83 mg/g),whereas Mg exhibited the inverse pattern(3.64±1.09 and 10.11±2.51 mg/g,respectively).The effect of forest types was only significant on forest floor Ca,and Ca concentrations were higher in broadleaf and mixed forests than in coniferous forests.Overall,Ca and Mg concentrations in forest floor and topsoil increased with latitudes while decreased with elevations,and the significance of the trends varied among forest types.Forest floor Ca and Mg were mainly influenced by environmental variables aboveground,i.e.,basal area(BA)and mean annual precipitation(MAP),respectively;topsoil Ca and Mg were more affected by soil properties(soil C/N and pH,respectively).Those suggested a depletion of Ca belowground was associated with forest growth and enriched soil nitrogen,and the leaching of mobile Mg was correlated with rainfall and soil acidification.Besides,the impact of environmental variables on Ca-Mg balance(Ca/Mg ratio)belowground was primarily through the regulation of Ca.Elucidating the influence of environmental variables will improve our ability to predict future changes in base cations and thus forest soil health in the greening vegetated Loess Plateau.
文摘In this study,sawdust served as a carbon source and urea as a nitrogen source to synthesize carbonsupported,nitrogen-doped TiO_(2)composites via a one-pot solvothermal method.The composites were characterized using FTIR,powder X-ray diffraction,X-ray photoelectron spectroscopy,ultraviolet-visible diffuse reflectance spectroscopy,thermogravimetry-derivative thermogravimetry,scanning electron microscopy-energy dispersive spectroscopy,and transmission electron microscopy.Results indicated that all synthesized composites exhibit the anatase phase,with those calcined at 800℃ demonstrating enhanced crystallinity.Nitrogen is incorporated into the TiO_(2)lattice,while carbon is predominantly located on the surface.Photodegradation experiments showed that 20 mg of composite N-TiO_(2)/C-800 achieved degradation rates of 93.4% for methylene blue(20 mg·L^(-1),50 mL)and 99.4% for oxytetracycline(20 mg·L^(-1),50 mL)within 30 min.Free radical capture experiments indicated that h+was the primary active species in the photocatalytic degradation process.
基金supported by the National Natural Science Foundation of China(52561042)the Industrial Support Plan Project of Gansu Provincial Education Department(2024CYZC-22)。
文摘Conventional electrocatalytic urea synthesis via CO_(2)+N_(2) or CO_(2)+NO_(3)^(-)coelectrolysis generally suffers from poor reactants coactivation,low C-N coupling efficiency,and serious competing reactions.To overcome these limitations,we implement HCOOH+NO_(3)^(-)coelectrolysis to urea using a Fe-Pd dual-atom catalyst(Fe_(1)Pd_(1)-DAC).Operando spectroscopic measurements and theoretical computations collectively reveal that Pd_(1) selectively dehydrogenates HCOOH to^(*)COOH,while Fe_(1) selectively activates NO_(3)^(-)to^(*)NH_(2).Specifically,the spatial proximity and electrophilic-nucleophilic synergy of^(*)COOH and^(*)NH_(2) enable the high C-N coupling efficiency and well-suppressed competing reactions.Consequently,Fe_(1)Pd_(1)-DAC assembled in a flow cell delivers the unprecedented urea yield rate up to 448.1 mmol h^(-1) g^(-1) and Faradaic efficiency of 78.3%at an industrial-level current density of-215 mA cm^(-2),far outperforming those obtained from CO_(2)+N_(2) or CO_(2)+NO_(3) coelectrolysis.Further techno-economic analysis demonstrates Fe_(1)Pd_(1)-DAC as a promising catalyst for economically feasible urea production via HCOOH+NO_(3)^(-)coelectrolysis.
基金supported by the National Key R&D Program of China(Grant No.2023YFA1406200)the National Science Foundation of China(Grant No.U2032215)+1 种基金Jilin Province Major Science and Technology Program,China(Grant No.20240211002GX)the Science and Technology Development Project of Jilin Province(Grant No.SKL202402004).
文摘Graphite and hexagonal boron nitride(h-BN),despite their structural similarity,exhibit opposing electronic properties,namely,metallic conductivity and wide-bandgap insulation,respectively.In recent years,graphene-h-BN heterostructures have attracted significant research interest,with the resulting hybrid B-C-N atomic-layer systems exhibiting distinctive electronic properties.Notably,interface effects play a decisive role in governing the performance of these heterostructures.Nevertheless,owing to the lack of high-quality composites,the interfacial structure in B-C-N materials and the correlation with critical properties such as charge transport and band structure modulation are not fully clear.Here,we report the direct synthesis of a millimeter-sized hexagonal B-C-N composite via a solvent method under high-pressure and high-temperature conditions.Structural characterization reveals that the synthesized B-C-N composite contains isolated graphite and h-BN.Compared with pure h-BN,the B-C-N composite has a narrower bandgap and shows a pronounced photoelectric response in the visible light region.More interestingly,we find a graphite-like B-C compound with a thickness of about 30 nm at the graphite-h-BN interface,which forms Schottky junctions with graphite,thus realizing rectification properties.Our findings provide a method for synthesizing highquality B-C-N composites and offer new insights into the structure of the graphite-h-BN interface.
