Herein,3‑aminopropyltriethoxysilane(APTES)was used to modify F‑containing silica slag(SS)by simple grafting and served as a multifunctional barrier layer.The amino group(—NH2)in the amino‑modified SS(NH2‑SS)forms lig...Herein,3‑aminopropyltriethoxysilane(APTES)was used to modify F‑containing silica slag(SS)by simple grafting and served as a multifunctional barrier layer.The amino group(—NH2)in the amino‑modified SS(NH2‑SS)forms ligand bonds or hydrogen bonds with sulfur ions in lithium polysulfides(LiPSs),thus inhibiting the shuttle effect.Electrochemical analyses demonstrated that lithium‑sulfur(Li‑S)batteries employing the NH2‑SS interlayer exhibited discharge specific capacities of 1048 and 789 mAh·g^(-1) at 0.2C and 2C,respectively,and even at 4C,the initial discharge specific capacity remained at 590 mAh·g^(-1),outperforming the Li‑S battery with unmodified SS as the interlayer.展开更多
It is crucial to develop arsenic removal adsorbents with strong sulfur resistance under middle-low-temperature flue gas conditions(<400℃).In this work,five Fe-Ce-La oxides were prepared by co-precipitation method,...It is crucial to develop arsenic removal adsorbents with strong sulfur resistance under middle-low-temperature flue gas conditions(<400℃).In this work,five Fe-Ce-La oxides were prepared by co-precipitation method,and FeCeLaO/SiO_(2)-Al_(2)O_(3) composite adsorbents were prepared by coupling fly ash-based Si-Al carriers.The active components Fe-Ce-La oxides and Si-Al carriers were characterized by TPD,TG,XRF,BET and XPS,respectively.The effects of temperature,Si/Al ratio and FeCeLaO loading rate on the sulfur resistance were investigated.Results show that the SO_(2) promotes the arsenic removal of Fe_(2)O_(3),CeLaO and FeCeLaO.At 400℃,the arsenic removal efficiencies of the three oxides increase from 45.3%,72.5% and 81.3% without SO_(2) to 62.6%,80.5%and 91.0%,respectively.The SO_(2) inhibits the arsenic removal of La_(2)O_(2)CO_(3) and FeLaO,and the inhibition effect is pronounced at high temperatures.The sulfur poisoning resistance of Si-Al carriers increases with the increase of Si/Al ratio.When the Si/Al ratio is increased to 9.74,the arsenic removal efficiency in the SO_(2) environment is 13.9% higher than that in the absence of SO_(2).Introducing FeCeLaO active components is beneficial for enhancing the SO_(2) poisoning resistance of Si-Al carriers.The strong sulfur resistance of the FeCeLaO/SiO_(2)-Al_(2)O_(3) composite adsorbent results from multiple factors:protective effects of Ce on Fe,La and Al;sulfation-induced generation of Ce^(3+)and surface-adsorbed oxygen;and strong surface acidity of SiO_(2).展开更多
Sulfur is closely associated with various types of ore deposits,particularly orogenic gold(Au)systems,where sulfur-bearing melts and fluids play a critical role in transporting oreforming elements essential for ore fo...Sulfur is closely associated with various types of ore deposits,particularly orogenic gold(Au)systems,where sulfur-bearing melts and fluids play a critical role in transporting oreforming elements essential for ore formation.The widely accepted metamorphic devolatilization model suggests that compositionally fertile sedimentary rocks serve as potential gold sources.Therefore,understanding sulfur behavior during prograde metamorphism is essential for elucidating the mechanisms underlying metal activation and mobility.In this study,we conducted in-situ sulfur isotope(δ^(34)S)analyses using secondary ion mass spectrometry(SIMS)on samples from the Hongshankou area,a representative Barrovian-type metamorphic sequence characterized by intermediate pressure-temperature(P-T)conditions.This sequence comprises the biotite,garnet,staurolite,and kyanite zones.Our results show a systematic increase in δ^(34)S values(from 3.1‰ to 5.5‰)coupled with a progressive decrease in total sulfur content(from 320 ppm to 165 ppm)as metamorphic grade increases.The most pronounced sulfur mobilization occurs between the garnet and staurolite zones.In all analyzed samples,Au or Au-bearing minerals predominantly occur along the edges or within pyrite grains,highlighting the critical role of pyrite breakdown in controlling gold mobility.Thus,sulfur isotope fractionation provides robust constraints for quantitatively assessing sulfur mobility during metamorphism.These findings reinforce the concept that metasedimentary rocks and their metamorphic fluids represent fertile sources of Au and other metals enriched in orogenic gold deposits.展开更多
Sluggish kinetics coupled with parasitic shuttling reactions are pivotal challenges hindering the performance of lithium-sulfur(Li-S)batteries.Improving areal capacity and cyclability of Li-S batteries can be achieved...Sluggish kinetics coupled with parasitic shuttling reactions are pivotal challenges hindering the performance of lithium-sulfur(Li-S)batteries.Improving areal capacity and cyclability of Li-S batteries can be achieved by addressing these challenges.A composite sulfur host material is synthesized herein by in situ anchoring ultrafine cobalt-iron phosphide nanoparticles(5-7 nm)onto a hollow mesoporous carbon sphere(HMCS)framework.This strategy achieved exceptional spatial restriction and a high density of catalytically active sites through the encapsulation of sulfur within a hollow-structured framework.Specifically,HMCS expedites rapid Li_(2)S nucleation kinetics,while CoFeP facilitates robust Li_(2)S dissolution kinetics by mitigating decomposition barriers.This synergistic integration equips CoFeP@HMCS with robust bi-directional catalytic activity,significantly promoting interracial charge-transfer,facilitate sulfu r multistep catalytic conversion,and inhibiting shuttling.Consequently,the battery exhibits excellent rate performance(991 mA h g^(-1) at 5.0 C)and retains a high areal capacity of 6.06 mA h cm^(-2) after 200 cycles under a high areal sulfur loading of 8.2 mg cm^(-2) but a low electrolyte/sulfur ratio of 4.8μL mg^(-1).This work contributes to enhancing the practical specific capacity of lithium-sulfur batteries and deepens the understanding of catalysts enabling bidirectional electrocatalytic sulfur conversion.展开更多
Hard carbon(HC)in sodium-ion batteries is searched by numerous investigations,which can offer the excellent performance of reversible Na^(+)insertion and extraction.The covalent heteroatom doping in HC is recently wor...Hard carbon(HC)in sodium-ion batteries is searched by numerous investigations,which can offer the excellent performance of reversible Na^(+)insertion and extraction.The covalent heteroatom doping in HC is recently worth concentrating,which can dilate the interlayer spacing of graphite to adjust the electrochemical storage performance in carbon anodes.However,the reported doping strategies of the modified HC have only resulted in limited improvement,especially unobvious effects on tuning porous structure.In this study,tannin extract and K_(2)SO_(4) are respectively utilized as carbon source and sulfur source for the fabrication of HC,in which K_(2)SO_(4) can contribute to the heteroatom doping,and the pore forming as well.The tannin-derived sulfur-doped carbon anode shows the excellent cycle stability,achieving a high reversible capacity of 520.5 mAh/g at a current density of 100 mA/g.Even after 500 cycles at a current density of 3 A/g,a high specific capacity of 236.7 mAh/g and a capacity retention rate of 92.6%can be reserved.Compared with the initial carbon,the adsorption energy of Na^(+)is multifold times higher,whereas Na^(+)diffusion energy barriers manyfold decrease.Moreover,the full battery assembled with Na_(3)V_(2)(PO_(4))_(3)/tannin-based HC demonstrates a stable cycling performance.This work can manifest the potentiality of the tannin-based electrode as anode for a high-performance sodium-ion batteries(SIBs),which could especially offer an explanation of Na^(+)storage and solid-electrolyte interface(SEI)stability to the electrochemical performance.展开更多
A novel method for the synthesis of 2,4-disubstituted thiophenes via the reactions of N,N-disubstituted enaminones and elemental sulfur is developed.By simply heating the substrates in pure water in the presence of Na...A novel method for the synthesis of 2,4-disubstituted thiophenes via the reactions of N,N-disubstituted enaminones and elemental sulfur is developed.By simply heating the substrates in pure water in the presence of NaOH,the thiophene annulation practically takes place via the generation of one C-C and two C-S bonds via cascade dual C-H functionalization and C-N bond thiolation without using any transition metal reagent.展开更多
Ferroptosis has exhibited great potential in therapies and intracellular reducing agents of sulfur species(RSSs) in the thiol-dependent redox systems are crucial in ferroptosis.This makes the simultaneous detection of...Ferroptosis has exhibited great potential in therapies and intracellular reducing agents of sulfur species(RSSs) in the thiol-dependent redox systems are crucial in ferroptosis.This makes the simultaneous detection of multiple RSSs significant for evaluating ferroptosis therapy.However,the traditional techniques,including fluorescent(FL) imaging and electrospray ionization-based mass spectrometry(MS) detection,cannot achieve the discrimination of different RSSs.Herein,simultaneous MS detection of multiple RSSs,including cysteine(Cys),homocysteine(Hcy),glutathione(GSH) and hydrogen sulfide(H_(2)S),was obtained upon enhancing ionization efficiency by a fluorescent probe(NBD-O-1).Based on the interaction between NBD-O-1 and RSSs,the complex of RSSs with a fragment of NBD-O-1 can be generated,which can be easily ionized for MS detection in the negative mode.Therefore,the intracellular RSSs can be well detected upon the incubation of He La cells with the probe of NBD-O-1,exhibiting the total RSS levels by the FL imaging and further providing expression of each RSS by enhanced MS detection.Furthermore,the RSSs during ferroptosis in He La cells have been evaluated using the present strategy,demonstrating the potential for ferroptosis examinations.This work has made an unconventional application of a fluorescent probe to enhance the detection of multiple RSSs by MS,providing significant molecular information for addressing the ferroptosis mechanism.展开更多
The development of catalytic multicomponent reactions for constructing complex organic scaffolds from readily accessible commodity chemicals is a key pursuit in contemporary synthetic chemistry.Current methods for syn...The development of catalytic multicomponent reactions for constructing complex organic scaffolds from readily accessible commodity chemicals is a key pursuit in contemporary synthetic chemistry.Current methods for synthesizing thioesters primarily rely on the acylation of thiols,which produces substantial waste and requires malodorous,unstable sulfur sources.In this work,we introduce a photocatalyzed hydrogen transfer strategy that enables a three-component synthesis of thioesters using abundant primary alcohols,easily available alkenes and elemental sulfur under mild conditions.This protocol demonstrates broad applicability and high chemo-and regioselectivity for both primary alcohols and alkenes,highlighting the advantage and potential of photo-mediated hydrogen transfer in facilitating multicomponent reactions using primary alcohol and elemental sulfur feedstocks.展开更多
Lithium-sulfur(Li-S)batteries require efficient catalysts to accelerate polysulfide conversion and mitigate the shuttle effect.However,the rational design of catalysts remains challenging due to the lack of a systemat...Lithium-sulfur(Li-S)batteries require efficient catalysts to accelerate polysulfide conversion and mitigate the shuttle effect.However,the rational design of catalysts remains challenging due to the lack of a systematic strategy that rationally optimizes electronic structures and mesoscale transport properties.In this work,we propose an autogenously transformed CoWO_(4)/WO_(2) heterojunction catalyst,integrating a strong polysulfide-adsorbing intercalation catalyst with a metallic-phase promoter for enhanced activity.CoWO_(4) effectively captures polysulfides,while the CoWO_(4)/WO_(2) interface facilitates their S-S bond activation on heterogenous catalytic sites.Benefiting from its directional intercalation channels,CoWO_(4) not only serves as a dynamic Li-ion reservoir but also provides continuous and direct pathways for rapid Li-ion transport.Such synergistic interactions across the heterojunction interfaces enhance the catalytic activity of the composite.As a result,the CoWO_(4)/WO_(2) heterostructure demonstrates significantly enhanced catalytic performance,delivering a high capacity of 1262 mAh g^(−1) at 0.1 C.Furthermore,its rate capability and high sulfur loading performance are markedly improved,surpassing the limitations of its single-component counterparts.This study provides new insights into the catalytic mechanisms governing Li-S chemistry and offers a promising strategy for the rational design of high-performance Li-S battery catalysts.展开更多
Photo-assisted lithium–sulfur batteries(PALSBs)offer an eco-friendly solution to address the issue of sluggish reaction kinetics of conventional LSBs.However,designing an efficient photoelectrode for practical implem...Photo-assisted lithium–sulfur batteries(PALSBs)offer an eco-friendly solution to address the issue of sluggish reaction kinetics of conventional LSBs.However,designing an efficient photoelectrode for practical implementation remains a significant challenge.Herein,we construct a free-standing polymer–inorganic hybrid photoelectrode with a direct Z-scheme heterostructure to develop high-efficiency PALSBs.Specifically,polypyrrole(PPy)is in situ vapor-phase polymerized on the surface of N-doped TiO_(2) nanorods supported on carbon cloth(N-TiO_(2)/CC),thereby forming a well-defined p–n heterojunction.This architecture efficiently facilitates the carrier separation of photo-generated electron–hole pairs and significantly enhances carrier transport by creating a built-in electric field.Thus,the PPy@N-TiO_(2)/CC can simultaneously act as a photocatalyst and an electrocatalyst to accelerate the reduction and evolution of sulfur,enabling ultrafast sulfur redox dynamics,as convincingly validated by both theoretical simulations and experimental results.Consequently,the PPy@N-TiO_(2)/CC PALSB achieves a high discharge capacity of 1653 mAh g^(−1),reaching 98.7%of the theoretical value.Furthermore,5 h of photo-charging without external voltage enables the PALSB to deliver a discharge capacity of 333 mAh g^(−1),achieving dual-mode energy harvesting capabilities.This work successfully integrates solar energy conversion and storage within a rechargeable battery system,providing a promising strategy for sustainable energy storage technologies.展开更多
Renewable electricity-driven production of value-added sulfur and H_(2)via electrocatalytic H_(2)S decomposition represents a sustainable route to conventional thermocatalysis.Both the electrocatalyst and electrolyte ...Renewable electricity-driven production of value-added sulfur and H_(2)via electrocatalytic H_(2)S decomposition represents a sustainable route to conventional thermocatalysis.Both the electrocatalyst and electrolyte solution strongly impact the H_(2)S decomposition performance.Despite significant progress in developing sophisticated electrocatalysts,a well-designed electrolyte solution in conjunction with industrial catalysts is an attractive strategy to advance the industrialization process of electrocatalytic H_(2)S decomposition,but remains unexplored.Here,for the first time,we design a solid-liquid-gas three-phase indirect electrolysis system based on a kind of CS_(2)-N electrolyte solution and Ni-Mo_(2)C that can efficiently enable H_(2)S decomposition into valuable H_(2)and sulfur.Specifically,the solid-phase Ni-Mo_(2)C as a heterogeneous redox mediator presents excellent electrocatalytic efficiency for the H_(2)S removal efficiency of up to 99%,and the formation of liquid-phase sulfur product(CS_(2)-N electrolyte solution dissolves sulfur,yield up to 95%)with the generation of gas-phase H_(2)product(~1.32 mL min^(-1)),resulting in an interesting three-phase indirect electrolysis system.Remarkably,it enables the scale-up production(~6 g in a batch experiment)of sulfur with continuous operation for 120 h without attenuation.This work may inaugurate a new electrocatalytic H_(2)S decomposition avenue to explore porous metal materials and electrolyte systems in simultaneous production of value-added sulfur and H_(2).展开更多
The rate capability and cycling stability of sodium metal batteries taking FeS_(2) or sulfur as cathode are limited due to their low reaction kinetics and severe shuttle effect.Herein,we rationally design a novel sing...The rate capability and cycling stability of sodium metal batteries taking FeS_(2) or sulfur as cathode are limited due to their low reaction kinetics and severe shuttle effect.Herein,we rationally design a novel single-atom-dispersed S_(2)-FeNC/FeS_(2) nanocluster heterojunction embedded in carbon spheres(SFNC/FeS_(2)) for the electrode material of sodium metal batteries.Interestingly,during the discharging process,the Na^(+) is inserted into FeS_(2) to generate Na_(2)S,as well as the unique electrochemical reaction between S_(2)-FeNC and Na^(+) to form Na_(2)S.Meanwhile,the FeNC can adsorb Na_(2)S and catalyze the conversion from Na_(2)S and Fe to FeS_(2) or from Na_(2)S and FeNC to S_(2)-FeNC for suppressing the shuttle effect and promoting the distinct hybrid reversible electrochemical behavior,which improves performance tremendously.Notably,the SFNC/FeS_(2) electrode delivers a specific capacity of 338.7 mAh g^(-1) after superlong 2000 cycles at a current density of 5.0 A g^(-1) and achieves a high energy density of 430.1 Wh Kg^(-1) at a current density of 0.05 A g^(-1).This work presents a novel approach to studying sodium metal batteries with hybrid behavior for excellent high energy density and cycling stability.展开更多
In this work,ofloxacin(OFL),a kind of frequently detected antibiotic in groundwater,was selected to explore its impact(at ng/L-μg/L-level)on denitrification performance in an autotrophic denitrification system driven...In this work,ofloxacin(OFL),a kind of frequently detected antibiotic in groundwater,was selected to explore its impact(at ng/L-μg/L-level)on denitrification performance in an autotrophic denitrification system driven by pyrite/sulfur(FeS2/S0).Results showed that OFL restrained nitrate removal efficiency,and the inhibition degree was positively related to the concentration of OFL.After being exposed to increased OFL(200 ng/L-100μg/L)for 69 days,higher inhibition of electron transport activity(ETSA),enzyme activities of nitrate reductase(NAR),and nitrite reductase(NIR)were acquired.Meanwhile,the extracellular protein(PN)content of sludge samples was remarkably stimulated by OFL to resist the augmented toxicity.OFL contributed to increased microbial diversity and sulfur/sulfide oxidation functional genes in ng/L-level bioreactors,whereas led to a decline inμg/L level experiments.With OFL at concentrations of 200 ng/L and 100μg/L,the whole expression of 10 key denitrification functional genes was depressed,and the higher the OFL concentration,the lower the expression level.However,no significant proliferation of antibiotic resistance genes(ARGs)either in 200 ng/L-OFL or 100μg/L-OFL groups was observed.Two-factor correlation analysis results indicated that Thiobacillus,Anaerolineae,Anaerolineales,and Nitrospirae might be the main hosts of existing ARGs in this system.展开更多
Lithium-sulfur (Li-S) batteries have gained great attention due to the high theoretical energy density and low cost,yet their further commercialization has been obstructed by the notorious shuttle effect and sluggish ...Lithium-sulfur (Li-S) batteries have gained great attention due to the high theoretical energy density and low cost,yet their further commercialization has been obstructed by the notorious shuttle effect and sluggish redox dynamics.Herein,we supply a strategy to optimize the electron structure of Ni_(2)P by concurrently introducing B-doped atoms and P vacancies in Ni_(2)P (Vp-B-Ni_(2)P),thereby enhancing the bidirectional sulfur conversion.The study indicates that the simultaneous introduction of B-doped atoms and P vacancies in Ni_(2)P causes the redistribution of electron around Ni atoms,bringing about the upward shift of d-band center of Ni atoms and effective d-p orbital hybridization between Ni atoms and sulfur species,thus strengthening the chemical anchoring for lithium polysulfides (LiPSs) as well as expediting the bidirectional conversion kinetics of sulfur species.Meanwhile,theoretical calculations reveal that the incorporation of B-doped atoms and P vacancies in Ni_(2)P selectively promotes Li2S dissolution and nucleation processes.Thus,the Li-S batteries with Vp-B-Ni_(2)P-separators present outstanding rate ability of 777 m A h g^(-1)at 5 C and high areal capacity of 8.03 mA h cm^(-2)under E/S of 5μL mg^(-1)and sulfur loading of 7.20 mg cm^(-2).This work elucidates that introducing heteroatom and vacancy in metal phosphide collaboratively regulates the electron structure to accelerate bidirectional sulfur conversion.展开更多
Titanium-bearing blast furnace slag(Ti-BFS)is an industrial solid waste rich in titanium,magnesium and aluminum.However,it is difficult to utilize Ti,Mg and Al from Ti-BFS for the strong stability and poor reaction ac...Titanium-bearing blast furnace slag(Ti-BFS)is an industrial solid waste rich in titanium,magnesium and aluminum.However,it is difficult to utilize Ti,Mg and Al from Ti-BFS for the strong stability and poor reaction activity of Ti-BFS.A comprehensive utilization route of Ti,Mg and Al from Ti-BFS was proposed.Ti-BFS was firstly roasted with H_(2)SO_(4)to realizes the conversion of Ti,Mg and Al to their corresponding sulphates.The sulphates were leached by dilute H_(2)SO_(4)solution to extraction Ti,Mg and Al from roasted Ti-BFS.The roasting conditions were optimized as follows,sulfuric acid concentration of 85%(mass),temperature of 200℃,acid-slag ratio of 5.5,particle size of Ti-BFS<75μm,and reaction time of 1 h.The extraction rates of titanium,aluminum,and magnesium reached 82.42%,88.78%and 90.53%,respectively.The leachate was hydrolyzed at 102℃for 5 h with a titanium hydrolysis ratio of 96%.After filtration and calcination,TiO_(2)with a purity of 97%(mass)was obtained.Al in the leachate was converted to NH_(4)Al(SO_(4))_(2)·12H_(2)O by the neutralization of ammonia water at pH=4.5.Al_(2)O_(3) was obtained by the calcination of NH_(4)Al(SO_(4))_(2)·12H_(2)O.The residual solution can be used to prepare products of magnesium sulfate.In the proposed process,Ti,Mg and Al were extracted from Ti-BFS and utilized comprehensively to prepare valuable products.The leaching behavior of roasted Ti-BFS with water was also studied.It followed the unreacted shrinking core model.The apparent activation energy was 26.07 kJ·mol^(-1).This research not only provides a viable method for recovering valuable metals in Ti-BFS,but also provides a strategy to comprehensive utilize the valuable elements in Ti-BFS.展开更多
0 INTRODUCTION Sulfur(S)and carbon(C)are essential volatile elements in both interior and surficial systems of the Earth.The cycling of S and C in subduction zones plays a fundamental role in modulating global S-C flu...0 INTRODUCTION Sulfur(S)and carbon(C)are essential volatile elements in both interior and surficial systems of the Earth.The cycling of S and C in subduction zones plays a fundamental role in modulating global S-C fluxes and exerts a significant influence on the climate evolution,mantle's redox budget,and ore deposit formation(Bekaert et al.,2021).展开更多
Potassium hydroxide(KOH)was introduced into the molybdenite roasting process to convert molybdenum(Mo)and sulfur(S)into water-soluble potassium molybdate(K_(2)MoO_(4))and potassium sulfate(K_(2)SO_(4)).Roasting with a...Potassium hydroxide(KOH)was introduced into the molybdenite roasting process to convert molybdenum(Mo)and sulfur(S)into water-soluble potassium molybdate(K_(2)MoO_(4))and potassium sulfate(K_(2)SO_(4)).Roasting with a 1.8-fold excess of KOH at 400℃ for 3 h enabled the leaching of over 99%of Mo from the molybdenum calcine using water.A precipitation method involving potassium–magnesium(K-Mg)salts was proposed for impurity removal.Under the conditions of pH 11,30℃,excess coefficient of 1.7 for Mg salts,and a duration of 1 h,98.37%of phosphorus(P)was removed from the K_(2)MoO_(4) solution.With post-purification,over 99%of Mo crystallized upon adjustment of pH to 1.Subsequently,S and K were recovered as K_(2)SO_(4) fertilizer from the crystalline mother liquor.An environmentally sustainable approach was proposed to conduct molybdenite production and ensure the efficient recovery of both Mo and S.展开更多
High performances of Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)solar cells are heavily influenced by the quality of heterojunctions.Herein,an oxygen(O)doping of CZTSSe/CdS heterojunction is performed to suppress the formation of th...High performances of Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)solar cells are heavily influenced by the quality of heterojunctions.Herein,an oxygen(O)doping of CZTSSe/CdS heterojunction is performed to suppress the formation of the defects by an ultraviolet ozone(UV-O_(3))treatment for the efficient flexible CZTSSe solar cells.The introduction of O reduces the non-radiative recombination and increases the carrier concentration of the CdS films.Furthermore,the defect density of the CdS film has been reduced from 8.24×10^(16)to2.91×10^(16)cm^(-3)by the O-doping.The results indicate that the electron transport is effectively promoted due to the decreased conduction band offset(CBO)at the heterojunction interface.As a result,the champion flexible CZTSSe solar cell achieves a power conversion efficiency(PCE)of 11.21%,with a significantly improved short circuit current density.The study for improving the CZTSSe/CdS heterojunction through O-doping treatment provides a new insight for enhancing the PCE of the flexible CZTSSe solar cells.展开更多
The use of lithium-sulfur(Li-S)batteries is limited by sulfur redox reactions involving multi-phase transformations,especially at low-temperatures.To address this issue,we report a material(FCNS@NCFs)consisting of nit...The use of lithium-sulfur(Li-S)batteries is limited by sulfur redox reactions involving multi-phase transformations,especially at low-temperatures.To address this issue,we report a material(FCNS@NCFs)consisting of nitrogen-doped carbon fibers loaded with a ternary metal sulf-ide((Fe,Co,Ni)_(9)S_(8))for use as the sulfur host in Li-S batteries.This materi-al was prepared using transfer blot filter paper as the carbon precursor,thiourea as the source of nitrogen and sulfur,and FeCl_(3)·6H_(2)O,CoCl_(2)·6H_(2)O and NiCl_(2)·6H_(2)O as the metal ion sources.It was synthesized by an impreg-nation method followed by calcination.The nitrogen doping significantly in-creased the conductivity of the host,and the metal sulfides have excellent catalytic activities.Theoretical calculations,and adsorption and deposition experiments show that active sites on the surface of FCNS@NCFs selectively adsorb polysulfides,facilitate rapid adsorption and conversion,prevent cathode passivation and inhib-it the polysulfide shuttling.The FCNS@NCFs used as the sulfur host has excellent electrochemical properties.Its initial dis-charge capacity is 1639.0 mAh g^(−1) at 0.2 C and room temperature,and it remains a capacity of 1255.1 mAh g^(−1) after 100 cycles.At−20~C,it has an initial discharge capacity of 1578.5 mAh g^(−1) at 0.2 C,with a capacity of 867.5 mAh g^(−1) after 100 cycles.Its excellent performance at both ambient and low temperatures suggests a new way to produce high-performance low-temper-ature Li-S batteries.展开更多
A transformative beryllium metallurgy theory and method was proposed based on the low-temperature dissociation of hydrofluoric acid and purification by exploiting the large difference of fluoride solubility.Hydrofluor...A transformative beryllium metallurgy theory and method was proposed based on the low-temperature dissociation of hydrofluoric acid and purification by exploiting the large difference of fluoride solubility.Hydrofluoric acid can quickly dissociate berylum ore powder directly at low or room temperature with more than 99%dissociation rate.The solubility of AlF_(3),FeF_(3) CrF_(3) and MgF_(2),is low.Coupled with common ion effect,99.9%-purity beryllium products can be prepared without chemical purification.For high-purity beryllium products of grade 4N or higher,they can be prepared through the superior property that the pH intervals of iron,chromium,and other hydroxide precipitates are distinctly different from those corresponding to Be(OH)_(2),precipitates.This new method can be used to prepare most of the beryllium products that are prepared by modern beryllium metallurgy.展开更多
文摘Herein,3‑aminopropyltriethoxysilane(APTES)was used to modify F‑containing silica slag(SS)by simple grafting and served as a multifunctional barrier layer.The amino group(—NH2)in the amino‑modified SS(NH2‑SS)forms ligand bonds or hydrogen bonds with sulfur ions in lithium polysulfides(LiPSs),thus inhibiting the shuttle effect.Electrochemical analyses demonstrated that lithium‑sulfur(Li‑S)batteries employing the NH2‑SS interlayer exhibited discharge specific capacities of 1048 and 789 mAh·g^(-1) at 0.2C and 2C,respectively,and even at 4C,the initial discharge specific capacity remained at 590 mAh·g^(-1),outperforming the Li‑S battery with unmodified SS as the interlayer.
文摘It is crucial to develop arsenic removal adsorbents with strong sulfur resistance under middle-low-temperature flue gas conditions(<400℃).In this work,five Fe-Ce-La oxides were prepared by co-precipitation method,and FeCeLaO/SiO_(2)-Al_(2)O_(3) composite adsorbents were prepared by coupling fly ash-based Si-Al carriers.The active components Fe-Ce-La oxides and Si-Al carriers were characterized by TPD,TG,XRF,BET and XPS,respectively.The effects of temperature,Si/Al ratio and FeCeLaO loading rate on the sulfur resistance were investigated.Results show that the SO_(2) promotes the arsenic removal of Fe_(2)O_(3),CeLaO and FeCeLaO.At 400℃,the arsenic removal efficiencies of the three oxides increase from 45.3%,72.5% and 81.3% without SO_(2) to 62.6%,80.5%and 91.0%,respectively.The SO_(2) inhibits the arsenic removal of La_(2)O_(2)CO_(3) and FeLaO,and the inhibition effect is pronounced at high temperatures.The sulfur poisoning resistance of Si-Al carriers increases with the increase of Si/Al ratio.When the Si/Al ratio is increased to 9.74,the arsenic removal efficiency in the SO_(2) environment is 13.9% higher than that in the absence of SO_(2).Introducing FeCeLaO active components is beneficial for enhancing the SO_(2) poisoning resistance of Si-Al carriers.The strong sulfur resistance of the FeCeLaO/SiO_(2)-Al_(2)O_(3) composite adsorbent results from multiple factors:protective effects of Ce on Fe,La and Al;sulfation-induced generation of Ce^(3+)and surface-adsorbed oxygen;and strong surface acidity of SiO_(2).
基金supported by the National Natural Science Foundation of China(Nos.42225301 and 42330304)。
文摘Sulfur is closely associated with various types of ore deposits,particularly orogenic gold(Au)systems,where sulfur-bearing melts and fluids play a critical role in transporting oreforming elements essential for ore formation.The widely accepted metamorphic devolatilization model suggests that compositionally fertile sedimentary rocks serve as potential gold sources.Therefore,understanding sulfur behavior during prograde metamorphism is essential for elucidating the mechanisms underlying metal activation and mobility.In this study,we conducted in-situ sulfur isotope(δ^(34)S)analyses using secondary ion mass spectrometry(SIMS)on samples from the Hongshankou area,a representative Barrovian-type metamorphic sequence characterized by intermediate pressure-temperature(P-T)conditions.This sequence comprises the biotite,garnet,staurolite,and kyanite zones.Our results show a systematic increase in δ^(34)S values(from 3.1‰ to 5.5‰)coupled with a progressive decrease in total sulfur content(from 320 ppm to 165 ppm)as metamorphic grade increases.The most pronounced sulfur mobilization occurs between the garnet and staurolite zones.In all analyzed samples,Au or Au-bearing minerals predominantly occur along the edges or within pyrite grains,highlighting the critical role of pyrite breakdown in controlling gold mobility.Thus,sulfur isotope fractionation provides robust constraints for quantitatively assessing sulfur mobility during metamorphism.These findings reinforce the concept that metasedimentary rocks and their metamorphic fluids represent fertile sources of Au and other metals enriched in orogenic gold deposits.
基金financially supported by the Nation Key R&D Program China(2018YFA0703200)the Key Research and Development Program of Hubei Province(2022BAA026)+1 种基金the National Natural Science Foundation of China(51772110)the Open Research Fund(2024JYBKF01)of Key Laboratory of Material Chemistry for Energy Conversion and Storage(HUST),Ministry of Education。
文摘Sluggish kinetics coupled with parasitic shuttling reactions are pivotal challenges hindering the performance of lithium-sulfur(Li-S)batteries.Improving areal capacity and cyclability of Li-S batteries can be achieved by addressing these challenges.A composite sulfur host material is synthesized herein by in situ anchoring ultrafine cobalt-iron phosphide nanoparticles(5-7 nm)onto a hollow mesoporous carbon sphere(HMCS)framework.This strategy achieved exceptional spatial restriction and a high density of catalytically active sites through the encapsulation of sulfur within a hollow-structured framework.Specifically,HMCS expedites rapid Li_(2)S nucleation kinetics,while CoFeP facilitates robust Li_(2)S dissolution kinetics by mitigating decomposition barriers.This synergistic integration equips CoFeP@HMCS with robust bi-directional catalytic activity,significantly promoting interracial charge-transfer,facilitate sulfu r multistep catalytic conversion,and inhibiting shuttling.Consequently,the battery exhibits excellent rate performance(991 mA h g^(-1) at 5.0 C)and retains a high areal capacity of 6.06 mA h cm^(-2) after 200 cycles under a high areal sulfur loading of 8.2 mg cm^(-2) but a low electrolyte/sulfur ratio of 4.8μL mg^(-1).This work contributes to enhancing the practical specific capacity of lithium-sulfur batteries and deepens the understanding of catalysts enabling bidirectional electrocatalytic sulfur conversion.
基金supported by National Natural Science Foundation of China(Nos.32271791,32171709 and 22475053)Hunan Provincial Natural Science Foundation of China(No.2024JJ7643)Natural Science Foundation of Shanghai(No.22ZR1404100).
文摘Hard carbon(HC)in sodium-ion batteries is searched by numerous investigations,which can offer the excellent performance of reversible Na^(+)insertion and extraction.The covalent heteroatom doping in HC is recently worth concentrating,which can dilate the interlayer spacing of graphite to adjust the electrochemical storage performance in carbon anodes.However,the reported doping strategies of the modified HC have only resulted in limited improvement,especially unobvious effects on tuning porous structure.In this study,tannin extract and K_(2)SO_(4) are respectively utilized as carbon source and sulfur source for the fabrication of HC,in which K_(2)SO_(4) can contribute to the heteroatom doping,and the pore forming as well.The tannin-derived sulfur-doped carbon anode shows the excellent cycle stability,achieving a high reversible capacity of 520.5 mAh/g at a current density of 100 mA/g.Even after 500 cycles at a current density of 3 A/g,a high specific capacity of 236.7 mAh/g and a capacity retention rate of 92.6%can be reserved.Compared with the initial carbon,the adsorption energy of Na^(+)is multifold times higher,whereas Na^(+)diffusion energy barriers manyfold decrease.Moreover,the full battery assembled with Na_(3)V_(2)(PO_(4))_(3)/tannin-based HC demonstrates a stable cycling performance.This work can manifest the potentiality of the tannin-based electrode as anode for a high-performance sodium-ion batteries(SIBs),which could especially offer an explanation of Na^(+)storage and solid-electrolyte interface(SEI)stability to the electrochemical performance.
基金supported by the National Natural Science Foundation of China(No.22261026).
文摘A novel method for the synthesis of 2,4-disubstituted thiophenes via the reactions of N,N-disubstituted enaminones and elemental sulfur is developed.By simply heating the substrates in pure water in the presence of NaOH,the thiophene annulation practically takes place via the generation of one C-C and two C-S bonds via cascade dual C-H functionalization and C-N bond thiolation without using any transition metal reagent.
基金supported by the National Key Research and Development Program of China (No.2024YFA1509600)National Natural Science Foundation of China (Nos.22474010 and 22274012)the Fundamental Research Funds for the Central Universities (No.2233300007)。
文摘Ferroptosis has exhibited great potential in therapies and intracellular reducing agents of sulfur species(RSSs) in the thiol-dependent redox systems are crucial in ferroptosis.This makes the simultaneous detection of multiple RSSs significant for evaluating ferroptosis therapy.However,the traditional techniques,including fluorescent(FL) imaging and electrospray ionization-based mass spectrometry(MS) detection,cannot achieve the discrimination of different RSSs.Herein,simultaneous MS detection of multiple RSSs,including cysteine(Cys),homocysteine(Hcy),glutathione(GSH) and hydrogen sulfide(H_(2)S),was obtained upon enhancing ionization efficiency by a fluorescent probe(NBD-O-1).Based on the interaction between NBD-O-1 and RSSs,the complex of RSSs with a fragment of NBD-O-1 can be generated,which can be easily ionized for MS detection in the negative mode.Therefore,the intracellular RSSs can be well detected upon the incubation of He La cells with the probe of NBD-O-1,exhibiting the total RSS levels by the FL imaging and further providing expression of each RSS by enhanced MS detection.Furthermore,the RSSs during ferroptosis in He La cells have been evaluated using the present strategy,demonstrating the potential for ferroptosis examinations.This work has made an unconventional application of a fluorescent probe to enhance the detection of multiple RSSs by MS,providing significant molecular information for addressing the ferroptosis mechanism.
基金National Natural Science Foundation of China (Nos.22071185 and 22271224)the Fundamental Research Funds for the Central Universities (No.2042019kf0008)Wuhan University startup funding for financial support。
文摘The development of catalytic multicomponent reactions for constructing complex organic scaffolds from readily accessible commodity chemicals is a key pursuit in contemporary synthetic chemistry.Current methods for synthesizing thioesters primarily rely on the acylation of thiols,which produces substantial waste and requires malodorous,unstable sulfur sources.In this work,we introduce a photocatalyzed hydrogen transfer strategy that enables a three-component synthesis of thioesters using abundant primary alcohols,easily available alkenes and elemental sulfur under mild conditions.This protocol demonstrates broad applicability and high chemo-and regioselectivity for both primary alcohols and alkenes,highlighting the advantage and potential of photo-mediated hydrogen transfer in facilitating multicomponent reactions using primary alcohol and elemental sulfur feedstocks.
基金support of the National Natural Science Foundation of China(22075131 and 22078265)the Shaanxi Fundamental Science Research Project for Mathematics and Physics under Grants(No.22JSZ005)the State-Key Laboratory of Multiphase Complex Systems(No.MPCS-2021-A).
文摘Lithium-sulfur(Li-S)batteries require efficient catalysts to accelerate polysulfide conversion and mitigate the shuttle effect.However,the rational design of catalysts remains challenging due to the lack of a systematic strategy that rationally optimizes electronic structures and mesoscale transport properties.In this work,we propose an autogenously transformed CoWO_(4)/WO_(2) heterojunction catalyst,integrating a strong polysulfide-adsorbing intercalation catalyst with a metallic-phase promoter for enhanced activity.CoWO_(4) effectively captures polysulfides,while the CoWO_(4)/WO_(2) interface facilitates their S-S bond activation on heterogenous catalytic sites.Benefiting from its directional intercalation channels,CoWO_(4) not only serves as a dynamic Li-ion reservoir but also provides continuous and direct pathways for rapid Li-ion transport.Such synergistic interactions across the heterojunction interfaces enhance the catalytic activity of the composite.As a result,the CoWO_(4)/WO_(2) heterostructure demonstrates significantly enhanced catalytic performance,delivering a high capacity of 1262 mAh g^(−1) at 0.1 C.Furthermore,its rate capability and high sulfur loading performance are markedly improved,surpassing the limitations of its single-component counterparts.This study provides new insights into the catalytic mechanisms governing Li-S chemistry and offers a promising strategy for the rational design of high-performance Li-S battery catalysts.
基金the financial support from the National Natural Science Foundation of China (22109127)the Chinese Postdoctoral Science Foundation (2021M702666)+2 种基金the Research Fund of the State Key Laboratory of Solidification Processing (NPU),China (Grant No.2023-TS-02)The financial support from the Youth Project of"Shaanxi High-level Talents Introduction Plan"the Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) are also sincerely appreciated
文摘Photo-assisted lithium–sulfur batteries(PALSBs)offer an eco-friendly solution to address the issue of sluggish reaction kinetics of conventional LSBs.However,designing an efficient photoelectrode for practical implementation remains a significant challenge.Herein,we construct a free-standing polymer–inorganic hybrid photoelectrode with a direct Z-scheme heterostructure to develop high-efficiency PALSBs.Specifically,polypyrrole(PPy)is in situ vapor-phase polymerized on the surface of N-doped TiO_(2) nanorods supported on carbon cloth(N-TiO_(2)/CC),thereby forming a well-defined p–n heterojunction.This architecture efficiently facilitates the carrier separation of photo-generated electron–hole pairs and significantly enhances carrier transport by creating a built-in electric field.Thus,the PPy@N-TiO_(2)/CC can simultaneously act as a photocatalyst and an electrocatalyst to accelerate the reduction and evolution of sulfur,enabling ultrafast sulfur redox dynamics,as convincingly validated by both theoretical simulations and experimental results.Consequently,the PPy@N-TiO_(2)/CC PALSB achieves a high discharge capacity of 1653 mAh g^(−1),reaching 98.7%of the theoretical value.Furthermore,5 h of photo-charging without external voltage enables the PALSB to deliver a discharge capacity of 333 mAh g^(−1),achieving dual-mode energy harvesting capabilities.This work successfully integrates solar energy conversion and storage within a rechargeable battery system,providing a promising strategy for sustainable energy storage technologies.
基金supported by the National Natural Science Foundation of China(No.22278439 and 21776313).
文摘Renewable electricity-driven production of value-added sulfur and H_(2)via electrocatalytic H_(2)S decomposition represents a sustainable route to conventional thermocatalysis.Both the electrocatalyst and electrolyte solution strongly impact the H_(2)S decomposition performance.Despite significant progress in developing sophisticated electrocatalysts,a well-designed electrolyte solution in conjunction with industrial catalysts is an attractive strategy to advance the industrialization process of electrocatalytic H_(2)S decomposition,but remains unexplored.Here,for the first time,we design a solid-liquid-gas three-phase indirect electrolysis system based on a kind of CS_(2)-N electrolyte solution and Ni-Mo_(2)C that can efficiently enable H_(2)S decomposition into valuable H_(2)and sulfur.Specifically,the solid-phase Ni-Mo_(2)C as a heterogeneous redox mediator presents excellent electrocatalytic efficiency for the H_(2)S removal efficiency of up to 99%,and the formation of liquid-phase sulfur product(CS_(2)-N electrolyte solution dissolves sulfur,yield up to 95%)with the generation of gas-phase H_(2)product(~1.32 mL min^(-1)),resulting in an interesting three-phase indirect electrolysis system.Remarkably,it enables the scale-up production(~6 g in a batch experiment)of sulfur with continuous operation for 120 h without attenuation.This work may inaugurate a new electrocatalytic H_(2)S decomposition avenue to explore porous metal materials and electrolyte systems in simultaneous production of value-added sulfur and H_(2).
基金financially supported by the National Natural Science Foundation of China (No. 22579095)the Beijing-Tianjin-Hebei Basic Research Cooperation Special Project (B2024204027)+2 种基金the Youth Top-notch Talent Foundation of Hebei Provincial Universities (BJK2022023)the Natural Science Foundation of Hebei Province (B2023204006)the talent training project of Hebei province (No. B20231004)。
文摘The rate capability and cycling stability of sodium metal batteries taking FeS_(2) or sulfur as cathode are limited due to their low reaction kinetics and severe shuttle effect.Herein,we rationally design a novel single-atom-dispersed S_(2)-FeNC/FeS_(2) nanocluster heterojunction embedded in carbon spheres(SFNC/FeS_(2)) for the electrode material of sodium metal batteries.Interestingly,during the discharging process,the Na^(+) is inserted into FeS_(2) to generate Na_(2)S,as well as the unique electrochemical reaction between S_(2)-FeNC and Na^(+) to form Na_(2)S.Meanwhile,the FeNC can adsorb Na_(2)S and catalyze the conversion from Na_(2)S and Fe to FeS_(2) or from Na_(2)S and FeNC to S_(2)-FeNC for suppressing the shuttle effect and promoting the distinct hybrid reversible electrochemical behavior,which improves performance tremendously.Notably,the SFNC/FeS_(2) electrode delivers a specific capacity of 338.7 mAh g^(-1) after superlong 2000 cycles at a current density of 5.0 A g^(-1) and achieves a high energy density of 430.1 Wh Kg^(-1) at a current density of 0.05 A g^(-1).This work presents a novel approach to studying sodium metal batteries with hybrid behavior for excellent high energy density and cycling stability.
基金supported by the National Natural Science Foundation of China(No.42377083)the Natural Science Foundation of Sichuan Province,China(No.2025 ZNSFSC0433).
文摘In this work,ofloxacin(OFL),a kind of frequently detected antibiotic in groundwater,was selected to explore its impact(at ng/L-μg/L-level)on denitrification performance in an autotrophic denitrification system driven by pyrite/sulfur(FeS2/S0).Results showed that OFL restrained nitrate removal efficiency,and the inhibition degree was positively related to the concentration of OFL.After being exposed to increased OFL(200 ng/L-100μg/L)for 69 days,higher inhibition of electron transport activity(ETSA),enzyme activities of nitrate reductase(NAR),and nitrite reductase(NIR)were acquired.Meanwhile,the extracellular protein(PN)content of sludge samples was remarkably stimulated by OFL to resist the augmented toxicity.OFL contributed to increased microbial diversity and sulfur/sulfide oxidation functional genes in ng/L-level bioreactors,whereas led to a decline inμg/L level experiments.With OFL at concentrations of 200 ng/L and 100μg/L,the whole expression of 10 key denitrification functional genes was depressed,and the higher the OFL concentration,the lower the expression level.However,no significant proliferation of antibiotic resistance genes(ARGs)either in 200 ng/L-OFL or 100μg/L-OFL groups was observed.Two-factor correlation analysis results indicated that Thiobacillus,Anaerolineae,Anaerolineales,and Nitrospirae might be the main hosts of existing ARGs in this system.
基金Institute of Technology Research Fund Program for Young Scholars21C Innovation Laboratory Contemporary Amperex Technology Co.,Limited,Ninde, 352100, China (21C–OP-202314)。
文摘Lithium-sulfur (Li-S) batteries have gained great attention due to the high theoretical energy density and low cost,yet their further commercialization has been obstructed by the notorious shuttle effect and sluggish redox dynamics.Herein,we supply a strategy to optimize the electron structure of Ni_(2)P by concurrently introducing B-doped atoms and P vacancies in Ni_(2)P (Vp-B-Ni_(2)P),thereby enhancing the bidirectional sulfur conversion.The study indicates that the simultaneous introduction of B-doped atoms and P vacancies in Ni_(2)P causes the redistribution of electron around Ni atoms,bringing about the upward shift of d-band center of Ni atoms and effective d-p orbital hybridization between Ni atoms and sulfur species,thus strengthening the chemical anchoring for lithium polysulfides (LiPSs) as well as expediting the bidirectional conversion kinetics of sulfur species.Meanwhile,theoretical calculations reveal that the incorporation of B-doped atoms and P vacancies in Ni_(2)P selectively promotes Li2S dissolution and nucleation processes.Thus,the Li-S batteries with Vp-B-Ni_(2)P-separators present outstanding rate ability of 777 m A h g^(-1)at 5 C and high areal capacity of 8.03 mA h cm^(-2)under E/S of 5μL mg^(-1)and sulfur loading of 7.20 mg cm^(-2).This work elucidates that introducing heteroatom and vacancy in metal phosphide collaboratively regulates the electron structure to accelerate bidirectional sulfur conversion.
基金the Pangang Group Company Limited for its financial supportthe support from the Fundamental Research Funds for the Central Universities(SCU2024D009)。
文摘Titanium-bearing blast furnace slag(Ti-BFS)is an industrial solid waste rich in titanium,magnesium and aluminum.However,it is difficult to utilize Ti,Mg and Al from Ti-BFS for the strong stability and poor reaction activity of Ti-BFS.A comprehensive utilization route of Ti,Mg and Al from Ti-BFS was proposed.Ti-BFS was firstly roasted with H_(2)SO_(4)to realizes the conversion of Ti,Mg and Al to their corresponding sulphates.The sulphates were leached by dilute H_(2)SO_(4)solution to extraction Ti,Mg and Al from roasted Ti-BFS.The roasting conditions were optimized as follows,sulfuric acid concentration of 85%(mass),temperature of 200℃,acid-slag ratio of 5.5,particle size of Ti-BFS<75μm,and reaction time of 1 h.The extraction rates of titanium,aluminum,and magnesium reached 82.42%,88.78%and 90.53%,respectively.The leachate was hydrolyzed at 102℃for 5 h with a titanium hydrolysis ratio of 96%.After filtration and calcination,TiO_(2)with a purity of 97%(mass)was obtained.Al in the leachate was converted to NH_(4)Al(SO_(4))_(2)·12H_(2)O by the neutralization of ammonia water at pH=4.5.Al_(2)O_(3) was obtained by the calcination of NH_(4)Al(SO_(4))_(2)·12H_(2)O.The residual solution can be used to prepare products of magnesium sulfate.In the proposed process,Ti,Mg and Al were extracted from Ti-BFS and utilized comprehensively to prepare valuable products.The leaching behavior of roasted Ti-BFS with water was also studied.It followed the unreacted shrinking core model.The apparent activation energy was 26.07 kJ·mol^(-1).This research not only provides a viable method for recovering valuable metals in Ti-BFS,but also provides a strategy to comprehensive utilize the valuable elements in Ti-BFS.
基金financially supported by the National Natural Science Foundation of China(Nos.92355301,42302061)the China Postdoctoral Science Foundation(No.2023M743471)+1 种基金the Key Research Program of the Institute of Geology and Geophysics,Chinese Academy of Sciences(No.IGGCAS-202204)the Youth Innovation Promotion Association of Chinese Academy of Sciences(No.Y2021026)。
文摘0 INTRODUCTION Sulfur(S)and carbon(C)are essential volatile elements in both interior and surficial systems of the Earth.The cycling of S and C in subduction zones plays a fundamental role in modulating global S-C fluxes and exerts a significant influence on the climate evolution,mantle's redox budget,and ore deposit formation(Bekaert et al.,2021).
基金financially supported by the National Natural Science Foundation of China(No.52174340)the National Key Research and Development Project of China(No.2022YFC2904505)the Hunan FURONG Scholars Project and the Basic Science Centre of the National Natural Science Foundation of China(No.72088101)。
文摘Potassium hydroxide(KOH)was introduced into the molybdenite roasting process to convert molybdenum(Mo)and sulfur(S)into water-soluble potassium molybdate(K_(2)MoO_(4))and potassium sulfate(K_(2)SO_(4)).Roasting with a 1.8-fold excess of KOH at 400℃ for 3 h enabled the leaching of over 99%of Mo from the molybdenum calcine using water.A precipitation method involving potassium–magnesium(K-Mg)salts was proposed for impurity removal.Under the conditions of pH 11,30℃,excess coefficient of 1.7 for Mg salts,and a duration of 1 h,98.37%of phosphorus(P)was removed from the K_(2)MoO_(4) solution.With post-purification,over 99%of Mo crystallized upon adjustment of pH to 1.Subsequently,S and K were recovered as K_(2)SO_(4) fertilizer from the crystalline mother liquor.An environmentally sustainable approach was proposed to conduct molybdenite production and ensure the efficient recovery of both Mo and S.
基金supported by the National Natural Science Foundation of China(62474043,62074037,52372183)the Fujian Science&Technology Innovation Laboratory for Optoelectronic Information of China(2021ZZ124)+1 种基金Fujian Provincial Natural Science Foundation of China(2024J09015)the Foundation of Fujian Provincial Department of Industry and Information Technology of China(82318075)。
文摘High performances of Cu_(2)ZnSn(S,Se)_(4)(CZTSSe)solar cells are heavily influenced by the quality of heterojunctions.Herein,an oxygen(O)doping of CZTSSe/CdS heterojunction is performed to suppress the formation of the defects by an ultraviolet ozone(UV-O_(3))treatment for the efficient flexible CZTSSe solar cells.The introduction of O reduces the non-radiative recombination and increases the carrier concentration of the CdS films.Furthermore,the defect density of the CdS film has been reduced from 8.24×10^(16)to2.91×10^(16)cm^(-3)by the O-doping.The results indicate that the electron transport is effectively promoted due to the decreased conduction band offset(CBO)at the heterojunction interface.As a result,the champion flexible CZTSSe solar cell achieves a power conversion efficiency(PCE)of 11.21%,with a significantly improved short circuit current density.The study for improving the CZTSSe/CdS heterojunction through O-doping treatment provides a new insight for enhancing the PCE of the flexible CZTSSe solar cells.
基金partially supported by National Natural Science Foundation of China(52172250)Institute of Process Engineering(IPE)Project for Frontier Basic Research(QYJC-2023-06)。
文摘The use of lithium-sulfur(Li-S)batteries is limited by sulfur redox reactions involving multi-phase transformations,especially at low-temperatures.To address this issue,we report a material(FCNS@NCFs)consisting of nitrogen-doped carbon fibers loaded with a ternary metal sulf-ide((Fe,Co,Ni)_(9)S_(8))for use as the sulfur host in Li-S batteries.This materi-al was prepared using transfer blot filter paper as the carbon precursor,thiourea as the source of nitrogen and sulfur,and FeCl_(3)·6H_(2)O,CoCl_(2)·6H_(2)O and NiCl_(2)·6H_(2)O as the metal ion sources.It was synthesized by an impreg-nation method followed by calcination.The nitrogen doping significantly in-creased the conductivity of the host,and the metal sulfides have excellent catalytic activities.Theoretical calculations,and adsorption and deposition experiments show that active sites on the surface of FCNS@NCFs selectively adsorb polysulfides,facilitate rapid adsorption and conversion,prevent cathode passivation and inhib-it the polysulfide shuttling.The FCNS@NCFs used as the sulfur host has excellent electrochemical properties.Its initial dis-charge capacity is 1639.0 mAh g^(−1) at 0.2 C and room temperature,and it remains a capacity of 1255.1 mAh g^(−1) after 100 cycles.At−20~C,it has an initial discharge capacity of 1578.5 mAh g^(−1) at 0.2 C,with a capacity of 867.5 mAh g^(−1) after 100 cycles.Its excellent performance at both ambient and low temperatures suggests a new way to produce high-performance low-temper-ature Li-S batteries.
基金National Key Research and Development Program of China(2021YFC2902301,2021YFC2902302)。
文摘A transformative beryllium metallurgy theory and method was proposed based on the low-temperature dissociation of hydrofluoric acid and purification by exploiting the large difference of fluoride solubility.Hydrofluoric acid can quickly dissociate berylum ore powder directly at low or room temperature with more than 99%dissociation rate.The solubility of AlF_(3),FeF_(3) CrF_(3) and MgF_(2),is low.Coupled with common ion effect,99.9%-purity beryllium products can be prepared without chemical purification.For high-purity beryllium products of grade 4N or higher,they can be prepared through the superior property that the pH intervals of iron,chromium,and other hydroxide precipitates are distinctly different from those corresponding to Be(OH)_(2),precipitates.This new method can be used to prepare most of the beryllium products that are prepared by modern beryllium metallurgy.
