Defects‑Rich Heterostructures Trigger Strong Polarization Coupling in Sulfides/Carbon Composites with Robust Electromagnetic Wave Absorption

Defects-rich heterointerfaces integrated with adjustable crystalline phases and atom vacancies,as well as veiled dielectric-responsive character,are instrumental in electromagnetic dissipation.Conventional methods,however,constrain their delicate constructions.Herein,an innovative alternative is proposed:carrageenan-assistant cations-regulated(CACR)strategy,which induces a series of sulfides nanoparticles rooted in situ on the surface of carbon matrix.This unique configuration originates from strategic vacancy formation energy of sulfides and strong sulfides-carbon support interaction,benefiting the delicate construction of defects-rich heterostructures in M_(x)S_(y)/carbon composites(M-CAs).Impressively,these generated sulfur vacancies are firstly found to strengthen electron accumulation/consumption ability at heterointerfaces and,simultaneously,induct local asymmetry of electronic structure to evoke large dipole moment,ultimately leading to polarization coupling,i.e.,defect-type interfacial polarization.Such“Janus effect”(Janus effect means versatility,as in the Greek two-headed Janus)of interfacial sulfur vacancies is intuitively confirmed by both theoretical and experimental investigations for the first time.Consequently,the sulfur vacancies-rich heterostructured Co/Ni-CAs displays broad absorption bandwidth of 6.76 GHz at only 1.8 mm,compared to sulfur vacancies-free CAs without any dielectric response.Harnessing defects-rich heterostructures,this one-pot CACR strategy may steer the design and development of advanced nanomaterials,boosting functionality across diverse application domains beyond electromagnetic response.

Comparative study on the hydrogen storage performance of as-milled MgRENi rapid quenched alloy catalyzed by metal sulfides

The composites of Mg_(20)Pr_(1)Sm_(3)Y_(1)Ni_(10)as-quenched alloy and 3 wt.%M(M=CoS,CoS_(2),MoS_(2))catalyst were prepared by high-speed vibration ball mill.The effects of metal sulfides on the hydrogenation and dehydrogenation dynamics of alloys were compared.The results show that the as-milled composites contain a large number of amorphous embedded by a small amount of nanocrystals,and there are many point defects.After ball milling,the crystal grain size in the composites containing CoS is relatively larger,followed by CoS_(2)and MoS_(2)again.After hydrogenation,the amorphous phase is crystallized to form Mg_(2)NiH_(4),YH_(3),Pr_(8)H_(18.96),Sm_(3)H_7,Mg,Co or Mo phases,however,Mg_(2)Ni,YH_(2),PrH_(2)and Ni_(3)Y phases appeared after dehydrogenation.The maximum hydrogenation capacity of the composites containing CoS,CoS_(2)and MoS_(2)are 3.939,4.265 and 4.507 wt.%,respectively.The hydrogenation saturation ratio of composite containing MoS_(2)is higher than that of the composites containing CoS and CoS_(2).The dehydrogenation activation energy of the composites containing CoS,CoS_(2)and MoS_(2)is 107.76,68.43 and 63.28 kJ.mol^(-1).H_(2).On the improvement of hydrogen storage performance of Mg_(20)Pr_(1)Sm_(3)Y_(1)Ni_(10)alloy,the catalytic effect of MoS_(2)sulfide is better than that of CoS_(2)sulfide,and which is better than CoS sulfide.

Hydrogen sulfide reduces oxidative stress in Huntington's disease via Nrf2

The pathophysiology of Huntington's disease involves high levels of the neurotoxin quinolinic acid. Quinolinic acid accumulation results in oxidative stress, which leads to neurotoxicity. However, the molecular and cellular mechanisms by which quinolinic acid contributes to Huntington's disease pathology remain unknown. In this study, we established in vitro and in vivo models of Huntington's disease by administering quinolinic acid to the PC12 neuronal cell line and the striatum of mice, respectively. We observed a decrease in the levels of hydrogen sulfide in both PC12 cells and mouse serum, which was accompanied by down-regulation of cystathionine β-synthase, an enzyme responsible for hydrogen sulfide production. However, treatment with NaHS(a hydrogen sulfide donor) increased hydrogen sulfide levels in the neurons and in mouse serum, as well as cystathionine β-synthase expression in the neurons and the mouse striatum, while also improving oxidative imbalance and mitochondrial dysfunction in PC12 cells and the mouse striatum. These beneficial effects correlated with upregulation of nuclear factor erythroid 2-related factor 2 expression. Finally, treatment with the nuclear factor erythroid 2-related factor 2inhibitor ML385 reversed the beneficial impact of exogenous hydrogen sulfide on quinolinic acid-induced oxidative stress. Taken together, our findings show that hydrogen sulfide reduces oxidative stress in Huntington's disease by activating nuclear factor erythroid 2-related factor 2,suggesting that hydrogen sulfide is a novel neuroprotective drug candidate for treating patients with Huntington's disease.

Research progress in enhanced bioleaching of copper sulfides under the intervention of microbial communities

Compared with the traditional pyrometallurgical process, copper bioleaching has distinctive advantages of high efficiency and lower cost, enabling efficiently extracts of valuable metal resources from copper sulfides. Moreover, during long-term industrial applications of bioleaching, many regulatory enhancements and technological methods are used to accelerate the interfacial reactions. With advances in microbial genetic and sequencing technologies, bacterial communities and their mechanisms in bioleaching systems have been revealed gradually. The bacterial proliferation and dissolution of sulfide ores by a bacterial community depends on the pH, temperature, oxygen, reaction product regulation, additives, and passivation substances, among other factors. The internal relationship among the influencing factors and the succession of microorganism diversity are discussed and reviewed in this paper. This paper is intended to provide a good reference for studies related to enhanced bioleaching.

REE Geochemistry of Sulfides from the Huize Zn-Pb Ore Field, Yunnan Province: Implication for the Sources of Ore-forming Metals

REE abundances in sulfides from the Huize Zn-Pb ore field were determined with the ICPMS after preconcentration. The REE abundances in 26 sulfide samples （including pyrite, galena and sphalerite） are very low, with the ~REE ranging from 1.6×10^-9 to 166.8×10^-9. Their LREE/HREE ratios range from 7.6 to 98, showing LREE enrichment relatively. The JEu values are below 1, indicating that they were deposited from an Eu-depleted and reducing fluid-system. Similar to the ore-hosting carbonate strata, calcite separates from carbonate veinlets filling in the fractures or faults crosscutting the carbonate strata also show clear Eu-depletion. This indicates that the carbonate veinlets and their parent fluid was possibly sourced from the strata and inherited the REE geochemical features of the strata. Therefore, REE-geochemical characteristics of both the sulfides and calcites, which were deposited from an ore-forming hydrothermal system, are similar to those of carbonate strata, and strongly suggest that the ore metals were mainly sourced from carbonate strata.

Petrophysical characteristics of rocks and sulfides from the SWIR hydrothermal field

Study of petrophysical properties of rocks in seafioor hydrothermal fields has great significance for inves- tigation of seafloor hydrothermal activities, especially for polymetallic sulfides prospecting. In the present study, based on the current experimental conditions, we conducted systematic experiments to measure the magnetic susceptibility, electrical resistivity, porosity, density, as well as acoustic wave velocity of seafloor rocks and sulfides. Subsequently, we measured the physical characteristics of hydrothermal sulfides, basalts and peridotites which were collected from newly discovered seafloor hydrothermal fields at 49.6°E, 50.5°E, 5 1°E, 63.5°E, and 63.9°E of the Southwest Indian Ridge （SWIR）. Previously available and newly collected data were combined to characterize the physical differences between polymetallic sulfides and rocks. We also discussed the impact of hydrothermal alteration on the bedrock and demonstrated how these petrophysical properties of rocks can help in geophysical prospecting of seafloor hydrothermal fields as indicators.

Synthesis of rare earth sulfides and their UV-vis absorption spectra

Rare earth sulfides were systematically synthesized via the sulfurization of their commercial oxide powders using CS2 gas to shorten sulfurization time, and their UV-vis absorption spectra were investigated. The appropriate sulfurization conditions were studied. For the rare earth sulfides with the same crystal structure, the sulfurization temperature showed increasing tendency with the decrease of rare earth element atomic radii. The UV-vis absorption spectra of rare earth sulfides did not depend on the crystal structure of rare earth sulfides, but on the 4f electronic structure of rare earth element. The data showed that the optical band gaps of rare earth sulfides were irregular, and the values ranged from 1.65 to 3.75 eV.

The application of nanostructured transition metal sulfides as anodes for lithium ion batteries

With wide application of electric vehicles and large-scale in energy storage systems, the requirement ofsecondary batteries with higher power density and better safety gets urgent. Owing to the merits of hightheoretical capacity, relatively low cost and suitable discharge voltage, much attention has been paid tothe transition metal sulfides. Recently, a large amount of research papers have reported about the appli-cation of transition metal sulfides in lithium ion batteries. However, the practical application of transitionmetal sulfides is still impeded by their fast capacity fading and poor rate performance. More well-focusedresearches should be operated towards the commercialization of transition metal sulfides in lithium ionbatteries. In this review, recent development of using transition metal sulfides such as copper sulfides,molybdenum sulfides, cobalt sulfides, and iron sulfides as electrode materials for lithium ion batteriesis presented. In addition, the electrochemical reaction mechanisms and synthetic strategy of transitionmetal sulfides are briefly summarized. The critical issues, challenges, and perspectives providing a fur-ther understanding of the associated electrochemical processes are also discussed.

Influence of Metal Sulfides as Anode Catalysts on Performance of H_2S SOFC

Two anode catalysts with Pt, MoS2 and composite metal sulfides (MoS2+NiS), are investigated for electrochemical oxidation of hydrogen sulfide in solid oxide fuel cell (SOFC) at temperatures 750-850℃. The catalysts comprising MoS2 and MoSa+NiS exhibited good electrical conductivity and catalytic activity. MoS2 and composite catalysts were found to be more active than Pt, a widely used catalyst for high temperature H2S/O2 fuel cell at 750-850℃. However, MoS2 itself sublimes above 450℃. In contrast, composite catalysts containing both Mo and transition metal (Ni) are shown to be stable and effective in promoting the oxidation of H2S in SOFC up to 850℃. However, electric contact is poor between the platinum current collecting layer and the composite metal sulfide layer, so that the cell performance becomes worse. This problem is overcome by adding conductive Ag powder into the anode layer (forming MoS2+NiS+Ag anode material) to increase anode electrical conductance instead of applying a thin layer of platinum on the top of anode.

Helium, neon and argon isotope compositions of fluid inclu-sions in massive sulfides from the Jade hydrothermal field, the Okinawa Trough

Helium, neon and argon isotope compositions of fluid inclusions have been measured in massive sulfide samples from theJade hydrothermal field in the central Okinawa Trough. Fluid-inclusion 3He/4He ratios are between 6.2 and 10.1 times theair value (Ra), and with a mean of 7.8Ra, which are consistent with the mid-ocean ridge basalt values [3He/4He≈(6Ra^11Ra)]. Values for 20Ne/22Ne are from 10.7 to 11.3, which are significantly higher than the atmospheric ratio (9.8).And the fluid-inclusion 40Ar/36Ar ratios range from 287 to 334, which are close to the atmosperic values (295.5). Theseresults indicate that the noble gases of trapped hydrothermal fluids in massive sulfides are a mixture of mantle- andseawater-derived components, and the helium of fluid inclusions is mainly from mantle, the nelium and argon isotopecompositions are mainly from seawater.

Geochemical Features of Sulfides from the Deyin-1 Hydrothermal Field at the Southern Mid-Atlantic Ridge near 15?S

In this study, geochemical compositions of elements in sulfide samples collected from the Deyin-1 hydrothermal field near the 15?S southern Mid-Atlantic Ridge(SMAR) were analyzed by the X-ray fluorescence spectrometry(XRF) and inductively coupled plasma mass spectrometry(ICP-MS) to examine the enrichment regulations of ore-forming elements and hydrothermal mineralization. These sulfide precipitates can be classified macroscopically into three types: Fe-rich sulfide, Fe-Cu-rich sulfide and Fe-Zn-rich sulfide, and are characterized by the enrichment of base metal elements along with a sequence of Fe>Zn>Cu. Compared with sulfides from other hydrothermal fields on MAR, Zn concentrations of sulfides in the research area are significantly high, while Cu concentrations are relatively low. For all major, trace or rare-earth elements(REE), their concentrations and related characteristic parameters exhibit significant variations(up to one or two orders of magnitude), which indicates the sulfides from different hydrothermal vents or even a same station were formed at different stages of hydrothermal mineralization, and suggests the variations of chemical compositions of the hydrothermal fluid with respect to time. The hydrothermal temperatures of sulfides precipitation decreased gradually from station TVG10(st.TVG10) to st.TVG12, and to st.TVG11, indicating that the precipitation of hydrothermal sulfides is subjected to conditions changed from high temperature to low temperature, and that the hydrothermal activity of study area was at the late stage of a general trend of evolution from strong to weak. The abnormally low concentrations of REE in sulfides and their similar chondrite-normalized REE patterns show that REEs in all sulfides were derived from a same source, but underwent different processes of migration or enrichment, or sulfides were formed at different stages of hydrothermal mineralization. The sulfides collected from the active hydrothermal vent were mainly attributed to precipitating directly from the hydrothermal fluid, while those collected from the extinct hydrothermal chimney might have already been altered by the seawater. Generally, ore-forming elements in the sulfides can be divided into three groups: Fe-based element group, Cu-based element group and Zn-based element group. The first group includes Fe, Mn, Cr, Mo, Sn, Rb and bio-enriching elements, such as P and Si, reflecting the similar characteristics to Fe in the study area. And the second group contains Cu, W, Co, Se, Te and Bi, suggesting the similar behavior with Cu. Moreover, the third group includes Zn, Hf, Hg, Cd, Ta, Ga, Pb, As, Ag, Ni and Sb, which indicates the geochemical characteristics of most dispersed trace elements controlled by Zn-bearing minerals to some extent.

Selective and mild oxidation of sulfides to sulfoxides by H_2O_2 using DBUH-Br_3 as catalyst

DBUH-Br_3 catalyzed selective conversion of sulfides to sulfoxides in the presence of H_2O_2 as oxidizing agent is described.The reaction was performed selectively at room temperature and relatively short reaction times.

Synthesis of 3D Hexagram-Like Cobalt–Manganese Sulfides Nanosheets Grown on Nickel Foam: A Bifunctional Electrocatalyst for Overall Water Splitting

The exploration of low-cost and efficient bifunctional electrocatalysts for oxygen evolution reaction and hydrogen evolution reaction through tuning the chemical composition is strongly required for sustainable resources. Herein, we developed a bimetallic cobalt–manganese sulfide supported on Ni foam(CMS/Ni) via a solvothermal method. It has discovered that after combining with the pure Co_9S_8 and Mn S, the morphologies of CMS/Ni have modulated. The obtained three-dimensionally hexagram-like CMS/Ni nanosheets have a significant increase in electrochemical active surface area and charge transport ability. More than that, the synergetic effect of Co and Mn has also presented in this composite. Benefiting from these, the CMS/Ni electrode shows great performance toward hydrogen evolution reaction and oxygen evolution reaction in basic medium, comparing favorably to that ofthe pure Co_9S_8/Ni and Mn S/Ni. More importantly, this versatile CMS/Ni can catalyze the water splitting in a twoelectrode system at a potential of 1.47 V, and this electrolyzer can be efficiently driven by a 1.50 V commercial dry battery.

Surface-treatment of Alkaline Earth Sulfides Based Phosphor

A series of alkaline earth sulfides based phosphors Ca_ 0.8 Sr_ 0.2 S∶Eu 2+ ,Tm 3+ were covered with a layer of protective coating with alkaline earth fluorides by heating the mixture of phosphor and NH_4HF_2 at elevated temperatures. The coatings were characterized by means of XRD and SEM. The optical properties of the coated phosphors and the influences of the coating on their properties have been discussed extensively. The stabilities of the coated and uncoated phosphors have been compared.

Influence of sulfides on the tribological properties of composites produced by pulse electric current sintering

Self-lubricating A1203-15wt% ZrO2 composites with sulfides, such as molybdenum disulfide （MoS2） and tungsten disulfide （WSz） serving as solid lubricants, were fabricated by using the pulse electric current sintering （PECS） technique. The coefficient of friction （COF） of the A1203-15wt% ZrO2 composite without/with sulfides was in the range of 0.37-0.48 and 0.27-0.49, respectively. As the amoant of sul- fides increased, the COF and the wear rate decreased. The reduction in COF and wear rate of the sulfide-containing composite is caused by a reduction in shear stresses between the specimen and the tribological medium due to the formation of a lubricating film resulting from the lamellar structure of sulfides located on the worn surface.

Fe(NO_3)_3·9H_2O/Fe(HSO_4)_3:An efficient reagent system for the oxidation of alcohols,thiols and sulfides in the absence of solvent

Fe（NO3）3-9H2O/Fe（HSO4）3 was used as an efficient reagent system for the oxidation of alcohols to their corresponding carbonyl compounds. All reactions were performed in the absence of solvent in good to high yields. Under the same reaction conditions, thiols and sulfides were also converted to their corresponding disulfides and sulfoxides, respectively. 2007 Farhad Shirini. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

Chemical compositions of sulfides in the porphyry Cu ores,Yangla Cu deposit,Yunnan,China:implication for ore genesis

The Yangla Cu deposit is the largest ore deposit in the Jinshajiang polymetallic metallogenic belt,northwest Yunnan,China.There is no consensus on the genesis of the ore deposit owing to the limited studies on the chemical compositions of sulfides.This study used an electron probe micro-analyzer to constrain the chemical compositions of pyrite,chalcopyrite,molybdenite,and sphalerite in the porphyry Cu ore of the Yangla Cu deposit and compared them with the chemical compositions of sulfides in the skarn Cu ore.The trace element contents and their occurrences were used to estimate the metallogenic temperature and infer the genesis of the Yangla deposit.The results show that the sulfides in the porphyry Cu ores have variations of ore element concentrations relative to their theoretical values.Pyrite is depleted in S but elevated in Fe;chalcopyrite is depleted in Cu,Fe,and S;and molybdenite and sphalerite are enriched in S whilst depleted in Mo and Zn.The concentrations of the main metallogenic elements Cu,Fe,Mo,Zn,and S in the porphyry are generally lower than those in skarn,suggesting that the porphyry ore was formed in a moderate to moderate-high temperature metallogenic environment.The formation time may also be slightly later than that of the skarn Cu ore.Elements such as As,Co,Cu.Pb,Zn,Mo,Cd,and Ni mainly exist as isomorphic replacements and mineral inclusions in the sulfides of both porphyry and skarn Cu ores.The trace element features of sulfides in the two ore bodies show that the Yangla Cu deposit may be a composite super imposed ore deposit,and让s formation has undergone the process of exhalative-sedimentary to skarnporphyry mineralization.

Methods of electrochemical study of natural metal sulfides

The history of electrochemical flotation was reviewed. Potentiometry, voltammetry, rotating disk electrode and spectral electrochemical methods for electrochemical studies of sulfides and sulfide flotation were introduced. The methodology of electrochemical research was expatiated on. Some research of sulfides done by these methods was demonstrated. Their results give good inosculation to the flotation practice. The mixed potential concept leads to an understanding of collector action in terms of well established electrochemical principles. At last, the trend of flotation electrochemistry was predicted.

Bifunctional oxygen electrode cobalt–nickel sulfides catalysts originated from intercalated LDH precursors

Bimetallic cobalt-nickel sulfide nanoparticles anchored on S-,N-codoped holey carbon nanosheets(CoNiS-T@NCFs)with a hydrangea-like morphology,were synthesized via a confinement synthesis route,in which an intercalated LDH precursor was subjected to the interlayer-confined carbonization and host-layer sulfurization.The phase transformation and structure evolution(e.g.,atom site occupancy,crystallite size,and cell volume)of the CoNi-S-T@NCFs electrocatalysts,as a function of sulfurization temperatures,were confirmed by X-ray diffraction and Rietveld analyses.The sulfur vacancies effectively enhance the electrocatalytic activity,while the synergistic effect of(Co,Ni)7 S8 alloy and S,N-codoped carbon matrix facilitates the electron transfer and accelerates reaction kinetics,making CoNi-S-900@NCFs an efficient and stable bifunctional electrocatalyst for oxygen reduction reaction(ORR).The rich highvalence Co(Ⅲ)and Ni(Ⅲ)of CoNi-S-900@NCFs facilitates the in-situ transformation of the metal(oxy)hydroxides intermediates with high catalytic activity for oxygen evolution reaction(OER).Thus,with a bifunctional parameter,ΔE,of 0.75 V(E_(j=10,OER)-E_(1/2,ORR)),this electrocatalyst slightly outperforms the state-of-the-art commercial Pt/C+RuO_(2)/C catalyst(ΔE=0.76 V)in alkaline medium.This work demonstrates the influence that the sulfurization temperature has on the relationship between the structure and electrocatalytic performance of bimetallic sulfides prepared by the synthesis strategy using the intercalated LDH precursor.This strategy can be extended to prepare other chalcogenides with binary or ternary transition metals.

Thiol-free route to diaryl sulfides by Cu catalyzed coupling of sodium thiosulfate with aryl halides

A method for the synthesis of diaryl sulfides from aryl halides in polyethylene glycol was reported.Inodorous Na2S2O3·5H2O,which is readily available as a stable salt,is an effective source of sulfur in the presence of Cu I as catalyst.