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Nickel-iron sulfide has shown attractive activity in electrocatalytic oxygen evolution reaction (OER). However, the effects of low valence sulfur (S 2− ) and metal species on OER in binary nickel-iron sulfide have rarely been systematically studied. Works based on post-catalysis characterization have led to the assumption that the real active species are nickel-iron oxyhydroxide, and that nickel-iron sulfide acts only as a precatalyst. Therefore, to study the role of S, Ni, and Fe for the development of nickel-iron sulfide catalyst is of self-evident importance. Herein, a facile solvothermal method is used to synthesize acetylene black coated with nickel-iron sulfide nanosheets. Electrochemical tests show that the presence of low valence S species makes the catalyst have faster OER kinetics, larger active area, and intermediate active species adsorption area. Therefore, the present study reveals the enhancing effect of low valence sulfur species (S 2− ) on OER in binary nickel-iron sulfide. In situ Raman spectroscopy shows that the generation of γ-NiOOH intermediate is essential and Fe does not directly participate in the oxygen production. Density functional theory (DFT) calculation shows that Ni-OH deprotonation is a rate-determining step for both binary nickel-iron sulfide and nickel sulfide. The addition of Fe into NiS x lightly increases the charge transfer of Ni atom to O atom, which makes deprotonation easier and thereby improves the OER performance.

Porous FeS nanofibers with numerous nanovoids for use as anode materials for sodium-ion batteries were prepared by electrospinning and subsequent sulfidation. The post-treatment of the as-spun Fe（acac）3-polyacrylonitrile composite nanofibers in an air atmosphere yielded hollow Fe2O3 nanofibers due to Ostwald ripening. The ultrafine Fe2O3 nanocrystals formed at the center of the fiber diffused toward the outside of the fiber via Ostwald ripening. On sulfidation, the Fe2O3 hollow nanofibers were transformed into porous FeS nanofibers, which contained numerous nanovoids. The formation of porosity in the FeS nanofibers was driven by nanoscale Kirkendall diffusion. The porous FeS nanofibers were very structurally stable and had superior sodium-ion storage properties compared with the hollow Fe2O3 nanofibers. The discharge capacities of the porous FeS nanofibers for the Ist and 150th cycles at a current density of 500 mA.g-1 were 561 and 592 mA.h-g-1, respectively. The FeS nanofibers had final discharge capacities of 456, 437, 413, 394, 380, and 353 mA-h.g-1 at current densities of 0.2, 0.5, 1.0, 2.0, 3.0, and 5.0 A.g-1, respectively.

An enhanced concentration of phosphorus has been found at the stratigraphic level of the disappearance of Ediacaran taxa in two areas, the Cis-Dniester region and the Moscow syneclise, on the East European Platform (EEP). The isotope composition of neodymium was determined in Fe sulphide and phosphorite in the same beds. Measured ε Nd(t) values in diagenetic phosphate nodules are similar to those in iron sulphide from the same layer. During the Ediacaran − Early Cambrian, accumulation of radiogenic Nd in the epeiric basins on the EEP increased progressively from −17.9 and −19.4 in pyrite from the sequence bottom to −7.9 and −8.5 in the Early Cambrian pyrite of the central part of the EEP. The Ediacaran phosphate nodules show ε Nd(t) ranging from −12.9 to −15.0, while that in the Early Cambrian nodules is typically c. −9.0. These data indicate the secular change in Nd isotope composition of the water reservoir on the EEP from Ediacaran to Cambrian.

PurposeThis field study aimed to guide the planning of iron amendments for phosphorus retention by investigating the long-term fate of iron added to two urban lakes (Plötzensee and Groß Glienicker See) in Berlin, Germany. The contributions of iron dosing to improve lake status as well as the relevance of competing processes for management success were evaluated.MethodsSediment stratigraphy, as well as occurrence of iron minerals, and fluxes between water and sediment were examined using geochemical analyses (i.e. element composition, sequential extraction, X-ray diffraction, and pore water analyses). A one-box lake model was used to relate these fluxes to monitoring data from the water column and to sediment inventories.ResultsIn both lakes, the added iron was preserved in the sediment. Whereas phosphorus retention increased following the addition of iron to Groß Glienicker See, sulphur was retained by the excess iron in Plötzensee. This contrasting effect is attributed to significantly different sulphate reduction rates in two lakes (Wilcoxon rank sum test: W = 25, p = 0.008). According to the one-box model, sulphate reduction explained both the decrease in measured sulphate concentrations after iron application as well as the observed increase in sulphur deposition in the sediments.ConclusionManagement interventions involving iron amendments to enhance phosphorus retention must consider the competing process of iron sulphide formation during the entire management plan period, and additional iron may need to be applied to account for this effect.

Metal sulfides have shown great potential as the anodes of the asymmetric supercapacitors ascribed to their superior theoretical specific capacitance. However, their specific capacitance and rate performances are still far from the expectation due to the intrinsic poor electronic conductivity and sluggish kinetics. Herein, we employ the anion and cation double‐substitution strategy to prepare iron sulfide nanoparticles on graphene composite (denoted as NiFeSP/G) to improve the electronic conductivity of FeS2. The NiFeSP/G composite exhibits greatly improved electrochemical performances with a high specific capacity of 765 C g−1 (765 F g−1) at 5 A g−1 and a remarkable rate capability of 65% at 100 A g−1. Moreover, an aqueous asymmetric supercapacitor is fabricated with the NiFeSP/G as anode and NiCo‐LDH/graphene as cathode presents an impressively high energy density up to 109 Wh kg−1 at 1591 W kg−1 and cycling performance (89% of the initial capacity retained after 8000 cycles). The effective strategy of anion (P) and cation (Ni) double‐substitution along with the incorporation of graphene nanosheets greatly improves the electrochemical performances of iron sulfide. An aqueous asymmetric supercapacitor is fabricated with the NiFeSP/G and NiCo‐LDH/G as the anode and cathode, respectively.

Recently, iron-based sulfides, including iron sulfide minerals and biological iron sulfide clusters, have attracted widespread interest, owing to their excellent biocompatibility and multi-functionality in biomedical applications. As such, controlled synthesized iron sulfide nanomaterials with elaborate designs, enhanced functionality and unique electronic structures show numerous advantages. Furthermore, iron sulfide clusters produced through biological metabolism are thought to possess magnetic properties and play a crucial role in balancing the concentration of iron in cells, thereby affecting ferroptosis processes. The electrons in the Fenton reaction constantly transfer between Fe2+ and Fe3+, participating in the production and reaction process of reactive oxygen species (ROS). This mechanism is considered to confer advantages in various biomedical fields such as the antibacterial field, tumor treatment, biosensing and the treatment of neurodegenerative diseases. Thus, we aim to systematically introduce recent advances in common iron-based sulfides.

In this study, the role of iron sulfide (FeS) content on the structural and optical properties of graphene/polyvinyl alcohol (Gr/PVA) blend has been examined for environmental-friendly applications. Gr/PVA blend filled with FeS (0 to 10 wt%) were equipped using the casting technique. The prepared samples were studied via a scanning electron microscope, X-ray diffractometer, FT-IR and UV–visible-NIR spectrophotometers. XRD analysis shows that the crystallinity increases with increasing FeS concentration in the host Gr/PVA blend. UV–visible-NIR analysis shows that the direct optical bandgap of composite blends shrinks from 5.37 to 4.68 eV as FeS content is increased to 10 wt%. Also, it confirms that the refractive index and optical conductivity of Gr/PVA blend could be significantly enhanced via FeS filling. FeS filled Gr/PVA blends are recommended eco-friendly applications.

In this study, iron sulphide thin films were prepared by simple and low-cost chemical spray-pyrolysis method using tilt deposition with a spraying angle of 45° and substrates temperature of 200°C. The precursors were iron chloride salt (FeCl 3 ) and thiourea. After the preparation process, some of the samples are annealed at a temperature 400°C for 30 min. It was found that the as-deposited iron sulphide thin films (without annealing) had an amorphous structure, which gave higher absorption coefficient (2 × 10 5  cm −1 ) for thin film thickness 400 nm. This study also presents a novel method to obtain polycrystalline FeS 2 thin films with pyrite phase and optimum energy bandgap and high absorption coefficient. A thin film of iron sulphide was also deposited on fluorine-doped tin oxide glass to work as a counter electrode for dye-sensitized solar cells.

In this work, FeS supported SBA-15 mesoporous silica catalyst (FeS@SBA-15) was synthesized successfully, characterized and first applied to persulfate (PS) activation for the degradation of imidacloprid in wastewater. The as-prepared 3.5-FeS@SBA-15 presented an impressive imidacloprid removal efficiency of 93.1% and reaction stoichiometric efficiency (RSE) of 1.82% after 5 min, ascribed to the synergetic effects of improved FeS dispersion and abundant surface sites by SBA-15. Electron paramagnetic resonance spectra and quenching experiments proved that both SO 4 ·- and ·OH were produced in FeS@SBA-15/PS system, and SO 4 ·- played a dominant role in the degradation process. The S 2- can accelerate the cycling of Fe(III)/Fe(II) during activation and increase the steady-state concentration of Fe(II). More importantly, the constructed heterogeneous system exhibited an efficient and stable catalytic activity over a wide range of pH (3.0-9.0), temperature (283K-313K), inorganic ion (NO 3 - ) and humic acid (1-20 mg/L). Moreover, the density functional theory calculations were conducted to predict the potential reaction sites of imidacloprid. Based on eighteen identified intermediates, four main degradation pathways were proposed: hydroxylation, dechlorination, hydrolysis, and the ring cleavage of the imidazolidine. ECOSAR analysis indicated hydroxylation and dechlorination played a key role in the detoxification of the formed compounds. These findings would provide new insights into the application of FeS@SBA-15 catalyst in wastewater treatment and the removal mechanism of imidacloprid from wastewater.

AbstractCobalt–iron sulfides supported on N-doped carbon were synthesized as energy storage material using ball milling followed by carbonization. As-synthesized materials were structurally analyzed by X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, scanning electron microscopy, and high-resolution transmission electron microscopy. Furthermore, cobalt–iron sulfides supported on N-doped carbon were coated on Ni foam, and their electrochemical performance was tested in a 3-M KOH electrolyte. The as-fabricated Co–Fe–S-2 electrode registered a specific capacitance of 1252 F g−1 at 1 A g−1 and also showed capacitance retention of 66.4% at 20 A g−1. In addition, asymmetric supercapacitors (ASC) were fabricated using the as-synthesized electrode materials and it had a voltage window of 0–1.6 V. Among them, the activated carbon (AC)//Co–Fe–S-2 ASC device showed maximum specific capacitance of 169.3 F g−1 at 1 A g−1, and it registered maximum energy density of 59.6 Wh kg−1 at power density of 0.796 kW kg−1. The AC//Co–Fe–S-2 device delivered a rate capability of 55.6% at 30 A g−1, and it reveals a capacitance retention of 76.3% over 5000 cycles. Herein we also found that ball-milling-assisted synthesis of Co–Fe–S-2 electrode material is a promising candidate for high-performance ASCs.Graphic abstract