Design and Fabrication of Biomass Derived Black Carbon Modified g-C3N4/FeIn2S4 Heterojunction as Highly Efficient Photocatalyst for Wastewater Treatment.

The environmental deterioration caused by dye wastewater discharge has received considerable attention in recent decades. One of the most promising approaches to addressing the aforementioned environmental issue is the development of photocatalysts with high solar energy consumption efficiency for the treatment of dye-contaminated water. In this study, a novel low-cost π-π biomass-derived black carbon modified g-C3N4 coupled FeIn2S4 composite (i.e., FeInS/BC-CN) photocatalyst is successfully designed and fabricated that reveals significantly improved photocatalytic performance for the degradation of Eosin Yellow (EY) dye in aqueous solution. Under dark and subsequent visible light irradiation, the amount optimized composite reveals 99% removal performance for EY dye, almost three-fold compared to that of the pristine FeInS and BC-CN counterparts. Further, it is confirmed by means of the electron spin resonance spectrometry, quenching experiments, and density functional theory (DFT) calculations, that the hydroxyl radicals (•OH) and superoxide radicals (•O2 -) are the dominant oxidation species involved in the degradation process of EY dye. In addition, a systematic photocatalytic degradation route is proposed based on the resultant degradation intermediates detectedduring liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis. This work provides an innovative idea for the development of advanced photocatalysts to mitigate water pollution.

Enhanced visible light photocatalytic performance of a novel FeIn2S4 microsphere/BiOBr nanoplate heterojunction with a Z-scheme configuration.

The rational design of heterojunction photocatalysts is an effective way to improve semiconductor photocatalytic activity. The simple solvothermal method was used to successfully prepare visible light-driven FeIn2S4 microsphere/BiOBr nanoplate binary heterojunction photocatalysts with varying FeIn2S4 contents. The crystal structure, morphology, surface composition, specific surface area, charge separation, and optical properties of the as-prepared photocatalysts were investigated using a variety of analytical methods. In the photocatalytic degradation of rhodamine B, the FeIn2S4/BiOBr photocatalysts obtained a degradation efficiency of 96% within 60 min, which was approximately 5.33 and 2.59 times higher than pure FeIn2S4 and BiOBr, respectively. Radical trapping experiments and ESR measurements revealed the main active species (·OH, ·O2-, and h+) produced during photocatalytic degradation. The increased photocatalytic activity was due to the formation of Z-scheme heterojunctions between FeIn2S4 and BiOBr, which contributed to the improved effective charge separation of photogenerated charge carriers, augmented specific surface area, and enhanced redox capacity. It is expected that our current study will provide a hopeful way for future environmental remediation research.

Interface ion-exchange strategy of MXene@FeIn2S4 hetero-structure for super sodium ion half/full batteries.

Herein, a well-designed hierarchical architecture of bimetallic transition sulfide FeIn2S4 nanoparticles anchoring on the Ti3C2 MXene flakes has been prepared by cation exchange and subsequent high-temperature sulfidation processes. The introduction of MXene substrate with excellent conductivity not only accelerates the migration rate of Na+ to achieve fast reaction dynamics but provides abundant deposition sites for the FeIn2S4 nanoparticles. In addition, this hierarchical structure of MXene@FeIn2S4 can effectively restrain the accumulation of MXene to guarantee the maximized exposure of redox active sites into the electrolyte, and simultaneously relieve the volume expansion in the repeated discharging/charging processes. The MXene@FeIn2S4 displays outstanding rate capability (448.2 mAh g-1 at 5 A g-1) and stable long cycling performance (428.1 mAh g-1 at 2 A g-1 after 200 cycles). Moreover, the Nay-In6S7 phase detected by ex-situ XRD and XPS characterization may be regarded as a "buffer" to maintain the stability of the Fe-based components and enhance the reversibility of the electrochemical reaction. This work confirms the practicability of constructing the hierarchical structure bimetallic sulfides with the promising electrochemical performance.