Enhanced efficiency of AgAlO2/g-C3N4 binary composite to degrade organic pollutants for environmental remediation under visible light irradiation.

This study explores the utilization of semiconductor-based photocatalysts for environmental remediation through photocatalytic degradation, harnessing solar energy for effective treatment. The primary focus is on the application of photocatalytic technology for the degradation of 2-chlorophenol and methylene blue, critical pollutants requiring remediation. The research involves the synthesis of binary AgAlO2/g-C3N4 nanocomposites through an exchange ion method, subsequent calcination, and sonication. This process enhances the transfer of photogenerated electrons from AgAlO2 to g-C3N4, resulting in a significantly increased reductive electron charge on the surface of g-C3N4. The photocatalytic activity of the synthesized composites is comprehensively examined in the degradation of 2-chlorophenol and methylene blue through detailed crystallographic, electron-microscopy, photoemission spectroscopy, electrochemical, and spectroscopic characterizations. Among the various composites, AgAlO2/20% g-C3N4 emerges as the most active photocatalyst, achieving an impressive 98% degradation of methylene blue and 97% degradation of 2-chlorophenol under visible light. Notably, AgAlO2/20% g-C3N4 surpasses bare AgAlO2 and bare g-C3N4, exhibiting 1.66 times greater methylene blue degradation and constant rate (k) values of 20.17 × 10-3 min-1, 4.18 × 10-3 min-1 and 3.48 × 10-3 min-1, respectively. The heightened photocatalytic activity is attributed to the diminished recombination rate of electron-hole pairs. Scavenging evaluations confirm that O2•- and h+ are the primary photoactive species steering methylene blue photodegradation over AgAlO2/g-C3N4 in the visible region. These findings present new possibilities for the development of efficient binary photocatalysts for environmental remediation.

Highly photoactive novel NiS/BiOI nanocomposite photocatalyst towards efficient visible light organic pollutant degradation and carcinogenetic Cr (VI) reduction for environmental remediation.

Heterojunction engineering in catalyst structures is a promising approach for solving the main restriction of the narrow photoabsorption range and quick recombination of photogenerated charge carriers in the photocatalysts. Herein, a simple, eco-friendly, non-toxic, and novel Z-scheme heterojunction of nanoflower-like NiS/BiOI was systematically designed using the low-temperature solvothermal and precipitation methods. The physicochemical and photo-electrochemical properties of the as-synthesized nanomaterials were characterized using XRD, FESEM, FT-IR, XPS, BET, UV-vis, PL, and EIS. NiS/BiOI nanomaterials exhibited a wide photoabsorption range (200-1000 nm), a narrow bandgap energy (1.76 eV), a large surface area (35.82 m2 g-1), and a low charge carrier recombination rate because of the synergistic effects of the NiS and BiOI photocatalysts, which could be the basis for superior photocatalytic efficiency. Particularly, the optimal 40% NiS/BiOI nanocomposite exhibited better stability and efficiency than the pure NiS and BiOI. The maximum degradation efficiency of rhodamine B (RhB) was 99.8% after 200 min, tetracycline (TC) was 96.3% after 140 min, and the photoreduction of Cr(VI) was 92.8% after 180 min rather than the pure NiS and BiOI under visible light irradiation. The constant rate (k) of RhB was approximately 10 and 4, TC was 12 and 4, and Cr(VI) was 10 and 8 times that of pristine NiS and BiOI, respectively. Radical trapping experiments and Tauc plot analysis proposed the design of the plausible Z-scheme reaction mechanism between NiS and BiOI, which has a crucial role in the rate of transportation and separation of electron/hole pairs. This investigation provides a venue for the design of a photoactive NiS-based nanocomposite for environmental remediation.