The adaptability, distribution, ecological function and restoration application of biological soil crusts on metal tailings: A critical review.

A large amount of metal tailings causes many environmental issues. Thus, the techniques for their ecological restoration have garnered extensive attention. However, they are still in the exploratory stage. Biological soil crusts (BSCs) are a coherent layer comprising photoautotrophic organisms, heterotrophic organisms and soil particles. They are crucial in global terrestrial ecosystems and play an equal importance in metal tailings. We summarized the existing knowledge on BSCs growing on metal tailings. The main photosynthetic organisms (cyanobacteria, eukaryotic algae, lichens, and mosses) of BSCs exhibit a high heavy metal(loid) (HM) tolerance. BSCs also have a strong adaptability to other adverse conditions in tailings, such as poor structure, acidification, and infertility. The literature about tailing BSCs has been rapidly increasing, particularly after 2022. The extensive literature confirms that the BSCs distributed on metal tailings, including all major types of metal tailings in different climatic regisions, are common. BSCs perform various ecological functions in tailings, including HM stress reduction, soil structure improvement, soil nutrient increase, biogeochemical cycle enhancement, and microbial community restoration. They interact and accelerate revegetation of tailings (at least in the temperate zone) and soil formation. Restoring tailings by accelerating/inducing BSC formation (e.g., resource augmentation and inoculation) has also attracted attention and achieved small-scale on-site application. However, some knowledge gaps still exist. The potential areas for further research include the relation between BSCs and HMs, large-scale quantification of tailing BSCs, application of emerging biological techniques, controlled laboratory experiments, and other restoration applications.

Doping engineering in S-scheme composite for Regulating the selectivity of photocatalytic CO2 reduction.

Regulating product selectivity in photocatalytic CO2 reduction to enhance the yield of valuable hydrocarbons remains a formidable challenge because of the diversity of reduction products and the competitive reduction of H2O. Herein, ultrathin Bi2O3/ Co-doped SrBi4Ti4O15 S-scheme photocatalysts (Co-BS) were synthesized using a hydrothermal method. The Bi2O3/Co-doped SrBi4Ti4O15 photocatalyst exhibited significantly higher selectivity for CH4 (62.3 µmolg-1) and CH3OH (54.1 µmolg-1) in CO2 reduction compared with pure SrBi4Ti4O15 (27.2 and 0.8 µmolg-1) and the Bi2O3/SrBi4Ti4O15 S-scheme without Co (30.2 and 0 µmolg-1). The experimental results demonstrated that the inclusion of Co into SrBi4Ti4O15 expanded the range of light absorption and generated an internal electric field between Co-doped SrBi4Ti4O15 and Bi2O3. Density functional theory calculations and other experimental findings confirmed the formation of a new doping energy level in the Bi2O3/SrBi4Ti4O15 S-scheme heterojunction after Co doping. The valence band electrons of Bi2O3/SrBi4Ti4O15 transitioned to the Co-doped level because of the interconversion between Co3+ and Co2+ under the action of the internal electric field. Furthermore, the corresponding characterizations revealed that the adsorption and electron transfer rates of the surface active sites were accelerated after Co doping, enhancing electron involvement in the photocatalytic reaction process. This study presented a metal-doped S-scheme heterojunction approach for CO2 reduction to produce high-value products, enhancing the conversion of solar energy into energy resources.

Efficient simultaneous removal of tetracycline hydrochloride and Cr(VI) through photothermal-assisted photocatalytic-Fenton-like processes with CuOx/γ-Al2O3.

Advanced oxidation processes (AOPs) based on photo-Fenton reaction has been widely used in refractory organic wastewater treatment. However, the mineralization rate and H2O2 utilization in AOPs is relatively low. Herein, a photothermal-assisted photocatalytic-Fenton-like process with CuOx/γ-Al2O3 catalyst was designed to solve the above issues. The utilization rate of H2O2 and mineralization rate of tetracycline hydrochloride (TC) in the 3%-CuOx/γ-Al2O3/H2O2/full spectrum light system were significantly increased to 72.0% and 74.3%, respectively, which were ascribed to the synergy of photothermal effect and photocatalytic-Fenton-like reaction. During the simultaneous removal of TC and Cr(VI), the reaction efficiency of 3%-CuOx/γ-Al2O3/H2O2/light system was much higher than that of 3%-CuOx/γ-Al2O3/H2O2 system. In addition, the 3%-CuOx/γ-Al2O3/H2O2/light system was not only active in wider pH range (3-9), but also effective in various organic pollutants and Cr(VI) coexisted solutions as well as different water conditions. More importantly, a possible photothermal-assisted photocatalytic-Fenton-like reaction mechanism for the simultaneous removal of TC and Cr(VI) in the CuOx/γ-Al2O3/H2O2/light system was proposed. This work may pave a new way for efficient simultaneous removal of refractory organic pollutants and heavy metals in wastewater.

A novel Fe-rectorite composite catalyst synergetic photoinduced peroxymonosulfate activation for efficient degradation of antibiotics.

Developing a low-cost and efficient photocatalysts activated peroxymonosulfate (PMS) for organic pollutants degradation are recognized as an importance way for dealing with environmental pollution. In this work, Fe-rectorite catalyst was synthesized by a simple impregnation-calcine method to synergetic photo activate PMS for antibiotics degradation. As expected, the Fe-rectorite/PMS/Light system exhibits superior catalytic performance for tetracycline (TC) removal, which achieving 96.4% removal rate of TC (30 mg/L) under light within 60 min. Fe-retorite has better degradation performance for TC than rectorite under photo-mediation. The enhancement of the degradation performance of TC by Fe-retorite can be attributed to the improvement of the separation efficiency of photogenerated electrons and holes in the rectorite by the loading of Fe2O3, and the accelerated active Fe(Ⅱ)/Fe(Ⅲ) cycle on the surface under photo-mediation. The large specific surface area and abundant hydroxyl groups of rectorite can also provide active sites for PMS activation. The quenching experiment and electron paramagnetic resonance (EPR) test were indicated that the h+, SO4•-, •OH, and O2-• all contributed to TC degradation. And the possible degradation pathway was proposed by LC-MS. This work helps induced a novel direction that design green, efficient, and recyclable heterogeneous catalysts to synergetic photoinduced PMS activation for enhanced degradation of TC.

The fabrication of two-dimensional g-C3N4/NaBiO3·2H2O heterojunction for improved photocatalytic CO2 reduction: DFT study and mechanism unveiling.

Photocatalytic CO2 reduction is typically limited by the separation efficiency of photogenerated carriers for a single semiconductor. Thus, fabricating a two-dimensional/two-dimensional (2D/2D) heterojunction photocatalyst with high separation efficiency of photogenerated carriers has become a research priority. Here, a 2D/2D g-C3N4/NaBiO3·2H2O (CN/NBO) heterojunction photocatalyst was successfully synthesized for CO2 photoreduction. With the assistance of the nature of CN, the 10CN/NBO composite showed the best performance with the production yield rates of 110.2 and 43.8 µmol g-1 for CO and CH4, respectively. Our experiments showed that the introduction of CN in CN/NBO composites, which is under the step-scheme (S-step) transfer direction of photogenerated carriers, could greatly inhibit the recombination of photogenerated e--h+ pairs to prolong the carriers' lifetime, which was further confirmed by analysis of photoluminescence and photochemical characterization. As we expected, the CN/NBO composites show improved photocatalytic CO2 reduction activity. The in situ infrared spectroscopy was also performed to study the intermediate products of the photocatalytic CO2 reduction process. This study provides a way to design CN-based heterojunction photocatalysts for CO2 photoreduction.