Dimensional and Doping Engineering of Chiral Perovskites with Enhanced Spin Selectivity for Green Emissive Spin Light-Emitting Diodes.

Chiral perovskites play a pivotal role in spintronics and optoelectronic systems attributed to their chiral-induced spin selectivity (CISS) effect. Specifically, they allow for spin-polarized charge transport in spin light-emitting diodes (LEDs), yielding circularly polarized electroluminescence at room temperature without external magnetic fields. However, chiral lead bromide-based perovskites have yet to achieve high-performance green emissive spin-LEDs, owing to limited CISS effects and charge transport. Herein, we employ dimensional regulation and Sn2+-doping to optimize chiral bromide-based perovskite architecture for green emissive spin-LEDs. The optimized (PEA)x(S/R-PRDA)2-xSn0.1Pb0.9Br4 chiral perovskite film exhibits an enhanced CISS effect, higher hole mobility, and better energy level alignment with the emissive layer. These improvements allow us to fabricate green emissive spin-LEDs with an external quantum efficiency (EQE) of 5.7% and an asymmetry factor |gCP-EL| of 1.1 × 10-3. This work highlights the importance of tailored perovskite architectures and doping strategies in advancing spintronics for optoelectronic applications.

Mitigated N2O emissions from submerged-plant-covered aquatic ecosystems on the Changjiang River Delta.

Submerged plants affect nitrogen cycling in aquatic ecosystems. However, whether and how submerged plants change nitrous oxide (N2O) production mechanism and emissions flux remains controversial. Current research primarily focuses on the feedback from N2O release to variation of substrate level and microbial communities. It is deficient in connecting the relative contribution of individual N2O production processes (i.e., the N2O partition). Here, we attempted to offer a comprehensive understanding of the N2O mitigation mechanism in aquatic ecosystems on the Changjiang River Delta according to stable isotopic techniques, metagenome-assembly genome analysis, and statistical analysis. We found that the submerged plant reduced 45 % of N2O emissions by slowing down the dissolved inorganic nitrogen conversion velocity to N2O in sediment (Vf-[DIN]sed). It was attributed to changing the N2O partition and suppressing the potential capacity of net N2O production (i.e., nor/nosZ). The dominated production processes showed a shift with increasing excess N2O. Meanwhile, distinct shift thresholds of planted and unplanted habitats reflected different mechanisms of stimulated N2O production. The hotspot zone of N2O production corresponded to high nor/nosZ and unsaturated oxygen (O2) in unplanted habitat. In contrast, planted habitat hotspot has lower nor/nosZ and supersaturated O2. O2 from photosynthesis critically impacted the activities of N2O producers and consumers. In summary, the presence of submerged plants is beneficial to mitigate N2O emissions from aquatic ecosystems.

Short-branched alkyl sulfobetaine-passivated CsPbBr3 nanocrystals for efficient green light emitting diodes.

Inorganic cesium lead bromide nanocrystals (CsPbBr3 NCs) hold promising prospects for high performance green light-emitting diodes (LEDs) due to their exceptional color purity and high luminescence efficiency. However, the common ligands employed for passivating these indispensable NCs, such as long-chain organic ligands like oleic acid and oleylamine (OA/OAm), display highly dynamic binding and electronic insulating issues, thereby resulting in a low efficiency of the as-fabricated LEDs. Herein, we report a new zwitterionic short-branched alkyl sulfobetaine ligand, namely trioctyl(propyl-3-sulfonate) ammonium betaine (TOAB), to in situ passivate CsPbBr3 NCs via a feasible one-step solution synthesis, enabling efficiency improvement of CsPbBr3 NC-based LEDs. The zwitterionic TOAB ligand not only strengthened the surface passivation of CsPbBr3 NCs with a high photoluminescence quantum yield (PLQY) of 97%, but also enhanced the carrier transport in the fabricated CsPbBr3 NC thin films due to the short-branched alkyl design. Consequently, CsPbBr3 NCs passivated with TOAB achieved a green LED with an external quantum efficiency (EQE) of 7.3% and a maximum luminance of 5716 cd m-2, surpassing those of LEDs based on insulating long-chain ligand-passivated NCs. Our work provides an effective surface passivation ligand design to enhance the performance of CsPbBr3 NC-based LEDs.

Fabrication of the flower-like Z-scheme heterojunction photocatalyst Bi-BiOI/UiO 66 for enhanced photodegradation of acetaminophen in simulated wastewater.

Acetaminophen is a representative contaminant of emerging persistent organic pollutants that can cause environmental problems when it enters municipal wastewater. An innovative flower-like Z-scheme photocatalyst Bi-BiOI/UiO 66 heterojunction composite was designed and constructed via a one-step solvothermal method. Investigations demonstrated that the Z-scheme structure strongly contributes to increasing the degradation efficiency of micropollutants. The results indicate that the bandgap energy (Eg) of the Bi-BiOI/UiO 66 composite decreases significantly from 3.22 eV to 2.43 eV, in comparison with that of pure copper-based UiO 66. Under suitable conditions (5 mg/L Ace, pH 3, 0.05 g/L), the organic pollutants in the water can be removed completely. A k value of 5.67 × 10-2 min-1 for the Bi-BiOI/UiO 66 heterojunction composite was found to effectively represent the acetaminophen photodegradation process. The reaction mechanism of acetamide in aqueous solution is also discussed. The Bi in Bi-BiOI can use surface plasmon resonance to form an electric field and accelerate the separation of photogenerated electrons and holes. This study highlights the potential of a novel photocatalyst for practical application.

Helical-caging enables single-emitted large asymmetric full-color circularly polarized luminescence.

Colorful circularly polarized luminescence materials are desired for 3D displays, information security and asymmetric synthesis, in which single-emitted materials are ideal owing to self-absorption avoidance, evenly entire-visible-spectrum-covered photon emission and facile device fabrication. However, restricted by the synthesis of chiral broad-luminescent emitters, the realization and application of high-performing single-emitted full-color circularly polarized luminescence is in its infancy. Here, we disclose a single-emitted full-color circularly polarized luminescence system (spiral full-color emission generator), composed of whole-vis-spectrum emissive quantum dots and chiral liquid crystals. The system achieves a maximum luminescence dissymmetry factor of 0.8 and remains an order of 10-1 in visible region by tuning its photonic bandgap. We then expand it to a series of desired customized-color circularly polarized luminescence, build chiral devices and further demonstrate the working scenario in the photoinduced enantioselective polymerization. This work contributes to the design and synthesis of efficient chiroptical materials, device fabrication and photoinduced asymmetric synthesis.

[Iron-based Bimetallic Catalysts for Persulfate Activation to Remove Antibiotics in Water: A Review].

In recent years, antibiotic residues are commonly detected in a variety of water bodies, causing serious threat to water ecosystems and human health. The removal of antibiotic contaminants from water based on the advanced oxidation process of activated persulfate has become a hot research topic due to its strong oxidative properties, high selectivity, and wide pH applicability range. Iron-based bimetallic materials with low cost, high stability, and excellent catalytic performance can effectively activate persulfate, which makes up for the defects of being a single iron activator, such as easy deactivation, low efficiency, and producing secondary pollution easily. Three typical Fe-based bimetallic catalysts, namely spinel ferrite, Fe-based layered double hydroxides, and Fe-based Prussian blue analogues, were investigated and analyzed for their activation of persulfate for antibiotic degradation. Several intrinsic mechanisms of persulfate activation by Fe-based bimetallic catalysts are systematically discussed, including the generation of free radicals, singlet oxygen, and high-valent metals; the process of electron transfer; and the direct oxidation process of persulfate. Finally, the general degradation pathways of four typical antibiotics, including fluoroquinolones, sulfonamides, tetracyclines, and ß-lactam antibiotics, are summarized to act as a reference for future studies on the application of Fe-based bimetallic catalysts and their modifications, derivatives, and complexes in the activating technology of persulfate.

Fabrication, characterization, and application of BiOI@ZIF-8 nanocomposite for enhanced photocatalytic degradation of acetaminophen from aqueous solutions under UV-vis irradiation.

This work investigates the use of novel BiOI@ZIF-8 nanocomposite for the removal of acetaminophen (Ace) from synthetic wastewater. The samples were analyzed using FTIR, XRD, XPS, DRS, PL, FESEM-EDS, and ESR techniques. The effects of the loading capacity of ZIF-8 on the photocatalytic oxidation performance of bismuth oxyiodide (BiOI) were studied. The photocatalytic degradation of Ace was maximized by optimizing pH, reaction time and the amount of photocatalyst. On this basis, the removal mechanisms of the target pollutant by the nanocomposite and its photodegradation pathways were elucidated. Under optimized conditions of 1 g/L of composite, pH 6.8, and 4 h of reaction time, it was found that the BiOI@ZIF-8 (w/w = 1:0.01) nanocomposite exhibited the highest Ace removal (94%), as compared to that of other loading ratios at the same Ace concentration of 25 mg/L. Although this result was encouraging, the treated wastewater still did not satisfy the required statutory of 0.2 mg/L. It is suggested that the further biological processes need to be adopted to complement Ace removal in the samples. To sustain its economic viability for wastewater treatment, the spent composite still could be reused for consecutive five cycles with 82% of regeneration efficiency. Overall, this series of work shows that the nanocomposite was a promising photocatalyst for Ace removal from wastewater samples.

Insight into the microbial nitrogen cycle in riparian soils in an agricultural region.

Riparian zones are considered as an effective measure on preventing agricultural non-point source nitrogen (N) pollution. However, the mechanism underlying microbial N removal and the characteristics of N-cycle in riparian soils remain elusive. In this study, we systematically monitored the soil potential nitrification rate (PNR), denitrification potential (DP), as well as net N2O production rate, and further used metagenomic sequencing to elucidate the mechanism underlying microbial N removal. As a whole, the riparian soil had a very strong denitrification, with the DP 3.17 times higher than the PNR and 13.82 times higher than the net N2O production rate. This was closely related to the high soil NO3--N content. In different profiles, due to the influence of extensive agricultural activities, the soil DP, PNR, and net N2O production rate near the farmland edge were relatively low. In terms of N-cycling microbial community composition, the taxa of denitrification, dissimilatory nitrate reduction, and assimilatory nitrate reduction accounted for a large proportion, all related to NO3--N reduction. The N-cycling microbial community in waterside zone showed obvious differences to the landside zone. The abundances of N-fixation and anammox genes were significantly higher in the waterside zone, while the abundances of nitrification (amoA&B&C) and urease genes were significantly higher in the landside zone. Furthermore, the groundwater table was an important biogeochemical hotspot in the waterside zone, the abundance of N-cycle genes near the groundwater table was at a relative higher level. In addition, compared to different soil depths, greater variation in N-cycling microbial community composition was observed between different profiles. These results reveal some characteristics of the soil microbial N-cycle in the riparian zone in an agricultural region and are helpful for restoration and management of the riparian zone.

Insight into suppression of dibutyl phthalate on DOM removal during municipal sewage treatment using fluorescence spectroscopy with PARAFAC and moving-window 2D-COS.

Dibutyl phthalate (DBP) has been widely detected in municipal and industrial wastewater, which could indirectly inhibit pollutant removals, especially degradation of dissolved organic matter (DOM). Here, the inhibition of DBP on DOM removal from wastewater in pilot-scale A2O-MBR system was investigated by fluorescence spectroscopy with two-dimensional correlation (2D-COS) and structural equation modeling (SEM). Seven components were extracted from DOM using parallel factor analysis, i.e., tryptophan-like (C1 and C2), fulvic-like (C4), tyrosine-like (C5), microbial humic-like (C6) and heme-like (C7). The tryptophan-like had a blue-shift at DBP occurrence, defined as blue-shift tryptophan-like (C3). DBP with 8 mg L-1 exhibited a stronger inhibition on removals of DOM fractions, extraordinarily tyrosine-like and tryptophan-like in anoxic unit than DBP of 6 mg L-1 by moving-window 2D-COS. The indirect removals of C1 and C2 through the C3 removal were more strongly inhibited by 8 mg L-1 DBP than those by 6 mg L-1 DBP, while the former exhibited a weaker inhibition on the direct degradation of C1 and C2 than the latter via SEM. Based on metabolic pathways, abundances of key enzymes secreted by microorganism in anoxic unit, degrading tyrosine-like and tryptophan-like, were higher in wastewater with 6 mg L-1 DBP than those with 8 mg L-1 DBP. These could provide a potential approach for online monitoring of DBP concentrations in wastewater treatment plants, which could rectify operating parameters, and then enhance the treatment efficiencies.

A LaCl3-based lithium superionic conductor compatible with lithium metal.

Inorganic superionic conductors possess high ionic conductivity and excellent thermal stability but their poor interfacial compatibility with lithium metal electrodes precludes application in all-solid-state lithium metal batteries1,2. Here we report a LaCl3-based lithium superionic conductor possessing excellent interfacial compatibility with lithium metal electrodes. In contrast to a Li3MCl6 (M = Y, In, Sc and Ho) electrolyte lattice3-6, the UCl3-type LaCl3 lattice has large, one-dimensional channels for rapid Li+ conduction, interconnected by La vacancies via Ta doping and resulting in a three-dimensional Li+ migration network. The optimized Li0.388Ta0.238La0.475Cl3 electrolyte exhibits Li+ conductivity of 3.02 mS cm-1 at 30 °C and a low activation energy of 0.197 eV. It also generates a gradient interfacial passivation layer to stabilize the Li metal electrode for long-term cycling of a Li-Li symmetric cell (1 mAh cm-2) for more than 5,000 h. When directly coupled with an uncoated LiNi0.5Co0.2Mn0.3O2 cathode and bare Li metal anode, the Li0.388Ta0.238La0.475Cl3 electrolyte enables a solid battery to run for more than 100 cycles with a cutoff voltage of 4.35 V and areal capacity of more than 1 mAh cm-2. We also demonstrate rapid Li+ conduction in lanthanide metal chlorides (LnCl3; Ln = La, Ce, Nd, Sm and Gd), suggesting that the LnCl3 solid electrolyte system could provide further developments in conductivity and utility.

Activated carbon enhanced traditional activated sludge process for chemical explosion accident wastewater treatment.

With the development of industries, explosion accidents occur frequently during production, transportation, usage and storage of hazard chemicals. It remained challenging to efficiently treat the resultant wastewater. As an enhancement of traditional process, the activated carbon-activated sludge (AC-AS) process has a promising potential in treating wastewater with high concentrations of toxic compounds, chemical oxygen demand (COD) and ammonia nitrogen (NH4+-N), etc. In this paper, activated carbon (AC), activated sludge (AS) and AC-AS were used to treat the wastewater produced from an explosion accident in the Xiangshui Chemical Industrial Park. The removal efficiency was assessed by the removal performances of COD, dissolved organic carbon (DOC), NH4+-N, aniline and nitrobenzene. Increased removal efficiency and shortened treatment time were achieved in the AC-AS system. To achieve the same COD, DOC and aniline removal (90%), the AC-AS system saved 30, 38 and 58 h compared with the AS system, respectively. The enhancement mechanism of AC on the AS was explored by metagenomic analysis and three-dimensional excitation-emission-matrix spectra (3DEEMs). More organics, especially aromatic substances were removed in the AC-AS system. These results showed that the addition of AC promoted the microbial activity in pollutant degradation. Bacteria, such as Pyrinomonas, Acidobacteria and Nitrospira and genes, such as hao, pmoA-amoA, pmoB-amoB and pmoC-amoC, were found in the AC-AS reactor, which might have played important roles in the degradation of pollutants. To sum up, AC might have enhanced the growth of aerobic bacteria which further improved the removal efficiency via the combined effects of adsorption and biodegradation. The successful treatment of Xiangshui accident wastewater using the AC-AS demonstrated the potential universal characteristics of the process for the treatment of wastewater with high concentration of organic matter and toxicity. This study is expected to provide reference and guidance for the treatment of similar accident wastewaters.

Overestimation of 1O2 role in N-doped carbon materials/peroxymonosulfate system: The misleading of furfuryl alcohol quenching effect.

Singlet oxygen (1O2) is frequently observed in persulfate-based advanced oxidation processes (PS-AOPs), however its significance in the removal of organic compounds is debatable. To evaluate the role of 1O2, some organic pollutants that have been proven to be successfully degraded by 1O2 in earlier research were selected as the targeted pollutants of this study. In the activation of peroxymonosulfate (PMS) using Co-BTC (a type of metal-organic framework)/melamine derived nitrogen-doped carbon material (Co-BTC/10MNC) as the catalyst, 1O2 and surface-bound SO4•- are discovered, however only surface-bound SO4•- was the dominant species. The degree of inhibition of furfuryl alcohol (FFA) on the removal of organics is reliant on the reaction rates of SO4•- and organics, rather than on the quenching impact of FFA on 1O2. The lower kSO4•- organics have, the easier it is for FFA to inhibit their removal. In short, the quenching effect of FFA is not solid evidence to identify 1O2. Besides, it is found that the influence of HCO3- is related to the second order reaction rate constant (kHCO3•) between HCO3• and organics, implying that the selective removal of some organics is due to that corresponding inorganic radicals (Cl•, NO3•, HCO3• or HPO4•-) have good ability to degrade these organics, rather than 1O2 as the key reactive oxygen species.

Nitrogen-doped carbon materials prepared using different organic precursors as catalysts of peroxymonosulfate to degrade sulfamethoxazole: First-time performance leading to the incorrect selection of the best catalyst.

Nitrogen-doped carbon materials are effective catalysts for peroxymonosulfate (PMS) activation to eliminate organic contaminants. In this research, the activity of nitrogen-doped carbon materials was significantly improved by optimizing the carbon source, and the reusability of the catalyst is used to select the best catalyst instead of depending on the performance in the first use, for avoiding the "short-life" catalyst with great initial activity. Fixing ferric nitrate nonahydrate and melamine as the metal and nitrogen sources, four catalysts were prepared using glucose, glucosamine hydrochloride, dopamine, and trimesic acid as the carbon sources, respectively. Based on the performance in PMS activation for sulfamethoxazole (SMX) removal, in the first use, the activity was Fe-DA-CN (carbon source: dopamine) > Fe-BTC-CN (carbon source: trimesic acid) > Fe-GLU-CN (carbon source: glucosamine) > Fe-DGLU-CN (carbon source: glucose). With no washing for the second time use, the activity was Fe-BTC-CN (0.135 min-1) â‰« Fe-DA-CN (0.037 min-1) > Fe-GLU-CN (0.032 min-1) > Fe-DGLU-CN (0.017 min-1). The large specific surface area, superior graphitization, and high CO/C-N group content endow Fe-BTC-CN with high ability in PMS activity. Surface-bound radicals are responsible for SMX elimination, and most of the SMX degradation intermediates have lower ecotoxicity than SMX.

Recovery iron from cyanide tailings by anaerobic roasting-persulfate leaching: effect of roasting temperature.

Anaerobic roasting combined with the persulfate-leaching process was used to treat cyanide tailings. In this study, the effect of the roasting conditions on the iron leaching rate was investigated by the response surface methodology. Additionally, this study was focusing on the effect of roasting temperature on the physical phase transformation of cyanide tailings and the persulfate-leaching process of roasted products. The results showed that roasting temperature had significant influences on the leaching of iron. The roasting temperature determined the physical phase changes of iron sulfides in roasted cyanide tailings, which in turn affected the leaching of iron. At the temperature of 700 °C, all pyrite was converted to pyrrhotite, and the leaching rate of iron reached a maximum of 93.62%. At this point, the weight loss rate of cyanide tailings and the recovery rate of sulfur were 43.50% and 37.73%, respectively. The sintering of the minerals became more severe when the temperature raised to 900 °C, and the iron leaching rate gradually decreased. The leaching of iron was mainly attributed to the indirect oxidation by SO4-˙ and OH˙ rather than the direct oxidation by S2O82-. The oxidation of iron sulfides by persulfate produced iron ions along with a certain amount of SO4-˙. Iron ions continuously activated persulfate to produce SO4-˙ and OH˙ under the mediation of sulfur ions in iron sulfides.

High-Density Microarray Analysis of Microbial Community Structures in Membrane Bioreactor at Short Sludge Retention Time.

Membrane bioreactors (MBR) have become prevalent in wastewater treatment because of their high effluent quality and low sludge generation. Sludge retention time (SRT) is an important parameter in the operation of MBR, and it has a direct effect on the microbial community. In this study, microarrays were used to analyze the microbial communities of three different MBRs at short SRTs. The results showed that MBR at SRT 5 days (CS5) has the highest operational taxonomic units (OTUs) richness, but the lowest diversity and uniformity compared to SRT 3 days at continuous CS3 and the sequencing batch (SS3). Proteobacteria were the dominant phylum of three reactors. Bacteroidetes were the second dominant phylum in MBRs at the continuous model, instead of Actinobacteria at the sequencing model. At the class level, the dominant group of Proteobacteria exhibited a remarkable difference between the three MBRs. γ-Proteobacteria was the dominant group in CS5 and CS3, while α-Proteobacteria was the main group in SS3. The samples from the three MBRs had similar compositions of α-, ß- and δ-Proteobacteria. However, γ-Proteobacteria showed different community compositions at the order level between the three MBRs. Enterobacteriales were the dominant group in CS5 and CS3, while Pseudomonadales were the dominant group in SS3. The bacterial community concentration of SRT 5 days was generally higher than that of the other two MBRs. The community composition of CS5 was significantly different from that of CS3 and SS3, and the phylogenetic relationships of the three MBRs were relatively different.

Impacts of dibutyl phthalate on bacterial community composition and carbon and nitrogen metabolic pathways in a municipal wastewater treatment system.

Dibutyl phthalate (DBP) is a typical toxic and hazardous pollutant in pharmaceutical wastewater, affecting the metabolism of microbial flora, leading to decreased treatment efficiency, and deteriorated effluent quality in municipal wastewater treatment plants (WWTPs). This study conducted a long-term experiment with 6 operational stages in a pilot-scale A2O-MBR system, analyzing the effect of DBP on the bacterial community and their carbon and nitrogen metabolic pathways. 16S rRNA gene amplicon sequencing analysis and principal components analysis (PCA) showed that DBP at 8 mg/L significantly influenced the structure of bacterial community (P < 0.05), resulting in reduced bacterial community diversity. Metagenomic analysis was used to explore the embedded carbon and nitrogen metabolic pathways. At the presence of DBP, the metabolism of saccharides, lipids, and aromatic compounds were blocked owing to the vanishment of key enzyme (such as acetylaminohexosyltransferase (EC 2.4.1.92) and UDP-sugar pyro phosphorylase (EC 2.7.7.64)) encoding genes, resulting in weakened carbon metabolism, and thus reduced COD removal performance. The resultant deficiency of the genes such as those encoding hydroxyproline dehydrogenase (EC 1.5.5.3) gave rise to interrupted metabolic pathways of amino acid (arginine, proline, tyrosine, and tryptophan), resulting in declined function of nitrogen metabolism and thus reduced TN removal efficiency. The uncovery of the mechanisms by which DBP affects wastewater treatment system efficiency and microbial metabolism is of theoretical importance for the efficient operation of municipal and pharmaceutical wastewater treatment systems.

Optimization and trade-off framework for coupled green-grey infrastructure considering environmental performance.

Implementing runoff control infrastructure has been regarded as an efficacious measure in stormwater management. The issue of its cost-effectiveness is a primary concern for decision makers since it is an exorbitant investment. However, most of existed studies only concentrated on the cost-effectiveness optimization of runoff control infrastructure, especially green infrastructure, between hydrological and economic aspects, and therefore, the potential layout scenarios with high extra environmental benefits could be neglected in the traditional two-dimensional frameworks. In this study, a novel carbon dioxide equivalent-based index was quantified to represent the extra environmental benefits of runoff control infrastructure besides stormwater management and was further integrated into the assessment framework. The effectiveness of green and grey infrastructure was comprehensively evaluated and traded off between hydrological, environmental and economic aspects. The results demonstrated that grey infrastructure is a better measure than green infrastructure when only hydrological (HF index) and economic (CI index) performances were considered. Nevertheless, the environmental performance (EROI index) of green infrastructure prevails over grey infrastructure, and when optimizing green and grey infrastructure simultaneously in the three-dimensional framework considering environmental effectiveness, green infrastructure is comparable with grey infrastructure. Furthermore, an appropriate composition of coupled green-grey infrastructure is requisite, which could achieve an optimal trade-off between hydrological and environmental effectiveness. The sources of environmental benefits were also identified and analyzed from three representative preference scenarios. The findings of the study could serve as a trade-off basis between green and grey infrastructure, as well as between EROI and HF.

Insight into the key role of oxygen dopants over ball-milled boron nitride for efficient degradation of PFOS alternative 6:2 fluorotelomer sulfonic acid.

6:2 Fluorotelomer sulfonic acid (6:2 FTS) has been identified as an alternative to perfluorooctane sulfonic acid but has been proven to cause potential threats to humans and the environment. In this study, boron nitride (BN) photocatalysis was explored for 6:2 FTS degradation with 100% removal (kobs=1.8 h-1) and desulfurization rate of 100% as well as the defluorination rate of 57.3%. The superior performance of BN was primarily related to oxygen dopants defects (O-dopants). In addition, O-dopants contribution was confirmed by ball-milled BN (B-BN), which introduced more O-dopants and exhibited an increased 6:2 FTS degradation rate of 2.88 h-1. The decomposition of 6:2 FTS was attributed to holes (h+), hydroxyl radicals (•OH), and superoxide (•O2-) and proceeded via two pathways, the hydrogen abstraction from ethyl carbons by •OH and the C-S bond activation by h+ and •OH. To the best of our knowledge, this is the first study demonstrating that h+, •OH, and •O2- played significant roles in the heterogeneous photocatalytic degradation of 6:2 FTS.

Study on the Changes in the Microcosmic Environment in Forward Osmosis Membranes to Reduce Membrane Resistance.

Osmotic microbial fuel cells (OsMFCs) are an emerging wastewater treatment technology in bioelectricity generation, organic substrate removal, and wastewater reclamation. To address this issue, proton-conductive sites were strengthened after using the forward osmosis (FO) membrane by reducing the membrane resistance. The mechanism of improving electricity generation was attributed mainly to the unique characteristics of the membrane material and the water flux characteristics of the FO membrane. In particular, only when the concentration of catholyte was greater than 0.3 M was the membrane resistance the main contributor to the overall internal resistance. Meanwhile, through the simulation of the concentration inside the membrane, the changes in the membrane thickness direction and the phase transition of the internal structure of the membrane from the dry state (0% water content) to the expansion state (>50%water content) were analyzed, which were influenced by the water flux, further explaining the important role of the membrane's microenvironment in reducing the membrane impedance. This further opens a novel avenue for the use of OsMFCs in practical engineering applications.

Forward Osmosis Technology and Its Application on Microbial Fuel Cells: A Review.

As a new membrane technology, forward osmosis (FO) has aroused more and more interest in the field of wastewater treatment and recovery in recent years. Due to the driving force of osmotic pressure rather than hydraulic pressure, FO is considered as a low pollution process, thus saving costs and energy. In addition, due to the high rejection rate of FO membrane to various pollutants, it can obtain higher quality pure water. Recovering valuable resources from wastewater will transform wastewater management from a treatment focused to sustainability focused strategy, creating the need for new technology development. An innovative treatment concept which is based on cooperation between bioelectrochemical systems and forward osmosis has been introduced and studied in the past few years. Bioelectrochemical systems can provide draw solute, perform pre-treatment, or reduce reverse salt flux to help with FO operation; while FO can achieve water recovery, enhance current generation, and supply energy sources for the operation of bioelectrochemical systems. This paper reviews the past research, describes the principle, development history, as well as quantitative analysis, and discusses the prospects of OsMFC technology, focusing on the recovery of resources from wastewater, especially the research progress and existing problems of forward osmosis technology and microbial fuel cell coupling technology. Moreover, the future development trends of this technology were prospected, so as to promote the application of forward osmosis technology in sewage treatment and resource synchronous recovery.