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Purification is a separated post-treatment step after the synthesis of nanocrystals (NCs) in order to exclude excess ligands and monomers in NC solution. The common purification process involves many manipulations, such as concentrating, addition of anti-solvents and centrifugation, which are troublesome and time consuming. In this work, we originally integrate NC synthesis and NC purification in one-pot via selecting water-ethanol co-environment for NC synthesis and NC purification. Our research shows that NCs can grow in water-ethanol mixture. When growing into critical size, NCs will automatically precipitate from the solution. Element analysis demonstrates that precipitates fraction fits well with stoichiometric of ligand-capped NCs. Excess monomers are left in supernatant, and thus achieving automatically purification of NCs in the water-ethanol co-environment. By adjusting the volume ratios of water and ethanol in bi-solvent system, different-sized purified NCs can be controlled. Besides, this water-ethanol co-environment can be used in both thermal-promoted and hydrazine-promoted growth.

To remove membrane fouling, a bio-electrochemical system that can generate a micro-electric field and micro-current was constructed. After 11 days of operation, the trans-membrane pressure difference of membrane modules in the open- and closed-circuit groups increased by 35.8 kPa and 6.2 kPa, respectively. The concentrations of total polysaccharide and protein in the open-circuit group were 1.8 and 1.1 times higher than those in the closed-circuit group, respectively. In addition, X-ray photoelectron spectroscopy and thermogravimetric analysis showed that inorganic crystals such as calcium carbonate were present on the membrane surface, and the concentration of calcium ion in the control group was 14.7 times that of the experimental group. High-throughput sequencing demonstrated that the enrichment of some electroactive bacteria and other microorganisms has a positive effect on the control of membrane fouling. Therefore, this system can effectively alleviate membrane fouling of a bioreactor, by targeting the membrane foulants.

AbstractReview: 268 refs.

In this study, we constructed a three-chamber microbial fuel cell (TC-MFC) that avoided the adverse effects of H+ diffusion on anode microorganisms in the acidic catholyte and the precipitation of heavy metals in the soil near the cathode side (S4), while also achieving migration of copper from the soil and reduction of Cu2+ in the catholyte. The removal efficiency of acid-soluble Cu from the soil near the anode region reached 42.5% after 63 days of operation at an external resistance of 100 Ω and electrode spacing of 10 cm, and Cu2+ in the catholyte was completely removed within 21 days. Heavy metal mobility index (MF) values indicated that the bioavailability and mobility of heavy metals were reduced by the TC-MFC. We found that changing the cathode potential and external circuit current in TC-MFC would affect the type (via XRD) and morphology (via SEM) of cathode deposits and the average removal rate of heavy metals. At the meantime, it should be noted that the interaction between the electric-field-dependent soil heavy metal migration and electron-dependent copper reduction in TC-MFC occurred, which was confirmed to have a relationship with the negative correlation between voltage and current during the test.

A coupled system consisting of a double-anode microbial fuel cell (MFC) unit and a biofilm electrode reactor (BER) has been applied to degrade the azo dye reactive brilliant red X-3B. In this system, the MFC effluent was used as the input of the BER. The MFC preliminarily degraded X-3B while generating electricity, and the BER obtained electrons from the MFC through the external circuit to continue degrading pollutants without the need for an external power supply. The X-3B removal efficiency was 41.93% higher in the coupled system than the control when the X-3B concentration was 3000 mg/L. The analysis of intermediate products showed that the azo bond of X-3B broke in the MFC, generating a large number of complex intermediates such as anthraquinones, which were further degraded into simple organic compounds in the BER. Meanwhile, the abundance of microbial taxa related to the degradation of refractory organics in the MFC was high, as was that of microbial taxa related to the degradation of simple organics in the BER. Furthermore, the abundance of microorganisms related to power generation in the MFC increased. These results provided an efficient strategy for improving electron utilization efficiency in the coupling system of bioelectrochemical system.

Several studies have identified threats that originate in areas surrounding protected areas (PAs). While there have been various efforts to integrate PAs with their surroundings, considerable challenges remain. Here we summarize these efforts to date, discuss their effectiveness, and provide recommendations for future research. Based on a broad literature review of theoretical and applied approaches, we have outlined 68 models for balancing conservation and sustainable development in PAs. We comprehensively analyzed 23 of these models for integrating PAs with their surroundings. They were divided into two categories: area-oriented and process-oriented approaches. This review reveals the absolute necessity of combining these two approaches for future conservation and sustainable development of PAs.

AbstractSolar evaporation is a facile and promising technology to efficiently utilize renewable energy for freshwater production and seawater desalination. Here, the fabrication of self‐regenerating hydrogel composed of 2D‐MXenes nanosheets embedded in perovskite La 0.6Sr 0.4Co 0.2Fe 0.8O3−δ (LSCF)/polyvinyl alcohol hydrogels for efficient solar‐driven evaporation and seawater desalination is reported. The mixed dimensional LSCF/Ti3C2 composite features a localized surface plasmonic resonance effect in the polymeric network of polyvinyl alcohol endows excellent evaporation rates (1.98 kg m−2 h−1) under 1 k Wm−2 or one sun solar irradiation ascribed by hydrophilicity and broadband solar absorption (96%). Furthermore, the long‐term performance reveals smooth mass change (13.33 kg m−2) during 8 h under one sun. The composite hydrogel prompts the dilution of concentrated brines and redissolves it back to water (1.2 g NaCl/270 min) without impeding the evaporation rate without any salt‐accumulation. The present research offers a substantial opportunity for solar‐driven evaporation without any salt accumulation in real‐life applications.

The carbon neutrality strategy marks that green electricity will replace fossil energy as the main power source in the future power system. The trading varieties in the electricity market will be more diverse, and the demand for green electricity by consumers will grow significantly. This paper innovatively proposes a provincial market framework for voluntary flexible trading of green electricity while elaborating on the conceptual design of differentiated green electricity trading processes in a systematic way for Zhejiang province. The proposed framework can not only reflect the carbon emission reduction attributes of green electricity but also fully exploit its commercial and social values. Moreover, the proposed green electricity trading certificate can realize the authoritative certification of green electricity consumption and help the construction of a carbon traceability mechanism. The proposed trading mechanism is expected to give rise to a new green electricity service industry and deepen the reform of the carbon and electricity synergy mechanism. The experience of green electricity trading in the Zhejiang province is expected to reveal the promotive impact of the electricity market on the carbon neutrality strategy.