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Lithium-sulfur (Li-S) batteries are considered as promising energy storage systems due to the high energy density of 2600 W h kg-1. However, the practical application of Li-S batteries is hindered by the inadequate conductivity of sulfur and Li2S, as well as the shuttle effect caused by polysulfides during the charge-discharge process. Introducing a conductive interlayer between the cathode and the separator to physically resist polysulfides represents an effective and straightforward approach to mitigate the shuttle effect in Li-S batteries. In this paper, an ultrathin (<1 µm) 2D-2D MXene-LDH interlayer with high polysulfide adsorption ability was introduced to Li-S batteries. The synergistic effect between MXene and layered double hydroxide greatly improved the adsorption effect of the interlayers: the conductive Ti3C2Tx MXene chemically adsorbs polysulfides and promotes their fast transfer, and the NiCo-LDH alleviates the restack of MXene and facilitates Li+ diffusion. After inserting the MXene-LDH interlayer, the Li-S batteries exhibit an enhanced specific capacity of 1137.6 mA h g-1 at 0.1 C and retain 622.6 mA h g-1 after 100 cycles. The ultrathin 2D-2D interlayer offers a feasible way for the development of highly efficient and lightweight interlayers in Li-S batteries.

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Li-O2 batteries (LOBs) have sparked significant interest due to their fascinating high theoretical energy density. However, the large overpotential for the formation and oxidation of Li2O2 during charge and discharge process seriously hinders the further development and application of LOBs. In this work, metal-organic frameworks (MOFs) with different metal clusters (Fe, Ti, Zr) are successfully synthesized, and they are employed as the photoelectrodes for the photo-assisted LOBs. The special dual excitation pathways of Fe-MOF under illumination and the superior separation efficiency of photocarriers, which significantly enhance the activation of O2/Li2O2, improving the catalytic activity of oxygen reduction reaction and oxygen evolution reaction. Moreover, compared to traditional inorganic semiconductor crystals, Fe-MOF exhibits large specific surface area and excellent O2 adsorption ability. Therefore, the LOB with Fe-MOF as the cathode exhibits large specific capacity, ultralow charge/discharge overpotential of 0.22 V at 0.05 mA cm-2 and excellent stability of 195 cycles under illumination. This study provides an environmentally friendly and highly efficient photocatalyst for LOBs, and a new strategy for designing photoelectrodes.

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Nonaqueous Li - O2 battery (LOB) is considered one of the most promising energy storage system due to its ultrahigh theoretical specific capacity (3500 Wh kg-1). Introducing vacancies in CoMn2O4 catalysts is regarded as an effective strategy to enhance the electrochemical performances of LOB. However, the relation between vacancy types in CoMn2O4 and catalytic performances in the LOB remains ambiguous. Herein, ordered porous CoMn2O4 with oxygen and metal vacancies is obtained via solvothermal reaction followed by temperature-controlled calcination using polystyrene spheres as templates. The increase in treatment temperature reduces the content of oxygen vacancies while increasing that of the metal vacancies. Notably, experimental results and theoretical calculations show that oxygen vacancies in CoMn2O4 have a greater influence than metal vacancies in modulating the LiO2 adsorption during the reaction processes and reducing the overpotential. CoMn2O4 synthesized at 500 ℃ (CoMnO-500) with higher oxygen vacancies exhibits stronger adsorption onto the LiO2, facilitating the formation of film-like Li2O2. Therefore, an LOB with the CoMnO-500 catalyst presents the lowest overpotential of 1.2 V and longest cycle lifespan of 286 cycles at a current density of 200 mA g-1. This study offers insights into the effect of CoMn2O4 vacancies on the formation pathway of Li2O2 discharge products.

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Taking advantage of the strong adsorption characteristics of coffee grounds (CGs) and coffee ground biochar (CGB), this research employed equal amounts of 2%, 4%, 6%, and 8% CGs and CGB to replace cement. This study thereby examined the impacts of CGs and CGB on cement compressive strength, as well as their abilities to adsorb chloride ions and formaldehyde. X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TG-DTG), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) were employed to investigate the hydration mechanism and characterize the microscopic structure. The results show the following: (1) The presence of a substantial quantity of organic compounds in CGs is found to have an adverse effect on both the compressive strength and hydration degree of the sample. The use of CGB after high-temperature pyrolysis of phosphoric acid can effectively improve the negative impact of organic compounds on the sample. (2) The addition of CGs reduces the adsorption of chloride ions by cement, primarily due to the presence of fewer hydration products. However, when CGB was incorporated into cement, it enhanced the ability to adsorb chloride ions. (3) Cement containing 8% CGB content can slightly enhance the adsorption of formaldehyde. However, the cement sample with 8% CGB content exhibited the most significant ability to adsorb formaldehyde.

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The cathodic polysulfides electrocatalyst, such as Mo2C, offers a promising approach to mitigate the shuttling effect by providing strong polysulfide adsorption and catalyst abilities to improve the electrochemical performance of Lithium-sulfur (Li-S) batteries. However, according to the Sabatier principle, excessive adsorption of Mo2C undermines the conversion of polysulfides. This undesirable effect can be mitigated by forming the heterostructure of Mo2C-MoP. Even more importantly, the introduction of MoP can prevent the surface gelation of Mo2C and expose more active sites. Consequently, the Li-S batteries with the Mo2C-MoP sulfur host exhibit outstanding long-term cycling stability, showcasing a mere 0.035% capacity decay per cycle over 800 cycles at 1 C. This work on the balance between adsorption capacity and catalytic active of cathodic polysulfides electrocatalyst provides a new vision for realizing a high-performance Li-S batteries.

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In order to further clarify the regulation of tannic acid on the off-flavor in starch-based algal oil emulsions, the effect of different starch matrix (OSA starch and OSA starch-tannic acid complex) on the release capacities of aldehydes (pentanal, hexanal, heptanal, nonanal) were investigated. The adsorption and retention ability, thermodynamic parameters, and hydrophobicity of aldehydes in the starch matrix were analyzed. Nonanal exhibited the strongest adsorption ability (65.01%-85.69%) with the starch matrix, followed by heptanal, hexanal, and pentanal, which accounted for the structures of aldehydes. Furthermore, aldehydes had a higher affinity with complex (16.33%-83.67%) than OSA starch (9.70%-66.71%) because the tannic acid altered the structure of OSA starch. Isothermal titration calorimetry suggested that the interaction between the starch matrix and aldehydes was an entropy-driven spontaneous endothermic reaction, and hydrophobic interactions were the predominant driving forces. Altogether, these results lay a theoretical foundation for facilitating the regulation of flavor in starch foods.

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The discharge of wastewater containing hexavalent chromium (Cr(VI)) into the environment is very harmful to living things. Therefore, before effluent that contains Cr(VI) can be discharged into the environment, this toxin should be removed from the contaminated water. In this study, corn stalk biochar was investigated to evaluate the Cr(VI) removal efficiency from an aqueous solution. The effects of pH (2-10), biochar concentration (0.5 to 10 g/L), Cr(VI) concentration (10-500 mg/L), and contact time (10-1440 min) were studied. The actual experimental value of the Cr(VI) removal efficiency was 28.67%, largely consistent with the predicted model value of 29.31%, under the optimal conditions of a Cr(VI) concentration of 60 g/L, pH 4, contact time of 270 min, and a biochar concentration of 4.5 g/L. A significant interaction between the Cr(VI) concentration and pH was observed, along with significance in the interaction between Cr(VI) concentration and biochar concentration, which had a greater impact on the removal of Cr(VI). Biosorption onto corn stalk biochar is an affordable and economical adsorption process to treat wastewater contaminated with Cr(VI). The aim of this study is to provide data to serve as a basis for future studies on the use of raw agricultural waste to remove Cr(VI).

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Two-dimensional MXene with high conductivity has metastable Ti atoms and inert functional groups on the surface, greatly limiting application in surface-related electrocatalytic reactions. A surface-functionalized nitrogen-doped two-dimensional TiO2/Ti3C2Tx heterojunction (N-TiO2/Ti3C2Tx) was fabricated theoretically, with high conductivity and optimized electrocatalytic active sites. Based on the conductive substrate of Ti3C2Tx, the heterojunction remained metallic and efficiently accelerated the transfer of Li+ and electrons in the electrode. More importantly, the precise regulation of active sites in the N-TiO2/Ti3C2Tx heterojunction optimized the adsorption for LiO2 and Li2O2, facilitating the sluggish kinetics with a lowest theoretical overpotential in both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Employed as an electrocatalyst in a Li-oxygen battery (Li-O2 battery), it demonstrated a high specific capacity of 15 298 mAh g-1 and a superior cyclability with more than 200 cycles at 500 mA g-1, as well as the swiftly reduced overpotential. Furthermore, combined with the in situ differential electrochemical mass spectrometry, ex situ Raman spectra, and SEM tests, the N-TiO2/Ti3C2Tx heterojunction electrode presented a superior stability and reduced side reaction along with the high performance toward the ORR and OER. It provides an efficient insight for the design of high-performance electrocatalysts for metal-oxygen batteries.

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The slow redox kinetics during cycling process and the serious shuttle effect caused by the solubility of lithium polysulfides (LiPSs) dramatically hinder the practical application of Li-S batteries. Herein, a facile and scalable spray-drying strategy is presented to construct conductive polar Mo2 C quantum dots-decorated carbon nanotube (CNT) networks (MCN) as an efficient absorbent and electrocatalyst for Li-S batteries. The results reveal that the MCN/S electrode exhibits a high specific capacity of 1303.3 mAh g-1 at 0.2 C, and ultrastable cycling stability with decay of 0.019% per cycle even at 1 C. Theoretical simulation uncovers that Mo2 C exhibits much stronger binding energies for S8 and Li2 Sn . The energy barrier for the conversion between Li2 S4 and Li2 S2 decreases from 1.02 to 0.72 eV when hybriding with Mo2 C. Furthermore, in situ discharge/charge-dependent Raman spectroscopy shows that long-chain Li2 S8 configuration is generated via S8 ring opening near the first plateaus at ≈2.36 V versus Li/Li+ and the S6 2- configuration in CNT/S electrode is maintained below the potential of ≈2.30 V versus Li/Li+ , indicating that the shuttle of soluble LiPSs happens during the whole discharge process. This work provides deep insights into the polar nanoarchitecture design and scalable fabrication for advanced Li-S batteries.

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An electrochemical sensor for Pb(II) is described that exploits (a) the outstanding adsorption ability of chitosan modified with quaternary ammonium groups (CQAS; cationic) and of lignosulfonate (LSN; anionic), and (b) the good electrical conductivity of polypyrrole nanoparticles (PPy NPs). A glassy carbon electrode (GCE) was modified with PPy NPs and polydopamine, and CQAS and LSN are used as dispersants in PPy. The modified GCE exhibits high selectivity and sensitivity for Pb(II) in the 0.1 to 50 µM concentration range, with a 55 nM detection limit (3σ method). The redox potentials for Pb(II) is around -0.55 V, and the sensor is not interfered by the presence of Hg(II) and Cu(II). The time dependent stability test showed that this sensor can maintain good reproducibility for one month. This sensor was applied to the determination of Pb(II) in wastewater samples. An electrochemical sensor for lead(II) is described that exploits the outstanding adsorption ability of chitosan that carries quaternary ammonium groups (CQAS), of lignosulfonate (LSN), and the good electrical conductivity of polypyrrole nanoparticles. CQAS and LSN are used as dispersants in PPy. The sensor exhibits high selectivity and sensitivity for Pb(II) in the range of 0.1 to 50 µM with a 55 nM detection limit.

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The advanced treatment of industrial wastewater often calls upon the use of highly-efficient treatment methods to remove hazardous pollutants prior to the effluent discharge. Adsorption can be used towards removing micro-pollutants. Congo Red dye is widely used in the paper and textile industry, and residual quantities are present in the process effluents. Adsorbing metal oxide nanoparticles have abundant pores of appropriate size, a large specific surface area, and can efficiently remove organic pollutants from waste water. FexCo3-xO4 nanoparticle adsorbents were synthesized. Their magnetic properties facilitate their recovery. Experiments were conducted for different Congo Red concentrations and FexCo3-xO4 nanoparticles dosage. The maximum Congo Red adsorption capacity of FexCo3-xO4 nanoparticles at equilibrium was 128.6 mg/g. The adsorption yield of Congo Red decreased from 86.12% to 79.53% when the initial concentration of Congo Red increased from 10 mg/L to 30 mg/L, Adsorption results were modeled to define essential parameters such as the adsorption mechanisms and kinetics. A pseudo-first-order kinetic model fitted the results. The equilibrium adsorption data were moreover fitted by isotherm models, with both the Langmuir and Freundlich equations shown appropriate. The re-use of the nanoparticle adsorbent was moreover investigated for 5 successive adsorption cycles, without loss of adsorption capacity. A case study for the adsorption of Congo Red on the FexCo3-xO4 nanoparticles demonstrates that the required mass of adsorbent can be calculated for any amount of Congo Red to be removed. It was demonstrated that the fairly cheap and environmentally friendly FexCo3-xO4 nanoparticles have a strong adsorption and removal ability for dyes and are easy to recycle.

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Two ferromanganese oxide-biochar composites (FMBC1 and FMBC2) were prepared by an impregnation method to promote the adsorption of As on red soil. Maximum adsorption capacities (Qm) of 0.687 and 0.712 mg g-1 were observed for FMBC1 and FMBC2, respectively, corresponding to increases of 104 and 111% relative to the control treatment (Qm = 0.337 mg g-1). Treatment with FMBC1 increased the pH of red soil, whereas a reverse trend was observed for FMBC2. A variety of analytical techniques were used to explain the differences between FMBC1 and FMBC2, revealing that the oxidation of As(III) to As(V) by Mn and Fe oxides was aided by interactions with the oxygen-containing functional groups of the ferromanganese oxide-biochar composites. Thus, red soil supplemented with the ferromanganese oxide-biochar composites mainly adsorbed As by chemisorption, thereby projecting ferromanganese oxide-biochar composites as potential absorbents for effectively remediating As-polluted red soil.

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Recently, antibiotics pollution has attracted more interests from many researches which causes potential risks on the ecosystem and human health. Herein, the porous carbons (PCs) was prepared by directly simultaneous carbonization/self-activation of potassium citrate at 750-900°C for chloramphenicol (CAP) removal from aqueous solution. The batch experiments were studied, which indicated that PCs prepared at 850°C, namely PCPCs-850, possessed excellent adsorption ability for CAP with a maximum adsorption amount of 506.1mgg-1. Additionally, PCPCs-850 showed a large BET surface area of 2337.06m2g-1 and microporosity of 89.11% by N2 adsorption-desorption experiment. The Langmuir and pseudo-second-order model could more precisely describe the experimental data. And thermodynamic analysis illustrated that CAP adsorption onto PCPCs-850 was an endothermic and spontaneous process. Importantly, the adsorbent exhibited good stability and regeneration after four times cycles. Based on these excellent performance, it is potential that PCPCs-850 can be used as a promising adsorbent for treating contaminants in wastewater.

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A three-dimensional hemin-functionalized graphene hydrogel (Hem/GH) was prepared by a facile self-assembly approach. The as-prepared Hem/GH showed good mechanical strength with a storage modulus of 609-642 kPa and a high adsorption capacity to organic dye contaminants (341 mg g-1 for rhodamine B). Moreover, Hem/GH could be used as a photosensitizer for the photocatalytic degradation of organic dyes and displayed superior photodegradation activity of methylene blue (MB). This result was better than that of counterparts such as graphene hydrogel (GH) and commercial catalyst P25. The excellent cycling performance of the Hem/GH was well maintained even after multiple cycles on adsorption process and photocatalytic reaction. Interestingly, after the photodegradation of MB, a light-induced pH change of the solution from alkaline pH 8.99 to acidic pH 3.82 was observed, and 10 wt % total organic carbon remained. The liquid chromatography/time-of-flight mass spectrometry (LC/TOF-MS) analysis confirmed the generation of acidic degradation products. The photocatalytic mechanism was further investigated by trapping experiments, which revealed that the MB degradation was driven mainly by the participation of O2•- radicals in the photocatalytic reaction. As an extended application, visually intuitive observation showed the as-prepared Hem/GH also had strong antibacterial properties. These results suggest that Hem/GH could be potentially used for practical application due to its high adsorption ability, excellent photocatalytic activity, and strong antibacterial properties.

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This study investigated PM2.5 adsorption by leaves of six tree species (Pinus bungeana, Pinus tabuliformis, Salix babylonica, Acer mono, Ginkgo biloba, Populus davidiana) in the West Mountain of Beijing. An aerosol generator was used for quantitative determination of PM2.5 adsorption. Atomic force microscopy (AFM) was used to determine micro morphology characteristics on the leaf surface, including roughness parameters and the PM2.5 absorption mechanism of tree leaves. The results showed that the PM2.5 adsorption capacity per unit leaf area was as follows: P. bungeana (2.44±0.22 µg·cm-2) > P. tabuliformis (2.40±0.23 µg·cm-2) > S. babylonica (1.62±0.09 µg·cm-2) > A. mono (1.23±0.01 µg·cm-2) > G. biloba (1.00±0.07 µg·cm-2) > P. davi-diana (0.97±0.03 µg·cm-2). In autumn, PM2.5 adsorption capacity per unit leaf area was as follows: November (2.33±0.43 µg·cm-2) > October (1.62±0.64 µg·cm-2) > September (1.51±0.50 µg·cm-2). The leaves of P. bungeana and P. tabuliformis were rugged with many recesses and protrusions, large relative height difference, and high roughness, and their absorption ability of PM2.5 was strong. The leaves of S. babylonica and A. mono had folded leaf lamina and were covered by fine hairs, and their roughness was relatively high, with many protrusions and fillisters on the leaf surface. Since G. biloba and P. davidiana had smooth leaves, mostly oblong stomata and low roughness, their PM2.5 absorption ability was weaker. The ranking of average roughness on the ada-xial and abaxial side of the leaves was as follows: P. bungeana (149.91±16.38 nm) > P. tabuliformis (124.47±10.52 nm) > S. babylonica (98.85±5.36 nm) > A. mono (93.74±21.75 nm) > G. biloba (80.84±0.88 nm) > P. davidiana (67.72±8.66 nm). This accorded with PM2.5 adsorption per unit leaf area, and leaf roughness had a significant positive correlation with PM2.5 adsorption amount per unit leaf area as well (R2=0.9498). To improve the environmental effects of city vegetation, tree species with leaf surface morphology that facilitates absorption of PM2.5 and other particles should be selected.

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