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The utilization or improvement of tumor microenvironment (TME) has become a breakthrough in emerging oncology therapies. To address the limited therapeutic efficacy of single modality, a multi-functional integrated nanoplatform based on a TME-responsive PtAu/MnO 2 cascade nanoreactor with multi-enzymatic activities was developed for multimodal synergistic tumor therapy. Benefiting from the slightly acidic environment and high-level glutathione (GSH) in TME, PtAu/MnO 2 cascade nanoreactor consumed GSH, followed by the reductive generation of manganese ion (Mn 2+ ) and the release of PtAu nanoparticles (NPs). Then, the multimodal synergistic tumor therapy was activated as follows. First, GSH depletion inhibited the activity of glutathione peroxidase 4 and led to the accumulation of lipid peroxidation, thereby inducing tumor cell ferroptosis. Second, PtAu NPs exhibited catalase-like, glucose oxidase-like and nicotinamide adenine dinucleotide (NADH) oxidase-like activities, which generated oxygen for the cascade reaction to alleviate hypoxia and further depleted glucose, NADH and adenosine triphosphate, leading to the inhibition of tumor cell proliferation via starvation therapy. Third, the production of reactive oxygen species by the oxidase- and peroxidase-like activities of PtAu NPs and the Fenton-like reaction of Mn 2+ simultaneously induced tumor cell apoptosis via chemodynamic therapy. Briefly, the in vitro and in vivo results confirmed that the multi-functional integrated nanoplatform based on a PtAu/MnO 2 cascade nanoreactor with five nanozyme activities demonstrated outstanding biocompatibility and greater inhibition of tumor growth via synergistic ferroptosis/starvation therapy/apoptosis., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Aqueous zinc ion batteries (AZIBs) face significant challenges stemming from Zn dendrite growth and water-contact attack, primarily due to the lack of a well-designed solid electrolyte interphase (SEI) to safeguard the Zn anode. Herein, we report a bio-mass derived polymer of chitin on Zn anode (Zn@chitin) as a novel and robust artificial SEI layer to boost the Zn anode rechargeability. The polymeric chitin SEI layer features both zincophilic and hydrophobic characteristics to target the suppressed dendritic Zn formation as well as the water-induced side reactions, thus harvesting a dendrite-free and corrosion-resistant Zn anode. More importantly, this polymeric interphase layer is strong and flexible accommodating the volume changes during repeated cycling. Based on these benefits, the Zn@chitin anode demonstrates prolonged cycling performance surpassing 1300 h under an ultra-large current density of 20 mA cm -2 , and a long cycle life of 680 h with a record-high zinc utilization rate of 80 %. Besides, the assembled Zn@chitin/V 2 O 5 full batteries reveal excellent capacity retention and rate performance under practical conditions, proving the reliability of our proposed strategy for industrial AZIBs. Our research offers valuable insights for constructing high-performance AZIBs, and simultaneously realizes the high-efficient use of cheap biomass from a "waste-to-wealth" concept., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Microstructural engineering is regarded as a promising option for fabricating high-performance carbon anodes. Hence, a facile solvothermal-assisted low-temperature calcination strategy was employed to modulate the microstructure of semicoke-derived carbon anodes. Owing to the effective pseudo-graphite phase modulation, the modified carbon anode exhibited a significant increase in capacity, cycling stability and ion kinetics in both lithium-ion batteries and sodium-ion batteries. Kinetic analysis and in-situ X-ray diffraction confirmed the "adsorption and intercalation" energy storage mechanism of the obtained carbon electrodes. In addition, by investigating the energy storage mechanism, we found that increasing the pseudo-graphite phase proportion played different roles in lithium and sodium ions storage. For lithium-ion storage, the pseudo-graphitic phase preferentially promotes lithium-ion transport kinetics. Conversely, during sodium-ion storage, this particular structure markedly augments the embedding capacity of sodium. Theoretical calculations demonstrate that different patterns of variation in the activation energy with the carbon layer spacing of lithium/sodium intercalation compounds lead to differences in performance enhancement. This study not only offers a low-cost approach for preparing carbon anodes enriched with a pseudo-graphitic phase, but also provides new insight into the discrepancy between lithium ion and sodium ion storage., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

The coexistence of antibiotic resistance genes (ARGs) and antibiotic-resistant bacteria (ARB) in the environment poses a potential threat to public health. In our study, we have developed a novel advanced oxidation process for simultaneously removing ARGs and ARB by two types of iron and nitrogen-doped biochar derived from rice straw (FeN-RBC) and sludge (FeN-SBC). All viable ARB (approximately 10 8 CFU mL -1 ) was inactivated in the FeN-RBC/ peroxymonosulfate (PMS) system within 40 min and did not regrow after 48 h even in real water samples. Flow cytometry identified 96.7 % of dead cells in the FeN-RBC/PMS system, which verified the complete inactivation of ARB. Thorough disinfection of ARB was associated with the disruption of cell membranes and intracellular enzymes related to the antioxidant system. Whereas live bacteria (approximately 200 CFU mL -1 ) remained after FeN-SBC/PMS treatment. Intracellular and extracellular ARGs (tetA and tetB) were efficiently degraded in the FeN-RBC/PMS system. The production of active species, primarily •OH, SO 4 •- and Fe (IV), as well as electron transfer, were essential to the effective disinfection of FeN-RBC/PMS. In comparison with FeN-SBC, the better catalytic performance of FeN-RBC was mainly ascribed to its higher amount of pyridine-N and Fe 0 , and more reactive active sites (such as CO group and Fe-N sites). Density functional theory calculations indicated the greater adsorption energy and Bader charge, more stable Fe-O bond, more easily broken OO bond in FeN-RBC/PMS, which demonstrated the stronger electron transfer capacity between FeN-RBC and PMS. To encapsulate, our study provided an efficient and dependable method for the simultaneous elimination of ARGs and ARB in water., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

A high-temperature-resistance insulating layer with high thermal conductivity is the key component for fabricating the instant metal-based electric heating tube. However, it is still a challenge for materials to possess excellent high-temperature resistance, superior insulating property, and high thermal conductivity at the same time. Here, a novel SiO 2 bridged AlN/MSR composite based on methylphenyl silicone resin (MSR) and AlN filler was reported. MSR with a high thermal decomposition temperature of 452.0 °C and a high withstand voltage of 5.6 kV was first synthesized by adjusting the contents of alkyl and phenyl groups. The superior high-temperature resistant insulating property is 3.7 and 2.4 times higher than the national standard requirement of 1.5 kV and commercial silicone resin, respectively. The hydrogen bonds formed between SiO 2 , AlN, and MSR and the electrostatic adsorption between SiO 2 and AlN can remarkably improve the uniform dispersion of AlN in MSR and thus enhance the insulating property, thermal conductivity, and thermal stability. With the addition of 2 wt% SiO 2 and 50 wt% AlN, the SiO 2 -AlN/MSR composite exhibits an extremely high withstand voltage of 7.3 kV, a high thermal conductivity of 0.553 W·m -1 ·K -1 , and an enhanced decomposition temperature of 475 °C. The superior insulating property and thermal conductivity are 4.9 and 1.3 times higher than the national standard requirement and pure MSR, respectively. This novel composite shows great potential for application in the fields requiring integrated superior insulating property, high-temperature resistance, and high thermal conductivity., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Lowering the operating temperatures of solid-oxide fuel cells (SOFCs) is critical, although achieving success in this endeavor has proven challenging. Herein, Bi 0.15 Sr 0.85 Co 0.8 Fe 0.2 O 3-δ (BiSCF) is systematically evaluated as a carbon dioxide (CO 2 )-tolerant and highly active cathode for SOFCs. BiSCF, which features Bi 3+ with an ionic radius similar to Ba 2+ , exhibits activity (e.g., 0.062 Ω cm 2 at 700 °C) comparable to that of Ba 0.5 Sr 0.5 Co 0.8 Fe 0.2 O 3-δ and PrBaCo 2 O 5+δ , while demonstrating a considerable advantage over Bi-doped cathodes. Moreover, BiSCF exhibits long-term stability over a period of 500 h, and an anode-supported cell with BiSCF achieves a power density of 912 mW cm -2 at 650 °C. The CO 2 -poisoned BiSCF exhibits quick reversibility or slight activation after returning to normal conditions. The exceptional CO 2 tolerance of BiSCF can be attributed to its reduced basicity and high electronegativity, which effectively restrict surface Sr diffusion and hinder subsequent carbonate formation. These findings highlight the substantial potential of BiSCF for SOFCs operating below 700 °C., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

After resection of bone tumour, the risk of cancer recurrence and numerous bone defects continues to threaten the health of patients. To overcome the challenge, we developed a novel multifunctional scaffold material consisting mainly of nano-hydroxyapatite particles (n-HA), MXene nanosheets and g-C 3 N 4 to prevent tumour recurrence and promote bone formation. N-HA has the potential to restrict the growth of osteosarcoma cells, and the combination of MXene and g-C 3 N 4 enables the scaffolds to produce photodynamic and photothermal effects simultaneously under near infrared (NIR) irradiation. Surprisingly, n-HA can further enhance the synergistic anti-tumour function of photodynamic and photothermal, and the scaffolds can eradicate osteosarcoma cells in only 10 min at a mild temperature of 45 ℃. Moreover, the scaffold exhibit exceptional cytocompatibility and possesses the capacity to induce osteogenic differentiation of bone marrow mesenchymal stem cells. Therefore, this multifunctional scaffold can not only inhibits the proliferation of bone tumour cells and rapidly eradicate bone tumour through NIR irradiation, but also enhances osteogenic activity. This promising measure can be used to treat tissue damage after bone tumour resection., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Chitosan microparticles are frequently used for the encapsulation of ingredients, owing to their pH-responsive, renewable, biocompatible and antimicrobial properties. Herein, pH-responsive antibacterial encapsulation carriers in chitosan-phytate (CS-PA) microparticles with various morphologies were prepared by gas-shearing microfluidics. Microparticles sizes were tuned by gas flow rate in production, and the CS and PA concentration significantly dominated the morphology of microparticles. Additionally, microparticles exhibit great storage stability, lyophilizing rehydration performance, pH-responsive behavior, as well as antibacterial and biocompatible effect, indicating that CS-PA microparticles are expected to become an ideal carrier for the actives encapsulation in pharmaceutical, food and cosmetic industries., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Graphitic carbon nitride (g-C 3 N 4 ) has received much attention as a metal-free polymeric two-dimensional photocatalyst for antibiotic-free antibacterial application. However, the weak photocatalytic antibacterial activity of pure g-C 3 N 4 stimulated by visible light limits its applications. Herein, g-C 3 N 4 is modified with Zinc (II) meso-tetrakis (4-carboxyphenyl) porphyrin (ZnTCPP) by amidation reaction to enhance the utilization of visible light and reduce the recombination of electron-hole pairs. The composite (ZP/CN) is used to treat bacterial infection under visible light irradiation with a high efficacy of 99.99% within 10 min due to the enhanced photocatalytic activity. Ultraviolet photoelectron spectroscopy and density flooding theory calculations indicate the excellent electrical conductivity between the interface of ZnTCPP and g-C 3 N 4 . The formed built-in electric field is responsible for the high visible photocatalytic performance of ZP/CN. In vitro and in vivo tests have demonstrated that ZP/CN not only possesses excellent antibacterial activity upon visible light irradiation, but also facilitates the angiogenesis. In addition, ZP/CN also suppresses the inflammatory response. Therefore, this inorganic-organic material can serve as a promising platform for effective healing of bacteria-infected wounds., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Nowadays, it is a global problem to recycle LiCoO 2 from waste lithium-ion batteries (LIBs) due to the deficiency of high business cost and environmental pollution. Here, a novel three-channel ion recovery device based on a Zn-air desalination battery (ZADB) is proposed which can supply energy while separating Li + and Co 2+ from the recovered solution. The three-channel ZADB device consists of a Zn foil anode chamber with ZnSO 4 anolyte stream, an intermediate chamber with Li + and Co 2+ recovered stream and an air cathode chamber with LiOH and Co(OH) 2 catholyte stream, chambers are separated by anion exchange membrane (AEM) and cation exchange membrane (CEM) respectively. It can be described by the finite element simulation (FES) of physics field that, the Li + and Co 2+ in the recovered solution move to the cathode chamber, where the OH - are produced by absorbing O 2 from the air combined with electronic in the discharge process. At the same time, the SO 4 2- moves to the other end of the Zn foil anode chamber according to the law of charge conservation, which combined with the Zn 2+ removed from the Zn foil. The results show that the recovery efficiency of the ZADB device is closely related to the discharge current density and the concentration of the recovered stream. The best recovery effect has achieved when 0.2 mol L -1 recovered solution is run for 24 h at the discharge current density of 0.2 mA cm -2 . The average recovery rate is 0.275 mg min -1 with the highest recovery rate is 40.73 mg h -1 , and the output energy density is 102.5 Wh Kg -1 during the experiment process. In addition, the ZADB device has the excellent long-term cycling performance and recycling stability. By comparing this device with other ion recovery methods, which provides that it is a splendid way to recycle Li + and Co 2+ from waste LIBs., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

PNIPAM as a stimuli-responsive polymer has generated extreme interests due to its versatile applications. However, there is no research report on whether PNIPAM micro/nano-particles can be extracted from its suspension after phase separation. In the present work, LCST-type phase separation in self-synthesized PNIPAM/water system was investigated in depth by dividing the DLS testing process into four stages. In addition to quenching duration, temperature rise process, quenching temperature and PNIPAM concentration all have a great influence on particle size of the suspension. Meanwhile, the steady-state rheology and dynamic viscoelasticity results show that PNIPAM micro/nano-particles in the suspension are "soft" that can deform. Finally, FE-SEM was used to observe the morphology of dehydrated PNIPAM extracted by sessile droplet evaporation under different conditions. The results indicate that these "soft" particles are easier to fuse together, do not have sufficient mechanical strength to maintain their spherical morphology after dehydration. But the above fusion can be suppressed by adjusting evaporation conditions to acquire smaller PNIPAM particles which have sufficient mechanical properties to keep their basic particle morphology. Further, by changing evaporation pressure to positive or negative pressure, dehydrated PNIPAM micro/nano-particles with excellent uniformity and separation can be obtained. This work will provide guidance for extracting micro/nano-particles from polymer/diluent systems with LCST., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Recently, carbon materials have attracted much attention in activating persulfate (PS) for the removal of organic pollutants. Seeking a greener, lower-cost, and higher-performance carbon material has become an important aspect of research. In this study, candle soot was innovatively used as a nanocarbon material, and its performance for PS activation was improved by simple ammonium ferric citrate modification. The optimal catalytic performance was achieved using 0.15 g/L modified candle soot (AS) and only 0.1 mM PS, with sulfamethoxazole (SMX) removal efficiency up to 95.5% within 120 min. Quenching tests, together with electron paramagnetic resonance measurements, showed that O 2 - and 1 O 2 were the main reactive species for SMX degradation. Meanwhile, electron transfer pathway was also occurred. Various characterization results showed that graphitic N and carbonyl group were the main active sites for PS activation. Moreover, AS/PS system exhibited high catalytic activity and stability for SMX degradation over a wide initial pH range (3∼9), or even in the presence of Cl - , H 2 PO 4 - and NO 3 - . This work not only taps the potential of candle soot as an environmental functional material, but also showcases the roadmap for the discovery, design, and resource utilization of other waste carbon materials in wastewater treatment., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier Inc.)

As one of the tactics to produce reactive oxygen radicals, the Fenton-like process has been widely developed to solve the increasingly severe problem of environmental pollution. However, establishing advanced mediators with sufficient stability and activity for practical application is still a long-term objective. Herein, we proposed a facile strategy through polymeric carbon nitride (pCN) in-situ growth single cobalt atom for efficient degradation of antibiotics by peroxymonosulfate (PMS) activation. X-ray absorption spectroscopy and high-angle annular dark field-scanning transmission electron microscopy prove the single cobalt atoms are successfully anchored on pCN. Moreover, extended X-ray absorption fine structure analysis shows that the embedded cobalt atoms are constructed by covalently forming the Co-N bond and Co-O bond, which endow the single-atom cobalt catalyst with high stability. Experiment results indicate that the prepared single-atom cobalt catalyst can be used for efficient PMS activation catalytic degradation of tetracycline with a high degradation rate of 98.7 % in 60 min. And the CoN/O sites with single cobalt atoms serve as the active site for generating active radical species (singlet oxygen) from PMS activation. This work may expand the strategy for constructing single-atom catalysts and extend its application for the advanced oxidation process., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier Inc.)

Oxygen evolution reaction (OER) and urea oxidation reaction (UOR) play important roles in the field of hydrogen energy preparation and pollution treatment. In this work, by merging bimetallic Co-Mo oxides with metallic Co on the graphite felt (GF), we effectively manufacture a 3D bifunctional and highly efficient electrocatalyst (CoMoO@Co/GF) with multi-site functionality for the simultaneous reduction of water and the oxidation of urea in an alkaline medium. The presence of metallic Co causes Co-Mo oxides to evolve from amorphous to crystalline structures. The coupling interface produced between metallic Co and Co-Mo oxides is proven to facilitate electron transport in addition to extensively accessible and highly electroactive Co-Mo oxide nanoflower architecture. The experimental results reveal that the overpotentials for OER and UOR in the CoMoO@Co/GF electrode require only 269 and 115 mV to obtain a current density of 10 mA cm -2 , respectively. Furthermore, with the aid of urea, the overpotential for HER at the current density of 10 mA cm -2 is lowered to 155 mV. Most notably, the constructed CoMoO@Co/GF-based electrolytic cell only requires a 1.5 V dry battery to achieve effective H 2 evolution and noteworthy stability, outperforming the commercial catalyst-based device and many previous results. The combination of experiments and theoretical calculations further clarifies the active sites in the catalyst. What's more, the pathway of electron transfer in the catalytic process is defined., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021. Published by Elsevier Inc.)

Unevenly distributed polypyrrole (PPy) films/coatings with extensive "dead volumes" via electrodeposition have emerged as a main challenge for high energy density flexible supercapacitor. In this work, we have fabricated a phytic acid-guided graphite carbon felt/polypyrrole (GF@PA@PPy) 3D porous composite with less "dead volumes" via electrodeposition. After the activation of phytic acid (PA), the quantity and content of defects and oxygen-containing groups on the surface of carbon felt (GF) have increased. First, these functional groups improve the hydrophilicity of the surface of GF, resulting in the preferential uniform distribution of pyrrole monomer (Py). While significantly, the synergistic effects between the defects and oxygen-containing groups boost the attraction of pyrrole ring, and thus promotes the formation of perfect PPy films with less "dead volume" on GF. Finally, the supercapacitor assembled from the GF@PA@PPy-40 displays a high areal energy density of 0.0732 mWh cm -2 , exceeding the previously reported PPy-based electrodes values. The deeper understanding of the role for the defects and oxygen-containing groups in the synthesis of PPy/carbon materials offers a new strategy to construct advanced PPy-based supercapacitors., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021. Published by Elsevier Inc.)

Bacterial infections are considered as a critical healthcare concern worldwide. Timely infection detection is crucial to effective antibiotic administration which can reduce the severity of infection and the occurrence of antibiotic resistance. We have developed label-free polydiacetylene (PDA) liposome-based colorimetric biosensor to detect and identify bacterial cultures at the genus and species level with naked eyes by simple color change. We found that among the various liposomal systems, moderate concentration of PDA, phospholipids and cholesterol in liposome assemblies can greatly influence the sensitivity to different bacteria, exhibiting unique chromatic properties of each bacterial strain. The strikingly different chromatic color change was due to the various mechanisms of interactions between bacterial toxins and biomimetic lipid bilayers. Furthermore, increase of cholesterol in liposome assemblies greatly enhanced the sensitivity of bacterial strains related to membrane destruction mediated by pore-formation mechanism such as S. aureus and E.coli, whereas the detection of the two bacterial strains was believed to rely on the specific recognition elements coupled with PDA moiety. As a proof of concept, a colorimetric finger-print array for distinguishing 6 bacterial species was studied. Particularly, the proposed bacterial detection platform is achieved through the interaction between bacterially secreted toxins and liposome bilayers instead of specific recognition of receptors-ligands. The results of both response time and sensitivity of label-free-liposome-based system show superior to previous reports on chromatic bacterial detection assays. By combing these results, the label-free-liposome-based colorimetric sensing platform shows great importance as a bacterial-sensing and discrimination platform., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

The booming development of carbon materials is of great value for diverse applications, owing to their superior electron conductivity, unique structures, and excellent cycle lifetime. This study presents two hierarchically structured amorphous carbon materials for asymmetric supercapacitor (ASC) device: i) the MOFs-derived urchin-like amorphous carbon anchored on nickel foam (UAC@NF) as positive electrode; ii) high temperature activated graphite carbon felt (GF500) as negative electrode. This ASC device achieves a higher energy density of 0.036 mWh cm -3 at a power density of 0.984 mW cm -3 and demonstrates better cycling performance with 91.4% capacitance retention after 10,000 cycles, compared with the other carbon-based supercapacitor. In addition, the UAC@NF after 10,000 cycles displays much better adsorption performance for Pb (II) compared with the unused UAC@NF. We have demonstrated the relationship between carbon materials' structure and performance by combining experiment and theoretical calculation. Predominantly, our work can provide a new direction for the common development of amorphous carbon materials in the field of energy and environment., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

Hypothesis: Stimuli-responsive Pickering emulsions have attracted considerable interest due to their widespread potential applications. Especially pH-responsive behavior could be easily implemented. In this work, we reported a pH-responsive Pickering emulsion based on amphiphilic graphene quantum dots at a low concentration which shows a great potential from the environmental and economic perspective. The stimuli responsive properties would make the smart Pickering emulsifiers recyclable and reusable., Experiments: The amphiphilic-adaptable graphene quantum dots functionalized by alkyl groups (C-GQDs) were synthesized by a facile one-step pyrolysis method. The pH-responsive emulsion performances were investigated, and the mechanism of pH-responsive of C-GQDs was studied by dynamic light scattering., Findings: The amphiphilicity of C-GQDs could be acquired controllably and effectively by this facile one-step pyrolysis method, which are able to stabilize Pickering emulsion at a very low concentration (0.001%). The amphiphilicity of C-GQDs are capable of changing in response to environmental stimuli. When the pH value of aqueous solution adjusts to 2, these C-GQDs aggregate in contrast to their stability in neutral condition due to the alternation of surface charges. The pH-responsive aggregation/ dispersion behavior of C-GQDs allows us to tune the interactions between oil-in-water emulsion droplets without introduction of destabilization agents. This will provide huge economic benefits in industrial applications in the future., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

The use of nanoscale metal-organic frameworks (MOFs) as drug delivery vehicles has attracted considerable attention in tumor therapy. In this study, novel biocompatible MOF-based nanocarriers were used as part of a facile and reproducible strategy for precision cancer theranostics. Both diagnostic (Mn 2+ ) and therapeutic compounds (doxorubicin, DOX) were incorporated into the multifunctional MOF-based nanocarriers, which exhibited high colloidal stability and promoted T 1 -weighted proton relaxivity and low-pH-activated drug release. The obtained MOF-based nanocarriers exhibited significantly high cellular uptake and efficient intracellular drug delivery into cancer cells, which resulted in high apoptosis and cytotoxicity, in addition to effectively inhibiting the migration of 4T1 breast cancer cells. Moreover, the MOF-based nanocarriers could intensively deliver diagnostic and therapeutic agents to tumors to enable precise visualization of the nanocarrier accumulation and accurate tumor positioning, diagnosis, and imaging-guided therapy using magnetic resonance imaging (MRI). In addition, the functional MOF-based nanocarriers exhibited effective ablation of the primary breast cancer, as well as significant inhibition of lung metastasis with a high survival rate. Therefore, the developed nanocarriers represent a viable platform for cancer theranostics., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Recently, the application of cheap, easily available biochar (BC) in advanced oxidation processes (AOPs) has received widespread attention. However, it is still a challenge to seek effective modification methods to prepare BC with high catalytic performance. In this study, a novel and environmentally friendly graphitized BC (WGBC) derived from wood chip was prepared, which exhibited excellent performance towards persulfate (PS) activation for sulfamethoxazole (SMX) removal as compared to original BC. Series characterizations confirmed that such improved catalytic performance was attributed to the well-established graphitic carbon structure and surface functionalized CO group. Free radical quenching and electron paramagnetic resonance (EPR) experiments qualitatively demonstrated that SO 4 ·- , ·OH, 1 O 2 and O 2 ·- were involved in the degradation of SMX, of which 1 O 2 and O 2 ·- played the dominant roles. Moreover, a non-radical process in the WGBC/PS system was also proposed, in which WGBC worked as an electron transfer bridge for allowing electrons to transfer from SMX to PS to participate in SMX degradation. The WGBC/PS system exhibited a high anti-interference ability to Cl - , H 2 PO 4 - , NO 3 - , and humic acid (HA)-containing environments. This study provides a new idea for designing and constructing environmentally friendly and efficient biochar towards organic pollutants removal., (Copyright © 2020 Elsevier Inc. All rights reserved.)

The integration of multiscale micro- and macroenvironment has been demonstrated as a critical role in designing biomimetic scaffolds for peripheral nerve tissue regeneration. While it remains a remarkable challenge for developing a biomimetic multiscale scaffold for enhancing 3D neuronal maturation and outgrowth. Herein, we present a 3D bioprinted multiscale scaffold based on a modular bioink for integrating the 3D micro- and macroenvironment of native nerve tissue. Gelatin methacryloyl (GelMA)/Chitosan Microspheres (GC-MSs) were prepared by a microfluidic approach, and the effect of these microspheres on enhancing neurite outgrowth and elongation of PC12 cells was demonstrated. The 3D multiscale composite scaffolds were bioprinted based on microspheres and hydrogel as the modular bioink. The co-culture of PC12 cells and RSC96 Schwann cells within these 3D biomimetic scaffolds were investigated to evaluate such a 3D multiscale environment for neurite outgrowth and Schwann cell proliferation. These results indicate that such multiscale composite scaffold with hydrogel microspheres provided a suitable 3D microenvironment for enhancing neurite growth, and the 3D printed hydrogel network provided a 3D macroenvironment mimicking the epineurium layer for Schwann cells proliferation and nerve cell organization, which is promising for the great potential applications in nerve tissue engineering., Competing Interests: Declaration of Competing Interest The authors declare no conflict of interest., (Copyright © 2020 Elsevier Inc. All rights reserved.)

It is important to develop a simple, facile and environmentally friendly strategy for improving the properties of materials in various energy storage systems. Herein, a binder-free anode based on self-assembled nanowires structures with GeSe particles is formed through a rapid box thermal deposition and first reported as an advanced anode for lithium/sodium-ion batteries. For LIBs, it delivers an excellent energy storage performance with high specific capacity (~815.49 mAh g -1 at 200 mA g -1 after 300 cycles), superior rate capability (~578.49 mAh g -1 for 10 cycles at 4000 mA g -1 ) and outstanding cycling stability (~87.78% of capacity retention after 300 cycles). It even shows a high reversible capacity of 359.5 mAh g -1 at 500 mA g -1 after 2000 cycles. For SIBs, it shows good cycling stability (~433.4 mAh g -1 at 200 mA g -1 after 50 cycles with ~85.3% capacity retention) and rate performance (~299.7 mAh g -1 for 10 cycles at 1000 mA g -1 ). In this electrode, GeSe nanowires (GeSe-NWs) consist of nanoparticles with voids between them that shorten the diffusion length for lithium/sodium ions and electrons and buffer the volumetric variation during the lithium/sodium ion insertion/extraction process. In addition, the introduction of Ni foam frameworks enhances the electrical conductivity of the electrode and retains the structural integrity upon cycling. This approach provides a new perspective for investigating and synthesizing various novel and suitable materials for energy storage fields., Competing Interests: Declaration of Competing Interest There are no conflicts of interest to declare., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Hypothesis: Membrane filtration is a promising technology for the treatment of alkali/surfactant/polymer (ASP) flooding oilfield wastewater, which contains high concentration of salt, surfactant, polymer and crude oil. The interactions of key foulants may influence the degree of membrane fouling. By comparing flux decline and interfacial free energies, it should be possible to derive the foulants governing the interactions with the membrane., Experiments: Polytetrafluoroethylene microfiltration membrane was employed to treat eleven types of model solutions to understand the effect of the interactions of key foulants on membrane fouling. The extended Derjaguin-Landau-Verwey-Overbeek theory was used to quantify the foulant-membrane and foulant-foulant interaction energies. The cake models were implemented to analyze the fouling form. Fourier transform infrared spectroscopy, atomic force microscopy, and contact angle were used to study the surface properties of various membranes., Findings: Microfiltration experiments and thermodynamic analysis revealed that both ions and sodium dodecylbenzenesulfonate could mitigate membrane fouling caused by anionic polyacrylamide (APAM) and crude oil. Moreover, APAM would produce a "shielding effect" on crude oil fouling. In addition, complete pore blocking, which primarily occurred on the membrane surface and formed a fouling layer, was the dominant form of membrane fouling., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Inc. All rights reserved.)

At present, environmental pollution caused by refractory organic pollutants becomes more serious. Semiconductor-based photocatalysis technology, an idea and continuable technology by solar-light-driven, is widely employed to address this situation. Here, oxygen-vacancy rich WO 3 decorated monolayer Bi 2 WO 6 nanosheet composite as an atomic scale heterojunction with high active species and ultrafast charge carrier transfer was rationally constructed. The atomic scale V o -WO 3 /Bi 2 WO 6 composite displayed remarkable photoactivity comparing with pristine V o -WO 3 and Bi 2 WO 6 ultrathin nanosheet, and about 79.5% of Ciprofloxacin can be degraded within 120 min under visible light irradiation when 40 mg of photocatalyst was added into CIP solution (10 mg/L). The promoted photoactivity can be ascribed to the following points: (1) the composite possesses enormous surface pit, thereby expanding the species surface area and exposing more active site to promote antibiotic absorption; (2) the presence of abundant oxygen vacancy can facilitate the formation of more electrons, which can be consumed by adsorbed molecular oxygen to produce superoxide radical, thereby accelerating degradation organic pollutant; (3) ultrathin V o -WO 3 nanosheet decorated monolayer Bi 2 WO 6 can shorten the charge carrier transfer distance and enlarge interface contact area, then ensuring remarkable photodegradation efficiency. The reasons for promoted photodegradation efficiency were elaborated based on experiments results and ESR analysis and the degradation pathways of CIP were recorded via [(LC-MS)/MS]. After 5 run for the degradation of CIP, V o -WO 3 /Bi 2 WO 6 composite also exhibited great photodegradation efficiency, thereby demonstrating its excellent stability and reusability., (Copyright © 2019 Elsevier Inc. All rights reserved.)

As a sustainable and cost-efficient technique, photocatalytic technology provides an ideal method for energy utilization and environmental pollution control. The current photocatalyst is commonly based on single charge transfer approach, which cannot meet the demand of rapidly charge transfer to improve the photocatalytic performance. Herein, a novel Ag 3 PO 4 /MWCNT/Bi 2 WO 6 Z-scheme heterojunction photocatalyst with multiple charge-carrier transfer channels was successfully prepared by a simple hydrothermal and deposition procedure, which possessed remarkable charge carriers separation efficiency and broad photoabsorption: (i) Z-scheme charge transfer channel was formed by Ag 3 PO 4 , Bi 2 WO 6 and Ag; (ii) Ag showed the "electron sink" property and surface plasmon resonance (SPR) effect; (iii) multi-walled carbon nanotube (MWCNT) can act as electron accepter to improve the transfer efficiency of photoinduced electron. Ag 3 PO 4 /MWCNT/Bi 2 WO 6 composite shows excellent visible light drive photocatalytic performance for organic pollution degradation. And the degradation pathways of tetracycline (TC) were investigated at length. In addition, the cyclic experiments confirmed that the photocatalytic stability of Ag 3 PO 4 /MWCNT/Bi 2 WO 6 . The hole (h + ) and superoxide radical (O 2 - ) radicals were confirmed that played a key role in the photodegradation system. This work provides inspiration for rational fabrication of excellent photocatalyst with multi-charge carrier transfer channels to meet increasing environmental requirements., (Copyright © 2019 Elsevier Inc. All rights reserved.)

Traditional method to functionalize mesoporous silica nanoparticles with organic groups for removal of contaminants from wastewater was surface modification. However, this surface modification could not cover the entire surface, leading to incomplete utilization of the high surface area of MSNs. In this work, we designed and prepared a novel inorganic-organic hybrid nanomaterial: ferrocene incorporated mesoporous organosilica nanoparticles (MONs). Owing to the mesoporous structure, large surface area and the ferrocene group in the framework, MONs could adsorb phosphate anion more efficiently with adsorption capacities up to 1299 mg/g than surface modified MSNs (SiO 2 -Fe) (488 mg/g). Congo red (CR) and Pb 2+ were also used as the model contaminants, and the results indicated that MONs is a superior absorbent comparing with ferrocene surface modified MSNs., (Copyright © 2019 Elsevier Inc. All rights reserved.)

High-quality Cu 2 ZnSnS 4 (CZTS) thin films prepared by spray pyrolysis on a Mo-coated glass substrate were used for solar water splitting in this study. Modification of a CdS layer under CZTS improved the photocatalysis efficiency by forming a pn junction between CdS and CZTS, effectively separating the photoexcited carriers without recombination. However, the photocorrosive nature of CdS induces poor stability of the CdS/CZTS photocathode. Surface protection of a CdS-covered CZTS photocathode by a ZnS layer resulted in efficient photoelectrochemical water splitting with a maximum half-cell solar to hydrogen (HC-STH) efficiency of 2.1% and without showing appreciable degradation. The ZnS layer acts as a mediator for efficient electron transport to Pt deposits and as a protective layer, preventing contact between the CdS layer and the outer electrolyte solution., (Copyright © 2018 Elsevier Inc. All rights reserved.)

A green synthesized gold-catalyst (PDA-g-C 3 N 4 /Au) for highly efficient reduction of nitroaromatics by NaBH 4 was proposed. Polydopamine (PDA) served as the reductant and stabilizer for AuNPs reduction, avoiding the use of chemical reductant and stabilizer that may result in secondary contamination. g-C 3 N 4 not only acted as the support but also provided compatibility for AuNPs deposition, enhancing the stability and deposition of AuNPs, which improved the catalytic activity. Different experimental parameters including the amount of Au loading, concentration of NaBH 4 , and dosage of catalyst were studied. Results showed that PDA-g-C 3 N 4 /Au (3) revealed higher catalytic activity with a rate constant of 0.0514 s -1 and TOF of 545.60 h -1 for 4-NP reduction. In addition, the catalyst was highly efficient in reduction of other nitroaromatics and the reduction rates of these compounds were found as the sequence: methyl orange > 2-nitrophenol > 2, 4-dinitrophenol > Erichrome Black T > Congo red. Moreover, the PDA-g-C 3 N 4 /Au (3) catalyst kept high stability and excellent conversion efficiency over ten reduction cycles. The practical application on different real water samples suggests that this Au catalyst has promising application in environmental water purification. The simple and green synthetic Au catalyst expands the range of application and provides potential application on environmental remediation., (Copyright © 2018 Elsevier Inc. All rights reserved.)

The reduction of nitrobenzene (NB) by Zn-substituted magnetite coupled with aqueous Fe(II) was studied. A series of Zn-substituted magnetites (Fe 3- x Zn x O 4 , x = 0, 0.25, 0.49, 0.74, and 0.99) were synthesized by a coprecipitation method followed by systematic analysis of the variation in structure and physicochemical properties of magnetite using XRD, TEM, TG, BET and XAFS. All of the samples had a spinel structure by Zn substitution. Zn 2+ primarily occupied the tetrahedral sites, but a portion of them moved to the octahedral sites at higher Zn level. Zn substitution increased the BET specific surface area and surface hydroxyl amount. The electron balance indicated that the NB reduction was primarily through the heterogeneous reaction by Fe 3- x Zn x O 4 and adsorbed Fe(II), where NB in aqueous solution was reduced by structural Fe 2+ in magnetite recharged by adsorbed Fe(II). Various factors, such as aqueous Fe(II) concentration, magnetite stoichiometry and Zn level, were investigated to illustrate their effects on the reduction processes. Both the rate constant k obs and electron transfer amount illustrated that Zn substitution generally improved the reduction activity of the Fe 3- x Zn x O 4 /Fe(II) system, while overdose of Zn retarded the process. This issue was attributed to the variation in electron conductivity of Fe 3- x Zn x O 4 and Zn 2+ occupancy., (Copyright © 2018 Elsevier Inc. All rights reserved.)

A novel adsorbent based on steel converter slag (SCS), useful for adsorbing cationic pollutants from water was prepared by a simple method. The characterization showed that salicylic acid-methanol (SAM) modification selectively removed calcium silicate minerals from the surface of SCS and lead to a prominent increase in the specific surface areas. The maximum adsorption capacity of SAM-modified SCS for methylene blue (MB) at initial pH of 7.0 and temperature of 293 K was 41.62 mg/g, which is 35.2-times higher than that of SCS (1.15 mg/g). Adsorption kinetics and isotherms of MB on the SAM-modified SCS can be satisfactorily fitted by pseudo-second order kinetic and Langmuir model, respectively, which suggest that single-layer chemical adsorption was mainly responsible for MB removal. Further studies showed that pH value and ionic strength of wastewater have minimal effects on the adsorption capacity of SAM-modified SCS. A small decrease (<10%) was found in the adsorption capacity of SAM-modified SCS after five cycles. These findings indicate that SAM-modified SCS is a promising adsorbent for the efficient removal of MB from aqueous solution due to its low cost, good thermal stability, excellent adsorption performance and simple separation., (Copyright © 2018 Elsevier Inc. All rights reserved.)

Magnetic chlorapatite nanoparticles (MNCLAP) was synthesized and used as adsorbent to remove Zn 2+ , Cd 2+ and Pb 2+ from aqueous solutions. The synthesized MNCLAP was characterized by scanning electron microscopy (SEM), energy dispersive analysis system of X-ray (EDAX), transmission electron microscopy (TEM) X-ray powder diffraction (XRD) and magnetization curves. Influence of different sorption parameters, such as equilibration time, initial heavy metal concentration, the amount of MNCLAP, pH values and competition adsorption were investigated in this study. Moreover, the desorption experiment was also carried out to explore the adsorption property of MNCLAP. The adsorption kinetic data has a very high correlation coefficient (R 2 =0.9999) with the pseudo-second-order kinetic model, and the Langmuir model was used in describing adsorption isotherms. The maximum adsorption capacities of MNCLAP adsorbent towards Zn 2+ , Cd 2+ and Pb 2+ were 1.1769, 1.1022 and 1.1546mmolg -1 , respectively. EDTA solution was the best efficient eluant for heavy metal desorption with 25.94%, 22.95% and 32.84% released rate of Zn 2+ , Cd 2+ and Pb 2+ , respectively. Experimental results revealed that the prepared MNCLAP combined both the properties of chlorapatite and magnetic material and it showed remarkable advantages in heavy metal removal from aqueous solutions., (Copyright © 2017 Elsevier Inc. All rights reserved.)

In this study, Cr(VI) removal by Zn-substituted magnetite coupled with aqueous Fe(II) through adsorption and reduction was investigated. A series of Zn-substituted magnetites (Fe 3- x Zn x O 4 , x=0, 0.25, 0.49, 0.74 and 0.99) were synthesized by a coprecipitation method, followed by systematic characterization, e.g., X-ray diffraction (XRD), thermogravimetry (TG), specific surface area and surface acid/base titration. The characterization results show that all samples had a spinel structure without an obvious alternation by Zn substitution. The BET surface area and surface site density gradually increased with Zn substitution. During Cr removal under neutral pH value, Cr(VI) was first adsorbed on the magnetite surface and then reduced to Cr(III) by Fe 3- x Zn x O 4 and adsorbed Fe(II); finally, it was immobilized on the Fe 3- x Zn x O 4 surface, which was verified via X-ray photoelectron spectroscopy (XPS) and X-ray absorption near edge spectroscopy (XANES) analyses and desorption experiment. With the increase in the Zn content in magnetite, the Cr removal efficiency initially decreased; then, it improved, which was ascribed to the decreasing Cr(VI) reduction and increasing Cr(VI) adsorption. This variation in activity by Zn substitution was discussed in terms of the reaction mechanism as well as the cationic microstructure and surface properties of Fe 3- x Zn x O 4 ., (Copyright © 2017 Elsevier Inc. All rights reserved.)

Based on rapid adsorption and incomplete reduction in Pd (II) ions by yeast, Pichia pastoris (P. pastoris) GS115, the effects of pretreatment on adsorption and reduction of Pd (II) ions and the catalytic properties of Pd NP/P. pastoris catalysts were studied. Interestingly, the results showed that the adsorption ability of the cells for Pd (II) ions was greatly enhanced after they were pretreated with aqueous HCl, aqueous NaOH and methylation of amino group. For the reduction in the adsorbed Pd (II) ions, more slow reduction rates by pretreated P. pastoris cells were displayed compared with the cells without pretreatment. Using the reduction of 4-nitrophenol as a model reaction, the Pd NP/P. pastoris catalysts based on the cells after pretreatment with aqueous HCl, aqueous NaOH and methylation of amino group exhibited higher stability than the unpretreated cells. The enhanced stability of the Pd catalysts can be attributed to smaller Pd NPs, better dispersion of the Pd NPs, and stronger binding forces of the pretreated P. pastoris for preparing the Pd NPs. This work exemplifies enhancing the stability of Pd catalysts through pretreatments., (Copyright © 2014 Elsevier Inc. All rights reserved.)

Ordered mesoporous carbon (Fe-CMK-3) with iron magnetic nanoparticles was prepared by a casting process via SBA-15 silica as template and anthracene as carbon source, was used as a magnetic adsorbent for the removal of anionic dye Orange II (O II) and cationic dye methylene blue (MB) from aqueous solution. TEM and magnetometer images showed that the iron magnetic nanoparticles were successfully embedded in the interior of the mesoporous carbon. The effect of various process parameters such as temperature (25-45°C), initial concentration (100-500 mg L(-1)) and pH (2-12) were performed. Equilibrium adsorption isotherms and kinetics were also studied. The equilibrium experimental data were analyzed by the Langmuir, Freundlich, Temkin and Redlich-Peterson model. The equilibrium data for two dyes adsorption was fitted to the Langmuir, and the maximum monolayer adsorption capacity for O II and MB dyes were 269 and 316 mg g(-1), respectively. Pseudo-first-order and pseudo-second-order kinetic and intraparticle diffusion model were used to evaluate the adsorption kinetic data. The kinetic data of two dyes could be better described by the pseudo second-order model. Thermodynamic data of the adsorption process were also obtained. It was found that the adsorption process of the two dyes were spontaneous and exothermic., (Copyright © 2014 Elsevier Inc. All rights reserved.)