Synthesis and characterization of TiO2/hydrochar matrix composites for enhanced ammonia degradation.

This study explores the limitations of TiO2 as a photocatalyst, focusing on its narrow bandwidth and high electron-hole complexation probabilities that restrict its applications. A novel one-pot synthesis method for TiO2/hydrochar matrix composites is presented, with variations achieved through control of hydrothermal temperature, time, and loading concentration. The efficacy of these composites in ammonia removal is investigated, revealing optimal performance for the composite denoted as 3Ti-160-7, synthesized with a titanium salt concentration of 0.3 mol L-1, a hydrothermal temperature of 160 °C, and a hydrothermal time of 7 hours. Comparative analyses with commercial TiO2 (P25) and hydrochar demonstrate superior performance of 3Ti-160-7, exhibiting significantly lower ammonia concentration and reduced NO and NO2 concentrations. This research underscores the cost-effectiveness and application potential of TiO2/hydrochar matrix composites, offering valuable insights for the enhancement of photocatalytic activity and broader applicability in addressing TiO2-related challenges.

Shape Control of Carbon Nanoparticles via a Simple Anion-Directed Strategy for Precise Endoplasmic Reticulum-Targeted Imaging.

Herein, small-sized fluorescent carbon nanoparticles (CNs) with tunable shapes ranging from spheres to various rods with aspect ratios (ARs) of 1.00, 1.51, 1.89, and 2.85 are prepared using a simple anion-directed strategy for the first time. Based on comprehensive morphological and structural characteristics of CNs, along with theoretical calculations of density functional theory and molecular dynamics simulations, their shape-control mechanism is attributed to interionic interactions-induced self-assembly, followed by carbonization. The endoplasmic reticulum-targeting accuracy of CNs is gradually enhanced as their shape changes from spherical to higher-AR rods, accompanied by a Pearson's correlation coefficient up to 0.90. This work presents a facile approach to control the shape of CNs and reveals the relationship between the shape and organelle-targeting abilities of CNs, thereby providing a novel idea to synthesize CNs that serve as precise organelle-targeted fluorescent probes.

Tunable Organelle Imaging by Rational Design of Carbon Dots and Utilization of Uptake Pathways.

Employing one-step hydrothermal treatment of o-phenylenediamine and lysine to exploit their self- and copolymerization, four kinds of CDs (ECDs, NCDs, GCDs, and LCDs) are synthesized, possessing different surface groups (CH3, C-O-C, NH2, and COOH) and lipophilicity which endow them with various uptake pathways to achieve tunable organelle imaging. Specifically, highly lipophilic ECDs with CH3 group and NCDs with C-O-C group select passive manner to target to endoplasmic reticulum and nucleus, respectively. Amphiphilic GCDs with CH3, C-O-C and NH2 groups prefer caveolin-mediated endocytosis to locate at Golgi apparatus. Highly hydrophilic LCDs with CH3, NH2 and COOH groups are involved in clathrin-mediated endocytosis to localize in lysosomes. Besides, imaging results of cell division, three-dimensional reconstruction and living zebrafish demonstrate that the obtained CDs are promising potential candidates for specific organelle-targeting imaging.

ß-Naphthothiazolium-based ratiometric fluorescent probe with ideal pKa for pH imaging in mitochondria of living cells.

The weakly alkaline microenvironment (pH ~8.0) in mitochondria plays a vital role in maintaining its morphology and function. Thus monitoring mitochondrial pH (pHmito) is of great significance. Herein, a ratiometric fluorescent probe (ENBT) for pHmito imaging in mitochondria of living cells is reported. pH variation closely correlates to intramolecular charge transfer (ICT) from naphthol to ß-naphthothiazolium. ENBT exhibits a remarkable decrease on ratiometric fluorescence at λem1/λem2 = F595/F700 in response to pH variation within 6.30-9.29. In addition, ENBT has an ideal pKa value of 7.94 ± 0.08, which is advantageous in accurate sensing of pHmito. Moreover, ENBT has a Stokes shift of >150 nm, which effectively eliminates the potential interference from the excitation irradiation. ENBT shows excellent capability for specific staining of mitochondria with low cytotoxicity, which is most suitable for pHmito imaging in live cells. The probe was applied for monitoring pHmito variation in mitochondria of live cells caused by H2O2, NAC (N-Acetyl-l-cysteine), NH4Cl, carbonyl cyanide m-chlorophenyl hydrazone (CCCP) and lactate/pyruvate. The morphological alterations of mitochondria in living cells after treatment by CCCP were further evaluated.

Correction: Carbon dots with tunable dual emissions: from the mechanism to the specific imaging of endoplasmic reticulum polarity.

Correction for 'Carbon dots with tunable dual emissions: from the mechanism to the specific imaging of endoplasmic reticulum polarity' by Shuang E et al., Nanoscale, 2020, 12, 6852-6860, DOI: .

Green synthesis of aluminum-hydrochar for the selective isomerization of glucose to fructose.

Hydrochar microspheres supported Al catalysts with hierarchically porous structure (Al/HPHMs) for glucose to fructose isomerization were fabricated. Superior catalytic selectivity (93.3%) and fructose yield (32.6%) were achieved in aqueous under 160 °C for 20 min. Hierarchically porous structure was formed after KHCO3 and K2CO3 activation and the roles of KHCO3 and K2CO3 in controlling the Al phase and tailoring morphology of hydrochar supported Al were evaluated. The major active sites were characterized as Al hydroxides including ß-Al(OH)3, γ-Al(OH)3, γ-AlO(OH), Al-C-O linkages. Active sites by KHCO3 activation with high contents of Al-C-O and Al(OH)3 have better selectivity. Oxygen-containing functional groups including aluminum­oxygen groups on the hydrochar microspheres have contributed to the formation of hydrogen bond and π-π interactions between glucose and Al species. Green process synthesized aluminum-hydrochars have potential for their application as a variety of stable, recyclable, and efficient catalysts for lignocellulosic biorefining.

Corn stover valorization by one-step formic acid fractionation and formylation for 5-hydroxymethylfurfural and high guaiacyl lignin production.

One-step fractionation with concentrated formic acid at elevated temperatures with short retention time was investigated for corn stover valorization. Crude pulp (CP) with high purity of cellulose and FA-lignin (FAL) with high guaiacyl content were fractionated through one-step mild pretreatment. Formylation reaction on both CP and FAL fractions occurred during the pretreatment and improved the hydrophobicity and thermal stability of CPs and FALs. The presence of formyl group on CPs significantly inhibited the enzymatic hydrolysis efficiency for sugar production, however, the formylated cellulose showed super high reactivity and selectivity for HMF production through catalysis by maleic acid and aluminum chloride in acetonitrile-water co-solvent system. In addition, the fractionated FAL fraction exhibited a loose structure which is prominent for its further catalytic conversion into chemicals and energy.

Regulating the properties of carbon dots via a solvent-involved molecule fusion strategy for improved sensing selectivity.

Carbon dots (CDs) were prepared by a solvent-involved molecular fusion strategy using o-phenylenediamine (OPD) as the carbon source and formamide as the reaction solvent. The CDs possessed not only the functional groups inherited from the carbon source and the reaction solvent, but also numerous C=N groups in the structure, resulting from the Schiff base reaction between -NH2 of OPD and C=O of formamide. These functional groups endowed the final CDs with a favorable soft-base property, leading to the high tolerance level toward hard-acid type metal ions and prominent detection selectivity toward Ag+. Moreover, the obtained CDs displayed outstanding biocompatibility and low cytotoxicity, and demonstrated potential as an effective photoluminescence probe for intercellular Ag+ and Cys imaging, preventing the interference of autofluorescence from living tissues. This study focused on the solvent-involved molecular fusion strategy could provide new insights into the design of novel carbon-based nanostructures and optimization of the structure-property relationship of CDs.

Facile synthesis of metal-organic framework-derived SiW12@Co3O4 and its peroxidase-like activity in colorimetric assay.

Over the past few years, artificial enzymes have attracted enormous attention due to their high stabilities and cost-effective productions. In this work, metal-organic framework-derived SiW12@Co3O4 was synthesized in large quantities by stirring the mixture at ambient temperature and calcination. The obtained SiW12@Co3O4 exhibited a highly inherent peroxidase-like activity and excellent stability. Kinetic studies demonstrated that the synthesized SiW12@Co3O4 had a strong binding affinity to 3,3',5,5'-tetramethylbenzidine (TMB), stronger than HRP had. Specifically, the peroxidase-like activity of SiW12@Co3O4 in an aqueous solution was well maintained after incubation at an elevated temperature, at an extreme pH and for a long time. A SiW12@Co3O4-based method was further developed for H2O2 and one-pot glucose detection with good sensitivity and reliability. The facile synthesis approach is expected to facilitate the practical use of metal-organic frameworks and their derivatives as enzyme mimics in the future.