Comparable Characterization of Nanocellulose Extracted from Bleached Softwood and Hardwood Pulps

In this study, the characteristics of nanocellulose extracted from bleached softwood and hardwood pulps by formic acid hydrolysis followed by TEMPO-mediated oxidation were compared using transmission electron microscopy (TEM), atomic force microscopy (AFM), Fourier transform infrared analysis (FT-IR), X-ray diffraction (XRD), and thermal gravimetric analysis (TGA). The experimental results showed that the nanocellulose products derived from spruce pulp exhibited a relatively larger particle size, higher crystallinity, and higher thermal stability, compared with the corresponding products obtained from aspen pulp under the same conditions. Furthermore, the study helped establish that the properties of the nanocellulose products were highly dependent on the nature of the starting materials under identical processing conditions.     

A viewpoint on the gastrointestinal fate of cellulose nanocrystals

BackgroundCellulose nanocrystalline (CNC) particles possess unique functional properties such as vastly modifiable surface, considerable mechanical strength and acid resistance, as well as, high aspect ratio. CNCs have received great attention for application in diverse fields of technology including (composite) hydrogels fabrication for the gastric protection and enteral delivery of drugs and nutraceuticals.Scope and approachThe orogastrointestinal digestibility and absorbability of the orally administered CNCs is overviewed in the current article. At first, some surface charge-related characteristics of acid-isolated CNCs are communicated. Then, the biocompatibility and biodegradability of CNCs and CNC-reinforced hydrogels are reviewed, followed by presenting credible digestion and absorption scenarios. Finally, the post-absorption metabolism of CNCs is briefly debated.Key findings and conclusionsBacterial cellulose shows good biocompatibility and hemocompatibility. CNC oxidation provides biologically beneficial impacts; for instance, the TEMPO- and periodate-oxidized CNCs have been shown to regulate some blood metabolic variables and improve the degradability in simulated human blood plasma, respectively. Spherical and carboxyl-bearing cellulose nanoparticles can be isolated through ammonium persulfate digestion. The sphericity of particles results in faster cellular uptake. Negatively-charged CNCs are non-mucoadhesive and thus upon ingestion can penetrate into the buccal and intestinal mucosa. One may augment the absorption of CNCs by targeted receptor-mediated endocytosis. It was postulated that sodium bicarbonate secretion into the duodenum can alter CNCs surface chemistry and influence CNC interaction with gut microbiota.     

Carbon membrane bridged ZnSe and TiO2 nanotube arrays: Fabrication and promising application in photoelectrochemical water splitting

In this work, a cascade structure among ZnSe, carbon membrane and TiO₂ NTAs was constructed precisely. This carbon membrane bridged ZnSe and TiO₂ composite exhibits excellent H₂ evolution activity, the H₂ evolution rate of ZnSe/C/TiO₂ NTAs (866.76 μmol/cm²) is about 6.95 times higher than that of pure TiO₂ NTAs (124.64 μmol/cm²) after 200 min irradiation. The introduction of carbon membrane can greatly facilitate the electron transfer from ZnSe to TiO₂, ZnSe/C/TiO₂ ternary composite exhibits the highest transient photocurrent density (1.05 mA/cm²) and the lowest impedance (677.6 Ω) among all the samples. Besides, the contact between TiO₂ and electrolyte is improved after introducing carbon membrane, therefore C/TiO₂ NTAs shows more positive flat band potential of (1.86 V) compared with TiO₂ NTAs (0.50 V). It is also found that pure carbon powder can achieve H₂ production under visible light irradiation, its sensitization effect can further improve photocurrent density of the composite under 500 nm light radiation, the electrons produced in carbon film can inject into TiO₂, and holes from TiO₂ can quickly transfer to carbon film, leading to excellent H₂ evolution efficiency.     

碱性溶液中非晶/纳米晶Ni-Mo合金的形成机制研究

针对碱性溶液中Ni-Mo合金的形成机制,采用极谱法和循环伏安法进行研究。实验发现:Ni,Mo原子为多步氧化还原反应,Ni-Mo合金的形成过程为异常共沉积与诱导共沉积的复合沉积过程,进而形成致密光滑的结构镀层。非晶/纳米晶Ni-Mo合金具有一定的储氢能力,其化学活性较高,是较好的电极材料。     

II3V2 (II: Zn,Cd; V: P,As) Semiconductors: From Bulk Solids to Colloidal Nanocrystals

II₃V₂ semiconductors have become increasingly popular for a variety of applications including solar light harvesting, near‐IR imaging, and low energy light detection. The bulk physical and electronic structure of these materials is highlighted, followed by an in‐depth survey on progress in synthesizing these semiconductors as colloidal nanocrystals. Interestingly, no universal synthetic approach has yet been developed to access all compounds within this family. A discussion on how the complex crystal structure of these materials translates to small domain sizes will highlight current challenges in the characterization of II₃V₂ nanocrystals. Finally, potential avenues for further research will be proposed as a way to advance this field towards greater utilization in light harvesting applications.     

Structural,linear and third-order nonlinear optical properties of Cu nanocrystal in sodium borosilicate glass

Cu nanocrystals embedded in sodium borosilicate glass of varied Cu contents from 0.5 to 1.5 wt% have been successfully prepared through a sol–gel process. According to the results of X-ray diffraction (XRD) and the energy dispersive X-ray spectrometry (EDS), the metal Cu nanocrystals in cubic crystal system were well distributed inside glass matrix. Fourier Transform Infrared (FTIR) indicated the sodium borosilicate matrix had no major structural change for gels with different Cu contents. The optical absorption peaks due to the surface plasmon resonance of Cu particles were observed in the wavelength range of 550–600 nm. The absorption peak showed a red-shift trend with increasing Cu contents from 0.5 to 1.5 wt%. Transmission electron microscopy (TEM) revealed the existence of spherical Cu nanocrystals in the matrix. The diameter of Cu nanocrystals varied from 1 to 3.5 nm. Furthermore, the third-order nonlinear optical properties were investigated by Z-scan technique at 800 nm. Experimental results indicated the Cu nanocrystals have obvious positive refractive nonlinearities and reverse saturated absorption performance.     

Nanocrystallization and optical properties of CsPbBr3−xIx perovskites in chalcogenide glasses

The confinement of CsPbX₃ (X = Cl, Br, and I) perovskite nanocrystals (NCs) in a stabilized inorganic glass matrix is a new strategy for improving their long-term stability and promoting their applications in the optoelectronic field. Here, in situ nanocrystallization strategy is developed to precipitate CsPbBr_3?xI_x NCs with arbitrary I/Br ratio among an elaborately designed GeS₂–Sb₂S₃-based chalcogenide glass matrix. Spherical CsPbBr_3?xI_x NCs are homogeneously distributed in the glass matrix after thermal treatment. The photoluminescence (PL) spectra show that the emission peaks of CsPbBr_3?xI_x NCs can be tuned from 570 nm to 722 nm with the replacement of Br by I. The fs transient absorption (TA) spectra reveal that there exists some structural defects in the NCs, leading to short PL decay life. This work would shed light on confining CsPbX₃ NCs into glassy matrices, facilitating their future applications in photoelectronic fields.     

Microstructure and synthesis mechanism of dysprosia-stabilized zirconia nanocrystals via chemical coprecipitation

In this study, zirconia (ZrO₂) and dysprosia-stabilized zirconia (DySZ) nanocrystals were synthesized using a chemical coprecipitation method. The crystal structure and micromorphology of the as-synthesized powders, as well as the structural evolution from precursors to oxides were investigated, and the synthesis mechanism was also examined. Results show that pure ZrO₂ powders mainly comprise the monoclinic ZrO₂ phase with trace tetragonal ZrO₂, while the DySZ powders exhibit a tetragonal ZrO₂ structure. In addition, the crystal growth rate of DySZ is far slower than that of the pure ZrO₂ under elevated calcination temperature. The addition of Dy could significantly improve the phase stability of DySZ powder and effectively inhibit the crystal growth of DySZ. In the DySZ precursor, the binding energy of chemical bonds is significantly difference than in the ZrO₂ precursor. A composite hydroxide can be formed with -Zr-OH-Dy- and -Zr-OH-Zr- units in the tetramer structure because of the in-situ substitution of Zr by Dy atoms. Both the ZrO₂ and DySZ precursors exhibit analogous dehydration and crystallization behaviours in calcination process. Dy-doping plays a significant role in stabilizing both the intermediate product and the DySZ crystal.