A Surface Matrix of Au NPs Decorated Graphdiyne for Multifunctional Laser Desorption/Ionization Mass Spectrometry.

The development of the valid strategy to enhance laser desorption/ionization efficiency gives rise to widespread concern in surface-assisted laser desorption/ionization mass spectrometry (SALDI-MS) technology. Herein, a hybrid of Au NP-decorated graphdiyne (Au/GDY) was fabricated and employed as the SALDI-MS matrix for the first time, and a mechanism based on photothermal and photochemical energy conversions was proposed to understand LDI processes. Given theoretical simulations and microstructure characterizations, it was revealed that the formation of a coupled thermal field and internal electric field endow the as-prepared Au/GDY matrix with superior desorption and ionization efficiency, respectively. Moreover, laser-induced matrix ablation introduced strain and defect level into the Au/GDY hybrid, suppressing the recombination of charge carriers and thereby facilitating analyte ionization. The optimized Au/GDY matrix allowed for reliable detection of trace sulfacetamide and visualization of exogenous/endogenous components in biological tissues. This work offers an integrated solution to promote LDI efficiency based on collaborative photothermal conversion and internal electric field, and may inspire the design of novel semiconductor-based surface matrices.

Breathable Bactericide Piezocatalyst Integrating Anode-Cathode Heterojunction Capacitance on a Piezoelectric-Conductive Film.

Piezocatalysis has received great attention in recent years. However, despite the great promise therein, high-performance piezocatalysts are still rare and the principles in designing high-performance piezocatalysts remain lacking. We demonstrate here a novel piezocatalyst design by integrating the oxidizing and reducing reaction sites heterojunction on a piezoelectric and conductive matrix. The catalytic composite generates reactive oxidizing species with unprecedented high capabilities. The •O2- yield is over 400% that of previously reported catalysts and for the first time realized effective piezocatalytic bactericidal effects over 99%. A range of structural features, including proper energy band alignments, high capacitance, patterned high conductivity, voltage-regulated wettability, and effective piezoelectrical capability, are believed to synergize for their high piezocatalytic performance. This study has extended the piezocatalysts with new design principles, effective descriptors of merits, new applications, and effective performance capabilities.

Au NPs decorated holey g-C3N4 as a dual-mode sensing platform of SERS and SALDI-MS for selective discrimination of L-cysteine.

Development of reliable sensing strategy combining surface-enhanced Raman scattering (SERS) and surface-assisted laser desorption/ionization-mass spectrometry (SALDI-MS) is of significant interest to distinguish cysteine enantiomers in body fluid for understanding their physiological roles and toxicity hazards. In this work, a SERS/SALDI-MS dual-mode sensing platform of gold nanoparticles (Au NPs) decorated holey carbon nitride (hg-C3N4) was fabricated for sensitive detecting cysteine. The designed Au@hg-C3N4 matrix featured a uniform distribution of Au NPs with the help of anchoring effect of hg-C3N4 holey structure, which was conducive to produce highly repeatable signals. Moreover, the combination of Au NPs and holey g-C3N4 endowed this matrix with superior enrichment capacity, enhanced charge transfer and strong UV absorption. These merits allowed the matrix to acquire high sensitivity and enhanced reproducibility for l-cysteine by means of SERS/SALDI-MS. Likewise, reliable detection of l-cysteine and efficient recognition of d-cysteine in human serum jointly revealed its prospect for detecting cysteine enantiomers in body fluids. This work offers a reliable SERS/SALDI-MS strategy for determining L/D-cysteine enantiomers, and the designed Au@hg-C3N4 matrix becomes a potential application candidate for selective detection of bio-enantiomers.

Double-side effect of B/C ratio on BDD electrode detection for heavy metal ion in water.

BDD (Boron-doped Diamond) electrode may hold a promising application to detect heavy metal ions for actual water monitoring and early warning, but a poor understanding of influence mechanism of B/C ratio on detection performance is in the way of its fabrication and application. This work is intended to reveal the double-side effect of B/C ratio on detection performance of BDD electrode so as to facilitate its actual application. SBDD (Self-supported Boron-doped Diamond) electrode is introduced for the first time to get rid of the interference factors such as substrate. A systematic investigation is conducted for the influence of B/C ratio on microstructure and electrochemical behavior of SBDD electrodes. With the increase of B/C ratio, the grain size continuously increases, and the preferred orientation gradually changes from plane (220) to (111). The gradual increasing of impurity phase content indicates a deterioration of diamond phase quality. In addition, the electrode electrochemical behavior initially gets better then worse. SBDD electrode with a B/C ratio of 1/500 has the largest active surface area of 2.1 cm2, the smallest diffusion resistance and the highest signal response. Under optimal parameter set, the SBDD electrode enjoys a sensitivity of 0.42 µA L µg-1 cm-2 and a detection limit of 1.12 µg L-1 in a wide linear range of 5-120 ppb. The phase quality and grain morphology jointly contribute to the double-side effect. A suitable B-sp3-C content, preferred orientation of (111) and small particle size may make the performance improvement of BDD electrode available.

Influence of Alloy Substrate Treatment on Microstructure and Surface Performances of Arc-Ion Plated Gold-Like Film.

Three typical surface pretreatment strategies (grind, drawing, polishing) are employed to explore the influence of alloy substrate treatment on microstructure and surface performances of arc-ion plated TiN and ZrN films. The luminance and color of the films are measured by the color coordinate value of CIELab system (a color system which is defined by the International Commission on illumination). The crystal phases, morphology and microstructure are characterized and analyzed by scanning electron microscope (SEM) and X-ray powder diffraction (XRD). In addition, the anti-alkali, salt corrosion and anti-oxidation performances of films are systematically researched. The results show that the films with grinding pretreatment are more like gold color, "L" values are 77.27 cd/m² and 80.30 cd/m². The "b" value of TiN film is 29.96, which is the same as that of pure gold. The "a" value of ZrN film is 0.31, which is the same as pure silver. The density of TiN and ZrN films is the best, and both TiN and ZrN films were crystalline. They have the best anti-alkali and anti-oxidation performance. The films with drawing pretreatment show slant red color and have medium brightness values (74.07⁻76.37 cd/m²), worse compactness, obvious furrows and holes in their microstructures and worse salt corrosion and anti-oxidation performances. However, the TiN films are in amorphous states. The films with polishing pretreatment have the lowest brightness (72.66 cd/m²), gold-like color, superior compactness and best salt corrosion performance, which have a small number of holes. The TiN films with polishing pretreatment are also in amorphous state. Above all, alloy substrate pretreatment by grinding has the best gold-like color, brightness, compactness and corrosion resistance performance. This work exclusively sheds new light on surface pretreatment of alloy substrate by arc-ion plated films and also provides a reference for corrosion resistance performance of gold-like films.

Overexpression of HMGB1 A-box reduced lipopolysaccharide-induced intestinal inflammation via HMGB1/TLR4 signaling in vitro.

AIM: To investigate the inhibitory effects and mechanism of high mobility group box (HMGB)1 A-box in lipopolysaccharide (LPS)-induced intestinal inflammation. METHODS: Overexpression of HMGB1 A-box in human intestinal epithelial cell lines (SW480 cells) was achieved using the plasmid pEGFP-N1. HMGB1 A-box-overexpressing SW480 cells were stimulated with LPS and co-culturing with human monocyte-like cell lines (THP-1 cells) using a Transwell system, compared with another HMGB1 inhibitor ethyl pyruvate (EP). The mRNA and protein levels of HMGB1/toll-like receptor (TLR) 4 signaling pathways [including HMGB1, TLR4, myeloid differentiation factor88 (MYD88), Phosphorylated Nuclear Factor κB (pNF-κB) p65] in the stimulated cells were determined by real-time polymerase chain reaction and Western blotting. The levels of the proinflammatory mediators [including HMGB1, interleukin (IL)-1ß, IL-6 and tumor necrosis factor (TNF)-α] in the supernatants of the stimulated cells were determined by ELISA. RESULTS: EP downregulated the mRNA and protein levels of HMGB1, inhibited the TLR4 signaling pathways (TLR4, MYD88 and pNF-κB p65) and reduced the secretion of proinflammatory mediators (HMGB1, IL-1ß, IL-6 and TNF-α) in the SW480 and THP-1 cells activated by LPS but not in the unstimulated cells. Activated by LPS, the overexpression of HMGB1 A-box in the SW480 cells also inhibited the HMGB1/TLR4 signaling pathways and reduced the secretion of these proinflammatory mediators in the THP-1 cells but not in the transfected and unstimulated cells. CONCLUSION: HMGB1 A-box, not only EP, can reduce LPS-induced intestinal inflammation through inhibition of the HMGB1/TLR4 signaling pathways.