Publications by authors named "Dai Yitao"

α-Proteobacteria have been repeatedly isolated from marine sponges and proposed to be beneficial to the host. Bacterial motility is known to contribute to host colonization. We have previously identified pseudovibriamides A and B, produced in culture by Ab134, and shown that pseudovibriamide A promotes flagellar motility.

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Although Pb-based metal halide perovskites (MHPs) have excellent photoelectric characteristics, their toxicity remains a limiting factor for their widespread application. In the paper, a series of CsCuClxBr3-x (x = 1, 2, 3) MHP microcrystals were developed and their hydrogen evolution performance in ethanol and HX (X = Cl, Br) was also studied. Among them, CsCuCl3 microcrystals exhibit high hydrogen evolution performance in both HX and ethanol, attributed to their longest average lifetime and suitable band structure.

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Article Synopsis
  • Selective hydrogenation is key for creating valuable chemicals and fuels, addressing fossil fuel issues and promoting green chemistry.
  • Understanding the efficiency of inexpensive, nonprecious metal catalysts is essential for improving industrial processes.
  • This review highlights recent advancements in synthesizing these catalysts for various hydrogenation methods and discusses ongoing challenges and future research directions.
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Niobium oxide (NbO) is a versatile semiconductor material with photochromic properties. This study investigates the local structure of noncrystalline, short-range-ordered niobium oxide synthesized via a sol-gel method. X-ray atomic pair distribution function analysis unravels the structural arrangements within the noncrystalline materials at a local scale.

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Hydrogen spillover widely occurs in a variety of hydrogen-involved chemical and physical processes. Recently, metal-organic frameworks have been extensively explored for their integration with noble metals toward various hydrogen-related applications, however, the hydrogen spillover in metal/MOF composite structures remains largely elusive given the challenges of collecting direct evidence due to system complexity. Here we show an elaborate strategy of modular signal amplification to decouple the behavior of hydrogen spillover in each functional regime, enabling spectroscopic visualization for interfacial dynamic processes.

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Near-infrared (NIR) photothermal therapy (PTT) is attractive for cancer treatment but is currently restricted by limited availability and insufficient NIR-II photoactivity of photothermal agents, for which artificial nanomaterials are usually used. Here, we report the first use of biogenic nanomaterials for PTT application. A fine-controlled extracellular biosynthesis of copper selenide nanoparticles (bio-CuSe) by MR-1 was realized.

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Halide perovskite materials, especially lead-based perovskites, have been widely used for optoelectronic and catalytic applications. However, the high toxicity of the lead element is a major concern that directs the research work toward lead-free halide perovskites, which could utilize bismuth as a promising candidate. Until now, the replacement of lead by bismuth in perovskites has been well studied by designing bismuth-based halide perovskite (BHP) nanomaterials with versatile physical-chemical properties, which are emerging in various application fields, especially heterogeneous photocatalysis.

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Photocatalysis is a promising yet challenging approach for the selective oxidation of hydrocarbons to valuable oxygenated chemicals with O under mild conditions. In this work, we report an atomically precise material model to address this challenge. The key to our solution is the rational incorporation of Fe species into polyoxotitanium cluster to form a heterometallic Ti Fe cocrystal.

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The groundwater environment often undergoes the transition from anoxic to oxic due to natural processes or human activities, but the influence of this transition on the fate of groundwater contaminates are not entirely understood. In this work, the degradation of tribromophenol (TBP) in the presence of environmentally relevant iron (oxyhydr)oxides (green rust, GR) and trace metal ions Cu(II) under anoxic/oxic-alternating conditions was investigated. Under anoxic conditions, GR-Cu(II) reduced TBP to 4-BP completely within 7 h while GR only had an adsorption effect on TBP.

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Reductive dechlorination of chlorinated organic pollutants (COPs) by Fe(II) occurs in natural environments and engineered systems. Fe(II) ions undergo hydroxylation in aqueous solutions to form Ferrous Hydroxyl Complex (FHC), which plays an essential role in Fe(II)-mediated reductive dechlorination. However, how hydroxyl groups of FHC bridge the electron transfer from Fe(II) to COPs is still not fully understood.

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Owing to the easy over-oxidation, it is a promising yet challenging task to explore renewable carbon resources to control the sunlight-driven selective catalytic oxidation of biomass-derived 5-hydroxymethylfurfural (HMF), producing important chemical feedstocks, namely, less-oxidized 2,5-diformylfuran (DFF) and 5-hydroxymethyl-2-furancarboxylic acid (HMFCA). Herein, we have developed a photocatalyst by anchoring a Ru complex on CdS quantum dots, which achieves selective oxidation of HMF toward DFF or HMFCA with high conversion (>81 %) and selectivity (>90 %), based on the controllable generation of two oxygen radicals under different atmospheres. Such selective conversion can also work well outside the laboratory by using natural sunlight.

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The aim of this study is to demonstrate the feasibility of a commercially available Auto-Planning module for the radiation therapy treatment planning for locally advanced nasopharyngeal carcinoma (NPC). 22 patients with locally advanced NPC were included in this study. For each patient, volumetric modulated arc therapy (VMAT) plans were generated both manually by an experienced physicist and automatically by the Auto-Planning module.

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Herein, we present a novel bottom-up preparation route for heptazine-based polymers (melon), also known as graphitic carbon nitride. The growth characteristics of isolated 1D melon strings in microporous templates are presented and studied in detail. Removal of the microporous silicate template via etching is accompanied by the self-assembly of a 1D melon to stacked 3D structures.

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Amorphous Ti O with high surface area has attracted significant interest as photocatalyst with higher activity in ultraviolet (UV) light-induced water splitting applications compared to commercial nanocrystalline TiO . Under photocatalytic operation conditions, the structure of the molecular titanium alkoxide precursor rearranges upon hydrolysis and leads to higher connectivity of the structure-building units. Structurally ordered domains with sizes smaller than 7 Å form larger aggregates.

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Although swarming motility and biofilms are opposed collective behaviors, both contribute to bacterial survival and host colonization. Pseudovibrio bacteria have attracted attention because they are part of the microbiome of healthy marine sponges. Two-thirds of Pseudovibrio genomes contain a member of a nonribosomal peptide synthetase-polyketide synthase gene cluster family, which is also found sporadically in Pseudomonas pathogens of insects and plants.

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The concept of being able to urinate in a cup and screen for colorectal cancer (CRC) is fascinating to the public at large. Here, a simple and label-free urine test based on surface-enhanced Raman spectroscopy (SERS) was employed for CRC detection. Significant spectral differences among normal, stages I-II, and stages III-IV CRC urines were observed.

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The exact formation mechanism of tantalum oxides (and in general, metal/mixed metal oxides) from alkoxide precursors is still not fully understood, particularly when forming cluster-like or amorphous materials. The structural evolution of Ta-based oxides was studied in detail using X-ray total scattering experiments along with subsequent pair distribution function (PDF) analyses. Starting from a tantalum alkoxide precursor (Ta(OEt)), the formation of hydrolysed TaOH clusters in highly diluted aqueous solution was analysed.

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Purpose: To develop and evaluate an automatic intensity-modulated radiation therapy (IMRT) program for cervical cancer, including a Convolution Neural Network (CNN)-based prediction model and an automated optimization strategy.

Methods: A CNN deep learning model was trained to predict a patient-specify set of IMRT objectives based on overlap volume histograms (OVH) and high-quality plan of previous patients. A total of 140 cervical cancer patients were enrolled in this study, including 100 patients in the training set, 20 patients in the validation set and 20 patients in the testing set.

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Background: To investigate the feasibility of a knowledge-based automated intensity-modulated radiation therapy (IMRT) planning technique for locally advanced nasopharyngeal carcinoma (NPC) radiotherapy.

Methods: One hundred forty NPC patients treated with definitive radiation therapy with the step-and-shoot IMRT techniques were retrospectively selected and separated into a knowledge library (n = 115) and a test library (n = 25). For each patient in the knowledge library, the overlap volume histogram (OVH), target volume histogram (TVH) and dose objectives were extracted from the manually generated plan.

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Although considerable progress has been achieved in the preparation of uniform hydrous TiO spheres (HTS) through the sol-gel process, there is plenty of room left in tailoring the size and morphology of HTS on the deep-submicron scale or even nanoscale since the diameters of the so far reported HTS are mostly on the (sub)micron scale (0.3-1.2 μm).

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Direct selective oxidation of hydrocarbons to oxygenates by O is challenging. Catalysts are limited by the low activity and narrow application scope, and the main focus is on active C-H bonds at benzylic positions. In this work, stable, lead-free, Cs Bi Br halide perovskites are integrated within the pore channels of mesoporous SBA-15 silica and demonstrate their photocatalytic potentials for C-H bond activation.

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Herein, an innovative approach was developed by using stable, lead-free halide perovskite for solar-driven organic synthesis. The ring-opening reaction of epoxides was chosen as a model system for the synthesis of value-added β-alkoxy alcohols, which require energy-intensive process conditions and corrosive, strong acids for conventional synthesis. The developed concept included the in situ preparation of Cs Bi Br and its simultaneous application as photocatalyst for epoxide alcoholysis under visible-light irradiation in air at 293 K, with exceptional high activity and selectivity ≥86 % for β-alkoxy alcohols and thia-compounds.

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The selective oxidation of primary alcohols to aldehydes by O instead of stoichiometric oxidants (for example, Mn , Cr , and Os ) is an important but challenging process. Most heterogeneous catalytic systems (thermal and photocatalysis) require noble metals or harsh reaction conditions. Here we show that the Bi O Br (OH) photocatalyst is very efficient in the selective oxidation of a series of aliphatic (carbon chain from C to C ) and aromatic alcohols to their corresponding aldehydes/ketones under visible-light irradiation in air at room temperature, which would be challenging for conventional thermal and light-driven processes.

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Nanozymes, nanoparticles that mimic the natural activity of enzymes, are intriguing academically and are important in the context of the Origin of Life. However, current nanozymes offer mimicry of a narrow range of mammalian enzymes, near-exclusively performing redox reactions. We present an unexpected discovery of non-proteinaceous enzymes based on metals, metal oxides, 1D/2D-materials, and non-metallic nanomaterials.

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