Publications by authors named "Qiurong Shi"

Article Synopsis
  • * The synthesis involves a quick reduction method using sodium borohydride to develop nanoparticle nests on a graphene support, which boosts performance due to improved catalytic activity and conductivity.
  • * NiFe NNG shows impressive efficiency with a low overpotential of 292.3 mV and stability, matching the performance of commercial catalysts, and its unique properties suggest it's promising for future energy storage and conversion applications.
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  • Fe-N-C single-atomic metal site catalysts (SACs) are being explored as alternatives to platinum-based catalysts for oxygen reduction reactions in fuel cells.
  • Researchers aim to enhance the efficiency of these catalysts by modifying the electronic structure of their active sites, particularly through the use of heteroatom doping.
  • The study introduces chlorine as a near-range coordinator to improve the Fe-N active center, resulting in a catalyst (FeNCl SAC) that shows higher ORR activity compared to traditional FeN SAC, supported by theoretical calculations and experimental results.
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  • * A new sensor was created to detect diaminochlorotriazine (DACT), a significant metabolite of the widely used herbicide atrazine, using a lateral flow immunoassay (LFIA) based on gold-platinum-palladium nanoparticles.
  • * This detection method demonstrates high sensitivity with a limit of 0.7 ng/mL, achieving even lower detection at 11 pg/mL, and includes a 3D printed device for real-time monitoring of color intensity related to pesticide exposure.
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We elucidate the structural evolution of CoN sites during thermal activation by developing a zeolitic imidazolate framework (ZIF)-8-derived carbon host as an ideal model for Co ion adsorption. Subsequent in situ X-ray absorption spectroscopy analysis can dynamically track the conversion from inactive Co-OH and Co-O species into active CoN sites. The critical transition occurs at 700 °C and becomes optimal at 900 °C, generating the highest intrinsic activity and four-electron selectivity for the oxygen reduction reaction (ORR).

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Noble metal-based nanomaterials offer great potential as cargoes for multifunctional cancer treatment. In this research, Au eyeball-like nanoparticles (NPs) with open-mouthed Pd shells were synthesized and their surface was functionalized with cell-targeting ligand folic acid (FA) and photodynamic agent Chlorin e6 (Ce6). Due to the broad near-infrared (NIR) absorption band of eyeball-like bimetallic Au and Pd, the photothermal therapy effects of this nanomaterial were studied in MCF-7 cancer cells.

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Atomically dispersed and nitrogen coordinated single metal sites (M-N-C, M=Fe, Co, Ni, Mn) are the popular platinum group-metal (PGM)-free catalysts for many electrochemical reactions. Traditional wet-chemistry catalyst synthesis often requires complex procedures with unsatisfied reproducibility and scalability. Here, we report a facile chemical vapor deposition (CVD) strategy to synthesize the promising M-N-C catalysts.

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  • * Recent advancements have identified atomically dispersed transition metal and nitrogen co-doped carbon (M-N-C) catalysts as promising PGM alternatives, focusing on improving catalyst activity and stability for oxygen reduction reactions (ORR).
  • * Progress involves innovative synthetic strategies to enhance catalyst performance by optimizing active site density and structural design, although insights into how these catalysts translate to better membrane electrode assembly (MEA) performance remain limited.
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  • Recent advancements in electrocatalysts using single metal atoms supported by conductive carbon show potential to replace expensive platinum for oxygen reduction reactions in fuel cells and batteries.
  • Researchers developed a cost-effective method to synthesize isolated iron atoms using carbon nanotubes, which included a simple one-pot polymerization followed by pyrolysis.
  • The resulting electrocatalyst exhibited superior performance in oxygen reduction, surpassing commercial platinum-based catalysts in both alkaline and acidic solutions.
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Conventional lateral flow biosensing technologies face the dual formidable challenges of poor sensitivity and cumbersome quantitative devices. Here, we developed a Au@Pd nanopopcorn and aptamer nanoflower assisted lateral flow strip (ANAN-LFS) with a thermal signal output to improve detection sensitivity. Moreover, a smartphone-based thermal reader was designed and meticulously optimized to hand-held style, realizing the essential portability of this quantitative device.

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Substantial progress has been made in applying nanotubes in biomedical applications such as bioimaging and drug delivery due to their unique architecture, characterized by very large internal surface areas and high aspect ratios. However, the biomedical applications of organic nanotubes, especially for those assembled from sequence-defined molecules, are very uncommon. In this paper, the synthesis of two new peptoid nanotubes (PepTs1 and PepTs2) is reported by using sequence-defined and ligand-tagged peptoids as building blocks.

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  • Excessive use of herbicides and insecticides can lead to increased toxicity in the environment, necessitating rapid testing methods for residue detection.
  • A new two-dimensional (2D) nanosheet-based lateral flow immunoassay (LFI) was developed to detect the pesticides acetochlor and fenpropathrin simultaneously, utilizing smartphone technology for easier results interpretation.
  • The platform showed high sensitivity with detection limits of 0.63 ng/mL and 0.24 ng/mL for each pesticide, and its performance was verified by comparisons to gas chromatography, demonstrating reliability and potential for on-site applications.
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  • Nanomaterials known as 'nanozymes' are gaining attention for their low cost and ease of production, but they generally have lower catalytic activity compared to natural enzymes, limiting their applications in fields like sensing and biomedicine.
  • Researchers have developed a Fe-N-C single-atom nanozyme (SAN) that achieves high peroxidase-mimicking activity, nearly matching that of natural horseradish peroxidase (HRP), by utilizing atomically dispersed iron within a porous carbon structure.
  • The Fe-N-C SAN demonstrates exceptional stability and robustness in challenging environments, making it a promising alternative for sensitive biosensing applications, such as detecting butyrylcholinesterase (BChE) activity.
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Here, a label-free fluorescent sensor was developed for detection Fe (III) by utilizing the quenching effect of Fe (III) on the fluorescence of the hydroxyl functionalized metal-organic framework MIL-53(Fe)-(OH), which was synthesized by using a one-step solvothermal method. The specific binding interaction between Fe (III) and hydroxyl facilitated the absorption of free Fe (III) to MIL-53(Fe)-(OH) which leads to rapid fluorescent intensity quenching effect. The potential quenching mechanism was proved to be the photo-induced electron transfer (PET) from electron-rich ligands of MIL-53(Fe)-(OH) to the half-filled 3d orbitals of free Fe (III) in the sample solution.

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The oxygen evolution reaction (OER) is a kinetically sluggish anodic reaction and requires a large overpotential to deliver appreciable current. Despite the fact that non-precious metal-based alkaline water electrocatalysts are receiving increased attention, noble metal-based electrocatalysts (NMEs) applied in proton exchange membrane water electrolyzers still have advantageous features of larger current and power densities with lower stack cost. Engineering NMEs for OER catalysis with high efficiency, durability and utilization rate is of vital importance in promoting the development of cost-effective renewable energy production and conversion devices.

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  • A new method for removing ReO from water using electrically switched ion exchange (ESIX) with a composite material made from activated carbon and polypyrrole (AC-PPy) has been developed.
  • The AC-PPy composite demonstrated high capacity and stability for absorbing and releasing ReO ions quickly, accomplishing the process in just 60 seconds.
  • This method's effectiveness was supported by various characterization techniques, showing that the uptake and release of ReO can be precisely controlled by adjusting the electrochemical potential of the AC-PPy material.
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The conversion reaction-based lithium-sulfur battery features an attractive energy density of 2600 W h/kg. Nevertheless, the unsatisfied performance in terms of poor discharge capacity and cycling stability still hinders its practical applications. Recently, porous carbon materials have been widely reported as promising sulfur reservoirs to promote the sluggish reaction kinetics of sulfur conversion, tolerate volume expansion of sulfur, and suppress polysulfide shuttling.

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  • Researchers developed Fe-S-N codoped hollow and porous carbon nanorods (Fe-S-N HPCNRs) to enhance the performance of Fe-N-C catalysts for oxygen reduction reactions (ORR) by optimizing their composition and structure.
  • The HPCNRs were created using a method involving cysteine, Fe salt, and polydopamine-encapsulated ZnO nanorods, verified through various analytical techniques like electron microscopy and X-ray diffraction.
  • The new catalysts demonstrated superior ORR activity, long-term stability, and methanol tolerance compared to standard platinum (Pt/C) catalysts, indicating their potential for practical applications.
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In the conventional non-invasive cancer treatments, such as photodynamic therapy (PDT) and photothermal therapy (PTT), light irradiation is precisely focused on tumors to induce apoptosis via the generation of reactive oxygen species (ROS) or localized heating. However, overconsumption of oxygen and restricted diffusion distance of ROS limit the therapeutic effects on hypoxic tumors. Herein, we developed a platform for the rapid uptake of multifunctionalized Au@Pt nanoparticles (NPs) by mitochondria in cancer cells.

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  • Rational design of nonprecious metal catalysts for the oxygen evolution reaction (OER) is crucial for improving the water splitting process's efficiency and cost-effectiveness.
  • Transition-metal-based nanomaterials, specifically Co P@Co/nitrogen-doped carbon (Co P@Co/N-C), are highlighted for their high activity, low cost, and robust performance, developed through a simple sugar-blowing method and low-temperature phosphorization.
  • Co P@Co/N-C demonstrates superior OER performance compared to other alternatives, with significant stability and increased catalytic activity observed during testing, making it promising for broader applications, including methanol and glucose electrooxidation.
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  • Recent years have seen a surge in sustainable energy production, but current electrochemical systems face performance limitations, prompting research into more efficient electrocatalysts.
  • Single-atom catalysts (SACs) have gained attention due to their exceptional catalytic activity, stability, and complete atom utilization, making them promising for various reactions.
  • This Review highlights new synthesis and characterization methods for SACs, focusing on their applications in reactions like oxygen reduction, hydrogen evolution, and fuel cell resources, aiming to enhance electrocatalytic performance at the atomic level.
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Self-assembled M-N-doped carbon nanotube aerogels with single-atom catalyst feature are for the first time reported through one-step hydrothermal route and subsequent facile annealing treatment. By taking advantage of the porous nanostructures, 1D nanotubes as well as single-atom catalyst feature, the resultant Fe-N-doped carbon nanotube aerogels exhibit excellent oxygen reduction reaction electrocatalytic performance even better than commercial Pt/C in alkaline solution.

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  • Researchers synthesized bimetallic aerogels (PdCu, PtCu, AuCu) through a process that speeds up hydrogel formation by using higher temperatures.
  • The resulting PdCu aerogel features ultra-thin nanowire networks which significantly improve its ability to catalyze reactions.
  • This material shows strong potential for use in fuel cells, particularly for oxidizing ethanol.
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  • Porous 3D graphene-based hybrid materials (3D GBHMs) are innovative nanomaterials with enhanced properties used for energy storage and conversion, particularly as electrode materials.* -
  • Various synthesis methods enable the production of 3D GBHMs, allowing for precise control over their architecture, such as pore sizes and doping elements.* -
  • The review examines advancements in 3D GBHM applications in fuel cells, supercapacitors, and batteries, while addressing challenges and future directions for their practical implementation.*
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Morphology control is a promising strategy to improve the catalytic performance of Pt-based catalysts. In this work, we reported a facile synthesis of PtCu bimetallic alloy nanodendrites using Brij 58 as a template. The highly branched structures and porous features offer relatively large surface areas, which is beneficial to the enhancement of the catalytic activity for oxygen reduction reactions in fuel cells.

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Currently, Pt-based nanomaterials with tailorable shapes, structures, and morphologies are the most popular electrocatalysts for oxygen reduction reaction, which is a significant cathode reaction in fuel cells for renewable energy applications. We have successfully synthesized mesoporous core-shell Au@PtNi ternary metallic nanoparticles through a one-pot reduction method for cathodic materials used as oxygen reduction reaction catalysts. The as-synthesized nanoparticles exhibited superior catalytic activities and long-term stabilities compared with mesoporous core-shell Au@Pt nanoparticles and commercial Pt/C.

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