Publications by authors named "Fuhua Zhao"

All-solid-state lithium sulfide-based batteries (ASSLSBs) have drawn much attention due to their intrinsic safety and excellent performance in overcoming the polysulfide shuttle effect. However, the sluggish kinetics of LiS cathode severely impede commercial utilization. Here, a Cu, I co-doping strategy is employed to activate the kinetics of LiS to construct high-performance ASSLSBs.

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Background: Verticillium wilt, caused by the fungus Verticillium dahliae, is a soil-borne vascular fungal disease, which has caused great losses to cotton yield and quality worldwide. The strain KRS010 was isolated from the seed of Verticillium wilt-resistant Gossypium hirsutum cultivar "Zhongzhimian No. 2.

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A collaborative manipulation strategy of proper heat treatment and self-customized hydrofluoroether-based electrolyte design has been proposed for boosting the sodium-ion storage kinetics of Prussian white cathodes. Improved monoclinic phase stability and electrolyte-cathode compatibility are responsible for an impressive discharge capacity of 148.4 mA h g and excellent electrode reversibility.

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Sulfide solid-state electrolytes have garnered considerable attention owing to their notable ionic conductivity and mechanical properties. However, achieving an electrolyte characterized by both high ionic conductivity and a stable interface between the electrode and electrolyte remains challenging, impeding its widespread application. In this work, we present a novel sulfide solid-state electrolyte, LiPZnSF, prepared through a solid-phase reaction, and explore its usage in all-solid-state lithium sulfur batteries (ASSLSBs).

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Due to the high energy density, high safety, and low cost of sulfur, all-solid-state lithium-sulfur batteries (ASSLSBs) are considered one of the most promising next-generation energy storage devices. Nevertheless, the insufficient interfacial contact between solid electrolytes (SEs) and the active material of sulfur leads to inadequate electronic and ionic conduction, which increases interfacial resistance and capacity decay. In this paper, commercial carbon nanotubes (CNTs) are activated to form porous-CNTs (P-CNTs), which are used as sulfur-bearing matrix, forming S@P-CNTs-based composite cathodes for ASSLSBs.

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The pharmacokinetic profiles and bioequivalence of two cyclosporine oral solutions were investigated in cats. Twenty-four cats were randomly allocated to two equally sized treatment groups in a randomized four-cycle, and dual-sequence cross-over design. Test and reference articles were orally administered in a single dose of 7 mg/kg Bodyweight.

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To analyze the clinical features and the prognostic factors of early-stage external auditory canal carcinoma. Data from 36 patients with early-stage external auditory canal carcinoma(T1, T2) treated in Department of Otolaryngology, Xijing Hospital, Air Force Military Medical University from January 2008 to June 2020 were reviewed retrospectively, including clinical manifestations, surgical and treatment methods, pathological types and disease status. The relationship between survival rate and the prognostic factors was compared using Kaplan-Meier method, and the independent risk factors were analyzed by Cox proportional hazards model.

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This study proposes a one-step method for growing superhydrophobic carbon nanothorn arrays (NTAs) directly on various substrates. The fabricated carbon material (named methyl-substituted graphdiyne (MGDY)) comprises sp and sp carbons in a conjugated-backbone form, as well as methyl groups introduced into the framework as hydrophobic-enhanced functional groups. MGDY NTAs exhibit excellent hydrophobicity (contact angle ≥152°), substantial long-period hydrophobic durability (the contact angle decreased by only 3.

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The properties of graphdiyne (GDY), such as energy gap, morphology, and affinity to alkali metals, can be adjusted by including electron-withdrawing/donating groups. The push-pull electron ability and size differences of groups play a key role on the partial property adjusting of GDY derivatives MeGDY, HGDY, and CNGDY. Cyano groups (electron-withdrawing) and methyl groups (electron-donating) decrease the band gap and increase the conductivity of the GDY network.

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Here, a new approach to further improve graphdiyne (GDY) based materials by using benzyl disulfide (BDS) as the sulfur source is demonstrated. The S radicals, generated from the homolysis of BDS, can react with the acetylenic bonds and be well confined in the triangle-like pores of GDY, forming S-GDY. The as-prepared S-GDY, which possesses numerous heteroatom defects and active sites, is suitable for applications in many electronic devices, such as lithium ion batteries (LIBs).

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On account of the high-cost of platinum, researchers are working to develop a new catalyst that is cheaper and has a catalytic effect equivalent to platinum. Herein, owing to the unique acetylenic bonds in graphdiyne, iron, nitrogen co-doped graphdiyne (Fe-N-GDY) is a promising nonprecious metal catalyst, which has been developed with just a small amount of iron precursor with the plan to substitute it for Pt-based catalysts. The as-synthesized Fe-N-GDY composited catalyst shows excellent catalytic performance with the onset potential of 0.

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Non-symmetric 1,3-substituted imidazopyridin-2-ones are a common structural scaffold found among many biologically active molecules. Herein we report an efficient, mild, and transition-metal free C-H amidation strategy to access such a pyrido-fused cyclic urea framework in good yields and with a broad functional group tolerance.

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A versatile controlled-release method was developed for the in situ growth of graphdiyne on arbitrary substrates. Cu2+-Ions escaped from the polyvinylpyrrolidone/copper acetate film on the surface of various substrates (e.g.

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Boron-graphdiyne (BGDY), which has a unique π-conjugated structure comprising an sp-hybridized carbon skeleton and evenlydistributed boron heteroatoms in a well-organized 2D molecular plane, is prepared through a bottom-up synthetic strategy. Excellent conductivity, a relatively low band gap and a packing mode of the planar BGDY are observed. Notably, the unusual bonding environment of the all sp-carbon framework and the electron-deficient boron centers generates affinity to metal atoms, and thus provides extra binding sites.

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Chlorine-substituted graphdiyne (Cl-GDY) is prepared through a Glaser-Hay coupling reaction on the copper foil. Cl-GDY is endowed with a unique π-conjugated carbon skeleton with expanded pore size in two dimensions, having graphdiyne-like sp- and sp - hybridized carbon atoms. As a result, the transfer tunnels for lithium (Li) ions in the perpendicular direction of the molecular plane are enlarged.

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Enzyme immobilization is believed to provide an excellent base for increasing environmental tolerance of enzyme and considerable period of time. In this work, a kind of nonporous silica nanoparticles functionalized with amino group was synthesized to immobilize proline-specific endoprotease (PSEP). PSEP is known to specifically cleave peptides (or esters) at the carboxyl side of proline, thus can prevent the formation of haze and prolong the shelf life of beer.

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A method was presented for fabricating the fluorescent nanocomposites containing CdTe quantum dots (QDs) and montmorillonite (MMT)-chitosan (CS). MMT-CS/CdTe QDs nanocomposites were prepared via a simple, versatile and robust approach combination of covalent and electrostatic assembly methods (Scheme 1). The negatively charged MMT was initially modified with positively charged CS through electrostatic assembly, followed by incorporation of CdTe-QDs into the MMT-CS nanosheets by covalent connections between the amino groups of CS and the carboxylic acid groups of thioglycollic acid (TGA).

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In this work, novel hybrid microbeads composed of chemically reduced graphene oxide (CRGO) and alginate were fabricated, which could encapsulate enzymes by a simple non-covalent adsorption-entrapment method. Compared with alginate gel beads, the intervention of CRGO in the alginate gel enhanced its mechanical strength, effectively prevented the leakage of enzyme, and greatly enhanced the stability and environmental tolerance. Compared with free enzymes or those on a single carrier, the enzyme encapsulated in these hybrid microbeads can retain its optimum activity within a broad range (temperature 45-60 °C, pH 4-6).

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A bio-based hybrid film containing chitosan (CS) and silver nanowires (AgNWs) has been prepared by a simple casting technique. X-ray diffraction (XRD), Fourier infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and UV-visible spectroscopy were employed to characterize the structure of bio-based film. The bio-based hybrid film showed unique performance compared with bare chitosan film.

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We demonstrate a novel method for fabricating glass microlens (arrays) with single step on conventional lens surface. In this method, the glass microlens can be achieved by only one step with sol gel glass material. The microlens aperture and focus length can be controlled easily and uniformly.

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