Publications by authors named "Guowang Diao"

During the reaction process in lithium-sulfur batteries, Lewis acidic lithium polysulfides (LiPSs) affect ion distribution and overall electrolyte stability, degrading battery performance and product distribution (e.g., LiS).

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Article Synopsis
  • Commercial graphite anodes are widely used due to their low potential and high conductivity, but they have a limited theoretical capacity of 372 mA h g.
  • Silicon (Si) anodes offer much higher capacity but face challenges like significant volume changes and low electronic conductivity.
  • The newly developed Si/RGtO@C composite anode shows improved performance, maintaining a discharged capacity of 367.6 mA h g after 300 cycles, indicating its potential for high-energy lithium-ion battery applications.
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Recently, research on polyoxometalates (POMs) has gained significant momentum. Owing to their properties as electronic sponges, POMs catalyst harbor substantial potential in lithium-sulfur battery research. However, POMs undergo a transformation into reduced heteropoly blue (HPB) during electrochemical reactions, which then dissolve into the electrolyte, resulting in catalyst loss.

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The advancement of Zn-Se batteries has been hindered by significant challenges, such as the sluggish kinetics of Se cathodes, limited Se loading, and uncontrollable formation of Zn dendrites. In this study, a bidirectional optimization strategy is devised for both cathode and anode to bolster the performance of Zn-Se batteries. A novel bowl-in-ball structured carbon (BIBCs) material is synthesized to serve as a nanoreactor, in which tin-based materials are grown and derived in situ to construct cathodes and anodes.

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Article Synopsis
  • High-performance rechargeable aluminum-sulfur batteries (RASB) show promise due to their high capacity, abundance of sulfur, and safety features, but face challenges like polysulfide diffusion and low sulfur efficiency.
  • Researchers developed a copper heterogeneous metal oxide catalyst, Cu/MoO@C, to improve sulfur utilization and electrical conductivity, effectively reducing the shuttle effect.
  • The new RASB boasts an impressive initial capacity of 875 mAh/g at 500 mA/g, maintaining 967 mAh/g even at elevated temperatures of 50°C, thanks to its unique nanostructure.
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Controlled aggregation is of great significance in designing nanodevices with high electrochemical performance. In this study, an aggregation strategy with cyclodextrin polymer (CDP) was employed to prepare polyaniline (PANI)/MXene (MX) composites. MXene served as a two-dimensional structure template.

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The electrocatalytic reduction of NO (NORR) holds promise as a sustainable pathway to both promoting the development of emerging NH economies and allowing the closing of the NO loop. Highly efficient electrocatalysts that could facilitate this complex six-electron transfer process are urgently desired. Herein, tremella-like CoNi-LDH intercalated by cyclic polyoxometalate (POM) anion PW (PW/CoNi-LDH) prepared by a simple two-step hydrothermal-exfoliation assembly method is proposed as an effective electrocatalyst for NO to NH conversion.

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Lithiumsulfur (Li-S) batteries are considered as promising candidates for next-generation batteries due to their high theoretical energy density. However, the practical application of Li-S batteries is still hindered by several challenges, such as the polysulfide shuttle and the growth of lithium dendrites. Herein, we introduce a bifunctional KPWO/graphene oxide-modified polypropylene separator (KPW/GO/PP) as a highly effective solution for mitigating polysulfide diffusion and protecting the lithium anode in Li-S batteries.

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Limited by preparation time and ligand solubility, synthetic protocols for cyclodextrin-based metal-organic framework (CD-MOF), as well as subsequent derived materials with improved stability and properties, still remains a challenge. Herein, an ultrafast, environmentally friendly, and cost-effective microwave method is proposed, which is induced by graphene oxide (GO) to design CD-MOF/GOs. This applicable technique can control the crystal size of CD-MOFs from macro- to nanocrystals.

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Al-S battery (ASB) is a promising energy storage device, notable for its safety, crustal abundance, and high theoretical energy density. However, its development faces challenges due to slow reaction kinetics and poor reversibility. The creation of a multifunctional cathode material that can both adsorb polysulfides and accelerate their conversion is key to advancing ASB.

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Developing polyoxometalate-cyclodextrin cluster-organic supramolecular framework (POM-CD-COSF) still remains challenging due to an extremely difficult task in rationally interconnecting two dissimilar building blocks. Here we report an unprecedented POM-CD-COSF crystalline structure produced through the self-assembly process of a Krebs-type POM, [Zn (WO ) (SbW O ) ] , and two β-CD units. The as-prepared POM-CD-COSF-based battery separator can be applied as a lightweight barrier (approximately 0.

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Aqueous zinc-ion batteries (AZIBs) are expected to be an attractive alternative in advanced energy storage devices due to large abundance and dependable security. Nevertheless, the undesirable energy density and operating voltage still hinder the development of AZIBs, which is intimately associated with the fundamental properties of the cathode. In this work, polyvinylpyrrolidone (PVP) intercalated Mn VO (PVP-MnVO) with a large interlayer spacing of 13.

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In this study, a strategy for the rapid and simple preparation of porous carbon (PC) using the microwave method was proposed. Oxygen-rich PC was synthesized by microwave irradiation in air, where potassium citrate and ZnCl served as the carbon source and microwave absorber, respectively. ZnCl achieves microwave absorption through dipole rotation, which uses ion conduction to convert heat energy in the reaction system.

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A novel supramolecular complex LiCl[(HPWO)(HCO)(CHCN)] {CR-PW12} was confirmed first to apply as a sulfur host in lithium-sulfur batteries. The {CR-PW12}@S cathode exhibits a reversible capacity of 1120 mA h g at 1.0 C and excellent cycle stability.

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Diphenylguanidine (DPG) is a widely used secondary accelerator for the vulcanization of natural rubber (NR) latex. However, its low water solubility and high toxicity limit its use in high-end NR products. In this study, a water-soluble inclusion complex of DPG and a -cyclodextrin polymer (-CDP), termed DPG--CDP, was prepared through supramolecular interactions and characterized using Fourier-transform infrared spectroscopy, H NMR, scanning electron microscopy, and UV-vis spectroscopy techniques.

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Vulcanization is an essential process to obtain high-performance rubber products. Diphenylguanidine (DPG) is often used as the secondary accelerator in the vulcanization process of natural rubber (NR) latex. However, DPG would make NR latex emulsion exhibit gelation, resulting in the negative vulcanization efficiency.

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In lithium-sulfur batteries, a serious obstacle is the dissolution and diffusion of long-chain polysulfides, resulting in rapid capacity decay and low Coulombic efficiency. At present, a common practice is designing cathode materials to solve this problem, but this gives rise to reduced gravimetric and volumetric energy densities. Herein, we present a thiodimolybdate [MoS] cluster as sulfur host material that can effectively confine the shuttling of polysulfides and contribute its own capacity in Li-S cells.

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By introducing a heteroatom into carbon material, an effective improvement in capacitance can be realized owing to surface oxidation and reduction reactions of pseudocapacitors. Herein, a simple one-pot carbonization activation method was proposed to convert potassium citrate into three-dimensional interconnected porous carbon (PC). Then, an effective double heteroatom doping method by thiourea was used to prepare nitrogen-sulfur-doped PC (N,S-PC).

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Reducing material accumulation and designing reasonable sizes are critical strategies for increasing the rate and cycling stability of electrode materials. Herein, we presented a double-walled hollow carbon spheres (DWHCSs) loading strategy for achieving ultrafine SnS nanosheet adhesion by utilizing three-sided active sites of the interior/exterior carbon walls. The structure effectively shortened the electron/ion transport path, increased the effective contact between electrolyte and electrode material, and promoted ion diffusion kinetics.

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Wearable supercapacitors based on carbon materials have been emerging as an advanced technology for next-generation portable electronic devices with high performance. However, the application of these devices cannot be realized unless suitable flexible power sources are developed. Here, an effective electrospinning method was used to prepare the one-dimensional (1D) and nano-scale carbon fiber membrane based on potassium citrate/polyacrylonitrile (PAN), which exhibited potential applications in supercapacitors.

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Engineering hierarchical nanostructures with enhanced charge storage capacity and electrochemical activity are vital for the advancement of energy devices. Herein, a highly ordered mesoporous three-dimensional (3D) nano-assembly of Nickel Cobalt Sulphide/Polyaniline @Polyoxometalate/Reduced Graphene Oxide (NiCoS/PANI@POM/rGO) is prepared first time via a simple route of oxidative polymerization followed by a hydrothermal method. Morphological analysis of the resulting hybrid reveals the sheet-like structures containing a homogeneous assembly of PANI@POM and NiCoS on the graphene exterior maintaining huge structural integrity, large surface area and electrochemically active centres.

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Dimeric mixed-ligand oxidovanadium complexes [VO(1,3-pdta)(bpy)]·9HO () and [VO(1,3-pdta)(phen)]·6HO () feature a symmetric binuclear structure bridged by 1,3-pdta, which is different from our previous reported asymmetric binuclear complex [VO(edta)(phen)]·11HO ().In this study, a wide range of analytical techniques were carried out to fully characterize the complexes and and further investigate their structural stabilities. Density functional theory calculations of and also suggest that they might have good reactivity with biomolecules as anticancer agents.

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Recently, electrochemistry- and photoelectrochemistry-based biosensors have been regarded as powerful tools for trace monitoring of carcinoembryonic antigen (CEA) due to the fact of their intrinsic advantages (e.g., high sensitivity, excellent selectivity, small background, and low cost), which play an important role in early cancer screening and diagnosis and benefit people's increasing demands for medical and health services.

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Lithium-sulfur batteries are one of the most promising next-generation energy storage systems. The efficient interconversion between sulfur/lithium polysulfides and lithium sulfide is a performance-determining factor for lithium-sulfur batteries. Herein, a novel strategy to synthesize a unique tube-in-tube CNT-wired sulfur-deficient MoS nanostructure embedding cobalt atom clusters as an efficient polysulfide regulator is successfully conducted in Li-S batteries.

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The rational design of hierarchical hollow nanomaterials is of critical significance in energy storage materials. Herein, dual-wall hollow nanospheres (DWHNS) Sn/MoS@C are constructed by confined growth and interface engineering. The inner hollow spheres of Sn/MoS are formed by atomic soldering MoS nanosheets with liquid Sn at high temperature.

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