Publications by authors named "Yang-Fan Xu"

Article Synopsis
  • Stable metal nitrides (MN) hold potential for creating "green" ammonia through catalysis and chemical looping, but their reduction to ammonia is hindered by stable M-NH surface species under mild conditions.
  • Researchers found that using supported platinum (Pt-Pt) atoms can help overcome the buildup of Ti-NH on titanium nitride (TiN), enabling the effective conversion of Ti-NH into free ammonia.
  • This study's insights could lead to the advancement of MN materials for more efficient ammonia production, challenging the traditional fossil fuel-driven Haber-Bosch process.
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Cobalt ferrite (CoFe O ) spinel has been found to produce C -C hydrocarbons in a single-step, ambient-pressure, photocatalytic hydrogenation of CO with a rate of 1.1 mmol g  h , selectivity of 29.8 % and conversion yield of 12.

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Halide perovskite single-crystals have recently been widely highlighted to possess high light harvesting capability and superior charge transport behaviour, which further enable their attractive performance in photovoltaics. However, their application in photoelectrochemical cells has not yet been reported. Here, a methylammonium lead bromide MAPbBr single-crystal thin film is reported as a photoanode with potential application in photoelectrochemical organic synthesis, 2,5-dimethoxy-2,5-dihydrofuran.

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Akin to single-site homogeneous catalysis, a long sought-after goal is to achieve reaction site precision in heterogeneous catalysis for chemical control over patterns of activity, selectivity and stability. Herein, we report on metal phosphides as a class of material capable of realizing these attributes and unlock their potential in solar-driven CO hydrogenation. Selected as an archetype, NiP affords a structure based upon highly dispersed nickel nanoclusters integrated into a phosphorus lattice that harvest light intensely across the entire solar spectral range.

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The performances of electron-transport-layer (ETL)-free perovskite solar cells (PSCs) are still inferior to ETL-containing devices. This is mainly due to severe interfacial charge recombination occurring at the transparent conducting oxide (TCO)/perovskite interface, where the photo-injected electrons in the TCO can travel back to recombine with holes in the perovskite layer. Herein, we demonstrate for the first time that a non-annealed, insulating, amorphous metal oxyhydroxide, atomic-scale thin interlayer (ca.

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The utilization of solar energy and the development of its related optoelectronic devices have become more important than ever. Solar cells or photoelectrochemical (PEC) cells that require the design of light harvesting assemblies for efficiently converting solar light into electricity or solar fuels are of particular interest. Semiconductor TiO, serving as the photoelectrode for photovoltaic devices (e.

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Though coating CsPbBr nanocrystal (NC) with an outer layer has been regarded as an effective strategy to address its instability issues, deep investigations into the electronic interaction between CsPbBr NC and coating layer have yet to be conducted. In this study, the dynamics of hot carrier and charge carrier of CsPbBr nanocrystal with various MO (M = Si, Ti, Sn) coating layers have been comprehensively studied. Combined transient optical characterizations (time-resolved photoluminescence and ultrafast transient absorption) and photoelectrochemical measurements reveal that coating with insulating SiO accelerates the hot carrier relaxation and enhances the radiative recombination by passivating surface traps, whereas efficient charge-carrier separation and extraction are observed after coating with SnO and TiO.

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Article Synopsis
  • The study investigates the controversial use of antioxidants, specifically glutathione (GSH), in combination with the chemotherapy drug doxorubicin (DOX), focusing on its effects on toxicity and efficacy during treatment.* -
  • Research using both animal models and cancer cell lines reveals that while GSH can reduce the cardiotoxic and hepatotoxic effects of DOX, it also diminishes DOX's anticancer effectiveness without affecting the drug's concentration in tumors.* -
  • The findings suggest that combining GSH with DOX in chemotherapy should generally be avoided, except in situations where DOX has caused significant liver or heart damage.*
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Lead halide perovskite nanocrystals (NCs) have demonstrated great potential as appealing candidates for advanced optoelectronic applications. However, the toxicity of lead and the intrinsic instability toward moisture hinder their mass production and commercialization. Herein, to solve such thorny problems, novel lead-free Cs AgBiBr double perovskite NCs fabricated via a simple hot-injection method are reported, which exhibit impressive stability in moisture, light, and temperature.

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Among the somatostatin analogues, octreotide (OCT) is the most commonly used in clinic via intravenous or subcutaneous injection to treat various diseases caused by increased secretion of growth hormone, gastrin or insulin. In order to assesse the feasibility of developing oral formulations of OCT, we conducted systematical pharmacokinetic and pharmacodynamic analyses of OCT in several animal models. The pharmacokinetic studies in rats showed that intragastric administration of OCT had extremely low bioavailability (<0.

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Transition metal phosphides have recently been regarded as robust, inexpensive electrocatalysts for both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). Thus far, tremendous scientific efforts have been applied to improve the catalytic activity of the catalyst, whereas the scale-up fabrication of morphology-controlled catalysts while maintaining their desired performance remains a great challenge. Herein, we present a facile and scalable approach to fabricate the macroporous NiP/nickel foam electrode.

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Halide perovskite quantum dots (QDs), primarily regarded as optoelectronic materials for LED and photovoltaic devices, have not been applied for photochemical conversion (e.g., water splitting or CO reduction) applications because of their insufficient stability in the presence of moisture or polar solvents.

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Cupric oxide (CuO), a narrow-bandgap semiconductor, has a band alignment that makes it an ideal photocathode for the renewable production of solar fuels. However, the photoelectrochemical performance of CuO is limited by its poor conductivity and short electron diffusion lengths. Herein, a three-dimensional (3D) architecture consisting of CuO nanosheets supported onto transparent conducting macroporous antimony-doped tin oxide (mpATO@CuONSs) is designed as an excellent photocathode for promoting the hydrogen evolution reaction (HER).

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Utilizing photoelectrochemical (PEC) cells to directly collecting solar energy into chemical fuels (e.g., H via water splitting) is a promising way to tackle the energy challenge.

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The scrupulous design of nanoarchitectures and smart hybridization of specific active materials are closely related to the overall photovoltaic performance of an anode electrode. Here we present a solution-based strategy for the fabrication of well-aligned metal oxide-based nanowire-nanosheet-nanorod hyperbranched arrays on transparent conducting oxide substrates. For these hyperbranched arrays, we observe a twofold increment in dye adsorption and enhanced light trapping and scattering capability compared with the pristine titanium dioxide nanowires, and thus a power conversion efficiency of 9.

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An unprecedented attempt was conducted on suitably functionalized integration of three-dimensional hyperbranched titania architectures for efficient multistack photoanode, constructed via layer-by-layer assembly of hyperbranched hierarchical tree-like titania nanowires (underlayer), branched hierarchical rambutan-like titania hollow submicrometer-sized spheres (intermediate layer), and hyperbranched hierarchical urchin-like titania micrometer-sized spheres (top layer). Owing to favorable charge-collection, superior light harvesting efficiency and extended electron lifetime, the multilayered TiO2-based devices showed greater J(sc) and V(oc) than those of a conventional TiO2 nanoparticle (TNP), and an overall power conversion efficiency of 11.01% (J(sc) = 18.

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Light-harvesting and charge collection have attracted increasing attention in the domain of photovoltaic cells, and can be facilitated dramatically by appropriate design of a photonic nanostructure. However, the applicability of current light-harvesting photoanode materials with single component and/or morphology (such as, particles, spheres, wires, sheets) is still limited by drawbacks such as insufficient electron-hole separation and/or light-trapping. Herein, we introduce a universal method to prepare hierarchical assembly of macroporous material-nanowire coated homogenous or heterogeneous metal oxide composite electrodes (TiO2 -TiO2 , SnO2 -TiO2 , and Zn2 SnO4 -TiO2 ; homogenous refers to a material in which the nanowire and the macroporous material have the same composition, i.

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The vertically oriented anatase single crystalline TiO2 nanostructure arrays (TNAs) consisting of TiO2 truncated octahedrons with exposed {001} facets or hierarchical TiO2 nanotubes (HNTs) consisting of numerous nanocrystals on Ti-foil substrate were synthesized via a two-step hydrothermal growth process. The first step hydrothermal reaction of Ti foil and NaOH leads to the formation of H-titanate nanowire arrays, which is further performed the second step hydrothermal reaction to obtain the oriented anatase single crystalline TiO2 nanostructures such as TiO2 nanoarrays assembly with truncated octahedral TiO2 nanocrystals in the presence of NH4F aqueous or hierarchical TiO2 nanotubes with walls made of nanocrystals in the presence of pure water. Subsequently, these TiO2 nanostructures were utilized to produce dye-sensitized solar cells in a backside illumination pattern, yielding a significant high power conversion efficiency (PCE) of 4.

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Hierarchical macroporous Zn(2)SnO(4) consisting of nanoparticles has been synthesized for the first time through an in situ hydrothermal and a following annealing process in the presence of a polystyrene (PS) template. Zn(2)SnO(4) macropore sizes are tuned in the range of 180-650 nm by selecting the appropriate size of PS spheres, and the building unit size of the Zn(2)SnO(4)macropore is 4.2 nm regardless of the PS sizes.

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Macroporous SnO2 composed of small SnO2 nanoparticles with diameters around 10 nm is prepared via a reflux process. This novel structure is designed as the photoanode in dye-sensitized solar cells (DSSCs), intending to improve the light utilization efficiency with its excellent light scattering ability. Though the dye adsorption of macroporous SnO2 (14.

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We report the innovative development of a double layered photoanode made of hierarchical TiO2 flowers (HTFs) as the overlayer and TiO2 nanoparticles (TNPs) as the underlayer, for dye-sensitized solar cells (DSSCs). They were prepared via a mild and simple one-step hydrothermal reaction of TiO2 nanoparticles/FTO glass substrate in an alkaline solution. The underlayer made of TNPs with a small size (20 nm in diameter) serves as a transparent photoanode for efficient dye adsorption.

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Hierarchical anatase TiO(2) nano-architecture arrays consisting of long TiO(2) nanowire trunk and numerous short TiO(2) nanorod branches on transparent conductive fluorine-doped tin oxide glass are successfully synthesized for the first time through a facile one-step hydrothermal route without any surfactant and template. Dye-sensitized solar cells based on the hierarchical anatase TiO(2) nano-architecture array photoelectrode of 18 μm in length shows a power conversion efficiency of 7.34% because of its higher specific surface area for adsorbing more dye molecules and superior light scattering capacity for boosting the light-harvesting efficiency.

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