Xiaolong Deng

Morphology-modulation of SnO2 Hierarchical Architectures by Zn Doping for Glycol Gas Sensing and Photocatalytic Applications.

The morphology of SnO2 nanospheres was transformed into ultrathin nanosheets assembled architectures after Zn doping by one-step hydrothermal route. The as-prepared samples were characterized in detail by various analytical techniques including scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and nitrogen adsorption-desorption technique. The Zn-doped SnO2 nanostructures proved to be the efficient gas sensing materials for a series of flammable and explosive gases detection, and photocatalysts for the degradation of methyl orange (MO) under UV irradiation. It was observed that both of the undoped and Zn-doped SnO2 after calcination exhibited tremendous gas sensing performance toward glycol. The response (S = Ra/Rg) of Zn-doped SnO2 can reach to 90 when the glycol concentration is 100 ppm, which is about 2 times and 3 times higher than that of undoped SnO2 sensor with and without calcinations, respectively. The result of photocatalytic activities demonstrated that MO dye was almost completely degraded (~92%) by Zn-doped SnO2 in 150 min, which is higher than that of others (MO without photocatalyst was 23%, undoped SnO2 without and with calcination were 55% and 75%, respectively).

Effects of architectures and H2O2 additions on the photocatalytic performance of hierarchical Cu2O nanostructures

Cu2O hierarchical nanostructures with different morphologies were successfully synthesized by a solvothermal method using copper (II) nitrate trihydrate (Cu(NO3)2⋅3H2O) and ethylene glycol (EG) as initial reagents. The obtained nanostructures were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) specific surface area test, and UV-vis spectroscopy. The synthesis conditions (copper source, temperature, and reaction time) dominated the compositions and the formation of crystals with different morphologies. The visible light photocatalytic properties of as-prepared Cu2O nanostructures were investigated with and without hydrogen peroxide (H2O2), and the effect of H2O2 were evaluated by monitoring the degradation of methyl orange (MO) with various amounts of H2O2. It was revealed that the degree of the photodegradation of MO depends on the amount of H2O2 and the morphology of Cu2O.

One-pot synthesis of Zn-doped SnO2 nanosheet-based hierarchical architectures as a glycol gas sensor and photocatalyst

Zn-doped SnO2 hierarchical architectures (ZSHAs) with controllable size have been prepared using a facile hydrothermal method, which are composed of two dimensional (2D) nanosheets with a thickness of about 40 nm. The properties of ZSHAs have been explored by gas sensing and photocatalysis testing. A sensor response (S = Ra/Rg) of 43 can be achieved at 100 ppm glycol, and the detection limit can reach down to the 5 ppm level with a response of about 5, combined with a low operating temperature of 240 °C, suggesting a promising application of ZSHAs in glycol gas sensing. Besides, the photocatalytic activities of ZSHAs have been evaluated by the degradation measurement of methylene blue (MB), methylene orange (MO), and rhodamine B (RhB). As a result, the ZSHAs demonstrate a much higher selectivity on the degradation of MB (91%) than that of MO (40%) and RhB (60%) in 60 min of measurement.

Constructing the novel ultrafine amorphous iron oxyhydroxide/g-C 3 N 4 nanosheets heterojunctions for highly improved photocatalytic performance

Ultrafine particles, more heterojunction interfaces and amorphous materials can effectively enhance the photocatalytic activity of photocatalysts. In this work, a facile in-situ precipitation method was developed to prepare ultrafine amorphous iron oxyhydroxide/ultrathin g-C3N4 nanosheets heterojunction composites. The amorphous iron oxyhydroxide possessed an ultrafine particle size and a wide range of visible light absorption. In this process, the ultrafine particles not only shortened the diffusion distance of photogenerated carriers, but also facilitated the formation of more heterojunctions with ultrathin g-C3N4 nanosheets. The photocatalytic activities were evaluated using rhodamine B, methylene blue, and methyl orange as pollution models under visible light irradiation. Notably, the optimal photocatalytic activity of a-FeOOH/CNNS-800 composite is ~17.8 times higher than that of CNNS towards the degradation of rhodamine B under visible light. The outstanding photocatalytic activities were ascribed to the narrower band gap, the enhanced visible light absorbance, abundant heterojunction interfaces, and the effective separation of the photogenerated charges driven by the matched band edge in the heterostructures. We trusted that the facile and easy-to-extend synthesis method can be further expanded to synthesize other ultrafine semiconductors coupled with g-C3N4 for enhancing the photocatalytic activities.

NiCo2O4-Based Supercapacitor Nanomaterials

In recent years, the research on supercapacitors has ushered in an explosive growth, which mainly focuses on seeking nano-/micro-materials with high energy and power densities. Herein, this review will be arranged from three aspects. We will summarize the controllable architectures of spinel NiCo2O4 fabricated by various approaches. Then, we introduce their performances as supercapacitors due to their excellent electrochemical performance, including superior electronic conductivity and electrochemical activity, together with the low cost and environmental friendliness. Finally, the review will be concluded with the perspectives on the future development of spinel NiCo2O4 utilized as the supercapacitor electrodes.

Stabilizing the Electrode/Electrolyte Interface of LiNi0.8Co0.15Al0.05O2 through Tailoring Aluminum Distribution in Microspheres as Long-Life, High-Rate, and Safe Cathode for Lithium-Ion Batteries

The unstable electrode/electrolyte interface of high-capacity LiNi0.8Co0.15Al0.05O2 (NCA) cathodes, especially at a highly delithiated state, usually leads to the transformation of layered to spinel and/or rock-salt phases, resulting in drastic capacity fade and poor thermal stability. Herein, the Al-increased and Ni-,Co-decreased electrode surface is fabricated through tailoring element distribution in micrometer-sized spherical NCA secondary particles via coprecipitation and solid-state reactions, aimed at stabilizing the electrode/electrolyte interface during continuous cycles. As expected, it shows much extended cycle life, 93.6% capacity retention within 100 cycles, compared with that of 78.5% for the normal NCA. It also delivers large reversible capacity of about 140 mAh g-1 even at 20 C, corresponding to energy density of around 480 Wh kg-1, which is enhanced by 45% compared to that of the normal NCA (about 330 Wh kg-1). Besides, the delayed heat emission temperature and reduced heat generation mean remarkably improved thermal stability. These foregoing improvements are ascribed to the Al-increased spherical secondary particle surface that stabilizes the electrode/electrolyte interface by protecting inner components from directly contacting with electrolyte and suppressing the side reaction on electrode surface between high oxidizing Ni4+ and electrolyte.

Low-temperature solution synthesis of CuO/Cu2O nanostructures for enhanced photocatalytic activity with added H2O2: synergistic effect and mechanism insight

CuxO (CuO, CuO/Cu2O, and Cu2O) nanostructures have been controllably synthesized through a facile low-temperature solution method. The morphologies and compositions of CuxO nanostructures were well controlled by tuning the reductant amount of hydroxylamine hydrochloride, which experienced the transformation of nanosheets to octahedrons as well as the phase change of CuO to Cu2O. The as-grown samples showed photodegradation selectivity to MO (maximum photocatalytic efficiency of 52% for methyl orange (MO) and 16% for rhodamine B (RhB) after 180 min photodegradation) and different photocatalytic activities in the absence or presence of H2O2 (62% without H2O2 and 82% with H2O2). The morphological transformations of as-grown samples were observed after the photocatalytic measurement in the presence of H2O2. The structural and morphological features after photodegradation were studied by XPS, SEM, and TEM investigations, revealing the possible mechanism of the as-prepared samples whereby the photodegradation of organic dyes occurred on the surface with respect to the adsorption ability, structure, and morphology of CuxO. In addition, H2O2 played an important role in the photodegradation of organic dyes.

Rare earth ion doped phosphors for dye-sensitized solar cells applications

Dye-sensitized solar cells (DSSCs) have attracted extensive attention as one of the promising alternatives to silicon solar cells. However, DSSCs have a maximum absorption in the visible light of solar spectrum, which confines their power conversion efficiency. Lots of research efforts have been focused on extending light absorption to enhance the conversion efficiency. Rare earth ion doped up/down conversion materials is an available approach to compensate for the non-absorbable wavelength region of DSSCs via converting ultraviolet and near-infrared radiation to visible emission. In addition to the light-harvesting enhancement, light-scattering effect and recombination loss can also be achieved in DSSCs by utilizing upconversion (UC) or downconversion (DC) materials. Moreover, the introduction of UC or DC facilitates to improve the stability of solar cells. In this review paper, the performance of dye-sensitized solar cells based on up or down conversion materials will be introduced.

One-pot hydrothermal synthesis of CdS decorated CuS microflower-like structures for enhanced photocatalytic properties

CdS decorated CuS structures have been controllably synthesized through a one-pot hydrothermal method. The morphologies and compositions of the as-prepared samples could be concurrently well controlled by simply tuning the amount of CdCl2 and thiourea. Using this strategy, the morphology of the products experienced from messy to flower-like morphologies with multiple porous densities, together with the phase evolution from pure CuS to the CdS/CuS composites. Serving as a photocatalyst, the samples synthesized with the addition of 1 mmol cadmium chloride and 3 mmol thiourea during synthetic process, showed the best photocatalytic activity, which could reach a maximum photocatalytic efficiency of 93% for methyl orange (MO) photodegradation after 150 min. The possible mechanism for the high photocatalytic efficiency of the sample was proposed by investigating the composition, surface area, structure, and morphology before and after photocatalytic reaction.

One-Step Solvothermal Method to Prepare Ag/Cu2O Composite With Enhanced Photocatalytic Properties.

Ag/Cu2O microstructures with diverse morphologies have been successfully synthesized with different initial reagents of silver nitrate (AgNO3) by a facile one-step solvothermal method. Their structural and morphological characteristics were carefully investigated by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), and the experimental results showed that the morphologies transformed from microcubes for pure Cu2O to microspheres with rough surfaces for Ag/Cu2O. The photocatalytic activities were evaluated by measuring the degradation of methyl orange (MO) aqueous solution under visible light irradiation. The photocatalytic efficiencies of MO firstly increased to a maximum and then decreased with the increased amount of AgNO3. The experimental results revealed that the photocatalytic activities were significantly influenced by the amount of AgNO3 during the preparation process. The possible reasons for the enhanced photocatalytic activities of the as-prepared Ag/Cu2O composites were discussed.