ELECTROCHIMICA ACTA
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2014
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IF 4.086
Shengjun Li,Zeng Chen,Tao Li,Huiping Gao,Chaochao Wei,Wei Li,Wenping Kong,Weifeng Zhang
Employing vertical nanosheet-structured films as photoanodes of quantum dot sensitized solar cells (QDSCs) might provide a direct pathway for the photo-exited electrons. Here, the vertical ZnO, ZnO/TiO 2 and TiO 2 nanosheet-structured films were prepared by a feasible deposition processes . These films were sensitized with CdS quantum dots and assembled with CuS counter electrodes to fabricate QDSCs. The photoelectric properties of ZnO/TiO 2 composite films were superior to both pure ZnO and TiO 2 films. The effects of TiO 2 coating were investigated using electrochemical impedance spectroscopy (EIS). It was found that the photo-excited electron lifetimes in the photoanode were significantly improved with TiO 2 layer. The optimum power conversion efficiency was about 1.95% under AM 1.5 G illumination (100 mW cm −2 ), with a short circuit current density, open circuit voltage, and fill factor of 6.11 mA cm −2 , 0.562 V and 0.57, respectively.
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ELECTROCHIMICA ACTA
·
2018
·
IF 5.116
Jianqing Zhou,Qiancheng Zhu,Hao Hu,Wenjuan Chen,Ying Yu
Spinel Li 4 Ti 5 O 12 known as a “zero-strain” anode material for Li-ion battery has attracted much attention because of its superior safety and stability. Herein, we report a novel H 2 O 2 -assisted one-step hydrothermal method to synthesize different ratio Li 4 Ti 5 O 12 /TiO 2 composites with the same amount of raw materials. For the first time, Li 4 Ti 5 O 12 was prepared directly from commercial titania with the presence of H 2 O 2 , and different proportion Li 4 Ti 5 O 12 /TiO 2 composites were fabricated only by adjusting the amount of H 2 O 2 . The reaction mechanism of the novel H 2 O 2 -assisted method was clearly investigated, and H 2 O 2 plays a crucial role in the formation of intermediate Li 1.81 H 0.19 Ti 2 O 5 ·2H 2 O. Further, the electrochemical performance of different ratio Li 4 Ti 5 O 12 /TiO 2 composites have been investigated. This facile method is also applicable for the preparation of Na 2 Ti 6 O 13 /TiO 2 material, and provides us the new way to fabricate composite materials.
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APPLIED SURFACE SCIENCE
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2015
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IF 2.711
Chongyi Li,Feng Xue,Enyong Ding,Xiaoling He
A unique organic–inorganic hybrid nanocomposite was designed and synthesized by chemically anchoring the cationic collagen-based derivatives onto the surface of Fe 3+ /TiO 2 nanospheres for the significant enhancement in photocatalytic activity under the visible light irradiation. The NMR analysis suggested the successful fabrication of cationic collagen-g-PDMC as grafted materials. In addition, the chemical structures, morphologies and properties of these samples were systematically characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Raman spectrum, ultra violet–visible spectroscopy (UV–vis), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and photoluminescence (PL). And obtained results clearly demonstrated that Fe 3+ ions diffusing into TiO 2 lattice could be responsible for slightly reducing the average diameter of nanospheres to about 125 nm, promoting phase transition from anatase to rutile to some extent and extending the light harvesting range into visible region markedly. Meanwhile, the achievement that collagen-g-PDMC molecules had been covalently immobilized onto the surface of Fe 3+ /TiO 2 nanoparticles was also well supported by the information acquired. Furthermore, the photocatalytic activities of all the as-prepared products were carefully evaluated by adopting photocatalytic decoloration of methyl orange (MO) solution under the solar direct irradiation, and the sample CFT-3 performed the best in the photocatalytic degradation process, which was mainly attributed to the energetic synergistic effect brought about by Fe 3+ ions doping and collagen-g-PDMC molecules immobilized on the surface.
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
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2022
·Vol. 169
·期 7
·076502
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IF 4.386
Zhuangzhuang Yin,Shihan Qi,Shangkun Deng,Jun Guo,Wei Gan,Peng Chen,Chunsheng Ding,Ziliang Li,Jianrou Li,Yuqing Lu,Ziwei Zhao,Qi Ling,Miao Zhang,Zhaoqi Sun
Transition metal sulfides are widely used for the modification of TiO2 to improve its light absorption range due to their small bandgaps. In this work, novel CoS/CuS/TiO2 was synthesized via a simple one-pot hydrothermal preparation method. Using various characterization techniques, CoS/CuS/TiO2 was found to demonstrate excellent photoelectrochemical performance and photocatalytic activity for the degradation of tetracycline hydrochloride. The CoS/CuS/TiO2 catalyst showcased a maximum photocurrent density of 55 μA cm−2, which was 7.8 times higher than that of unmodified TiO2 nanorods. Under visible light irradiation using Xe lamp, the photocatalytic degradation efficiency of CoS/CuS/TiO2 on tetracycline hydrochloride was found to be significantly improved, where it recorded an excellent degradation rate of 64.0% at 90 min. The charge transfer mechanism of the proposed material was also investigated.
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MICROPOROUS AND MESOPOROUS MATERIALS
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2016
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IF 3.349
Mingming Zou,Honghong Liu,Lu Feng,Fengqiang Xiong,Tiju Thomas,Minghui Yang
A simple solvothermal approach with post-calcination is used to obtain (Ag, Ag 2 O) co-loaded TiO 2 microspheres with high specific surface area (43.8 m 2 g -1 ) and desirable visible light photocatalytic degradation (64% after 2 h visible light irradiation). Generally, N-doping of TiO 2 via nitridation using NH 3 improves the visible light absorption property of material. However, nitridation of (Ag, Ag 2 O) co-loaded TiO 2 results in a deleterious impact on the photocatalytic performance (around 20% after 2 h visible light irradiation). This is because nitridation of Ag-Ag 2 O-TiO 2 results in (a) reduction of Ag 2 O to Ag and (b) Ag agglomeration and grain growth on TiO 2 particles. These results in fact imply that in as-synthesized (Ag, Ag 2 O) co-loaded TiO 2 systems, local surface plasmonic resonance (associated with of 5–12 nm Ag particles) aids in enhanced broad band visible light absorption; furthermore the heterojunction between TiO 2 and Ag 2 O improves efficiency with which photogenerated carriers become available for photocatalysis . In all cases we show through selective radical quenching experiments that singlet oxygen is the primary reason for the dye degradation observed.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
·
IF 5.518
Zhixuan Huang,Kaifeng Yu,Doudou Wang,Ye Zhang,Lili Li,Ce Liang
Herein, a facile way was reported for fabrication of the anode nanocomposites with efficient lithium/sodium storage and excellent cycling stability. Iron phytate nanoparticles embedded in TiO 2 (IP/TiO 2 ) was prepared by coaxial electrospinning with the aid of PAN and PVP. N, P-doped Fe 2 P@TiO 2 core-shell carbon nanofibers (Fe 2 P@TiO 2 /CNF) was prepared after heat treatment. When Fe 2 P@TiO 2 /CNF were introduced as a self-supporting anode in lithium/sodium-ion batteries, Fe 2 P core supplied high energy density , and N, P-doped carbon fiber could induce the structural defects, facilitate electron transport and improve electrical conductivity . Moreover, TiO 2 shell inhibited volumetric expansion and pulverization of Fe 2 P core and improved the cycling stability of the anode. The Fe 2 P@TiO 2 /CNF electrode exhibited a large reversible capacity (LIB: 1175.7 and SIB: 519.8 mAh g −1 ), excellent cycling ability and outstanding rate performance. As anode in LIBs for Fe 2 P@TiO 2 /CNF, capacitance and diffusion control played important roles in Li + intercalation and deintercalation, simultaneously. When Fe 2 P@TiO 2 /CNF anode was used in SIBs, capacitive control behavior occupied a major role and displayed outstanding electrochemical performance . This work offers a possibility for designing anode nanocomposite with outstanding capacity and cycling stability in lithium/sodium-ion batteries.
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ACS Applied Materials & Interfaces
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2023
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IF 9.5
Liang Dan,Hui Wang,Xiaobao Yang,Jiangwen Liu,Liuzhang Ouyang,Min Zhu
The practical applications of MgH2 as a high-density hydrogen carrier depend heavily on efficient and low-cost catalysts to accelerate the dehydriding/hydriding reactions at moderate temperatures. In the present work, this issue is addressed by synthesizing Nb-doped TiO2 solid-solution-type catalysts that dramatically improve the hydrogen sorption performances of MgH2. The catalyzed MgH2 can absorb 5 wt % of H2 even at room temperature for 20 s, release 6 wt % of H2 at 225 °C within 12 min, and the complete dehydrogenation can be achieved at 150 °C under a dynamic vacuum atmosphere. Density functional theory calculations reveal that Nb doping introduces Nb 4d orbitals with stronger interaction with H 1s into the density of states of TiO2. This considerably enhances both the adsorption and dissociation ability of the H2 molecule on the catalysts surface and the hydrogen diffusion across the specific Mg/Ti(Nb)O2 interface. The successful implementation of solid solution-type catalysts in MgH2 offers a demonstration and inspiration for the development of high-performance catalysts and solid-state hydrogen storage materials.
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CURRENT APPLIED PHYSICS
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2022
·
IF 2.856
Yuchen Fei,Xiaofang Ye,Aseel Shaker Al-Baldawy,Jing Wan,Jinshen Lan,Jingtian Zhao,Ziyun Wang,Shanzhi Qu,Rongdun Hong,Shengshi Guo,Shengli Huang,Shuping Li,Junyong Kang
Noble metal particles have been embedded in semiconductors to improve photocatalysis efficiently, but the high cost made this approach difficult to apply widely in industry. Herein titanium dioxide/reduced graphene oxide (TiO 2 /rGO) nanowires in a core-shell structure were prepared. The physicochemical properties and photocatalytic performance of the specimen were characterized in comparison with TiO 2 and TiO 2 /Pt nanowires. The rGO layer and Pt nanoparticles increased chemical states of the components, reduced bandgap energy of the nanowires, enhanced visible light absorption , improved conductance and capacitance significantly. The methylene blue as catalyzed by TiO 2 /Pt and TiO 2 /rGO nanowires was degraded to 7.9% and 8.4% in an hour, but retained 25.7% by the TiO 2 nanowires. The properties and function of TiO 2 /rGO nanowires were close to those of TiO 2 /Pt nanowires, while the rGO price was much lower than that of Pt, which was of great significance for the photocatalytic application of TiO 2 heterojunction materials in industry.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2020
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IF 7.489
Jianing Li,Qiancheng Zhang,Juming Liu,Mengran Yu,Huiyan Ma,Jucai Yang,Sheng Ye,Tomas Ramirez Reina,Jian Liu
It still remains challenge for expanding the photo-response range of TiO 2 with dominant {0 0 1} facets due to the hardly achieving modification of the electronic structure without destroying the formation of TiO 2 high energy facets. Herein, we report the construction of carboxylate species modified TiO 2 nanosheets with dominant {0 0 1} facets by employing ethanol as a carbon source through a low-temperature (300 °C) carbonization method. The as-obtained samples were investigated in detail by using various characterization techniques. The results indicate that the carboxylate species derived from the oxidation and carbonization of ethanol are coordinated to the {0 0 1} facets in a bidentate bridging mode. The electron-withdrawing carboxylate species induce TiO 2 to form a lower valence band edge and a narrower bandgap, which enhances the oxidation ability of photogenerated holes and expands the photo-response range. The partially carbonized carboxylate species can also act as a photosensitizer to induce visible-light photocatalytic activity of TiO 2 nanosheets. In addition, the carboxylate species can further promote the separation of photogenerated charge carriers. The findings of this work may provide a new perspective for tuning the band structure of TiO 2 with dominant {0 0 1} facets and improving its photocatalytic performance.
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JOURNAL OF PHYSICS-CONDENSED MATTER
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2019
·Vol. 31
·期 39
·395403
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IF 2.711
Fang Liu,Zhaohui Dong,Lijia Liu
Nanostructured anatase TiO2 undergoes pressure-induced phase transformation, and the transformation sequence is significantly different from the bulk counterpart. The size and the morphology are found both playing a critical role in the phase transformation behavior. In this work, we prepare anatase TiO2 microspheres using a hydrothermal method. By controlling the reaction time, hollow and solid spheres of similar diameters are prepared. TEM and XRD analysis reveals that these microspheres are aggregates of anatase nanocrystalline of size between 15–16 nm. The phase transformation behaviour under high temperature is examined in situ using both Raman spectroscopy and synchrotron x-ray diffraction. We find that although both solid and hollow spheres are micron-sized, they undergo phase transformation sequence similar to nanomaterials with size of several tens of nanometers. Hollow spheres exhibit a higher compressibility than the solid spheres. A detailed analysis based on the formation mechanism of the spheres is performed to explain the unique phase transformation behavior of these materials.
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JOURNAL OF MEMBRANE SCIENCE
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2017
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IF 6.035
Huiqing Wu,Yuejun Liu,Long Mao,Chunhai Jiang,Jiaming Ang,Xuehong Lu
To prepare an ultrafiltration membrane with simultaneous self-cleaning and self-protection abilities, TiO 2 -polydopamine (PDA) nanohybrid are facilely prepared and used to functionalize polysulfone (PSf) membrane matrix. In the TiO 2 -PDA nanohybrid , PDA spheres acts as an adhesive substrate to hold densely covered photocatalytic TiO 2 nanoparticles , and also serves as a free-radical scavenger to protect PSf membrane against the damage by free radicals produced by TiO 2 during UV exposure treatment. The spherical-shaped TiO 2 -PDA can be easily doped into PSf membrane via phase inversion method, which allows the hydrophilic TiO 2 -PDA spheres migrating to the hydrophobic PSf surface and benefiting the antifouling ability. As a result, the TiO 2 -PDA/PSf hybrid membrane exhibits excellent overall performances in separation efficiency, remarkable self-cleaning property and performance stability under UV irradiation, in comparison with PSf and TiO 2 /PSf membrane. The influence of TiO 2 -PDA content on the membrane properties is also investigated, and it is found the hybrid membrane with 0.8 wt% TiO 2 -PDA possesses the optimal performance.
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CERAMICS INTERNATIONAL
·
2022
·
IF 5.532
Xufeng Zhang,Huidan Zeng,Xin Wang,Weichang Li,Lili Hu,Shubin Chen
MgO–Al 2 O 3 –SiO 2 glass-ceramics have been widely used in military, industrial, and construction applications. The nucleating agent is one of the most important factors in the production of glass-ceramics as it can control the crystallization temperature or the grain size. In this study, we investigated the effect of replacing P 2 O 5 with different amounts of TiO 2 on the crystallization, structure, and mechanical properties of an MgO–Al 2 O 3 –SiO 2 system. The crystallization and microstructure were investigated by differential scanning calorimetry , Raman spectroscopy , X-ray diffraction, scanning electron microscopy, and transmission electron microscopy . The mechanical properties were investigated by measuring the Vickers hardness , Young's modulus , and fracture toughness. The results showed that adding TiO 2 favored the precipitation of fine grains and significantly increased the Vickers hardness, Young's modulus, and fracture toughness of the glasses. Introducing an appropriate amount of TiO 2 can make a glass structure more compact, promote crystallization, and improve the mechanical properties of MgO–Al 2 O 3 –SiO 2 glass-ceramics.
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