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TiO2
Journal of Materials Chemistry A · 2018 ·Vol. 6 ·期 17 ·7409-7419 · IF 9.931

15% efficient carbon based planar-heterojunction perovskite solar cells using a TiO2/SnO2 bilayer as the electron transport layer

Zhiyong Liu,Bo Sun,Xingyue Liu,Jinghui Han,Haibo Ye,Yuxue Tu,Chen Chen,Tielin Shi,Zirong Tang,Guanglan Liao

Perovskite solar cells (PSCs) are one of the most promising lab-scale technologies to deliver inexpensive solar electricity. Low-temperature printable carbon counter electrode based planar-heterojunction PSCs are particularly suitable for future large-scale manufacturing, but suffer from an inferior efficiency. Here, we demonstrate a TiO2/SnO2 bilayer as the electron transport layer (ETL) for carbon counter electrode based planar-heterojunction PSCs together with micromolecule Cu-phthalocyanine (CuPc) as the hole transport layer (HTL), yielding a high power conversion efficiency of 15.39% and an excellent stability over 1200 h. The improved performances are attributed to a better energy level transition, a suppressed electron–hole recombination, and a wider depletion region of the TiO2/SnO2 bilayer. Our work represents a great advancement in the fabrication and popularization of carbon counter electrode based PSCs. More importantly, the whole devices are processed at a temperature below 200 °C, providing potential application of PSCs in monolithic tandem devices and paving the way for the development of carbon based flexible PSCs.

✓ 已验证 DOI 高影响因子
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Journal of Materials Chemistry A · 2017 ·Vol. 5 ·期 21 ·10591-10598 · IF 8.867

A novel architecture of dandelion-like Mo2C/TiO2 heterojunction photocatalysts towards high-performance photocatalytic hydrogen production from water splitting

Xinzheng Yue,Shasha Yi,Runwei Wang,Zongtao Zhang,Shilun Qiu

In the development of photocatalytic hydrogen (H2) production, designing and optimizing photocatalyst nanostructures with efficient charge transfer and separation for catalytically active sites are still a great challenge. Herein, a well-controlled synthetic strategy is developed to prepare an Mo2C/TiO2 hetero-nanostructure, in which the TiO2 3D hierarchical configuration is loaded with highly dispersed Mo2C nanoparticles. This heterostructure achieves the excellent photocatalytic activity of 39.4 mmol h−1 g−1 with its rate ∼25 times higher than that of pristine TiO2. Also, our photocatalysts process excellent long-term durability (>20 h). The impressive photocatalytic H2 activity of Mo2C/TiO2 indicates favourable charge carrier dynamics, as determined by the results of photoluminescence (PL), time-resolved photoluminescence (TRPL), surface photovoltage (SPV), and open circuit potential (OCP) decay curves. Moreover, this study provides a guide for researchers to design new functional materials with excellent hydrogen production activity.

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Frontiers in Chemistry · 2022 · IF 5.545

Arrays of Ag-nanoparticles decorated TiO2 nanotubes as reusable three-dimensional surface-enhanced Raman scattering substrates for molecule detection

Zhai Haichao,Zhu Chuhong,Wang Xiujuan,Yuan Yupeng,Tang Haibin

Three-dimensional surface-enhanced Raman scattering (SERS) substrates usually provide more hot spots in the excitation light beam and higher sensitivity when compared with the two-dimensional counterpart. Here a simple approach is presented for the fabrication of arrays of Ag-nanoparticles decorated TiO2 nanotubes. Arrays of ZnO nanorods were fabricated in advance by a hydrothermal method. Then TiO2 nanotube arrays were achieved by immersing the arrays of ZnO nanorods in an aqueous solution of (NH4)2TiF6 for 1.5 h. Vertically aligned TiO2 nanotube arrays were modified with dense Ag nanoparticles by Ag mirror reaction. High density of Ag nanoparticles decorated on the fabricated TiO2 nanotubes provide plenty of hotspots for Raman enhancement. In addition, the fabricated array of Ag nanoparticles modified TiO2 nanotubes can serve as a reusable SERS substrate because of the photocatalytic activity of the TiO2 nanotubes. The SERS substrate adsorbed with analyte molecules can realize self-cleaning in deionized water after UV irradiation for 2.5 h. The sensitivity of the fabricated SERS substrate was investigated by the detection of organic dye molecules. The detectable concentration limits of rhodamine 6G (R6G), malachite green (MG) and methylene blue (MB) were found to be 10−12 M, 10−9 M and 10−8 M, respectively. The enhancement factor (EF) of the three-dimensional SERS substrate was estimated to be as high as ∼1.4×108. Therefore, the prepared Ag nanoparticles modified TiO2 nanotube arrays have promising potentials to be applied to rapid and trace SERS detection of organic chemicals.

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MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING · 2021 · IF 5.234

High-performance copper-matrix materials reinforced by nail board-like structure 2D Ti3C2Tx MXene with in-situ TiO2 particles

Lu Liu,Guobing Ying,Dong Wen,Yuexia Li,Kaicheng Zhang,Huihua Min,Cong Hu,Cheng Sun,Cheng Wang

Two-dimensional (2D) nanomaterials based on MXenes have gained increasing importance in the field of strength reinforcement. However, the easy oxidation of MXenes has long been deemed unfavorable for reinforcement in high-temperature processing. Herein, high-shear mixing was used in present work for simple and efficient dispersion of MXenes in copper powders. Partial MXene sheets were also in-situ oxidized to TiO 2 particles to form nail board-like structure reinforcement (NSR) during spark plasma sintering (SPS) process at 600 °C, which allowed one to significantly improve the yield strength of copper matrix by up to 70.3%. Experimental characterization and modeling simulations enabled one to identify second phase strengthening as the main reason for increased yield strength of the composites. In particular, the mechanical engagement of NSR played an important role in strengthening. Meanwhile, the hardness of TiO 2 particles on NSR was found to be higher than that of the copper matrix, leading to enhancement in compressive yield strength. Also, the presence of MXene sheets on NSR slightly reduced the resistance of copper matrix composites . In sum, these findings look promising for designing novel MXene reinforced metal matrix composites with improved mechanical properties.

✓ 已验证 DOI 高影响因子
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2021 · IF 8.128

Visible light-driven photoelectrocatalysis for simultaneous removal of oxytetracycline and Cu (II) based on plasmonic Bi/Bi2O3/TiO2 nanotubes

Jin Qin,Shangshi Ye,Kai Yan,Jingdong Zhang

A visible light-driven photoelectrocatalytic system was constructed based on Bi/Bi 2 O 3 /TiO 2 nanotubes (NTs) to treat wastewater containing oxytetracycline and Cu 2+ mixed pollutants. The surface morphology , crystal phase, elemental composition , light absorption property and photoelectrochemical activity of the synthesized Bi/Bi 2 O 3 /TiO 2 NTs were investigated. The composite film , Bi/Bi 2 O 3 /TiO 2 NTs was used for the photoelectrochemical removal of oxytetracycline, and it had excellent visible light photoelectrocatalytic performance. Under optimal conditions, the composite film was simultaneously used to remove coexisting oxytetracycline-Cu 2+ . The study results show that the reduction of Cu 2+ on cathode was promoted by oxytetracycline while the degradation of oxytetracycline on photoanode was slightly suppressed by Cu 2+ . Also, possible photoelectrocatalytic degradation pathways for oxytetracycline-Cu 2+ were analyzed by HPLC-MS.

✓ 已验证 DOI 高影响因子
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MOLECULES · 2022 ·Vol. 27 ·期 13 ·4291 · IF 4.927

Vanadium-Substituted Dawson-Type Polyoxometalate–TiO2 Nanowire Composite Film as Advanced Cathode Material for Bifunctional Electrochromic Energy-Storage Devices

Yu Fu,Yanyan Yang,Dongxue Chu,Zefeng Liu,Lili Zhou,Xiaoyang Yu,Xiaoshu Qu

Polyoxometalates (POMs) demonstrate potential for application in the development of integrated smart energy devices based on bifunctional electrochromic (EC) optical modulation and electrochemical energy storage. Herein, a nanocomposite thin film composed of a vanadium-substituted Dawson-type POM, i.e., K7[P2W17VO62]·18H2O, and TiO2nanowires were constructed via the combination of hydrothermal and layer-by-layer self-assembly methods. Through scanning electron microscopy and energy-dispersive spectroscopy characterisations, it was found that the TiO2nanowire substrate acts as a skeleton to adsorb POM nanoparticles, thereby avoiding the aggregation or stacking of POM particles. The unique three-dimensional core−shell structures of these nanocomposites with high specific surface areas increases the number of active sites during the reaction process and shortens the ion diffusion pathway, thereby improving the electrochemical activities and electrical conductivities. Compared with pure POM thin films, the composite films showed improved EC properties with a significant optical contrast (38.32% at 580 nm), a short response time (1.65 and 1.64 s for colouring and bleaching, respectively), an excellent colouration efficiency (116.5 cm2C−1), and satisfactory energy-storage properties (volumetric capacitance = 297.1 F cm−3at 0.2 mA cm−2). Finally, a solid-state electrochromic energy-storage (EES) device was fabricated using the composite film as the cathode. After charging, the constructed device was able to light up a single light-emitting diode for 20 s. These results highlight the promising features of POM-based EES devices and demonstrate their potential for use in a wide range of applications, such as smart windows, military camouflage, sensors, and intelligent systems.

✓ 已验证 DOI 高影响因子
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2022 ·Vol. 33 ·期 22 ·17587-17598 · IF 2.779

Preparation of visible light responsive g-C3N4/H-TiO2 Z-scheme heterojunction with enhanced photocatalytic activity for RhB degradation

Yu Bo,Miao Chun,Wang Dandan,Li Hongji,Sun Dongshu,Jiang Wei,Liu Chunbo,Che Guangbo

The development of high-efficiency heterojunction with improved photocatalytic property is regarded as a promising way to decontaminate wastewater. In this study, Z-Scheme g-C 3 N 4 /H-TiO 2 heterojunctions with different proportions were synthesized. The photocatalytic degradation of rhodamine B (RhB) was studied under visible light irradiation. Among them, 10% g-C 3 N 4 /H-TiO 2 photocatalyst had the best performance, and the degradation rate of RhB was 65% within 120 min. In addition, 10% g-C 3 N 4 /H-TiO 2 photocatalyst had high stability, and its photocatalytic activity did not decrease significantly after four cycles. Through photocurrent analysis, it is found that the photogenerated carriers have obviously excellent separation and transfer characteristics, which makes the 10% g-C 3 N 4 /H-TiO 2 photocatalyst have good degradation performance. Electron paramagnetic resonance (ESR) experiments showed that ·OH and ·O 2 − were active radicals during degradation.

✓ 已验证 DOI 高影响因子
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DALTON TRANSACTIONS · 2022 ·Vol. 51 ·期 7 ·2855-2862 · IF 4.569

A hierarchically porous TiO2@C membrane with oxygen vacancies: a novel platform for enhancing the catalytic conversion of polysulfides

Sheng-You Qiu,Chuang Wang,Liang-Liang Gu,Ke-Xin Wang,Xiao-Tian Gao,Jian Gao,Zaixing Jiang,Jian Gu,Xiao-Dong Zhu

In cases involving high levels of sulfur loading or high levels of current discharge, constructing sulfur composite cathodes via traditional coating preparation processes is an unsuitable way to overcome intractable problems relating to cathodes for use in lithium–sulfur batteries, such as poor conductivity, severe volume expansion, and the detrimental shuttle effect. Herein, a novel three-dimensional self-supported TiO2@C membrane with hierarchical interlinked porosity and oxygen vacancies was prepared via a phase-inversion method to act as a sulfur host. The procured TiO2−x@C membrane facilitates the infiltration of electrolyte, provides fast lithium-ion and electron transport channels and abundant sulfur loading sites, and shows superb structural buffering against the large volume changes during the conversion process between sulfur and lithium sulfide. More importantly, the introduction of oxygen vacancies not only enhances the conductivity of the original TiO2, but it also improves the corresponding adsorption abilities toward polysulfides and the subsequent transformation dynamics. Therefore, the TiO2−x@C membrane can significantly inhibit the polysulfide shuttle effect through polar chemisorption and conversion catalysis. Based on the above superiorities, the TiO2−x@C/S membrane electrode exhibits an impressive lifespan of more than 500 cycles at 2 C with a prominent ultimate specific discharge capacity of 715.2 mA h g−1.

✓ 已验证 DOI 高影响因子
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NPG Asia Materials · 2022 ·Vol. 14 ·期 1 ·1-11 · IF 10.761

High energy density of BaTiO3@TiO2 nanosheet/polymer composites via ping-pong-like electron area scattering and interface engineering

Jian Gang,Jiao Yong,Feng Liang,Meng Qingzhen,Yang Ning,Zhu Shangtao,Lü Minfeng,Wong Ching-Ping

Dielectric substances exhibit great potential for high-power capacitors due to their high stability and fast charge–discharge; however, a long-term challenge is to enhance energy density. Here, we propose a poly(vinylidene fluoride) (PVDF) composite utilizing BaTiO 3 nanoparticle@TiO 2 nanosheet (BT@TO ns) 2D nanohybrids as fillers, aiming at combining the interfacial strategy of using a core–shell filler and the electron scattering of a 2D filler to improve the energy density. With 4 wt% filler, the composite possesses the largest breakdown strength ( E b ) of 561.2 MV m −1 , which is significantly enhanced from the 407.6 MV m −1 of PVDF, and permittivity of 12.6 at 1 kHz, which is a 23% increase from that of PVDF. A superhigh energy density of 21.3 J cm −3 with an efficiency of 61% is obtained at 550 MV m −1 . The 2D BT@TO ns-filled composite exhibits a higher energy density than composites filled with core–shell 1D BT@TO nws or non-core–shell 0D BT, 1D TO, or 2D TO particles. The E b and energy density improvements are attributed to the buffer layer-based interface engineering and enhanced area scattering of electrons caused by the 2D hybrids, an effect similar to that of a ping-pong paddle to scatter electric field-induced charge migrations in composites. Thus, an effective hybrid strategy is presented for achieving high-performance polymer composites that can be used in energy storage devices.

✓ 已验证 DOI 高影响因子
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ULTRASONICS SONOCHEMISTRY · 2020 · IF 6.513

Enhanced photocatalytic degradation of organic dyes by ultrasonic-assisted electrospray TiO2/graphene oxide on polyacrylonitrile/β-cyclodextrin nanofibrous membranes

Rong Zhang,Yanlan Ma,Wenting Lan,Dur E Sameen,Saeed Ahmed,Jianwu Dai,Wen Qin,Suqing Li,Yaowen Liu

Polyacrylonitrile (PAN)/β-cyclodextrin (β-CD) composite nanofibrous membranes immobilized with nano-titanium dioxide (TiO 2 ) and graphene oxide (GO) were prepared by electrospinning and ultrasonic-assisted electrospinning. Scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), and X-ray diffraction (XRD) confirmed that TiO 2 and GO were more evenly dispersed on the surface and inside of the nanofibers after 45 min of ultrasonic treatment. Adding TiO 2 and GO reduced the fiber diameter; the minimum fiber diameter was 84.66 ± 40.58 nm when the mass ratio of TiO 2 -to-GO was 8:2 (PAN/β-CD nanofibrous membranes was 191.10 ± 45.66 nm). Using the anionic dye methyl orange (MO) and the cationic dye methylene blue (MB) as pollutant models, the photocatalytic activity of the nanofibrous membrane under natural sunlight was evaluated. It was found that PAN/β-CD/TiO 2 /GO composite nanofibrous membrane with an 8:2 mass ratio of TiO 2 -to-GO exhibited the best degradation efficiency for the dyes. The degradation efficiency for MB and MO were 93.52 ± 1.83% and 90.92 ± 1.52%, respectively. Meanwhile, the PAN/β-CD/TiO 2 /GO composite nanofibrous membrane also displayed good antibacterial properties and the degradation efficiency for MB and MO remained above 80% after 3 cycles. In general, the PAN/β-CD/TiO 2 /GO nanofibrous membrane is eco-friendly, reusable, and has great potential for the removal of dyes from industrial wastewaters.

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APPLIED CATALYSIS B-ENVIRONMENTAL · 2020 · IF 16.683

Fluorinated TiO2 coupling with α-MnO2 nanowires supported on different substrates for photocatalytic VOCs abatement under vacuum ultraviolet irradiation

Yingguang Zhang,Muyan Wu,Yifei Wang,Yu Ho Kwok,Wending Pan,Wai Szeto,Haibao Huang,Dennis Y.C. Leung

The particular role of fluorine (F) doping in the photocatalytic activity of nanocrystalline titanium dioxide (TiO 2 ) towards toluene degradation was systematically studied. TiO 2 nanosheet catalysts doped with different amounts of F − (denoted by F-TiO 2 ) were synthesized by hydrothermal method. For comparison, calcination was performed on the catalyst to remove F - . The photocatalytic oxidation (PCO) of toluene over F-TiO 2 was found to be much higher than those of TiO 2 and commercial P25 under the irradiation of vacuum ultraviolet (VUV) light, with a high toluene degradation efficiency of about 90 %. Moreover, the toluene degradation efficiency increased to 96 % with the addition of only 1 wt.% α-MnO 2 nanowires, and the residual ozone (O 3 ) in the system can be completely eliminated. In addition, four different substrates were explored for catalyst coating to facilitate the operation and minimize catalyst loading, which can provide a promising strategy for practical volatile organic compounds (VOCs) abatement in industrial applications.

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APPLIED SURFACE SCIENCE · 2023 · IF 6.7

Pt-modified TiO2 nanorod array films on FTO with enhanced CO sensitivity: A combined experimental and first-principle study

Bowen Zhang,Chongyang Wang,Saisai Zhang,Xiangli An,Zhiyong Zhao,Hari Bala,Zhanying Zhang

In this work, highly regular TiO 2 array films consisting of nanorods with a diameter of ∼119 nm were grown on FTO via a facile hydrothermal method. Then Pt nanoparticles with a size of ∼5 nm were modified on the surface of TiO 2 nanorods via an in-situ reduction process. The gas-sensing performances of pristine TiO 2 and Pt-modified TiO 2 samples were systematically tested. The introduction of Pt nanoparticles could enhance the response and stability toward CO gas and decrease the optimal operating temperature from 400 °C to 360 °C. And the Pt/TiO 2 -based sensor with a Pt content of 1.5 wt% exhibits the maximum CO sensitivity. Furthermore, the adsorption energies of Pt-modified or Pt-doped TiO 2 for CO molecules were calculated using first-principles calculations. The chemical sensitivity of Pt to CO molecules may be responsible for the improved CO sensitivity. Additionally, the unique nanorod array structure of Pt/TiO 2 and the nano-Schottky junction generated between them are helpful in enhancing the gas-sensing property.

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