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TiO2纳米颗粒
Polymers · 2021 ·Vol. 13 ·期 3 ·336 · IF 4.329

Novel TiO2 Nanoparticles/Polysulfone Composite Hollow Microspheres for Photocatalytic Degradation

Shangying Zhang,Qi Wang,Fengna Dai,Yangyang Gu,Guangtao Qian,Chunhai Chen,Youhai Yu

Nanosized titanium oxide (TiO2) material is a promising photocatalyst for the degradation of organic pollutants, whereas the difficulty of its recycling hinders its practical application. Herein, we reported the preparation of a novel titanium oxide/polysulfone (TiNPs/PSF) composite hollow microspheres by the combination of Pickering emulsification and the solvent evaporation technique and their application for the photodegradation of methyl blue (MB). P25 TiO2nanoparticles dispersed on the surface of PSF microspheres. The porosity, density and photoactivity of the TiNPs/PSF composite microsphere are influenced by the TiO2loading amount. The composite microsphere showed good methyl blue (MB) removal ability. Compared with TiO2P25, and PSF, a much higher MB adsorption speed was observed for TiNPs/PSF microspheres benefited from their porous structure and the electrostatic attractions between the MB+ and the negatively charged PSF materials, and showed good degradation efficiency. For TiNPs/PSF composite microsphere with density close to 1, a 100% MB removal (10 mg L−1) within 120 min at a catalyst loading of 2.5 g L−1can be obtained under both stirring and static condition, due to well dispersing of TiO2particles on the microsphere surface and its stable suspending in water. For the non-suspended TiNPs/PSF composite microsphere with density bigger than 1, the 100% MB removal can be only obtained under stirring condition. The removal efficiency of MB for the composite microspheres retained 96.5%, even after 20 cycles. Moreover, this composite microsphere also showed high MB removal ability at acidic condition. The high catalysis efficiency, excellent reusability and good stability make this kind of TiNPs/PSF composite microsphere a promising photocatalyst for the water organic pollution treatment.

研究领域: 材料科学 · 环境科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS · 2013 · IF 1.527

TiO2 nanoparticles with high ability for selective adsorption and photodegradation of textile dyes under visible light by feasible preparation

Yan-Fang Li,Wen-Pei Zhang,Xiangru Li,Ying Yu

Particular TiO 2 nanoparticles with high selective photocatalytic oxidation of anionic dyes are prepared by a feasible hydrothermal method . Moreover, its photocatalytic selectivity can be easily switched to cationic dyes by a simple post-treatment in ammonia solution, which makes the prepared TiO 2 have bi-directional selectivity in dye photodegradation. Based on the photocatalytic performances and the structure and surface characteristics of the catalyst, the bi-directional selectivity of the catalysts is found to be closely related to the adsorption selectivity. The adsorption selectivity originates from surface charge groups, which are introduced during the preparation and post-treatment progresses. This study provides a facile and economical approach towards selective degradation of dyes with high efficiency by the special TiO 2 nanoparticles synthesized through a simple hydrothermal method , which may be used practically in the future.

CAS / MDL: 989-38-8
研究领域: 材料科学 · 环境科学
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TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA · 2017 · IF 1.342

Enhanced photocatalytic activity of TiO2 nanoparticles using WS2/g-C3N4 hybrid as co-catalyst

Li-li ZHENG,Xin-yan XIAO,Yang LI,Wei-ping ZHANG

TiO 2 /WS 2 /g-C 3 N 4 composite photocatalysts were synthesized by a liquid-exfoliation-solvothermal method. In this process, the WS 2 /g-C 3 N 4 nano-sheets were prepared by liquid-exfoliation method from the bulk WS 2 and C 3 N 4 in the alcohol system, and then the TiO 2 nanoparticles (NPs) grew on the WS 2 /g-C 3 N 4 nano-sheets by in-situ synthesized technique. The photocatalytic activity of the as-prepared samples was evaluated by photocatalytic degradation of methyl orange (MO). The results showed that the as-prepared samples exhibited higher photocatalytic activities as compared to the pure TiO 2 , g-C 3 N 4 and TiO 2 /g-C 3 N 4 composite. The enhanced photocatalytic activities of TiO 2 /WS 2 /g-C 3 N 4 photocatalysts could be attributed to the synergistic effect of heterostructure between TiO 2 NPs and WS 2 /g-C 3 N 4 nano-sheets, which could efficiently improve the separation of photogenerated electron/hole pairs and utilization efficiency of photons. The quenching tests of radicals indicated that ·O − 2 had crucial effect on degradation of MO, which demonstrated that ·O − 2 was the main active radical in photocatalytic reaction process.

CAS / MDL: 100-21-0 12138-09-9
研究领域: 材料科学 · 环境科学
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Acta Biomaterialia · 2014 · IF 5.684

Potential application of functional porous TiO2 nanoparticles in light-controlled drug release and targeted drug delivery

Tianyi Wang,Haitao Jiang,Long Wan,Qinfu Zhao,Tongying Jiang,Bing Wang,Siling Wang

Novel multifunctional porous titanium dioxide (TiO 2 ) nanoparticles modified with polyethylenimine (PEI) were developed to explore the feasibility of exploiting the photocatalytic property of titanium dioxide to achieve ultraviolet (UV) light triggered drug release. Additionally, in order to further realize targeting delivery, folic acid , which chemically conjugated to the surface of the functionalized multifunctional porous TiO 2 nanoparticles through amide linkage with free amine groups of PEI, was used as a cancer-targeting agent to effectively promote cancer-cell-specific uptake through receptor-mediated endocytosis . And a typical poorly water-soluble anti-cancer drug, paclitaxel, was encapsulated in multifunctional porous TiO 2 nanoparticles. The PEI on the surface of multifunctional porous TiO 2 nanoparticles could effectively block the channel to prevent premature drug release, thus providing enough circulation time to target cancer cells. Following UV light radiation, PEI molecules on the surface were cut off by the free radicals (OH and O 2 −) that TiO 2 produced, and then the drug loaded in the carrier was released rapidly into the cytoplasm. Importantly, the amount of drug released from multifunctional porous TiO 2 nanoparticles can be regulated by the UV-light radiation time to further control the anti-cancer effect. This multifunctional porous TiO 2 nanoparticle exhibits a combination of stimuli-triggered drug release and cancer cell targeting. The authors believe that the present study will provide important information for the use of porous TiO 2 nanomaterials in light-controlled drug release and targeted therapy.

CAS / MDL: 9002-98-6 3326-32-7
研究领域: 纳米医学 · 生物材料 · 肿瘤学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Fabrication of polymer@TiO2 NPs hybrid membrane based on covalent bonding and coordination and its mechanism of enhancing photocatalytic performance

Zihan Tian,Shixiao Wang,Yilin Wu,Feng Yan,Shuhao Qin,Jingkui Yang,Jianxin Li,Zhenyu Cui

PVDF@TiO 2 NPs hybrid membranes with different hybrid modes were fabricated. The chemical structure , surface characteristic features and optical properties of the hybrid membranes were characterised. The effects of different hybrid modes on photocatalytic performance are discussed for the first time. The results indicated that the membrane with both chemical bonding and coordination between TiO 2 NPs and polymer matrix showed the best photocatalytic performance. Furthermore, the aggregation tendency of TiO 2 NPs on the hybrid membrane surface was effectively suppressed and the band gap of TiO 2 NPs was significantly reduced. The photogenerated electron-hole recombination rate was significantly decreased by the strongly electronegative fluorine (F), carboxyl and ester groups. Additionally, the negatively charged carboxyl groups on the surface of hybrid membrane facilitated the adsorption of methylene blue (MB) dye and promoted the adsorption-photocatalytic degradation of the MB. The photocatalytic degradation efficiency ( η ) of MB was higher than 95.4% and the η remained greater than 90% after 5 recycling cycles. Compared with membranes prepared by dip coating or blending, the grafted membrane exhibited higher degradation efficiency and improved recyclability. Therefore, this membrane provided a simple method for preparing stable hybrid membranes with better photocatalytic performance.

CAS / MDL: 538-75-0 1122-58-3
研究领域: 材料科学 · 环境科学
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WATER RESEARCH · 2020 · IF 9.13

Responses of freshwater biofilm formation processes (from colonization to maturity) to anatase and rutile TiO2 nanoparticles: Effects of nanoparticles aging and transformation

Kun Li,Jin Qian,Peifang Wang,Chao Wang,Bianhe Lu,Wen Jin,Xixian He,Sijing Tang,Chao Zhang,Pan Gao

Most of the current studies on the toxicology of pristine nanoparticles (NPs) are environmentally irrelevant, because their ‘‘aging’’ process accompanied by the physicochemical transformation is inevitable in the environment. Considering aging phenomenon will gain a better understanding of the toxicity and fate of NPs in the environment. Here, we focused on the physicochemical transformation of anatase-NPs (TiO 2 -A) and rutile-NPs (TiO 2 -R) after 90 days of aging and investigated the responses of freshwater biofilm formation to the stress changes of naturally aged TiO 2 -NPs (aTiO 2 -NPs). We found that after aging, the TiO 2 -NPs underwent sophisticated physicochemical transformations in the original morphology and microstructure owing to organic and crystal salts inclusions, such as energy band changes and the formation of Ti 3+ on the NPs surfaces. These comprehensive transformations increased the stability of NPs in the exposed suspension. However, the physicochemical transformations were crystal-forms-dependent, and aging did not change the crystal structure and crystallinity . Interestingly, compared to pristine NPs, aTiO 2 -NPs showed much lower cytotoxicity and had the weaker ability to promote or inhibit the biofilm formation (p < 0.05) owing to the passivation of photoactivity caused by the comprehensive effect of the inclusions, especially for aTiO 2 -A. Regardless of aging or not of crystal forms, responses of biofilm formation were exposure-concentration-dependent, namely low concentration promotion (0.1 mg/L) and high concentration inhibition (10 mg/L), e.g., role transition of the pioneers (algae or bacteria) in initial colonization, extracellular polymeric substances (EPS) secretion and compositions of development stages with polysaccharide (PS)-rich and protein (PRO)-rich stages, and biomass and cell activity at different depths of mature biofilms. The reactive oxygen species (ROS) induced by TiO 2 -NPs showed typical hormesis. The changing trends of the autoinducers (c-di-GMP and quorum sensing signals including AHL and AI-2) were highly consistent with the growth stages of biofilms and were stimulated or suppressed by TiO 2 -NPs. The NPs crystal-dependently changed the microorganism community structures, while the UPGMA clustering of bacteria was based on the growth stages of the biofilms. The toxic mechanisms revealed that photoactivity and nanoscale retention of particles are the main reasons for the differences in the ecological stress capacity of four kinds of TiO 2 -NPs. Aging reduced characteristic differences of two pristine NPs and even reversed their relative stresses levels (p > 0.05). However, the toxicity of high-concentration aTiO 2 -NPs (10 mg/L) remained serious in a water environment. This study provides a better understanding for the water environmental risks evaluation and policy control of nanoparticles, that is, the effect of time aging has to be considered.

研究领域: 环境科学 · 纳米技术 · 生态毒理学 · 微生物学 · 水生生态学
✓ 已验证 DOI PubMed 高影响因子
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MATERIALS RESEARCH BULLETIN · 2020 · IF 4.019

Investigation of the TiO2 nanoparticles aggregation with high light harvesting for high-efficiency dye-sensitized solar cells

Zhongwei Ge,Chenglei Wang,Zhiyan Chen,Tong Wang,Tao Chen,Rui Shi,Shengqing Yu,Jianqiang Liu

The TiO 2 nanoparticles aggregation (TNA) was synthesized by a novel one-step hydrothermal method in this work. And for the first time we prepared a kind of jelly pastes of TNA used as photoanode for high-efficiency dye-sensitized solar cells (DSSCs). The prepared TNA provides larger specific surface area of 79.34 m 2 g −1 compared with P25 nanoparticles (49.25 m 2 g −1 ), which is beneficial of absorbing more dye molecules and contributes to high current densities. Moreover, the high scattering effect of TNA caused a strong absorption in the visible-light range increasing the number of excited charges and reducing the energy loss. The effect of various concentrations of TNA pastes for DSSCs was studied to explore the superiority of concentrated TNA pastes. The result shows the DSSC based on high-concentration pastes and double-layer film achieved the best power conversion efficiency (PCE) of 8.34 % corresponding the current density of 17.97 mA cm -2 .

研究领域: 材料科学 · 能源科学
✓ 已验证 DOI 高影响因子
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Nanoscience and Nanotechnology Letters · 2017 ·Vol. 9 ·期 9 ·1356-1362 · IF 1.889

Fabrication and Electrocatalytic Activity of Hierarchically Nanoporous Ti–SiO2/Ni–Mo Composite Electrode for Hydrogen Evolution

Xu Jianxiong,Xie Shaowen,Feng Yahui,Du Jingjing,Xu Lijian

TiO2 nanoparticles with average diameter of 510 nm were prepared by sol–gel surfactants, and the hierarchically nanoporous Ti–SiO2 particles were further prepared using in-situ method. The hierarchically nanoporous Ti–SiO2 particles with hollow structure were analyzed by transmission electron microscope (TEM), energy dispersive spectrometer (EDS), scanning electron microscope (SEM), nitrogen adsorption stripping curves and Barrett-Joyner-Halenda (BJH) pore size distribution curves. Finally, the hierarchically nanoporous Ni–Mo composite electrodes were prepared using the TiO2 nanoparticles or nanoporous Ti–SiO2 particles as composite particles respectively, and the influence of the concentration of composite particles on the electrocatalytic activities of Ni–Mo composite electrodes for hydrogen evolution were investigated by polarization curves. The results showed that the diameter of Ti–SiO2 particles was from 200 nm to 500 nm, and specific surface area was 573 m2/g with pore volume of 1.19 cm3/g and mesopore size of 3.2 nm. The TiO2/Ni–Mo and Ti–SiO2/Ni–Mo composite electrodes were fabricated by electrodeposition with TiO2 nanoparticles and nanoporous Ti–SiO2 particles as composite particles respectively. The electrocatalytic activities of TiO2/Ni–Mo and Ti–SiO2/Ni–Mo composite electrodes for hydrogen evolution were investigated. Results showed that the electrocatalytic activities of TiO2/Ni–Mo and Ti–SiO2/Ni–Mo composite electrodes for hydrogen evolution reached the optimal value when the concentration of particles was 4 g/L and 2 g/L respectively. The electrocatalytic activities of TiO2/Ni–Mo and Ti–SiO2/Ni–Mo composite electrodes were greater than that of Ni–Mo alloy electrode, and the Ti–SiO2/Ni–Mo composite electrode showed the best electrocatalytic activity.

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

In-situ creating elastic lattice OO bonds over semicrystalline yellow TiO2 nanoparticles for significantly enhanced photocatalytic H2 production

Qingping Wu,Yao Cheng,Feng Huang,Xiao Li,Xiangshui Cui,Ju Xu,Yuansheng Wang

Atomic defects (e.g., Ti 3+ , oxygen vacancies) have been intenstively investigated for modifying TiO 2 in order to reach visible light active photocatalytic H 2 production. However, the atomic defects within TiO 2 could easily act as photo-generated charge-carrier recombination centers, resulting in relatively low H 2 conversion efficiency. In this paper, semicrystalline yellow TiO 2 nanoparticles rich of superoxide ions are new synthesized by a simple aqueous solution method. Instead of introducing atomic defects, we show for the first time that catalytic performance can also be significantly improved via in-situ creating lattice O O bonds within metastable semicrystalline TiO 2 . The synthesized semicrystalline yellow TiO 2 exhibits significantly enhanced photocatalytic activity for H 2 production after cycle tests. The formaldehyde in aqueous solution is used as target pollutant to simulate industrial wastewater. In-situ created elastic lattice O O bonds are proposed to improve catalytic performance through facilitating the breakage of C H bonds of HCHO. A series of internally consistent reaction equations is proposed that describes the role of in-situ created lattice O O bonds for improving the catalytic performance. This is strongly supported by that the H 2 production rate at the end of the fourth cycle test is significantly more than that of the beginning of the first cycle test.

研究领域: 材料科学 · 环境科学 · 化学工程
✓ 已验证 DOI 高影响因子
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Scientific Reports · 2015 ·Vol. 5 ·期 1 ·1-10 · IF 5.578

Anatase TiO2 Nanoparticles with Exposed {001} Facets for Efficient Dye-Sensitized Solar Cells

Chu Liang,Qin Zhengfei,Yang Jianping,Li Xing’ao

Anatase TiO 2 nanoparticles with exposed {001} facets were synthesized from Ti powder via a sequential hydrothermal reaction process. At the first-step hydrothermal reaction, H-titanate nanowires were obtained in NaOH solution with Ti powder and at second-step hydrothermal reaction, anatase TiO 2 nanoparticles with exposed {001} facets were formed in NH 4 F solution. If the second-step hydrothermal reaction was carried out in pure water, the H-titanate nanowires were decomposed into random shape anatase-TiO 2 nanostructures, as well as few impurity of H 2 Ti 8 O 17 phase and rutile TiO 2 phase. Then, the as-prepared TiO 2 nanostructures synthesized in NH 4 F solution and pure water were applied to the photoanodes of dye-sensitized solar cells (DSSCs), which exhibited power conversion efficiency (PCE) of 7.06% ( V OC of 0.756 V, J SC of 14.80 mA/cm 2 , FF of 0.631) and 3.47% ( V OC of 0.764 V, J SC of 6.86 mA/cm 2 , FF of 0.662), respectively. The outstanding performance of DSSCs based on anatase TiO 2 nanoparticles with exposed {001} facets was attributed to the high activity and large special surface area for excellent capacity of dye adsorption.

研究领域: 材料科学 · 能源科学
✓ 已验证 DOI 高影响因子
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Materials Science & Engineering C-Materials for Biological Applications · 2017 · IF 4.164

808 nm light triggered black TiO2 nanoparticles for killing of bladder cancer cells

Wenjun Ni,Meng Li,Jiayi Cui,Zipeng Xing,Zhenzi Li,Xiaoyan Wu,Erlin Song,Mancheng Gong,Wei Zhou

The black TiO 2 nanoparticles are synthesized via a facile calcination method combined with an in-situ controllable solid-state reaction approach. The results indicate that the photocatalyst with a narrow band gap of ~   2.32 eV extends the photoresponse to visible light and near infrared region. And thus more reactive oxygen species can be obtained to induce the cell-killing under 808 nm light triggering. The as-obtained black TiO 2 nanoparticles exhibiting low toxicity, good biocompatibility and high anticancer effect in vitro, is demonstrated as efficient photosensitizers for phototherapy to kill the bladder cancer cells. These findings suggest that the facile synthetic black TiO 2 nanomaterials will have broad application in biomedicine.

研究领域: 纳米技术 · 癌症研究 · 生物医学工程 · 材料科学
✓ 已验证 DOI PubMed 高影响因子
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Results in Physics · 2018 · IF 2.147

Effect of TiO2 size factor on the electrical properties of polyethylene matrix dielectrics

Qingguo Chi,Xubin Wang,Wei Zhao,Changhai Zhang,Tiandong Zhang,Xuan Wang,Qingquan Lei

In this study, the TiO 2 nanoparticles and TiO 2 nanofibers were chosen as inorganic fillers to dope into the linear low density polyethylene (LLDPE). The TiO 2 nanofibers were prepared by the electrospinning method, the diameter and length of TiO 2 nanofibers were about 100 nm–200 nm and 3 μm–4 μm, respectively, and the size of the purchased TiO 2 nanoparticles was about 100 nm–200 nm. The microstructure of TiO 2 fillers and their composites was analyzed by the X-ray diffraction (XRD) and scanning electron microscopy (SEM). The breakdown field strength and space charge characteristics of the LLDPE/TiO 2 nanoparticles and LLDPE/TiO 2 nanofiber composites with different sizes of inorganic fillers were investigated. The results showed that the LLDPE/TiO 2 nanofiber composites had higher breakdown strength than LLDPE/TiO 2 nanoparticle composites at the same doping content. The breakdown strength of 0.5 wt% LLDPE/TiO 2 nanofiber composites (237 kV/mm) was higher than that of pure LLDPE (223 kV/mm) and 0.5 wt% LLDPE/TiO 2 nanoparticle composites (205 kV/mm). In addition, the space charge accumulation and electric field distortion in the composites were significantly relieved by doping TiO 2 nanofibers compared with that of doping TiO 2 nanoparticles.

CAS / MDL: 62-31-7 77-86-1
研究领域: 材料科学 · 电气工程
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