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ENVIRONMENTAL SCIENCE & TECHNOLOGY · 2025 · IF 11.3

Tuning Pt-TiO2 Interactions to Switch Inhibition to Synergy in Toluene–Acetone Mixture Combustion

Yuqin Lu,Hua Deng,Xueshan Zhang,Jianguo Ding,Sijia Bai,Lian Wang,Hong He

The inhibitory interactions among various volatile organic compounds (VOCs) during combustion in industrial exhaust gases pose a significant challenge for catalytic technologies, primarily due to a lack of effective approaches to counter these adverse effects. The interaction between Pt and TiO2 was readily tuned through hydrogen reduction of the TiO2 matrix (Pt/TiO2-800), which ultimately transformed the inhibitory effect into a synergistic effect in a toluene–acetone mixture. Optimal catalytic activity was achieved at 0.6 wt % Pt loading, with 0.6Pt/TiO2-800 lowering reaction temperatures by 21 °C for toluene and 24 °C for acetone in mixed VOC oxidation. Characterization reveals that Pt/TiO2-800 possesses abundant oxygen vacancy clusters, enhancing TiO2-Pt electron transfer, diversifying Pt nanoparticle sizes, stabilizing low-valent Pt species, and improving oxidative capacity. DFT calculations further underscore the role of oxygen vacancy in modulating the Pt electronic environment and enhancing defect-enhanced adsorption. This work advances Pt-TiO2 interaction understanding and offers an effective catalyst for VOCs abatement, addressing inhibitory effects in mixed VOCs systems.

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NANO · 2025 · IF 1.1

Enhanced Photocatalytic Degradation of Methylene Blue using La3+ and Mo6+ Co-doped TiO2 Nanotubes

Yi Gou,Jinghong Du,Zilong Wang,Shengyang He,Jiahao Lv

La 3+ single-doped and La 3+ -Mo 6+ co-doped TiO 2 nanotubes were synthesized via anodic oxidation combined with a two-step electrochemical process. Their crystalline structure, microstructure, and light absorption properties were characterized using XRD, SEM, and UV-Vis spectroscopy, followed by methylene blue photocatalytic degradation experiments. The results indicate that both La 3+ single-doping and La 3+ -Mo 6+ co-doping can suppress the transformation of the anatase phase to the rutile phase and inhibit grain growth. The diameters of both types of nanotubes range between 60-80 nm, with La and Mo uniformly distributed throughout the nanotubes. Both La 3+ single-doped and La 3+ -Mo 6+ co-doped induced red shifts in the TiO 2 light absorption peaks. The most pronounced red shift in the light absorption band edges occurred at a La 3+ -Mo 6+ ratio of 3:7, reducing the bandgap width to its minimum value of 2.99 eV. Both La 3+ single-doped and La 3+ -Mo 6+ co-doped TiO 2 exhibited first-order photocatalytic degradation of methylene blue. As the La 3+ single-doped concentration increased or the La 3+ -Mo 6+ co-doped ratio varied from 1:9 to 9:1, both the methylene blue degradation rate and photocatalytic reaction rate initially increased before decreasing, while the half-life initially decreased before increasing. At a La 3+ -Mo 6+ co-doped ratio of 3:7, the photocatalytic activity of the TiO 2 nanotubes was optimal, achieving a maximum degradation rate of 89.73% within 8 hours-a 52% improvement over pure TiO 2 nanotubes.

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CERAMICS INTERNATIONAL · 2025 · IF 5.6

Low-temperature sintered Li2ZnSiO4-Bi2O3-TiO2 ceramics with improved dielectric properties and temperature stability

Keyu Chen,Yu He,Bixuan Zhu,Chuanyezi Cai,Jiacheng Guo,Ruiqi He,Xi Chen,Lu Ye,Jianjun Zhang,Sude Ma

As the communications industry continues to develop, low temperature co-fired ceramics are used as resonators in multilayer chip components of integrated circuits. In order to co-fire with the metal, it is necessary to reduce the sintering temperature of ceramics to below 960 °C. In order to rule out the impact of changes in the operating temperature of the ceramic material, we need to adjust the resonant frequency temperature coefficient to near zero. This paper discusses the application of a temperature-stable low-temperature sintered dielectric material derived from Li 2 ZnSiO 4 (LZS) in low-temperature co-fired ceramics (LTCC). The addition of the low melting point oxide Bi 2 O 3 resulted in a significant reduction of the sintering temperature and improvement of the densification of LZS ceramics, where the sintering temperature was reduced from 1200 °C to 900 °C. The relative density and microwave dielectric properties (dielectric constant ε r , quality factor Q × f and temperature coefficient of resonant frequency τ ƒ ) of LZS- x Bi 2 O 3 ( x  = 0, 3, 6, 9, 12 mol%) ceramics sintered at different temperatures increase and then decrease with increasing Bi 2 O 3 content. The best performance was obtained when the Bi 2 O 3 addition was 9 mol% (ε r  = 6.87, Q × f = 28,151 GHz, τ ƒ  = - 85.2 ppm/°C). By increasing the amount of TiO 2 added to LZS-9 mol%Bi 2 O 3 , the τ ƒ value of the ceramic system can be continuously increased, which is effectively adjusted to near zero. The best integrated dielectric properties of the LZS-Bi 2 O 3 -TiO 2 ceramic system (ε r  = 8.9, Q × f = 22.982 GHz, τ ƒ  = - 8.34 ppm/°C) are obtained when the TiO 2 addition is 30 wt%. This suggests that LZS-Bi 2 O 3 -TiO 2 ceramics have potential for low-temperature co-fired ceramics (LTCC) applications.

CAS / MDL: 1304-76-3 13463-67-7
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ACS Applied Nano Materials · 2025 · IF 5.5

TiO2-Coated BiOCl Nanosheet p-n Heterojunctions for Photocatalytic H2O2 Production under Simulated Sunlight

Mingming Du,Anxian Peng,Hongyue Liu,Huimei Chen,Qiyun Li,Zheng Fang,Ganning Zeng,Rongjun Yan

The well-designed internal electric field (IEF) with band bending effects will effectively accelerate the separation and transfer of photogenerated charges to foster a photocatalytic performance. Hence, in this work, the IEF-induced BiOCl/TiO2 p-n heterojunctions are prepared through the hydrothermal method for photocatalytic H2O2 production. The BiOCl/2TiO2 composite performed a superior H2O2 yield of 4.75 mM h–1, which is 4 times higher than that of pristine BiOCl. The p-n heterojunction mechanism was investigated via XPS and photoelectrochemical property tests, in which BiOCl/2TiO2 showed the highest photogenerated charge separation efficiency for boosting photocatalytic activity. This work provided an effective strategy for the design of p-n heterojunction photocatalysts to enhance photocatalytic performance.

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FUEL · 2025 · IF 7.5

Ru/TiO2-photocatalysed synthesis of γ-butyrolactone from a furfural derivative under mild conditions

Yang Peng,Haikuan Yang,Ting Zhang,Songsong Zhou,Haiwei Jiang,Yongjie Zheng,Weiran Yang

Synthesis of γ -butyrolactone (GBL) from renewable biomass resources under mild reaction condition with catalysis is attractive but challenging. Herein, we report the photocatalytic oxidation of the biomass-based furfural derivative tetrahydrofurfuryl alcohol (THFAL) to prepare GBL under light irradiation (365 nm) in air at room temperature. Utilising Ru/TiO 2 as the photocatalyst and air as the oxidant, a GBL yield as high as 73 % was achieved. The reaction mechanism was studied rigorously by performing photocatalyst performance evaluation, material characterisation, free-radical quenching reactions and electron spin resonance (ESR). In situ diffuse reflectance infrared Fourier transform spectroscopy was employed to detect intermediate products and elucidate the mechanism at the molecular level. Based on the in-situ monitoring results, we propose a pathway for the oxidation decarbonylation of THFAL to produce CO 2 and GBL.

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SENSORS AND ACTUATORS B-CHEMICAL · 2025 · IF 7.7

UV-activated TiO2 nanoparticles for sensitively detecting ppb-level dimethyl sulfide at room temperature

Dandan Rong,Gang Meng,Longqing Mi,Meng Li,Ruofan Zhang,Xiaohua Ji,Tiantian Dai,Hongtao Li,Xiaodong Fang,Libing You,Zanhong Deng

Dimethyl sulfide (DMS) is one kind of volatile sulfur compounds (VSCs) possessing disagreeable odor, with a low olfactory threshold around 20 ppb. Highly sensitive detection of DMS at room temperature (RT) is critically needed for emerging application with low power consumption, but it remains a significant challenge owing to its low reactivity. Herein, UV photoactivated titanium dioxide (TiO 2 ) nanoparticles (NPs) have been employed for detecting DMS at RT. An eco-friendly ultrasonic crushing solution spray technique was developed to prepare TiO 2 based sensors. An ultrahigh response of 30–500 ppb DMS and a low experimental limit of detection ( R a / R g = 2.7@50 ppb) could be achieved at RT under UV light activation. This work opens a new avenue to achieve highly sensitive, energy-efficient sensors for trace VSCs detection at RT in ambient odor monitoring.

CAS / MDL: 13463-67-7
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JOURNAL OF MATERIALS CHEMISTRY · 2012 ·Vol. 22 ·期 11 ·4847-4854 · IF 5.968

Novel preparation method for a new visible light photocatalyst: mesoporous TiO2 supported Ag/AgBr

Desong Wang,Yandong Duan,Qingzhi Luo,Xueyan Li,Jing An,Leilei Bao,Lei Shi

A new method for the preparation of mesoporous TiO2 with a surface deposited with nanoparticles of Ag and AgBr was developed. Cetyltrimethylammonium bromide (CTAB) was used as both a template agent and bromine source in the preparation process of the mesoporous TiO2. Mesoporous TiO2 containing CTAB was synthesized by a sol–gel method, and was dipped into AgNO3 solution to form a mesoporous AgBr/TiO2 nanocomposite. The AgBr/TiO2 nanocomposite was irradiated by visible light to accelerate photolysis of AgBr, forming mesoporous Ag/AgBr/TiO2 photocatalyst. The Ag/AgBr/TiO2 photocatalyst was characterized by small angle X-ray diffraction (SAXRD), wide angle X-ray diffraction (WAXRD), transmission electron microscopy (TEM), UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS), X-ray photoelectron spectroscopy (XPS), Auger electron spectroscopy (AES) and N2 isothermal adsorption–desorption. Ag/AgBr/TiO2 exhibits high photocatalytic activity for the degradation of methyl orange under visible light irradiation. The photocatalytic reaction follows the first-order kinetics and the rate constant (k) for the degradation of methyl orange photocatalyzed by Ag/AgBr/TiO2 is 63.6, 36.1 and 2.7 times that of mesoporous TiO2 (M-TiO2), commercial TiO2 (P-25), and Ag/AgBr/SiO2, respectively. The recycling runs experiment shows that the photocatalytic stability of the Ag/AgBr/TiO2 photocatalyst is excellent. The visible light photocatalytic mechanism of Ag/AgBr/TiO2 is also discussed.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2017 · IF 3.133

Branched open-ended TiO2 nanotubes for improved efficiency of flexible dye-sensitized solar cells

Lixin Song,Yangyang Zhou,Yingli Guan,Pingfan Du,Jie Xiong,Frank Ko

The anatase branched open-ended titanium dioxide (TiO 2 ) nanotubes (NTs) are prepared using a combined method of electrospinning, hydrothermal processing and calcination . The branched open-ended TiO 2 NT (BOTNT) is composed a trunk of a large sized NT, from which out growth many branches consisting of single-crystalline TiO 2 nanosheets (NSs) and small NTs. The morphology and microstructure of the BOTNTs can be controlled by varying with the hydrothermal treatment time. When it is used in flexible dye-sensitized solar cells (FDSSCs) as multifunctional layer covering on the carbon nanotubes (CNTs) incorporated TiO 2 (CNTs/TiO 2 ) nanorods (NRs) layer, a high conversion efficiency of 4.70% is obtained. This efficiency is much higher than that of the cell assembled by the single-layer CNTs/TiO 2 NRs film. This is attributed to the great increase in light harvesting efficiency , resulting from excellent light-scattering ability and high specific surface area for dye loading of the BOTNTs. Furthermore, the excellent electron transport ability of the BOTNTs due to their high level of interconnectivity , improves the performance of FDSSCs.

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ACS Applied Materials & Interfaces · 2016 · IF 7.145

Highly Efficient Photocatalytic Hydrogen Evolution in Ternary Hybrid TiO2/CuO/Cu Thoroughly Mesoporous Nanofibers

Huilin Hou,Minghui Shang,Fengmei Gao,Lin Wang,Qiao Liu,Jinju Zheng,Zuobao Yang,Weiyou Yang

Development of novel hybrid photocatalysts with high efficiency and durability for photocatalytic hydrogen generation is highly desired but still remains a grand challenge currently. In the present work, we reported the exploration of ternary hybrid TiO2/CuO/Cu thoroughly mesoporous nanofibers via a foaming-assisted electrospinning technique. It is found that by adjusting the Cu contents in the solutions, the unitary (TiO2), binary (TiO2/CuO, TiO2/Cu), and ternary (TiO2/CuO/Cu) mesoporous products can be obtained, enabling the growth of TiO2/CuO/Cu ternary hybrids in a tailored manner. The photocatalytic behavior of the as-synthesized products as well as P25 was evaluated in terms of their hydrogen evolution efficiency for the photodecomposition water under Xe lamp irradiation. The results showed that the ternary TiO2/CuO/Cu thoroughly mesoporous nanofibers exhibit a robust stability and the most efficient photocatalytic H2 evolution with the highest release rate of ∼851.3 μmol g–1 h–1, which was profoundly enhanced for more than 3.5 times with respect to those of the pristine TiO2 counterparts and commercial P25, suggesting their promising applications in clean energy production.

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Journal of Physical Chemistry C · 2014 · IF 4.835

Catalytic Behavior of Flame-Made Pd/TiO2 Nanoparticles in Methane Oxidation at Low Temperatures

Fang Niu,Shuiqing Li,Yichen Zong,Qiang Yao

A controlled one-step synthesis of titania-supported palladium (Pd/TiO2) nanoparticles is demonstrated by using a premixed stagnation swirl flame with an ultrafine spray feeding system. The new method produces well-dispersed palladium clusters on the surface of TiO2 particle. The low-temperature methane catalytic oxidation indicates that the flame-made Pd/TiO2 possesses activity apparently higher than that of the impregnated one under the same Pd loading. For the first time, we observe a special pinched hysteresis loop of catalytic activity of Pd/TiO2 nanoparticles from the curves of CH4 conversion versus temperature during heating–cooling cycles. Thermal stability analysis confirms the complex coexistence and transformation of metallic Pd and PdO in Pd/TiO2 particles. Further morphological characterization reveals the oxidation rate is controlled by the metallic Pd content on the particle surface, whereas the deactivation of the catalysts is mainly due to the Pd dispersion decrement. The competition between the Pd dispersion decrement and the PdO reduction at the surface may result in the pinched hysteresis loop of Pd/TiO2 catalysts during low-temperature methane combustion.

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JOURNAL OF MATERIALS SCIENCE · 2013 ·Vol. 48 ·期 24 ·8386-8392 · IF 2.163

Photocatalytic degradation of Rhodamine B using electrospun TiO2 and ZnO nanofibers: a comparative study

Du Pingfan,Song Lixin,Xiong Jie,Cao Houbao

TiO 2 and ZnO nanofibers were fabricated through a facile electrospinning method. The obtained nanofibers were characterized by a variety of analytical means including FESEM, TEM, SAED, XRD, UV–Vis, and PL. Compared with nanoparticles, nanofibers can be recycled more easily when they are used as photocatalysts. The photocatalytic activities of these two nanofibers were investigated and compared by evaluating the photodegradation of hazardous dye Rhodamine B. Although, ZnO nanofibrous photocatalyst exhibits better initial activity than TiO 2 nanofibrous counterpart, its photocatalytic performance is inferior to that of the latter on the whole. The photo-instability arising from photocorrosion may be responsible for its rapid deterioration in activity. The difference in the photocatalytic properties between TiO 2 and ZnO nanofibers was discussed, and a possible photodegradation mechanism of organic dyes in the presence of the nanofibrous photocatalyst was proposed. This work offers a direct insight into the comparison of photocatalysis of electrospun TiO 2 and ZnO nanofibers.

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Desalination and Water Treatment · 2024 · IF 1

Application and mechanism study of TiO2/MXene nanocomposites in photocatalytic degradation of methyl orange

Runlin Han,Yongli Xie

In this work, TiO 2 /MXene nanocomposites have been explored with hydrothermal synthesis during the dye photocatalytic degradation process. They worked as photocatalyst with high efficiency. The degradation of organic dye methyl orange with MXene under ultraviolet (UV) light and visible light was studied in detail. The methyl orange can be degraded efficiently especially at acid condition. When the nanocomposites/dye ratio was fixed at 5, most of the dye (close to 99.9%) was degraded under UV and visible light irradiation in 3 h. When MXene was recycled to treat methyl orange, the degradation rate was kept at 96% after 2 cycles under UV light. It was found that the composite material showed improved photocatalytic performance under long time ultraviolet treatment. Scanning electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy characterizations of Ti 3 AlC 2 and MXene were carried to investigate the possible reasons for high degradation efficiency. MXene worked as a cocatalyst which enhanced the separation of electron hole pairs and catalytic performance.

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