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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Enhanced visible-light photocatalytic performance of black TiO2/SnO2 nanoparticles

Yufang Li,Yangchun Feng,Hang Bai,Jinsong Liu,Dayuan Hu,Jiyu Fan,Honglie Shen

In recent years, large and small industries have discharged a multitude of organic pollutants into the environment, causing environmental pollution. Titanium dioxide (TiO 2 ) materials is very important photocatalyst as a result of its outstanding applications to remove organic contaminants from the environment. Nonetheless, the low utilization rate of visible light of TiO 2 has limited its application. To begin with, Black TiO 2 is produced by the magnesium thermal reduction method to promote the absorption of visible light, Subsequently, The black TiO 2 /SnO 2 composites are synthesized by chemical synthesis method to form a hetero-junction to augment the photocatalytic activity. The morphology, chemical composition, phase structure and photocatalytic degradation of Rhodamine B (RhB) under visible light irradiation were investigated. The morphological properties demonstrated that a Ti 3+ self-doped disorder layer forms on the surface of TiO 2 nanophase, and black TiO 2 nanoparticles are well decorated with SnO 2 nanoparticles. After 90 min of visible light irradiation, RhB has a photocatalytic degradation efficiency of 96.62%, which is 1.597 times that of TiO 2 nanoparticles, and its cycle stability is well beyond our expectation. The ameliorated photocatalytic degradation performance of TiO 2 /SnO 2 composite is ascribed to the formation of a "type Ⅱ heterojunction", which not only reinforces the absorption of visible light of black TiO 2 /SnO 2 nanoparticles, but also heightens the separation and transfer efficiency of the photogenerated carriers.

研究领域: 环境科学 · 材料科学
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ACS Sustainable Chemistry & Engineering · 2022 · IF 9.224

Deactivation and Stabilization Mechanism of Photothermal CO2 Hydrogenation over Black TiO2

Yang Li,Zhaojian Zeng,Yuanming Zhang,Yong Chen,Wenjing Wang,Xiaoming Xu,Mengyang Du,Zhaosheng Li,Zhigang Zou

Photothermal catalytic reduction of CO2 is a powerful way to promote carbon neutralization goals. However, there are few reports on the deactivation of the photothermal CO2 reduction reaction. Here, we observed an interesting deactivation phenomenon of photothermal CO2 conversion over TiO2–xHx (black TiO2). Despite the presence of a reducing atmosphere of H2, the oxygen vacancy concentration of TiO2–xHx is reduced, resulting in the deactivation of photothermal CO2 reduction. After Ni is modified onto TiO2–xHx, Ni can activate H2 to form Hs, and the oxygen vacancy concentration of Ni/TiO2–xHx may be maintained, thus solving the deactivation problem in photothermal CO2 hydrogenation.

研究领域: 化学工程 · 材料科学 · 环境科学
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CATALYSIS LETTERS · 2020 ·Vol. 151 ·期 6 ·1755-1765 · IF 2.482

CrOx Anchored on the Black-TiO2 Surface via Organic Carboxylic Acid Ligand and Its Catalysis in Oxidation of NO

Meng Fanyu,Zhang Mingjia,Zhou Fayang,Zou Haocheng,Zhu Boming,Zeng Yiqing,Zhang Shule,Zhong Qin

Abstract CrO x /black-TiO 2 catalysts were prepared by ligand-assisted (citric acid, oxalic acid and ethylenediaminetetraacetic acid) impregnation method. These catalysts were characterized in detail by means of X-ray diffraction, Raman, BET, X-ray photoelectron spectroscopy, H 2 and O 2 (NO) temperature programmed reduction or desorption and in-suit DFTIR spectra. The results indicated that ligands assistance was beneficial for CrO x interacted with oxygen vacancies and O–Ti–O structures. Among all the catalysts, CrO x /black-TiO 2 /CA (modified by citric acid) revealed excellent catalytic activity and stability for NO oxidation in the temperature range of 200–450 °C. The characterization results exhibited that the interaction existed between CrO x and oxygen vacancies resulting in more Cr 6+ . Moreover, the strong interaction between CrO x and O–Ti–O was attributed to the modification of carboxylic acid, which increased the content of Cr 3+ and chemical adsorption oxygen. High content of chemical adsorption oxygen promoted the adsorption ability of O 2 , and Cr 6+ enhanced the adsorption capacity of NO. Hence, chemical adsorption oxygen and Cr 6+ synergistically promoted the NO oxidation. Graphic Abstract

研究领域: 催化材料科学 · 环境化学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Microwave-assisted synthesis of RuTe2/black TiO2 photocatalyst for enhanced diclofenac degradation: Performance, mechanistic investigation and intermediates analysis

Chenghong Qiang,Nan Li,Shixiang Zuo,Zhimin Guo,Wei Zhan,Zhengping Li,Jiangquan Ma

Seeking active and low-cost cocatalysts is a vital task for solving the sluggish kinetics of photocatalysis process in environmental management. Herein, we report a novel and high-efficiency crystallized RuTe 2 cocatalyst, and loaded it onto black TiO 2 to form photocatalytic heterostructure (denoted as RuTe 2 /B-TiO 2 ) for diclofenac (DCF) degradation. To the best of our knowledge, the RuTe 2 as a cocatalyst for photocatalysis based on swift electron capture has not been documented yet. The degradation efficiency of DCF over 0.5% RuTe 2 /B-TiO 2 reached 95.2% for 120 min, which is 1.2 times higher than that of pure B-TiO 2 . In addition, the effects of different calcination temperatures, catalyst amounts, DCF concentrations and solution pH of the as-prepared catalysts were also investigated in depth. Spectroscopy/electrochemistry showed that 0.5% RuTe 2 /B-TiO 2 exhibited a narrower band gap, more active sites and better electrical conductivity than pure B-TiO 2 . Experiments with trapping agents have shown that O 2 – was the main active substance under irradiation. Furthermore, intermediates for the photodegradation of DCF were detected by liquid chromatography mass system (LC-MS) and density functional theory (DFT) calculations. Finally, the degradation pathway was rationalized and a possible photocatalytic mechanism for 0.5% RuTe 2 /B-TiO 2 was proposed.

研究领域: 环境科学 · 材料科学
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Journal of CO2 Utilization · 2023 · IF 7.7

Black TiO2-supported copper nanoparticles for efficient photocatalytic N-formylation of N-methylaniline with CO2

Shibo Yuan,Peng Bai,Yi He,Jiafa Chen,Yicheng Zhao,Yongdan Li

Photocatalytic N-formylation of amines with CO 2 is a promising strategy to convert CO 2 into value-added chemicals sustainably. In this work, a black TiO 2 -supported Cu photocatalyst is prepared through a solvothermal method for the N-formylation of N-methylaniline with NaBH 4 as the reducing agent. Cu nanoparticles and oxygen vacancies are formed on the surface of the photocatalyst after reduction with H 2 , which decreases the band-gap energy and promotes the separation of photogenerated electrons and holes, thereby improving the photocatalytic activity remarkably. A 100 % conversion is achieved after 9 h radiation, and the yield of N -methylformanilide reaches 81 %. Both the amount of NaBH 4 and the pressure of CO 2 show important influences on the activity and selectivity of the photocatalytic process, and the carbon and hydrogen in the aldehyde group are from CO 2 and NaBH 4 , respectively. The photocatalyst also shows promising cycling durability.

研究领域: 材料科学 · 化学工程
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JOURNAL OF MATERIALS SCIENCE · 2018 ·Vol. 53 ·期 14 ·10302-10312 · IF 2.993

Synthesis of metal-phase-assisted 1T@2H-MoS2 nanosheet-coated black TiO2 spheres with visible light photocatalytic activities

Fan Hongmei,Wu Rong,Liu Haiyang,Yang Xi,Sun Yanfei,Chen Chu

Hybrid-phase-MoS 2 (1T@2H-MoS 2 ) nanosheet-coated black TiO 2 spheres (1T@2H-MoS 2 /B-TiO 2 ) were prepared using a hydrothermal method and a chemical reduction method under an argon atmosphere. X-ray diffraction, transmission electron microscope, Raman spectra and X-ray photoelectron spectroscopy indicated the generation of the 1T@2H-MoS 2 and black TiO 2 . The efficiency of the 1T@2H-MoS 2 /B-TiO 2 core–shell structure degradation of rhodamine B (RhB) reached 98.0%. The high photocatalytic activity was due to the presence of 1T-MoS 2 , which accelerated the electron transfer to participate in the redox reaction. In addition, the presence of B-TiO 2 suppressed the undesirable electron–hole recombination. Finally, the synergistic effect between 1T@2H-MoS 2 and B-TiO 2 promoted the separation of the photoelectron–hole pairs. Moreover, scavenger studies found that the hydroxyl radical ( • OH) was the dominant reactive oxygen species in the degradation of RhB under visible light irradiation. The possible growth mechanism and photocatalytic mechanism are discussed in detail. The results of this study will contribute to the improvement in the visible light absorption and photocatalytic degradation of catalysts.

研究领域: 材料科学 · 环境科学
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RSC Advances · 2019 ·Vol. 9 ·期 63 ·36907-36914 · IF 3.049

Mesoporous hollow black TiO2 with controlled lattice disorder degrees for highly efficient visible-light-driven photocatalysis

Xiongrui Jiang,Zhiyao Yan,Jing Zhang,Junzheng Gao,Wanxia Huang,Qiwu Shi,Hengzhong Zhang

Black TiO2 has received tremendous attention because of its lattice disorder-induced reduction in the TiO2 bandgap, which yields excellent light absorption and photocatalytic ability. In this report, a highly efficient visible-light-driven black TiO2 photocatalyst was synthesized with a mesoporous hollow shell structure. It provided a higher specific surface area, more reaction sites and enhanced visible light absorption capability, which significantly promoted the photocatalytic reaction. Subsequently, the mesoporous hollow black TiO2 with different lattice disorder-engineering degrees were designed. The structure disorder in the black TiO2 obviously increased with reduction temperature, leading to improved visible light absorption. However, their visible-light-driven photocatalytic efficiency increased first and then decreased. The highest value can be observed for the sample reduced at 350 °C, which was 2-, 1.4- and 5-fold that of the samples reduced at 320 °C, 380 °C and 400 °C, respectively. This contradiction can be ascribed to the varied functions of the surface defects with different concentrations in the black TiO2 during the catalytic process. In particular, the defects at low concentrations boost photocatalysis but reverse photocatalysis at high concentrations when they act as charge recombination centers. This study provides significant insight for the fabrication of high-efficiency visible-light-driven catalytic black TiO2 and the understanding of its catalysis mechanism.

CAS / MDL: 100-21-0 78-10-4
研究领域: 材料科学 · 光催化技术 · 纳米技术
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Journal of Materials Chemistry B · 2018 ·Vol. 6 ·期 22 ·3800-3810 · IF 4.776

Controllable synthesis of Fe3O4 nanoflowers: enhanced imaging guided cancer therapy and comparison of photothermal efficiency with black-TiO2

Madiha Saeed,M. Zubair Iqbal,Wenzhi Ren,Yuanzhi Xia,Chuang Liu,Waheed S. Khan,Aiguo Wu

Photothermal therapy (PTT) has emerged as one of the promising cancer therapy approaches. However, nanoparticles (NPs) which are used for PTT might be biopersistent and potentially toxic. The current research explores the promising use of Fe3O4 nanoflowers as nontoxic, efficient photothermal, and strong T2 type magnetic resonance imaging (MRI) contrast agents for imaging-guided photothermal cancer therapy. In this study, a facile solvothermal method is used to fabricate PEG-coated Fe3O4 nanoflowers with controllable dimensions. Their successful fabrication, the effect of the reaction parameters, and their magnetic properties are investigated in depth. The therapeutic performance of the Fe3O4 nanoflowers (Fe-NFs) is evaluated and compared with commercially available black TiO2 nanoparticles (b-TiO2) under an 808 nm laser. The photothermal therapy efficiency of the Fe-NFs is observed to be better than that of the reported Fe3O4 nanoparticles. In vitro and in vivo investigation demonstrates that the therapeutic performance of the Fe-NFs is comparable to that of b-TiO2. Moreover, the Fe-NFs show excellent magnetic properties and magnetic resonance imaging capability to monitor therapeutic performance.

研究领域: 生物医学工程 · 材料科学 · 医学影像学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2021 · IF 5.455

Hollow structured black TiO2 with thickness-controllable microporous shells for enhanced visible-light-driven photocatalysis

Zhiyao Yan,Wanxia Huang,Xiongrui Jiang,Junzheng Gao,Yiwen Hu,Hengzhong Zhang,Qiwu Shi

Black TiO 2 has attracted great attentions due to its wide application potentials in visible-light photocatalysis , solar-thermal conversion for water evaporation, photothermal therapy and so on because of its controllable band gap using lattice disorder engineering. In this work, we proposed the design of microporous hollow structure in black TiO 2 with thickness-controllable nano-shells to further optimize its photocatalytic ability. The hollow shells were produced from the evaporation-induced self-assembly (EISA) followed by NaBH 4 reduction, and the shell thicknesses could be adjusted from ~20 to ~145 nm. The prepared microporous hollow shells showed excellent light absorption and enhanced photocatalysis performance with decreased shell thickness. Under visible light irradiation, the photocatalytic efficiency of the 20-nm shells was ~8 times higher than that of the 145-nm shells, revealing the strong promotion effect of the nano-shell design on the photocatalytic activity of hollow black TiO 2 . This great effect can be attributed to the higher surface area, more catalytic active sites and less diffusing distance in pore channels of the thinner shells. Our work demonstrates a scheme for the porous hollow structural design of black TiO 2 with ultrathin nano-shell, and provides significant insights for its applications in higher efficiency of visible-light utilization and photocatalysis.

CAS / MDL: 78-10-4
研究领域: 材料科学 · 环境科学
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Flame-assisted combustion preparation of highly efficient black TiO2 microspheres photocatalysts under visible light

Yahui Zhou,Xiaohua Cheng,Zijian Duan,Xin Liu,Huiyu Yang,Bo Deng

Black TiO 2 microspheres photocatalysts with high light absorption intensity and photosensitive activity were prepared by a simple two-step method of flame-assisted combustion hydrolysis of tetrabutylorthotitanate (TBOT) and NaBH 4 reduction. The black TiO 2 microspheres photocatalysts were characterized by XRD, TEM, XPS, EELS , and UV-Vis absorption spectroscopy . The results show that the reduced TiO 2 exhibits a unique core-shell composite structure with a large number of oxygen vacancies and defects in the outer layer due to Ti 3+ , which effectively reduces the band gap of the photocatalyst. Compared with the commercial P25 catalyst, B-TiO 2 (1:7) showed higher removal of carbamazepine (CBZ) under visible light and its photocatalytic activity was 1.7 times higher than that of P25. This high photocatalytic activity is due to the efficient separation of electron-hole pairs, creating a greater number of active species. B-TiO 2 (1:7) maintained high activity after five repeated cycles and achieved 89.7 % removal of CBZ.

CAS / MDL: 298-46-4
研究领域: 材料科学 · 环境科学
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ChemPlusChem · 2019 ·Vol. 84 ·期 5 ·474-480 · IF 3.441

An Efficient Photocatalyst Based on Black TiO2 Nanoparticles and Porous Carbon with High Surface Area: Degradation of Antibiotics and Organic Pollutants in Water

Yu Fang,Yuanyuan Li,Feng Zhou,Peiyang Gu,Jiadi Liu,Dongyun Chen,Najun Li,Qingfeng Xu,Jianmei Lu

Graphical Rapid removal : A photocatalyst comprising black TiO 2 nanoparticles (BTNs) grown in situ on a porous carbon material (PC) can be used for the efficient photocatalytic degradation of antibiotics and pollutants. Under visible-light irradiation, the photogenerated electrons of BTNs react with O 2 to generate . O 2 − radical species and holes (h + ) which can decompose the adsorbed antibiotics. The PC allows a more efficient adsorption as well as rapid transport of charge carriers and provides more active sites. Porous carbon (PC) materials with high surface area can separate electron–hole pairs and adsorb organic pollutants more effectively. A series of nanocomposites were prepared by anchoring black TiO 2 nanoparticles (BTN) onto PC through a calcination process. Chemical and structural features of samples were examined by X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, powder X-ray diffraction (P-XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses. The resulting adsorption-photocatalysis synergistic effect led to a dramatically improved photocurrent for BTN@PCs, thus indicating the high photocatalytic performance toward water-soluble organic species. For instance, the degradation of tetracycline under visible light reached 90 %, which is higher than that for activated carbon doped onto BTN (57 %) without any additional agents. Moreover, the degradation of other antibiotics (such as oxytetracycline and ciprofloxacin) and methylene blue were also studied, thus showing that this system has the potential to be used for water treatment.

研究领域: 环境科学 · 材料科学
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Materials Research Express · 2017 ·Vol. 4 ·期 12 ·125503 · IF 1.068

Fabrication of photo-absorption enhanced black TiO2–SiO2 by flame spraying

Jiaxi Liu,Gang He,Nan Lu,Jiangtao Li

Photo-absorption enhanced black TiO2–SiO2 microspheres were prepared by flame spraying synthesis. The phase composition, microstructure, infrared absorption, and emission property of the synthesized samples were investigated. Compared with the rutile TiO2 raw material, the visible light and near-infrared absorptivity of the flame sprayed TiO2 is significantly enhanced. The addition of SiO2 promotes the rutile-to-anatase phase transformation and appearance of Ti3+ species. The prepared sample with a composition of 40 at.% TiO2–60 at.% SiO2 exhibits the highest absorption of above 95% in 0.79–2.5 µm, and the highest emissivity of above 0.96 in 3–5 µm and 8–14 µm. The black TiO2–SiO2 microspheres with enhanced photo-absorption properties can be used as a promising optical-thermal conversion material.

研究领域: 材料科学 · 光学
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