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NANO · 2018 · IF 1.1

Fabrication of Novel n-SrTiO3/p-BiOI Heterojunction for Degradation of Crystal Violet Under Simulated Solar Light Irradiation

Yongmei Xia,Zuming He,Jiangbin Su,Ya Liu,Bin Tang,Xiaoping Li

Novel n-SrTiO 3 /p-BiOI heterojunction composites were successfully fabricated by loading SrTiO 3 particles onto the surface of BiOI nanoflakes via a two-step method. The as-prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FE-SEM), energy-disperse X-ray spectroscopy (EDS), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET), diffuse reflectance spectroscopy (DRS) and electrochemical measurements. The results show that the n-SrTiO 3 /p-BiOI heterojunction composites are composed of perovskite structure SrTiO 3 and tetragonal phase BiOI. The composites exhibit excellent photocatalytic performance for the degradation of crystal violet (CV) solution under simulated solar light irradiation, which is superior to that of pristine BiOI and SrTiO 3 . The 30 wt.%SrTiO 3 /BiOI composite is found to be the optimal composite, over which the dye degradation reaches 92.5% for 30 min of photocatalysis. The photocatalytic activity of the 30 wt.%SrTiO 3 /BiOI composite is found to be 3.94 times and 28.2 times higher than that of bare BiOI and SrTiO 3 , respectively. The reactive species trapping experiments suggest that • O 2 − and holes are the main active species responsible for the CV degradation. In addition, the electrochemical measurements elucidate the effective separation of photoinduced electron–hole pairs. Moreover, on the basis of experimental and theoretical results, a possible mechanism for the enhanced photocatalytic performance of the SrTiO 3 /BiOI heterojunction composites is also proposed.

研究领域: 材料科学 · 环境科学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2017 · IF 9.446

Carbon dots-TiO2 nanosheets composites for photoreduction of Cr(VI) under sunlight illumination: Favorable role of carbon dots

Yaru Li,Zhongmin Liu,Yongchuan Wu,Jitao Chen,Jingyu Zhao,Fengmin Jin,Ping Na

Carbon dots-TiO 2 nanosheets (CDs-TNs) composites were synthesized by hydrothermal method and applied for the first time in photoreduction of Cr(VI) under sunlight illumination. The materials were characterized by transmission electron microscope, X-ray diffraction, thermogravimetric analysis, Fourier transform infrared spectrometer, and X-ray photoelectron spectroscopy analysis. The results confirmed that CDs are successfully incorporated with TNs through Ti O C bonds. With the introduction of CDs, CDs-TNs composites exhibit excellent photoreduction performance of Cr(VI), which is higher than that of TNs, P25 and CDs-P25. The unique upconversion property and electron transfer property of CDs play essential roles on light harvesting and charge carriers transferring in the photoreduction process. Most importantly, CDs could facilitate the formation of H 2 O 2 , leading to the consumption of holes. As a result, the recombination of photoinduced electron-hole pairs is hindered and photoreduction activity of CDs-TNs is promoted.

研究领域: 材料科学 · 环境科学 · 光催化
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Environmental Chemistry · 2012 ·Vol. 9 ·期 6 ·558-563 · IF 2.57

Photochlorination of aniline in Fe3+-containing saline water under simulated solar light irradiation

Lei Wu,Xuefeng Hu,Lei Wu,Xuefeng Hu

Environmental context Aromatic amines are widely used chemicals, which show enhanced toxicity and longer environmental persistence when halogenated. We investigated the chlorination of aniline in seawater and in natural aqueous solutions containing Fe3+ and Cl–, under simulated sunlight irradiation. The results increase our understanding of the transformation pathway of typical nitrogen-containing aromatic contaminants in the environment. Photochlorination of aniline was observed in aqueous solutions containing dissolved FeIII and chloride ions under simulated solar light irradiation. Effects of O2, Cl–, Fe3+ and pH on the formation of chloroanilines (CAs) were investigated. para-chloroaniline (4CA) was identified as the main chlorinated product. The formation of 4CA is enhanced with increased concentrations of Cl– or Fe3+, and decreased pH, whereas oxygen plays a negligible role in the process. The results indicate that, Cl• is formed mainly by the photodissociation of FeCl2+–FeCl2+ complexes, and reacts with Cl– to produce Cl2•–. Aniline is then oxidised by Cl2•– into an anilino radical cation, which further reacts with Cl2•– to generate CAs. The photochlorination of aniline in natural seawater was also observed. Other phototransformation products of aniline were detected and a transformation pathway was proposed. This work provides evidence for the photochemical chlorination path of aniline-based aromatic amines in aqueous solutions.

研究领域: 环境科学 · 化学
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CATALYSIS COMMUNICATIONS · 2019 · IF 3.674

Synthesis of Ni2P/Zn3In2S6 hierarchical heterostructure for improving photocatalytic H2 evolution

Li-Li Chu

2D-3D noble-metal-free Ni 2 P/Zn 3 In 2 S 6 hierarchical composites were fabricated firstly by the hydrothermal method and characterized by the relative techniques. The average H 2 evolution rate over the optimized Ni 2 P/Zn 3 In 2 S 6 under simulated sunlight can reach up to 6.4 mmol g −1  h −1 , which is about 3.4 and 2.6 times higher than that of pure Zn 3 In 2 S 6 and Pt/Zn 3 In 2 S 6 hybrid. The excellent photocatalytic performance can be attributed to the interaction between the well-dispersed ultrafine Ni 2 P cocatalyst and the 2D-3D Zn 3 In 2 S 6 hierarchical structure, which contributes to the separation and transportation of the photoinduced charge carriers.

研究领域: 材料科学 · 能源科学
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CATALYSIS TODAY · 2018 · IF 4.667

Ag2MoO4 nanoparticles encapsulated in g-C3N4 for sunlight photodegradation of pollutants

Ming Wu,Hongying Lv,Teng Wang,Zhimin Ao,Hongqi Sun,Chengyin Wang,Taicheng An,Shaobin Wang

Graphitic carbon nitride (g-C 3 N 4 ), a promising metal-free photocatalyst, shows a high thermal stability, excellent chemical stability, and great optical absorption of solar light. However, a short life of activated electron-hole pairs limits g-C 3 N 4 in practical applications. In this work, Ag 2 MoO 4 nanoparticles encapsulated in g-C 3 N 4 (Ag 2 MoO 4 /g-C 3 N 4 ) was synthesized with a facile in-situ precipitation method. A variety of characterization techniques were applied for analyzing the compositions, morphologies and optical properties of Ag 2 MoO 4 /g-C 3 N 4 . The band structure of Ag 2 MoO 4 produces a synergistic effect with g-C 3 N 4 , which can efficiently increase solar light absorption and reduce the recombination rate of the photo-induced electron-hole pairs. Therefore, this hybrid catalyst presents a much higher photocatalytic activity for the degradation of various organic pollutants (bisphenol A, acyclovir, and methyl orange) and strong stability under both artifical and real sunlight, which is promising for practical application.

研究领域: 材料科学 · 环境科学
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY · 2021 ·Vol. 329 ·期 2 ·1125-1133 · IF 1.371

The enhanced photocatalytic reduction of uranium(VI) by ZnS@g-C3N4 heterojunctions under sunlight

Wu Fan,Zhang Zhibin,Cheng Zhongping,Zhou Runze,Lin Yuling,Liu Yuhui,Wang Youqun,Cao Xiaohong,Liu Mingguang,Liu Yunhai

The photocatalytic reduction of soluble \({\text{UO}}_{2}^{2 + }\) from radioactive wastewater is becoming an effective method to reduce radioactive pollution, while available catalysts are considerable limitation. Herein, the ZnS@g-C 3 N 4 (ZSGCN) heterojunctions complexes were compounded as catalysts to reduce \({\text{UO}}_{2}^{2 + }\) . The results from TEM, XRD, XPS, EIS, DRS and PL showed that the ZnS nanoparticles combined with graphite carbon nitride (GCN), which is the construction of heterojunctions broadened the absorption range of sunlight. The ZSGCN-5 presented the optimal photocatalytic reduction activity to \({\text{UO}}_{2}^{2 + }\) , which was 4.34 times than that of pristine GCN. The ZSGCN-5 heterojunction becomes a promising photocatalyst for radioactive environment remediation.

研究领域: 环境科学 · 材料科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Effect of TiO2 crystal phase on the construction of TiO2/g-C3N4 heterojunction photocatalyst for efficient sunlight photodegradation of naphthalene

Yu Huang,Xinyang Xu,Guangjian Fan,Xiaoxuan Zhu,Lin Zhu,Xi Chen

The effect of TiO 2 crystal phase on the photocatalytic properties of TiO 2 /g-C 3 N 4 heterojunction photocatalyst under sunlight irradiation was investigated through experiments and theoretical calculations. Results reveal that for TiO 2 /g-C 3 N 4 heterojunction photocatalyst, anatase phase TiO 2 can adjust the band edge positions to ensure the generation of strongly oxidizing radical species (·O 2- and ·OH), and rutile phase TiO 2 can effectively reduce the band gap to more efficiently utilize sunlight. Consequently, the combination of g-C 3 N 4 with P25 TiO 2 composed of both anatase and rutile phases is the most favorable combination for sunlight-driven photocatalyst among the obtained three TiO 2 /g-C 3 N 4 heterojunction photocatalyst. P25 TiO 2 and g-C 3 N 4 form a type-II/type-II heterostructure with stepped heterojunction and concave heterojunction. The P/CN photocatalyst exhibits excellent photocatalytic activity with degradation efficiencies for naphthalene reaching 100% within 120 min of sunlight irradiation, as well as considerable stability. The combination of P25 TiO 2 and g-C 3 N 4 has shown significant potentials in improving the separation and transfer efficiency of photogenerated electron-hole pairs, as well as enhancing the utilization of sunlight in photocatalytic process. This work provides a promising strategy for the preparation of highly active TiO 2 /g-C 3 N 4 heterojunction photocatalyst for the effective treatment of naphthalene from water.

CAS / MDL: 13463-67-7
研究领域: 环境科学 · 材料科学
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CATALYSIS LETTERS · 2025 ·Vol. 155 ·期 4 ·1-19 · IF 2.4

g-C3N4 Enhanced Fe3+/ Fe2+ Cycling to Activate PMS for Pharmaceuticals Degradation Under Solar Irradiation

Cheng Liu,Zhu Zhexin,Wang Gangqiang,Du Shiting

Since Peroxymonosulfate (PMS) is readily available and can produce sulfate radicals with a stronger oxidation capacity, the Fenton-like system Fe 2+ /PMS has gradually replaced Fe 2+ /H 2 O 2 system in organic pollutants degradation. However, the Fe 3+ /PMS system has almost no degradation effects, with the conversion of Fe 2+ to Fe 3+ being the rate-limiting step in the Fe 3+ /PMS system. In this paper, graphite-like phase carbon nitride (g-C 3 N 4 ) was employed to activate PMS using trace amounts of Fe 3+ for the treatment of water pollution under sunlight, and the Fe 3+ /g-C 3 N 4 /PMS system demonstrated the ability to rapidly degrade a wide range of difficult-to-degrade organic pollutants. The Fe 3+ /g-C 3 N 4 /PMS system was able to completely degrade carbamazepine (CBZ) within 30 min under sunlight. The fundings indicated that this system effectively improved the stringent limitations typically associated with Fenton process regarding the feed ratio of metal ions to oxidants, and could efficiently degrade CBZ across a broad pH range. In addition, the Fe 3+ concentration of 6.17 × 10 −6 M was used in the experiments to avoid the generation of large amounts of “iron sludge”. The trap burst experiments, DMSO oxidation experiments and electron paramagnetic resonance spectroscopy experiments indicated that O 2 · − and 1 O 2 exerted the major effectiveness in the photocatalytic degradation reaction of CBZ, and SO 4 · − and · OH jointly promoted the CBZ degradation. Graphical

研究领域: 环境科学 · 化学
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CHINESE JOURNAL OF CHEMISTRY · 2021 ·Vol. 39 ·期 5 ·1310-1318 · IF 6

Facile Construction of Carbon Dots Layer and Oxygen Vacancies Simultaneously onto TiO2 to Enhance Photoreduction Activity

Jingyu Zhao,Yaru Li,Ping Na

Main observation and conclusion We reported a facile and green hydrothermal strategy to tailor the carbon dots layer (CDL) and oxygen vacancies (Vo) modified on TiO 2 , by using ascorbic acid as CDL precursor and Vo regulator. The amorphous CDL was uniformly coated on the surface of the as prepared CDL@TiO 2– x composites by Ti-O-C bond. With the increase of carbon content, the amorphous CDL gradually became thicker, while the Vo concentration first increased and then decreased. 1.5 CDL@TiO 2– x possessed the highest Vo concentration. With the decoration of CDL and Vo, the photoreduction properties of CDL@TiO 2– x composites were significantly improved. Under simulated solar light and visible light, the reaction rates of 1.5 CDL@TiO 2– x were 9.6 times and 216 times higher than that of pure TiO 2 , respectively. Interestingly, the results discovered that CDL and Vo influenced the properties of CDL@TiO 2– x composites in different ways. The primary function of CDL was to improve the utilization of solar light, and the enhancement of the charge transfer ability was decided by Vo and CDL together. Our work provides a new strategy for the modification of TiO 2 and sheds new light on the respective role of CDL and Vo when they coexist in the catalyst.

CAS / MDL: 140-22-7 9003-99-0
研究领域: 材料科学 · 环境科学
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ENVIRONMENTAL POLLUTION · 2020 · IF 6.793

Extensive solar light harvesting by integrating UPCL C-dots with Sn2Ta2O7/SnO2: Highly efficient photocatalytic degradation toward amoxicillin

Shukun Le,Weishan Yang,Gonglai Chen,Aoyu Yan,Xiaojing Wang

The carbon dots (C-dots) mediated Sn 2 Ta 2 O 7 /SnO 2 heterostructures with spongy structure were successfully assembled by simple hydrothermal route. The photocatalytic removal efficiency of amoxicillin (AMX, 20 mg L −1 ) over C-dots/Sn 2 Ta 2 O 7 /SnO 2 was estimated to reach up 88.3% within 120 min simulated solar light irradiating. Meanwhile, the HPLC-MS/MS analysis and density functional theory (DFT) computation were examined to clarify the photo-degradation pathway of AMX. The mechanism investigation proposed that with the modification of C-dots, the photocatalysts improves the utilization of solar energy by harvesting the long wavelength solar light due to their unique up-converted photoluminescence (UCPL). In addition, the porous spongy structure and plenty of tiny C-dots promote the ability of adsorption by enlarged specific surface area. Furthermore, the C-dots mediated Z-type heterojunction of Sn 2 Ta 2 O 7 /SnO 2 facilitates the efficient separation and transfer of photo-induced carriers. Our work affords a promising approach for the design of the high-efficient photocatalysts to remedy poisonous antibiotics in aqueous environment.

研究领域: 环境科学 · 材料科学 · 化学工程
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Inactivation of Microcystis aeruginosa using piezoelectric T-BaTiO3/Ag3PO4-PVDF composite photocatalyst: Characterization, performance and mechanism

Yang Tao,Gongduan Fan,Xin Lin,Chenjian Cai,Xingfeng Cao,Zhimin He,Jing Luo,Kai-Qin Xu

To mitigate the profound impact of Microcystis aeruginosa algal bloom outbreaks on aquatic ecosystems and human health, a piezoelectric T-BaTiO 3 /Ag 3 PO 4 -PVDF composite photocatalyst (T-BTO/AP-PVDF) was successfully synthesized in this study. The catalyst inactivated 97.12% of Microcystis aeruginosa within 4 h by the combined effect of ultrasound and sunlight, and the inactivation rate remained above 88% after five cycles of reuse, which exhibits excellent inactivation effectiveness and stability. Under the conditions of piezo-photocatalytic, the analysis of the physiological properties of algal cells showed that T-BTO/AP-PVDF produced a large amount of •OH, which were active species that could effectively inactivate the algal cells and promote the degradation of organic matter, thus preventing the occurrence of secondary pollution. The composite photocatalysts were characterized using XRD, SEM, XPS, FTIR, PFM, and WCA. Combined with the results of quenching experiments, possible mechanisms for the inactivation of Microcystis aeruginosa by T-BTO/AP-PVDF were proposed. The application results in actual water bodies further proved that T-BTO/AP-PVDF is a new method for effectively inhibiting cyanobacterial bloom outbreaks and shows promising potential for application.

CAS / MDL: 12047-27-7
研究领域: 环境科学 · 微生物学
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APPLIED SURFACE SCIENCE · 2015 · IF 2.711

Adsorption and photocatalytic degradation of pharmaceuticals by BiOClxIy nanospheres in aqueous solution

Xiaoning Wang,Wenlong Bi,Pingping Zhai,Xiaobing Wang,Hongjing Li,Gilles Mailhot,Wenbo Dong

BiOCl x I y nanospheres have been synthesised via precipitation method in ethylene glycol (EG)-water (H 2 O) mixed solvent at 80   °C and ambient pressure. Results of BiOCl x I y characterisation showed that these composite materials well combined BiOCl with BiOI crystals, which displayed flower-like hierarchical nanospheres consisted of numerous nanosheets and possessed smaller particle size, higher surface area than those in previous papers. The great surface area resulted in its high adsorption abilities of hydroxyphenylacetic acid (p-HPA) in the dark, the adsorption process could be suitably described by a pseudo-second-order kinetics model and the adsorption isotherms could be well fitted with Freundlich and Langmuir equations. The photocatalytic degradation of p-HPA and acetaminophen (ACTP) were investigated under simulated solar and visible irradiation using BiOCl x I y catalyst for the first time. The combination of BiOCl and BiOI to a certain extent has largely improved the remove efficiency, and BiOCl 0.75 I 0.25 was the optimal catalyst with almost 100% removal of p-HPA and 80% removal of ACTP under solar light for 3   h. Experimental results demonstrated that the photocatalytic degradation of p-HPA and ACTP followed pseudo-first-order kinetics and O 2 − and dissolved oxygen play predominant roles in photocatalytic process efficiency. This research will supply an environment-friendly photocatalyst for pharmaceutical wastewater treatment under sunlight.

CAS / MDL: 156-38-7 298-83-9
研究领域: 环境科学 · 材料科学
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