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JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

Enhanced interface charge transfer via n-n WO3/Ti–Fe2O3 heterojunction formation for water splitting

Qiannan Wu,Qijing Bu,Shuo Li,Yanhong Lin,Xiaoxin Zou,Dejun Wang,Tengfeng Xie

Inevitable drawbacks on α-Fe 2 O 3 photoanodes , such as poor conductivity, short hole diffusion length , high electron-hole recombination rate, limit their photoelectrochemical (PEC) performance for water oxidation . The construction of heterojunction is an effective approach to improve the PEC performance of photoanodes. Herein, we report the design of the WO 3 /Ti–Fe 2 O 3 heterojunction photoanodes, which are synthesized by two simple hydrothermal method . The optimized WO 3 /Ti–Fe 2 O 3 photoanode shows remarkably improved photocurrent of 2.15 mA/cm 2 at 1.23 V versus reversible hydrogen electrode (RHE) without additional cocatalyst , which is higher than that of previous literatures. The improvement benefits from reduced charge transfer resistance in the bulk of Ti–Fe 2 O 3 photoanode and improved charge separation efficiency, which can been further confirmed by electrochemical impedance spectroscopy (EIS), the transient photovoltage (TPV) and the work function (WF) measurement. The present work also provide new opportunities in developing high performance photoanodes for PEC water splitting .

研究领域: 材料科学 · 物理化学 · 能源科学 · 半导体光电化学 · 纳米材料
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Materials Research Express · 2018 ·Vol. 6 ·期 2 ·025517 · IF 1.151

Synthesis of flexible CuxS-CNT/Ti counter electrodes for improved quantum dots sensitized solar cells

Qingqing Pei,Zeng Chen,Shuo Wang,Di Zhang,Pin Ma,Shengjun Li

In this study, flexible CuxS-CNT/Ti counter electrodes (CEs) were prepared through successive ionic layer adsorption followed by reaction technique (SILAR). The electrocatalytic activities of the obtained CuxS-CNT/Ti CEs were investigated by electrochemical impedance spectroscopy (EIS) and Tafel polarization measurements. The results indicated that the catalytic activities of CNT/Ti films significantly improved after deposition of CuxS nanoparticles. CuxS-CNT/Ti flexible CEs were then assembled with CdS and CdSe QDs co-sensitized TiO2 film electrodes to prepare simple QDSCs. The optimized QDSCs based on CuxS-CNT/Ti flexible CEs delivered photovoltaic conversion efficiencies reaching ca. 6.20%. These values were ca. 48.7% higher than those based on CNT/Ti CEs.

研究领域: 材料科学 · 能源技术 · 纳米技术
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CARBON · 2022 · IF 11.307

Ti doped SiOC precursor to activate gyroid sensing structures

Shixiang Zhou,Li Yao,Tong Zhao,Hui Mei,Laifei Cheng,Litong Zhang

Ti-doped polymer-derived SiOC ceramic has multi-functional sensing capability due to its semiconductive properties. Their mechanical and chemical stability provide reliable support for their long-term service and safe operation in extreme environments. The sensing properties of Ti-doped SiOC (SiTiOC) can be optimized by modulation carrier concentration. Meanwhile, it can be fabricated by 3D printing as structural-strengthened components, promising for abnormal environmental signals warning under harsh conditions. In this work, SiTiOC gyroid structures were constructed by vat photopolymerization. The resulting components had thermistor characteristics with a negative temperature coefficient . After the Ti doping, the structures exhibited a high conductivity of 1.10 S/m, as the Ti ions formed an efficient percolation network by introducing acceptor impurities. The structures also had piezoresistive capability as the conductive phases can generate a tunneling-percolation conduction effect. They can detect a strain of less than 0.5%. Furthermore, the structures can realize n-butanol sensing for their p-type semiconductor properties . The components also had an excellent mechanical performance with the compressive strength and Young's modulus of 92.83 MPa and 4.28 GPa, respectively, ensuring reliable service under pressure loading.

研究领域: 材料科学 · 传感技术 · 增材制造
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2023 · IF 22.1

Amino-rich Ag-NWs/NH2-MIL-125(Ti) hybrid heterostructure via LSPR effect for photo-assist uranium extraction from fluorine-containing uranium wastewater without sacrificial agents

Boyuan Tu,Kaifu Yu,Dengjiang Fu,Li Zhou,Ruixiang Wang,Xinying Jiang,Huanhuan Liu,Xin Cao,Xiang Gong,Rong He,Yongjian Tang,Tao Chen,Wenkun Zhu

Photo-assist uranium extraction from fluorine-containing uranium wastewater by building semiconductor-plasma material heterostructure is a forward-looking strategy, which not only effectively accelerates F-U separation via the LSPR effect but also impacts the intensity of binding between U (VI) and site. Here, we developed an amino-rich Ag-NWs/NH 2 -MIL-125(Ti) (AgNW/N-M(Ti)) hybrid nanowires with LSPR effect for photo-assist uranium extraction. Accordingly, the AgNW/N-M(Ti) hybrid nanowires presented 90.4% removal efficiency for U(VI) without a sacrificial agent at the U: F molar ratio of 1:20. By virtue of In-situ KPFM, we identify hot electrons generated over AgNW were transferred to amino-rich N-M(Ti) to efficiently reduce the U(VI) adsorbed on the N-M(Ti), which effectively enhances the excellent uranium removal performance of AgNW/N-M(Ti) hybrid nanowires. This strategy may open a paradigm for the development of advanced heterojunctions with the LSPR effect as catalysts for photo-assisted uranium extraction from fluorine-containing uranium wastewater.

研究领域: 材料科学 · 环境科学
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RSC Advances · 2014 ·Vol. 4 ·期 29 ·15216-15224 · IF 3.708

An improved kinetic model for cellulose hydrolysis to 5-hydroxymethylfurfural using the solid SO42−/Ti-MCM-41 catalyst

Chong-Wen Jiang,Xin Zhong,Zheng-Hong Luo

5-Hydroxymethylfurfural (5-HMF) which can be produced from cellulose is considered as one of the promising green platform chemicals. In this work, the conversion of cellulose to 5-HMF was carried out through hydrolysis in a batch reactor using the SO42−/Ti-MCM-41 catalyst at a temperature of 463–503 K. Two analytical techniques including the 3,5-dinitrosalicylic acid (DNS) method and high performance liquid chromatography (HPLC) were employed to track the time evolution of the main reagents, i.e., cellulose, 5-HMF and reducing sugar. Based on the typical kinetic experiments for the cellulose hydrolysis, a comprehensive hydrolysis mechanism was introduced to describe the heterogeneous hydrolysis of cellulose to 5-HMF. A corresponding kinetic model was proposed on the basis of the hydrolysis mechanism and the mass balance law. The results show that the predicted data obtained via the suggested model agree well with the experimental results. In addition, some data from the open reports were referred for further model verification in this work. The kinetic model suggested in this work is a mechanism model for the heterogeneous catalytic cellulose hydrolysis process, which is different from the previous first-order kinetic model.

研究领域: 化学工程 · 可再生化学
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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2025 · IF 6.2

Low-temperature dielectric relaxation and microwave-terahertz dielectric response of Ca-Sm-Ti-O perovskite ceramics

Weijia Guo,Yutian Lu,Chongyang Zhang,Zhenxing Yue

Low-loss (high- Q × f , where Q = 1/tan δ ) dielectric ceramics can help achieve efficient microwave signal transmission and reduce heat generation. In the traditional Ca-Ln-Ti-O perovskite system (where Ln = rare earth) with the general formula of Ca 1– x Ln 2 x /3 TiO 3 (CST x ), the sharp decline in the Q × f value when x  > 0.5 remains unexplained, posing a challenge for designing low-loss ceramics. In this study, CST x ceramics ( x  ≤ 0.7) are synthesized via the solid-state reaction method, with a focus on their structure, defects, and broadband dielectric properties. A significant discrepancy between the Q × f values in the microwave and terahertz bands is found when x  ≥ 0.6, suggesting the presence of additional loss mechanisms in the microwave band beyond ion displacement depolarization. Meanwhile, the low-frequency dielectric spectra show a weak dielectric relaxation in the low-temperature region, attributed to the partially ordered A -site vacancies. Therefore, this relaxation can act on the microwave frequency band at room temperature, resulting in a sharp decline in Q × f values. Such low-frequency and low-temperature dielectric relaxation should not be ignored in the research of microwave dielectric ceramics. These findings provide a crucial theoretical reference for developing low-loss microwave dielectric ceramics.

CAS / MDL: 12060-58-1 471-34-1
研究领域: 材料科学 · 电子工程
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JOURNAL OF CATALYSIS · 2023 · IF 7.3

Ti-MWW synthesis via acid-modulated isomorphous substitution of ERB-1 for efficient ethylene oxidative hydration to ethylene glycol

Yuexia Wang,Qibin Yao,Bowen Xu,Kehang Lin,Mengshan Deng,Xinqing Lu,Rui Ma,Yanghe Fu,Weidong Zhu

Although the oxidative hydration of ethylene with hydrogen peroxide (H 2 O 2 ) to ethylene glycol (EG) over Ti-MWW zeolites take advantages of step-saving and facile operation, both H 2 O 2 utilization efficiency and EG yield are relatively low, because some extra-framework octahedral Ti species are usually formed in the Ti-MWW zeolites synthesized by prevailing methods, which are detrimental to selective oxidation . In the present work, an acid-modulated isomorphous substitution method, i.e. , layered borosilicate MWW-type zeolite (ERB-1) treated with HNO 3 aqueous solution containing tetrabutyl orthotitanate (TBOT), is developed to synthesize a Ti-MWW zeolite without extra-framework octahedral Ti species under the optimized synthesis conditions. In combination with the results from extensive characterizations for the synthesized zeolites, it is found that in the zeolite prepared by the currently developed synthesis method there are more open Ti(OSi) 3 OH sites formed, resulting in the stronger Lewis acidity that is very helpful to EG production from the oxidative hydration of ethylene with H 2 O 2 , compared to the one synthesized by the prevailing method. Moreover, the developed catalyst is recyclable after the regeneration of the deactivated zeolite by calcination at high temperatures. Therefore, it is anticipated that the currently developed Ti-MWW might be industrially applicable in the one-pot synthesis of EG from ethylene with H 2 O 2 .

研究领域: 化学工程 · 催化材料科学
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FUEL · 2022 · IF 8.035

Catalytic peroxone process for low-temperature denitration with enhanced Ti-OOH formation on P-TiO2: Experimental, DFT, and semi-in-situ UV–vis studies

Mingjia Zhang,Shule Zhang,Fanyu Meng,Mengjie Hu,Zhongyu Wang,Yiqing Zeng,Qin Zhong

Promoting the formation of Ti-OOH in the TiO 2 -based-catalyst/H 2 O 2 /O 3 system is critical to further develop the catalytic peroxone process for low-temperature flue gas denitration. In this study, a series of phosphorus-doped TiO 2 with rich Lewis acid sites and high stability was designed and established, achieving 94 % NO oxidation efficiency with less oxidant (373 K, H 2 O 2 /NO = 1.2, O 3 /NO = 0.5) and high GHSV (1.2 × 10 5 h −1 ). Combining characterizations and DFT results, a possible mechanism was proposed: phosphorus-doping enhanced the Lewis acidity, which was conducive to the adsorption and activation of H 2 O 2 . Moreover, P-TiO 2 significantly promoted the H 2 O dissociation and Ti-OOH formation process by reducing the energy barrier, thereby promoting the synergistic effect between O 3 and Ti-OOH. The semi-in-situ UV–vis DRS demonstrated that the catalytic peroxone process occurs at the solid–liquid interface and the Ti-OOH is consumed in the catalytic process. We hope this work provide a new investigation method and insight into the catalyst design.

研究领域: 环境科学 · 材料科学
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Materials Research Express · 2021 ·Vol. 8 ·期 12 ·125006 · IF 1.62

One pot synthesis of Ti and O co-doped g-C3N4: a novel composite for efficient visible-light-driven photocatalytic inactivation of E. cloacae

Peng She,Chun Yao,Jun Li,Hegang Bao,Xiuquan Xu,Hong Zhou

Co-doping is one of the most facile and efficient strategies for boosting the photocatalytic performance of g-C3N4. Herein, a series of Ti and O co-doped g-C3N4 (Ti/OCN) composites with excellent photocatalytic inactivation activity of Enterobacter cloacae (E. cloacae) were successfully synthesized by simple calcination of urea/formic acid/TiCl4 precursor. The obtained Ti/OCN-3 possessed the optimal photocatalytic capability with complete inactivation of 6.20 log CFU·ml−1 E. cloacae under 60 min of visible light irradiation. The improved photocatalytic disinfection performance was probably attributed to the synergistic effect of Ti and O co-doping, which led to an extended visible light response and accelerated charge transport efficiency. Furthermore, scavenger trapping and electron spin resonance (ESR) experiments revealed that ·O2−, h+ and ·OH were responsible for the enhanced inactivation activity. Overall, this research provided a promising strategy for fabricating g-C3N4-based catalysts to efficiently deal with the hazards of pathogenic microorganisms.

研究领域: 环境科学 · 微生物学 · 材料科学
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Biomaterials Science · 2013 ·Vol. 1 ·期 7 ·703-710 · IF 0

Preparation of porous PLGA/Ti biphasic scaffold and osteochondral defect repair

Chaoyong Zhao,Hongfang Zhang,Bing Cai,Guanglin Wang,Hongsong Fan,Xingdong Zhang

In this study, a porous PLGA/Ti biphasic scaffold was prepared and its potential to repair osteochondral defects was evaluated. The microstructure and mechanical properties of porous PLGA and porous Ti and their interface were characterized. The as-prepared biphasic scaffolds were implanted into rabbit knees for 1 and 3 months (PLGA/Ti group), and the porous PLGA (PLGA group) or empty defect (Untreated group) was also used. The results showed that both porous PLGA and porous Ti had an interconnected porous structure. The mechanical strength of porous PLGA and porous Ti was similar to that of cartilage and subchondral bone, respectively. The interface analysis revealed that the as-prepared biphasic scaffold had good overall integrity and interface stability. The gross observation and histological evaluation of specimens showed that hyaline-like cartilage filled the defects to a certain extent at 3 months for both PLGA/Ti and PLGA groups while the defects remained in an untreated group. In the PLGA/Ti group, better cartilage and subchondral bone repair was observed, and quantitative macroscopic and histological score evaluations confirmed this result, indicating that the porous biphasic PLGA/Ti scaffold had good biocompatibility and the best osteochondral defect repair ability in this study. The as-prepared porous biphasic scaffold showed the potential to be used in osteochondral tissue engineering for osteochondral defect repair.

CAS / MDL: 7761-88-8
研究领域: 组织工程 · 骨科 · 生物材料
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APPLIED SURFACE SCIENCE · 2024 · IF 6.3

Inkless printing and advanced dynamic information anti-counterfeiting via photochromic system based on solid-state Zr/Ti-MOF@WO3 heterojunctions

Bingbing Cui,Guodong Fu

Given that heterojunction engineering is an effective method for improving the separation efficiency of photoexcited electrons in WO 3 -based photochromic systems, a series of solid-state photochromic Zr/Ti-MOF@WO 3 heterojunctions prepared via a facile hydrothermal strategy, where Zr/Ti-MOF with photosensitivity and chemical stability was selected as template to load WO 3 . Zr/Ti-MOF@WO 3 heterojunctions were verified as nanoparticles filled with thin layer structure and WO 3 was diffused into the Zr/Ti-MOF planar. The appropriate conductive band energies facilitate the transport of photostimulated electrons from Zr/Ti-MOF to WO 3 , resulting in a fast photresponse in color changes (it only takes 1 s). In addition, a carrier for information storage and data dynamic encryption was developed on the basis of the photochromic Zr/Ti-MOF@WO 3 heterojunctions. This work presents a promising way to improve the electron/holes separation efficiency by constructing unique heterojunctions and further explore novel WO 3 -based photochromic systems and broaden their applications in rewritable media and data security.

研究领域: 材料科学 · 光学工程
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CHINESE JOURNAL OF CHEMICAL ENGINEERING · 2022 · IF 3.898

Efficient, continuous oxidation of durene to pyromellitic dianhydride mediated by a V-Ti-P ternary catalyst: The remarkable doping effect

Da Ke,Minjia Wang,Jiancheng Ruan,Xinzhi Chen,Shaodong Zhou

Continuous preparation of pyromellitic dianhydride (PMDA) from durene has been studied using a fixed-bed reactor. The reaction was performed using a phosphorus-vanadium-titanium ternary catalyst. Relatively high selectivity and yield of PMDA was obtained. The in-situ characterization was combined with theoretical calculation to reveal the reaction mechanisms, and the remarkable doping effect was discussed.

CAS / MDL: 7803-55-6
研究领域: 化学工程 · 催化化学
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