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Z-scheme CdS/WO on a carbon cloth enabling effective hydrogen evolution

《能源前沿（英文）》 2021年第15卷第3期页码 678-686 doi: 10.1007/s11708-021-0768-6

摘要： Photocatalytic water splitting for hydrogen (H₂) generation is a potential strategy to solve the problem of energy crisis and environmental deterioration. However, powder-like photocatalysts are difficult to recycle, and the agglomeration of particles would affect the photocatalytic activity. Herein, a direct Z-scheme CdS/WO₃ composite photocatalyst was fabricated based on carbon cloth through a two-step process. With the support of carbon cloth, photocatalysts tend to grow uniformly for further applications. The experimental results showed that the H₂ yield of adding one piece of CdS/WO₃ composite material was 17.28 μmol/h, which was 5.5 times as compared to that of pure CdS-loaded carbon cloth material. A cycle experiment was conducted to verify the stability of the as-prepared material and the result demonstrated that the H₂ generation performance of CdS/WO₃ decreased slightly after 3 cycles. This work provides new ideas for the development of recyclable photocatalysts and has a positive significance for practical applications.

关键词： photocatalysis CdS/WO₃ carbon cloth Z-scheme hydrogen evolution

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Photoelectrocatalytic generation of H and S from toxic HS by using a novel BiOI/WO nanoflake array photoanode

《能源前沿（英文）》 2021年第15卷第3期页码 744-751 doi: 10.1007/s11708-021-0775-7

摘要： In this paper, a photoelectrocatalytic (PEC) recovery of toxic H₂S into H₂ and S system was proposed using a novel bismuth oxyiodide (BiOI)/ tungsten trioxide (WO₃) nano-flake arrays (NFA) photoanode. The BiOI/WO₃ NFA with a vertically aligned nanostructure were uniformly prepared on the conductive substrate via transformation of tungstate following an impregnating hydroxylation of BiI₃. Compared to pure WO₃ NFA, the BiOI/WO₃ NFA promotes a significant increase of photocurrent by 200%. Owing to the excellent stability and photoactivity of the BiOI/WO₃ NFA photoanode and I^–/

I 3 −

catalytic system, the PEC system toward splitting of H₂S totally converted S^2– into S without any polysulfide (

S x n −

) under solar-light irradiation. Moreover, H₂ was simultaneously generated at a rate of about 0.867 mL/(h·cm). The proposed PEC H₂S splitting system provides an efficient and sustainable route to recover H₂ and S.

关键词： bismuth oxyiodide (BiOI)/ tungsten trioxide (WO₃) nano-flake arrays (NFA) photoelectrocatalytic (PEC) H₂S splitting H₂ S

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WO₃ nanomaterials synthesized via a sol-gel method and calcination for use as a CO gas sensor

Diah SUSANTI,A.A. Gede Pradnyana DIPUTRA,Lucky TANANTA,Hariyati PURWANINGSIH,George Endri KUSUMA,Chenhao WANG,Shaoju SHIH,Yingsheng HUANG

《化学科学与工程前沿（英文）》 2014年第8卷第2期页码 179-187 doi: 10.1007/s11705-014-1431-0

摘要： Carbon monoxide is a poisonous and hazardous gas and sensitive sensor devices are needed to prevent humans from being poisoned by this gas. A CO gas sensor has been prepared from WO synthesized by a sol-gel method. The sensor chip was prepared by a spin-coating technique which deposited a thin film of WO on an alumina substrate. The chip samples were then calcined at 300, 400, 500 or 600 °C for 1 h. The sensitivities of the different sensor chips for CO gas were determined by comparing the changes in electrical resistance in the absence and presence of 50 ppm of CO gas at 200 °C. The WO calcined at 500 °C had the highest sensitivity. The sensitivity of this sensor was also measured at CO concentrations of 100 ppm and 200 ppm and at operating temperatures of 30 and 100 °C. Thermogravimetric analysis of the WO calcined at 500 °C indicated that this sample had the highest gas adsorption capacity. This preliminary research has shown that WO can serve as a CO gas sensor and that is should be further explored and developed.

关键词： WO₃ nanomaterial sol-gel calcinations CO gas sensor sensitivity

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Design and synthesis of ZnCoO/CdS for substantially improved photocatalytic hydrogen production

《化学科学与工程前沿（英文）》 2023年第17卷第5期页码 606-616 doi: 10.1007/s11705-022-2233-4

摘要： In this study, the hydrogen evolution performance of CdS nanorods is improved using ZnCo₂O₄. ZnCo₂O₄ nanospheres are synthesized using the hydrothermal and calcination methods, and CdS nanorods are synthesized using the solvothermal method. From the perspective of morphology, numerous CdS nanorods are anchored on the ZnCo₂O₄ microspheres. According to the experimental results of photocatalytic hydrogen evolution, the final hydrogen evolution capacity of 7417.5 μmol∙g^–1∙h^–1 is slightly more than two times that of the single CdS, which proves the feasibility of our study. Through various characterization methods, it is proved that the composite sample has suitable optoelectronic properties. In addition, ZnCo₂O₄ itself exhibits good conductivity and low impedance, which shortens the charge-transfer path. Overall, the introduction of ZnCo₂O₄ expands the adsorption range of light and improves the performance of photocatalytic hydrogen evolution. This design can provide reference for developing high-efficiency photocatalysts.

关键词： ZnCo₂O₄ nanosphere CdS nanorods photocatalytic hydrogen evolution

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Hydrogen production from water splitting on CdS-based photocatalysts using solar light

Xiaoping CHEN, Wenfeng SHANGGUAN

《能源前沿（英文）》 2013年第7卷第1期页码 111-118 doi: 10.1007/s11708-012-0228-4

摘要： Hydrogen energy has been regarded as the most promising energy resource in the near future due to that it is a clean and sustainable energy. And the heterogeneous photocatalytic hydrogen production is increasingly becoming a research hotspot around the world today. As visible light response photocatalysts for hydrogen production, cadmium sulfide (CdS) is the most representative material, the research of which is of continuing popularity. In the past several years, there has been significant progress in water splitting on CdS-based photocatalysts using solar light, especially in the development of co-catalysts. In this paper, recent researches into photocatalytic water splitting on CdS-based photocatalysts are reviewed, including controllable synthesis of CdS, modifications with different kinds of cocatalysts, solid solution, intercalated with layered nanocomposites and metal oxides, and hybrids with graphenes etc. Finally, the problems and future challenges in photocatalytic water splitting on CdS-based photocatalysts are described.

关键词： hydrogen photocatalysis solar conversion cadmium sulfide (CdS) complex

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growth of a-few-layered MoS on CdS nanorod for high efficient photocatalytic H production

《能源前沿（英文）》 2021年第15卷第3期页码 752-759 doi: 10.1007/s11708-021-0779-3

摘要： An ultrathin MoS₂ was grown on CdS nanorod by a solid state method using sulfur powder as sulfur source for photocatalytic H₂ production. The characterization result reveals that the ultrathin MoS₂ nanosheets loaded on CdS has a good contact state. The photoelectrochemical result shows that MoS₂ not only are beneficial for charge separation, but also works as active sites, thus enhancing photocatalytic activity. Compared with pure CdS, the photocatalytic activity of MoS₂ loaded CdS was significantly improved. The hydrogen evolution rate on m(MoS₂): m(CdS) = 1: 50 (m is mass) reaches 542 μmol/h, which is 6 times of that on pure CdS (92 μmol/h). This work provides a new design for photocatalysts with high photocatalytic activities and provides a deeper understanding of the effect of MoS₂ on enhancing photocatalytic activity.

关键词： photocatalytic H₂ production CdS MoS₂ cocatalyst charge separation

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Chemical deactivation of V

Xiaodong WU, Wenchao YU, Zhichun SI, Duan WENG

《环境科学与工程前沿（英文）》 2013年第7卷第3期页码 420-427 doi: 10.1007/s11783-013-0489-0

摘要： V O -WO /TiO catalyst was poisoned by impregnation with NH Cl, KOH and KCl solution, respectively. The catalysts were characterized by X-ray diffraction (XRD), inductively coupled plasma (ICP), N physisorption, Raman, UV-vis, NH adsorption, temperature-programmed reduction of hydrogen (H -TPR), temperature-programmed oxidation of ammonia (NH -TPO) and selective catalytic reduction of NO with ammonia (NH -SCR). The deactivation effects of poisoning agents follow the sequence of KCl>KOH>>NH Cl. The addition of ammonia chloride enlarges the pore size of the titania support, and promotes the formation of highly dispersed V=O vanadyl which improves the oxidation of ammonia and the high-temperature SCR activity. K ions are suggested to interact with vanadium and tungsten species chemically, resulting in a poor redox property of catalyst. More importantly, potassium can reduce the Br?nsted acidity of catalysts and decrease the stability of Br?nsted acid sites significantly. The more severe deactivation of the KCl-treated catalyst can be mainly ascribed to the higher amount of potassium resided on catalyst.

关键词： V₂O₅-WO₃/TiO₂ potassium chloride poisoning reducibility acid sites

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Cu-doped Bi/Bi₂WO₆ catalysts for efficient N₂ fixation by photocatalysis

《化学科学与工程前沿（英文）》 2023年第17卷第10期页码 1412-1422 doi: 10.1007/s11705-023-2312-1

摘要： In this paper, Cu-doped Bi₂WO₆ was synthesized via a solvothermal method and applied it in photocatalytic N₂ immobilization. Characterization results showed the presence of a small amount of metallic Bi in the photocatalyst, indicating that the synthesized photocatalyst is actually Bi/Cu-Bi₂WO₆ composite. The doped Cu had a valence state of +2 and most likely substituted the position of Bi³⁺. The introduced Cu did not affect the metallic Bi content, but mainly influenced the energy band structure of Bi₂WO₆. The band gap was slightly narrowed, the conduction band was elevated, and the work function was reduced. The reduced work function improved the transfer and separation of charge carriers, which mainly caused the increased photoactivity. The optimized NH₃ generation rates of Bi/Cu-Bi₂WO₆ reached 624 and 243 μmol·L^–1·g^–1·h^–1 under simulated solar and visible light, and these values were approximately 2.8 and 5.9 times higher those of Bi/Bi₂WO₆, respectively. This research provides a method for improving the photocatalytic N₂ fixation and may provide more information on the design and preparation of heteroatom-doped semiconductor photocatalysts for N₂-to-NH₃ conversion.

关键词： Bi₂WO₆ Cu doping work function photocatalytic N₂ fixation charge separation

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基于磁驱动正交悬臂探针的三维原子力显微镜技术开发 Article

张号, 耿俊媛, 高海波, 荣伟彬, 谢晖

《工程（英文）》 2023年第24卷第5期页码 84-93 doi: 10.1016/j.eng.2022.06.010

摘要： magnetically driven-orthogonal cantilever probes, MD-OCP）的三维原子力显微镜（three-dimensional atomic force microscopy, 3D-AFM该3D-AFM系统还配备了高精度旋转台，可实现360°全向成像。定制的MD-OCP包含水平悬臂、垂直悬臂和磁珠三部分，其中磁珠可在磁场中机械驱动OCP实现激振。通过对具有微梳结构的微机电系统（MEMS）器件进行3D表征，进一步证实了所提出的基于MD-OCP的3D-AFM技术的有效性。实验结果表明，所提出的方法可以高精度地获取三维结构的CD信息，相比难以获得侧壁信息的二维技术，该方法在3D微纳制造检测领域具有更好的潜力。

关键词：三维原子力显微镜磁驱动正交悬臂探针关键尺寸 360°表征三维形貌重建

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Comparison of the morphology and structure of WO

Diah Susanti, Stefanus Haryo N, Hasnan Nisfu, Eko Prasetio Nugroho, Hariyati Purwaningsih, George Endri Kusuma, Shao-Ju Shih

《化学科学与工程前沿（英文）》 2012年第6卷第4期页码 371-380 doi: 10.1007/s11705-012-1215-3

摘要： Tungsten (VI) oxide (WO ) nanomaterials were synthesized by a sol-gel method using WCl and C H OH as precursors followed by calcination or hydrothermal treatment. X-Ray diffraction (XRD), scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM) equipped with energy dispersive X-ray spectroscopy (EDX) were used to characterize the structure and morphology of the materials. There were significant differences between the WO materials that were calcinated and those that were subjected to a hydrothermal process. The XRD results revealed that calcination temperatures of 300°C and 400°C gave hexagonal structures and temperatures of 500°C and 600°C gave monoclinic structures. The SEM images showed that an increase in calcination temperature led to a decrease in the WO powder particle size. The TEM analysis showed that several nanoparticles agglomerated to form bigger clusters. The hydrothermal process produced hexagonal structures for holding times of 12, 16, and 20 h and monoclinic structures for a holding time of 24 h. The SEM results showed transparent rectangular particles which according to the TEM results originated from the aggregation of several nanotubes.

关键词： WO₃ nanomaterial sol-gel method calcination hydrothermal

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Morphological and mechanical characterization of a PMMA/CdS nanocomposite

Vishal MATHUR, Manasvi DIXIT, K.S. RATHORE, N. S. SAXENA, K.B. SHARMA

《化学科学与工程前沿（英文）》 2011年第5卷第2期页码 258-263 doi: 10.1007/s11705-010-1014-7

摘要： Thick film of poly(methyl methacrylate) (PMMA)/CdS nanocomposite have been synthesized by the solution casting process. The nanostructure of the CdS particles has been ascertained through the small angle X-ray scattering (SAXS) technique. The surface morphological characterization of the PMMA/CdS nanocomposite has been done through scanning electron microscopy (SEM) analysis. The variation of mechanical loss factor (Tan ) with temperature and tensile properties of prepared samples have been studied using Dynamic Mechanical Analyzer (DMA). This study reveals that the glass transition temperature ( ), Young’s modulus, and fracture energy of the PMMA/CdS nanocomposite are greatly influenced by the existence of interfacial energetic interaction between dispersed CdS nanoparticles and the matrix of PMMA.

关键词： poly(methyl methacrylate) (PMMA) filler nanoparticles polymer semiconducting nanocomposite tensile properties glass transition temperature

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Effective regeneration of thermally deactivated commercial V-W-Ti catalysts

Xuesong SHANG, Jianrong LI, Xiaowei YU, Jinsheng CHEN, Chi HE

《化学科学与工程前沿（英文）》 2012年第6卷第1期页码 38-46 doi: 10.1007/s11705-011-1167-z

摘要： An effective method for the regeneration of thermally deactivated commercial monolith SCR catalysts was investigated. Two types of regenerated solutions, namely NH Cl (1 mol/L) and dilute H SO (0.5 mol/L), were employed to treat the used catalyst. The effects of temperature and the regeneration process on the structural and textural properties of the catalysts were determined by X-ray diffraction, scanning electron microscopy, N adsorption/desorption, elemental analysis and Fourier transform infrared spectroscopy. The results suggest that the anatase phase of the used catalyst is maintained after exposure to high temperatures. Some of the catalytic activity was restored after regeneration. The catalyst regenerated by aqueous NH Cl had a higher activity than that of the catalyst treated by dilute H SO . The main reason is that the NH generated from the decomposition of NH Cl at high temperatures can be adsorbed onto the catalyst which promotes the reaction. The aggregated V O were partially re-dispersed during the regeneration process, and the intrinsic oxidation of ammonia with high concentrations of O is a factor that suppresses the catalytic activity.

关键词： V₂O₅-WO₃/TiO₂ catalysts thermal deactivation regeneration NH₄Cl dilute H₂SO₄ solution

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Morphology selective construction of

Maher Darwish, Ali Mohammadi, Navid Assi, Samer Abuzerr, Youssef Alahmad

《化学科学与工程前沿（英文）》 2020年第14卷第4期页码 561-578 doi: 10.1007/s11705-019-1808-1

摘要： Controlled growth of Bi WO nanorods with exposed [0 0 1] facets and the fabrication of an Fe O -Bi WO magnetic composite by a microwave-assisted polyol process, were achieved in this study. The adsorptivity and photocatalytic performance of the composite toward sunset yellow dye degradation were greatly enhanced by the -cyclodextrin cavities on its surface, firmly anchored through a cetyltrimethylammonium bromide linkage. A series of examinations and characterizations were carried out to determine the influence of various factors on the morphological modulation-photocatalytic behavior of the pure Bi WO prior to final functionalization. Changing the pH of the precursor solution impacted the formation of 0D, 2D, and 3D structures; however, the presence of hexamethylenetetramine surfactant induced the development of 1D nanorod structure. A reasonable crystal growth mechanism was proposed to elucidate the formation process. Conversely, the mechanism of the activity enhancement of -cyclodextrin functionalized Fe O -Bi WO , compared to that of the non-functionalized samples, could be realized with the assistance of chemical trapping experiments on sunset yellow, and was confirmed on the colorless antibiotic (sulfamethoxazole). The high performance and durability of this composite can be attributed to the facet-dependent activity, large adsorption capacity due to inclusion interactions, enhanced visible light absorption, and efficient charge separation.

关键词： β-cyclodextrin Bi₂WO₆ shape controlled nanorod sunset yellow

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Fabrication of highly efficient Bi

Wei Mao, Lixun Zhang, Tianye Wang, Yichen Bai, Yuntao Guan

《环境科学与工程前沿（英文）》 2021年第15卷第4期 doi: 10.1007/s11783-020-1344-8

摘要： Abstract • A novel Bi2WO6/CuS composite was fabricated by a facile solvothermal method. • This composite efficiently removed organic pollutants and Cr(VI) by photocatalysis. • The DOM could promoted synchronous removal of organic pollutants and Cr(VI). • This composite could be applied at a wide pH range in photocatalytic reactions. • Possible photocatalytic mechanisms of organic pollutants and Cr(VI) were proposed. A visible-light-driven Bi2WO6/CuS p-n heterojunction was fabricated using an easy solvothermal method. The Bi2WO6/CuS exhibited high photocatalytic activity in a mixed system containing rhodamine B (RhB), tetracycline hydrochloride (TCH), and Cr (VI) under natural conditions. Approximately 98.8% of the RhB (10 mg/L), 87.6% of the TCH (10 mg/L) and 95.1% of the Cr(VI) (15 mg/L) were simultaneously removed from a mixed solution within 105 min. The removal efficiencies of TCH and Cr(VI) increased by 12.9% and 20.4%, respectively, in the mixed solution, compared with the single solutions. This is mainly ascribed to the simultaneous consumption electrons and holes, which increases the amount of excited electrons/holes and enhances the separation efficiency of photogenerated electrons and holes. Bi2WO6/CuS can be applied over a wide pH range (2–6) with strong photocatalytic activity for RhB, TCH and Cr(VI). Coexisiting dissolved organic matter in the solution significantly promoted the removal of TCH (from 74.7% to 87.2%) and Cr(VI) (from 75.7% to 99.9%) because it accelerated the separation of electrons and holes by consuming holes as an electron acceptor. Removal mechanisms of RhB, TCH, and Cr(VI) were proposed, Bi2WO6/CuS was formed into a p-n heterojunction to efficiently separate and transfer photoelectrons and holes so as to drive photocatalytic reactions. Specifically, when reducing pollutants (e.g., TCH) and oxidizing pollutants (e.g., Cr(VI)) coexist in wastewater, the p-n heterojunction in Bi2WO6/CuS acts as a “bridge” to shorten the electron transport and thus simultaneously increase the removal efficiencies of both types of pollutants.

关键词： Photocatalysis Bi₂WO₆/CuS Organic pollutants Cr(VI) Synergistic effect

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Effective degradation of tetracycline by mesoporous Bi

Xiaolong CHU,Guoqiang SHAN,Chun CHANG,Yu FU,Longfei YUE,Lingyan ZHU

《环境科学与工程前沿（英文）》 2016年第10卷第2期页码 211-218 doi: 10.1007/s11783-014-0753-y

摘要： Bi WO was synthesized with a hydrothermal method at different pHs and used for the degradation of tetracycline (TC) in water. The mesoporous Bi WO prepared at pH 1 (BWO-1) displayed the highest adsorption and degradation capacity to TC due to its large surface area and more efficient capacity to separate photogenerated electrons and holes. 97% of TC at 20 mg·L was removed by BWO-1 at 0.5 g·L after 120 min irradiation under simulated solar light. Only 31% of the total organic carbon (TOC) was removed after 360 min irradiation although the TC removal reached 100%, suggesting that TC was mainly transformed to intermediate products rather than completely mineralized. The intermediates were identified by high-performance liquid chromatography-time of flight-mass spectrometry (HPLC-TOF-MS) and possible photodegradation pathways were proposed.

关键词： Bi₂WO₆ hydrothermal synthesis tetracycline (TC) photocatalysis