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Materials · 2015 ·Vol. 8 ·期 5 ·2043-2053 · IF 2.651

Biochemical Synthesis of Ag/AgCl Nanoparticles for Visible-Light-Driven Photocatalytic Removal of Colored Dyes

Xiyun Zhao,Jie Zhang,Binsong Wang,Amir Zada,Muhammad Humayun

Photocatalytic removal of organic pollution such as waste colored dyes was a promising technique for environment technique. However, effective photocatalysts were needed to enhance the photocatalytic efficiency. Ag/AgCl was regarded as high performance catalyst for photocatalytic degradation. Ag/AgCl nanoparticles were biochemically prepared with metabolin of living fungi which was used as reductant and characterized by X-Ray diffraction (XRD), UV-visible spectroscopy and transmission electron microscopy (TEM). The Ag/AgCl nanoparticle composites showed spherical aggregation shape with an average size of about 3–5 nm which is well inside the quantum regime. The UV-visible study showed that Ag/AgCl nanoparticles had strong visible light absorption and exhibited excellent visible-light-driven photocatalytic performance. Photocatalytic results indicated that the obtained Ag/AgCl nanoparticles were suitable for photocatalytic removal of RhB dye under visible light irradiation. The excellent photocatalytic activities could be attributed to the quantum size nanoparticles and the Plasmon resonance of Ag/AgCl composites.

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MATERIALS CHEMISTRY AND PHYSICS · 2018 · IF 2.21

The regulation on visible-light photocatalytic activity of CuInS2 by different Cu/In molar ratio

Xiaoying Lu,Fang Deng,Min Liu,Xubiao Luo,Aijie Wang

CuInS 2 semiconductor were synthesized by regulating Cu/In molar ratio via a hot solvent method. Different Cu/In molar ratio in reaction system had significant influence on the BET surface area , charge separation and photocatalytic activity of CuInS 2 . The CuInS 2 with optimal Cu/In ratio of 1:1.5 exhibits the most efficient charge separation and transfer, leading to the highest photocatalytic activity . The mineralization efficiency of pharmaceutical wastewater by CuInS 2 (Cu:In = 1:1.5) was 67.5% in 6 h, and CuInS 2 (Cu:In = 1:1.5) exhibited high stability, indicating that CuInS 2 has a promising prospect in real pharmaceutical wastewater treatment .

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DYES AND PIGMENTS · 2024 · IF 4.1

Anthracene derivatives with electron-transport units for non-doped blue fluorescent organic light-emitting diodes

Zhiming Zhong,Tingxin Chen,Feng Peng,Pengfei Niu,Jin Xu,Lei Ying

Blue organic light-emitting diodes with non-doped emissive layer (EML) structures have been garnered increasing interest due to their convenience of manufacturing process. For this purpose, we designed and synthesized two novel anthracene derivatives, PO2PhAnTz and PO2PhAnBI. Both derivatives exhibited bright blue electroluminescence emission and a relatively low operating voltage with a simple bilayer device structure. The PO2PhAnBI with triphenyl-phosphine oxide moiety as host, anthracene core as dopant and benzimidazole as electron transport group, realized a balanced bipolar transport and attained a maximum external quantum efficiency of 5.74 %. The findings shed light on the molecule design role toward high-efficiency non-doped blue OLEDs.

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NANOTECHNOLOGY · 2022 ·Vol. 33 ·期 17 ·175401 · IF 3.953

Silver nanoparticles embedded 2D g-C3N4 nanosheets toward excellent photocatalytic hydrogen evolution under visible light

Xiyu Deng,Xinya Kuang,Jiyang Zeng,Baoye Zi,Yiwen Ma,Ruihan Yan,Jin Zhang,Bin Xiao,Qingju Liu

Photocatalytic water splitting is considered to be a feasible method to replace traditional energy. However, most of the catalysts have unsatisfactory performance. In this work, we used a hydrothermal process to grow Ag nanoparticles in situ on g-C3N4 nanosheets, and then a high performance catalyst (Ag–g–C3N4) under visible light was obtained. The Ag nanoparticles obtained by this process are amorphous and exhibit excellent catalytic activity. At the same time, the local plasmon resonance effect of Ag can effectively enhance the absorption intensity of visible light by the catalyst. The hydrogen production rate promote to 1035 μmol g−1 h−1 after loaded 0.6 wt% of Ag under the visible light, which was 313 times higher than that of pure g-C3N4 (3.3 μmol g−1 h−1). This hydrogen production rate is higher than most previously reported catalysts which loaded with Ag or Pt. The excellent activity of Ag-g-C3N4 is benefited from the Ag nanoparticles and special interaction in each other. Through various analysis and characterization methods, it is shown that the synergy between Ag and g-C3N4 can effectively promote the separation of carriers and the transfer of electrons. Our work proves that Ag-g-C3N4 is a promising catalyst to make full use of solar energy.

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Journal of Materials Chemistry A · 2019 ·Vol. 7 ·期 14 ·8521-8526 · IF 10.733

An intelligent light-driven thermoelectric conversion system through the thermosensitive phase transition of vanadium dioxide

Yuang Zhang,Malik Muhammad Umair,Xin Jin,Rongwen Lu,Shufen Zhang,Bingtao Tang

Solar thermoelectric generation (STEG) is an environmentally-friendly, safe, and economical technique that can be used for sustainable solar energy utilization. Efficient and stable STEG depends on strong light absorption and stable temperature difference. Herein, we constructed a new intelligent light-driven thermoelectric conversion system with VO2, polystyrene/Fe2O3-graphene nanosheets (PS/Fe2O3-GNS), and a thermoelectric module. The system can realize light-thermal-electric conversion and obtain a stable current owing to the infrared light transmittance switch of the VO2 film, high visible-light absorbing ability of PS/Fe2O3-GNS, and thermoelectric effect of the thermoelectric module. Furthermore, the new system can operate normally under sunlight, indicating the prospect of practical application.

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Materials Today Communications · 2024 · IF 3.7

Constructing ZnIn2S4@WO3·H2O Z-type heterojunction to boost photocatalytic efficiency under visible-light irradiation

Ligang Ma,Yuqing Yang,Tianyu Zhu,Yihuan Ding,Chao Lin,Le Xu,Xiaoqian Ai

In this paper, hexagonal ZnIn 2 S 4 nanoflowers were grown in situ on tetragonal WO 3 ·H 2 O nanosheets, yielding a compact ZnIn 2 S 4 @WO 3 ·H 2 O (ZIS@WO) core-shell heterojunction. The formation of the ZIS@WO heterojunction was optimized by meticulously adjusting the quantity of WO 3 ·H 2 O nanosheets incorporated. The crystal structure and microstructure of ZIS@WO were comprehensively examined using XRD, TEM and EDS analyses. The photocatalytic properties of ZIS@WO heterojunctions were evaluated through the degradation of organic pollutants under visible light irradiation. The results demonstrated a marked enhancement in photocatalytic efficiency for the ZIS@WO heterojunction. Further investigation into the separation and transport of photogenerated carriers were performed using PL spectroscopy and photoelectrochemical measurement. Compared to the individual components of ZnIn 2 S 4 nanoflowers and WO 3 ·H 2 O nanosheets, the ZIS@WO heterojunction creates an internal electric field at the interface, along with a compact core-shell configuration. This internal electric field, in conjunction with the band structure of the heterojunction, effectively accelerates the separation of photogenerated electrons and holes. Additionally, a comprehensive analysis of the photocatalytic degradation mechanisms were presented, elucidating the intricate processes.

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JOURNAL OF ORGANIC CHEMISTRY · 2024 · IF 3.3

Visible Light-Induced, Nickel-Catalyzed Late-Stage 4-Alkylation of Hantzsch Esters with Alkyl Bromide

Yan-Ling Liu,Xian-Chen He,Jie Gao,Ke-Rong Li,Kai Chen,Hao-Yue Xiang,Hua Yang

Herein, visible light-induced, nickel-catalyzed direct functionalization of the Hantzsch esters (HEs) with readily accessible alkyl bromides has been successfully achieved by taking advantage of HE as the reductant and substrate through an aromatization-dearomatization process. In this strategy, the single electron reduction of alkyl bromides by reactive Ni(I) species is essential for the success of this late-stage transformation. A wide range of 4-alkyl-1,4-dihydropyridines were rapidly assembled in moderate to good yields under mild conditions, rendering this photoinduced approach attractive for synthetic and medicinal chemistry.

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APPLIED CATALYSIS B-ENVIRONMENTAL · 2020 · IF 16.683

Toward visible-light-assisted photocatalytic nitrogen fixation: A titanium metal organic framework with functionalized ligands

Hao Huang,Xu-Sheng Wang,Davin Philo,Fumihiko Ichihara,Hui Song,Yunxiang Li,Dan Li,Teng Qiu,Shengyao Wang,Jinhua Ye

The fixation of atmospheric dinitrogen to ammonia is one of the most essential processes for sustaining life. Since the N N bond in dinitrogen is one of the strongest bonds in chemistry, it remains a grand challenge to develop efficient catalysts for fixation of N 2 under ambient conditions. Herein we report for the first time on visible-light-assisted photocatalytic nitrogen fixation by metal organic framework material at room temperature and pressure. The Ti 3+ species induced by electron transfer from ligand-to-metal charge transfer process provide active sites for N 2 reduction. Furthermore, visible-light-assisted photocatalytic N 2 fixation is achieved by ligands functionalization which extend the light harvesting of the MOF to visible region. The integration of Ti sites and amine-functionalized linkers in NH 2 -MIL-125 (Ti) shows the highest visible light photocatalysis efficiency at a rate of 12.3 μmol g −1  h −1 . This Ti MOF system therefore shows a potential as a new design of combining light-harvesting and catalytic components in a single solid platform for green NH 3 production.

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KOREAN JOURNAL OF CHEMICAL ENGINEERING · 2015 ·Vol. 33 ·期 1 ·107-113 · IF 1.166

Preparation of titanium dioxide/tungsten disulfide composite photocatalysts with enhanced photocatalytic activity under visible light

Zheng Lili,Zhang Weiping,Xiao Xinyan

Titanium dioxide/tungsten disulfide (TiO 2 /WS 2 ) composite photocatalysts were fabricated via a one-step hydrothermal synthesis process, using TiCl 4 as titanium source and bulk WS 2 as sensitizer. The morphology, structure, specific surface area and optical absorption properties of the composite photocatalysts were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD), specific surface area analyzer and ultraviolet-visible diffuse reflection spectrum (UV-vis DRS), respectively. The photocatalytic activity of as-prepared photocatalysts was evaluated by the degradation of methyl orange (MO) under illumination of 500W Xenon lamp. The results indicated that TiO 2 /WS 2 composite photocatalysts possessed excellent photocatalytic activity, and ∼95% of the degradation rate for MO was reached when molar ratio of WS 2 to TiO 2 was 0.004 and the irradiation time was 60 min. Moreover, the carrier trapping experiment and fluorescence spectra showed that ·O − 2 was the key component in the photocatalytic degradation process and O 2 was reduced to be ·O − 2 by the electrons from the conduction band of TiO 2 and WS 2 for the degradation of MO.

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Materials Today Communications · 2022 · IF 3.662

Ti3C2 MXene derived (001)TiO2/Ti3C2 heterojunctions for enhanced visible-light photocatalytic degradation of tetracycline

Wei Qiang,Xiao Qu,Chuntao Chen,Lei Zhang,Dongping Sun

As a photocatalyst , titanium dioxide (TiO 2 ) suffers from the wide band gap and the quick carrier recombination process, thus leading to the inefficient use of solar energy and poor catalytic performance. Herein, in this work, TiO 2 /Ti 3 C 2 heterojunctions are designed to overcome these shortcomings via growing TiO 2 in situ on the titanium element of Ti 3 C 2 MXene . The TiO 2 /Ti 3 C 2 heterojunctions not only broaden the range of light absorption , but also hugely extend the lifetime of photogenerated carriers. Besides, the anatase TiO 2 with exposed (001) facets further enhances the catalytic properties. After optimizing the amount of TiO 2 /Ti 3 C 2 heterojunctions by controlling reaction time, 20 mg catalysts can degrade 97.6% of 30 mL tetracycline solution (15 mg/L) in 90 min under visible light . Even after five cycles, the degradation ability of TiO 2 /Ti 3 C 2 only changes from 97.6% to 94.3%. This paper offers another perspective on the synthesis of efficient and stable photocatalysts.

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CERAMICS INTERNATIONAL · 2024 · IF 5.1

Ultraviolet light charged and self-powered mechanoluminescence of KMgF3: Tb3+ glass ceramics in various media

Lili Li,Yingdan Song,Hongxin Song,Kaige Cheng,Qiang Xu,Lei Zhao

The light waveguiding effect of transparent glass ceramics (GCs) on mechanoluminescence (ML) signals is highly attractive for remote stress sensing and structural health monitoring applications. However, a prerequisite for generating ML in GCs is pre-irradiation with high-energy rays, which not only increases application costs but also poses a risk of GCs devitrification. Herein, we propose a safe, non-destructive, and convenient charging method for the ML of KMgF 3 : Tb 3+ GCs, namely ultraviolet (UV) light charging. By effectively filling the intrinsic defects in KMgF 3 : Tb 3+ nanocrystal using UV light, we achieved trap-controlled ML in rigid GCs. Moreover, this ML is attributed to thermoluminescence (TL) induced by frictional heating during mechanical stimulation. Additionally, when the GCs powder is combined with flexible polydimethylsiloxane (PDMS), a self-powered (without any pre-charging) ML induced by interfacial triboelectricity can also be achieved, which is similar to the results observed in most flexible ML systems. This work proposes a more straightforward and safer approach for applications such as mechanical sensing based on the ML of transparent GCs.

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iScience · 2022 · IF 6.107

Surface engineering of ZnO nanoparticles with diethylenetriamine for efficient red quantum-dot light-emitting diodes

Dandan Zhang,Yan-Hua Liu,Lianqing Zhu

Due to the outstanding electron injection/transport capability of ZnO nanoparticles (NPs), quantum-dot light-emitting diodes (QLEDs) are commonly constructed by employing a hybrid device structure with ZnO electron-transporting layer and organic hole-transporting layer. However, the emission quenching of quantum dots and excessive electron injection induced by ZnO NPs also limits the device efficiency and operational stability. Here, diethylenetriamine (DETA) molecules as the ligands are introduced to modify the surface of ZnO NPs, which not only passivate the surface defects of ZnO but also suppress the overwhelming electron injection in the QLED. As a result, the device based on the DETA-modified ZnO NPs exhibits a peak external quantum efficiency of 23.7%, corresponding to an enhancement factor of 129% in comparison with that of the device with as-synthesized ZnO as the electron-transporting layer. The easy and feasible strategy may also be applicable to other photoelectric devices, such as solar cells and photodetectors.

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