CHINESE CHEMICAL LETTERS
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2020
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IF 4.632
Xiao Zhang,Yaohua Xu,Hao Liu,Wenrui Zhao,Anjie Ming,Feng Wei
A homogeneous porous Co 3 O 4 -ZnO nanomaterial (Zn-CoO x ) was successfully fabricated by precipitation-annealing route. The as-prepared Zn-CoO x exhibited good response, reliable reversibility and good selectivity towards alcohols, which attributed to the porous structure and p-n heterojunction formed between Co 3 O 4 and ZnO. In particular, the different Fermi levels of Co 3 O 4 and ZnO leaded to a further increase the depth of the space charge layer, which improved the gas sensitivity of the material from 10% to 480%. Besides, the continuous Co 3 O 4 leaded to a relatively lower operating temperature and resistance. This material preparation method and bimetallic oxides could be widely used in the research and development of metal oxide gas sensitive materials and sensors.
研究领域:
材料科学
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传感器技术
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DOI
高影响因子
ACS Photonics
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2018
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IF 6.88
Pengqi Lu,Ruifeng Li,Ni Yao,Xusheng Dai,Zhenyu Ye,Kai Zheng,Weiguang Kong,Wei Fang,Shuang Li,Qinghua Xu,Huizhen Wu
Heavy-metal-free I–III–VI2 quantum dots (QDs) have recently emerged as favorable alternatives to toxic II–VI QDs for optoelectronic and biological applications, but low fluorescence efficiency is a key issue related to the promising nanocrystals. In this work, we demonstrate big enhancement of two-photon fluorescence efficiency and low threshold two-photon pumped amplification of spontaneous emission (ASE) of Zn-processed CuInS2 (CIS) QDs for the first time. The change of two-photon process caused by Zn2+ cation exchange in CIS QDs is systematically investigated. Two-photon ASE in Zn-processed CIS QDs films is achieved with a record of low threshold fluence of 5.7 μJ/cm2. With high two-photon fluorescence quantum yields and low threshold ASE, the Zn-processed CIS QDs could become a promising candidate for two-photon bioimaging, nonlinear optical and novel QDs laser devices.
研究领域:
材料科学
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光学
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生物成像
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产品关联
DOI
高影响因子
FUEL
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2021
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IF 6.609
Tao Pan,Sida Ge,Mengnan Yu,Yana Ju,Ran Zhang,Pei Wu,Kuanyu Zhou,Zhijie Wu
Zn modified ZSM-5 zeolite supported Ni bifunctional catalysts were prepared by in-situ hydrothermal synthesis (Zn-Ni-ZSM-5), co-impregnation method (Zn-Ni/ZSM-5) as well as combining in-situ hydrothermal synthesis of Zn-ZSM-5 and sequential impregnation of Ni (Ni/Zn-ZSM-5) and used for the selective converting olefin to aromatics applicable for FCC gasoline hydro-upgrading. The Lewis (L) acid sites generated by ZnOH + species and hydrogenation active sites from Ni 0 species were varied with preparation method, in which their locations at the external surface or micropores of zeolite changed the acid properties of catalysts. Comparing to the Zn-Ni/ZSM-5 from the co-impregnation method, direct in-situ hydrothermal method could incorporate Zn and Ni species within zeolite, which makes the strong interaction between the metal species and the framework Al to form medium-strong L acids (ZnOH + /NiOH + ). This leads to the decrease of ratio of Brønsted acid sites to L acid sites (B/L) from 0.40 to 0.12 and the difficulty in reducing of Ni cations to Ni 0 from 57% to 30% Ni 0 percent. Ni/Zn-ZSM-5 sample prepared by incorporating Zn species into micropores and sequential depositing Ni species at the external surface of zeolite possesses a low B/L ratio similar to Zn-Ni-ZSM-5 (0.20 versus 0.12) but a much higher Ni 0 percent (52% versus 30%). Zn-Ni-ZSM-5 shows closer intimacy between Zn and Ni species comparing to Zn-Ni/ZSM-5 and Ni/Zn-ZSM-5. For the 1-hexene aromatization, the formed iso -alkene at acid sites was quickly saturated to iso -alkanes by the adjacent Ni 0 particles over Ni-Zn-ZSM-5 catalyst in hydrogen steam. However, the location of aromatization active sites (ZnOH + , L acid sites) in micropores and hydrogenation active sites (Ni 0 species) on external surface of Ni/Zn-ZSM-5 makes the tandem conversion of n-alkene → iso -alkene → aromatics, rather than the n-alkene → iso -alkene → iso -alkane. Thus, Zn-Ni-ZSM-5 with close intimacy of ZnOH + and Ni 0 particles shows a high iso -alkane selectivity (27.9% iC 4 + ), while Ni/Zn-ZSM-5 exhibits a high aromatics selectivity (39.6 %) in the conversion of 1-hexene in hydrogen steam. Similar results have also found in the conversion of n-heptane. Here, the control of the intimacy of Zn and Ni in ZSM-5 zeolites has been realized to be a good protocol to adjust the selective conversion of olefins/alkanes to aromatics versus iso -alkanes.
研究领域:
催化化学
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材料科学
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产品关联
DOI
高影响因子
RSC Advances
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2018
·Vol. 8
·期 62
·35353-35359
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IF 2.936
Yanyan Zheng,Chengyan Liu,Lei Miao,Hong Lin,Jie Gao,Xiaoyang Wang,Junliang Chen,Shaohai Wu,Xin Li,Huanfu Cai
As promising candidates for the progress of low-temperature thermoelectric devices, MgAgSb-based thermoelectric materials have drawn a great deal of attention. However, due to complicated phase changes, high content of impurities and high volatilization of Mg, it is difficult to synthesize pure phase MgAgSb-based thermoelectric materials via conventional methods. Here, MgAgSb alloy was successfully synthesized by a combination of common planetary ball milling and spark plasma sintering. Furthermore, the introduction of Zn improved the purity of alloys, leading to optimization of the electrical transport properties. As a result, the power factor was improved from 1087 μW m−1 K−2 for MgAg0.9Sb0.95 to 1394 μW m−1 K−2 for Mg0.97Zn0.03Ag0.9Sb0.95 at 473 K, and the ZT reached ∼0.7 at 473 K. These results suggest that MgAgSb-based thermoelectric materials have a good thermoelectric application potential and this study can be used as guidance for the synthesis and performance improvement of other thermoelectric materials. Our synthesis route sets forth a new avenue for accelerating commercial applications of MgAgSb-based thermoelectric power generation or refrigeration.
研究领域:
材料科学
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能源技术
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DOI
高影响因子
INORGANIC CHEMISTRY
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2022
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IF 5.436
Lixiong Qian,Lei Yao,Yunpeng Liu,Hao Wang,Jiajun Zhong,Chao Liu,Guang Mo,Xueqing Xing,Zhongjun Chen,Zhonghua Wu
The formation mechanism of nanoparticles is of great significance for the controllable synthesis, structural design, and performance optimization of nanomaterials. In this paper, an economical hydrothermal method was used to synthesize zinc oxide (ZnO) nanorods. X-ray diffraction, X-ray absorption fine structure, and small-angle X-ray scattering techniques were used to probe the structural changes. Scanning electron microscopy and high-resolution transmission electron microscopy were used to observe the morphologies of the products. A self-designed in situ temperature–pressure sample cell was used to control the hydrothermal conditions. The results demonstrate that an unknown intermediate phase, Zn(HCO3)2·H2O, was first formed at 50 °C, having a morphology of nanoflakes with a average thickness of about 35 nm. The intermediate phase Zn(HCO3)2·H2O was determined to have a monoclinic structure with space group P1211 and the following lattice parameters: a = 11.567 Å, b = 3.410 Å, c = 5.358 Å, β = 96.0011°, and Z = 2. After a hydrothermal temperature of 140 °C, CO2 and H2O were evaporated from the Zn(HCO3)2·H2O intermediate product and the ZnO nanorods with a wurtzite structure were formed. The final ZnO nanorods have an average diameter of about 45 nm and an average length of about 2 μm. The axial direction of the ZnO nanorods is the [001] crystallographic direction. By virtue of understanding the formation mechanism, this work is helpful for the controllable synthesis of ZnO nanoparticles.
研究领域:
材料科学
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纳米技术
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产品关联
DOI
PubMed
高影响因子
MOLECULES
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2017
·Vol. 22
·期 2
·305
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IF 2.861
Jingwei Rui,Fei Liu,Rijie Wang,Yanfei Lu,Xiaoxia Yang
A series of Zn-modified NaY zeolites were prepared by the liquid-phase ion-exchange method with different Zn sources, including Zn(NO3)2, Zn(Ac)2and ZnSO4. The samples were tested as adsorbents for removing an organic sulfur compound from a model gasoline fuel containing 1000 ppmw sulfur. Zn(Ac)2-Y exhibited the best performance for the desulfurization of gasoline at ambient conditions. Combined with the adsorbents’ characterization results, the higher adsorption capacity of Zn(Ac)2-Y is associated with a higher ion-exchange degree. Further, the results demonstrated that the addition of 5 wt % toluene or 1-hexene to the diluted thiophene (TP) solution in cyclohexane caused a large decrease in the removal of TP from the model gasoline fuel. This provides evidence about the competition through the π-complexation between TP and toluene for adsorption on the active sites. The acid-catalyzed alkylation by 1-hexene of TP and the generated complex mixture of bulky alkylthiophenes would adsorb on the surface active sites of the adsorbent and block the pores. The regenerated Zn(Ac)2-Y adsorbent afforded 84.42% and 66.10% of the initial adsorption capacity after the first two regeneration cycles.Keywords:Zeolite;Zinc sources;adsorption;desulfurization;ion exchange
研究领域:
化学工程
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环境科学
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产品关联
DOI
PubMed
高影响因子
Frontiers in Chemistry
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2022
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IF 5.545
Zhang Xiaojuan,Yu Rongfei,Wang Dandan,Li Weihua,Zhang Yutao
A series of bimetallic Zn-Zr metal-organic frameworks (Zn-Zr MOFs) with different Zn:Zr molar ratios has been synthesized via a green hydrothermal method. The structures and morphologies of these photocatalysts have been characterized and analyzed by FTIR, XRD, SEM, and nitrogen adsorption-desorption. The prepared Zn-Zr MOFs had large specific surface areas and pore volumes, favoring the adsorption of pollutant molecules, which in turn led to an improved photocatalytic effect. The photocatalytic activities of the Zn-Zr MOFs under visible light irradiation have been studied towards rhodamine B (RhB) as a target pollutant. The extent of degradation of RhB in a 40 mg/L aqueous solution reached 97.4%. The optimal photocatalyst could also degrade other dyes, suggesting a certain degree of universality.
研究领域:
材料科学
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环境科学
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产品关联
DOI
PubMed
高影响因子
NEW JOURNAL OF CHEMISTRY
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2025
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IF 2.5
Yafeng Xu,Yu Li,Jian Yao,Xiang Liu,Shengbiao Zhang,Shihao Zhang,Shuqin Dong,Yue Yao,Xihong Ding,Meng Wang
Antimony sulfide (Sb2S3) is regarded as a promising candidate for next-generation photovoltaic technology. In recent years, the efficiency of Sb2S3 solar cells has shown significant improvement, however, there still exists a considerable gap from the theoretical efficiency. This is partially due to the relatively high resistivity and parasitic light absorption of the CdS buffer layer, as well as the unsatisfactory crystal orientation of Sb2S3. In this work, a Zn salt additive is added to chemical bath solution of CdS to regulate the growth of CdS film. Elemental analysis indicates that only a small amount of zinc is deposited into the CdS film. The introduction of the Zn salt additive significantly increases the grain size and electrical conductivity of CdS, while also leading to preferential growth of the [hk1] orientation in Sb2S3 film. The low-cost Sb2S3 solar cells with inexpensive carbon electrodes were fabricated. The enhanced quality of the junction, attributed to the Zn salt additive, leads to improved charge transport and suppressed charge recombination in the Sb2S3 solar cells. As a result, the efficiency increases from 4.90% to 5.74%. This work presents a straightforward and efficient approach for the fabrication of superior CdS buffer layers and Sb2S3 solar cells.
研究领域:
材料科学
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光伏技术
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产品关联
DOI
高影响因子
ACS Omega
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2020
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IF 2.87
Nina Zhang,Ruili Li,Ge Zhang,Le Dong,Dongyuan Zhang,Guojiang Wang,Tongtong Li
Different metal ions were used to modify Hβ zeolite adsorbents by an impregnation method to remove organic chlorides from the model naphtha. The dechlorination performance of different ion-modified adsorbents was evaluated using a microcoulometer. The effects of calcination time and temperature, metal loading, adsorption time and temperature, and dosage of adsorbent were investigated by batch adsorption experiments. The modified adsorbents were characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), NH3-temperature-programmed desorption (TPD), scanning electron microscopy (SEM), infrared spectroscopy of pyridine adsorption (Py-IR), and X-ray photoelectron spectroscopy (XPS). After modification, the modified Zn/Hβ zeolite exhibited the best dechlorination performance among the other metal-loaded zeolites. The removal percentage of organic chloride of the Zn/Hβ adsorbent prepared at optimum preparation and adsorption conditions can reach 72.54%, compared with 34.07% of Hβ zeolite. The Zn/Hβ adsorbent also maintained good dechlorination performance after regeneration by calcination for five times. The characterization results revealed that the concentration of the B acid sites in the zeolite decreased with the introduction of the metals, whereas that of the L acid sites increased. Zn/Hβ zeolite had the lowest B/L ratio but the best dechlorination performance, which meant that the type and amount of acidic sites present in zeolites played a significant role in dechlorination performance and L acid was beneficial for chloride compound removal.
研究领域:
化学工程
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环境科学
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材料科学
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产品关联
DOI
PubMed
高影响因子
FUEL
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2023
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IF 7.4
Xiao-Yan Zhao,Xue-Yu Ren,Yan-Jun Wang,Jing-Pei Cao,Zi-Meng He,Nai-Yu Yao,Hong-Cun Bai,Hou-Luo Cong
Direct conversion of lignite into light aromatics via catalytic fast pyrolysis is a great challenge because of severe catalyst deactivation and low aromatics yield. The tandem catalysis (1Zn@MCM-41 and ZSM-5) system was employed to promote the conversion of thermally-derived volatiles of lignite into aromatics at 600 °C. The mesoporous Zn-incorporated MCM-41 (xZn@MCM-41) with different doping amount of Zn was prepared with a one-pot hydrothermal procedure. The structure and the dispersion of Zn species of 1Zn@MCM-41 were systematically studied with XRD, SEM, BET, NH 3 -TPD and so on. The presence of 1Zn@MCM-41 significantly expands the lifetime of the microporous ZSM-5. Meanwhile, the yield of aromatics, especially benzene, is also increased to some extent. The content of the long-chain hydrocarbons and the phenolic compounds are decreased significantly after being cracked by the mesoporous 1Zn@MCM-41. More small molecules are able to contact with the active sites located in the micropores of ZSM-5 with the presence of Zn@MCM-41. In addition, the ZSM-5 in the tandem catalysts system presents an excellent stability. Therefore, this meso -microporous tandem catalysis system promotes the preferential cracking of macromolecular compounds, the cracked small molecules generated from which then contact with ZSM-5 to produce aromatics. This work provides a new perspective for the gradient catalyzing lignite-derived volatiles over a tandem catalysis system.
研究领域:
能源化学
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催化科学
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产品关联
DOI
高影响因子
Environmental Science-Nano
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2025
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IF 5.1
Shuoli Ma,Wen-Xiong Wang
The toxicity of environmental pollutants is often manifested through metabolic disruptions and damage to detoxification organs. However, current understanding is insufficient to explain the physiological response mechanisms of metabolically abnormal fish exposed to secondary pollutants in complex natural environments. This study established a fish model with non-alcoholic fatty liver to evaluate the effects of Zn oxide nanoparticles (nZnO) and Zn²⁺ on physiological metabolism using untargeted lipidomics and bioimaging techniques. Nile red and hematoxylin and eosin (H&E) staining indicated that increased Zn levels reduced the number of lipid droplets (LDs) and hepatocyte vacuolization in the livers of groupers. Non-targeted lipidomics, employing an unsupervised K-means clustering algorithm, identified key lipid profiles that differentiated the effects of nZnO and Zn, including TG (16:0/16:1/18:1), PC (18:2/22:6), TG (18:2/18:2/22:6), SM (d18:1/24:1), and TG (16:1/18:1/18:2). The increased content of SM (d18:1/24:0) indicated that fish liver cells internalized nZnO via lipid raft structures on the cell membrane, a process distinct from Zn ion uptake. Moreover, nZnO/Zn treatments significantly activated lipolysis regulation in fish liver experiencing oxidative stress. This study contributed to the use of non-targeted lipidomics to identify differential biomarkers of nZnO and Zn, as well as their compensatory mechanisms in metabolically abnormal fish. These findings provide novel insights into the effects of nanometal exposure on aquatic animal health in complex environments.
研究领域:
环境毒理学
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代谢组学
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水生生物学
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产品关联
DOI
高影响因子
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS
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2020
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IF 3.442
Jun Wang,Xiaofang Lei,Cong Huang,Lian Xue,Wei Cheng,Qiang Wu
Herein, a novel MoO 3 /Zn–Al LDHs composite photocatalyst was successfully prepared. Morphology, chemical composition, and photoelectrochemical properties of the prepared catalyst were explored by different characterization methods, including X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), Brunauer Emmett-Teller (BET), UV–Vis diffuse reflectance spectrometry (DRS) and Electron Spin Resonance (ESR). Using tetracycline as a target pollutant, the photocatalytic activity of MoO 3 (10 wt%)/Zn–Al LDHs composite was tested by photodegradation of tetracycline under visible light irradiation. The experimental results indicate that the MoO 3 (10 wt%)/Zn–Al LDHs composite exhibited higher photocatalytic removal efficiency than pure Zn–Al LDHs and MoO 3 . The removal efficiency of TC in 60 min could reach 90.5%. It was confirmed that the optimal conditions were a catalyst dosage of 1.0 g/L, an initial pH of 9, and an initial concentration of TC of 40 mg/L. In addition, a possible mechanism for the photodegradation of TC with MoO 3 (10 wt%)/Zn–Al LDHs composite was proposed. The introduction of MoO 3 facilitates the separation of electron-hole pairs. It could be seen that the MoO 3 (10 wt%)/Zn–Al LDHs composite has great application prospects for the treatment of antibiotic wastewater.
研究领域:
环境科学
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材料科学
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DOI
高影响因子
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