ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Xiaohui Niu,Simeng Yan,Rui Zhao,Hongxia Li,Xiaoyu Liu,Kunjie Wang
In the pursuit of chiral materials with significant chiral recognition effects and stability, various strategies have been explored, among which the integration of metal nanoparticles and chiral metal–organic frameworks (CMOFs) is highly promising. However, metal nanoparticles (MNPs)/CMOFs show high chiral properties but inferior stabilities due to the MNPs being easily detached from the outside layer under certain conditions. Sandwich MOFs@MNPs@CMOF chiral materials can overcome this dilemma because the sandwich structure can maximize the regulation of the chiral interface activity, while the controlled outer layer can stop the MNPs from falling off in the procedure of chiral recognition. Here, a novel sandwich chiral material (d-His-ZIF-8@Au@ZIF-8) was synthesized by a ligand-assisted strategy with a well-defined sandwich morphology and chiral recognition capabilities. The electrochemical chiral recognition showed that d-His-ZIF-8@Au@ZIF-8 was the most efficient for the enantiomer of phenylalanine (Phe). This experiment presents a novel perspective for the fabrication of a chiral electrochemical sensing platform based on a solid sandwich chiral nanocomposite.
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FOOD CHEMISTRY
·
2023
·
IF 8.8
Xiaorong Zhao,Qiulan Li,Hong Li,Yijie Wang,Feijian Xiao,Dezhi Yang,Qinghai Xia,Yaling Yang
In this work, cerium-doped carbon dots (Ce-CDs) both as a reducing agent and template hybrid gold nanoparticles (AuNPs) with weak oxidase-like (OXD) activity was synthesized for the detection of Hg 2+ and aflatoxin B 1 (AFB 1 ). The AuNPs can catalyze efficiently mercury ion (Hg 2+ ) reduction to the metallic (Hg 0 ) to form Au-Hg amalgam (Au@HgNPs). The obtained Au@HgNPs with strong OXD-like activity oxidize without Raman-active leucomalachite green (LMG) into the Raman-active malachite green (MG) and simultaneously as the SERS substrates by the formed Raman “hot spot” through MG-induced Au@HgNPs aggregation. While AFB 1 was introduced resulting in the SERS intensity decreasing due to Hg 2+ with AFB 1 via carbonyl group to inhibit the aggregation of Au@HgNPs. The work paves a new path for the design of a nanozyme-based SERS protocol for tracing Hg 2+ and AFB 1 residues in foodstuff analysis.
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International Journal of Electrochemical Science
·
2023
·
IF 1.5
Bo-Cai Liu,Wei-Yan Xia,Shang-Qing Wang,Chang-Wei Xu,Zi-Li Liu
Spinel oxide NiCo 2 O 4 firstly has been explored to promote activity of Au for glycerol electrooxidation, which is supported on a three-dimensional hierarchical porous graphene-like carbon (3D HPG) material. Addition NiCo 2 O 4 into the Au/HPG catalyst can significantly improve the catalytic performance for glycerol oxidation. When NiCo 2 O 4 is added to the Au/HPG, onset potential is more 108 mV negatively than that on the Au/HPG. Peak current density on the Au/NiCo 2 O 4 (wt 6:1)/HPG is 5.1 times as high as that on the Au(20wt%)/HPG. The Au/NiCo 2 O 4 in this work shows a great potential as electrocatalyst for glycerol electrooxidation in alkaline medium.
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ANALYTICA CHIMICA ACTA
·
2023
·
IF 6.2
Huasheng Lai,Gongke Li,Zhuomin Zhang
A bioinspired Au@Ag nanodome-cones array (Au@Ag NDCA) surface-enhanced Raman scattering (SERS) chip was developed for efficient residue analyses of food samples. The cicada wing inspired Au@Ag NDCA chip was fabricated by a bottom-up method, Au nanocones array was firstly grown onto nickel foil by displacement reaction and cetyltrimethylammonium bromide guidance growth, and then silver shell with controllable thickness was coated onto the Au nanocones array by magnetron sputtering . The Au@Ag NDCA chip exhibited good SERS performances with high enhancement factor of 1.2 × 10 8 , good uniformity with relative standard deviation (RSD) less than 7.5% (n = 25), good inter-batch reproducibility with RSD less than 9.4% (n = 9), and long-term stability over 9 weeks. By adapting a minimized sample preparation, Au@Ag NDCA chip combined with a 96-well plate could realize high-throughput SERS analyses of 96 samples with average analysis time less than 10 min. The substrate was applied for quantitative analyses of two food projects. One was 6-benzylaminopurine auxin residue in sprout samples with detection limit of 38.8 μg/L, recoveries of 93.3–105.4% and RSDs of 1.5–6.5%, and the other was an edible spice of 4-amino-5,6-dimethylthieno (2,3-d) pyrimidin-2(1H)-one hydrochloride additive in beverage samples with detection limit of 18.0 μg/L, recoveries of 96.2–106.6% and RSDs of 3.5–7.9%. All the SERS results were well confirmed by conventional high-performance liquid chromatographic methods with relative errors less than 9.7%. The robust Au@Ag NDCA chip exhibited good analytical performances possessed great potential for convenient and reliable analyses of food quality and safety.
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Nanoscale Horizons
·
2023
·Vol. 8
·期 6
·812-826
·
IF 9.7
Junqing Ye,Meizan Jing,Yu Liang,Wenjin Li,Wanting Zhao,Jianying Huang,Yuekun Lai,Weiyu Song,Jian Liu,Jian Sun
Exploring eco-friendly and cost-effective strategies for structure engineering at the nanoscale is important for boosting heterogeneous catalysis but still under a long-standing challenge. Herein, multifunctional polyphenol tannic acid, a low-cost natural biomass containing catechol and galloyl species, was employed as a green reducing agent, chelating agent, and stabilizer to prepare Au nanoparticles, which were dispersed on different-shaped CeO2 supports (e.g., rod, flower, cube, and octahedral). Systematic characterizations revealed that Au/CeO2-rod had the highest oxygen vacancy density and Ce(III) proportion, favoring the dispersion and stabilization of the metal active sites. Using isopropanol as a hydrogen-transfer reagent, deep insights into the structure–activity relationship of the Au/CeO2 catalysts with various morphologies of CeO2 in the catalytic nitrobenzene transfer hydrogenation reaction were gained. Notably, the catalytic performance followed the order: Au/CeO2-rod (110), (100), (111) > Au/CeO2-flower (100), (111) > Au/CeO2-cube (100) > Au/CeO2-octa (111). Au/CeO2-rod displayed the highest conversion of 100% nitrobenzene and excellent stability under optimal conditions. Moreover, DFT calculations indicated that nitrobenzene molecules had a suitable adsorption energy and better isopropanol dehydrogenation capacity on the Au/CeO2 (110) surface. A reaction pathway and the synergistic catalytic mechanism for catalytic nitrobenzene transfer hydrogenation are proposed based on the results. This work demonstrates that CeO2 structure engineering is an efficient strategy for fabricating advanced and environmentally benign materials for nitrobenzene hydrogenation.
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ACS Applied Materials & Interfaces
·
2023
·
IF 9.5
Xinyan Chen,Yu Qi,Bin He,Yu Liang,Yu Lei,Jian Sun
Au nanozymes are extensively researched for their photothermal effect and catalytic performance, but overcoming the inherent defects of poor dispersibility and thermal stability through complementary materials will expand their prospects for biological applications. Herein, several novel CAu nanozymes were fabricated by in situ reduction of chloroauric acid on hollow carbon nanospheres (HCNs). Through regulating the number of reductions, sesame ball-shaped CAu (sCAu) with highly dispersed Au nanoparticles and diversity-shaped CAu (dCAu) were obtained. The number and morphology of loaded Au nanoparticles, absorption spectra, and hydrophilicity of CAu nanozymes were systematically characterized to demonstrate the flexibility of this novel method. The high-efficiency peroxidase-like sCAu0.3 nanozyme with hyperthermia-activated property was then screened for later bio-application. It is worth mentioning that its photothermal-promoted peroxidase-like activity could be achieved under near-infrared laser irradiation. Moreover, sCAu0.3 could specifically achieve glutathione detection in human blood samples. This method will provide a protocol for the regulation of CAu nanozymes to adapt to bio-detection applications.
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FOOD AND AGRICULTURAL IMMUNOLOGY
·
2022
·
IF 3.268
Peizhen Li,Xiuhua Xia,Jiannan Chen,Hang Yu,Yunfei Xie,Yahui Guo,Weirong Yao,He Qian,Yuliang Cheng
Gold-coated silver core–shell nanoparticles (Ag@Au NPs) have been widely used for SERS analysis due to plasmon resonance performances. However, it is a great challenge to fabricate Ag@Au core–shell structures with specified morphology. In this paper, the size and shape of Ag NPs (core) were precisely controlled by a seed-mediated approach, and then the gold shell was completely coated on under the strong reduction of ascorbic acid, resulting in Ag@Au NPs with highly regulated morphology. The obtained Ag@Au NPs achieved a similar or even better SERS enhancement factor (EF) (up to 5.7 × 107) compared to Ag NPs, but significantly higher stability. For the rapid SERS detection of nitrofurantoin metabolite AHD, a limit of detection (LOD) as low as 1 × 10−10 M and a wide linear range from 1 × 10−4 to 1 × 10−8 M were obtained. Furthermore, recoveries for crayfish samples were from 90.5% to 108%, indicating a good performance of the presented method in real sample detection.
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Journal of Materials Chemistry A
·
2019
·Vol. 7
·期 7
·3408-3414
·
IF 10.733
Song Ma,Kai Chen,Yun-Hang Qiu,Li-Li Gong,Gui-Min Pan,Yong-Jie Lin,Zhong-Hua Hao,Li Zhou,Qu-Quan Wang
Substantial effort has been devoted to synthesizing plasmonic metal/semiconductor heteronanostructures with controlled morphology owing to their excellent performance ranging from photocatalysis to optical information processing. However, growing semiconductor heterojunctions with both counterparts in direct contact with the plasmonic metal nanostructures remains challenging. Herein, we report a three-step method to grow CdS–Cu2−xS lateral heteroshells on Au nanoparticles with all components directly connected with each other. Ag2S semi shells are initially grown on the Au nanoparticles as an interim layer, Cu2−xS semi shells are then grown on the uncovered surface of the Au nanoparticles, and CdS is generated by replacing Ag2S and the Au core complex with CdS–Cu2−xS lateral heteroshells Au/CdS–Cu2−xS is finally obtained. These complexes integrate the plasmon resonances of Au in the visible region and that of Cu2−xS in the near-infrared region, and therefore show improved photocatalytic activity and high photothermal efficiency. This study offers a synthetic approach to grow metal sulfides on Au nanostructures which have diverse applications in photocatalysis and photothermal therapy.
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CATALYSIS LETTERS
·
2019
·Vol. 149
·期 2
·361-372
·
IF 2.372
Liu Yanan,Yang Zhao,Zhang Xinyi,He Yufei,Feng Junting,Li Dianqing
Abstract A series of CeO 2 with the morphology of nanocube (NC), nanopolyhedron (NP) and nanorod (NR) were synthesized by hydrothermal method as substrates to support monometallic Au catalysts. Insight into support morphology-dependent the property of active component and catalytic behavior for the selective hydrogenation of phenylacetylene has been performed. Specifically, nanocube ceria could disperse monometallic Au nanoparticles due to a large amount of low coordinated sites that readily generated the strong interaction for anchoring active metal, whereas the polyhedron and rod-like ceria supported Au nanoparticles possessed large size and wide particle distribution. As expected, well-dispersed and stable Au/CeO 2 nanocube demonstrated 83% of selectivity towards styrene when the conversion of phenylacetylene reached 90%, which was much higher than that of others. Preferable activity was mainly ascribed to small size of Au nanoparticles, which facilitated the adsorption/dissociation of hydrogen considered as the rate-determining step. Enhanced selectivity was due to the electronic effect that caused by strong interaction between Au and cubic CeO 2 , which also contributed to good stability. This work not only provides a facile method for the preparation of highly dispersed and efficient Au/CeO 2 catalysts by modulating the morphology of support, but also offers a novel idea for the fabrication of other highly dispersed supported metal catalysts with enhanced behavior in heterogeneous catalysis. Graphical Abstract
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2018
·Vol. 30
·期 1
·855-861
·
IF 2.324
Yu Binglong,Wen Yu,Yang Xiaoxin,Cai Xiulan
The growth of metal mixed semiconductor particles was known to enhance their photocatalytic properties. In this study, a brand-new and simple one-pot polyol method was successfully used to synthesize metal gold embedded in ZnO nanoparticles (NPs), termed ZnO–Au microspheres. The physicochemical properties of ZnO–Au microspheres were analyzed by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy measurements, UV–Vis absorption espectroscopy and Fourier transform infrared espectroscopy. Applied to degradation of methylene blue under visible light, the ZnO–Au microspheres photocatalyst showed better photocatalytic activity than pure ZnO NPs. The reusability of ZnO–Au microspheres was also examined.
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NEW JOURNAL OF CHEMISTRY
·
2019
·Vol. 43
·期 20
·7613-7619
·
IF 3.069
Yuanjie Teng,Yuchao Zhang,Zeyu Ren,Zhenni Wang,Wenhan Liu,Kang Shao,Zaifa Pan
In this work, a facile surface-enhanced Raman scattering (SERS) substrate formed on a water/oil interface was prepared by adding n-hexane to Au colloids through simple vortex mixing without the involvement of any organic additives. In this process, the background SERS signal was reduced, which is good for the detection of adsorbed analyte molecules on the interfacial substrate. Furthermore, an Au monolayer nanofilm (Au MLF) spontaneously formed at the water/n-hexane interface after just a few seconds of simple vortex mixing, which is much shorter than the time required for self-assembly of nanoparticle films using organic additives. Transmission electron microscopy characterization results showed that the Au nanoparticles are close-packed and that the density of the Au nanoparticles on the interface could be controlled by varying the vortex mixing time and volume of n-hexane. The enhanced Raman signal was mainly as a result of the localized surface plasmon resonance and adsorption enrichment effects. The substrate showed good repeatability, with an relative standard deviation (RSD) of 5.02% (n = 6 × 8) by random selection and an RSD of 5.5% for an area of 4.0 μm × 4.0 μm. Finally, the proposed substrate was successfully applied in the detection of rhodamine B (RhB), malachite green (MG) and ciprofloxacin (CIP), with enhancement factors of 1.1 × 106 (RhB), 0.8 × 106 (MG), and 2.7 × 106 (CIP).
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CHEMISTRY-A EUROPEAN JOURNAL
·
2019
·Vol. 25
·期 23
·5904-5911
·
IF 5.16
Guoqiang Liu,Zhiqing Cui,Miaomiao Han,Shengbo Zhang,Cuijiao Zhao,Chun Chen,Guozhong Wang,Haimin Zhang
Graphical Room at the active site : A room-temperature redox approach is used to prepare a composite core–shell-structured Au@CeO 2 electrocatalyst (see figure) composed of small gold nanoparticles (<10 nm) and rich oxygen vacancies in CeO 2 nanoparticles to synergistically boost the electrocatalytic activity toward the N 2 reduction reaction (NRR) to NH 3 . Electrosynthesis of NH 3 through the N 2 reduction reaction (NRR) under ambient conditions is regarded as promising technology to replace the industrial energy- and capital-intensive Haber–Bosch process. Herein, a room-temperature spontaneous redox approach to fabricate a core–shell-structured Au@CeO 2 composite, with Au nanoparticle sizes below about 10 nm and a loading amount of 3.6 wt %, is reported for the NRR. The results demonstrate that as-synthesized Au@CeO 2 possesses a surface area of 40.7 m 2 g −1 and a porous structure. As an electrocatalyst, it exhibits high NRR activity, with an NH 3 yield rate of 28.2 μg h −1 cm −2 (10.6 μg h −1 mg −1 cat. , 293.8 μg h −1 mg −1 Au ) and a faradaic efficiency of 9.50 % at −0.4 V versus a reversible hydrogen electrode in 0.01 m H 2 SO 4 electrolyte. The characterization results reveal the presence of rich oxygen vacancies in the CeO 2 nanoparticle shell of Au@CeO 2 ; these are favorable for N 2 adsorption and activation for the NRR. This has been further verified by theoretical calculations. The abundant oxygen vacancies in the CeO 2 nanoparticle shell, combined with the Au nanoparticle core of Au@CeO 2 , are electrocatalytically active sites for the NRR, and thus, synergistically enhance the conversion of N 2 into NH 3 .
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