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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2022 · IF 5.518

Exploration of nisin-directed gold nanoclusters employed for detecting thiourea and the sensing mechanism

Lu Zhao,Jie Liu,Yunfeng Bai,Yaqiong Wen,Xiaoming Yang

In this study, we successfully synthesized the red-fluorescence gold nanoclusters (AuNCs@nisin) while employing nisin as the template, and AuNCs@nisin showed the uniform particle size of around 3.5 ± 0.5 nm, and the corresponding excitation and emission wavelengths were 493 nm and 644 nm, respectively. Meanwhile, AuNCs@nisin was mainly composed by the elements of C, N, O, Au as well as S, and it was equipped with the functional groups of hydroxyl and amino. Significantly, the fluorescence of AuNCs@nisin showed the obvious response to thiourea based on the interaction between the metal core of AuNCs@nisin and thiourea, thus leading to the formation of Au-S bond and affecting the fluorescence intensity of AuNCs@nisin. Consequently, we achieved to establishing the detection of thiourea by AuNCs@nisin, and the corresponding linear range between the fluorescence intensity of AuNCs@nisin and the concentration of thiourea was 2 mmol/L-4 mol/L with a detection limit of 0.74 μmol/L. Consequently, the prepared AuNCs@nisin exhibited the potential of serving as a fluorescent probe for determining thiourea.

CAS / MDL: 10031-53-5
研究领域: 分析化学 · 生物化学
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TALANTA · 2016 · IF 4.035

Modification-free and N-acetyl-L-cysteine-induced colorimetric response of AuNPs: A mechanistic study and sensitive Hg2+ detection

Jie Tang,Peng Wu,Xiandeng Hou,Kailai Xu

A facile yet sensitive and selective method was proposed for Hg 2+ detection based on N-acetyl-L-cysteine(NAC)-induced colorimetric response of AuNPs. The proposed method can be easily performed by introducing the premixing of NAC and Hg 2+ into as-prepared citrate-capped AuNPs solution. A combination of experimental and theoretical studies was applied to illustrate the mechanism of this AuNPs colorimetric system. The strong interaction of NAC and AuNPs through Au–S bond could lead to the aggregation of AuNPs, but the formation of NAC-Hg-NAC complex decreased the affinity between NAC and AuNPs and resulted in an anti-aggregation effect. Therefore, the color of the AuNPs solution would progress from purple to red with the increase of Hg 2+ concentration. The proposed method had a high sensitivity with a limit of detection of 9.9   nM. Coexistent metal ions , including Cd 2+ , Mn 2+ , Al 3+ , Ag + , K + , Mg 2+ , Ca 2+ , Cr 3+ , Cu 2+ , Fe 3+ , Pb 2+ , Ni 2+ and Zn 2+ , did not interfere with the detection of Hg 2+ . This method can be used to monitor Hg 2+ in tap water.

CAS / MDL: 16903-35-8
研究领域: 分析化学 · 环境科学
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JOURNAL OF CATALYSIS · 2022 · IF 8.047

Boosting photoelectrochemical water splitting by Au@Pt modified ZnO/CdS with synergy of Au-S bonds and surface plasmon resonance

Songbo Wang,Pengjie Liu,Chengzhen Meng,Yidan Wang,Lei Zhang,Lun Pan,Zhen Yin,Na Tang,Ji-Jun Zou

Photoelectrochemical (PEC) water splitting is a promising approach to solve the current energy and environmental crises. Herein, we developed a “one stone, two birds” strategy to construct Au@Pt decorated ZnO/CdS heterojunctions (ZCAP) with Au-S bond and surface plasmon resonance (SPR) effect for promoted PEC water splitting. The optimized ZCAP structure exhibited the highest photocurrent density of 4.23 mA/cm 2 at 1.23 V vs. RHE and hydrogen evolution rate of 72.3 μmol·cm −2 ·h −1 , which is magnitude higher than pure ZnO. In-depth investigations indicate that SPR effect can afford hot electrons, whereas Au-S bonds over interface act as transmission bridge for facilitated electron transfer, the synergy of them achieves efficient charge separation and light utilization. Meanwhile, surface Pt nanoparticles serve as active sites for rapid charge transfer and promoted surface reaction. This article illustrates that the synergy of SPR and electron transfer bridge is an efficient strategy for promoted PEC performance.

研究领域: 材料科学 · 能源科学 · 化学工程 · 纳米技术
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Nature Communications · 2023 ·Vol. 14 ·期 1 ·1-7 · IF 16.6

The role of halogens in Au–S bond cleavage for energy-differentiated catalysis at the single-bond limit

Li Peihui,Hou Songjun,Wu Qingqing,Chen Yijian,Wang Boyu,Ren Haiyang,Wang Jinying,Zhai Zhaoyi,Yu Zhongbo,Lambert Colin J.,Jia Chuancheng,Guo Xuefeng

The transformation from one compound to another involves the breaking and formation of chemical bonds at the single-bond level, especially during catalytic reactions that are of great significance in broad fields such as energy conversion, environmental science, life science and chemical synthesis. The study of the reaction process at the single-bond limit is the key to understanding the catalytic reaction mechanism and further rationally designing catalysts. Here, we develop a method to monitor the catalytic process from the perspective of the single-bond energy using high-resolution scanning tunneling microscopy single-molecule junctions. Experimental and theoretical studies consistently reveal that the attack of a halogen atom on an Au atom can reduce the breaking energy of Au−S bonds, thereby accelerating the bond cleavage reaction and shortening the plateau length during the single-molecule junction breaking. Furthermore, the distinction in catalytic activity between different halogen atoms can be compared as well. This study establishes the intrinsic relationship among the reaction activation energy, the chemical bond breaking energy and the single-molecule junction breaking process, strengthening our mastery of catalytic reactions towards precise chemistry.

研究领域: 催化 · 化学物理 · 材料科学 · 纳米技术
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MICROCHIMICA ACTA · 2021 ·Vol. 188 ·期 2 ·1-8 · IF 5.833

Determination of β-amyloid oligomer using electrochemiluminescent aptasensor with signal enhancement by AuNP/MOF nanocomposite

Yin Lixiu,Wang Yueju,Tan Rong,Li Huiling,Tu Yifeng

In order to effectively and conveniently detect the β-amyloid oligomer (AβO) for earlier diagnosis of Alzheimer’s disease (AD), a disposable aptamer biosensor has been developed with high performance, facile operation, and low cost. Using a nanocomposite by in situ reduction of chloroauric acid to decorate Au nanoparticles (AuNPs) on Fe-MIL-88NH 2 material via Au–N bond to effectively enhance the electrochemiluminescence (ECL) of luminol, the functioned basal electrode provides adequate background for sensing response. When the aptamer is linked via Au–S bond on the surface, the sensor gets the ability of specific recognition and coalescence toward the target (AβO). After incubating the sample on the aptasensor, its ECL signal is inhibited owing to the steric hindrance of the AβO macromolecules. The relative inhibition ratio linearly depends to the logarithm of AβO concentration in the range 0.1 pM to 10 pM, with an LOD of 71 fM. The aptasensor has high selectivity to AβO among its analogs. The recoveries in human serum were 98.9–105.4%. This research provides a new approach for sensitive detection of AβO in clinic laboratories for investigation and diagnosis of AD. Graphical abstract

CAS / MDL: 13822-56-5
研究领域: 生物医学工程 · 分析化学 · 纳米技术 · 诊断学
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ANALYST · 2011 ·Vol. 136 ·期 22 ·4770-4773 · IF 3.913

N-1-(2-Mercaptoethyl)thymine modification of gold nanoparticles: a highly selective and sensitive colorimetric chemosensor for Hg2+

Ling Chen,Tingting Lou,Chunwei Yu,Qi Kang,Lingxin Chen

An approach for mercury ions (Hg2+) sensing based on the Hg2+-induced aggregation of thymine (T)–SH-functionalized gold nanoparticles (AuNPs) has been reported. The T–SH ligands that we synthesized can easily be coupled to the surface of AuNPs through the Au–S bond and can recognize Hg2+ with high selectivity by forming a T–Hg–T complex with strong affinity. For the T–SH-functionalized AuNPs (T–S-AuNPs) sensor, upon addition of Hg2+, the formation of the T–Hg–T complex induces aggregation of T–S-AuNPs and results in a significant change of color and UV-Vis absorption spectra. Thus, our method can be used for the rapid, easy and reliable screening of Hg2+ in aqueous solution, with high sensitivity (2.8 nM) and selectivity over competing analytes. The developed method is successfully applied to the sensing of Hg2+ in real environmental samples.

CAS / MDL: 65-71-4
研究领域: 分析化学 · 环境科学 · 纳米技术
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ANALYTICA CHIMICA ACTA · 2022 · IF 6.911

Antifouling zwitterionic peptide hydrogel based electrochemical biosensor for reliable detection of prostate specific antigen in human serum

Qiushu Du,Wenqi Wang,Xianghua Zeng,Xiliang Luo

An electrochemical biosensor based on the antifouling zwitterionic peptide hydrogel (CFEFKFC) and the poly(3,4-ethylenedioxythiophene) (PEDOT) was fabricated to accurately detect prostate specific antigen (PSA) in complex human serum. The electrode was modified with the conducting polymer PEDOT and gold nanoparticles (AuNPs) in sequence through electrodeposition , and then the designed zwitterionic peptide hydrogel prepared through self-assembly was immobilized onto the modified electrode surface via the Au–S bond. The zwitterionic peptide hydrogel with cysteine terminal is easy for immobilization onto the gold surface, and it is also suitable for the immobilization of biomolecules such as PSA antibody in this work, through the formation of covalent amide bonds. The peptide hydrogel possessed excellent antifouling property, and it was able to effectively prevent the adsorption of nonspecific proteins, cells and other biomolecules. The developed antifouling biosensor showed a linear response range from 0.1 ng mL −1 to 100 ng mL −1 , with a low limit of detection down to 5.6 pg mL −1 . These results encourage the wide use of zwitterionic peptide hydrogels as antifouling materials in various sensing and bio-sensing devices.

CAS / MDL: 126213-50-1 16903-35-8
研究领域: 生物传感器 · 电化学 · 纳米技术 · 分析化学 · 生物医学工程
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MICROCHIMICA ACTA · 2020 ·Vol. 187 ·期 3 ·1-12 · IF 6.232

Gold nanoparticles-functionalized monolithic column for enantioseparation of eight basic chiral drugs by capillary electrochromatography

Ma Mingxuan,Du Yingxiang,Yang Jiangxia,Feng Zijie,Ding Wen,Chen Cheng

Poly(glycidyl methacrylate)-co-(ethylene dimethacrylate) [poly(GMA-co-EDMA)] monoliths were prepared, and used as a support to attach gold nanoparticles (AuNP) via Au-S bond. Pepsin, acting as a chiral selector, was linked to the surface of the carboxyl-modified AuNP through a hydrochloride/N-hydroxysuccinimide coupling reaction. The material was characterized by scanning electron microscopy, energy dispersive X-ray spectrometry, transmission electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy and N 2 adsorption-desorption isotherm. The pepsin@AuNP@poly(GMA-co-EDMA) monolith showed preferable enantioselectivity for hydroxychloroquine (HCQ), chloroquine (CHQ), hydroxyzine (HXY), labetalol (LAB), nefopam (NEF), clenbuterol (CLE), amlodipine (AML) and chlorpheniramine (CHL) in capillary electrochromatography (CEC). These racemic drugs were monitored at the maximum absorption wavelength (220 nm for HXQ, CHQ, HXY, LAB, NEF; 240 nm for AML; 215 nm for CLE, CHL). In comparison with the pepsin@poly(GMA-co-EDMA) monolith loaded with 5 nm AuNP, the pepsin@poly(GMA-co-EDMA) monolith loaded with 13 nm AuNP shows significantly enhanced enantiomeric resolution (HCQ: 0.62 → 3.45; CHQ: 0.60 → 2.11; HXY: 0.49 → 2.30; LAB: 1.03 → 2.45, 1.45 → 3.46, 0 → 0.67; NEF: 0.53 → 1.29; CLE: 0.42 → 0.56; AML: 0 → 0.83; CHL: 0.24 → 0.55). Pepsin concentration, buffer pH value, buffer concentration and applied voltage were investigated in detail with (±) HCQ and (±) HXY as model analytes. The reproducibility of intra-day, inter-day and column-to-column were explored, and found to be satisfactory. Schematic presentation of the preparation of gold nanoparticles (AuNP) modified.

研究领域: 分析化学 · 纳米技术 · 药学 · 分离科学
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