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Citric acid based (CQDs/TiO2) nanocomposites against SARS-COV-2: theoretical, photocatalytic and computational studies
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-12-02 DOI: 10.1186/s11671-024-04117-2
Joina Gunjan Singh, Ankit Kumar Singh, Nurul Hidayah Mohamad Idris, Nattasa Kitchawengkul, Purim Jarujamrus, Hooi Ling Lee, Maria Grishina, Nadezhda Palko, Prateek Pathak, Amita Verma

In the last decade, carbon quantum dots (CQDs), a novel class of carbon-based nanomaterials, have received increasing attention due to their distinct properties. Carbon Quantum Dots/Titanium Dioxide (CQDs/TiO2) Nanocomposites were reported as potent compounds against SARS-COV-2. In this manuscript, citric acid is the carbon precursor used to synthesize carbon quantum dots (CQDs). Using a green approach, the synthesized CQD fabricates the Carbon Quantum Dots/Titanium Dioxide (CQDs/TiO2) Nanocomposites. Synthesized composites were characterized by using a UV–visible spectrophotometer, Fourier-transformed infrared (FTIR) spectrometry, X-ray diffractometry (XRD), and Scanning electron microscopy with energy dispersive X-ray analysis (SEM–EDX). Methylene blue was used to check the Photocatalytic activity of synthesized (CQDs/TiO2) nanocomposites of different concentrations. Computational modeling of agglomerates of CQD and TiO2 nanoparticles with the formula TiO2…….. Ti253O506 demonstrated two stages of the nanocomposite formation, including the formation of agglomerates with the neutral and salt-like structures with the total gain in the Gibbs free energy − 38.397 kcal/mole. In silico, Molecular docking studies of citric acid were evaluated against SARS-COV-2 protein to understand their mechanism and key amino acid interactions along with standard drug remdesivir. The photocatalytic activity of CQDs/TiO2 showed extremely promising results. Based on this study, the proposed mechanism of action of these compounds is reported. A detailed investigation of CQDs/TiO2 against SARS-CoV-2 is needed, which is another part of the research in our next manuscript.

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引用次数: 0
Hybrid layer-by-layer assembly of AuNPs/NSF composite for electrochemical detection of miRNA-196a 逐层混合组装 AuNPs/NSF 复合材料,用于电化学检测 miRNA-196a
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-26 DOI: 10.1186/s11671-024-04127-0
Jun Ji, Gaofan Shi, Jiayi Jiang, Shu Wu, Haoyuan Su, Hongzhi Pan, Dongdong Zeng

Detection of microRNA-196a (miRNA-196a) is crucial in cancer research, enabling early diagnosis and providing guidance for individualized treatment. In this work, we employed a naturally occurring negatively charged nano silk fibroin (NSF) with high mechanical properties, biocompatibility, and conductivity to be encapsulated with a positively charged gold nanoparticles (AuNPs) were used as film-forming materials for electrostatic layer-by-layer self-assembly to modify the working electrode of the screen-printed carbon electrode (SPCE). Under the optimized experimental conditions, the uniformly distributed AuNPs on the surface of the multilayer film modified SPCE (AuNPs/NSF)5.5/SPCE combined with the sulfhydryl-modified capture probe cp-DNA through gold-sulfur bonds. Furthermore, miRNA-196a is specifically captured through complementary base pairing to achieve highly sensitive and specific detection. (AuNPs/NSF)5.5/SPCE electrode can detect miRNA-196a in a concentration range of 1.0 × 10−13 to 1.0 × 10−6 M, and the calculated detection limit is 4.63 × 10−14 M when the signal-to-noise ratio is 3. The obtained results showed that the (AuNPs/NSF)5.5/SPCE has excellent selectivity and good stability over time.

微RNA-196a(miRNA-196a)的检测在癌症研究中至关重要,它可以实现早期诊断并为个体化治疗提供指导。在这项工作中,我们采用了一种具有高机械性能、生物相容性和导电性的天然负电荷纳米蚕丝纤维素(NSF),将其与带正电荷的金纳米颗粒(AuNPs)封装在一起,作为静电逐层自组装的成膜材料,对丝网印刷碳电极(SPCE)的工作电极进行改性。在优化的实验条件下,多层膜修饰 SPCE(AuNPs/NSF)5.5/SPCE 表面均匀分布的 AuNPs 通过金硫键与巯基修饰的捕获探针 cp-DNA 结合。此外,miRNA-196a 通过互补碱基配对被特异性捕获,实现了高灵敏度和特异性检测。(AuNPs/NSF)5.5/SPCE电极可在 1.0 × 10-13 至 1.0 × 10-6 M 的浓度范围内检测 miRNA-196a,当信噪比为 3 时,计算出的检测限为 4.63 × 10-14 M。
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引用次数: 0
Solid-state hydrogen storage materials 固态储氢材料
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-26 DOI: 10.1186/s11671-024-04137-y
M. R. Kalibek, A. D. Ospanova, B. Suleimenova, R. Soltan, T. Orazbek, A. M. Makhmet, Kh. S. Rafikova, N. Nuraje

The increasing global emphasis on sustainable energy alternatives, driven by concerns about climate change, has resulted in a deeper examination of hydrogen as a viable and ecologically safe energy carrier. The review paper analyzes the recent advancements achieved in materials used for storing hydrogen in solid-state, focusing particularly on the improvements made in both physical and chemical storage techniques. Metal–organic frameworks and covalent-organic frameworks are characterized by their porous structures and large surface areas, making them appropriate for physical adsorption. Additionally, the conversation centers on metal hydrides and complex hydrides because of their ability to form chemical bonds (absorption) with hydrogen, leading to substantial storage capacities. The combination of materials that adsorb and absorb hydrogen could enhance the overall efficiency. Moreover, the review discusses recent research, analyzes key factors that influence performance, and discusses the difficulties and strategies for enhancing material efficiency and cost-effectiveness. The provided observations emphasize the critical significance of improved materials in facilitating the transition towards a hydrogen-based economy. Furthermore, it is crucial to highlight the necessity for additional study and development in this vital field.

随着全球对可持续能源替代品的日益重视,以及对气候变化的担忧,人们开始深入研究氢这种可行且生态安全的能源载体。这篇综述论文分析了固态储氢材料的最新进展,尤其关注物理和化学储氢技术的改进。金属有机框架和共价有机框架具有多孔结构和大表面积的特点,适合物理吸附。此外,由于金属氢化物和复合氢化物能够与氢形成化学键(吸附),因而具有很强的储存能力,因此也成为人们讨论的焦点。将吸附和吸收氢的材料结合起来,可以提高整体效率。此外,综述还讨论了最新研究,分析了影响性能的关键因素,并讨论了提高材料效率和成本效益的困难和策略。所提供的意见强调了改良材料在促进向氢基经济过渡方面的重要意义。此外,还必须强调在这一重要领域开展更多研究和开发的必要性。
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引用次数: 0
Nucleus-targeted Silencer nanoplatform regulating ZEB1-AS1 in head and neck squamous cell carcinoma therapy 在头颈部鳞状细胞癌治疗中调控 ZEB1-AS1 的核靶向 Silencer 纳米平台
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-23 DOI: 10.1186/s11671-024-04148-9
Haojie Yang, Yangfan Zhang, Zicong Tan, Zihao Liu, Yingzhe Yan, Qin Li, Phei Er Saw, Ning Liufu, Fengtao Ji

Long noncoding RNAs have emerged as key players in the progression of head and neck squamous cell carcinoma (HNSC). Among them, ZEB1-AS1 was identified as an upregulated candidate in HNSC through comprehensive analysis of RNA-sequencing datasets. Here, elevated ZEB1-AS1 expression was correlated with poor prognosis in HNSC patients. Further investigations demonstrated that downregulation of ZEB1-AS1 induced epithelial-mesenchymal transition and increased sensitivity to cisplatin in Cal27 cells, while its upregulation reversed these effects, underscoring its pivotal role in tumor metastasis and cisplatin resistance in Cal27 cells. Mechanistically, ZEB1-AS1, located in cytoplasm and nucleus, directly regulated the expression of ZEB1, thereby influencing the expression of μ opioid receptor (MOR) and implicating in cancer progression. To advance clinical translation, we employed a nucleus-targeting nanoparticle platform for efficient delivery of a mixture of antisense oligonucleotides and siRNA (Silencer), effectively manipulating ZEB1-AS1 expression in vitro and in vivo. Besides, a predictive model for HNSC patients was developed by analyzing the expression levels of ZEB1-AS1, ZEB1, and MOR in the HNSC datasets. Our study underscored the critical role of ZEB1-AS1 in HNSC and its potential as a therapeutic target. By elucidating its functional mechanisms and utilizing a nucleus-targeting nanoparticle platform for efficient delivery, we proved the potential of ZEB1-AS1-targeted therapies in HNSC.

长非编码 RNA 已成为头颈部鳞状细胞癌(HNSC)恶化过程中的关键因素。通过对RNA测序数据集的综合分析,ZEB1-AS1被确定为HNSC中的上调候选RNA。在这里,ZEB1-AS1的高表达与HNSC患者的不良预后相关。进一步的研究表明,ZEB1-AS1的下调会诱导上皮-间充质转化,并增加Cal27细胞对顺铂的敏感性,而上调则会逆转这些效应,这突显了ZEB1-AS1在Cal27细胞肿瘤转移和顺铂耐药中的关键作用。从机理上讲,ZEB1-AS1位于细胞质和细胞核中,直接调控ZEB1的表达,从而影响μ阿片受体(MOR)的表达,并与癌症进展有关。为了推进临床转化,我们采用了一种细胞核靶向纳米粒子平台,高效递送反义寡核苷酸和siRNA(Silencer)的混合物,有效操纵了ZEB1-AS1在体外和体内的表达。此外,我们还通过分析HNSC数据集中ZEB1-AS1、ZEB1和MOR的表达水平,建立了HNSC患者的预测模型。我们的研究强调了ZEB1-AS1在HNSC中的关键作用及其作为治疗靶点的潜力。通过阐明ZEB1-AS1的功能机制并利用细胞核靶向纳米粒子平台进行高效递送,我们证明了ZEB1-AS1靶向疗法在HNSC中的潜力。
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引用次数: 0
Bismuth sensitized iron oxide on exfoliated graphene oxide (Bi–Fe2O3@GO) for oxygen evaluation reaction 用于氧气评估反应的剥离氧化石墨烯上的铋敏化氧化铁(Bi-Fe2O3@GO
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-23 DOI: 10.1186/s11671-024-04146-x
Akhtar Munir, Shaheer Jamal, Humaira Yasmeen Gondal, Javed Iqbal, Aamir Hussain, Arslan Aziz, Mahammad Nisar, Muhammad Zubair, Abdul Momin, Ali Haider

Electrochemical water splitting is a promising approach towards a sustainable and renewable energy source. However, the demand for high anodic potential and sluggish kinetics of oxygen evolution reaction (OER) restrict the efficiency and feasibility of the water-splitting process. In this quest, transition metal oxides and alloys are considered potential candidates owing to their natural occurrence and high redox potential for OER. However, many associated challenges in their use are still there to be addressed. Here, we designed a new class of bismuth-doped iron oxide on exfoliated graphene oxide by optimizing the metal loading on the conductive support to facilitate the flow of charge during catalysis. The catalytic ability of the synthesized Bi-doped nanocomposites was evaluated in activating the OER under extreme alkaline conditions (1 MKOH). On screening different combinations, 20Bi–Fe2O3@GO was identified as the most efficient and sustainable electrocatalyst even under harsh operating conditions, with an onset potential of 1.48 V and a Tafel slope of 65 mV/dec. The current study offers a new class of Bi-doped electrocatalysts, where the precise doping of Bi and the optimized loading of metal was found the key to achieving low onset potential and high current density to initiate OER.

Graphical abstract

电化学水分离是实现可持续和可再生能源的一种前景广阔的方法。然而,对高阳极电位的要求和缓慢的氧进化反应动力学限制了水分离过程的效率和可行性。在这一过程中,过渡金属氧化物和合金因其天然存在和高氧化还原电位而被认为是潜在的候选材料。然而,在使用过程中仍有许多相关挑战有待解决。在这里,我们在剥离的氧化石墨烯上设计了一类新的掺铋氧化铁,通过优化导电支撑上的金属负载来促进催化过程中的电荷流动。评估了合成的掺铋纳米复合材料在极碱性条件(1 MKOH)下激活 OER 的催化能力。在对不同组合进行筛选后,20Bi-Fe2O3@GO 被确定为即使在苛刻的操作条件下也是最高效、最可持续的电催化剂,其起始电位为 1.48 V,塔菲尔斜率为 65 mV/dec。目前的研究提供了一类新的掺铒电催化剂,发现精确的掺铒和优化的金属负载是实现低起始电位和高电流密度以启动 OER 的关键。
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引用次数: 0
Nature-inspired innovations: unlocking the potential of biomimicry in bionanotechnology and beyond 受大自然启发的创新:释放仿生技术及其他领域的生物模仿潜力
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-21 DOI: 10.1186/s11671-024-04153-y
Sergio A. Paniagua, Diego Batista Menezes, María Fernanda Camacho Murillo, Luis Castillo Henriquez, José Roberto Vega Baudrit

Bionanotechnology research has surged to the forefront of scientific innovation, propelling the exploration of cutting-edge technologies and interdisciplinary collaboration. Biomimicry, which harnesses nature's ingenuity, drives the development of novel research-based solutions in diverse fields such as vaccines, medicine, and biomedical devices. Nature's role is becoming increasingly pivotal in addressing complex challenges related to environmental conservation, human health, and pandemic preparedness, including those posed by SARS-CoV-2 and other emerging pathogens. Progress in this domain encompasses understanding nature´s mechanisms to develop advanced materials inspired by biological structures. Biomimetic innovations have the potential to revolutionize industries, reduce environmental impacts, and facilitate a more harmonious relationship between humans and nature while considering bioethics, underlining the necessity of conducting responsible research and implementing biomimetic advancements conscientiously. As biomimicry continues to grow, integrating ethical guidelines and policies will ensure these nature-inspired technologies' sustainable development and application, ultimately contributing to a more resilient and adaptive society. This mini-review article broadly overviews bionanotechnology applications based on natural examples.

Graphical Abstract

仿生技术研究已跃居科学创新的前沿,推动了尖端技术的探索和跨学科合作。仿生学利用大自然的聪明才智,在疫苗、医药和生物医学设备等不同领域推动了基于研究的新型解决方案的开发。在应对与环境保护、人类健康和大流行病防备(包括 SARS-CoV-2 和其他新出现的病原体)有关的复杂挑战方面,大自然的作用正变得越来越关键。在这一领域取得的进展包括了解自然机理,开发受生物结构启发的先进材料。生物仿生创新有可能给工业带来革命性的变化,减少对环境的影响,促进人与自然之间更加和谐的关系,同时考虑到生物伦理,强调了开展负责任的研究和认真实施生物仿生进步的必要性。随着生物仿生学的不断发展,整合伦理准则和政策将确保这些受大自然启发的技术得到可持续发展和应用,最终为建设一个更具复原力和适应力的社会做出贡献。这篇微型综述文章广泛概述了基于自然实例的仿生技术应用。
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引用次数: 0
Advances and challenges in dynamic photo-induced force microscopy 动态光诱导力显微镜的进展与挑战
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-21 DOI: 10.1186/s11671-024-04150-1
Hwi Je Woo, Mingu Kang, Yeonjeong Koo, Kyoung-Duck Park, Bongsu Kim, Eun Seong Lee, Junghoon Jahng

Photo-induced force microscopy (PiFM) represents a scanning probe technique renowned for its ability to provide high-resolution spectroscopic imaging at the nanoscale. It capitalizes on the amplification of tip motion by photo-induced forces, which are influenced by the response of the local medium, spanning from induced dipole interactions to thermal expansion. The behaviors of these force responses exhibit complexity in connection with both far-field and near-field effects, depending on their spectroscopic origins. In this review, we aim to provide a comprehensive overview of prior research endeavors, shedding light on their technical intricacies. We provide the perspectives of photo-induced dipole force and photo-induced thermal force, while exploring the dynamic PiFM modes associated with each scenario. Our article targets individuals newly venturing into this field, offering a blend of theoretical foundations and practical demonstrations covering a range from fundamental principles to advanced topics.

光诱导力显微镜(PiFM)是一种扫描探针技术,因其能够在纳米尺度上提供高分辨率光谱成像而闻名于世。它利用了光诱导力对针尖运动的放大作用,而光诱导力又受到局部介质反应的影响,包括诱导偶极相互作用和热膨胀。这些力响应的行为与远场和近场效应有关,表现出复杂性,这取决于它们的光谱起源。在这篇综述中,我们旨在全面概述之前的研究工作,揭示其技术的复杂性。我们提供了光诱导偶极力和光诱导热力的视角,同时探讨了与每种情况相关的动态 PiFM 模式。我们的文章针对刚刚涉足这一领域的人员,提供了理论基础和实践演示的融合,涵盖了从基本原理到高级主题的一系列内容。
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引用次数: 0
A review of new generation of dental restorative resin composites with antibacterial, remineralizing and self-healing capabilities 具有抗菌、再矿化和自修复功能的新一代牙科修复树脂复合材料综述
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-21 DOI: 10.1186/s11671-024-04151-0
Jinshuang Zhang, Yujin Yang, Yaqing Chen, Xu Chen, Ang Li, Juan Wang, Daojun Shen, Shunli Zheng

Dental restorative resin composites are widely used to repair tooth decay owing to attractive esthetics, adequate mechanical properties and minimally invasive tooth structure preparations. Nevertheless, dental restorative resin composites still face challenges because of their relatively high failure rate and short lifespan caused by secondary caries and bulk fracture. Thus, attempts have been carried out to explore a new generation of dental restorative resin composites with antibacterial, remineralizing, and self-healing capabilities to inhibit bacteria and lengthen the lifetime of the restorations. Such novel restorative composites can inhibit bacterial activity, reduce acid production, promote mineral regeneration and present a renewable advantage to achieve a higher performance, which are inspiring and provide support for further basic and clinical research. In this review, antibacterial dental restorative resin composites are first introduced, followed by remineralizing, self-healing, and multifunctional dental resin composites with two or more of the functions mentioned above. Meanwhile, we explain the mechanism of the corresponding dental restorative resin composites and describe their characteristics. Finally, we conclude and put forward prospects. This review will attract both researchers and clinicians in this field and help to provide innovative ideas to design new restorative resin composites for biomedical applications.

Graphical abstract

牙科修复树脂复合材料因其美观、适当的机械性能和微创的牙齿结构制备而被广泛用于修复蛀牙。然而,牙科修复用树脂复合材料仍然面临着挑战,因为二次龋坏和大量断裂导致其失效率相对较高,使用寿命较短。因此,人们开始尝试探索具有抗菌、再矿化和自愈合功能的新一代牙科修复树脂复合材料,以抑制细菌并延长修复体的使用寿命。这种新型修复复合材料可以抑制细菌活动、减少酸的产生、促进矿物质再生,并具有可再生的优势,从而实现更高的性能,这对进一步的基础和临床研究具有启发和支持作用。在这篇综述中,首先介绍了抗菌牙科修复树脂复合材料,然后介绍了具有上述两种或两种以上功能的再矿化、自修复和多功能牙科树脂复合材料。同时,我们解释了相应的牙科修复树脂复合材料的机理,并描述了它们的特点。最后,我们进行了总结并提出了展望。这篇综述将吸引该领域的研究人员和临床医生,并有助于为设计生物医学应用的新型修复树脂复合材料提供创新思路。
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引用次数: 0
Review on recent advancements in the role of electrolytes and electrode materials on supercapacitor performances 电解质和电极材料对超级电容器性能作用的最新进展综述
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-21 DOI: 10.1186/s11671-024-04053-1
Ashutosh Patel, Suresh Kumar Patel, R. S. Singh, R. P. Patel

Supercapacitors currently hold a prominent position in energy storage systems due to their exceptionally high power density, although they fall behind batteries and fuel cells in terms of energy density. This paper examines contemporary approaches aimed at enhancing the energy density of supercapacitors by adopting hybrid configurations, alongside considerations of their power density, rate capability, and cycle stability. Given that electrodes play a pivotal role in supercapacitor cells, this review focuses on the design of hybrid electrode structures with elevated specific capacitance, shedding light on the underlying mechanisms. Factors such as available surface area, porosity, and conductivity of the constituent materials significantly influence electrode performance, prompting the adoption of strategies such as nanostructuring. Additionally, the paper delves into the impact of novel bio-based hybrid electrolytes, drawing upon literature data to outline the fabrication of various hybrid electrode materials incorporating conducting polymers like polyaniline and polypyrrole, as well as metal oxides, carbon compounds, and hybrid electrolytes such as ionic liquids, gel polymers, aqueous, and solid polymer electrolytes. The discussion explores the contributions of different components and methodologies to overall capacitance, with a primary emphasis on the mechanisms of energy storage through non-faradic electrical double-layer capacitance and faradaic pseudo-capacitance. Furthermore, the paper addresses the electrochemical performance of hybrid components, examining their concentrations and functioning via diverse charge storage techniques.

目前,超级电容器因其超高的功率密度而在储能系统中占据重要地位,但在能量密度方面却落后于电池和燃料电池。本文研究了旨在通过采用混合配置提高超级电容器能量密度的现代方法,同时考虑了超级电容器的功率密度、速率能力和循环稳定性。鉴于电极在超级电容器电池中起着举足轻重的作用,本综述将重点关注具有较高比电容的混合电极结构的设计,并阐明其基本机制。组成材料的可用表面积、孔隙率和电导率等因素对电极性能有重大影响,促使人们采用纳米结构等策略。此外,论文还深入探讨了新型生物基混合电解质的影响,利用文献数据概述了各种混合电极材料的制造过程,其中包含聚苯胺和聚吡咯等导电聚合物、金属氧化物、碳化合物以及离子液体、凝胶聚合物、水性和固体聚合物电解质等混合电解质。讨论探讨了不同成分和方法对整体电容的贡献,主要重点是通过非法拉第双层电容和法拉第伪电容进行能量存储的机制。此外,论文还探讨了混合元件的电化学性能,通过不同的电荷存储技术研究了它们的浓度和功能。
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引用次数: 0
Waste upcycling of Sapota peels as a green route for the synthesis of silver nanoparticles and their application as catalytic and colorimetric detection of Co2+ and Hg2+ 将废弃的山榄皮作为合成银纳米粒子的绿色途径,并将其用于催化和比色检测 Co2+ 和 Hg2+
IF 5.5 3区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY Pub Date : 2024-11-21 DOI: 10.1186/s11671-024-04147-w
Anuradha Beniwal, Sushila Singh, Jyoti Rani, Monika Moond, Simran Kakkar, Seema Sangwan, Sachin Kumari

Biochemical synthesis of nanoparticles (NPs) using plant part extracts as capping and reducing agents has drawn considerable attention in research with a growing focus on green chemistry. The present study utilized Sapota (Manilkara zapota L.) peel extract to synthesize silver nanoparticles (SP-AgNPs) using ultrasonic vibration. Different characterization techniques such as UV-vis spectroscopy, dynamic light scattering, Fourier Transform Infrared Spectroscopy, Field emission scanning electron microscope, High resolution transmission electron microscopy, and X-ray diffraction were employed to check the production of SP-AgNPs. The AgNPs were crystalline in nature and had an average particle size of 27.906 nm. The research primarily focused on two aspects: the catalytic activity of SP-AgNPs in degrading environmental pollutants and their ability to act as colorimetric sensors for toxic metal ions. SP-AgNPs exhibited significant catalytic activity in the decomposition of various pollutants such as Methyl Orange (0.035 ± 0.090 min−1, 92.89 ± 1.79%), Crystal Violet (0.1097 ± 0.1016 min−1, 85.56 ± 2.21%) and Cosmic Brilliant Blue G-250 (0.0697 ± 0.0275 min−1, 79.56 ± 1.80%). The high degradation percentages and reaction rate constants indicate the efficiency of SP-AgNPs in pollutant degradation. Additionally, the study demonstrated the effectiveness of SP-AgNPs as sensors for detecting toxic metal ions, particularly Co2+ and Hg2+ with limits of detection 54.40 ± 1.43 µM and 10.70 ± 0.16 µM. With impressive sensitivity and low detection limits, SP-AgNPs showed promise in detecting these ions, which are often found in environmental contaminants. Moreover, their plant-based synthesis, low toxicity, and cost-effectiveness make them attractive options for environmental remediation efforts.

Graphical abstract

随着绿色化学日益受到关注,利用植物部分提取物作为封端剂和还原剂进行纳米粒子(NPs)的生化合成研究引起了广泛关注。本研究利用沙波塔(Manilkara zapota L.)果皮提取物,通过超声波振动合成银纳米粒子(SP-AgNPs)。采用了不同的表征技术,如紫外-可见光谱、动态光散射、傅立叶变换红外光谱、场发射扫描电子显微镜、高分辨率透射电子显微镜和 X 射线衍射,来检测 SP-AgNPs 的生产情况。AgNPs 呈结晶状,平均粒径为 27.906 nm。研究主要集中在两个方面:SP-AgNPs 降解环境污染物的催化活性及其作为有毒金属离子比色传感器的能力。SP-AgNPs 在分解甲基橙(0.035 ± 0.090 min-1,92.89 ± 1.79%)、水晶紫(0.1097 ± 0.1016 min-1,85.56 ± 2.21%)和宇宙亮蓝 G-250 (0.0697 ± 0.0275 min-1,79.56 ± 1.80%)等多种污染物时表现出显著的催化活性。较高的降解率和反应速率常数表明了 SP-AgNPs 在污染物降解方面的效率。此外,研究还证明了 SP-AgNPs 作为传感器检测有毒金属离子(尤其是 Co2+ 和 Hg2+)的有效性,其检测限分别为 54.40 ± 1.43 µM 和 10.70 ± 0.16 µM。SP-AgNPs 灵敏度高、检测限低,有望用于检测环境污染物中常见的这些离子。此外,SP-AgNPs 的植物合成、低毒性和成本效益使其成为环境修复工作中极具吸引力的选择。 图表摘要
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引用次数: 0
期刊
Nanoscale Research Letters
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