Phosphorene, a novel member of the two-dimensional nanomaterial family, has demonstrated great potential in biomedical applications, such as photothermal therapy, drug delivery and antibacterial. However, phosphorene is unstable and easily oxidized in an aerobic environment. In this paper, using larger-scale molecular dynamics simulations, we investigated the disruption of phosphorene oxide (PO) to the structure of a model protein, villin headpiece subdomain (HP35). It shows that the disruption of PO nanosheets to the protein structure is enhanced with increasing oxidation concentration of PO, while PO's oxidation mode has very little effect on the PO-HP35 interaction. PO with a low oxidation concentration has certain biocompatibility to HP35. Oxygen atoms filling into the groove region in the puckered surface of phosphorene enhance the dispersion interaction between phosphorene and HP35, which enhances the disruption of phosphorene to the structure of HP35. Compared with the dispersion interaction, the electrostatic interaction between PO and the protein has a negligible effect on the structural damage of HP35. These findings might shed light on the biological toxicity of PO nanosheets and would be helpful for future potential biomedical applications of PO nanosheets, such as nanodrugs and antibacterial agents.
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http://dx.doi.org/10.1039/d2cp04080h | DOI Listing |
Phys Chem Chem Phys
October 2024
Department of Chemistry, Faculty of Science, Arak University, Arak 3848177584, Iran.
We conducted a DFT study of the BN monolayer pairing with the O-containing volatile organic compounds (O-containing VOCs) in exhaled breath, acetone, ethanol, methanol, and formaldehyde. The most stable configuration of O-containing VOCs on the BN sheet is also considered and compared with the adsorbed HO on the desired monolayer. The adsorption energy when both water and O-containing VOC molecules are present shows that the O-containing VOC molecules can be effectively adsorbed on the surface of BN while maintaining stability in the presence of water molecules.
View Article and Find Full Text PDFMikrochim Acta
July 2024
Key Laboratory of Chemical Utilization of Plant Resources of Nanchang, Institute of Functional Materials and Agricultural Applied Chemistry, College of Chemistry and Material, Jiangxi Agricultural University, Nanchang, 330045, China.
The stability of black phosphorene (BP) and its preparation and modification for developing and applying devices have become a hot topic in the interdisciplinary field. We propose ultrasound-electrochemistry co-assisted liquid-phase exfoliation as an eco-friendly one-step method to prepare gold-silver bimetallic nanoparticles (Au-AgNPs)-decorated BP nanozyme for smartphone-based portable sensing of 4-nitrophenol (4-NP) in different water sources. The structure, morphology, composition, and properties of Au-AgNPs-BP nanozyme are characterized by multiple instrumental analyses.
View Article and Find Full Text PDFNanomaterials (Basel)
June 2024
Department of Materials Science and Engineering, Soongsil University, 369 Sangdo-ro, Dongjak-gu, Seoul 06978, Republic of Korea.
In this study, an omnidirectional and high-performance free-standing monopole patch radio-frequency antenna was fabricated using a urea-functionalized phosphorene/TiO/polypyrrole (UTP) nanocomposite. The UTP nanocomposite antenna was fabricated via ball milling of urea-functionalized phosphorene, chemical oxidative polymerization of the UTP nanocomposite, and mechanical pelletizing of the composite. Based on experiments, the proposed UTP nanocomposite-based antenna exhibited long-term stability in terms of electrical conductivity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2024
Key Laboratory of Precision and Intelligent Chemistry, Collaborative Innovation Center of Chemistry for Energy Materials (iChEM), School of Chemistry and Materials Science, University of Science and Technology of China, Hefei, 230026, China.
Phosphorene and fullerene are representative two-dimensional (2D) and zero-dimensional (0D) nanomaterials respectively, constructing their heterodimensional hybrid not only complements their physiochemical properties but also extends their applications via synergistic interactions. This is however challenging because of their diversities in dimension and chemical reactivity, and theoretical studies predicted that it is improbable to directly bond C onto the surface of phosphorene due to their strong repulsion. Here, we develop a facile electrosynthesis method to synthesize the first phosphorene-fullerene hybrid featuring fullerene surface bonding via P-C bonds.
View Article and Find Full Text PDFMolecules
May 2024
Department of Materials Science and Engineering, Soongsil University 369, Sangdo-ro, Dongjak-gu, Seoul 06978, Republic of Korea.
In this paper, we report a titanium dioxide/polypyrrole/phosphorene (TiO/PPy/phosphorene) nanocomposite as an active material for supercapacitor electrodes. Black phosphorus (BP) was fabricated by ball milling to induce a phase transition from red phosphorus, and urea-functionalized phosphorene (urea-FP) was obtained by urea-assisted ball milling of BP, followed by sonication. TiO/PPy/phosphorene nanocomposites can be prepared via chemical oxidative polymerization, which has the advantage of mass production for a one-pot synthesis.
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