Understanding the adsorption of dye molecules on nanostructured materials is important in regard to innovative potential applications, especially when the corresponding entities are combined. Here, we explore the interaction of methylene blue (MB) with graphene and hexagonal boron-nitride (h-BN) as two-dimensional nanosheets with unique electronic properties and high potential in technological applications. We study these interactions using quantum-based molecular simulations and probe these through the interaction properties and electronic struc-ture of the adsorbed MB on the considered monolayers and especially the specific role of the surrounding environment. We discuss the importance of the findings in view of contaminant removal from wastewater and specifically sensing applications of considered monolayers. Our dispersion-corrected density functional theory (DFT) results show that MB adsorbs strongly on both the graphene and h-BN with interaction energies of-47.454 and-45.072 kcal/mol, respectively, with equilibrium distances of about 3.2 angstrom between the aromatic rings of adsorbate and substrates. The accuracy of the DFT calculations is validated by the coupled-cluster with single, double (triple) excitations level of theory. The charge density and atom-in-molecule theory analyses reveal the existence of non-covalent and electrostatic interactions between MB and graphene/h-BN surface. The electronic structure analysis shows that the semiconducting graphene becomes metallic after MB adsorption while the h-BN monolayer retains its semiconducting characteristic upon the adsorption. Complementary assays using DFT-based molecular dynamic simulations demonstrate the strong binding of MB to both the graphene and h-BN surfaces in the presence of water molecules as competitive entities. These findings demonstrate the po-tential applications of graphene and h-BN for the efficient adsorption of dye molecules and for developing promising adsorbents for wastewater treatment and functionalized sensors.
机构:
Lawrence Livermore Natl Lab, Mat Sci Div, Livermore, CA 94550 USA
Lawrence Livermore Natl Lab, Lab Energy Applicat Future LEAF, Livermore, CA 94550 USALawrence Livermore Natl Lab, Mat Sci Div, Livermore, CA 94550 USA
Zhou, Yilong
Kucheyev, S. O.
论文数: 0引用数: 0
h-index: 0
机构:
Lawrence Livermore Natl Lab, Mat Sci Div, Livermore, CA 94550 USALawrence Livermore Natl Lab, Mat Sci Div, Livermore, CA 94550 USA
Kucheyev, S. O.
Wan, Liwen F.
论文数: 0引用数: 0
h-index: 0
机构:
Lawrence Livermore Natl Lab, Mat Sci Div, Livermore, CA 94550 USA
Lawrence Livermore Natl Lab, Lab Energy Applicat Future LEAF, Livermore, CA 94550 USALawrence Livermore Natl Lab, Mat Sci Div, Livermore, CA 94550 USA
机构:
Ajou Univ, Dept Phys, Suwon 16499, Gyeonggi, South Korea
Ajou Univ, Dept Energy Syst Res, Suwon 16499, Gyeonggi, South KoreaAjou Univ, Dept Phys, Suwon 16499, Gyeonggi, South Korea
机构:
Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
Univ Nebraska, Nebraska Ctr Mat & Nanosci, Lincoln, NE 68588 USAUniv Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Peoples R China
Zhao, Yu
Wu, Xiaojun
论文数: 0引用数: 0
h-index: 0
机构:
Univ Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Peoples R China
Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R ChinaUniv Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Peoples R China
Wu, Xiaojun
Yang, Jinlong
论文数: 0引用数: 0
h-index: 0
机构:
Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R ChinaUniv Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Peoples R China
Yang, Jinlong
Zeng, Xiao Cheng
论文数: 0引用数: 0
h-index: 0
机构:
Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
Univ Nebraska, Nebraska Ctr Mat & Nanosci, Lincoln, NE 68588 USAUniv Sci & Technol China, Dept Mat Sci & Engn, CAS Key Lab Mat Energy Convers, Hefei 230026, Peoples R China