Do you want to publish a course? Click here

Bispropylurea bridged polysilsesquioxane: A microporous MOF-like material for molecular recognition

58   0   0.0 ( 0 )
 Added by Dorian Hanaor
 Publication date 2021
  fields Physics
and research's language is English




Ask ChatGPT about the research

Microporous organosilicas assembled from polysilsesquioxane (POSS) building blocks are promising materials that are yet to be explored in-depth. Here, we investigate the processing and molecular structure of bispropylurea bridged POSS (POSS-urea), synthesised through the acidic condensation of 1,3-bis(3-(triethoxysilyl)propyl)urea (BTPU). Experimentally, we show that POSS-urea has excellent functionality for molecular recognition toward acetonitrile with an adsorption level of 74 mmol/g, which compares favourably to MOFs and zeolites, with applications in volatile organic compounds (VOC). The acetonitrile adsorption capacity was 132-fold higher relative to adsorption capacity for toluene, which shows the pores are highly selective towards acetonitrile adsorption due to their size and arrangement. Theoretically, our tight-binding density functional and molecular dynamics calculations demonstrated that this BTPU based POSS is microporous with an irregular placement of the pores. Structural studies confirm maximal pore sizes of around 1 nm, with POSS cages possessing an approximate edge length of approximately 3.16 Angstrom



rate research

Read More

We propose a new environment for information encoding and transmission via a novel type of molecular Quantum Dot Cellular Automata (QCA) wire, composed of a single row of head-to-tail interacting 2-dots molecular switches. While most of the research in the field refers to dots-bearing molecules bound on some type of surface, forming a bidimensional array of square cells capable of performing QCA typical functions, we propose here to embed the information bearing elements within the channels of a microporous matrix. In this way molecules would self-assemble in a row as a consequence of adsorption inside the pores of the material, forming an encased wire, with the crystalline environment giving stability and protection to the structure. DFT calculations on a diferrocenyl carborane, previously proposed and synthesized in the literature, were performed both in vacuum and inside the channels of zeolite ITQ-51, indicating that information encoding and trasmission is possible within the nanoconfined environment.
In the search of material properties out-of-equilibrium, the non-equilibrium steady states induced by electric current are an appealing research direction where unconventional states may emerge. However, the unavoidable Joule heating caused by flowing current calls for the development of new measurement protocols, with a particular attention to the physical properties of the background materials involved. Here, we demonstrate that localised heating can give rise to a large, spurious diamagnetic-like signal. This occurs due to the local reduction of the background magnetisation caused by the heated sample, provided that the background material has a Curie-like susceptibility. Our experimental results, along with numerical calculations, constitute an important building block for performing accurate magnetic measurements under the flow of electric current.
In this work, we propose a new auxetic (negative Poissons ratio values) structure, based on a $gamma$-graphyne structure, here named $Agamma G$ $structure$. Graphynes are 2D carbon allotropes with phenylic rings connected by acetylenic groups. The A$gamma$G structural/mechanical and electronic properties, as well as its thermal stability, were investigated using classical reactive and quantum molecular dynamics simulations. We found that A$gamma$G has a large bandgap of 2.48 eV and is thermally stable at a large range of temperatures. It presents a Youngs modulus that is an order of magnitude smaller than that of graphene or $gamma$-graphyne. The classical and quantum results are consistent and validate that the A$gamma$G is auxetic, both when isolated (vacuum) and when deposited on a copper substrate. We believe that this is the densest auxetic structure belonging to the graphyne-like families.
Metal organic framework (MOF) materials in general, and MOF-74 in particular, have promising properties for many technologically important processes. However, their instability under humid conditions severely restricts practical use. We show that this instability and the accompanying reduction of the CO$_2$ uptake capacity of MOF-74 under humid conditions originate in the water dissociation reaction H$_2$O$rightarrow$OH+H at the metal centers. After this dissociation, the OH groups coordinate to the metal centers, explaining the reduction in the MOFs CO$_2$ uptake capacity. This reduction thus strongly depends on the catalytic activity of MOF-74 towards the water dissociation reaction. We further show that-while the water molecules themselves only have a negligible effect on the crystal structure of MOF-74-the OH and H products of the dissociation reaction significantly weaken the MOF framework and lead to the observed crystal structure breakdown. With this knowledge, we propose a way to suppress this particular reaction by modifying the MOF-74 structure to increase the water dissociation energy barrier and thus control the stability of the system under humid conditions.
Two-dimensional (2D) materials with Dirac cones have been intrigued by many unique properties, i.e., the effective masses of carriers close to zero and Fermi velocity of ultrahigh, which yields a great possibility in high-performance electronic devices. In this work, using first-principles calculations, we have predicted a new Dirac cone material of silicon carbide with the new stoichiometries, named g-SiC6 monolayer, which is composed of sp2 hybridized with a graphene-like structure. The detailed calculations have revealed that g-SiC6 has outstanding dynamical, thermal, and mechanical stabilities, and the mechanical and electronic properties are still isotropic. Of great interest is that the Fermi velocity of g-SiC6 monolayer is the highest in silicon carbide Dirac materials until now. The Dirac cone of the g-SiC6 is controllable by an in-plane uniaxial strain and shear strain, which is promised to realize a direct application in electronics and optoelectronics. Moreover, we found that new stoichiometries AB6 (A, B = C, Si, and Ge) compounds with the similar SiC6 monolayer structure are both dynamics stable and possess Dirac cones, and their Fermi velocity was also calculated in this paper. Given the outstanding properties of those new types of silicon carbide monolayer, which is a promising 2D material for further exploring the potential applications.
comments
Fetching comments Fetching comments
Sign in to be able to follow your search criteria
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا