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تسجيل مستخدم جديدOne-pot green process to synthesize controllable surface terminations MXenes in molten salts
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Surface terminations for 2D MXene have dramatic impacts on physicochemical properties. The commonly etching methods usually introduce -F surface termination or metallic into MXene. Here, we present a new molten salt assisted electrochemical etching (MS-E-etching) method to synthesize fluorine-free Ti3C2Tx without metallics. Due to performing electrons as reaction agent, the cathode reduction and anode etching can be spatially isolated, thus no metallic presents in Ti3C2Tx product. Moreover, the Tx surface terminations can be directly modified from -Cl to -O and/or -S in one pot process. The obtained -O terminated MXenes exhibited capacitance of 225 and 205 F/g at 1 and 10 A/g, confirming high reversibility of redox reactions. This one-pot process greatly shortens the modification procedures as well as enriches the surface functional terminations. More importantly, the recovered salt after synthesis can be recycled and reused, which brands it as a green sustainable method.
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Nanolaminated materials are important because of their exceptional properties and wide range of applications. Here, we demonstrate a general approach to synthesize a series of Zn-based MAX phases and Cl-terminated MXenes originating from the replacem
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Molecular dynamics simulations of the temperature dependent crystal growth rates of the salts, NaCl and ZnS, from their melts are reported, along with those of a number of pure metals. The growth rate of NaCl and the FCC-forming metals show little ev
idence of activated control, while that of ZnS and Fe, a BCC forming metal, exhibit activation barriers similar to those observed for diffusion in the melt. Unlike ZnS and Fe, the interfacial inherent structures of NaCl and Cu and Ag are found to be crystalline. We calculate the median displacement between the interfacial liquid and crystalline states and show that this distance is smaller than the cage length, demonstrating that crystal growth in the fast crystallizers can occur via local vibrations and so largely avoid the activated kinetics associated with the larger displacements associated with particle transport.
New MAX phases Ti2(AlxCu1-x)N and Nb2CuC were synthesized by A-site replacement by reacting Ti2AlN and Nb2AlC, respectively, with CuCl2 or CuI molten salt. X-ray diffraction, scanning electron microscopy, and atomically-resolved scanning transmission
electron microscopy showed complete A-site replacement in Nb2AlC, which lead to formation of Nb2CuC. However, the replacement of Al in Ti2AlN phase was only close to complete at Ti2(Al0.1Cu0.9)N. Density-functional theory calculations corroborated the structural stability of Nb2CuC and Ti2CuN phases. Moreover, the calculated cleavage energy in these Cu-containing MAX phases are weaker than in their Al-containing counterparts, indicating that they are precursor candidates for MXene derivation.
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The family of MAX phases and their derivative MXenes are continuously growing in terms of both crystalline and composition varieties. In the last couple of years, several breakthroughs have been achieved that boosted the synthesis of novel MAX phases
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