Toxic gas whisperers: Sensing dynamics of pristine and alloyed Cu nanoclusters
Year: 2025
Type: article
Abstract: • A state-of-the-art Density Functional Theory (DFT) approach was employed to investigate the structural, electronic, and reactivity properties of pristine and transition metal-decorated clusters. • Adsorption of toxic gases such as CO, NO, and NH₃ on Ni- and Ag-doped Cu₄ and Cu₆ nanoclusters was systematically studied. • CO adsorption on the Cu₃Ni cluster demonstrates significant potential for CO gas sensing applications. • Pristine Cu₄, Cu₃Ag, and Cu₃Ni clusters show promising capability for the removal of NH₃ from the environment. The present study investigates the interactions of environmental pollutants, such as CO, NO, and NH₃, with copper nanoclusters Cuₙ ( n = 2–6), given their significant applications in catalysis and gas sensing. Among the nanoclusters studied, Cu₄ and Cu₆ demonstrated the strongest interactions with toxic gases and exhibited aromatic properties. When alloyed with silver (Ag) and nickel (Ni) to form bimetallic nanoclusters (Cu₃M and Cu₆M, where M = Ag, Ni), these clusters displayed enhanced catalytic activities for gas sensing, storage, and removal of harmful chemicals. The study calculated the structural stability, infrared activity, formation energy, and binding energies. Cu₄ and Cu₆ clusters substituted with Ag and Ni yields binding energy values of -2.82 eV, -3.26 eV, -3.32 eV, and -3.62 eV, respectively. These results indicate that interactions with transition metals (TMs) are energetically favorable. The calculated adsorption energies for CO gas on pristine Cu₄, Cu₃Ag, and Cu₃Ni were determined to be -0.60, -0.40, and -0.56 eV, respectively, indicating weak physisorption in the case of Cu₃Ag. Similarly, the adsorption energies for NO gas on Cu₄, Cu₆, and Cu₃Ag were -0.79, -0.21, and -0.77 eV, respectively. Furthermore, NH₃ adsorption on Cu₃Ag resulted in an energy of -1.11 eV, suggesting stronger interaction compared to other gases. The optimal adsorption energy obtained suggests promising recovery times for CO and NO on Cu₃Ni and Cu₆, measured at 2.20 and 2.70 s, respectively, underscoring their effectiveness in molecular sensing. For NH₃, the recovery time of 3.85 s highlights the potential of both doped and pristine clusters for efficient NH₃ removal from the environment. Additionally, the study analysed the density of states (DOS), revealing significant changes in molecular orbitals, particularly in the HOMO-LUMO gap, which further supports the enhanced reactivity of the nanoclusters.
Source: Chemical Physics Impact
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $1,520
OpenAlex ID: W4409670586