Hydrogen Dissociation Reaction on First-Row Transition Metal Doped Nanobelts

• Published in: Materials Vol. 16; no. 7; p. 2792
• Main Authors: Bayach, Imene, Sarfaraz, Sehrish, Sheikh, Nadeem S, Alamer, Kawther, Almutlaq, Nadiah, Ayub, Khurshid
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 31.03.2023; MDPI
• Subjects: Adsorbents; Adsorption; Catalysis; Catalysts; Catalytic activity; Comparative analysis; density functional theory; Dissociation; dissociation barrier; Efficiency; Electronic properties; Energy gap; Hydrocarbons; Hydrogen; hydrogen molecule; Hydrogenation; Investigations; Metals; molecular nanobelts; Molecular orbitals; Nitrogen; Perturbation; Stability analysis; transition metal; Transition metal compounds; Transition metals; dissociation barrier; hydrogen molecule; transition metal; density functional theory; molecular nanobelts
• ISSN: 1996-1944; 1996-1944
• DOI: 10.3390/ma16072792

Zigzag molecular nanobelts have recently captured the interest of scientists because of their appealing aesthetic structures, intriguing chemical reactivities, and tantalizing features. In the current study, first-row transition metals supported on an H -N -belt[6]arene nanobelt are investigated for the electrocatalytic properties of these complexes for the hydrogen dissociation reaction (HDR). The interaction of the doped transition metal atom with the nanobelt is evaluated through interaction energy analysis, which reveals the significant thermodynamic stability of TM-doped nanobelt complexes. Electronic properties such as frontier molecular orbitals and natural bond orbitals analyses are also computed, to estimate the electronic perturbation upon doping. The highest reduction in the HOMO-LUMO energy gap compared to the bare nanobelt is seen in the case of the Zn@NB catalyst (4.76 eV). Furthermore, for the HDR reaction, the Sc@NB catalyst displays the best catalytic activity among the studied catalysts, with a hydrogen dissociation barrier of 0.13 eV, whereas the second-best catalytic activity is observed for the Zn@NB catalyst (0.36 eV). It is further found that multiple active sites, i.e., the presence of the metal atom and nitrogen atom moiety, help to facilitate the dissociation of the hydrogen molecule. These key findings of this study enhance the understanding of the relative stability, electronic features, and catalytic bindings of various TM@NB catalysts.