Transition Metal-Doped C 20 Fullerene-Based Single-Atom Catalysts with High Catalytic Activity for Hydrogen Dissociation Reaction.
Sehrish SarfarazMuhammad YarNadeem S SheikhImene BayachKhurshid AyubPublished in: ACS omega (2023)
Hydrogen dissociation is a key step in almost all hydrogenation reactions; therefore, an efficient and cost-effective catalyst with a favorable band structure for this step is highly desirable. In the current work, transition metal-based C 20 (M@C 20 ) complexes are designed and evaluated as single-atom catalysts (SACs) for hydrogen dissociation reaction (HDR). Interaction energy ( E int ) analysis reveals that all the M@C 20 complexes are thermodynamically stable, whereas the highest stability is observed for the Ni@C 20 complex ( E int = -6.14 eV). Moreover, the best catalytic performance for H 2 dissociation reaction is computed for the Zn@C 20 catalyst ( E ads = 0.53 eV) followed by Ti@C 20 ( E ads = 0.65 eV) and Sc@C 20 ( E ads = 0.76 eV) among all considered catalysts. QTAIM analyses reveal covalent or shared shell interactions in H 2 * + M@C 20 systems, which promote the process of H 2 dissociation over M@C 20 complexes. NBO and EDD analyses declare that transfer of charge from the metal atom to the antibonding orbital of H 2 causes dissociation of the H-H bond. Overall outcomes of this study reveal that the Zn@C 20 catalyst can act as a highly efficient, low-cost, abundant, and precious metal-free SAC to effectively catalyze HDR.
Keyphrases
- electron transfer
- highly efficient
- transition metal
- visible light
- low cost
- metal organic framework
- room temperature
- genome wide
- magnetic resonance imaging
- single cell
- computed tomography
- heavy metals
- quantum dots
- reduced graphene oxide
- dna methylation
- gene expression
- type diabetes
- weight loss
- insulin resistance
- skeletal muscle
- risk assessment