Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 683, P. 170 - 177
Published: Dec. 10, 2024
Language: Английский
Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 683, P. 170 - 177
Published: Dec. 10, 2024
Language: Английский
ACS Catalysis, Journal Year: 2024, Volume and Issue: 14(21), P. 16434 - 16458
Published: Oct. 23, 2024
Thermo-catalytic CO2 hydrogenation to high-value oxygenates has been regarded as one of the most powerful strategies that can potentially alleviate excessive emissions. However, due high chemical stability and variability pathways, it is still challenging achieve highly active selective hydrogenation. Single atom catalysts (SACs) with ultrahigh metal utilization efficiency extraordinary electronic features have displayed growing importance for thermo-catalytic multiple developed improve performances. Here, we review breakthroughs in developing SACs efficient toward common (CO, HCOOH, CH3OH, CH3CH2OH) following order: first, an analysis reaction mechanisms thermodynamics challenges reactions; second, a summary SAs designed by dividing them into two categories single- dual-sites; third, discussion support effects focus on approaches regulating strong metal–support interaction (MSI). Summarily, current future perspectives develop higher-performance are presented. We expect this bring more design inspiration trigger innovation catalytic evolution materials eventually benefit achievement carbon-neutrality goal.
Language: Английский
Citations
7Molecular Catalysis, Journal Year: 2024, Volume and Issue: 569, P. 114550 - 114550
Published: Sept. 19, 2024
Language: Английский
Citations
5Applied Surface Science, Journal Year: 2025, Volume and Issue: 688, P. 162339 - 162339
Published: Jan. 8, 2025
Language: Английский
Citations
0Langmuir, Journal Year: 2025, Volume and Issue: unknown
Published: March 11, 2025
Single-atom catalysts (SACs) have displayed unprecedented activity and selectivity for electrochemical CO2 reduction reaction (CO2RR). Herein, a series of metal single atoms embedded on nitrogen-doped graphene (M–N4G, where M = In, Tl, Ge, Sn, Pb, Sb, Bi) is systematically evaluated as CO2RR electrocatalysts by density functional theory (DFT) calculations. The computational results show that most M–N4G exhibit better over the hydrogen evolution (HER). Ge/Pb–N4G exhibits excellent electrocatalytic performance in generation HCOOH from with low limiting potentials −0.292 −0.306 eV, which surpass vast majority electrocatalysts. Adsorption energy key intermediate *HCOO can be used an effective reactivity descriptor to screen promising catalysts. this work highlight ideal CO2RR.
Language: Английский
Citations
0Science Bulletin, Journal Year: 2025, Volume and Issue: unknown
Published: April 1, 2025
Language: Английский
Citations
0Published: Jan. 1, 2024
Language: Английский
Citations
0Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 683, P. 170 - 177
Published: Dec. 10, 2024
Language: Английский
Citations
0