First-Principles Study on the Molecular Mechanism of Solar-Driven CO2 Reduction on H-Terminated Si

• Solar-driven conversion of CO2 with H-terminated silicon has recently attracted increasing interest. However, the molecular mechanism of the reaction is still not well understood. A systematic study of the mechanism has been carried out with first-principles calculations. The formation energies of the intermediates are found to be insensitive to the structure of the surface. On the fully H-terminated Si(111) surface, several pathways for the conversion of CO2 into CO at a coordinatively saturated Si site are studied, including the conventional COOH* pathway and the direct insertion of CO2 into Si−H and Si−Si bonds. Although the barrier of the COOH* pathway is lowest among the three pathways, it is higher than that for OH* elimination, which suggests that CO2 should be converted by other types of active site. The reaction at the isolated and dual coordinatively unsaturated (CUS) Si sites, which can be generated by light illumination, heat, and Pd loading, are then studied. The results suggest that the most efficient pathway to convert CO2 is to convert it into CO and O* at an isolated CUS Si site before O* reacts with a terminating H* to form adsorbed OH* and generate new isolated CUS Si sites. Therefore, the CUS Si site catalyzes the reaction until all H* is converted into OH*. The results provide new insight into the mechanism of the reaction and should be helpful for the design of more efficient Si-based catalysts for CO2 conversion. 

Ämnesord

NATURVETENSKAP  -- Kemi -- Teoretisk kemi (hsv//swe)

NATURAL SCIENCES  -- Chemical Sciences -- Theoretical Chemistry (hsv//eng)

Nyckelord

CO2 reduction

density functional calculations

photocatalysis

reaction mechanisms

silicon

Calculations

Carbon dioxide

Co-ordinatively unsaturated

First-principles calculation

First-principles study

Formation energies

Light illumination

Molecular mechanism

Systematic study

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