Graphitic Carbon Nitride with Dopant Induced Charge Localization for Enhanced Photoreduction of CO2 to CH4

The photoreduction of CO 2 to hydrocarbon products has attracted much attention because it provides an avenue to directly synthesize value‐added carbon‐based fuels and feedstocks using solar energy. Among various photocatalysts, graphitic carbon nitride (g‐C 3 N 4 ) has emerged as an attractive metal‐free visible‐light photocatalyst due to its advantages of earth‐abundance, nontoxicity, and stability. Unfortunately, its photocatalytic efficiency is seriously limited by charge carriers′ ready recombination and their low reaction dynamics. Modifying the local electronic structure of g‐C 3 N 4 is predicted to be an efficient way to improve the charge transfer and reaction efficiency. Here, boron (B) is doped into the large cavity between adjacent tri‐s‐triazine units via coordination with two‐coordinated N atoms. Theoretical calculations prove that the new electron excitation from N (2p x , 2p y ) to B (2p x , 2p y ) with the same orbital direction in B‐doped g‐C 3 N 4 is much easier than N (2p x , 2p y ) to C 2p z in pure g‐C 3 N 4 , and improves the charge transfer and localization, and thus the reaction dynamics. Moreover, B atoms doping changes the adsorption of CO (intermediate), and can act as active sites for CH 4 production. As a result, the optimal sample of 1%B/g‐C 3 N 4 exhibits better selectivity for CH 4 with ≈32 times higher yield than that of pure g‐C 3 N 4 .

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