The successful separation of photoexcited charge carriers and their effective utilization are crucial for overcoming the slow kinetics of the four-electron process for photocatalytic oxygen evolution. Herein, a novel strategy utilizing urea as a source of N-doping on Ca 2 Nb 3 O 10 nanosheets is adopted, followed by the successful deposition of Co single atoms (Co-SAs) to achieve a synergistic effect. The presence of N-dopants and Co-SAs is validated via various experimental techniques. It is also observed that the presence of N-doping contributed towards the deposition of higher content of Co-SAs (0.21 wt%) in Ca 2 Nb 3 O 10− x N x -Co SA nanosheets compared to 0.15 wt% for non-doped Ca 2 Nb 3 O 10 -Co SA . The optimized Ca 2 Nb 3 O 10− x N x -Co SA nanosheets exhibited an impressive photocatalytic O 2 evolution of ∼727.22 µ mol g −1 h −1 via the synergy of N-dopants and Co-SAs. As a result, the O 2 evolution response of Ca 2 Nb 3 O 10− x N x -Co SA is 3.6 times higher than that of pristine Ca 2 Nb 3 O 10 nanosheets (201.26 µ mol g −1 h −1 ), 2.24 times better than Ca 2 Nb 3 O 10− x N x nanosheets (323.42 µ mol g −1 h −1 ), and 1.77 times higher compared to Ca 2 Nb 3 O 10 -Co SA , (409.33 µ mol g −1 h −1 ), which clearly demonstrated the synergistic effect of N-dopants and Co-SAs in Ca 2 Nb 3 O 10− x N x -Co SA nanosheets. Based on the findings of various characterization techniques, the co-presence of N-dopants and Co-SAs is observed to contribute towards better charge carrier separation, and utilization to achieve superior photocatalytic response. Thus, this study presents a novel approach for incorporating N-dopants and Co-SAs on Ca 2 Nb 3 O 10 nanosheets, which can be extended to a wide range of nanosheets produced by the soft chemical exfoliation method.
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Haq et al. (2024) studied this question.
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