Abstract

Abstract 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 Ca2Nb3O10 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. Besides, it is observed that the presence of N-doping contributed towards deposition of higher content of Co-SAs (0.21 wt%) in Ca2Nb3O10-xNx¬-CoSA nanosheets compared to 0.15 wt% for non-doped Ca2Nb3O10-CoSA. The optimized Ca2Nb3O10-xNx-CoSA nanosheets exhibited an impressive photocatalytic O2 evolution of ~727.22 µmol g-1 h-1 via the synergy of N-dopants and Co-SAs. As a result, O2 evolution response of Ca2Nb3O10-xNx-CoSA is 3.6 times higher than pristine Ca2Nb3O10 nanosheets (201.26 µmol g-1 h-1), 2.24 times better than Ca2Nb3O10-xNx nanosheets (323.42 µmol g-1 h-1), and 1.77 times higher compared to Ca2Nb3O10-CoSA, (409.33 µmol g-1 h-1), clearly demonstrated the synergistic effect of N-dopants and Co-SAs in Ca2Nb3O10-xNx-CoSA nanosheets. Base on the finding of various characterization techniques, the co-presence of N-dopants and Co-SAs is observed to contribute towards better charge carriers separation, and utilization to achieve superior photocatalytic response. Thus, this work presents a novel approach for incorporating N-dopants and Co-SAs on Ca2Nb3O10 nanosheets which can be extended to wide range of nanosheets produced by the soft chemical exfoliation method.

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