Constructing S-scheme charge separation in cobalt phthalocyanine/oxygen-doped g-C3N4 heterojunction with enhanced photothermal-assisted photocatalytic H2 evolution AITranslate
Abstract AITranslate
Hydrogen acquisition from solar energy is an effective way to address energy crisis,which makes the development of efficient photocatalysts become the main direction of scientific research.Herein,cobalt phthalocyanine/oxygen-doped g-C3N4(CoPc/OCN) S-scheme heterojunction photocatalyst was designed by coupling multi-step calcination with solvothermal method for enhanced photothermal-assisted photocatalytic H2 evolution.The multistep calcined g-C3N4 is easier for O-doping formation,and the ethanol solvothermal strategy is utilized to enhance the dispersion of CoPc on OCN nano sheet surface and forms sufficient S-scheme heterojunction through H-bonds.In addition,the active sites and excellent photothermal properties of CoPc itself further improve the integrated photocatalytic activity of CoPc/OCN S-scheme heterojunction.The optimal photocatalytic hydrogen evolution rate of CoPc/OCN S-scheme heterojunction photocatalyst reached 9.56 mmol·g-1·h-1,which is 2.69 and 1.23 times higher than that of CN and OCN,respectively.This work provides a valuable design idea and scheme for enhancing the multi-factor co-assisted photocatalytic H2 evolution performance.
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Basic Information:
DOI:
Chinese Library Classification Number:O643.36[理学—物理化学];O644.1[理学—物理化学];TQ116.2[化学工程—无机化工]
Citation Information:
Hydrogen acquisition from solar energy is an effective way to address energy crisis,which makes the development of efficient photocatalysts become the main direction of scientific research.Herein,cobalt phthalocyanine/oxygen-doped g-C3N4(CoPc/OCN) S-scheme heterojunction photocatalyst was designed by coupling multi-step calcination with solvothermal method for enhanced photothermal-assisted photocatalytic H2 evolution.The multistep calcined g-C3N4 is easier for O-doping formation,and the ethanol solvothermal strategy is utilized to enhance the dispersion of CoPc on OCN nano sheet surface and forms sufficient S-scheme heterojunction through H-bonds.In addition,the active sites and excellent photothermal properties of CoPc itself further improve the integrated photocatalytic activity of CoPc/OCN S-scheme heterojunction.The optimal photocatalytic hydrogen evolution rate of CoPc/OCN S-scheme heterojunction photocatalyst reached 9.56 mmol·g-1·h-1,which is 2.69 and 1.23 times higher than that of CN and OCN,respectively.This work provides a valuable design idea and scheme for enhancing the multi-factor co-assisted photocatalytic H2 evolution performance.
quote
| GB/T 7714-2015 | [1] Wei-Long Shi, Zheng Xu, Yu-Xing Shi, et al. Rare Metals, 2024(1): 198-211. |
| MLA | [1] Wei-Long Shi, et al., Rare Metals, no. 1, 2024, pp. 198-211. |
| APA | [1] Wei-Long Shi, Zheng Xu, Yu-Xing Shi, Ling-Ling Li, Jia-Lin Lu, Xin-Hai Sun, Xin Du, Feng Guo, & Chang-Yu Lu. (2024). Rare Metals(1), 198-211. |
| IEEE | [1] Wei-Long Shi, Zheng Xu, Yu-Xing Shi, Ling-Ling Li, Jia-Lin Lu, Xin-Hai Sun, Xin Du, Feng Guo, and Chang-Yu Lu, Rare Metals, no. 1, pp. 198-211, 2024. |
