Journal
SMALL
Volume 17, Issue 39, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202102699
Keywords
CdS; cyano groups; hydrogen evolution; photo-deposition; polymeric carbon nitride; Z-scheme mechanism
Categories
Funding
- National Natural Science Foundation of China [61764003]
- Major Science and Technology Planning Project of Hainan Province [ZDKJ201810]
- Hainan Academician Innovation Platform Funding
- US Department of Energy, Basic Energy Sciences, Division of Materials Science and Engineering [DE-AC02-07CH11358]
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A novel direct Z-scheme heterojunction of defective g-C3N4/CdS was designed in this study by introducing cyano groups as active bridge sites, which endows the photocatalyst with advantageous properties such as high light absorption ability, strong redox performance, satisfactory charge separation efficiency, and long lifetime of charge carriers. The resulting photocatalytic system exhibited more active performance than CdS and g-C3N4 under visible light, achieving an excellent hydrogen evolution rate and good stability after continuous testing.
g-C3N4/CdS heterojunctions are potential photocatalysts for hydrogen production but their traditional type-II configuration generally leads to weak oxidative and reductive activity. How to construct the novel Z-scheme g-C3N4/CdS counterparts to address this issue remains a great challenge in this field. In this work, a new direct Z-scheme heterojunction of defective g-C3N4/CdS is designed by introducing cyano groups (N(sic)C-) as the active bridge sites. Experimental observations in combination with density functional theory (DFT) calculations reveal that the unique electron-withdrawing feature of cyano groups in the defective g-C3N4/CdS heterostructure can endow this photocatalyst with numerous advantageous properties including high light absorption ability, strong redox performance, satisfactory charge separation efficiency, and long lifetime of charge carriers. Consequently, the resultant photocatalytic system exhibits more active performance than CdS and g-C3N4 under visible light and reaches an excellent hydrogen evolution rate of 1809.07 mu mol h(-1) g(-1), which is 6.09 times higher than pristine g-C3N4. Moreover, the defective g-C3N4/CdS photocatalyst maintains good stability after 40 h continuous test. This work provides new insights into design and construction of Z-scheme heterojunctions for regulating the visible-light-induced photocatalytic activity for H-2 evolution.
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