Sodium ion doped graphitic carbon nitride with high crystallinity for superior photocatalytic hydrogen evolution efficiency

被引:5
|
作者
Han, Xue [1 ]
Kang, Yuna [1 ]
Song, Shuang [1 ]
Lu, Rong [1 ]
Yu, Anchi [1 ]
机构
[1] Renmin Univ China, Dept Chem, Beijing 100872, Peoples R China
基金
中国国家自然科学基金;
关键词
EXCITON DISSOCIATION; G-C3N4; NANOSHEETS; ELECTRON-TRANSFER; H-2; PRODUCTION; WATER; CONSTRUCTION; MODULATION; ABSORPTION; DYNAMICS; STORAGE;
D O I
10.1039/d3ta02887a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
As a promising photocatalyst for solar-light driven H-2 generation, graphitic carbon nitride (GCN) has been intensively investigated for more than ten years. Herein, highly crystalline Na+-doped GCN (GCN-Na) and NH4Cl-assisted Na+-doped GCN (GCN-Na-NH4Cl) were successfully synthesized. A 25-fold and 65-fold increase in the photocatalytic hydrogen evolution (PHE) rate for GCN-Na and GCN-Na-NH4Cl was achieved compared with pristine GCN under visible light irradiation (& lambda; & GE; 420 nm). Furthermore, the short duration time of the long-lived electron for GCN-Na and GCN-Na-NH4Cl indicated their efficient electron utilization. Apart from the structure and optoelectronic property characterization, femtosecond transient absorption spectroscopy (fs-TAS) was performed to investigate the association between the crystallinity and the PHE performance. The fs-TAS measurements at low excitation density reveal a trap-assisted recombination (tens of picoseconds, ps) of the photogenerated electrons for GCN, GCN-Na and GCN-Na-NH4Cl dispersions, and further suggest that GCN-Na and GCN-Na-NH4Cl possess higher density of shallow-trap sites and their energy level is even closer to the conduction band when compared to that of GCN. Moreover, a strong pump density dependence of the photogenerated electron decay kinetics is observed for GCN-Na and GCN-Na-NH4Cl, indicating a rapid Auger recombination (less than 1 ps) occurring in them under intense illumination. Electrons from the shallower-trap-site as well as electrons from the Auger process would participate in PHE, resulting in a remarkably improved PHE activity for GCN-Na and GCN-Na-NH4Cl. This work not only provides insights into the superior PHE efficiency in highly crystalline GCN but also an NH4Cl-assisted calcination method for the preparation of metal-ion doped GCN with high crystallinity.
引用
收藏
页码:18213 / 18226
页数:14
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