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In situ grown TiN/N-TiO2 composite for enhanced photocatalytic H2 evolution activity
被引:17
|作者:
Liu, Dong
[1
]
Yan, Zhuqing
[2
]
Zeng, Peng
[1
]
Liu, Haoran
[2
]
Peng, Tianyou
[1
,2
]
Li, Renjie
[2
]
机构:
[1] Wuhan Univ Shenzhen, Res Inst, Shenzhen 518057, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
基金:
中国国家自然科学基金;
关键词:
photocatalytic H2 evolution;
TiN;
N-TiO2;
composite;
plasmonic effect;
in-situ nitridation;
HETEROJUNCTION PHOTOCATALYSTS;
HYDROGEN EVOLUTION;
CATALYTIC-ACTIVITY;
TITANIUM NITRIDE;
TIO2;
EFFICIENT;
WATER;
PERFORMANCE;
G-C3N4;
CHARGE;
D O I:
10.1007/s11708-021-0766-8
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
Titanium nitride (TiN) decorated N-doped titania (N-TiO2) composite (TiN/N-TiO2) is fabricated via an in situ nitridation using a hydrothermally synthesized TiO2 and melamine (MA) as raw materials. After the optimization of the reaction condition, the resultant TiN/N-TiO2 composite delivers a hydrogen evolution activity of up to 703 mu mol/h under the full spectrum irradiation of Xelamp, which is approximately 2.6 and 32.0 times more than that of TiO2 and TiN alone, respectively. To explore the underlying photocatalytic mechanism, the crystal phase, morphology, light absorption, energy band structure, element composition, and electrochemical behavior of the composite material are characterized and analyzed. The results indicate that the superior activity is mainly caused by the in situ formation of plasmonic TiN and N-TiO2 with intimate interface contact, which not only extends the spectral response range, but also accelerates the transfer and separation of the photoexcited hot charge carrier of TiN. The present study provides a fascinating approach to in situ forming nonmetallic plasmonic material/N-doped TiO2 composite photocatalysts for high-efficiency water splitting.
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页码:721 / 731
页数:11
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