Plasmonic Titanium Nitride/g-C3N4 with Inherent Interface Facilitates Photocatalytic CO2 Reduction

被引:11
|
作者
Nguyen, Duc-Trung [1 ]
Do, Trong-On [1 ]
机构
[1] Laval Univ, Dept Chem Engn, Quebec City, PQ G1V 0A6, Canada
关键词
titanium nitride; localized surface plasmon resonance; inherent interface; CO2; reduction; LIGHT; COPOLYMERIZATION; NANOPARTICLES; NANOSPHERES; WATER;
D O I
10.1021/acsaem.2c02303
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
Plasmonic metal nitride is a practical alternative for plasmonic gold nanoparticles owing to its low-cost, tunable plasmonic resonance in the visible-light and near-IR region. However, an efficient charge transfer between plasmonic metal nitride nanoparticles and graphitic carbon nitride g-C3N4 through the formation of chemical bonds remains challenging. Herein, a facile strategy for the fabrication of plasmonic titanium nitride/g-C3N4 with intimate contact toward an enhanced photocatalytic CO2 reduction is proposed. The functionalization of TiN nanoparticles with amino groups enables the copolymerization with g-C3N4 precursors, offering intimate contact between them by the covalent bonds. This intimate contact could facilitate the electron transfer between TiN nanoparticles and g-C3N4. Under optimized conditions, the representative g-C3N4-2.8TiN has the highest CO production rate of similar to 820 mu mol g-1 h-1 with an apparent quantum yield of 3.5% at 400 nm and even 0.43% at 550 nm, which are some of the highest reported values for g-C3N4-based materials. This work offers promising opportunities to fabricate low-cost plasmonic nanoparticle/semiconductor systems for solar energy applications.
引用
收藏
页码:89 / 98
页数:10
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