个人信息Personal Information
教授
博士生导师
硕士生导师
主要任职:无
其他任职:精细化工国家重点实验室副主任、大连理工大学-瑞典皇家工学院分子器件联合研究中心主任
性别:男
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:应用化学. 精细化工
办公地点:大连理工大学西部校区化工实验楼E-223
联系方式:0411-84986493
电子邮箱:sunlc@dlut.edu.cn
Perovskite-based nanocubes with simultaneously improved visible-light absorption and charge separation enabling efficient photocatalytic CO2 reduction
点击次数:
论文类型:期刊论文
发表时间:2016-12-01
发表刊物:NANO ENERGY
收录刊物:SCIE、EI、Scopus
卷号:30
页面范围:59-68
ISSN号:2211-2855
关键字:Perovskite; Band structure tuning; Charge separation; Nitrogen-doped graphene quantum dots; CO2 photoreduction
摘要:Finding an ideal model to disclose the role upon tuning band structure and charge separation of wide-bandgap perovskite semiconductors by introducing suitable heteroatoms remains a huge challenge in photocatalysis. Herein, we propose an efficient pathway to increase the light absorption and charge separation for nitrogen and oxygen-vacancy confined in sodium tantalate nanocubes (V-o-NaTaON) and nitrogen-doped graphene quantum dots (N-GQDs) grafted V-o-NaTaON nanocubes by solution-etching-induced phase-transition and in-situ reduction strategies. First-principles calculations demonstrate that the simultaneous incorporation of nitrogen and oxygen-vacancy in sodium tantalate can effectively regulate the electronic structure of sodium tantalate. The analysis of UV vis spectra and electron paramagnetic resonance reveal that the synergistic contribution of nitrogen and oxygen-vacancy endows the wide-bandgap perovskites tuning the band absorption region from UV (315 nm) to visible regime beyond 600 nm. As expected, an optimized V-o-NaTaON catalyst was developed, exhibiting superior broad spectrum photochemical reduction of CO2 to fuels. Moreover, N-GQDs/V-o-NaTaON heterojunctions further improve the broad spectrum CO2 photoreduction due to the synergetic catalytic effect of simultaneously improved light-absorption and charge separation. This work may open up more opportunities in the design of efficient photocatalysts for applications in solar photochemical conversion.