CO2 Preactivation in Photoinduced Reduction via Surface Functionalization of TiO2 Nanoparticles

被引:24
|
作者
Finkelstein-Shapiro, Daniel [1 ,2 ]
Petrosko, Sarah Hurst [3 ]
Dimitrijevic, Nada M. [2 ,3 ,6 ]
Gosztola, David [3 ]
Gray, Kimberly A. [2 ,5 ]
Rajh, Tijana [3 ]
Tarakeshwar, Pilarisetty [4 ]
Mujica, Vladimiro [1 ,3 ,4 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Inst Catalysis Energy Proc, Evanston, IL 60208 USA
[3] Argonne Natl Lab, Ctr Nanoscale Mat, Argonne, IL 60439 USA
[4] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[5] Northwestern Univ, Dept Civil & Environm Engn, Evanston, IL 60208 USA
[6] Argonne Natl Lab, Chem Sci & Engn Div, Argonne, IL 60439 USA
来源
基金
美国国家科学基金会;
关键词
CHARGE-TRANSFER; ADSORPTION; ANATASE; PHOTOREDUCTION; RUTILE; H2O;
D O I
10.1021/jz3020327
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
Salicylate and salicylic acid derivatives act as electron donors via charge-transfer complexes when adsorbed on semiconducting surfaces. When photoexcited, charge is injected into the conduction band directly from their highest occupied molecular orbital (HOMO) without needing mediation by the lowest unoccupied molecular orbital (LUMO). In this study, we successfully induce the chemical participation of carbon dioxide in a charge transfer state using 3-aminosalicylic acid (3ASA). We determine the geometry of CO2 using a combination of ultraviolet-visible spectroscopy (UV-vis), surface enhanced Raman scattering (SERS), C-13 NMR, and electron paramagnetic resonance (EPR). We find CO2 binds on Ti sites in a carbonate form and discern via EPR a surface Ti-centered radical in the vicinity of CO2, suggesting successful charge transfer from the sensitizer to the neighboring site of CO2. This study opens the possibility of analyzing the structural and electronic properties of the anchoring sites for CO2 on semiconducting surfaces and proposes a set of tools and experiments to do so.
引用
收藏
页码:475 / 479
页数:5
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