Oscillation in Excited State Lifetimes with Size of Sub-nanometer Neutral (TiO2)n Clusters Observed with Ultrafast Pump-Probe Spectroscopy

被引:17
作者
Garcia, Jacob M. [1 ,2 ]
Heald, Lauren F. [1 ,2 ]
Shaffer, Ryan E. [1 ,2 ]
Sayres, Scott G. [1 ,2 ]
机构
[1] Arizona State Univ, Sch Mol Sci, Tempe, AZ 85287 USA
[2] Arizona State Univ, Biodesign Ctr Appl Struct Discovery, Tempe, AZ 85287 USA
基金
美国国家科学基金会;
关键词
CHARGE-CARRIER DYNAMICS; ELECTRONIC-STRUCTURE; TIO2; NANOPARTICLES; ANATASE; RUTILE; NANOCLUSTERS;
D O I
10.1021/acs.jpclett.1c00840
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
Neutral titanium oxide clusters of up to 1 nm in diameter (TiO2)(n), with n < 10, are produced in a laser vaporization source and subsequently ionized by a sequence of femtosecond laser pulses. Using a 400 nm pump and 800 nm probe lasers, the excited state lifetimes of neutral (TiO2) n clusters are measured. All clusters exhibit a rapid relaxation lifetime of similar to 35 fs, followed by a sub-picosecond lifetime that we attribute to carrier recombination. The excited state lifetimes oscillate with size, with even-numbered clusters possessing longer lifetimes. Density functional theory calculations show the excited state lifetimes are correlated with charge carrier localization or polaron-like formation in the excited states of neutral clusters. Thus, structural rigidity is suggested as a feature for extending excited state lifetimes in titania materials.
引用
收藏
页码:4098 / 4103
页数:6
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