English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

A large number of studies have examined the origins of high-catalytic activities of nanoparticles, but very few have discussed the lifetime of high-energy electrons in nanoparticles. The lifetime is one of the factors determining electron transfer and thus catalytic activity. Much of the lifetime of electrons reported in the literature is too short for a high transfer-efficiency of photo-excited electrons from a catalyst to the attached molecules. We observed TiO2 nanoparticles using the femtosecond laser two-color pump-probe technique with photoemission electron microscopy having a 40 nm spatial resolution. A lifetime longer than 4 ps was observed together with a fast decay component of 100 fs time constant when excited by a 760 nm laser. The slow decay component was observed only when the electrons in an intermediate state pumped by the fundamental laser pulse were excited by the second harmonic pulse. The electronic structure for the asymmetry of the pump-probe signal and the origin of the two decay components are discussed based on the color center model of the oxygen vacancy.

Picosecond Lifetime Hot Electrons in TiO2 Nanoparticles for High Catalytic Activity