Ultrafast spectroscopy of plasmons and free carriers in 2D MXenes

TitleUltrafast spectroscopy of plasmons and free carriers in 2D MXenes
Publication TypeJournal Article
Year of Publication2023
AuthorsColin-Ulloa, E, Fitzgerald, A, Montazeri, K, Mann, J, Natu, V, Ngo, K, Uzarski, J, Barsoum, MW, Titova, LV
JournalAdvanced Materials
Volume35
Issue8
Date PublishedFEB
Type of ArticleArticle
ISSN0935-9648
Keywords2D properties, MXenes, Optical properties, plasmons, ultrafast spectroscopy
Abstract

2D MXenes have diverse and chemically tunable optical properties that arise from an interplay between free carriers, interband transitions, and plasmon resonances. The nature of photoexcitations and their dynamics in three different members of the MXene family, Ti3C2, Mo2Ti2C3, and Nb2C, are investigated using two complementary pump-probe techniques, transient optical absorption, and time-resolved terahertz (THz) spectroscopy. Measurements reveal pronounced plasmonic effects in the visible and near-IR in all three. Optical excitation, with either 400 or 800 nm pulses, results in a rapid increase in lattice temperature, evidenced by a pronounced broadening of the plasmon mode that presents as a plasmon bleach in transient absorption measurements. Observed kinetics of plasmon bleach recovery provide a means to monitor lattice cooling. Remarkably slow cooling, proceeding over hundreds of picoseconds to nanoseconds time scales, implies MXenes have low thermal conductivities. The slowest recovery kinetics are observed in the MXene with the highest free carrier density, viz. Ti3C2, that supports phonon scattering by free carriers as a possible mechanism limiting thermal conductivity. These new insights into photoexcitation dynamics can facilitate their applications in photothermal solar energy conversion, plasmonic devices, and even photothermal therapy and drug delivery.

DOI10.1002/adma.202208659
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

32.086

Divison category: 
Physical and Materials Chemistry
Database: 
Web of Science (WoS)

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