It is often taken for granted that in pump-probe experiments on the topological insulator (TI) BiSeusing IR pumping with a commercial Ti:sapphire laser [∼800 nm (1.55 eV photon energy)], the electrons are excited in the one-photon absorption regime, even when pumped with absorbed fluences in the mJ cmrange. Here, using UV-Vis transient absorption (TA) spectroscopy, we show that even at low-power Infrared (IR) pumping with absorbed fluences in theJ cmrange, the TA spectra of the TI BiSeextend across a part of the UV and the entire visible region. This observation suggests unambiguously that the two-photon pumping regime accompanies the usual one-photon pumping regime even at low laser powers applied. We attribute the high efficiency of two-photon pumping to the giant nonlinearity of Dirac fermions in the Dirac surface states (SS). On the contrary, one-photon pumping is associated with the excitation of bound valence electrons in the bulk into the conduction band. Two mechanisms of absorption bleaching were also revealed since they manifest themselves in different spectral regions of probing and cause the appearance of three different relaxation dynamics. These two mechanisms were attributed to the filling of the phase-space in the Dirac SS and bulk states, followed by the corresponding Pauli blocking.
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http://dx.doi.org/10.1088/1361-648X/ac90a7 | DOI Listing |
Chem Soc Rev
January 2025
School of Science, RMIT University, Melbourne, 3000, Australia.
Metal halide perovskites (MHPs) have emerged as the most promising materials due to superior optoelectronic properties and great applications spanning from photovoltaics to photonics. Absorption spectroscopy provides a broad and deep insight into the carrier dynamics of MHPs, and is a critical complement to fluorescence and scattering spectroscopy. However, absorption spectroscopy is often misunderstood or underestimated, being seen as UV-vis spectroscopy only, which can lead to various misinterpretations.
View Article and Find Full Text PDFACS Nano
December 2024
International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi'an Jiaotong University, Xi'an, Shaanxi 710049, China.
Photocatalytic CO conversion is a promising approach to simultaneously mitigate climate change and alleviate the energy crisis. However, infrared light, which constitutes nearly half of the solar energy, has not been effectively utilized yet. In this work, we discover a photogenerated charge transition mechanism in CuInS with intrinsic In antisite defects for synergistic utilization of full-spectrum photons.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
College of Materials Science and Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, Shaanxi, People's Republic of China; School of Chemistry and Chemical Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, Shaanxi, People's Republic of China. Electronic address:
Inorg Chem
December 2024
Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996, United States.
J Phys Chem B
December 2024
Institute of Physical and Theoretical Chemistry, Eberhard Karls University of Tübingen, Auf der Morgenstelle 18, D-72076 Tübingen, Germany.
We use femtosecond transient broadband absorption spectroscopy (TAS) to characterize Rose Bengal in water/methanol solutions and reveal a continuous tunability of intersystem crossing (ISC) times by changing the mole fraction of the solvents. We find that the transients of excited state absorptions (ESAs) in Rose Bengal at ∼430 nm can be attributed to transitions from the singlet state S, with decay times of 74 ps via ISC in pure water and up to 405 ps in pure methanol. TA measurements at near-infrared wavelengths, on the other hand, reveal the rise of an ESA at ∼1080 nm from the triplet state T with time constants of 68 and 491 ps in pure water and methanol, respectively, strongly supporting the associated UV-vis TAS data.
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