TY - JOUR
T1 - Photothermal behaviour of titanium nitride nanoparticles evaluated by transient X-ray diffraction
AU - Diroll, Benjamin T.
AU - Brumberg, Alexandra
AU - Leonard, Ariel A.
AU - Panuganti, Shobhana
AU - Watkins, Nicolas E.
AU - Cuthriell, Shelby A.
AU - Harvey, Samantha M.
AU - Kinigstein, Eli D.
AU - Yu, Jin
AU - Zhang, Xiaoyi
AU - Kanatzidis, Mercouri G.
AU - Wasielewski, Michael R.
AU - Chen, Lin X.
AU - Schaller, Richard D.
N1 - Funding Information:
†The submitted manuscript has been created by UChicago Argonne, LLC, Operator of Argonne National Laboratory (“Argonne”). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DE-AC02-06CH11357. The U.S. Government retains for itself, and others acting on its behalf, a paid-up nonexclusive, irrevocable worldwide license in said article to reproduce, prepare derivative works, distribute copies to the public, and perform publicly and display publicly, by or on behalf on the Government. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan. http://energy.gov/downloads/doe-public-access-plan. ‡Electronic supplementary information (ESI) available: Methods and additional data. See DOI: 10.1039/d0nr08202c. §These authors contributed equally.
Funding Information:
This material is based upon work supported by the National Science Foundation Graduate Research Fellowship Program under Grant No. DGE-1842165 (A.B., N.E.W., S.M.H.). This work was supported by the MSN program of the National Science Foundation (no. 1808590). This work was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Award DE-FG02-99ER14999 (M.R. W.). This work was performed, in part, at the Center for Nanoscale Materials, a U.S. Department of Energy Office of Science User Facility, and supported by the U.S. Department of Energy, Office of Science, under Contract No. DE-AC02-06CH11357. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. This work made use of the Jerome B. Cohen X-Ray Diffraction Facility supported by the MRSEC program of the National Science Foundation (DMR-1720139) at the Materials Research Center of Northwestern University and the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-1542205).
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2021
Y1 - 2021
N2 - The photothermal properties of metal nitrides have recently received significant attention owing to diverse applications in solar energy conversion, photothermal therapies, photoreactions, and thermochromic windows. Here, the photothermal response of titanium nitride nanoparticles is examined using transient X-ray diffraction, in which optical excitation is synchronized with X-ray pulses to characterize dynamic changes in the TiN lattice. Photoinduced diffraction data is quantitatively analyzed to determine increases in the TiN lattice spacing, which are furthermore calibrated against static, temperature-dependent diffraction patterns of the same samples. Measurements of 20 nm and 50 nm diameter TiN nanoparticles reveal transient lattice heating from room temperature up to ∼175 °C for the highest pump fluences investigated here. Increasing excitation intensity drives sublinear increases in lattice temperature, due to increased heat capacity at the higher effective temperatures achieved at higher powers. Temporal dynamics show that higher excitation intensity drives not only higher lattice temperatures, but also unexpectedly slower cooling of the TiN nanoparticles, which is attributed to heating of the solvent proximal to the nanoparticle surface.
AB - The photothermal properties of metal nitrides have recently received significant attention owing to diverse applications in solar energy conversion, photothermal therapies, photoreactions, and thermochromic windows. Here, the photothermal response of titanium nitride nanoparticles is examined using transient X-ray diffraction, in which optical excitation is synchronized with X-ray pulses to characterize dynamic changes in the TiN lattice. Photoinduced diffraction data is quantitatively analyzed to determine increases in the TiN lattice spacing, which are furthermore calibrated against static, temperature-dependent diffraction patterns of the same samples. Measurements of 20 nm and 50 nm diameter TiN nanoparticles reveal transient lattice heating from room temperature up to ∼175 °C for the highest pump fluences investigated here. Increasing excitation intensity drives sublinear increases in lattice temperature, due to increased heat capacity at the higher effective temperatures achieved at higher powers. Temporal dynamics show that higher excitation intensity drives not only higher lattice temperatures, but also unexpectedly slower cooling of the TiN nanoparticles, which is attributed to heating of the solvent proximal to the nanoparticle surface.
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U2 - 10.1039/d0nr08202c
DO - 10.1039/d0nr08202c
M3 - Article
C2 - 33496308
AN - SCOPUS:85100766310
SN - 2040-3364
VL - 13
SP - 2658
EP - 2664
JO - Nanoscale
JF - Nanoscale
IS - 4
ER -