TY - JOUR
T1 - Ultrafast Carrier Dynamics in 2D van der Waals CuTe2Cl Probed by Terahertz Spectroscopy
AU - Zhang, Jiali
AU - Shi, Bingxian
AU - Chen, Hongyu
AU - Zou, Yuqing
AU - Hu, Shanshan
AU - Song, Yiwen
AU - Li, Ziyang
AU - Dai, Hongtao
AU - Song, Yuna
AU - Zhang, Hao
AU - Jin, Q. Y.
AU - Cheng, Peng
AU - Zhang, Zongzhi
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/2/26
Y1 - 2026/2/26
N2 - The two-dimensional van der Waals material CuTe2Cl (CTC) has been theoretically predicted to possess exceptional charge separation, strong visible-light absorption, and robust dynamic stability, making it a promising candidate for high-performance optoelectronic devices. However, its carrier relaxation pathways and the experimental validation of these predicted properties remain underexplored. Here, we investigate the photocarrier dynamics of CTC flakes using ultrafast optical pump-terahertz probe spectroscopy at 1.55 and 3.1 eV. Sub-bandgap excitation (1.55 eV) yields three distinct relaxation components (lifetimes τ1 ≈ 2–4 ps, τ2 ≈ 17–34 ps, τ3 ≈ 418–667 ps), corresponding to ultrafast defect trapping, defect-mediated recombination, and three-carrier Auger recombination, respectively. In contrast, above-bandgap excitation (3.1 eV) suppresses the intermediate channel and accelerates Auger recombination due to enhanced absorption and reduced penetration depth, producing only τ1 and τ3. These findings provide critical insight into the carrier relaxation mechanisms of CTC, advancing its potential for next-generation optoelectronic applications.
AB - The two-dimensional van der Waals material CuTe2Cl (CTC) has been theoretically predicted to possess exceptional charge separation, strong visible-light absorption, and robust dynamic stability, making it a promising candidate for high-performance optoelectronic devices. However, its carrier relaxation pathways and the experimental validation of these predicted properties remain underexplored. Here, we investigate the photocarrier dynamics of CTC flakes using ultrafast optical pump-terahertz probe spectroscopy at 1.55 and 3.1 eV. Sub-bandgap excitation (1.55 eV) yields three distinct relaxation components (lifetimes τ1 ≈ 2–4 ps, τ2 ≈ 17–34 ps, τ3 ≈ 418–667 ps), corresponding to ultrafast defect trapping, defect-mediated recombination, and three-carrier Auger recombination, respectively. In contrast, above-bandgap excitation (3.1 eV) suppresses the intermediate channel and accelerates Auger recombination due to enhanced absorption and reduced penetration depth, producing only τ1 and τ3. These findings provide critical insight into the carrier relaxation mechanisms of CTC, advancing its potential for next-generation optoelectronic applications.
UR - https://www.scopus.com/pages/publications/105031250793
U2 - 10.1021/acs.jpclett.6c00114
DO - 10.1021/acs.jpclett.6c00114
M3 - 文章
C2 - 41686132
AN - SCOPUS:105031250793
SN - 1948-7185
VL - 17
SP - 2328
EP - 2334
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 8
ER -