Interface-Tailored Secondary Excitation and Ultrafast Charge/Energy Transfer in Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>-MoS<sub>2</sub> Heterostructure Films

Charge/energy separation across interfaces of plasmonic materials is vital for minimizing plasmonic losses and enhancing their performance in photochemical and optoelectronic applications. While heterostructures combining plasmonic two-dimensional transition metal carbides/nitrides (MXenes) and semiconducting transition metal dichalcogenides (TMDs) hold significant potential, the mechanisms governing plasmon-induced carrier dynamics at these interfaces remain elusive. Here, we uncover a distinctive secondary excitation phenomenon and an ultrafast charge/energy transfer process in heterostructure films composed of macro-scale Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> and MoS<sub>2</sub> films. Using Rayleigh-Bénard convection and Marangoni effect-induced self-assembly, we fabricate large-scale (square centimeters) Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> and MoS<sub>2</sub> films composed of edge-connected monolayer nanoflakes. These films are flexibly stacked in a controlled sequence to form macroscopic heterostructures, enabling the investigation and manipulation of excited-state dynamics using transient absorption and optical pump-terahertz probe spectroscopy. In the Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>-MoS<sub>2</sub> heterostructure, we observe a secondary excitation in MoS<sub>2</sub> driven by the surface plasmon resonance of Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>. This phenomenon, with a characteristic rise time constant of ∼70 ps, is likely facilitated by acoustic phonon recycling across the interface. Further interfacial thermal transport engineering─achieved by tailoring the sequence and combination of interfaces in trilayer heterostructures─allows extending the characteristic time to ∼175 ps. Furthermore, we identify a sub-150 fs ultrafast charge/energy transfer process from Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> to MoS<sub>2</sub>. The transfer efficiency is strongly dependent on the excitation photon energy, resulting in amplified photoconductivity in MoS<sub>2</sub> by up to ∼180% under 3.10 eV excitation. These insights are crucial for developing plasmonic MXene-based heterostructures, paving the way for advancements in photochemical and optoelectronic applications.

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Journal
Journal of the American Chemical Society
Published
2025-03-07
DOI
https://doi.org/10.1021/jacs.5c01826
Citations
21
Primary Topic
2D Materials and Applications
Type
article
Field-Weighted Citation Impact
10.87

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Interface-Tailored Secondary Excitation and Ultrafast Charge/Energy Transfer in Ti3C2Tx-MoS2 Heterostructure Films

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Journal of the American Chemical Society
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article

Interface-Tailored Secondary Excitation and Ultrafast Charge/Energy Transfer in Ti3C2Tx-MoS2 Heterostructure Films

Alexander Tahn, Giuseppe Maria Paternò, Francesco Scotognella, Mike Hambsch, Minghao Yu, Darius Pohl, Hao Xu, Hai I. Wang, Shuai Fu, Stefan C. B. Mannsfeld, Dongqi Li, Rafael Muñoz‐Mármol, Wenhao Zheng, Andrea Villa, Xinliang Feng, Xiaodong Li, Jiaxu Zhang, Quanquan Guo
article en
21 citations

Abstract

Charge/energy separation across interfaces of plasmonic materials is vital for minimizing plasmonic losses and enhancing their performance in photochemical and optoelectronic applications. While heterostructures combining plasmonic two-dimensional transition metal carbides/nitrides (MXenes) and semiconducting transition metal dichalcogenides (TMDs) hold significant potential, the mechanisms governing plasmon-induced carrier dynamics at these interfaces remain elusive. Here, we uncover a distinctive secondary excitation phenomenon and an ultrafast charge/energy transfer process in heterostructure films composed of macro-scale Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> and MoS<sub>2</sub> films. Using Rayleigh-Bénard convection and Marangoni effect-induced self-assembly, we fabricate large-scale (square centimeters) Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> and MoS<sub>2</sub> films composed of edge-connected monolayer nanoflakes. These films are flexibly stacked in a controlled sequence to form macroscopic heterostructures, enabling the investigation and manipulation of excited-state dynamics using transient absorption and optical pump-terahertz probe spectroscopy. In the Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>-MoS<sub>2</sub> heterostructure, we observe a secondary excitation in MoS<sub>2</sub> driven by the surface plasmon resonance of Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub>. This phenomenon, with a characteristic rise time constant of ∼70 ps, is likely facilitated by acoustic phonon recycling across the interface. Further interfacial thermal transport engineering─achieved by tailoring the sequence and combination of interfaces in trilayer heterostructures─allows extending the characteristic time to ∼175 ps. Furthermore, we identify a sub-150 fs ultrafast charge/energy transfer process from Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> to MoS<sub>2</sub>. The transfer efficiency is strongly dependent on the excitation photon energy, resulting in amplified photoconductivity in MoS<sub>2</sub> by up to ∼180% under 3.10 eV excitation. These insights are crucial for developing plasmonic MXene-based heterostructures, paving the way for advancements in photochemical and optoelectronic applications.

Journal of the American Chemical SocietyVol. 147(11)
University of Alicante (ES), Politecnico di Torino (IT), Utrecht University (NL), Center for NanoScience (DE), Italian Institute of Technology (IT), Max Planck Institute of Microstructure Physics (DE), Max Planck Institute for Polymer Research (DE), Center for Advancing Health (US), Center for Nano Science and Technology (IT), Center for Systems Biology Dresden (DE), Technische Universität Dresden (DE), Politecnico di Milano (IT)
Universidad de Alicante, Ministerio de Ciencia, Innovación y Universidades, Deutsche Forschungsgemeinschaft, China Scholarship Council, H2020 Future and Emerging Technologies, HORIZON EUROPE Digital, Industry and Space, HORIZON EUROPE European Innovation Council, HORIZON EUROPE European Research Council
Affordable and clean energy
Openalex Percentile: Top 1%
2D Materials and Applications
10.87
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