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Zhenjia Zhou

Publications and source records attributed to Zhenjia Zhou.

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Carrier-coupled ultrafast structural dynamics and interlayer energy transport of supported transition metal dichalcogenide heterostructures

Understanding the electronic coupling and energy flow across layered two-dimensional heterostructures (HSs) is crucial to the exploitation of carrier and phonon transports as well as thermal management in next-generation optoelectronic devices. By using reflection ultrafast electron diffraction, we directly examine photoinduced out-of-plane structural dynamics of supported MoS2/WS2 bilayer HSs and their individual monolayers. Experimental evidence reveals the launch of ultrafast carrier-coupled intralayer atomic motions due to interlayer charge transfer across the van der Waals (vdW) heterojunctions that is absent for individual monolayers. Such a notable carrier-lattice correlation is in addition to the electronic coupling manifested in the enhanced optical absorption for HSs. Also, different pathways of energy flow as a result of carrier-phonon coupling and phonon scattering are reported with the corresponding characteristic times. On longer timescales, relaxation of thermalized atomic motions can be sufficiently described by a thermal transport model. A higher thermal boundary conductance (TBC) across MoS2/WS2 HSs is obtained compared to those at the monolayer-substrate interfaces; however, the similar TBC values suggest comparable couplings of phonons across vdW contacts. These results further shed light on the optical, phonon, and interfacial thermal properties of vertically-stacked vdW HSs.

cond-mat.mes-hall

Ripple-assisted adsorption of noble gases on graphene at room temperature

Controllable gas adsorption is critical for both scientific and industrial fields, and high-capacity adsorption of gases on solid surfaces provides a significant promise due to its high-safety and low-energy consumption. However, the adsorption of nonpolar gases, particularly noble gases, poses a considerable challenge under atmospheric pressure and room temperature (RT). Here, we theoretically simulate and experimentally realize the stable adsorption of noble gases like xenon (Xe), krypton (Kr), argon (Ar), and helium (He) on highly rippled graphene at RT. The elemental characteristics of adsorbed Xe are confirmed by electron energy loss spectroscopy and X-ray photoelectron spectroscopy. The adsorbed gas atoms are crystalized with periodic arrangements. These adsorbed noble gases on graphene exhibit high stability at RT and can be completely desorbed at approximately 350 °C without damaging the intrinsic lattice of graphene. The structural and physical properties of graphene are significantly influenced by the adsorbed gas, and they fully recover after desorption. Additionally, this controllable adsorption could be generalized to other layered adsorbents such as NbSe2, MoS2 and carbon nanotubes. We anticipate that this ripple-assisted adsorption will not only re-define the theoretical framework of gas adsorption, but also accelerate advancements in gas storage and separation technologies, as well as enhance the applications in catalysis, surface modification, and other related fields.

cond-mat.mtrl-sci