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Fengfeng Ye

Publications and source records attributed to Fengfeng Ye.

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Two-dimensional vertically polarized Hg3AsSe4I monolayer for efficient photocatalytic water-splitting: promoting carrier separation by intrinsic electric field and Rashba effect

Efficient separation of photo-excited electron-hole pairs is essential for developing the high performance photocatalysts towards light-driven water-splitting applications. To this end, pho tocatalytic performances of two-dimensional (2D) semiconducting ferroelectric (FE) materials with out-of-plane polarizations have been extensively explored. However, out-of-plane polarizations in 2D FE materials are susceptible to the critical thickness limitation and can be easily compensated by surface adsorbates. On the other hand, 2D vertically polarized materials with stable and ir reversible out-of-plane polarizations may overcome the critical thickness limitation, enabling the practical advantage for spatial separation of photo-excited electron-hole pairs during the photo catalytic reactions. In the current work, 2D vertically polarized Hg3AsSe4I, an experimentally synthesized van der Waals (vdW) layered material, has been systematically investigated as a high performance 2D photocatalyst. Owing to its semiconducting band gap suitable for visible-light absorption, high carrier mobility, and desirable band edge alignment ideally matching water reduc tion and oxidation potentials, Hg3AsSe4I monolayer fulfills both optical and electronic prerequisites for photocatalytic water-splitting reactions. Besides the stable vertical polarization able to persist in Hg3AsSe4I monolayer, the dual mechanism for efficient separation of photo-excited carriers has also been demonstrated. Rashba spin-orbit coupling (SOC) of large strength emerges within 2D Hg3AsSe4I, splitting the band edges into spin-resolved band branches with unique spin-momentum locking characters.........

cond-mat.mtrl-sci

Distinguish the Orientation of Sliding Ferroelectricity by Second-Harmonic Generation

As the emerging ferroelectric (FE) materials, the ultrathin two-dimensional (2D) sliding ferroelectrics without phase-matching bottleneck, usually exhibit the pronounced second harmonic generation (SHG) responses. Despite the structural polarity of sliding ferroelectrics can be precisely detected via SHG characterizations, distinguishing the orientations of sliding ferroelectricity based on SHG responses has rarely been realized, as SHG intensities for upward and downward polarization states are supposed to be same. In current work, combining computational simulations and experimental characterizations, the orientation of sliding ferroelectricity is demonstrated to be readily distinguishable via SHG responses in 2D SnP2S6 (SnP2Se6), a new sliding FE material. Specifically, owing to the unique symmetry operation within FE-SnP2S6 (SnP2Se6), the intersection between \c{hi}xxx and \c{hi}yyy SHG susceptibility coefficients with opposite signs leads to the effective rotation of SHG polar directions upon switching of sliding ferroelectricity. Moreover, the remarkable dependence of SHG polar directions on the orientation of sliding ferroelectricity is further validated by experimental characterizations performed on SnP2S6 crystal in a single FE domain structural form. This work opens up the avenue for in-situ detecting the ferroelectricity orientation of 2D sliding ferroelectrics based on SHG nonlinear optical responses, and also demonstrates the controllable optical nonlinearly for new "slidetronics" applications.

cond-mat.mtrl-sci