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Wei-Tao Peng

Publications and source records attributed to Wei-Tao Peng.

4 recordsLinked to original sources

Atomic-scale tunable phonon transport at tailored grain boundaries and Their Impact on Thermal Conductivity

Grain boundaries (GBs) strongly influence thermal transport in crystalline solids by disrupting lattice periodicity and scattering phonons. Due to the atomic-level disorder and structural complexity, a fundamental understanding of how specific GB geometries regulate nanoscale phonon behavior and macroscopic thermal conductivity has remained elusive. Here, using emerging atomic-resolution vibrational spectroscopy, we directly correlate GB structure, defect-specific vibrational states, and thermal transport in bicrystal strontium titanate with controlled tilt and twist angles. The phonon characterizations and thermal conductivity data reveal two distinct regimes, where low-angle tilt GBs (2deg, 6deg, 10deg) substantially modulate phonon populations and mode frequencies, resulting in pronounced changes in thermal conductivity, whereas high-angle tilt GBs (22deg, 36deg) exhibit weak conductivity variation due to saturated structural disorder and scattering. In contrast, twist GBs introduce periodic defect motifs that only locally tailor phonon transport. Our results suggest tilt and twist angles as complementary knobs for coarse and fine control of phonon propagation and cross-GB thermal transport, providing a predictive framework for thermal engineering in materials.

cond-mat.mes-hall

Compositionally Complex Perovskite Oxides as a New Class of Li-Ion Solid Electrolytes

Compositionally complex ceramics (CCCs), including high-entropy ceramics (HECs) as a subclass, offer new opportunities of materials discovery beyond the traditional methodology of searching new stoichiometric compounds. Herein, we establish new strategies of tailoring CCCs via a seamless combination of (1) non-equimolar compositional designs and (2) controlling microstructures and interfaces. Using oxide solid electrolytes for all-solid-state batteries as an exemplar, we validate these new strategies via discovering a new class of compositionally complex perovskite oxides (CCPOs) to show the possibility of improving ionic conductivities beyond the limit of conventional doping. As an example (amongst the 28 CCPOs examined), we demonstrate that the ionic conductivity can be improved by >60% in (Li0.375Sr0.4375)(Ta0.375Nb0.375Zr0.125Hf0.125)O3-δ, in comparison with the state-of-art (Li0.375Sr0.4375)(Ta0.75Zr0.25)O3-δ (LSTZ) baseline, via maintaining comparable electrochemical stability. Furthermore, the ionic conductivity can be improved by another >70% via grain boundary (GB) engineering, achieving >270% of the LSTZ baseline. This work suggests transformative new strategies for designing and tailoring HECs and CCCs, thereby opening a new window for discovering materials for energy storage and many other applications.

cond-mat.mtrl-sci

Assessment of the LFAs-PBE exchange-correlation potential for high-order harmonic generation of aligned H2+ molecules

We examine the performance of our recently developed LFAs-PBE exchange-correlation (XC) potential [C.-R. Pan, P.-T. Fang, and J.-D. Chai, Phys. Rev. A, 2013, 87, 052510] for the high-order harmonic generation (HHG) spectra and related properties of H2+ molecules aligned parallel and perpendicular to the polarization of an intense linearly polarized laser pulse, employing the real-time formulation of time-dependent density functional theory (RT-TDDFT). The results are compared with the exact solutions of the time-dependent Schrodinger equation as well as those obtained with other XC potentials in RT-TDDFT. Owing to its correct (-1/r) asymptote, the LFAs-PBE potential significantly outperforms conventional XC potentials for the HHG spectra and the properties that are sensitive to the XC potential asymptote. Accordingly, the LFAs-PBE potential, which has a computational cost similar to that of the popular Perdew-Burke-Ernzerhof (PBE) potential, can be very promising for the study of the ground-state, excited-state, and time-dependent properties of large electronic systems, extending the applicability of density functional methods for a diverse range of applications.

physics.chem-ph

Assessment of asymptotically corrected model potential scheme for charge-transfer-like excitations in oligoacenes

We examine the performance of the asymptotically corrected model potential scheme on the two lowest singlet excitation energies of acenes with different number of linearly fused benzene rings (up to 5), employing both the real-time time-dependent density functional theory and the frequency-domain formulation of linear-response time-dependent density functional theory. The results are compared with the experimental data and those calculated by long-range corrected hybrid functionals and others. The long-range corrected hybrid scheme is shown to outperform the asymptotically corrected model potential scheme for charge-transfer-like excitations.

physics.chem-ph