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Zhiyu Pei

Publications and source records attributed to Zhiyu Pei.

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Quench dynamics in nonreciprocal Aubry-André-Harper model

The critical phase of a non-Hermitian quasicrystal can support stronger transport than its surrounding delocalized phase. We demonstrate this anomalous behavior in the one-dimensional nonreciprocal Aubry-André-Harper model through a combined study of dynamical quantum phase transitions (DQPTs) and wavepacket diffusion. Using a parity-sorted energy-spectrum classification that directly encodes the generalized $\mathcal{PT}$ symmetry, we find that DQPTs in this system are energy-resolved, in contrast to the energy-independent DQPTs of Hermitian quasicrystals. The energy-resolved features are most pronounced when the initial and final Hamiltonians belong to different phases (localized or extended), and they are tied to the even-odd index structure of the spectrum, which we exploit to organize the quench-dynamical landscape. For wavepacket dynamics after a single-site quench, the diffusion exponent $β$, extracted from the long-time power-law scaling of the root-mean-square displacement $σ(τ)$, partitions the phase diagram into four distinct regimes. In the Hermitian limit the extended phase is ballistic ($β=1$), the critical phase is normally diffusive ($β=0.5$), and the localized phase yields $β\to 0$. Nonreciprocity reverses this hierarchy: the extended phase becomes normally diffusive, while the critical phase turns ballistic. We trace the anomalous $β=1$ at criticality to the self-similar multifractal structure of the critical eigenstates, whose nodal positions are organized by the golden ratio. A finite-size scaling ansatz built on the wave-front propagation yields $σ(τ)\proptoτ$. The parity-resolved DQPTs and the $β$-phase diagram establish two complementary dynamical diagnostics of nonreciprocal quasicrystals, in which nonreciprocity promotes transport at the critical point and suppresses it in the delocalized phase.

cond-mat.mes-hall

Constructing a bifunctional platform based on Mn2+-doped Mg2Y8(SiO4)6O2 phosphors for multi-parameter optical thermometry and manometry

Series of the Mn2+-doped Mg2Y8(SiO4)6O2 phosphors were synthesized. Upon excitation at 408 nm, these phosphors exhibited intense orange emission originating from Mn2+, with concentration quenching observed beyond x = 0.07, and they also demonstrated excellent thermal stability. For optical thermometry, two independent parameters, emission band centroid (λ) and lifetime, were employed as thermal indicators, yielding sensitivities of dλ/dT = 0.053 nm K-1 and SR = 0.86% K-1, respectively. High-pressure in-situ X-ray diffraction revealed that the phosphors retained structural integrity under compression, accompanied by a progressive lattice contraction. With increasing pressure (0.13-10.89 GPa), a spectral red-shift was observed, corresponding to a pressure sensitivity of dλ/dp = 4.75 nm GPa-1. Additionally, pressure-dependent shifts in color coordinates allowed the development of a colorimetric manometric response, achieving a relative sensitivity of 3.27% GPa-1. Remarkably, the pressure-induced spectral shift of Mn2+ emission, characterized by low thermal cross-sensitivity, enabled a highly reliable ratiometric manometric strategy, with a relative sensitivity of 72% GPa-1. Notably, the system delivered the highest TIMF reported to date above 3 GPa, peaking at 1940 K GPa-1 at 7 GPa. These results position Mn2+-doped Mg2Y8(SiO4)6O2 phosphors as a highly promising bifunctional material for next-generation, multi-parameter optical sensing applications under extreme conditions.

cond-mat.mtrl-sci