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Wanli Yang

Publications and source records attributed to Wanli Yang.

34 records · Page 2Linked to original sources

Synthetic control over polymorph formation in the d-band semiconductor system FeS$_2$

Pyrite, also known as fool's gold is the thermodynamic stable polymorph of FeS$_2$. It is widely considered as a promising d-band semiconductor for various applications due to its intriguing physical properties. Marcasite is the other naturally occurring polymorph of FeS$_2$. Measurements on natural crystals have shown that it has similarly promising electronic, mechanical, and optical properties as pyrite. However, it has been only scarcely investigated so far, because the laboratory-based synthesis of phase-pure samples or high-quality marcasite single crystal has been a challenge until now. Here, we report the targeted phase formation via hydrothermal synthesis of marcasite and pyrite. The formation condition and phase purity of the FeS$_2$ polymorphs are systematically studied in the form of a comprehensive synthesis map. We, furthermore, report on a detailed analysis of marcasite single crystal growth by a space-separated hydrothermal synthesis. We observe that single phase product of marcasite forms only on the surface under the involvement of H$_2$S and sulphur vapor. The availability of high-quality crystals of marcasite allows us to measure the fundamental physical properties, including an allowed direct optical bandgap of 0.76 eV, temperature independent diamagnetism, an electronic transport gap of 0.11 eV, and a room-temperature carrier concentration of 4.14 $\times$ 10$^{18}$ cm$^{-3}$. X-ray absorption/emission spectroscopy are employed to measure the band gap of the two FeS$_2$ phases. We find marcasite has a band gap of 0.73 eV, while pyrite has a band gap of 0.87 eV. Our results indicate that marcasite -- that is now synthetically available in a straightforward fashion -- is as equally promising as pyrite as candidate for various semiconductor applications based on earth abundant elements.

cond-mat.mtrl-sci↗

Coulombically-stabilized oxygen hole polarons enable fully reversible oxygen redox

Stabilizing high-valent redox couples and exotic electronic states necessitate an understanding of the stabilization mechanism. In oxides, whether they are being considered for energy storage or computing, highly oxidized oxide-anion species rehybridize to form short covalent bonds and are related to significant local structural distortions. In intercalation oxide electrodes for batteries, while such reorganization partially stabilizes oxygen redox, it also gives rise to substantial hysteresis. In this work, we investigate oxygen redox in layered Na2-XMn3O7, a positive electrode material with ordered Mn vacancies. We show that coulombic interactions between oxidized oxide-anions and the interlayer Na vacancies can disfavor rehybridization and stabilize hole polarons on oxygen at 4.2 V vs. Na/Na+. These coulombic interactions provide thermodynamic energy saving as large as O-O covalent bonding and enable ~ 40 mV voltage hysteresis over multiple electrochemical cycles with negligible voltage fade. Our results establish a complete picture of redox energetics by highlighting the role of coulombic interactions across several atomic distances and suggest avenues to stabilize highly oxidized oxygen for applications in energy storage and beyond.

cond-mat.mtrl-sci↗

Disparate exciton-phonon couplings for zone center and boundary phonons in solid-state graphite

The exciton-phonon coupling in highly oriented pyrolytic graphite is studied using resonant inelastic X-ray scattering (RIXS) spectroscopy. With ~ 70 meV energy resolution, multiple low energy excitations associated with coupling to phonons can be clearly resolved in RIXS spectra. Using resonance dependence and the closed form for RIXS cross-section without considering the intermediate state mixing of phonon modes, the dimensionless coupling constant g is determined to be 5 and 0.4, corresponding to the coupling strength of 0.42 eV +/- 40 meV and 0.21 eV +/- 30 meV, for zone center and boundary phonons respectively. The reduced g value for zone-boundary phonon may be related to its double resonance nature.

cond-mat.mtrl-sci↗

Fingerprint oxygen redox reactions in batteries through high-efficiency mapping of resonant inelastic X-ray scattering (mRIXS)

Realizing reversible reduction-oxidation (Redox) reactions of lattice oxygen in batteries is a promising way to improve the energy and power density. However, conventional oxygen absorption spectroscopy fails to distinguish the critical oxygen chemistry in oxide-based battery electrodes. Therefore, high-efficiency full-range mapping of resonant inelastic X-ray scattering (mRIXS) has been developed as a reliable probe of oxygen redox reactions. Here, based on mRIXS results collected from a series of Li1.17Ni0.21Co0.08Mn0.54O2 electrodes at different electrochemical states and its comparison with peroxides, we provide a comprehensive analysis of five components observed in the mRIXS results. While almost all the components change upon electrochemical cycling, comparison with peroxide species show that only two evolving features correspond to the critical oxidized oxygen states. One is a specific feature at 531.0eV excitation and 523.7eV emission energy, the other is a low-energy loss feature. We show that both features evolve with electrochemical cycling of Li1.17Ni0.21Co0.08Mn0.54O2 electrodes, and could be used for characterizing oxygen redox states in battery electrodes. This work is the first benchmark for a complete assignment of all the important mRIXS features collected from battery materials, which provides guidelines for future studies in characterization, analysis and theoretical calculation for probing and understanding oxygen redox reactions.

physics.chem-ph↗

High Reversibility of Lattice Oxygen Redox in Na-ion and Li-ion Batteries Quantified by Direct Bulk Probes of both Anionic and Cationic Redox Reactions

The reversibility and cyclability of anionic redox in battery electrodes hold the key to its practical employments. Here, through mapping of resonant inelastic X-ray scattering (mRIXS), we have independently quantified the evolving redox states of both cations and anions in Na2/3Mg1/3Mn2/3O2. The bulk-Mn redox emerges from initial discharge and is quantified by inverse-partial fluorescence yield (iPFY) from Mn-L mRIXS. Bulk and surface Mn activities likely lead to the voltage fade. O-K super-partial fluorescence yield (sPFY) analysis of mRIXS shows 79% lattice oxygen-redox reversibility during initial cycle, with 87% capacity sustained after 100 cycles. In Li1.17Ni0.21Co0.08Mn0.54O2, lattice-oxygen redox is 76% initial-cycle reversible but with only 44% capacity retention after 500 cycles. These results unambiguously show the high reversibility of lattice-oxygen redox in both Li-ion and Na-ion systems. The contrast between Na2/3Mg1/3Mn2/3O2 and Li1.17Ni0.21Co0.08Mn0.54O2 systems suggests the importance of distinguishing lattice-oxygen redox from other oxygen activities for clarifying its intrinsic properties.

physics.chem-ph↗

Spectroscopic Signature of Oxidized Oxygen States in Peroxides

Recent debates on the oxygen redox behaviors in battery electrodes have triggered a pressing demand for the reliable detection and understanding of non-divalent oxygen states beyond conventional absorption spectroscopy. Here, enabled by high-efficiency mapping of resonant inelastic X-ray scattering (mRIXS) coupled with first-principles calculations, we report distinct mRIXS features of the oxygen states in Li2O, Li2CO3, and especially, Li2O2, which are successfully reproduced and interpreted theoretically. mRIXS signals are dominated by valence-band decays in Li2O and Li2CO3. However, the oxidized oxygen in Li2O2 leads to partially unoccupied O-2p states that yield a specific intra-band excitonic feature in mRIXS. Such a feature displays a specific emission energy in mRIXS, which disentangles the oxidized oxygen states from the dominating transition-metal/oxygen hybridization features in absorption spectroscopy, thus providing critical hints for both detecting and understanding the oxygen redox reactions in transition-metal oxide based battery materials.

physics.chem-ph↗

Characterizing Real-space Topology in Rice-Mele Model by Thermodynamics

The thermodynamic quantities which are related to energy-level statistics are used to characterize the real-space topology of the Rice-Mele model. Through studying the energy spectrum of the model under different boundary conditions, we found that the non-normalizable wave function for the infinite domain is reduced to the edge state adhered to the boundary. For the finite domain with symmetric boundary condition, the critical point for the topological phase transition is equal to the inverse of the domain length. In contrast, the critical point is zero for the semi-infinite domain. Additionally, the symmetry of the energy spectrum is found to be sensitive to the boundary conditions of the Rice-Mele model, and the emergence of the edge states as well as the topological phase transition can be reflected in the thermodynamic properties. A potentially practical scheme is proposed for simulating the Rice-Mele model and detecting the relevant thermodynamic quantities in the context of Bose-Einstein condensate.

cond-mat.other↗

Generation of stable entanglement between two cavity mirrors by squeezed-reservoir engineering

The generation of quantum entanglement of macroscopic or mesoscopic bodies in mechanical motion is generally bounded by the thermal fluctuation exerted by their environments. Here we propose a scheme to establish stationary entanglement between two mechanically oscillating mirrors of a cavity. It is revealed that, by applying a broadband squeezed laser acting as a squeezed-vacuum reservoir to the cavity, a stable entanglement between the mechanical mirrors can be generated. Using the adiabatic elimination and master equation methods, we analytically find that the generated entanglement is essentially determined by the squeezing of the relative momentum of the mechanical mirrors, which is transferred from the squeezed reservoir through the cavity. Numerical verification indicates that our scheme is within the present experimental state of the art of optomechanics.

quant-ph↗

Measurement of the spectral line shapes for orbital excitations in the Mott insulator CoO using high-resolution resonant inelastic x-ray scattering

We establish the spectral line shape of orbital excitations created by resonant inelastic X-ray scattering for the model Mott insulator CoO. Improved experimental energy resolution reveals that the line shapes are strikingly different from expectations in a first principles-based atomic multiplet model. Extended theoretical simulations are performed to identify the underlying physical origins, which include a pronounced thermal tail reminiscent of anti-Stokes scattering on the energy gain side of excitations, and an essential contribution from interatomic many-body dynamics on the energy loss side of excitations.

cond-mat.str-el↗

Multiplet resonance lifetimes in resonant inelastic X-ray scattering involving shallow core levels

Resonant inelastic X-ray scattering (RIXS) spectra of model copper- and nickel-based transition metal oxides are measured over a wide range of energies near the M-edge (h$ν$=60-80eV) to better understand the properties of resonant scattering involving shallow core levels. Standard multiplet RIXS calculations are found to deviate significantly from the observed spectra. However, by incorporating the self consistently calculated decay lifetime for each intermediate resonance state within a given resonance edge, we obtain dramatically improved agreement between data and theory. Our results suggest that these textured lifetime corrections can enable a quantitative correspondence between first principles predictions and RIXS data on model multiplet systems. This accurate model is also used to analyze resonant elastic scattering, which displays the elastic Fano effect and provides a rough upper bound for the core hole shake-up response time.

cond-mat.str-el↗

Spectroscopic fingerprints of valence and spin states in manganese oxides and fluorides

We performed a systematic study of soft X-ray absorption spectroscopy in various manganese oxides and fluorides. Both Mn L-edges and ligand (O and F) K-edges are presented and compared with each other. Despite the distinct crystal structure and covalent/ionic nature in different systems, the Mn-L spectra fingerprint the Mn valence and spin states through spectral lineshape and energy position consistently and evidently. The clear O- and F- K pre-edge features in our high resolution spectra enable a quantitative definition of the molecular orbital diagram with different Mn valence. In addition, while the binding energy difference of the O-1s core electrons leads to a small shift of the O-K leading edges between trivalent and quadrivalent manganese oxides, a significant edge shift, with an order of magnitude larger in energy, was found between divalent and trivalent compounds, which is attributed to the spin exchange stabilization of half- filled 3d system. This shift is much enhanced in the ionic fluoride system. This work provides the spectroscopic foundation for further studies of complicated Mn compounds.

cond-mat.mtrl-sci↗

No spin-localization phase transition in the spin-boson model without local field

We explore the spin-boson model in a special case, i.e., with zero local field. In contrast to previous studies, we find no possibility for quantum phase transition (QPT) happening between the localized and delocalized phases, and the behavior of the model can be fully characterized by the even or odd parity as well as the parity breaking, instead of the QPT, owned by the ground state of the system. Our analytical treatment about the eigensolution of the ground state of the model presents for the first time a rigorous proof of no-degeneracy for the ground state of the model, which is independent of the bath type, the degrees of freedom of the bath and the calculation precision. We argue that the QPT mentioned previously appears due to unreasonable treatment of the ground state of the model or of the infrared divergence existing in the spectral functions for Ohmic and sub-Ohmic dissipations.

quant-ph↗

Parity breaking and scaling behavior in the spin-boson model

We study the breaking of parity in the spin-boson model and demonstrate unique scaling behavior of the magnetization and entanglement around the critical points for the parity breaking after suppressing the infrared divergence existing inherently in the spectral functions for Ohmic and sub-Ohmic dissipations. Our treatment is basically analytical and of generality for all types of the bath. We argue that the conventionally employed spectral function is not fully reasonable and the previous justification of quantum phase transition for localization needs to be more seriously reexamined.

cond-mat.str-el↗

Comparison of different measures for quantum discord under non-Markovian noise

Two geometric measures for quantum discord were recently proposed by Modi et al. [Phys. Rev. Lett. 104, 080501 (2010)] and Dakic et al. [Phys. Rev. Lett. 105, 190502 (2010)]. We study the similarities and differences for total quantum correlations of Bell-diagonal states using these two geometry-based quantum discord and the original quantum discord. We show that, under non-Markovian dephasing channels, quantum discord and one of the geometric measures stay constant for a finite amount of time, but not the other geometric measure. However, all the three measures share a common sudden change point. Our study on critical point of sudden transition might be useful for keeping long time total quantum correlations under decoherence.

quant-ph↗

Parity-relevant Zitterbewegung and quantum simulation by a single trapped ion

Zitterbewegung (ZB), the trembling of free relativistic electrons in a vacuum could be simulated by a single trapped ion. We focus on the variations of ZB under different parity conditions and find no ZB in the case of odd or even parity. ZB occurs only for admixture of the odd and even parity states. We also show the similar role played by the parity operator for the trapped ion in Fock-state representation and the space inversion operator for a realistic relativistic electron. Although the ZB effect is invisible in a relativistic electron, preparation of the trapped ion in different parity states is a sophisticated job, which makes it possible to observe the parity relevant ZB effects with currently available techniques.

quant-ph↗

Anomalous Fermi-Surface Dependent Pairing in a Self-Doped High-Tc Superconductor

We report the discovery of a self-doped multi-layer high Tc superconductor Ba2Ca3Cu4O8F2(F0234) which contains distinctly different superconducting gap magnitudes along its two Fermi surface(FS) sheets. While formal valence counting would imply this material to be an undoped insulator, it is a self-doped superconductor with a Tc of 60K, possessing simultaneously both electron- and hole-doped FS sheets. Intriguingly, the FS sheet characterized by the much larger gap is the electron-doped one, which has a shape disfavoring two electronic features considered to be important for the pairing mechanism: the van Hove singularity and the antiferromagnetic (Pi/a, Pi/a) scattering.

cond-mat.supr-con↗