Understanding Large Negative Thermal Expansion of NdFe(CN)[subscript 6] through the Electronic Struc
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Engineering topics
Publications and source records attributed to Chen, Jun.
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A novel oxygen octahedral tilt engineering is used to design a new NaNbO 3 -based lead-free piezoceramic with thermal insensitive high piezoresponse.
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Experimental nuclear structure data from various reactions and decays are compiled and evaluated for all known nuclides with mass number A=48 (S, Cl, Ar, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni). For each nuclide, detailed evaluated nuclear structure information is presented for each individual reaction and decay, and the best values combining all available data are recommended for spectroscopic properties, such as level energies, half-lives, γ-ray energies and intensities, decay radiations. No excited states have been identified in 48 S, 48 Cl, 48 Co and 48 Ni, among which the first three even have no measured ground-state half-lives and decay modes. For 48 Fe, a level scheme with a sequence of excited states was established for the first time from a recent one-neutron removal measurement by 2021Ya33. Data for excited states in 48 Ar, 48 K and 48 Mn remain limited; no decay scheme has been measured for 48 Ar and 48 K yet, while the decay scheme for 48 Ni is incomplete due to unobserved levels. 48 Ti is the most studied nuclide through various reactions and decays, followed by 48 V, 40 Ca, 48 Sc, and 48 Cr, among which no decay event to 48 Sc has been observed and the decay schemes for 48 V and 48 Cr are considered as incomplete. Furthermore, this work supersedes the previous full evaluations of A=48: 2006Bu08, 1993Bu04, 1985Al14, 1978Be01.
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Highlights: • IR-induced mitochondrial damage accelerates HSC apoptosis. • CA attenuates mitochondrial damage and apoptosis of HSCs induced by IR. • CA protects against BM hematopoietic failure in mice after IR exposure. Hematopoietic stem cells (HSCs) are sensitive to ionizing radiation (IR) damage, and its injury is the primary cause of bone marrow (BM) hematopoietic failure and even death after exposure to a certain dose of IR. However, the underlying mechanisms remain incompletely understood. Here we show that mitochondrial oxidative damage, which is characterized by mitochondrial reactive oxygen species overproduction, mitochondrial membrane potential reduction and mitochondrial permeability transition pore opening, is rapidly induced in both human and mouse HSCs and directly accelerates HSC apoptosis after IR exposure. Mechanistically, 5-lipoxygenase (5-LOX) is induced by IR exposure and contributes to IR-induced mitochondrial oxidative damage through inducing lipid peroxidation. Intriguingly, a natural antioxidant, caffeic acid (CA), can attenuate IR-induced HSC apoptosis through suppressing 5-LOX-mediated mitochondrial oxidative damage, thus protecting against BM hematopoietic failure after IR exposure. These findings uncover a critical role for mitochondria in IR-induced HSC injury and highlight the therapeutic potential of CA in BM hematopoietic failure induced by IR.
The evaluated experimental data are presented and evaluated for 13 known nuclides of mass 64 (Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge, As, Se). For each nuclide, the best values combining all available data are recommended for spectroscopic properties. No excited states have been identified in 64 Ti, 64 As, and 64 Se. Only one excited state in 64 V as an isomer, and three in 64 Cr have been identified. Data for excited states in 64 Mn, 64 Fe, and 64 Co remain limited. 64 Ni, 64 Cu, and 64 Zn are the most studied nuclides through various reactions and decays, followed by 64 Ga and 64 Ge. In the opinion of the evaluators, there are several incomplete or discrepant aspects of the high-spin portion of the level scheme for 64 Zn above ≈5 MeV excitation which need to be resolved in further experiments using large γ-detector arrays. The decay schemes of 64 Ti β - , 64 As ε and 64 Se ε are unknown, while very little information is available for 64 V β - and 64 Cr β - . The decay schemes of 64 Mn β - , 64 Fe β - , 64 Co β - and 64Ge ε are somewhat better known, but still considered incomplete by evaluators. The decay scheme of 64 Ga ε decay is known in detail, however there is the possibility of additional levels populated above 4713 keV, as the Q(ε) value is 7171 keV. The β - , β + and ε decay modes of 64 Cu are well known, as this radionuclide is of great importance in applications, for example, as a dosimeter for neutron flux determination in nuclear reactors, and as a radiopharmaceutical for positron emission tomography (PET). This work supersedes earlier full evaluations of A=64 by 2007Si04, 1996Si12, 1991Si03, 1979Ha35 and 1974Au04.
Experimental nuclear structure and decay data are evaluated for all of 14 known nuclides of mass 194 (Ta, W, Re, Os, Ir, Pt, Au, Hg, Tl, Pb, Bi, Po, At, Rn). Detailed evaluated spectroscopic information is presented for each reaction and decay experiment, and by combining all the available data, recommended values are provided for energies, spins and parities and half-lives of levels, together with energies, branching ratios and multipolarities of gamma radiations from the levels, and characteristics of beta and alpha radiations in radioactive decays. No excited states have yet been identified in 194 Ta, 194 W, and 194 Rn. Only limited spectroscopic data are available for 194 Re, with a 45–μs isomer identified, but its absolute energy yet to be determined. Only two levels at unknown absolute energies are reported for 194 At, both of which are isomeric but neither can be unambiguously identified as the ground state. Data are scarce for 194 Os, 194 Bi and 194 Po, while 194 Pt, 194 Au, 194 Hg, 194 Tl and 194 Pb are well studied through decays and reactions. For 194 Ir, although a major (n, γ), E=thermal study and two particle-transfer studies provide large amounts of spectral data, still several problematic issues are found in the assignment of multipolarities for the secondary gamma transitions in the (n, γ) study by 2008Ba25, 1998Ba85 and 1998Ba42, all from the same group. Some issues have been resolved by the evaluators, but we suggest that further experimental work is needed on 194 Ir structure to resolve standing issues, and verify the conclusions made by 2008Ba25. Furthermore, our attempt to contact the prime authors of the 2008Ba25 paper was not successful. The present work supersedes all the earlier evaluations of A=194 nuclides by 2006Si17, 1996Br26, 1989Si01 and 1972Au11.
The existence of bridging domains in the vicinity of morphotropic phase boundaries brings an insight into the interplay of phase and domain and explains the excellent piezoelectric performance.
Zero thermal expansion (ZTE) alloys possess unique dimensional stability, high thermal and electrical conductivities. Their practical application under heat and stress is however limited by their inherent brittleness because ZTE and plasticity are generally exclusive in a single-phase material. Besides, the performance of ZTE alloys is highly sensitive to change of compositions, so conventional synthesis methods such as alloying or the design of multiphase to improve its thermal and mechanical properties are usually inapplicable. In this study, by adopting a one-step eutectic reaction method, we overcome this challenge. A natural dual-phase composite with ZTE and plasticity was synthesized by melting 4 atom% holmium with pure iron. The dual-phase alloy shows moderate plasticity and strength, axial zero thermal expansion, and stable thermal cycling performance as well as low cost. By using synchrotron X-ray diffraction, in-situ neutron diffraction and microscopy, the critical mechanism of dual-phase synergy on both thermal expansion regulation and mechanical property enhancement is revealed. These results demonstrate that eutectic reaction is likely to be a universal and effective method for the design of high-performance intermetallic-compound-based ZTE alloys.
Super Invar (SIV), i.e., zero thermal expansion of metallic materials underpinned by magnetic ordering, is of great practical merit for a wide range of high precision engineering. However, the relatively narrow temperature window of SIV in most materials restricts its potential applications in many critical fields. Here, we demonstrate the controlled design of thermal expansion in a family of R 2 (Fe,Co) 17 materials (R=rare Earth). We find that adjusting the Fe-Co content tunes the thermal expansion behavior and its optimization leads to a record-wide SIV with good cyclic stability from 3–461 K, almost twice the range of currently known SIV. In situ neutron diffraction, Mössbauer spectra and first-principles calculations reveal the 3d bonding state transition of the Fe-sublattice favors extra lattice stress upon magnetic ordering. On the other hand, Co content induces a dramatic enhancement of the internal molecular field, which can be manipulated to achieve “ultrawide” SIV over broad temperature, composition and magnetic field windows. Furthermore, these findings pave the way for exploiting thermal-expansion-control engineering and related functional materials.
Understanding how individual dopants or substitutional atoms interact with host lattices enables us to manipulate, control, and improve the functionality of materials. However, because of the intimate coupling among various degrees of freedom in multiferroics, the atomic-scale influence of individual foreign atoms has remained elusive. Here, we unravel the critical roles of individual Sc substitutional atoms in modulating ferroelectricity at the atomic scale of typical multiferroics, Lu 1–x Sc x FeO 3 , by combining advanced microscopy and theoretical studies. Atomic variations in polar displacement of intriguing topological vortex domains stabilized by Sc substitution are directly correlated with Sc atom-mediated local chemical and electronic fluctuations. The local FeO 5 trimerization magnitude and Lu/Sc–O hybridization strength are found to be significantly reinforced by Sc, clarifying the origin of the strong dependence of improper ferroelectricity on Sc content. We find that this study could pave the way for correlating dopant-regulated atomic-scale local structures with global properties to engineer emergent functionalities of numerous chemically doped functional materials.
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