We investigate vibrational properties and lattice distortion of negatively charged nitrogen-vacancy (NV − ) center in diamond. Using the first-principles electronic structure calculations, we show that the presence of NV − center leads to appearance of a large number of quasilocalized vibrational modes (qLVMs) with different degree of localization. The vibration patterns and the symmetries of the qLVMs are presented and analyzed in detail for both ground and excited orbital states of the NV − center. We find that in the high-symmetry (C3v) excited orbital state a pair of degenerate qLVMs becomes unstable, i.e. have formally negative frequencies, and the stable excited state has lower (C 1h ) symmetry. This is a direct indication of the Jahn-Teller effect, and our studies suggest that dynamical Jahn-Teller effect in the weak coupling regime takes place. We have also performed a detailed comparison of our results with the available experimental data on the vibrations involved in optical emission/absorption of the NV − centers. We have directly demonstrated that, among other modes, the qLVMs crucially impact the optical properties of the NV − centers in diamond, and identified the most important groups of qLVMs. Our results are important for deeper understanding of the optical properties and the orbital relaxation associated with lattice vibrations of the NV − centers.

Background Mental fatigue is usually caused by long-term cognitive activities, mainly manifested as drowsiness, difficulty in concentrating, decreased alertness, disordered thinking, slow reaction, lethargy, reduced work efficiency, error-prone and so on. Mental fatigue has become a widespread sub-health condition, and has a serious impact on the cognitive function of the brain. However, seldom studies investigate the differences of mental fatigue on electrophysiological activity both in resting state and task state at the same time. Here, twenty healthy male participants were recruited to do a consecutive mental arithmetic tasks for mental fatigue induction, and electroencephalogram (EEG) data were collected before and after each tasks. The power and relative power of five EEG rhythms both in resting state and task state were analyzed statistically. Results The results of brain topographies and statistical analysis indicated that mental arithmetic task can successfully induce mental fatigue in the enrolled subjects. The relative power index was more sensitive than the power index in response to mental fatigue, and the relative power for assessing mental fatigue was better in resting state than in task state. Furthermore, we found that it is of great physiological significance to divide alpha frequency band into alpha1 band and alpha2 band in fatigue related studies, and at the same time improve the statistical differences of sub-bands. Conclusions Our current results suggested that the brain activity in mental fatigue state has great differences in resting state and task state, and it is imperative to select the appropriate state in EEG data acquisition and divide alpha band into alpha1 and alpha2 bands in mental fatigue related researches.

A X B X t r r r r ), where r A , r B , and r X stand for the ionic radii of A, B, and X, respectively. For cubic or pseudo-cubic crystal structures, the ideal value for t is 1 or a wave between 0.813 and 1.107; tolerance values that deviate significantly from 1 lead to warping and destruction of the structure. [25,26] As reported by Shannon, [27] the ionic radii for Pb 2+ and Eu 2+ are 1.19 and 1.17 Å, respectively. The similarity in size between lead and europium suggests the potential to replace lead with the more environmental-friendly europium. In this vein, many CsEuX n (X = Cl, I) structures have been reported, including CsEuCl 3 , [28,29] CsEu 2 I 5 , [30] and CsEuI 3 . [30,31] Preparation Lead-based perovskite nanocrystals (NCs) are promising candidates for use in lighting and display applications; however, the toxicity of lead is one critical issue that needs to be solved for its commercialization. Consequently, less toxic tin and bismuth-based perovskite NCs have been developed, but these materials exhibit low photoluminescence quantum yields (PLQYs) and large full width at half maximum (FWHM) values. Due to their similarity in size for Eu 2+ and Pb 2+ , the more environmental-friendly europium shows the potential to replace lead. Herein, the synthesis of Eu 2+ doped CsBr NCs with an average size of 51.5 nm via a facile hot-injection method is reported. The prepared CsBr:Eu 2+ NCs exhibit an emission peak at 440 nm with an FWHM of 31 nm and PLQY up to 32.8%, which is persistent for at least 60 d. Moreover, the size and FWHM of CsBr:Eu 2+ NCs can be tuned to 18.9 and 29 nm, respectively, by co-doping of Ca 2+ ions into the NCs. It is also demonstrated that the prepared CsBr:Eu 2+ NCs can be employed as efficient color conversion materials for fabricating white light-emitting diodes.

Nutrient resorption from senescing leaves is a key mechanism of nutrient conservation for plants. The nutrient resorption efficiency is highly dependent on leaf nutrient status, species identity and soil nutrient availability. Nitrogen is a limiting nutrient in most ecosystems, it is widely reported that nitrogen resorption efficiency (NRE) was highly dependent on the soil nitrogen availability and vary with N deposition. The effects of nitrogen deposition on NRE and nitrogen concentration in green and senescing leaves have been well established for forests and grasslands; in contrast, little is known on how plants in shrublands respond to nitrogen deposition across the world. In this study, we conducted a two-year nitrogen addition manipulation experiment to explore the responses of nitrogen concentration in green and senescing leaves, and NRE of seven dominant species, namely, Vitex negundo, Wikstroemia chamaedaphne, Carex rigescens and Cleistogenes chinensis from the Vitex negundo community, and Spirea trilobata, Armeniaca sibirica, V. negundo, C. rigescens and Spodiopogon sibiricus from the Spirea trilobata community, to nitrogen deposition in two typical shrub communities of Mt. Dongling in northern China. Results showed that NRE varied remarkably among different life forms, which was lowest in shrubs, highest in grasses, and intermediate in forbs, implying that shrubs may be most capable of obtaining nitrogen from soil, grasses may conserve more nitrogen by absorption from senescing leaves, whereas forbs may adopt both mechanisms to compete for limited nitrogen supply from the habitats. As the N addition rate increases, N concentration in senescing leaves ([N]s) increased consistent from all species from both communities, that in green leaves ([N]g) increased for all species from the Vitex negundo community, while no significant responses were found for all species from the Spirea trilobata community; NRE decreased for all species except A. sibirica from the Vitex community and W. chamaedaphn from the Spirea community. Given the substantial interspecific variations in nutrient concentration, resorption and the potentially changing community composition, and the increased soil nutrient availability due to fertilization may indirectly impact nutrient cycling in this region.

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In a lithium-ion battery, electrons are released from the anode and go through an external electronic circuit to power devices, while ions simultaneously transfer through internal ionic media to meet with electrons at the cathode. Inspired by the fundamental electrochemistry of the lithium-ion battery, we envision a cell that can generate a current of ions instead of electrons, so that ions can be used for potential applications in biosystems. Based on this concept, we report an ‘electron battery’ configuration in which ions travel through an external circuit to interact with the intended biosystem whereas electrons are transported internally. As a proof-of-concept, we demonstrate the application of the electron battery by stimulating a monolayer of cultured cells, which fluoresces a calcium ion wave at a controlled ionic current. Electron batteries with the capability to generate a tunable ionic current could pave the way towards precise ion-system control in a broad range of biological applications.

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Heterostructures consisting of vertically stacked two-dimensional (2D) materials have recently gained large attention due to their highly controllable electronic properties and resulting quantum phases. In contrast to the mechanically stacked multilayered systems, which offer exceptional control over a stacking sequence or interlayer twist angles, the epitaxially grown 2D materials express unprecedented quality and stability over wafer-scale lengths. However, controlling the growth conditions remains a major obstacle toward the formation of complex, epitaxial heterostructures with well-defined electronic properties. Here, we synthesized a trilayer graphene heterostructure on the SiC(0001) substrate with two specific interlayer locations occupied by gadolinium. We applied multitechnique methodology based on low-temperature scanning tunneling microscopy/spectroscopy (STM/S) and angle-resolved photoelectron spectroscopy (ARPES) to determine the intercalant’s locations in the complex, epitaxial graphene heterostructure. Our approach relies on very high quality and large, micrometer-scale homogeneity of the synthesized system. The experimentally determined electronic structure is dominated by the two topmost graphene layers. Our spectroscopic results show quantitative agreement between global ARPES, local STM/S, and density functional theory predictions. The characterized electronic properties primarily reflect highly anisotropic doping levels between the two corresponding graphene layers, which significantly affect the band structure topology. Two pairs of hybridized massive Dirac bands from our initial synthesisthe bilayer graphene on the SiC­(0001) substrateare transformed upon Gd intercalation into two pairs of massless Dirac bands with a new hybridization region in between. Our results open perspectives in the realization of exotic 2D quantum materials via atomically precise synthesis of epitaxial, multilayered graphene–rare earth heterostructures.