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Exploring the unique physical properties of oxide perovskites necessitates their growth on diverse single‐crystal substrates. The thin‐film growth of perovskite SrMnO3 (SMO) has been a particular focus of research due to its emerging room‐temperature multiferroicity. Herein, the epitaxial thin films of (110)‐oriented SMO are grown on the piezoelectric (110)‐oriented (1–x)Pb(Mg1/3Nb2/3)O3–xPbTiO3 (PMN‐PT) substrate. The effects of the thickness and oxygen annealing on the crystal structure, stoichiometry, and ferroelectric properties of the SMO thin film are systematically investigated. The tensile strain produced by the lattice mismatch between the bulk SMO and the PMN‐PT substrate causes an expansion of the c‐lattice parallel to the in‐plane direction of the substrate. The films show larger a‐, b‐, and c‐lattice parameters than the bulk material, resulting in volume expansion of the unit cell. This lattice expansion is attributed to the generation of oxygen vacancies driven by the reduced formation energy caused by the high elastic strain. Piezoelectric force microscopy reveals that the SMO film contains domains with strain‐mediated in‐plane and vacancy‐mediated out‐of‐plane polarization. Furthermore, the piezoelectric response of the PMN‐PT substrate effectively modulates the biaxial tensile strain in the SMO film, offering a potential strategy for controlling the crystal structure and ferroelectric properties of SMO. [ABSTRACT FROM AUTHOR]

Electrolyte additives with multiple functions enable the interfacial engineering of Li‐metal batteries (LMBs). Owing to their unique reduction behavior, additives exhibit a high potential for electrode surface modification that increases the reversibility of Li‐metal anodes by enabling the development of a hierarchical solid electrolyte interphase (SEI). This study confirms that an adequately designed SEI facilitates the homogeneous supply of Li+, nonlocalized Li deposition, and low electrolyte degradation in LMBs while enduring the volume fluctuation of Li‐metal anodes on cycling. An in‐depth analysis of interfacial engineering mechanisms reveals that multilayered SEI structures comprising mechanically robust LiF‐rich species, electron‐rich P–O species, and elastic polymeric species enabled the stable charge and discharge of LMBs. The polymeric outer SEI layer in the as‐fabricated multilayered SEI could accommodate the volume fluctuation of Li‐metal anodes, significantly enhancing the cycling stability Li||LiNi0.8Co0.1Mn0.1O2 full cells with an electrolyte amount of 3.6 g Ah−1 and an areal capacity of 3.2 mAh cm−2. Therefore, this study confirms the ability of interfacial layers formed by electrolyte additives and fluorinated solvents to advance the performance of LMBs and can open new frontiers in the fabrication of high‐performance LMBs through electrolyte‐formulation engineering. [ABSTRACT FROM AUTHOR]

Sodium metal (Na) anodes are considered the most promising anode for high‐energy‐density sodium batteries because of their high capacity and low electrochemical potential. However, Na metal anode undergoes uncontrolled Na dendrite growth, and unstable solid electrolyte interphase layer (SEI) formation during cycling, leading to poor coulombic efficiency, and shorter lifespan. Herein, a series of Na‐ion conductive alloy‐type protective interface (Na‐In, Na‐Bi, Na‐Zn, Na‐Sn) is studied as an artificial SEI layer to address the issues. The hybrid Na‐ion conducting SEI components over the Na‐alloy can facilitate uniform Na deposition by regulating Na‐ion flux with low overpotential. Furthermore, density functional study reveals that the lower surface energy of protective alloys relative to bare Na is the key factor for facilitating facile ion diffusion across the interface. Na metal with interface layer facilitates a highly reversible Na plating/stripping for ≈790 h, higher than pristine Na metal (100 h). The hybrid self‐regulating protective layers exhibit a high mechanical flexibility to promote dendrite free Na plating even at high current density (5 mA cm−2), high capacity (10 mAh cm−2), and good performance with Na3V2(PO4)3 cathode. The current study opens a new insight for designing dendrite Na metal anode for next generation energy storage devices. [ABSTRACT FROM AUTHOR]

Activation of metal oxides by light is a robust yet facile approach to manipulating their surface chemistry for favorable reactions with target molecules in heterogeneous catalysis and gas sensors. However, a limited understanding of interface chemistry and the involved mechanism impedes the development of a rational design of oxide interfaces for light‐activated gas sensing. Herein, the TiOx‐assisted photosensitization of In2O3 toward NO2 sensing is investigated as a case study to elucidate the detailed mechanism of light‐activated surface chemistry at the metal/gas interface. The resultant heterogeneous oxides exhibit outstanding NO2 sensing performance under light irradiation thanks to abundant photoexcited electrons and holes that serve as adsorption and desorption sites, respectively, to accelerate both surface reactions. Furthermore, the facile transfer of electrons and holes across the TiOx‐In2O3 interface contributes to improving the reversibility of sensing kinetics. Through this study, the mechanistic understanding is established of how the surface chemistry of metal oxide surfaces can be tuned by light activation providing an effective route to the design fabrication of high‐performance gas sensors. [ABSTRACT FROM AUTHOR]

Engineering active sites of metal nanoparticle‐based heterogeneous catalysts is one of the most prerequisite approaches for the efficient production of chemicals, but the limited active sites and undesired oxidation on the metal nanoparticles still remain as key challenges. Here, it is reported that the negatively charged surface of copper nanoparticles on the 2D [Ca2N]+∙e− electride provides the unrestricted active sites for catalytic selective sulfenylation of indoles and azaindoles with diaryl disulfides. Substantial electron transfer from the electride support to copper nanoparticles via electronic metal–support interactions results in the accumulation of excess electrons at the surface of copper nanoparticles. Moreover, the surface‐accumulated excess electrons prohibit the oxidation of copper nanoparticle, thereby maintaining the metallic surface in a negatively charged state and activating both (aza)indoles and disulfides under mild conditions in the absence of any further additives. This study defines the role of excess electrons on the nanoparticle‐based heterogeneous catalyst that can be rationalized in versatile systems. [ABSTRACT FROM AUTHOR]

The well‐known ferromagnetic oxide, NiFe2O4, was studied as a potential candidate for room‐temperature Type II magnetoelectrics. A spin canting as one of the essential requirements for Type II multiferroics was induced by breaking the stoichiometry, that is, intentionally subtracting Fe ions. We observed that Fe ions were first subtracted exclusively from the tetrahedral sites, leading to an increase in the magnetoelectric coupling owing to an increasing degree of spin canting. The enhancement in the magnetoelectric coupling culminated beyond the subtraction level of ~30 at.%, at which Fe ions started to be removed from the octahedral sites. Alongside, we observed that the subtraction of Fe ions gives rise to a ferroelectricity due to the formation of defect complexes that establish an internal bias field. [ABSTRACT FROM AUTHOR]

Ferroelectricity in HfO2 thin films can be utilized for fast, power‐efficient, and highly scalable non‐volatile memories. However, the required wake‐up process for inducing ferroelectricity/ achieving higher polarization is one of the major hurdles that hinder HfO2‐based thin films from developing reliable electronic devices. The wake‐up effect is believed to originate from i) phase transformation from non‐ferroelectric to ferroelectric, ii) movement of defect entities (mainly oxygen vacancy defects) near the film‐electrode interface, and iii) heterogeneity of the electrode interfaces. In the present study, an experimental strategy is designed to overcome these sources of the wake‐up process. A multi‐step deposition and annealing process is carried out to induce wake‐up‐free ferroelectricity in Yttrium doped HfO2 (Y:HfO2) thin film directly grown on Si‐substrate. Furnace annealing is utilized instead of the standard rapid thermal annealing process to reduce the oxygen deficiencies and stimulate the direct growth of the polar Y:HfO2. The oxygen‐vacancy‐related defects are found to be the dominating source of wake‐up effect in Y‐doped HfO2 films. The step‐wise deposition and annealing in the oxygen atmosphere facilitate direct growth of the polar phase, reduce the oxygen vacancies, and induce wake‐up‐free ferroelectricity in Y:HfO2. [ABSTRACT FROM AUTHOR]

Hafnium zirconium oxide (HZO) has been studied intensively due to its potential application to memory and logic devices based on its outstanding dielectric and ferroelectric properties. Because many process factors can significantly impact the properties of HZO thin film, an optimized process or post‐treatment is necessary to ensure its performance. Herein, the effect of hydrogen on HZO thin film can make the film degraded. Analysis of the polarization–voltage hysteresis loops and I–V measurements indicate a leaky behavior in the film. To address this issue, post‐oxygen‐plasma treatment is performed on the film, which results in the decrease in hydrogen ions inside the film and consequently reduces the leakage current density. This finding can provide new insight into the effect of hydrogen incorporation for HZO thin films and methodology to remove leaky components inside ferroelectric films using O2 plasma treatment. [ABSTRACT FROM AUTHOR]

The prediction of the climate change effect on plant distribution has become a primary research field for conservation practices and planning. The present research predicted future distributions of warm-adapted evergreen trees, Neolitsea sericea (Blume) Koidz. and Camellia japonica L., under climate change in the Korean Peninsula (KP) using an ensemble approach and quantified the predictive uncertainty. For these purposes, we used nine modeling algorithms and the pre-evaluation weighted ensemble method in modelling the current distributions of those evergreen trees; furthermore, we predicted their future distributions under 20 climate change scenarios and averaged the future predictions for ensemble forecasts. The results suggest that both species would expand to the northern part of KP under climate changes; however, the spatial pattern and rate of expansions would be different. C. japonica showed a faster expansion than N. sericea. While C. japonica showed both inland and northward expansions under climate change, N. sericea was mostly distributed in coastal areas. In addition, the highly suitable habitats of N. sericea and C. japonica will decline or shift to the north under climate change. This may indicate that climate change will degrade habitat suitability of those species within the distribution boundary and may restrict their continuous range expansions under further climate changes. Considering the lack of research on the climate-related range shifts of plants in Asia including KP, the present study provides fundamental and practical knowledge for a better understanding of climate-related vegetation changes in Asia as well as in KP. [ABSTRACT FROM AUTHOR]

Here, we demonstrate a novel process to convert TiO2 nanotubes into ferroelectric nanohoneycombs, comprised of vertically aligned PbTiO3 nanotubes. Tube bottom opening process enabled effective infiltration of lead acetate precursor into the nanotubes. Nanohoneycombs, which were converted via additional lead supplement process, showed uniform conversion and well-defined ferroelectric properties with the effective piezoelectric coefficient of approximately 20 pm/V, which was measured by piezoresponse force microscopy. [ABSTRACT FROM AUTHOR]

ABSTRACT We have fabricated vertically aligned ferroelectric PVDF mesoscale rod arrays comprising β and γ phases using a 200 nm diameter anodized aluminum oxide (AAO) as the porous template. We could synthesize the ferroelectric phase in mesoscale rod forms by combining the well-established recipe for crystallizing the β phase using dimethyl sulfoxide (DMSO) at low temperature and template-guided infiltration processing for the rods using AAO. We measured the dimensions of the PVDF rods by scanning electron microscopy and identified the polymorph phases by X-ray diffraction and Fourier transform infrared spectroscopy. The length of the rods varied from 3.82 μm to 1.09 μm and the diameter from 232 nm to 287 nm when the volume ratio between DMSO and acetone changed from 5 : 5 to 10 : 0. We obtained well-defined piezoresponse hysteresis loops for all rods with remnant piezoresponse ranging from 2.12 pm/V to 5.04 pm/V and coercive voltage ranging from 2.29 V to 2.71 V using piezoresponse force microscopy. Our results serve as a processing platform for flexible electronic devices that need high capacitance and piezoelectric functionalities such as flexible memory devices or body energy harvesting devices for intelligent systems. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3842-3848, 2013 [ABSTRACT FROM AUTHOR]

Nanoscale ferroelectric honeycombs, comprised of vertically aligned PbTiO3 nanotubes, are fabricated by vapor phase reaction between lead acetate-infiltrated TiO2 nanotubes and PbO vapor. PbTiO3 nanohoneycombs converted by vapor phase reaction at 550°C showed well-aligned nanoscale structure with alignment angle less than 1° and well-defined ferroelectric properties with the effective piezoelectric coefficient of 44 pm/V. This novel nanoscale structure is expected to facilitate high efficiency sensing of electromechanical and electrochemical stimuli. [ABSTRACT FROM AUTHOR]

In this study, a mechanically flexible structure, a cuboctahedral metal‐organic polyhedra (MOP) Cu24[5‐(octyloxy) isophthalic acid]24 Cu (II) paddlewheel clusters coordinated with (5‐(octyloxy) isophthalate), resulting in significantly enhanced hydrolytic stability are prepared. It should be noted that CuMOP‐1 exhibits evenly and symmetrically distributed non‐polar long alkyl chains and polar hydroxy groups, facilitating self‐assembly into higher‐order structures reminiscent of amphiphiles. Furthermore, the resultant CuMOP‐1 undergoes a phase change at 150–160 °C as confirmed temperature‐dependent Raman spectroscopy (RS), thermogravimetric analysis and Differential Scanning Calorimetry (TGA‐DSC). The possible use of Cu‐MOP‐1 for capturing mechanical energy is demonstrated by creating a flexible hybrid piezoelectric‐triboelectric nanogenerator (HP‐TENG). The resultant CuMOP‐1@ Polyvinylidene fluoride(PVDF) membrane‐based HP‐TENG demonstrates enhanced triboelectric output voltage of 547.5 V, current density of 15.16 µAcm−2, and power density of 2.8 mWcm−2 due to its increased surface charge density and a substantial rise in the dielectric constant. Furthermore, the amphiphiles and phase change in CuMOP‐1 lead to ∽73% increase in voltage and 60% in current density of HP‐TENG in high‐temperature (140 °C) environments. HP‐TENG also exhibits exceptional temperature‐ and pressure‐sensing abilities, with sensitivities of 1.81 V°C−1 and 7.12 V°kPa−1, respectively, showcasing its feasibility over a wide range of temperatures and pressures. [ABSTRACT FROM AUTHOR]

Multiferroic materials have driven significant research interest due to their promising technological potential. Developing new room‐temperature multiferroics and understanding their fundamental properties are important to reveal unanticipated physical phenomena and potential applications. Here, a new room temperature multiferroic nanocomposite comprised of an ordered ferrimagnetic spinel α‐LiFe5O8 (LFO) and a ferroelectric perovskite BiFeO3 (BFO) is presented. It is observed that lithium (Li)‐doping in BFO favors the formation of LFO spinel as a secondary phase during the synthesis of LixBi1−xFeO3 ceramics. Multimodal functional and chemical imaging methods are used to map the relationship between doping‐induced phase separation and local ferroic properties in both the BFO‐LFO composite ceramics and self‐assembled nanocomposite thin films. The energetics of phase separation in Li doped BFO and the formation of BFO‐LFO composites are supported by first principles calculations. These findings shed light on Li's role in the formation of a functionally important room temperature multiferroic and open a new approach in the synthesis of light element doped nanocomposites for future energy, sensing, and memory applications. [ABSTRACT FROM AUTHOR]

Recently, in electric mobilities and stationary energy storage device applications, the development of long‐lasting, low‐cost, and high‐safety lithium‐ion batteries (LIBs) is widely studied. LiFePO4 (LFP) is a core cathode material for LIBs owing to its cost‐effectiveness and high safety. However, it exhibits low electronic conductivity and sluggish Li+ diffusion, hindering the application of LFP cathodes in high‐power battery industries. Herein, a triazole‐motivated electrolyte additive, 1‐(trimethylsilyl)−1H‐benzotriazole (TMSBTA) is presented, for mitigating iron dissolution via HF scavenging, reinforcing the robustness of the solid electrolyte interphase and constructing a cathode–electrolyte interface (CEI) to balance the ion and electron conduction of the CEI on the LFP cathode. Scanning probe microscopy performed in the conductive atomic force microscopy mode indicates that the electronically conductive CEI created by the oxidative decomposition of TMSBTA enables rapid and homogeneous lithiation and delithiation during cycling without morphological changes in the LFP particles. This study elucidates the design principles of the CEI on the LFP cathode and is expected to guide integrated electrolyte additive engineering for LFP‐containing LIBs. [ABSTRACT FROM AUTHOR]