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Probing and manipulating the intriguing nonlinear optical responses in van der Waals (vdW) ferroelectrics offer opportunities for their applications in nanophotonics. Here, we report the observation of giant and tunable second-harmonic generation (SHG) in ferroelectric CuInP 2 S 6 (CIPS) and CIPS/MoS 2 heterostructures. The results show that CIPS, ranging from multilayer to bulk-like samples, all exhibit strong SHG with giant anisotropy. The SHG anisotropy is attributed to the local strain along the a -axis that naturally exists in CIPS, as evidenced by piezoresponse force microscopy measurement. We further realized the strong modulation of SHG in CIPS by interfacing with monolayer MoS 2 . A combination of polarization, temperature, and thickness-dependent SHG and photoluminescence analyses shows that the nonlinear optical signal control in CIPS/MoS 2 heterostructures is unrelated to the polar symmetry of CIPS and MoS 2 but is driven by light absorption-mediated interfacial coupling. Our study provides a material platform based on vdW ferroelectric heterostructures for achieving dynamic control of nonlinear optical responses, which shows great potential applications in modern nanophotonics.

Metal-semiconductor interfaces are crucial components of optoelectronic and electrical devices, the performance of which hinges on intricate dynamics involving charge transport and mechanical interaction at the interface. Nevertheless, structural changes upon photoexcitation and subsequent carrier transportation at the interface, which crucially impact hot carrier stability and lifetime, remain elusive. To address this long-standing problem, they investigated the electron dynamics and resulting structural changes at the Au/TiO 2 interface using ultrafast electron diffraction (UED). The analysis of the UED data reveals that interlayer electron transfer from metal to semiconductor generates a strong coupling between the two layers, offering a new way for ultrafast heat transfer through the interface and leading to a coherent structural vibration that plays a critical role in propagating mechanical stress. These findings provide insights into the relationship between electron transfer and interfacial mechanical and thermal properties., (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

Rechargeable non-aqueous lithium-oxygen batteries (LOBs) have garnered increasing attention owing to their high theoretical energy density. However, their slow cathodic kinetics hinder efficient battery reactions. Nanoscale catalysts can effectively enhance electrocatalytic activity and atomic utilization efficiency. However, the agglomeration of nanoscale catalysts (such as cluster and single atoms) during continuous discharge/charge cycles leads to decreased electrochemical performance and poor cyclic stability. Herein, the ruthenium (Ru) atomic sites anchored on an O-doped molybdenum disulfide (O-MoS 2 ) catalyst (designated as Ru/O-MoS 2 ) was fabricated using a facile impregnation and calcination method. Strong Ru-O coupling between Ru atoms and the O-MoS 2 substrate optimizes the localized electronic structure, resulting in improved electrochemical performance and enhanced resistance to Ostwald ripening. When employed as a cathode catalyst for LOBs, Ru/O-MoS 2 catalyst exhibits a high reversible specific capacity (18700.5 (±59.8) mAh g -1 ), good rate capability, and enhanced long-term stability (115 cycles, 1200 h). This study encourages facile and efficient strategies for the development of effective and stable electrocatalysts for use in LOBs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Nickel-based catalysts are suitable for water splitting to generate hydrogen. However, the low conductivity and weak stability have always been urgent issues to be addressed in nickel-based catalysts. Fe-doped nickel oxide/nickel phosphide (Fe-NiO/Ni 2 P) was prepared as a bifunctional electrocatalyst by doping metal and constructing heterogeneous interface. The introduction of Fe contributed to the reinforced interfacial coupling effect of NiO/Ni 2 P to promote charge transfer and accelerate reaction kinetics. The heterojunction regulated the interfacial charge density between NiO and Ni 2 P to improve the electronic environment of Ni 2+ and enhance conductivity. The O-Fe-P bond at the heterogeneous interface induced the directional transfer of electrons and ensured the structure stability. The synergistic effect of Fe doping and heterogeneous interface increased the adsorption energy of *O and coordinated the adsorption energy of *H, advancing the catalytic performance. Fe-NiO/Ni 2 P exhibited the overpotential of 242 mV and 141 mV at 10 mA cm -2 for oxygen and hydrogen evolution, respectively., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Due to promising functionalities that may dramatically enhance spintronics performance, antiferromagnets are the subject of intensive research for developing the next-generation active elements to replace ferromagnets. In particular, the recent experimental demonstration of tunneling magnetoresistance and electrical switching using chiral antiferromagnets has sparked expectations for the practical integration of antiferromagnetic materials into device architectures. To further develop the technology to manipulate the magnetic anisotropies in all-antiferromagnetic devices, it is essential to realize exchange bias through the interface between antiferromagnetic multilayers. Here, the first observation on the omnidirectional exchange bias at an all-antiferromagnetic polycrystalline heterointerface is reported. This experiment demonstrates that the interfacial energy causing the exchange bias between the chiral-antiferromagnet Mn 3 Sn/collinear-antiferromagnet MnN layers is comparable to those found at the conventional ferromagnet/antiferromagnet interface at room temperature. In sharp contrast with previous reports using ferromagnets, the magnetic field control of the unidirectional anisotropy is found to be omnidirectional due to the absence of the shape anisotropy in the antiferromagnetic multilayer. The realization of the omnidirectional exchange bias at the interface between polycrystalline antiferromagnets on amorphous templates, highly compatible with existing Si-based devices, paves the way for developing ultra-low power and ultra-high speed memory devices based on antiferromagnets., (© 2024 The Authors. Advanced Materials published by Wiley‐VCH GmbH.)

The generally nonpolar SrTiO 3 has attracted more attention recently because of its possibly induced novel polar states and related paraelectric-ferroelectric phase transitions. By using controlled pulsed laser deposition, high-quality, ultrathin, and strained SrTiO 3 layers were obtained. Here, transmission electron microscopy and theoretical simulations have unveiled highly polar states in SrTiO 3 films even down to one unit cell at room temperature, which were stabilized in the PbTiO 3 /SrTiO 3 /PbTiO 3 sandwich structures by in-plane tensile strain and interfacial coupling, as evidenced by large tetragonality (∼1.05), notable polar ion displacement (0.019 nm), and thus ultrahigh spontaneous polarization (up to ∼50 μC/cm 2 ). These values are nearly comparable to those of the strong ferroelectrics as the PbZr x Ti 1- x O 3 family. Our findings provide an effective and practical approach for integrating large strain states into oxide films and inducing polarization in nonpolar materials, which may broaden the functionality of nonpolar oxides and pave the way for the discovery of new electronic materials.

The disadvantages of layered double hydroxides (LDHs) such as easy stacking, poor inherent conductivity, and limited versatility hinder their application in splitting water and zinc-air batteries (ZABs). Interface engineering to regulate the electron distribution of LDHs by introducing another component is a way to compensate for the poor electron transport capacity of LDHs during catalysis. Herein, a hierarchical structure is synthesized by assembling CoFe-LDH nanosheets onto the surface of layered N-doped porous carbon (NPC), CoFe-LDH@NPC, by using an interface engineering strategy. CoFe-LDH@NPC has high catalytic activity for the oxygen/hydrogen evolution reaction (OER/HER) with overpotentials of 280/100 mV, respectively. The two-electrode water splitting catalyzed by CoFe-LDH@NPC only needs 1.61 V to drive a current density of 10 mA cm -2 for 60 h. The theoretical results show that there is an electron-deficient/electron-rich interface between the NPC substrate and the CoFe-LDH in CoFe-LDH@NPC. The electrons on the coupling interface are easily transferred, which results in a change of the adsorption behavior of the reaction intermediates and improves the catalytic activity for the OER and HER. In addition, CoFe-LDH@NPC-catalyzed rechargeable flexible ZABs have excellent performance with low charge-discharge polarization (0.87 V) and a long-term stability of 65 h.

Van der Waals materials and their interfaces play critical roles in defining electrical contacts for nanoelectronics and developing vehicles for mechanoelectrical energy conversion. In this work, we propose a vertical strain engineering approach by enforcing pressure across the heterostructures. First-principles calculations show that the in-plane band structures of 2D materials such as graphene, h-BN, and MoS 2 as well as the electronic coupling at their contacts can be significantly modified. For the graphene/h-BN contact, a band gap in graphene is opened, while at the graphene/MoS 2 interface, the band gap of MoS 2 and the Schottky barrier height at contact diminish. Changes and transitions in the nature of contacts are attributed to localized orbital coupling and analyzed through the redistribution of charge densities, the crystal orbital Hamilton population, and electron localization, which yield consistent measures. These findings offer key insights into the understanding of interfacial interaction between 2D materials as well as the efficiency of electronic transport and energy conversion processes., (© 2023 IOP Publishing Ltd.)

Tin selenide (SnSe 2 ) is considered a promising anode of the lithium-ion battery because of its tunable interlayer space, abundant active sites, and high theoretical capacity. However, the low electronic conductivity and large volume variation during the charging/discharging processes inevitably result in inadequate specific capacity and inferior cyclic stability. Herein, a high-throughput wet chemical method to synthesize SnSe 2 /SnSe heterostructures is designed and used as anodes of lithium-ion batteries. The hierarchical nanoflower morphology of such heterostructures buffers the volume expansion, while the built-in electric field and metallic feature increase the charge transport capability. As expected, the superb specific capacity (≈911.4 mAh g -1 at 0.1 A g -1 ), high-rate performance, and outstanding cyclic stability are obtained in the lithium-ion batteries composed of SnSe 2 /SnSe anodes. More intriguingly, a reversible specific capacity (≈374.7 mAh g -1 at 2.5 A g -1 ) is maintained after 1000 cycles. The internal lithium storage mechanism is clarified by density functional theory (DFT) calculations and in situ characterizations. This work hereby provides a new paradigm for enhancing lithium-ion battery performances by constructing heterostructures., (© 2022 The Authors. Advanced Science published by Wiley-VCH GmbH.)

We designed an edge-sites 2D/0D/2D based TiO 2 @Au/g-C 3 N 4 Z-scheme photocatalytic system consists of highly exposed (001) TNSs@Au edge-site heterojunction, and the Au/g-C 3 N 4 interfacial heterojunction. The designed photocatalyst was prepared by a facile and controlled hydrothermal synthesis strategy via in-situ nanoclusters-to-nanoparticles deposition technique and programable calcination in N 2 atmosphere to get edge-site well-crystalline interface, followed by chemically bonded thin overlay of g-C 3 N 4 . Photocatalytic performance of the prepared TNSs@Au/g-C 3 N 4 catalyst was evaluated by the photocatalytic degradation of organic pollutants in water under visible light irradiation. The results obtained from structural and chemical characterization conclude that the inter-facet junction between highly exposed (001) and (101) TNSs surface, and TNSs@Au interfacial heterojunction formed by a direct contact between highly crystalline TNSs and Au, are the key factors to enhance the separation efficiency of photogenerated electrons/holes. On coupling with overlay of g-C 3 N 4 2D NSs synergistically offer tremendous reactive sites for the potential photocatalytic dye degradation in the Z-scheme photocatalyst. Particularly in the designed photocatalyst, Au nanoparticles accumulates and transfer the photo-stimulated electrons originated from anatase TNSs to g-C 3 N 4 via semiconductor-metal heterojunction. Because of the large exposed reactive 2D surface, overlay g-C 3 N 4 sheets not only trap photoelectrons, but also provide a potential platform for increased adsorption capacities for organic contaminants. This work establishes a foundation for the development of high-performance Z-scheme photocatalytic systems., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2022 Hong, Anwer, Wu, Deng and Qian.)

Metal-organic frameworks (MOFs) fillers are emerging for composite polymer electrolytes (CPEs). Enhancing Lewis acid-base interaction (LABI) among MOFs, polymer and Li-salt is expected to promote Li + -transport. However, it is unclear how to customize a strong LABI interface. The large surface-area of classical MOFs also interferes with clarifying the LABI influence on Li + -transport. Herein, Bi 3+ as metal centers to design colloidal-dispersed nonporous MOFs (Bi/HMT-MOFs) nanowire with a surface-area of only 17.13 m 2 g -1 to prepare polyethylene oxide (PEO)-based CPEs (BMCPE) is chosen. The nonporous feature can exclude the surface-area effect on Li + -transport. More interestingly, Bi 3+ is a typical borderline acid, which can interact with both hard-basic PEO and soft-basic Li-salt anion. Accordingly, Bi/HMT-MOFs are uniformly dispersed in the BMCPE to form a strong LABI interface with PEO and Li-salt, promoting Li-salt dissociation and providing rapid Li + -transport channels. Despite the ultralow surface-area of Bi/HMT-MOFs, BMCPE exhibits significantly enhanced ion-conductivity and Li + transference number, which completely rival traditional MOFs-filled CPEs. BMCPE also enables symmetric and full cells with excellent high-rate performance and long-term cycling stability. In contrast, when Bi 3+ sites are obscured, electrochemical performances are obviously decreased. Therefore, employing borderline metal centers will be an effective strategy to construct a LABI interface for high-performance MOFs-filled CPEs., (© 2022 Wiley-VCH GmbH.)

The construction of heterostructures is a versatile tactic to enhance catalytic activity. However, it is still elusive to realize the modulation of the interlayer spacing in this way to further improve the performance. Here, strong interfacial coupling between CoSe 2 and MoSe 2 by constructing CoSe 2 /MoSe 2 heterostructures is achieved. The interlayer spacing of MoSe 2 is compressed by 0.3 Å. The enhanced charge transfer is validated by X-ray absorption spectroscopy and X-ray photoelectron spectroscopy. Coupled with the morphology of hollow microtubes, which can facilitate the exposure of active sites, CoSe 2 /MoSe 2 heterostructures reported here exhibit high activity (119 mV at 10 mA cm -2 ) and excellent stability with small degradation after 50 h operation, surpassing other analogous powdered electrocatalysts. This work sheds light on the importance of tuning the interlayer spacing to improve electrocatalytic activity., (© 2022 Wiley-VCH GmbH.)

Developing efficient electrocatalysts to realize the nitrate reduction reaction (eNO 3 - RR) for ammonia synthesis as an alternative to the traditional Haber-Bosch production process is of great significance. Herein, the heterostructured Bi 2 S 3 /MoS 2 nanoarrays were successfully synthesized by Bi 2 S 3 nanosheets. Owing to the interfacial coupling effect, both particular surface area and exposure active sites increase. Density functional theory further uncovered that the excellent activity originates from charge transfer of the interface and a low potential barrier of 0.58 eV for hydrogenation of *NO to *NOH on Bi 2 nanosheets. Owing to the interfacial coupling effect, both particular surface area and exposure active sites increase. Density functional theory further uncovered that the excellent activity originates from charge transfer of the interface and a low potential barrier of 0.58 eV for hydrogenation of *NO to *NOH on Bi 2 S 3 /MoS 2 . Compared with pure Bi 2 S 3 and MoS 2 catalysts, the heterostructured Bi 2 S 3 /MoS 2 nanoarrays exhibit a superior NH 3 yield of 15.04 × 10 -2 mmol·h -1 ·cm -2 and a Faraday efficiency of 88.4% at -0.8 V versus the reversible hydrogen electrode. This work provides a new avenue to explore advanced electrocatalysts, which is expected to shorten the distance from the practical application of the eNO 3 - RR technology.

The development of hydrogen sensors is of paramount importance for timely leak detection and remains a crucial unmet need. Palladium-based materials, well known as hydrogen sensors, still suffer from poisoning and deactivation. Here, a hybrid hydrogen sensor consisting of a Pd nanocluster (NC) film, a metal-organic framework (MOF), and a polymer, are proposed. The polymer coating, as a protection layer, endows the sensor with excellent H 2 selectivity and CO-poisoning resistance. The MOF serves as an interface layer between the Pd NC film and the polymer layer, which alters the nature of the interaction with hydrogen and leads to significant sensing performance improvements, owing to the interfacial electronic coupling between Pd NCs and the MOF. The strategy overcomes the shortcomings of retarded response speed and degraded sensitivity induced by the polymer coating of a Pd NC film-polymer hybrid system. This is the first exhibition of a hydrogen-sensing enhancement mechanism achieved by engineering the electronic coupling between Pd and a MOF. The work establishes a deep understanding of the hydrogen-sensing enhancement mechanism at the nanoscale and provides a feasible strategy to engineer next-generation gas-sensing nanodevices with superior sensing figures of merit via hybrid material systems., (© 2022 Wiley-VCH GmbH.)

The use of cheap and efficient electrocatalyst for the production of hydrogen is the key to solving the current energy crisis. Herein, we used a two-step hydrothermal process to fabricate noble-metal-free 3D net-like Ni 3 (VO 4 ) 2 ultrathin nanosheets coupled with MoS 2 @CFC interface. Unlike the traditional two-dimensional composite materials, Ni 3 (VO 4 ) 2 ultrathin nanosheets intersect with MoS 2 nanosheets grown on CFC in a 3D net-like structure (Ni 3 (VO 4 ) 2 /MoS 2 @CFC). Due to the mutual combination of structures and the interfacial coupling cooperation effect between Ni 3 (VO 4 ) 2 nanosheet and MoS 2 @CFC, the catalytically active area was expanded, and the intrinsic activity toward HER was significantly improved. Ni 3 (VO 4 ) 2 /MoS 2 @CFC showed high activity at the industrial temperature (75 °C), with an overpotential of 77 mV (10 mA/cm 2 ) and a 65 mV/dec Tafel slope. This material showed good stability at 0.5 M H 2 SO 4 . This work provides a heterostructure scheme for the construction of a novel noble metal-free electrocatalyst to promote hydrogen evolution reaction., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

The half-metallic manganite oxide La 2/3 Sr 1/3 MnO 3 (LSMO) has a very high spin polarization of ∼100%, making it ideal for ferromagnetic electrodes to realize tunneling magnetoresistance (TMR). Because of the in-plane magnetic anisotropy of the ferromagnetic LSMO electrode, which leads to the density limit of memory, realizing perpendicular tunneling in manganite-based magnetic tunnel junctions (MTJ) is critical for future applications. Here, we design and fabricate manganite-based MTJs composed of alternately stacked cobaltite and manganite layers that demonstrate strong perpendicular magnetic anisotropy (PMA) induced by interfacial coupling. Moreover, spin-dependent tunneling behaviors with an out-of-plane magnetic field were observed in the perpendicular MTJs. We found that the direct tunneling effect plays a dominant role in the low bias region during the transport behavior of devices, which is associated with thermionic emission of electrons or oxygen vacancies in the high bias region. Our works of realizing perpendicular tunneling in manganite-based MTJs lead to new approaches for designing and developing all-oxide spintronic devices.

In recent years, two-dimensional (2D) magnetic heterostructures have captured widespread interest as they provide a fertile ground for exploring the novel properties induced by interfacial magnetic coupling, modulating the intrinsic magnetism of the 2D magnet, and exploiting new spintronic device applications. In this Spotlight on Applications, dominating synthetic strategies employed to fabricate 2D magnetic heterostructures are introduced first. Notably, we then concentrate on two different kinds of magnetic interfaces, namely, the magnetic-nonmagnetic interface and the magnetic-magnetic interface. Specifically, various interface modulated magnetisms such as valley splitting and the anomalous Hall effect as well as their related device applications such as magnetic tunnel junctions have been further reviewed and discussed. Finally, we briefly summarize the recent progress of 2D magnetic heterostructures and outline the future development direction of this booming field.

A comprehensive understanding of the roles of various nanointerfaces in thermal transport is of critical significance but remains challenging. A two-dimensional van der Waals (vdW) heterostructure with tunable interface lattice mismatch provides an ideal platform to explore the correlation between thermal properties and nanointerfaces and achieve controllable tuning of heat flow. Here, we demonstrate that interfacial engineering is an efficient strategy to tune thermal transport via systematic investigation of the thermal conductance ( G ) across a series of large-area four-layer stacked vdW materials using an improved polyethylene glycol-assisted time-domain thermoreflectance method. Owing to its rich interfacial mismatch and weak interfacial coupling, the vertically stacked MoSe 2 -MoS 2 -MoSe 2 -MoS 2 heterostructure demonstrates the lowest G of 1.5 MW m -2 K -1 among all vdW structures. A roadmap to tune G via homointerfacial mismatch, interfacial coupling, and heterointerfacial mismatch is further demonstrated for thermal tuning. Our work reveals the roles of various interfacial effects on heat flow and highlights the importance of the interfacial mismatch and coupling effects in thermal transport. The design principle is also promising for application in other areas, such as the electrical tuning of energy storage and conversion and the thermoelectricity tuning of thermoelectronics.

The interfacial chemistry of nanocomposite materials is of overarching importance in the separation and purification science; moreover, its understanding helps to guide synthesis, clarify structure-property relationship and unearth novel applications. However, the composites feature rather complicated local structures and hydrogen bonds are often involved in the interface and the vicinity of active sites. In this regard, density functional theory first-principle calculations associated with experimental study have synergistically examined two-dimensional (2D) magnesium hydroxide material with different layers and their adsorption toward cellobiose. Hydrogen bonds are found responsible for the interfacial coupling, which make it vital to cover the dispersion correction in the calculation. The average adsorption energy ranges from -0.29 to -0.35 eV, falling well within the range of reported hydrogen-bonding strength. On the basis of calculated structural/interfacial properties and experimental findings, the 2D Mg(OH) 2 in terms of three-layer model was unraveled to substitute toxic Cd 2+ ion and sorb radioactive UO 2 2+ that is coordinated by water and hydroxyl groups. These reactions are thermodynamically feasible. The ion-exchanging mechanism was proposed for cadmium removal and the outer-sphere adsorption one for uranium extraction., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Rational design and highly efficient dual-functional catalyst are still difficult to develop for electrocatalytic oxygen evolution reaction and degradation of RhB dye pollutant. Herein, we report a highly efficient "bandgap matching and interfacial coupling" strategy to synthesize nano-assembled ultrathin layered MoS 2 @NiFe 2 O 4 (MS@NiFeO) bifunctional catalyst constructed by the hydrothermal route and subsequently amine-hydrolysis. The OER performance of the prepared MS@NiFeO catalyst delivers a low overpotential of 290 mV at 10 mA/cm 2 and Tafel slope is 69.2 mV dec -1 in an alkaline solution. In addition, the nano-assembled ultrathin layered structure of MS@NiFeO showed a highly efficient (96.37%) RhB dye degradation performance than that of MoS 2 nanosheets and NiFe 2 O 4 nanostructures. Unique nanostructure of ultrathin layered MS@NiFeO with suitable band matching, interfacial charge transfer, high surface area and more active sites favored for the enhancement of the catalytic activity. This work presents an unpretentious construction and low-cost production strategy to synthesize bifunctional hybrid catalyst for oxygen evolution reaction as well as degradation of organic pollutant with superior efficiency and longer stability., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Inc. All rights reserved.)

It is of great importance to develop useful methods to evaluate interfacial coupling strength noninvasively for exploring and optimizing heterointerface functionality. Recently, organic-inorganic van der Waals (vdW) heterostructures (HSs) composed of organic semiconductors and transition-metal dichalcogenides (TMD) have shown great potential for developing next-generation flexible optical, electrical, and optoelectrical devices. Since vdW coupling dominates the property of such a vdW HS, it is crucial to develop a method to evaluate its interfacial coupling strength noninvasively. In this work, by combining electrical force microscopy (EFM) and Raman and photoluminescence spectroscopic measurements, we were able to directly probe the coupling strength between monolayer MoSe 2 and a copper phthalocyanine (CuPc) thin film. Especially, we also found a new Raman mode in HS due to the Davydov splitting of the CuPc thin film via strong interfacial coupling between the two materials. This new Raman mode was thus utilized as a probe to reveal the modulation of the coupling strength by changing post-treatment conditions. All of these results indicate that the method developed here is capable of evaluating the coupling strength of the MoSe 2 /CuPc HS effectively and innovatively, which aids in providing deep insights into such hybrid vdW HSs for future optical and optoelectrical applications.

We characterize the magnetic interfacial coupling of the Fe/FeGe heterostructure and its influence on the magnetic damping via ferromagnetic resonance in the temperature range of 200-300 K. When the temperature is below the critical temperature of FeGe, the interfacial coupling rises. The strength of the magnetic interfacial coupling is determined as a function of the temperature and reaches up to 0.194 erg/cm 2 at 200 K. Meanwhile, the Gilbert damping of the Fe layer is enhanced from 0.035 at 300 K to 0.050 at 200 K. The enhancement is linearly proportional to the strength of magnetic interfacial coupling. We attribute the enhancement to the interfacial coupling that transfers spin angular momentum from Fe to FeGe via the exchange interaction. Our results reveal that the interfacial coupling is an effective approach to inject spin current into the chiral spin texture.

The oxygen octahedral rotation around the out-of-plane axis is explored to study its effect on metastable status, magnetic cluster glass in manganite. The antiphase rotation around the out-of-plane axis (TiO 6 a 0 a 0 c - ) of SrTiO 3 substrate on material properties is obvious with a large irreversible MR effect for thin films, which fades away with the increase in film thickness. At 10 K, the irreversible MR is 0.91 for the 12 nm film and 0.22 for the 30 nm film. This work extends current understanding on interfacial coupling to metastable status and could help explore other systems in the perovskite structure with octahedral rotation.0.67 Sr 0.33 MnO 3 film on the (001) SrTiO 3 substrate, which together promote the formation of magnetic cluster-glassiness and enlarges the irreversible magnetoresistance (MR) effect with enhanced relaxation time of charge carriers. The effect of TiO 6 a 0 a 0 c - in the SrTiO 3 substrate on material properties is obvious with a large irreversible MR effect for thin films, which fades away with the increase in film thickness. At 10 K, the irreversible MR is 0.91 for the 12 nm film and 0.22 for the 30 nm film. This work extends current understanding on interfacial coupling to metastable status and could help explore other systems in the perovskite structure with octahedral rotation.

Disorder-induced magnetoresistance (MR) effect is quadratic at low perpendicular magnetic fields and linear at high fields. This effect is technologically appealing, especially in 2D materials such as graphene, since it offers potential applications in magnetic sensors with nanoscale spatial resolution. However, it is a great challenge to realize a graphene magnetic sensor based on this effect because of the difficulty in controlling the spatial distribution of disorder and enhancing the MR sensitivity in the single-layer regime. Here, a room-temperature colossal MR of up to 5000% at 9 T is reported in terraced single-layer graphene. By laminating single-layer graphene on a terraced substrate, such as TiO 2 -terminated SrTiO 3 , a universal one order of magnitude enhancement in the MR compared to conventional single-layer graphene devices is demonstrated. Strikingly, a colossal MR of >1000% is also achieved in the terraced graphene even at a high carrier density of ≈10 12 cm -2 . Systematic studies of the MR of single-layer graphene on various oxide- and non-oxide-based terraced surfaces demonstrate that the terraced structure is the dominant factor driving the MR enhancement. The results open a new route for tailoring the physical property of 2D materials by engineering the strain through a terraced substrate., (© 2020 Wiley-VCH GmbH.)

Highly efficient oxygen evolution driven by abundant sunlight is a key to realize overall water splitting for large-scale conversion of renewable energy. Here, we report a strategy for the interfacial atomic and electronic coupling of layered CoOOH and BiVO 4 to deactivate the surface trapping states and suppress the charge-carrier recombination for high photoelectrochemical (PEC) water oxidation activity. The successful synthesis of a 3D ultrathin-CoOOH-overlayer-coated coral-like BiVO 4 photoanode effectively tailors the migration route of photocarriers on the semiconductor/liquid interface to realize a great increase of ∼200% in the photovoltage relative to bare BiVO 4 , consequently decreasing the corresponding onset potential of PEC water splitting from 0.60 to 0.20 V RHE . As a result, the unique CoOOH/BiVO 4 photoanode could efficiently perform PEC water oxidation in a neutral aqueous solution (pH = 7) with a high photocurrent density of 4.0 mA/cm 2 at 1.23 V RHE and a prominent quantum efficiency of 65% at 450 nm. Electronic structural characterizations and theoretical calculations reveal that the combination of layered CoOOH and BiVO 4 forming interfacial oxo-bridge bonding could greatly eliminate surface trapping states and promote the direct transfer of photogenerated holes from the valence band to the surface water redox potential for water oxidation.

Interfaces with subtle differences in atomic and electronic structures in perovskite ABO3 heterostructures often yield intriguingly different properties, yet their exact roles remain elusive. Here, we report an integrated study of unusual transport, magnetic, and structural properties of Pr0.67Sr0.33MnO3 film on SrTiO3 substrate. The variations in the out-of-plane lattice constant and BO6 octahedral rotation across the Pr0.67Sr0.33MnO3/SrTiO3 interface strongly depend on the thickness of the Pr0.67Sr0.33MnO3 film. In the 12 nm film, a new interface-sensitive ferromagnetic polaronic insulator (FI') phase is formed during the cubic-to-tetragonal phase transition of SrTiO3, apparently due to the enhanced electron-phonon interaction and atomic disorder in the film. The transport properties of the FI' phase in the 30 nm film are masked because of the reduced interfacial coupling and smaller interface-to-volume ratio. This work demonstrates how thickness-dependent interfacial coupling leads to the formation of a theoretically predicted ferromagnetic-polaronic insulator, as illustrated in a new phase diagram, that is otherwise ferromagnetic metal (FM) in bulk form.

The magnetic properties of the all-oxide multiferroic heterostructures composed of orthorhombic YMnO3 (YMO) with E-type antiferromagnetic and double-exchange ferromagnetic (FM) La0.6Sr0.4MnO3 (LSMO) were studied. An orientation-modulated exchange bias effect, which is related to the interfacial Mn-O-Mn bond angle, was discovered. Because of the large bond angle in YMO/LSMO(100) heterostructures, a strong exchange coupling at the interface is formed. This strong exchange coupling sustains an FM phase in YMO at the interface region. The FM phase with strong magnetocrystalline anisotropy contributes to the vertical shift and exchange bias effect in (100) orientation heterostructures. When LSMO (110) and (111) were layered with YMO, the Mn-O-Mn bond angle was reduced, leading to a weakened exchange coupling at the interface, and only a relatively small exchange bias at low temperatures was visible.

The superlattice of energetically stable La2/3Sr1/3MnO3 and tetragonal BiFeO3 is investigated by means of density functional theory. The superlattice as a whole exhibits a half-metallic character, as is desired for spintronic devices. The interfacial electronic states and exchange coupling are analyzed in details. We demonstrate that the interfacial O atoms play a key role in controlling the coupling. The higher ferroelectricity of tetragonal BiFeO3 and stronger response to the magnetic moments in the La2/3Sr1/3MnO3/BiFeO3 superlattice show a strongly enhanced electric control of the magnetism as compared to the rhombohedral one. Therefore, it is particularly practical interest in the magnetoelectrically controlled spintronic devices.