A Facile and Effective Design for Dynamic Thermal Management Based on Synchronous Solar and Thermal Radiation Regulation.

Passive solar heating and radiative cooling have attracted great interest in global energy consumption reduction due to their unique electricity-free advantage. However, static single radiation cooling or solar heating would lead to overcooling or overheating in cold and hot weather, respectively. To achieve a facile, effective approach for dynamic thermal management, a novel structured polyethylene (PE) film was engineered with a switchable cooling and heating mode obtained through a moisture transfer technique. The 100 µm PE film showed excellent solar modulation from 0.92 (dried state) to 0.32 (wetted state) and thermal modulation from 0.86 (dried state) to 0.05 (wetted state). Outdoor experiments demonstrated effective thermal regulation during both daytime and nighttime. Furthermore, our designed PE film can save 1.3-41.0% of annual energy consumption across the whole country of China. This dual solar and thermal regulation mechanism is very promising for guiding scalable approaches to energy-saving temperature regulation.

Extreme lithium-metal cycling enabled by a mixed ion- and electron-conducting garnet three-dimensional architecture.

The development of solid-state Li-metal batteries has been limited by the Li-metal plating and stripping rates and the tendency for dendrite shorts to form at commercially relevant current densities. To address this, we developed a single-phase mixed ion- and electron-conducting (MIEC) garnet with comparable Li-ion and electronic conductivities. We demonstrate that in a trilayer architecture with a porous MIEC framework supporting a thin, dense, garnet electrolyte, the critical current density can be increased to a previously unheard of 100 mA cm-2, with no dendrite-shorting. Additionally, we demonstrate that symmetric Li cells can be continuously cycled at a current density of 60 mA cm-2 with a maximum per-cycle Li plating and stripping capacity of 30 mAh cm-2, which is 6× the capacity of state-of-the-art cathodes. Moreover, a cumulative Li plating capacity of 18.5 Ah cm-2 was achieved with the MIEC/electrolyte/MIEC architecture, which if paired with a state-of-the-art cathode areal capacity of 5 mAh cm-2 would yield a projected 3,700 cycles, significantly surpassing requirements for commercial electric vehicle battery lifetimes.

Optical and Photocatalytic Properties of Cobalt-Doped LuFeO3 Powders Prepared by Oxalic Acid Assistance.

B-site cobalt (Co)-doped rare-earth orthoferrites ReFeO3 have shown considerable enhancement in physical properties compared to their parent counterparts, and Co-doped LuFeO3 has rarely been reported. In this work, LuFe1-xCoxO3 (x = 0, 0.05, 0.1, 0.15) powders have been successfully prepared by a mechanochemical activation-assisted solid-state reaction (MAS) method at 1100 °C for 2 h. X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy studies demonstrated that a shrinkage in lattice parameters emerges when B-site Fe ions are substituted by Co ions. The morphology and elemental distribution were investigated by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). The UV-visible absorbance spectra show that LuFe0.85Co0.15O3 powders have a narrower bandgap (1.75 eV) and higher absorbance than those of LuFeO3 (2.06 eV), obviously improving the light utilization efficiency. Additionally, LuFe0.85Co0.15O3 powders represent a higher photocatalytic capacity than LuFeO3 powders and can almost completely degrade MO in 5.5 h with the assistance of oxalic acid under visible irradiation. We believe that the present study will promote the application of orthorhombic LuFeO3 in photocatalysis.

3D Asymmetric Bilayer Garnet-Hybridized High-Energy-Density Lithium-Sulfur Batteries.

Lithium garnet Li7La3Zr2O12 (LLZO), with high ionic conductivity and chemical stability against a Li metal anode, is considered one of the most promising solid electrolytes for lithium-sulfur batteries. However, an infinite charge time resulting in low capacity has been observed in Li-S cells using Ta-doped LLZO (Ta-LLZO) as a solid electrolyte. It was observed that this cell failure is correlated with lanthanum segregation to the surface of Ta-LLZO that reacts with a sulfur cathode. We demonstrated this correlation by using lanthanum excess and lanthanum deficient Ta-LLZO as the solid electrolyte in Li-S cells. To resolve this challenge, we physically separated the sulfur cathode and LLZO using a poly(ethylene oxide) (PEO)-based buffer interlayer. With a thin bilayer of LLZO and the stabilized sulfur cathode/LLZO interface, the hybridized Li-S batteries achieved a high initial discharge capacity of 1307 mA h/g corresponding to an energy density of 639 W h/L and 134 W h/kg under a high current density of 0.2 mA/cm2 at room temperature without any indication of a polysulfide shuttle. By simply reducing the LLZO dense layer thickness to 10 µm as we have demonstrated before, a significantly higher energy density of 1308 W h/L and 257 W h/kg is achievable. X-ray diffraction and X-ray photoelectron spectroscopy indicate that the PEO-based interlayer, which physically separates the sulfur cathode and LLZO, is both chemically and electrochemically stable with LLZO. In addition, the PEO-based interlayer can adapt to the stress/strain associated with sulfur volume expansion during lithiation.

Electronic properties and interfacial contact of graphene/CrSiTe3 van der Waals heterostructures.

The electronic properties and interfacial contact of the graphene-based heterostructure graphene/CrSiTe3 (Gr/CrSiTe3) are modulated by tuning the interfacial distance, along with application of an external electric field. Our first-principles calculations show that the gap is enlarged to 27.6 meV in Gr/CrSiTe3 when the interfacial distance is reduced to a distance of 2.75 Å. Gr/CrSiTe3 changes from an n-type to a p-type Schottky contact with a decrease in interfacial space. The most significant effect of applying a positive electric field is the presence of a p-type Schottky contact along with an increase of interfacial charge transfer to graphene, while an electric field in the opposite direction enhances the n-type Schottky contact effectively with a decrease of interfacial charge transfer to graphene. The Schottky contact transforms into an Ohmic contact when a positive electric field of 0.41 eV Å-1 is applied to this interface. The work proposes an approach to manipulate the interfacial properties, which can be very useful for future experimental studies and graphene-based interfaces.

H2S detection at low temperatures by Cu2O/Fe2O3 heterostructure ordered array sensors.

2D heterostructures are promising gas sensor materials due to their surface/interface effects and hybrid properties. In this research, Cu2O/Fe2O3 heterostructure ordered arrays were synthesized using an in situ electrodeposition method for H2S detection at low temperatures. These arrays possess a periodic long range ordered structure with horizontal multi-heterointerfaces, leading to superior gas sensitivity for synergistic effects at the heterointerfaces. The sensor based on the Cu2O/Fe2O3 heterostructure ordered arrays exhibits a dramatic improvement in H2S detection at low temperatures (even as low as -15 °C). The response is particularly significant at room and human body temperatures since the conductivity of the arrays can change by up to three orders of magnitude in a 10 ppm H2S atmosphere. These good performances are also attributed to the formation of metallic Cu2S conducting channels. Our results imply that the Cu2O/Fe2O3 heterostructure ordered arrays are promising candidates for high-performance H2S gas sensors that function at low temperatures as well as breath analysis systems for disease diagnosis.

Topological edge states in high-temperature superconductiving FeSe/SrTiO3 films with Te substitution.

Using first principles theory, we investigated the behavior of the one-dimensional (1D) topological edge states of high temperature superconductiviing FeSe/SrTiO3 films with Te atoms substitution to Se atoms in the bottom (top) layer in single-layer FeSe, as a function of strain. It was discovered that the 1D topological edge states are present in single-unit-cell FeSe film on SrTiO3, but are absent when more than 50% Se atoms are replaced by Te atoms. Stress induced displacive phase transformation exists in FeSe/SrTiO3 film when Te atoms substitute Se atoms in the bottom (top) layer in single-layer FeSe under 3% strain respectively. The 1D topological edge states are present under 3% (1.8%) strain in FeSe/SrTiO3 films with Te substitution Se in the bottom (top) layer in single-layer FeSe, even up to 5%, respectively. This indicates that the bonding angle of Se-Fe-Se (Te) and the distance of Te (or Se) atoms to the Fe plane are correlated with the topological edge states. Our findings provide an effective interface system that provides both superconducting and topological states, opening a new route for realizing 2D topological superconductors with proximity effect.

Prevention of Hydrogen Damage Using MoS2 Coating on Iron Surface.

The prevention of hydrogen penetration into steels can effectively protect steels from hydrogen damage. In this study, we investigated the effect of a monolayer MoS2 coating on hydrogen prevention using first-principles calculations. We found that monolayer MoS2 can effectively inhibit the dissociative adsorption of hydrogen molecules on an Fe(111) surface by forming a S⁻H bond. MoS2 coating acts as an energy barrier, interrupting hydrogen penetration. Furthermore, compared with the H-adsorbed Fe(111) film, the work function of the MoS2-coated film significantly increases under both equilibrium and strained conditions, indicating that the strained Fe(111) film with the MoS2 coating also becomes more corrosion resistant. The results reveal that MoS2 film is an effective coating to prevent hydrogen damage in steels.

Full Dissolution of the Whole Lithium Sulfide Family (Li2 S8 to Li2 S) in a Safe Eutectic Solvent for Rechargeable Lithium-Sulfur Batteries.

The lithium-sulfur battery is an attractive option for next-generation energy storage owing to its much higher theoretical energy density than state-of-the-art lithium-ion batteries. However, the massive volume changes of the sulfur cathode and the uncontrollable deposition of Li2 S2 /Li2 S significantly deteriorate cycling life and increase voltage polarization. To address these challenges, we develop an ϵ-caprolactam/acetamide based eutectic-solvent electrolyte, which can dissolve all lithium polysulfides and lithium sulfide (Li2 S8 -Li2 S). With this new electrolyte, high specific capacity (1360 mAh g-1 ) and reasonable cycling stability are achieved. Moreover, in contrast to conventional ether electrolyte with a low flash point (ca. 2 °C), such low-cost eutectic-solvent-based electrolyte is difficult to ignite, and thus can dramatically enhance battery safety. This research provides a new approach to improving lithium-sulfur batteries in aspects of both safety and performance.

Improved visible-light absorbance of monolayer MoS2 on AlN substrate and its angle-dependent electronic structures.

In this paper, we performed density functional theory (DFT) calculations to investigate the geometric structures, electronic structures and visible-light absorbance of MoS2/AlN heterostructure based on van der Waals interaction. The calculated formation energy indicated that the designed MoS2/AlN heterostructure could be experimentally prepared. The Mo-N stacked MoS2/AlN heterostructure exhibited more considerable optical absorption in visible-light region than MoS2 and AlN monolayers. More interestingly, the band gaps were sensitive to strain, which led to an obvious shift of optical absorption spectra along the direction of the infrared region. The two most energetically favorable twisted MoS2/AlN heterostructures (Mo-N and Mo-HAl) had similar band structures, which were different from the non-twisted MoS2/AlN heterostructure. With different rotation angles, their band structures all exhibited an indirect band gap and almost had the same values of indirect band gaps, indicating that the indirect band gaps had no clear dependence on rotation angles.

First-principles prediction of two-dimensional metal bis(dithiolene) complexes as promising gas sensors.

The recently synthesized two-dimensional metal bis(dithiolene) complex (MDT), a kind of metal-organic framework with a kagome lattice structure, has been found to be a promising material for electronic devices. Here we report the surface adsorption effects of gas molecules on the electronic properties and transport behaviors of two-dimensional MDT (M = Fe, Co, Ni, Pd, and Pt) films. The first-principles results reveal that the MDT nanosheets are selectively sensitive to different adsorbed molecules, such as CO, NO, and O2 molecules. All the studied gas molecules can be chemically adsorbed on the ferromagnetic FeDT and CoDT nanosheets, whereas the non-magnetic PdDT and PtDT films are only sensitive to NO molecules, showing quite weak interaction with CO and O2. The physisorption of CO on PdDT and PtDT originates from the mismatch of energy levels between the metal dz2 orbitals and the CO σ orbitals. In contrast, the Pd and Pt dxz and dyz orbitals can well align with the NO π* orbitals, causing strong chemisorption. More importantly, the adsorption of NO on PdDT and PtDT not only induces a magnetism of 1.0 µB for the two films but also greatly enhances the conductivity. In the case of PtDT, we observe a transition from the semiconducting to the metallic phase on NO adsorption. This significant change in the electronic structure can be understood from the adsorption-induced interfacial charge transfer and the strong orbital hybridization between the metal d states and the NO π* states. Our results suggest the potential application of the PdDT and PtDT nanosheets in gas sensing and spintronics.

Strain induced band inversion and topological phase transition in methyl-decorated stanene film.

The researches for new quantum spin Hall (QSH) insulators with large bulk energy gap are of much significance for their practical applications at room temperature in electronic devices with low-energy consumption. By means of first-principles calculations, we proposed that methyl-decorated stanene (SnCH3) film can be tuned into QSH insulator under critical tensile strain of 6%. The nonzero topological invariant and helical edge states further confirm the nontrivial nature in stretched SnCH3 film. The topological phase transition originates from the s-p xy type band inversion at the Γ point with the strain increased. The spin-orbital coupling (SOC) induces a large band gap of ~0.24 eV, indicating that SnCH3 film under strain is a quite promising material to achieve QSH effect. The proper substrate, h-BN, finally is presented to support the SnCH3 film with nontrivial topology preserved.

Effect of Cr-doping on the electronic structure and work function of α-Fe2O3 thin films.

We investigate the effect of Cr-doping on the properties of α-Fe2O3(001) thin films with Fe termination using the local density approximation plus a Hubbard U correction. We find that both the doping site and concentration of Cr atoms dramatically affect the electronic structure and work function (WF) of α-Fe2O3 films. The results demonstrate that it is most energetically favorable for Cr atoms to substitute the Fe atoms in the sub-surface of α-Fe2O3 thin films. The doping of Cr atoms in the sub-surface not only lowers the band gap of the film but also greatly enhances the work function by 0.9 eV with respect to the pure α-Fe2O3 film. The increase of WF correlates with the reduction of occupied O px/py states at the top valence band which leads to a decrease of the Fermi energy. As the Cr concentration changes from 4.2% to 16.7%, the WF firstly increases, and then drops. The WF reaches a maximum of 6.61 eV for the Cr concentration of 8.3%. These results suggest that doping Cr atoms in a α-Fe2O3(001) thin film can increase the corrosion potential and benefits the protection of steel from corrosion.

Strain Effect on Electronic Structure and Work Function in α-Fe2O3 Films.

We investigate the electronic structure and work function modulation of α-Fe2O3 films by strain based on the density functional method. We find that the band gap of clean α-Fe2O3 films is a function of the strain and is influenced significantly by the element termination on the surface. The px and py orbitals keep close to Fermi level and account for a pronounced narrowing band gap under compressive strain, while unoccupied dz2 orbitals from conduction band minimum draw nearer to Fermi level and are responsible for the pronounced narrowing band gap under tensile strain. The spin polarized surface state, arising from localized dangling-bond states, is insensitive to strain, while the bulk band, especially for pz orbital, arising from extended Bloch states, is very sensitive to strain, which plays an important role for work function decreasing (increasing) under compressive (tensile) strain in Fe termination films. In particular, the work function in O terminated films is insensitive to strain because pz orbitals are less sensitive to strain than that of Fe termination films. Our findings confirm that the strain is an effective means to manipulate electronic structures and corrosion potential.

Highly sensitive H2S sensors based on Cu2O/Co3O4 nano/microstructure heteroarrays at and below room temperature.

Gas sensors with high sensitivity at and below room temperature, especially below freezing temperature, have been expected for practical application. The lower working temperature of gas sensor is better for the manufacturability, security and environmental protection. Herein, we propose a H2S gas sensor with high sensitivity at and below room temperature, even as low as -30 °C, based on Cu2O/Co3O4 nano/microstructure heteroarrays prepared by 2D electrodeposition technique. This heteroarray was designed to be a multi-barrier system, and which was confirmed by transmission electron microscopy, scanning electron microscopy, X-ray photoelectron spectroscopy and scanning probe microscopy. The sensor demonstrates excellent sensitivity, sub-ppm lever detection, fast response, and high activity at low temperature. The enhanced sensing property of sensor was also discussed with the Cu2O/Co3O4 p-p heterojunction barrier modulation and Cu2S conductance channel. We realize the detection of the noxious H2S gas at ultra-low temperature in a more security and environmental protection way.

Asthma control and severe exacerbations in patients with moderate or severe asthma in Jilin Province, China: a multicenter cross-sectional survey.

BACKGROUND: No systemic evaluation of asthma control in Jilin Province has been reported. Asthma control might provide the basis for asthma management in this region. A multicenter hospital-based cross-sectional study was performed to investigate the asthma control and related factors for severe asthma exacerbations in patients with moderate or severe asthma in Jilin Province, China. METHODS: The study enrolled 1546 patients in five grade one general hospitals from January to December 2013. Asthma medication, patient self-management, asthma control test (ACT) scores and frequency of severe asthma exacerbations during the follow-up (12 months) were collected via a follow-up questionnaire. RESULTS: In the study, 889 patients provided a complete follow-up questionnaire. Severe asthma exacerbations occurred in 54.89 % of patients. ACT score ≤15, asthma medication ≤ 3 months, severe asthma, income level lower than average Per Capita Disposable Income (PCDI) and a lower educational level were risk factors of a severe exacerbation. CONCLUSIONS: Poor adherence to asthma medication, poor asthma symptom control, lower income, a low educational level might be possible reasons for the high incidence of severe asthma exacerbations and poor asthma control in Jilin Province of China.

Quantum phase transitions in Sn bilayer based interfacial systems by an external strain.

Using first-principle calculations, we report for the first time, the changes in electronic structures of a single bilayer Sn stacked on a single bilayer Sb(Bi) and on a single quintuple layer Sb2Te3 induced by both interface polarization and strain. With BL Bi and QL Sb2Te3 substrates, the stanene tends to have a low-buckled configuration, whereas with BL Sb substrate, the stanene prefers to form high-buckled configurations. For strained Sn/Sb(Bi) system, we find that the Dirac cone state is not present in the band gap, whereas in strained Sn/Sb2Te3 system, spin-polarized Dirac cone can be introduced into the band gap. We discuss why tensile strain can result in the Dirac cone emerging at the K point based on a tight-binding lattice model. This theoretical study implies the feasibility of realizing quantum phase transitions for Sn thin films on suitable substrates. Our findings provide an effective manner in manipulating electronic structures and topological states in interfacial systems by using interface polarization and strain, which opens a new route for realizing atomically thin spintronic devices.

Quantum spin Hall insulator in halogenated arsenene films with sizable energy gaps.

Based on first-principles calculations, the electronic and topological properties of halogenated (F-, Cl-, Br- and I-) arsenene are investigated in detail. It is found that the halogenated arsenene sheets show Dirac type characteristic in the absence of spin-orbital coupling (SOC), whereas energy gap will be induced by SOC with the values ranging from 0.194 eV for F-arsenene to 0.255 eV for I-arsenene. Noticeably, these four newly proposed two-dimensional (2D) systems are verified to be quantum spin Hall (QSH) insulators by calculating the edge states with obvious linear cross inside bulk energy gap. It should be pointed out that the large energy gap in these 2D materials consisted of commonly used element is quite promising for practical applications of QSH insulators at room temperature.

CO2 sensing of La0.875Ca0.125FeO3 in wet vapor: a comparison of experimental results and first-principles calculations.

Experimental results show that with an increase of relative humidity, the resistance of La0.875Ca0.125FeO3 decreases at room temperature but increases at higher temperatures (140-360 °C). The humid effect at room temperature is due to the movement of H(+) or H3O(+) inside of the condensed water layer on the surface of La0.875Ca0.125FeO3. Regarding the humid effect at high temperatures, the density functional theory (DFT) calculations show that H2O can be adsorbed onto the La0.875Ca0.125FeO3 surface in the molecular and dissociative adsorption configurations, where the La0.875Ca0.125FeO3 surface gains some electrons from H2O or its dissociative products, consistent with our observation. Experimental results also show that CO2 sensing response at high temperatures decreases with an increase of room-temperature relative humidity. DFT calculations indicate that CO2 adsorbed onto the La0.875Ca0.125FeO3(010) surface, where high concentration oxygen adsorption occurs without water adsorption nearby, releases some electrons into the semiconductor surface, playing the role of a donor. The interaction between CO2 and the local La0.875Ca0.125FeO3(010) surface with pre-adsorption of H2O nearby results in some electron transfer from the La0.875Ca0.125FeO3 surface to CO2, which is responsible for the weakening of CO2 response at high temperatures for La0.875Ca0.125FeO3 with an increase of room-temperature relative humidity.