Well-defined ternary metal phosphide nanowires with stabilized Pt nanoclusters to boost alkaline hydrogen evolution reaction.

Designing low-content and high-activity Pt-based catalysts with the high durability for the electrochemical hydrogen production remains a challenge. In this study, a ternary metal phosphide (NiCoP) with 1D nanowire (NW) and 2D nanosheet (NS) morphologies incorporating Pt clusters (denoted as Ptcluster-NiCoP@NF NWs and Ptcluster-NiCoP@NF NSs, respectively) was prepared using a hydrothermal-phosphorization-electrodeposition method. Based on the "tip effect" of NWs and a high electrochemical surface area, the as-prepared Ptcluster-NiCoP@NF NWs display better hydrogen evolution reaction (HER) performance, with a low overpotential of 65 mV at a high current density of 100 mA cm-2 and a low Tafel slope of 38.86 mV dec-1, than the Ptcluster-NiCoP@NF NSs, with an overportential of 95 mV at 42.53 mV dec-1. This indicates that the NiCoP NW-based support exhibits faster HER kinetics. The mass activity (11.47 A mgPt-1) of the Ptcluster-NiCoP@NF NWs is higher than that of commercial Pt/C catalysts. Significantly, the Ptcluster-NiCoP@NF NWs display excellent cyclic stability with negligible losses for 5000 cycles and 30-h tests at a high current of 500 mA cm-2.

Preparation of a TiO2/PEDOT nanorod film with enhanced electrochromic properties.

The designed growth of titanium dioxide (TiO2)/poly(3,4-ethylenedioxythiophene) (PEDOT) nanorod arrays has been achieved by the combination of hydrothermal and electrodeposition methods. Due to the use of one-dimensional (1D) TiO2 nanorod arrays as the template of the nanocomposites (TiO2/PEDOT), the surface area of the active materials is enlarged and the diffusion distance of the ions is shortened. The nanorod structure also contributes to increasing the length of PEDOT conjugated chains and facilitates the transfer of electrons in the conjugated chains. Consequently, the TiO2/PEDOT film delivers a shorter response time (∼0.5 s), higher transmittance contrast (∼55.5%) and long-cycle stability compared to the pure PEDOT film. In addition, the TiO2/PEDOT electrode is further developed to be a smart bi-functional electrochromic device exhibiting energy storage performance. We expect that this work may lead to new designs for powerful intelligent electrochromic energy storage devices.

Efficient Charge Transfer and Effective Active Sites in Lead-Free Halide Double Perovskite S-Scheme Heterojunctions for Photocatalytic H2 Evolution.

The practical application of lead-free double perovskite Cs2 AgBiBr6 in photocatalytic H2 evolution is still restricted due to the low activity and poor stability. The rational design of lead-free halide double perovskites heterojunctions with efficient charge transfer and effective active sites is a potential route to achieve the ideal prospect. Herein, in this work an S-scheme heterojunction of Cs2 AgBiBr6 with enriched Br-vacancies and WO3 nanorods (VBr -Cs2 AgBiBr6 /WO3 ) obtaining excellent visible-light responsive photocatalytic H2 evolution performance and durable stability is reported. The S-scheme heterojunction driven by the unaligned Fermi levels of these two semiconductors ensures the efficient charge transfer at the interface, and density functional theory calculations reveal the enriched Br vacancies on Cs2 AgBiBr6 (022) surfaces introduced by atom thermal vibration provide effective active sites for hydrogen evolution. The optimized VBr -Cs2 AgBiBr6 /WO3 S-scheme photocatalyst exhibits the photocatalytic hydrogen evolution rate of 364.89 µmol g-1 h-1 which is 4.9-fold of bare VBr -Cs2 AgBiBr6 (74.44 µmol g-1 h-1 ) and presents long-term stability of 12 h continuous photocatalytic reaction. This work provides deep insights into the photocatalytic mechanism of VBr -Cs2 AgBiBr6 /WO3 S-scheme heterojunctions, which emerges a new strategy in the applications of perovskite-based photocatalysts.

Cuboid-like phosphorus-doped metal-organic framework-derived CoSe2 on carbon cloth as an advanced bifunctional oxygen electrocatalyst for rechargeable zinc-air batteries.

Zinc-air batteries (ZABs) are regarded as attractive devices for electrochemical energy storage and conversion due to their outstanding electrochemical performance, low price, and high safety. However, it remains a challenge to design a stable and efficient bifunctional oxygen catalyst that can accelerate the reaction kinetics and improve the performance of ZABs. Herein, a phosphorus-doped transition metal selenide/carbon composite catalyst derived from metal-organic frameworks (P-CoSe2/C@CC) is constructed by a self-supporting carbon cloth structure through a simple solvothermal process with subsequent selenization and phosphatization. The P-CoSe2/C@CC exhibits a low overpotential of 303.1 mV at 10 mA cm-2 toward the oxygen evolution reaction and an obvious reduction peak for the oxygen reduction reaction. The abovementioned electrochemical performances for the P-CoSe2/C@CC are attributed to the specific architecture, the super-hydrophilic surface, and the P-doping effect. Remarkably, the homemade zinc-air battery based on our P-CoSe2/C@CC catalyst shows an expected peak power density of 124.4 mW cm-2 along with excellent cycling stability, confirming its great potential application in ZABs for advanced bifunctional electrocatalysis.

Dual-Band Electrochromic Optical Modulation Improved by a Precise Control of Lithium Content in Li4+xTi5O12.

Dual-band electrochromic smart windows that can dynamically and independently control incident solar irradiation and visible light are envisioned as intelligent technology to reduce power consumption of buildings. However, there is still a great challenge to put the dual-band electrochromic technology into practice due to some limits in material systems and preparation techniques. Herein, a new electrochromic material of Li4Ti5O12 is developed to implement the dual-band optical modulation behavior, which could be further improved by a precise control of the lithium content in the active material. It could separately modulate the light and heat based on regulation of the transmittance of visible and near-infrared light. This enables Li4Ti5O12 to operate in three distinct modes of bright, cool, and dark, so as to meet various indoor needs. The optical transmittance contrast reaches over 60% at both visible- and near-infrared-light regions between different modes, and a large range of apparent temperature adjustments (7 °C) could be achieved. The prototype device based on dual-band electrochromic Li4Ti5O12 is further developed into a smart window of a house model, which exhibits good optical and thermal modulation behaviors in response to a high-temperature environment. This work provides a new material system for achieving dual-band electrochromic optical modulation toward smart energy-saving window applications.

Fabrication of Vertical-Standing Co-MOF Nanoarrays with 2D Parallelogram-like Morphology for Aqueous Asymmetric Electrochemical Capacitors.

Metal organic frameworks (MOFs) have been considered as one of the most promising electrode materials for electrochemical capacitors due to their large specific surface area and abundant pore structure. Herein, we report a Co-MOF electrode with a vertical-standing 2D parallelogram-like nanoarray structure on a Ni foam substrate via a one-step solvothermal method. The as-prepared Co-MOF on a Ni foam electrode delivered a high area-specific capacitance of 582.0 mC cm-2 at a current density of 2 mA cm-2 and a good performance rate of 350.0 mC cm-2 at 50 mA cm-2. Moreover, an asymmetric electrochemical capacitor (AEC) device (Co-MOF on Ni foam//AC) was assembled by using the as-prepared Co-MOF on a Ni foam as the cathode and a active carbon-coated Ni foam as the anode to achieve a maximum energy density of 0.082 mW cm-2 at a power density of 0.8 mW cm-2, which still maintained 0.065 mW cm-2 at a high power density of 11.94 mW cm-2. Meanwhile, our assembled device exhibited an excellent cycling stability with a capacitance retention of nearly 100% after 1000 cycles. Therefore, this work provides a simple method to prepare MOF-based material for the application of energy storage and conversion.

EMP3 negatively modulates breast cancer cell DNA replication, DNA damage repair, and stem-like properties.

Enhanced DNA damage repair capacity attenuates cell killing of DNA-damaging chemotherapeutic agents. In silico analysis showed that epithelial membrane protein 3 (EMP3) is associated with favorable survival, and negatively regulates cell cycle S-phase. Consistently, loss and gain of function studies demonstrated that EMP3 inhibits breast cancer cell S-phage entry, DNA replication, DNA damage repair, and stem-like properties. Moreover, EMP3 blocks Akt-mTOR signaling activation and induces autophagy. EMP3 negatively modulates BRCA1 and RAD51 expression, indicating EMP3 suppresses homologous recombination repair of DNA double-strand breaks. Accordingly, EMP3 sensitizes breast cancer cells to the DNA-damaging drug Adriamycin. EMP3 downregulates YTHDC1, a RNA-binding protein involved in m6a modification, which at least in part mediates the effects of EMP3 on breast cancer cells. Taken together, these data indicate that EMP3 is a putative tumor suppressor in breast cancer, and EMP3 downregulation may be responsible for breast cancer chemoresistance.

FZD5 prevents epithelial-mesenchymal transition in gastric cancer.

BACKGROUND: Frizzled (FZD) proteins function as receptors for WNT ligands. Members in FZD family including FZD2, FZD4, FZD7, FZD8 and FZD10 have been demonstrated to mediate cancer cell epithelial-mesenchymal transition (EMT). METHODS: CCLE and TCGA databases were interrogated to reveal the association of FZD5 with EMT. EMT was analyzed by investigating the alterations in CDH1 (E-cadherin), VIM (Vimentin) and ZEB1 expression, cell migration and cell morphology. Transcriptional modulation was determined by ChIP in combination with Real-time PCR. Survival was analyzed by Kaplan-Meier method. RESULTS: In contrast to other FZDs, FZD5 was identified to prevent EMT in gastric cancer. FZD5 maintains epithelial-like phenotype and is negatively modulated by transcription factors SNAI2 and TEAD1. Epithelial-specific factor ELF3 is a downstream effecter, and protein kinase C (PKC) links FZD5 to ELF3. ELF3 represses ZEB1 expression, further guarding against EMT. Moreover, FZD5 signaling requires its co-receptor LRP5 and WNT7B is a putative ligand for FZD5. FZD5 and ELF3 are associated with longer survival, whereas SNAI2 and TEAD1 are associated with shorter survival. CONCLUSIONS: Taken together, FZD5-ELF3 signaling blocks EMT, and plays a potential tumor-suppressing role in gastric cancer. Video Abstract.

Bulbophyllum papuaense (Orchidaceae), a new species from Indonesia.

A new species, Bulbophyllum papuaense, was described and illustrated from Indonesia. Bulbophyllum papuaense is similar to Bulbophyllum tortuosum and B. muscohaerens but differs from them by having rhizome and pseudobulbs covered with papillose scales, caudate and ciliate petals, linear and ciliate lip.

Improving Electrochromic Cycle Life of Prussian Blue by Acid Addition to the Electrolyte.

In this study, we examined the cyclic stability of Prussian blue (PB) films in electrolytes with acid. The cyclic stabilities of the PB films were investigated in K⁺ based electrolytes with different values of solution pH. The acidified KCl solution can significantly improve the durability of the film. Among the three pH values tested, the KCl solutions (pH = 2.15 and pH = 3.03) showed better performance. Furthermore, we investigated the cyclic stabilities of the PB films in LiClO4/PC electrolyte containing different acids. We found that the cyclic stability of PB film was significantly improved when a small amount of acetic acid was dissolved in LiClO4/PC electrolyte. The PB film exhibited stable optical modulation after up to 20,000 cycles in LiClO4/PC electrolyte containing acetic acid-a much higher result than those of some literatures. This suggests that the addition of acetic acid to LiClO4/PC electrolyte can promote the development of PB-based devices with improved stability.