Flexible aqueous Cr-ion hybrid supercapacitors with remarkable electrochemical properties in all climates.

The integration of hostless battery-like metal anodes for hybrid supercapacitors is a realistic design method for energy storage devices with promising future applications. With significant Cr element deposits on Earth, exceptionally high theoretical capacity (1546 mAh g-1), and accessible redox potential (-0.74 V vs. reversible hydrogen electrode) of Cr metals, the design of Cr anodes has rightly come into our focus. This work presents a breakthrough design of a flexible Cr-ion hybrid supercapacitor (CHSC) based on a porous graphitized carbon fabric (PGCF) substrate prepared by K2FeO4 activation. In the CHSC device, PGCF acts as both a current collector and cathode material due to its high specific surface area and superior conductivity. The use of a highly concentrated LiCl-CrCl3 electrolyte with high Cr plating/stripping efficiency and excellent antifreeze properties enables the entire PGCF-based CHSC to achieve well-balanced performance in terms of energy density (up to 1.47 mWh cm-2), power characteristics (reaching 9.95 mW cm-2) and durability (95.4% capacity retention after 30,000 cycles), while realizing it to work well under harsh conditions of -40 °C. This work introduces a new concept for low-temperature energy storage technology and confirms the potential application of Cr anodes in hybrid supercapacitors.

Urchin-like (NH4)2V10O25·8H2O hierarchical arrays with significantly expanded interlayer spacing for superior aqueous zinc-ion batteries.

The practical application of zinc ion batteries (ZIBs) can be facilitated by designing cathode materials with unique structures that can overcome the critical problems of slow reaction kinetics and large volume expansion associated with the intercalation reaction of divalent zinc ions. In this study, a novel urchin-like (NH4)2V10O25·8H2O assembled from nanorods was synthesized by a simple hydrothermal method, noted as U-NVO. The interlayer organic pillar of cetyltrimethylammonium cation (CTAB) has been intercalated between layers to regulate the interlayer microstructure and expand the interlayer spacing to 1.32 nm, which effectively increased the contact between the electrode and electrolyte interface and shortened the diffusion path of electrolyte ions. The interlayer pillars of structural H2O and NH4+ provide a flexible framework structure and enhance the cohesion of the layered structure, which helps to maintain structural stability during the charging and discharging process, resulting in long-term durability. These unique properties result in the U-NVO cathodes demonstrating high specific capacity (401.7 mA h g-1 at 0.1 A g-1), excellent rate capability (99.6 % retention from 0.1 to 5 A g-1 and back to 0.1 A g-1), and long-term cycling performance (∼87.5 % capacity retention after 2600 cycles). These results offer valuable insights into the design of high-performance vanadium oxide cathode materials.

The MYB transcription factor OsMYBxoc1 regulates resistance to Xoc by directly repressing transcription of the iron transport gene OsNRAMP5 in rice.

Bacterial leaf streak caused by Xanthomonas oryzae pv. oryzicola (Xoc) is a continuous threat to rice cultivation, leading to substantial yield losses with socioeconomic implications. Iron ions are essential mineral nutrients for plant growth, but little information is available on how they influence mechanisms of rice immunity against Xoc. Here, we investigated the role of the myeloblastosis-related (MYB) transcriptional repressor OsMYBxoc1 in modulation of rice resistance through control of iron ion transport. Overexpression of OsMYBxoc1 significantly increased rice resistance, whereas OsMYBxoc1 RNA-interference lines and knockout mutants showed the opposite result. Suppression of OsMYBxoc1 expression dampened the immune response induced by pathogen-associated molecular patterns. We demonstrated that OsMYBxoc1 binds specifically to the OsNRAMP5 promoter and represses transcription of OsNRAMP5. OsNRAMP5, a negative regulator of rice resistance to bacterial leaf streak, possesses metal ion transport activity, and inhibition of OsMYBxoc1 expression increased the iron ion content in rice. Activity of the ion-dependent H2O2 scavenging enzyme catalase was increased in plants with suppressed expression of OsMYBxoc1 or overexpression of OsNRAMP5. We found that iron ions promoted Xoc infection and interfered with the production of reactive oxygen species induced by Xoc. The type III effector XopAK directly inhibited OsMYBxoc1 transcription, indicating that the pathogen may promote its own proliferation by relieving restriction of iron ion transport in plants. In addition, iron complemented the pathogenicity defects of the RS105_ΔXopAK mutant strain, further confirming that iron utilization by Xoc may be dependent upon XopAK. In conclusion, our study reveals a novel mechanism by which OsMYBxoc1 modulates rice resistance by regulating iron accumulation and demonstrates that Xoc can accumulate iron ions by secreting the effector XopAK to promote its own infection.

A low-cost and efficient route for large-scale synthesis of NiCoSx nanosheets with abundant sulfur vacancies towards quasi-industrial electrocatalytic oxygen evolution.

Transition-metal sulfides (TMS) have piqued a great deal of interest due to their unprecious nature and high intrinsic catalytic activity for water splitting. In this work, a low-cost and efficient route was developed, which included electrodeposition to prepare Ni-Co layered double hydroxide (NiCo-LDH) followed by ion exchange to form nickel cobalt sulfide (NiCoSx). Electrochemical reduction was used to modulate sulfur vacancies in order to produce sulfur vacancies-rich NiCoSx with nanosheet arrays on -three-dimensional nickel foam (NiCoSx-0.4/NF) with a large area of more than 250 cm2. Combining data from experiments and density functional theoretical (DFT) calculations reveals that engineered sulfur vacancies change the electronic structure, electron transfer property, and surface electron density of NiCoSx, significantly improving the free energy of water adsorption and boosting electrocatalytic activity. The developed NiCoSx-0.4/NF has long-term stability of more than 300 h at 500 mA cm-2 in 1 M KOH at ambient temperature and only needs a 289 mV overpotential at 100 mA cm-2. Remarkably, the synthesized electrocatalyst rich in sulfur vacancies, exhibits exceptional performance with a high current density of up to 1.9 A cm-2 and 1 A cm-2 in 6 M KOH and leads to overpotentials of 286 mV at 80 °C and 358 mV at 60 °C, respectively. The catalyst's practicability under quasi-industrial conditions (60 °C, 6 M KOH) is further demonstrated by its long-term stability for 220 h with only a 3.9 % potential increase at 500 mA cm-2.

MoSe2 hollow nanospheres with expanded selenide interlayers for high-performance aqueous zinc-ion batteries.

Transition metal dichalcogenides (TMDs) as materials for aqueous zinc-ion batteries (ZIBs) have received a lot of interest because of their large theoretical capacity and unique layered structure. However, the sluggish kinetics and inferior cyclic stability limit the usefulness of ZIBs. In the present investigation, the interlayer spacing enlarged MoSe2 hollow nanospheres comprised of nanosheets with ultrathin shells have been successfully synthesized through a combined strategy of template assistance and anion-exchange reaction. The hierarchical ultrathin nanosheets and hollow structure effectively suppress the agglomeration of pure nanosheets and ameliorate volume fluctuations induced by ion migration during (dis)charging/charging. The interlayer expansion provides good channels for the transport of Zn2+ ions and speeds up the insertion/extraction of Zn2+. In addition, in-situ carbon modification can significantly improve electronic conductivity. Therefore, the electrode prepared from MoSe2 hollow nanospheres with enlarged interlayer spacing not only exhibits outstanding cycle stability (capacity retention of 94.5% after 1600 cycles) but also exhibits high-rate capability (266.1 mA h g-1 at 0.1 A g-1 and 203.6 mA h g-1 at 3 A g-1). This work could provide new insights into the design of cathode using TMDs of hollow structure for Zn2+ storage.

Ectopic Expression of OsJAZs Alters Plant Defense and Development.

A key step in jasmonic acid (JA) signaling is the ligand-dependent assembly of a coreceptor complex comprising the F-box protein COI1 and JAZ transcriptional repressors. The assembly of this receptor complex results in proteasome-mediated degradation of JAZ repressors, which in turn bind and repress MYC transcription factors. Many studies on JAZs have been performed in Arabidopsis thaliana, but the function of JAZs in rice is largely unknown. To systematically reveal the function of OsJAZs, in this study, we compared the various phenotypes resulting from 13 OsJAZs via ectopic expression in Arabidopsis thaliana and the phenotypes of 12 AtJAZs overexpression (OE) lines. Phylogenetic analysis showed that the 25 proteins could be divided into three major groups. Yeast two-hybrid (Y2H) assays revealed that most OsJAZ proteins could form homodimers or heterodimers. The statistical results showed that the phenotypes of the OsJAZ OE plants were quite different from those of AtJAZ OE plants in terms of plant growth, development, and immunity. As an example, compared with other JAZ OE plants, OsJAZ11 OE plants exhibited a JA-insensitive phenotype and enhanced resistance to Pst DC3000. The protein stability after JA treatment of OsJAZ11 emphasized the specific function of the protein. This study aimed to explore the commonalities and characteristics of different JAZ proteins functions from a genetic perspective, and to screen genes with disease resistance value. Overall, the results of this study provide insights for further functional analysis of rice JAZ family proteins.

Interfacial engineering of an FeOOH@Co3O4 heterojunction for efficient overall water splitting and electrocatalytic urea oxidation.

Constructing heterostructure is an efficient method to provide more active sites and optimize electronic structure for improving the oxygen evolution reaction (OER) and urea oxidation reaction (UOR) performance. Herein, the 3D FeOOH@Co3O4 heterostructure was constructed using FeOOH layer (10-20 nm) coated on the surface of Co3O4 nanoneedles through the strong hydrolysis of Fe3+. The FeOOH@Co3O4 heterostructure not only retains the nanoneedle structure with open frameworks, but also improves the specific surface area and expedites the charge transfer. The FeOOH@Co3O4-240 heterostructure affords a remarkable OER performance with low overpotential of 228 mV at 10 mA·cm-2 in 1 M KOH solution. The symmetrical urea electrolyzer using FeOOH@Co3O4-240 as both anode and cathode delivers 10 mA/cm2 at 1.43 V. Density functional theory (DFT) calculations unveil that the FeOOH@Co3O4-240 heterostructure could adjust the electronic structure and strengthen the conductivity. This work offered a facile strategy for designing heterojunction catalysts in an economic way.

Self-Supportive Mesoporous Ni/Co/Fe Phosphosulfide Nanorods Derived from Novel Hydrothermal Electrodeposition as a Highly Efficient Electrocatalyst for Overall Water Splitting.

Low cost and highly efficient bifuctional catalysts for overall water electrolysis have drawn considerable interests over the past several decades. Here, rationally synthesized mesoporous nanorods of nickel-cobalt-iron-sulfur-phosphorus composites are tightly self-supported on Ni foam as a high-performance, low cost, and stable bifunctional electrocatalyst for water electrolysis. The targeted designing and rational fabrication give rise to the nanorod-like morphology with large surface area and excellent conductivity. The NiCoFe-PS nanorod/NF can reach 10 mA cm-2 at a small overpotential of 195 mV with a Tafel slope of 40.3 mV dec-1 for the oxygen evolution reaction and 97.8 mV with 51.8 mV dec-1 for the hydrogen evolution reaction. Thus, this bifunctional catalyst shows low potentials of 1.52 and 1.76 V at 10 and 50 mA cm-2 toward overall water splitting with excellent stability for over 200 h, which are superior to most non-noble metal-based bifunctional electrocatalysts recently. This work provides a new strategy to fabricate multiple metal-P/S composites with the mesoporous nanorod-like structure as bifunctional catalysts for overall water splitting.