Nickel Phosphonate MOF Derived N-Doped Carbon-Coated Phosphorus-Vacancies-Rich Ni2 P Particles as Efficient Bifunctional Oxygen Electrocatalyst.

The design of non-noble metal bifunctional electrocatalysts with outstanding performance and remarkable stability for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is one of the most essential issues to the realization of rechargeable zinc-air battery, and transition metal phosphides (TMPs) have emerged as robust candidates for oxygen electrocatalysts. Herein, N-doped carbon-coated phosphorus-vacancies-rich Ni2 P particles (Vp -Ni2 P@NC) is proposed via simple carbonization and following Ar plasma treatment from a single nickel phosphonate metal-organic framework (MOF) without extra phosphine and nitrogen sources. The facile and rapid plasma treatment can achieve phosphorus vacancies which could modulate the electronic structure to enhance the inherent active and electrical conductivity. Meanwhile, the pyridine-N and graphitized-N produced during calcination also could provide more active sites and increase the electrical conductivity. The resultant Vp -Ni2 P@NC catalyst shows excellent bifunctional electrocatalytic activity (OER/ORR) based on synergistic effect of introducing P vacancies into Ni2 P and N-doped carbon. Vp -Ni2 P@NC catalyst shows more advantageous ΔE value (0.70 V) compared to Pt/C+RuO2 (0.73 V) and most reported catalysts. Additionally, the zinc-air bbatterie (ZAB) employing Vp -Ni2 P@NC as air cathode shows excellent performance. The maximum power density of 203.48 mW cm-2 , the cycling stability of more than 150 h at 10 mA cm-2 .

High-Efficient Ultrathin PdCuMo Porous Nanosheets with Abundant Defects for Oxygen Reduction Reaction.

To reduce the over-dependence on Pt, Pd-based catalysts have become one of the most effective candidates for oxygen reduction reaction (ORR). In order to further accelerate the ORR kinetics and strengthen the catalytic performance of Pd catalysts, component optimization and morphology design have been adopted. Although great progress has been made, it is still difficult to obtain porous ultrathin nanosheets with excellent performance by a simple method. Here, ultrathin PdCuMo porous nanosheets (PdCuMo NSs) were successfully prepared. This structure possessed a large specific surface area with rich cavities and structural defects, significantly enhancing its ORR performance. In special, the mass activity of PdCuMo NSs was 1.46 A mg-1 at 0.90 V, which was 12.2, 8.6, and 2.7 times as high as that of Pd/C, Pt/C, and PdCuMo nanoparticles (PdCuMo NPs), respectively. In addition, it had an excellent ability to resist CO poisoning and exhibited remarkable long-term stability.

Effects of sulfur application on selenium uptake and seed selenium speciation in soybean (Glycine max L.) grown in different soil types.

AIMS: The objective of the present study was to elucidate the effects of sulfur (S) application on selenium (Se) uptake and seed Se speciation in high-protein soybean (Glycine max L.) grown in different soil types. METHODS: Pot experiments were conducted with soybean plants grown in yellow-brown soil (pH 5.68) and in calcareous alluvial soil (pH 7.87). Sodium selenate (Na2SeO4, 2 mg kg-1) was applied to soil with or without S fertilizer (S, 100 mg kg-1). RESULTS: Soybean grain yield and total biomass in calcareous alluvial soil were both approximately 1.3-fold the levels in yellow-brown soil. Following Se application, seed Se concentration in calcareous alluvial soil was 3.2-fold the concentration in yellow-brown soil, although additional S application reduced the corresponding seed Se concentrations by 55.6% and 38.6%, respectively. Generally, Se application facilitated Se translocation and enrichment in soybean seeds. Organic Se accounted for 92% of seed total Se and Se-methionine (>90%) was always the major Se species. Available Se (soluble and exchangeable fractions) accounted for 50.7% (yellow-brown soil) and 70.1% (calcareous alluvial soil) of soil total Se under Se treatment, while additional S application decreased the corresponding proportion of soluble Se by 12.6% and 14.4%. CONCLUSIONS: The bioavailability of selenate in calcareous alluvial soil was higher than the bioavailability in yellow-brown soil and was more negatively affected by S application. Although S application inhibited Se uptake in soybean plants in both soil types, it did not influence seed Se speciation and Se-methionine was the major Se species.

1,2,4-triazole-assisted metal-organic framework-derived nitrogen-doped carbon nanotubes with encapsulated Co4N particles as bifunctional oxygen electrocatalysts for rechargeable zinc-air batteries.

The design of high-performance oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) dual-functional catalysts is not only important for the further applications of zinc-air batteries (ZABs) but also a major challenge in the field of energy conversion. The cheap 1,2,4-triazole (1,2,4-TZ) can be decomposed easily by heat, making it a high research value in carbon catalysts derived from metal-organic frameworks (MOFs). Here, Co4N particles encapsulated at the top of N-doped carbon nanotubes (Co4N@NCNTs) were conveniently prepared by 1,2,4-TZ-assisted pyrolysis of Co-MOF-74 for the first time. Owing to the excellent activity of Co4N particles and the highly graphitized N-doped carbon nanotubes (NCNTs), Co4N@NCNTs obtained at 900 °C (Co4N@NCNT-900) exhibited astonishing catalytic performance in both ORR and OER, and high reversible oxygen bifunctional activity (ΔE = 0.685 V). Moreover, Co4N@NCNT-900 displayed a larger discharge power density (122 mW cm-2), a better specific capacity (811.8 mAh g-1), and more excellent durability during the ZAB test, implying that Co4N@NCNT-900 can act as a bifunctional high active catalyst in ZABs.

Structurally-supported PtCuCo nanoframes as efficient bifunctional catalysts for oxygen reduction and methanol oxidation reactions.

Developing highly durable and active catalysts with the morphology of structurally robust nanoframes toward oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR) in acidic environment is crucial but still a great challenge to completely achieve in a single material. Herein, PtCuCo nanoframes (PtCuCo NFs) with internal support structures as enhanced bifunctional electrocatalysts were prepared by a facile one-pot approach. PtCuCo NFs exhibited remarkable activity and durability for ORR and MOR owing to the ternary compositions and the structure-fortifying frame structures. Impressively, the specific/mass activity of PtCuCo NFs were 12.8/7.5 times as large as that of commercial Pt/C for ORR in perchloric acid solution. For MOR in sulfuric acid solution, the mass/specific activity of PtCuCo NFs was 1.66 A mgPt-1/4.24 mA cm-2, which was 5.4/9.4 times as large as that of Pt/C. This work may provide a promising nanoframe material to develop dual catalysts for fuel cells.

The complete mitochondrial genome of Aulacochilus grouvellei Achard, 1923 (Coleoptera: Erotylidae: Erotylinae) with a phylogenetic analysis of Cucujoidea.

The complete mitochrondiral genome of Aulacochilus grouvellei Achard, 1923 was sequenced using an Illumina HiSeq platform. It represents the first mitochondrial genome of the subfamily Erotylinae. The mitogenome is a double-stranded circular molecule 15,607 bp in length with 22 transfer RNA genes, 13 protein-coding genes, 2 ribosomal RNA genes, and a control region. A Bayesian inference phylogenetic analysis including the new mitochondrial genome and a broad selection of other Cucujoidea recovered four major clades, including a 'Cryptophagidae-Laemophloeidae-Cucujidae' clade, a 'Monotomidae-Nitidulidae' clade, an Erotylidae clade, and a 'Coccinellidae-Silvanidae' clade. The family Erotylidae was recovered closely related to the 'Cryptophagidae-Laemophloeidae-Cucujidae' - 'Monotomidae -Nitidulidae' clade.

Bottom-Up Fabrication of a Sandwich-Like Carbon/Graphene Heterostructure with Built-In FeNC Dopants as Non-Noble Electrocatalyst for Oxygen Reduction Reaction.

High-performance non-noble electrocatalysts for oxygen reduction reaction (ORR) are the prerequisite for large-scale utilization of fuel cells. Herein, a type of sandwiched-like non-noble electrocatalyst with highly dispersed FeNx active sites embedded in a hierarchically porous carbon/graphene heterostructure was fabricated using a bottom-up strategy. The in situ ion substitution of Fe3+ in a nitrogen-containing MOF (ZIF-8) allows the Fe-heteroatoms to be uniformly distributed in the MOF precursor, and the assembly of Fe-doped ZIF-8 nano-crystals with graphene-oxide and in situ reduction of graphene-oxide afford a sandwiched-like Fe-doped ZIF-8/graphene heterostructure. This type of heterostructure enables simultaneous optimization of FeNx active sites, architecture and interface properties for obtaining an electron-catalyst after a one-step carbonization. The synergistic effect of these factors render the resulting catalysts with excellent ORR activities. The half-wave potential of 0.88 V vs. RHE outperforms most of the none-noble metal catalyst and is comparable with the commercial Pt/C (20 wt %) catalyst. Apart from the high activity, this catalyst exhibits excellent durability and good methanol-tolerance. Detailed investigations demonstrate that a moderate content of Fe dopants can effectively increase the intrinsic activities, and the hybridization of graphene can enhance the reaction kinetics of ORR. The strategy proposed in this work gives an inspiration towards developing efficient noble-metal-free electrocatalysts for ORR.