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81.
《Liver Transplantation》2018,8(25)
Herein, a novel and effective method to prepare n‐doped MoOx films with highly improved conductivity is reported. The MoOx films are readily prepared by spin‐coating an aqueous solution containing ammonium molybdate tetrahydrate and vitamin C (VC). As confirmed by UV–vis absorption, X‐ray photoelectron spectroscopy and ultraviolet photoelectron spectroscopy measurements, Mo(VI) is partially reduced to Mo(V) by VC, resulting in the n‐doping of MoOx. The conductivity of the n‐doped MoOx (H:V‐Mo) film can be enhanced by four orders of magnitude compared to pristine MoOx (H‐Mo), that is, from 1.2 × 10−7 to 1.1 × 10−3 S m−1. The device using a 10 nm H:V‐Mo anode interlayer (AIL) exhibits comparable photovoltaic performance to a poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate)‐modified device. More importantly, the hole transport and collection properties of the H:V‐Mo AILs show outstanding tolerance to thickness variation, that is, with increasing thickness of the H:V‐Mo AIL from 10 to 150 nm, the V oc and fill factor values of the devices remain unchanged. The device based on the blade‐coated H:V‐Mo AIL also has a high power conversion efficiency of 10.6%. To the best of the authors' knowledge, this work demonstrates the first example to prepare metal oxide AILs with outstanding tolerance to thickness, which is promising for the future large‐area manufacturing. 相似文献
82.
Nitrogen‐Doped Porous Molybdenum Carbide and Phosphide Hybrids on a Carbon Matrix as Highly Effective Electrocatalysts for the Hydrogen Evolution Reaction
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The efficient evolution of hydrogen through electrocatalysis is considered a promising approach to the production of clean hydrogen fuel. Platinum (Pt)‐based materials are regarded as the most active hydrogen evolution reaction (HER) catalysts. However, the low abundance and high cost of Pt hinders the large‐scale application of these catalysts. Active, inexpensive, and earth‐abundant electrocatalysts to replace Pt‐based materials would be highly beneficial to the production of cost‐effective hydrogen energy. Herein, a novel organoimido‐derivatized heteropolyoxometalate, Mo4‐CNP, is designed as a precursor for electrocatalysts of the HER. It is demonstrated that the carbon, nitrogen, and phosphorus sources derived from the Mo4‐CNP molecules lead to in situ confined carburization, phosphorization, and chemical doping on an atomic scale, thus forming nitrogen‐doped porous molybdenum carbide and phosphide hybrids, which exhibit remarkable electrocatalytic activity for the HER. Such an organically functionalized polyoxometalate‐assisted strategy described here provides a new perspective for the development of highly active non‐noble metal electrocatalysts for hydrogen evolution. 相似文献
83.
Leyla Najafi Sebastiano Bellani Reinier Oropesa‐Nuñez Alberto Ansaldo Mirko Prato Antonio Esau Del Rio Castillo Francesco Bonaccorso 《Liver Transplantation》2018,8(16)
2D transition metal‐dichalcogenides are emerging as efficient and cost‐effective electrocatalysts for the hydrogen evolution reaction (HER). However, only the edge sites of their trigonal prismatic phase show HER‐electrocatalytic properties, while the basal plane, which is absent of defective/unsaturated sites, is inactive. Herein, the authors tackle the key challenge of increasing the number of electrocatalytic sites by designing and engineering heterostructures composed of single‐/few‐layer MoSe2 flakes and carbon nanomaterials (graphene or single‐wall carbon nanotubes) produced by solution processing. The electrochemical coupling between the materials that comprise the heterostructure effectively enhances the HER‐electrocatalytic activity of the native MoSe2 flakes. The optimization of the mass loading of MoSe2 flakes and their electrode assembly via monolithic heterostructure stacking provides a cathodic current density of 10 mA cm?2 at overpotential of 100 mV, a Tafel slope of 63 mV dec?1, and an exchange current density (j0) of 0.203 µA cm?2. In addition, thermal and chemical treatments are exploited to texturize the basal planes of the MoSe2 flakes (through Se‐vacancies creation) and to achieve in situ semiconducting‐to‐metallic phase conversion, respectively, thus they activate new HER‐electrocatalytic sites. The as‐engineered electrodes show a 4.8‐fold enhancement of j0 and a decrease in the Tafel slope to 54 mV dec?1. 相似文献
84.
Fine Tuning Electronic Structure of Catalysts through Atomic Engineering for Enhanced Hydrogen Evolution
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Yichao Huang Jun Hu Haoxiang Xu Wei Bian Jingxuan Ge Dejin Zang Daojian Cheng Yaokang Lv Cheng Zhang Jing Gu Yongge Wei 《Liver Transplantation》2018,8(24)
An efficient, durable, and low‐cost hydrogen evolution reaction (HER) catalyst is an essential requirement for practical hydrogen production. Herein, an effective approach to facilitate the HER kinetics of molybdenum carbide (Mo2C) electrocatalysts is presented by tuning its electronic structure through atomic engineering of nitrogen implantation. Starting from the organoimido‐derivatized polyoxometalate nanoclusters with inherent Mo? N bonds, the formation of N‐implanted Mo2C (N@Mo2C) nanocrystals with perfectly adjustable amounts of N atoms is demonstrated. The optimized N@Mo2C electrocatalyst exhibits remarkable HER performance and good stability over 20 h in both acid and basic electrolytes. Further density functional theory calculations show that engineering suitable nitrogen atoms into Mo2C can regulate its electronic structure well and decrease Mo? H strength, leading to a great enhancement of the HER activity. It could be believed that this ligand‐controlled atomic engineering strategy might influence the overall catalyst design strategy for engineering the activation sites of nonprecious metal catalysts for energy conversions. 相似文献
85.
Doped‐MoSe2 Nanoflakes/3d Metal Oxide–Hydr(Oxy)Oxides Hybrid Catalysts for pH‐Universal Electrochemical Hydrogen Evolution Reaction
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Leyla Najafi Sebastiano Bellani Reinier Oropesa‐Nuñez Alberto Ansaldo Mirko Prato Antonio Esau Del Rio Castillo Francesco Bonaccorso 《Liver Transplantation》2018,8(27)
Clean hydrogen production is highly promising to meet future global energy demands. The design of earth‐abundant materials with both high activity for hydrogen evolution reaction (HER) and electrochemical stability in both acidic and alkaline environments is needed, in order to enable practical applications. Here, the authors report a non‐noble 3d metal Cl‐chemical doping of liquid phase exfoliated single‐/few‐layer flakes of MoSe2 for creating MoSe2/3d metal oxide–hydr(oxy)oxide hybrid HER‐catalysts. It is proposed that the electron‐transfer from MoSe2 nanoflakes to metal cations and the chlorine complexation‐induced neutralization, as well as the in situ formation of metal oxide–hydr(oxy)oxides on the MoSe2 nanoflakes' surface, tailor the proton affinity of the catalysts, increasing the number and HER‐kinetics of their active sites in both acidic and alkaline electrolytes. The electrochemical coupling between doped‐MoSe2/metal oxide–hydr(oxy)oxide hybrids and single‐walled carbon nanotubes heterostructures further accelerates the HER process. Lastly, monolithic stacking of multiple heterostructures is reported as a facile electrode assembly strategy to achieve overpotential for a cathodic current density of 10 mA cm?2 of 0.081 and 0.064 V in 0.5 m H2SO4 and 1 m KOH, respectively. This opens up new opportunities to address the current density versus overpotential requirements targeted in pH‐universal hydrogen production. 相似文献
86.
Cástor Menéndez Gabor Igloi Hanspeter Henninger Roderich Brandsch 《Archives of microbiology》1995,164(2):142-151
A gene homologous tomoaA, the gene responsible for the expression of a protein involved in an early step in the synthesis of the molybdopterin cofactor
ofEscherichia coli, was found to be located 2.7-kb upstream of the nicotine dehydrogenase (ndh) operon on the catabolic plasmid pAO1 ofArthrobacter nicotinovorans. The MoaA protein, containing 354 amino acids, migrated on an SDS-polyacrylamide gel with an apparent molecular weight of
40,000, in good agreement with the predicted molecular weight of 38,880. The pAO1-encodedmoaA gene fromA. nicotinovorans was expressed inE. coli as an active protein that functionally complementedmoaA mutants. Its reduced amino acid sequence shows 43% identity to theE. coli MoaA, 44% to the NarAB gene product fromBacillus subtilis, and 42% to the gene product of two contiguous ORFs fromMethanobacterium formicicum. N-terminal sequences, including the motif CxxxCxYC, are conserved among the MoaA and NarAB proteins. This motif is also
present in proteins involved in PQQ cofactor synthesis in almost all the NifB proteins reported so far and in thefixZ gene product fromRhizobium leguminosarum. Mutagenesis of any of these three conserved cysteine residues to serine abolished the biological activity of MoaA, while
substitution of the tyrosine by either serine, phenylalanine, or alanine did not alter the capacity of the protein to complement
themoaA mutation inE. coli. A second Cys-rich domain with the motif FCxxC(13x)C is found close to the C-terminus of MoaA and NarAB proteins. These two
Cys-rich sequences may be involved in the coordination of a metal ions. The pAO1 copy ofmoaA may not be unique in theA. nicotinovorans genome since the molybdopterin cofactor oxidation products were detected in cell extracts from a plasmidless strain. 相似文献
87.
Porphobilinogen deaminase and uroporphyrinogen III synthase: Structure,molecular biology,and mechanism 总被引:1,自引:0,他引:1
Peter M. Shoolingin-Jordan 《Journal of bioenergetics and biomembranes》1995,27(2):181-195
Porphobilinogen deaminase (hydroxymethylbilane synthase) and uroporphyrinogen III synthase (uroporphyrinogen III cosynthase) catalyze the transformation of four molecules of porphobilinogen, via the 1-hydroxymethylbilane, preuroporphyrinogen, into uroporphyrinogen III. A combination of studies involving protein chemistry, molecular biology, site-directed mutagenesis, and the use of chemically synthesized substrate analogs and inhibitors is helping to unravel the complex mechanisms by which the two enzymes function. The determination of the X-ray structure ofE. coli porphobilinogen deaminase at 1.76 Å resolution has provided the springboard for the design of further experiments to elucidate the precise mechanism for the assembly of both the dipyrromethane cofactor and the tetrapyrrole chain. The human deaminase structure has been modeled from theE. coli structure and has led to a molecular explanation for the disease acute intermittent porphyria. Molecular modeling has also been employed to simulate the spiro-mechanism of uroporphyrinogen III synthase. 相似文献
88.
Regulators of complement activity mediate inhibitory mechanisms through a common C3b‐binding mode
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Federico Forneris Jin Wu Xiaoguang Xue Daniel Ricklin Zhuoer Lin Georgia Sfyroera Apostolia Tzekou Elena Volokhina Joke CM Granneman Richard Hauhart Paula Bertram M Kathryn Liszewski John P Atkinson John D Lambris Piet Gros 《The EMBO journal》2016,35(10):1133-1149
Regulators of complement activation (RCA) inhibit complement‐induced immune responses on healthy host tissues. We present crystal structures of human RCA (MCP, DAF, and CR1) and a smallpox virus homolog (SPICE) bound to complement component C3b. Our structural data reveal that up to four consecutive homologous CCP domains (i–iv), responsible for inhibition, bind in the same orientation and extended arrangement at a shared binding platform on C3b. Large sequence variations in CCP domains explain the diverse C3b‐binding patterns, with limited or no contribution of some individual domains, while all regulators show extensive contacts with C3b for the domains at the third site. A variation of ~100° rotation around the longitudinal axis is observed for domains binding at the fourth site on C3b, without affecting the overall binding mode. The data suggest a common evolutionary origin for both inhibitory mechanisms, called decay acceleration and cofactor activity, with variable C3b binding through domains at sites ii, iii, and iv, and provide a framework for understanding RCA disease‐related mutations and immune evasion. 相似文献
89.
Legumes capable of fixing atmospheric N2 are abundant and diverse in many tropical forests, but the factors determining ecological patterns in fixation are unresolved. A long‐standing idea is that fixation depends on soil nutrients (N, P or Mo), but recent evidence shows that fixation may also differ among N2‐fixing species. We sampled canopy‐height trees across five species and one species group of N2‐fixers along a landscape P gradient, and manipulated P and Mo to seedlings in a shadehouse. Our results identify taxonomy as the major determinant of fixation, with P (and possibly Mo) only influencing fixation following tree‐fall disturbances. While 44% of trees did not fix N2, other trees fixed at high rates, with two species functioning as superfixers across the landscape. Our results raise the possibility that fixation is determined by biodiversity, evolutionary history and species–specific traits (tree growth rate, canopy stature and response to disturbance) in the tropical biome. 相似文献
90.
A dual system formed by the ARC and NR molybdoenzymes mediates nitrite‐dependent NO production in Chlamydomonas
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