6 research outputs found
Role of Sodium Ion on TiO<sub>2</sub> Photocatalyst: Influencing Crystallographic Properties or Serving as the Recombination Center of Charge Carriers?
There have been continuing debates
about the role of Na<sup>+</sup> on TiO<sub>2</sub> photocatalyst
in the past decades. Most researchers
accepted that Na<sup>+</sup> served as the recombination center of
photogenerated electrons and holes. Nevertheless, other opinions also
existed, such as Na<sup>+</sup> increased the crystallite size of
TiO<sub>2</sub>, Na<sup>+</sup> hampered the crystallization of anatase
TiO<sub>2</sub>, and Na<sup>+</sup> promoted the formation of brookite
TiO<sub>2</sub> or titanate sodium. In this research, we have systematically
investigated the role of Na<sup>+</sup> during the fabrication of
TiO<sub>2</sub> film and powder through the sol–gel method
and studied the influences of crystallinity and the content of Na<sup>+</sup> on the photocatalytic activities of TiO<sub>2</sub> film
and powder. It has been found that the existence of Na<sup>+</sup> in TiO<sub>2</sub> film and powder should influence their crystallographic
properties, in detail, inhibiting the crystallization and growth of
anatase phase in TiO<sub>2</sub> film and powder, promoting the formation
of brookite phase in TiO<sub>2</sub> film, and increasing the transformation
temperature of anatase to rutile phase in TiO<sub>2</sub> powder.
Even though the existence of Na<sup>+</sup> forms the Ti–O–Na
bond on the surface of TiO<sub>2</sub>, however, the widely adopted
hypothesis of Na<sup>+</sup> serving as the recombination center of
photogenerated electrons and holes is not correct
Easy Way To Create Stepped Surface: A Thought from Oriented Attachment
Easy Way To Create Stepped Surface: A Thought from
Oriented Attachmen
Image_4_Integrated transcriptomic and metabolomic analyses revealed the molecular mechanism of terpenoid formation for salicylic acid resistance in Pulsatilla chinensis callus.tif
As a kind of traditional Chinese medicine, Pulsatilla chinensis (Bunge) Regel is well known for its anti-inflammation and anti-cancer activities, which are attributed to its active components including total saponins and monomers. To clarify the synthesis and metabolism mechanisms of class components in callus terpenes of P. chinensis, a certain concentration of salicylic acid (SA) hormone elicitor was added to the callus before being analysed by transcriptomic and metabolomic techniques. Results showed that the content of Pulsatilla saponin B4 in the callus suspension culture was significantly increased up to 1.99% with the addition of SA. Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that the differentially expressed genes were mainly enriched in 122 metabolic pathways, such as terpenoid metabolism-related pathways: terpenoid skeleton synthesis pathway, monoterpenoid biosynthesis pathways, diterpenoid biosynthesis pathways, and ubiquinone and other terpenoid-quinone biosynthesis pathways. A total of 31 differentially accumulated metabolites were obtained from four differential groups. Amongst 21 kinds of known chemical components in P. chinensis, deoxyloganic acid was the only monoterpenoid; the others are triterpenoids. In summary, this study found that SA elicitors can affect the metabolic changes of terpenoids in P. chinensis callus, which provided a basis for analysing the genetic regulation of terpenoid components of leucons.</p
Comparison of Sedimentary PAHs in the Rivers of Ammer (Germany) and Liangtan (China): Differences between Early- and Newly-Industrialized Countries
As a proxy to trace the impact of anthropogenic activity,
sedimentary
polycyclic aromatic hydrocarbons (PAHs) are compared between the early
industrialized and newly industrialized countries of Germany and China,
respectively. Surface sediment samples in the Ammer River of Germany
and the Liangtan River of China were collected to compare concentration
levels, distribution patterns, and diagnostic plots of sedimentary
PAHs. Total concentrations of 16 PAHs in Ammer sediments were significantly
higher by a factor of ∼4.5 than those in Liangtan. This contrast
agrees with an extensive literature survey of PAH levels found in
Chinese versus European sediments. Distribution patterns of PAHs were
similar across sites in the Ammer River, whereas they were highly
varied in the Liangtan River. Pyrogenic sources dominated in both
cases. Strong correlations of the sum of 16 PAHs and PAH groups with
TOC contents in the Liangtan River may indicate coemission of PAHs
and TOC. Poor correlations of PAHs with TOC in the Ammer River indicate
that other factors exert stronger influences. Sedimentary PAHs in
the Ammer River are primarily attributed to input of diffuse sources
or legacy pollution, while sediments in the Liangtan River are probably
affected by ongoing point source emissions. Providing further evidence
of a more prolonged anthropogenic influence are the elevated black
carbon fractions in sedimentary TOC in the Ammer compared to the Liangtan.
This implies that the Liangtan River, like others in newly industrialized
regions, still has a chance to avoid legacy pollution of sediment
which is widespread in the Ammer River and other European waterways
Facile Synthesis of Mesoporous and Thin-Walled Ni–Co Sulfide Nanotubes as Efficient Electrocatalysts for Oxygen Evolution Reaction
Development of high-performance and
inexpensive electrocatalysts
for oxygen evolution reaction (OER) is of important significance for
sustainable energy conversion technologies. In this work, mesoporous
Co and Ni–Co sulfide nanotubes with ultrathin nanowalls are
designed and fabricated by a facile and template-free solvothermal
method. The obtained CoS<sub>1.097</sub> nanotubes can be used as
an OER electrocatalyst, and the incorporation of Ni into the CoS<sub>1.097</sub> lattice could further enhance the catalytic activity
of the catalysts. The best-performing Ni<sub>0.13</sub>ÂCo<sub>0.87</sub>S<sub>1.097</sub> nanotubes exhibit high performance for
OER with a small overpotential of 316 mV to achieve a current density
of 10 mA cm<sup>–2</sup> and excellent stability, which outperform
those of commercial IrO<sub>2</sub> and most of the studied Co-based
OER catalysts. Our work demonstrates a new strategy to design highly
efficient non-previous-metal OER electrocatalysts with unique structures
and can be extended to other transition-metal-based systems