20 research outputs found
Magnetic Field Enhancing the Electrocatalytic Oxygen Evolution Reaction of FeMn-Based Spinel Oxides
For the widespread application of electrolytic water
hydrogen production
technology, it is crucial to prepare electrolytic water catalysts
via inexpensive and abundant transition metals. Commercially, Mn3O4 can be utilized extensively since it is cheap,
abundant, and stable, but its electrocatalytic performance still needs
to be enhanced. In this paper, we adopted the conventional hydrothermal
method to introduce Fe atoms into Mn3O4 to form
spinel-structured FeMn oxides on Ni foam (marked as FexMn3–xO4); then, an external magnetic field was applied to further improve
its oxygen evolution reaction (OER) performance. The overpotential
of FeMn2O4 is 258 mV (current density at 20
mA·cm–2), and the Tafel slope is 28.7 mV·dec–1 when the magnetic field strength is 105 mT and the
angle between the electric field and the magnetic field is 45°.
The introduction of Fe and the synergistic effect of the mixed Mn
and Fe promote the reaction kinetics and thus improve the OER performance
of Mn3O4. The enhanced performance of FexMn3–xO4 under the magnetic field may mainly originate from the magnetohydrodynamic
(MHD) effect, charge transfer effect, and energy effect
Probing the Crystal Plane Effect of Co<sub>3</sub>O<sub>4</sub> for Enhanced Electrocatalytic Performance toward Efficient Overall Water Splitting
Identifying
effective methods to enhance the properties of catalysts is urgent
to broaden the scanty technologies, so far. Herein, we synthesized
four Co<sub>3</sub>O<sub>4</sub> crystals with different crystal planes
and explored the crystal planes’ effects on electrochemical
water splitting through theoretical and experimental studies for the
first time. The results illustrate that the correlation of catalytic
activity is established as {111} > {112} > {110} > {001}.
Co<sub>3</sub>O<sub>4</sub> crystals exposed with {111} facets show
the highest OER (oxygen evolution reaction) and HER (hydrogen evolution
reaction) activities. Upon fabrication in an alkaline electrolyzer,
the bifunctional {111}∥{111} couple manifests the highest catalytic
activity and satisfying durability for overall water splitting. Density
functional theory (DFT) explains that the {111} facet possesses the
biggest dangling bond density, highest surface energy, and smallest
absolute value of Δ<i>G</i><sub>H*</sub>, leading
to the enhanced electrocatalytic performance. This work will broaden
our vision to improve the activity of various electrocatalysts by
selectively exposing the specific crystal planes
New Efficient Electrocatalyst for the Hydrogen Evolution Reaction: Erecting a V<sub>2</sub>Se<sub>9</sub>@Poly(3,4-ethylenedioxythiophene) Nanosheet Array with a Specific Active Facet Exposed
To obtain catalysts
with remarkable activity for the hydrogen evolution
reaction (HER), rational design and synthesis of catalysts with rich
active sites are very urgent. Herein, we reported, for the first time,
V<sub>2</sub>Se<sub>9</sub> nanosheet arrays exposed with the highly
active (100) facet as a new efficient catalyst for HER. The highly
active but thermodynamically instable (100) facet was converted from
V<sub>2</sub>O<sub>5</sub> based on a low crystal-mismatch strategy.
Furthermore, conductive polyÂ(3,4-ethylenedioxythiophene) (PEDOT) acting
as a co-catalyst further contributed to the redistribution of charge
and reduction of hydrogen adsorption energy. Due to the strong synergistic
effect between V<sub>2</sub>Se<sub>9</sub> and PEDOT, the resulting
material, noted as V<sub>2</sub>Se<sub>9</sub>@PEDOT NSs/NF, exhibited
excellent electrocatalytic performance among selenide catalysts, for
example, a small overpotential of 72 mV at 10 mA cm<sup>–2</sup>, a low Tafel slope of 36.5 mV dec<sup>–1</sup>, and remarkable
durability. Simultaneously, density functional theory (DFT) computations
proved that the adsorption free energy of H* (Δ<i>G</i><sub>H*</sub>) for V<sub>2</sub>Se<sub>9</sub>@PEDOT NSs/NF (0.09
eV) is comparable to that of Pt (around 0.09 eV)
SNP distribution among scaffolds.
<p>The X-axis represents scaffold size (number of SNPs per scaffold)</p
Identification of expressed <i>Claudin</i> genes containing SNPs.
<p>Identification of expressed <i>Claudin</i> genes containing SNPs.</p
The genome distribution of the mapped reads.
<p>The genome distribution of the mapped reads.</p
Classification of putative SNPs.
<p>Inter-genic SNPs were identified from regions between genes, while Down_stream(+1 k) and Up_stream(−1 k) represents SNPs identified from regions of 1 kb downstream and upstream of the genes.</p
Distribution of minor allele frequencies (MAFs) of SNPs identified from the <i>T. rubirpes</i> swimbladder.
<p>The X-axis represents the SNP minor allele frequency in percentage, while the Y-axis represents the number of SNPs with given minor allele frequency</p
KEGG biochemical mappings for genes containing SNPs.
<p>KEGG biochemical mappings for genes containing SNPs.</p