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It is observed that higher water splitting temperature favors towards higher efficiencies.
The prepared NiO/Mo BiVO4 p n junction structure showed much higher water splitting activity than the pristine BiVO4 and Mo BiVO4.
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The resulting membrane has a low electrical resistance and a high "water splitting" efficiency.
A water electrolysis cell was fabricated using this cheap, easily-obtained, efficient and robust electrode as both anode and cathode to achieve high water splitting current density of 20 mA cm−2 at cell voltage around 1.50 V.
The basic approach in high-temperature water splitting is to heat up an oxidized metal to drive off oxygen, then add water.
It is expected to provide a novel route to prepare such a core-shell electrocatalyst with high performance for water splitting.
This result demonstrated high performance PEC water splitting as a potential route for the production of hydrogen gas using a single Cu-doped α-Fe2O3 photoelectrode without the need for other catalysts and hybrid structures.
The sluggish kinetics process derived from oxygen evolution reaction (OER), as the crucial half-reaction, is one of key and bottleneck issues for achieving high-efficiency electrochemical water splitting.
This paper describes a novel design of high-efficiency photoelectrochemical water splitting electrode, i.e., ordered TiO2 nanorod arrays (NRs) sensitized simultaneously with noble metal (Ag), binary metal sulfides (Ag2S) and ternary metal sulfides (Ag3CuS2) multiple photosensitizers for the first time.
In any case, the measured almost steplike improvement of the electrode performance by Fe exsolution emphasizes the high complexity of such a system but provides new directions in the search of novel oxide based electrodes for high-temperature electrochemical water splitting.
Additionally, the higher photocurrent densities for water splitting were obtained for the samples anodized at the highest anodization potential and under hydrodynamic conditions, increasing in a 71% for the nanostructures anodized at 1000 rpm when the anodization potential changes from 20 to 40 V.
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CEO of Professional Science Editing for Scientists @ prosciediting.com