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Chia-Ying Chiang

Researcher at National Taiwan University of Science and Technology

Publications -  39
Citations -  1338

Chia-Ying Chiang is an academic researcher from National Taiwan University of Science and Technology. The author has contributed to research in topics: Water splitting & Photoelectrochemical cell. The author has an hindex of 15, co-authored 35 publications receiving 993 citations. Previous affiliations of Chia-Ying Chiang include University of Maryland, College Park & Academia Sinica.

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Comparative study on MoS2 and WS2 for electrocatalytic water splitting

TL;DR: In this paper, the catalytic reactivity of both MoS2 and WS2 materials produced by one-step and scalable thermolysis from (NH4)2WS4 and (NH 4)2MoS4 precursors respectively was investigated.
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Copper oxide nanoparticle made by flame spray pyrolysis for photoelectrochemical water splitting – Part II. Photoelectrochemical study

TL;DR: A scalable method for hydrogen generation by splitting water via a photo-electrochemical cell was studied in this article, where flame spray pyrolysis and spin coating processing methods were used for preparing copper oxide nanoparticles and copper oxide photocathodes.
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Selective Electro-oxidation of Glycerol to Dihydroxyacetone by a Non-precious Electrocatalyst – CuO

TL;DR: In this article, an earth abundant and non-precious electrocatalyst, CuO, is developed for the high selectivity (∼60 %) towards the glycerol electro-oxidation to dihydroxyacetone (DHA) at high current density (3 mA/cm2) under mild basic condition, pH 9.
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Copper oxide photocathodes prepared by a solution based process

TL;DR: In this paper, the authors devised an economical solution-based route to photoelectrochemical (PEC) cells, taking copper nitrate as the copper ion source and adding an alkali hydroxide, here NaOH, to produce high aspect ratio (3.1-9.7) CuO nanoparticles.
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Three‐Dimensional Molybdenum Sulfide Sponges for Electrocatalytic Water Splitting

TL;DR: Electroactive MoSx catalysts on porous 3D sponges synthezied by a simple and scalable thermolysis process are proposed and are attributed to the large electrochemical surface area and their S-rich chemical structure.