Boosting Hydrogen Evolution Reaction by Phase Engineering and Phosphorus Doping on Ru/P-TiO2
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhou, Shizheng | ko |
dc.contributor.author | Jang, Haeseong | ko |
dc.contributor.author | Qin, Qing | ko |
dc.contributor.author | Hou, Liqiang | ko |
dc.contributor.author | Kim, Min Gyu | ko |
dc.contributor.author | Liu, Shangguo | ko |
dc.contributor.author | Liu, Xien | ko |
dc.contributor.author | Cho, Jaephil | ko |
dc.date.available | 2022-12-09T01:38:46Z | - |
dc.date.created | 2022-11-16 | ko |
dc.date.issued | 2022-11 | ko |
dc.identifier.citation | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.61, no.47 | ko |
dc.identifier.issn | 1433-7851 | ko |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/60114 | - |
dc.description.abstract | Synergistic optimization of the elementary steps of water dissociation and hydrogen desorption for the hydrogen evolution reaction (HER) in alkaline media is a challenge. Herein, the Ru cluster anchored on a trace P-doped defective TiO2 substrate (Ru/P-TiO2) was synthesized as an electrocatalyst for the HER; it exhibited a commercial Pt/C-like geometric activity and an excellent mass activity of 9984.3 mA mg(Ru)(-1) at -0.05 V vs. RHE, which is 34.3 and 18.7 times higher than that of Pt/C and Ru/TiO2, respectively. Experimental and theoretical studies indicated that using a rutile-TiO2-crystal-phase substrate enhanced the HER activity more than the anatase phase. Rich surface oxygen vacancies on rutile-TiO2 facilitated the adsorption and dissociation of water, while the partial substitution of Ti4+ with P5+ enhanced H-2 generation by facilitating hydrogen spillover from the Ru site to the surface P site, synergistically enhancing the HER activity. | ko |
dc.language | 영어 | ko |
dc.publisher | WILEY-V C H VERLAG GMBH | ko |
dc.title | Boosting Hydrogen Evolution Reaction by Phase Engineering and Phosphorus Doping on Ru/P-TiO2 | ko |
dc.type | ARTICLE | ko |
dc.identifier.scopusid | 2-s2.0-85140355077 | ko |
dc.identifier.wosid | 000871723400001 | ko |
dc.type.rims | ART | ko |
dc.identifier.doi | 10.1002/anie.202212196 | ko |
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