3D ordered RuO 2/WO 3 heterostructure inverse opal arrays for highly-active and stable acidic oxygen evolution reaction DOI Creative Commons

Runlong Jia,

Yan Tan,

Aoshuang Li

и другие.

Deleted Journal, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 8, 2024

Development of highly active and stable acidic oxygen evolution reaction catalyst is very important for efficient water splitting while remains challenging. Herein, we report a ordered RuO2/WO3 inverse opals (IOs) to address the bottleneck problem see-saw relationship between activity stability, in which crystalline corrosionresistant WO3 facilitates electron transport stabilizes RuO2, whereas lattice mismatch-induced amorphousdominated RuO2 provides abundant unsaturated coordination sites enhance (OER) activity. Consequently, IOs demonstrates outstanding OER performance terms low overpotential 180 mV reach 10 mA·cm–2, excellent stability maintaining 100 hours continuous test. Experimental characterizations density functional theory calculations reveal that interface coupling can spin polarization electrons increase overlaps electronic projected states Ru d orbitals metal O p intermediates, facilitating pathway switch from mechanism adsorbate mechanism, significantly decreases energy barrier process. Meanwhile, rich vacancies supports heterostructures could inhibit over-oxidation species, so as simultaneously.

Язык: Английский

Research progress of anionic vacancies in electrocatalysts for oxygen evolution reaction DOI

Yanan Xia,

Jing‐Qi Chi,

Junheng Tang

и другие.

CHINESE JOURNAL OF CATALYSIS (CHINESE VERSION), Год журнала: 2024, Номер 66, С. 110 - 138

Опубликована: Ноя. 1, 2024

Язык: Английский

Процитировано

3

3D ordered RuO 2/WO 3 heterostructure inverse opal arrays for highly-active and stable acidic oxygen evolution reaction DOI Creative Commons

Runlong Jia,

Yan Tan,

Aoshuang Li

и другие.

Deleted Journal, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 8, 2024

Development of highly active and stable acidic oxygen evolution reaction catalyst is very important for efficient water splitting while remains challenging. Herein, we report a ordered RuO2/WO3 inverse opals (IOs) to address the bottleneck problem see-saw relationship between activity stability, in which crystalline corrosionresistant WO3 facilitates electron transport stabilizes RuO2, whereas lattice mismatch-induced amorphousdominated RuO2 provides abundant unsaturated coordination sites enhance (OER) activity. Consequently, IOs demonstrates outstanding OER performance terms low overpotential 180 mV reach 10 mA·cm–2, excellent stability maintaining 100 hours continuous test. Experimental characterizations density functional theory calculations reveal that interface coupling can spin polarization electrons increase overlaps electronic projected states Ru d orbitals metal O p intermediates, facilitating pathway switch from mechanism adsorbate mechanism, significantly decreases energy barrier process. Meanwhile, rich vacancies supports heterostructures could inhibit over-oxidation species, so as simultaneously.

Язык: Английский

Процитировано

1