In situ X-ray spectroscopies beyond conventional X-ray absorption spectroscopy on deciphering dynamic configuration of electrocatalysts

被引:58
作者
Wang, Jiali [1 ,2 ]
Hsu, Chia-Shuo [1 ,2 ]
Wu, Tai-Sing [3 ]
Chan, Ting-Shan [3 ]
Suen, Nian-Tzu [4 ]
Lee, Jyh-Fu [3 ]
Chen, Hao Ming [1 ,2 ,3 ,5 ]
机构
[1] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan
[2] Natl Taiwan Univ, Ctr Emerging Mat & Adv Devices, Taipei 10617, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
[4] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Peoples R China
[5] Taipei Med Univ, Coll Biomed Engn, Grad Inst Nanomed & Med Engn, Taipei 11031, Taiwan
关键词
RESOLUTION FLUORESCENCE DETECTION; EMISSION SPECTROSCOPY; OXIDATION-STATE; FUEL-CELL; K-EDGE; OXYGEN REDUCTION; ADSORPTION SITES; IRON SITES; CATALYSTS; IDENTIFICATION;
D O I
10.1038/s41467-023-42370-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Realizing viable electrocatalytic processes for energy conversion/storage strongly relies on an atomic-level understanding of dynamic configurations on catalyst-electrolyte interface. X-ray absorption spectroscopy (XAS) has become an indispensable tool to in situ investigate dynamic natures of electrocatalysts but still suffers from limited energy resolution, leading to significant electronic transitions poorly resolved. Herein, we highlight advanced X-ray spectroscopies beyond conventional XAS, with emphasis on their unprecedented capabilities of deciphering key configurations of electrocatalysts. The profound complementarities of X-ray spectroscopies from various aspects are established in a probing energy-dependent "in situ spectroscopy map" for comprehensively understanding the solid-liquid interface. This perspective establishes an indispensable in situ research model for future studies and offers exciting research prospects for scientists and spectroscopists.
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页数:23
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