In situ Observation of Porosity Formation in Porous Single-crystalline TiO2 Monolith for Enhanced and Stable Catalytic CO Oxidation

被引:3
|
作者
Cheng, Fangyuan [1 ,4 ,5 ]
Zhang, Jie [1 ]
Xie, Kui [1 ,2 ,3 ,4 ,5 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Optoelect Mat Chem & Phys, Fuzhou 350002, Peoples R China
[2] Fujian Sci & Technol Innovat Lab Optoelect Informa, Fuzhou 350108, Fujian, Peoples R China
[3] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
[4] Adv Energy Sci & Technol Guangdong Lab, 29 Sanxin North Rd, Huizhou 116023, Guangdong, Peoples R China
[5] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
Porous single crystal; TiO2; In situ TEM; Solid-solid transformation; CO oxidation; TITANIUM-DIOXIDE; LARGE-AREA; FILMS; SURFACE; GROWTH; RUTILE; XPS; IR;
D O I
10.1002/anie.202300480
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Introducing pores in single crystals creates a new type of porous materials that incorporate porosity and structural coherence. Herein, we use in situ transmission electron microscopy to disclose the porosity formation by converting KTiOPO4 (KTP) single crystals into porous single-crystalline (PSC) TiO2 monoliths in a solid-solid transformation. The isolated crystalline nuclei of TiO2 clusters with identical lattice orientation on KTP surface moves TiO2/KTP interface toward mother phase for growing PSC TiO2 monoliths. The relative density in PSC TiO2 monoliths dominates porosity while the macroscopic dimensions remain unchanged in the transformation. The single-crystalline nature of porous architecture stabilizes oxygen vacancy to activate lattice oxygen while the three-dimensional percolation enhances species diffusion. PSC TiO2 monoliths with deposited Pt clusters show enhanced and stable catalytic CO oxidation in air at similar to 75 degrees C for 200 hours of operation.
引用
收藏
页数:7
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