Porous single crystalline-like titanium dioxide monolith with enhanced photoelectrochemical performance

Macro-sized porous single crystalline-like (PSC-like) TiO 2 is endowed with unique structural advantages due to its structural consistency and porosity in a large area, which would significantly enhance its photoelectrochemical function. However, there are significant technical challenges in the gro...

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Veröffentlicht in:Frontiers in materials 2023-04, Vol.10
Hauptverfasser: Liu, Kaipeng, Cheng, Fangyuan, Luo, Yunfei, Liu, Ling, Wang, Changtao, Xie, Kui, Luo, Xiangang
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Sprache:eng
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Zusammenfassung:Macro-sized porous single crystalline-like (PSC-like) TiO 2 is endowed with unique structural advantages due to its structural consistency and porosity in a large area, which would significantly enhance its photoelectrochemical function. However, there are significant technical challenges in the growth of porous single crystalline-like monoliths. The consistency of structure dominates the structure so that the grain boundary is reduced to the minimum, which is in contradiction with the three-dimensional percolation structure. Here we report a lattice reconstruction strategy based on solid-solid transformation to grow porous single crystal-like anatase TiO 2 dominated by (200) and (101) facets at 2 cm scale. In comparison with the traditional definition of porous single crystal, it has two different lattice orientations, but still has good photoelectrochemical properties. The band gap engineering introduces Ti 3+ gap into the lattice to generate Ti n O 2n−1 with Magneli phase, limiting the created active structure to the lattice with two-dimensional surface, which would open a new avenue to create highly active surfaces to capture photons and transport electrons stably. The PSC-like Ti n O 2n−1 provides enhanced exciton lifetime (3–5 ns) as a photocatalytic catalyst and shows significant visible light absorption. The independent PSC-like Ti n O 2n−1 delivers high photocurrent of 1.8–5.5 mA · cm −2 at room temperature and does not decay for 10 h.
ISSN:2296-8016
2296-8016
DOI:10.3389/fmats.2023.1177093