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Preparation of Pt-Intercalated KCa2Nb3O10 Nanosheets and Their Photocatalytic Activity for Overall Water Splitting
被引:15
|作者:
Oshima, Takayoshi
[1
,2
]
Lu, Daling
[3
]
Maeda, Kazuhiko
[1
]
机构:
[1] Tokyo Inst Technol, Sch Sci, Dept Chem, Meguro Ku, 2-12-1-NE-2, Tokyo 1528550, Japan
[2] Japan Soc Promot Sci, Chiyoda Ku, 5-3-1 Kojimachi, Tokyo 1020083, Japan
[3] Tokyo Inst Technol, Ctr Adv Mat Anal, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
来源:
关键词:
artificial photosynthesis;
heterogeneous photocatalysis;
nanosheets;
semiconductors;
water splitting;
RHODIUM HYDROXIDE NANOPARTICLES;
HYDROGEN-EVOLUTION;
OXIDE NANOSHEETS;
VISIBLE-LIGHT;
PEROVSKITE NANOSHEETS;
REACTION-MECHANISM;
DECOMPOSITION;
CATALYST;
NIOBATE;
D O I:
10.1002/cnma.201600072
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Pt-deposited KCa2Nb3O10 restacked nanosheets were studied as water splitting photocatalysts under UV and visible irradiation (lambda >= 300 nm). Nanoparticulate Pt species were intercalated into the gallery space of KCa2Nb3O10 restacked nanosheets by using the electrostatic interaction between the anionic nanosheets and a cationic Pt precursor, followed by H-2 reduction at 373-973 K. Although differences in the Pt size distribution were observed, Pt nanoparticles <2 nm in size were mainly deposited at temperatures below 673 K, owing to the suppression of Pt aggregation that originated from steric hindrance of the interlayer nanospace. On the other hand, the valence state of Pt varied from oxide to metal, accompanied with a change in the location from the interlayer space to the external surface, as the reduction temperature was increased. The highest water splitting activity was obtained at 473 K, where the Pt species were mainly loaded as nanoparticles that had <1 nm size and electron-deficient states.
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页码:748 / 755
页数:8
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