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author:

Chen, Jie (Chen, Jie.) [1] | Luo, Xingrui (Luo, Xingrui.) [2] | Fan, Ao (Fan, Ao.) [3] | Zhu, Wenhao (Zhu, Wenhao.) [4] | Chen, Kailin (Chen, Kailin.) [5] | Qiu, Qingqing (Qiu, Qingqing.) [6] | Bi, Lingling (Bi, Lingling.) [7] | Yang, Kai (Yang, Kai.) [8] | Liang, Tongxiang (Liang, Tongxiang.) [9]

Indexed by:

EI SCIE

Abstract:

The development of full-spectrum composite photocatalysts is a promising approach to enhance solar energy utilization. In this study, the FeTiO3/NaYF4: Yb, Dy, Nd (FNYDN) upconversion composite photocatalysts were successfully synthesized via the hydrothermal method. The upconversion effect of rare earth ions on nearinfrared light is utilized to broaden the absorption range of visible light, thereby further improving the efficiency of solar energy utilization. Compared to pure FeTiO3 (80.83 %) and NaYF4 (37.76 %), the 0.75 FNYDN (93.51 %) samples showed significantly higher photo-Fenton activity for degradating antibiotics under visiblenear infrared (Vis-NIR) light. The upconversion luminescence at 980 nm and visible near-infrared (UV-VisNIR) spectrophotometer indicate that the incorporation of NaYF4: Yb, Dy, Nd (NYDN) can broaden the utilization of near infrared light, enhancing the degradation activity of organic pollutants under the NIR-light irradiation. Particularly, in the NIR light condition, the degradation efficiency of TCH by 0.75 FNYDN can go up to 86.72 % due to upconversion function of rare earth ions. Besides, several characterizations suggest that the formation of Z-Scheme heterojunction between FeTiO3 and NYDN enables effective separation and transfer of photocarriers. Thus, the enhanced photo-Fenton activity of the 0.75 FNYDN heterojunction can be attributed to the synergistic effects of upconversion and the Z-Scheme heterojunction. This experimental investigation provides a sound basis for the preparation of efficient upconversion composite photocatalysts.

Keyword:

FeTiO3 NaYF4 Photo-Fenton catalyst Upconversion Z -Scheme heterojunction

Community:

  • [ 1 ] [Chen, Jie]Jiangxi Univ Sci & Technol, Coll Rare Earths, Engn Res Ctr Hydrogen Energy Mat & Devices, 86 Hong Qi Rd, Ganzhou 341000, Peoples R China
  • [ 2 ] [Luo, Xingrui]Jiangxi Univ Sci & Technol, Coll Rare Earths, Engn Res Ctr Hydrogen Energy Mat & Devices, 86 Hong Qi Rd, Ganzhou 341000, Peoples R China
  • [ 3 ] [Fan, Ao]Jiangxi Univ Sci & Technol, Coll Rare Earths, Engn Res Ctr Hydrogen Energy Mat & Devices, 86 Hong Qi Rd, Ganzhou 341000, Peoples R China
  • [ 4 ] [Zhu, Wenhao]Jiangxi Univ Sci & Technol, Coll Rare Earths, Engn Res Ctr Hydrogen Energy Mat & Devices, 86 Hong Qi Rd, Ganzhou 341000, Peoples R China
  • [ 5 ] [Chen, Kailin]Jiangxi Univ Sci & Technol, Coll Rare Earths, Engn Res Ctr Hydrogen Energy Mat & Devices, 86 Hong Qi Rd, Ganzhou 341000, Peoples R China
  • [ 6 ] [Qiu, Qingqing]Jiangxi Univ Sci & Technol, Coll Rare Earths, Engn Res Ctr Hydrogen Energy Mat & Devices, 86 Hong Qi Rd, Ganzhou 341000, Peoples R China
  • [ 7 ] [Liang, Tongxiang]Jiangxi Univ Sci & Technol, Coll Rare Earths, Engn Res Ctr Hydrogen Energy Mat & Devices, 86 Hong Qi Rd, Ganzhou 341000, Peoples R China
  • [ 8 ] [Bi, Lingling]Huaiyin Inst Technol, Coll Chem Engn, Natl & Local Joint Engn Res Ctr Mineral Salt Deep, Key Lab Palygorskite Sci & Appl Technol Jiangsu Pr, Huaian 223003, Peoples R China
  • [ 9 ] [Luo, Xingrui]Jiangxi Univ Sci & Technol, Sch Chem & Chem Engn, Ganzhou 341000, Jiangxi, Peoples R China
  • [ 10 ] [Yang, Kai]Fuzhou Univ, Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China

Reprint 's Address:

  • [Qiu, Qingqing]Jiangxi Univ Sci & Technol, Coll Rare Earths, Engn Res Ctr Hydrogen Energy Mat & Devices, 86 Hong Qi Rd, Ganzhou 341000, Peoples R China;;[Bi, Lingling]Huaiyin Inst Technol, Coll Chem Engn, Natl & Local Joint Engn Res Ctr Mineral Salt Deep, Key Lab Palygorskite Sci & Appl Technol Jiangsu Pr, Huaian 223003, Peoples R China

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Source :

JOURNAL OF ALLOYS AND COMPOUNDS

ISSN: 0925-8388

Year: 2025

Volume: 1036

5 . 8 0 0

JCR@2023

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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