4.8 Article

Carbon dots enhance the interface electron transfer and photoelectrochemical kinetics in TiO2 photoanode

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 304, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2021.120983

Keywords

TiO2 photoanode; Nitrogen-doped carbon dots; Photoelectrochemical activities; In-situ transient photovoltage

Funding

  1. National Key Research and Development Project of China [2020YFA0406101, 2020YFA0406104]
  2. National MCF Energy RD Program [2018YFE0306105]
  3. Key-Area Research and Development Program of GuangDong Province [2019B010933001]
  4. Innovative Research Group Project of the National Natural Science Foundation of China [51821002]
  5. National Natural Science Foundation of China [51725204, 21771132, 51972216, 52041202]
  6. Natural Science Foundation of Jiangsu Province [BK20190041]
  7. Collaborative Innova-tion Center of Suzhou Nano Science Technology
  8. Suzhou Key Laboratory of Functional Nano Soft Materials

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In this study, nitrogen-doped carbon dots (N-CDs) anchored TiO2 photoanodes were fabricated by one-step hydrothermal method, and the mechanism of how it improves the photoelectrochemical (PEC) performance was explained through in-situ characterization. The results showed that after anchoring N-CDs, the photo-generated charge separation efficiency and charge transfer efficiency of TiO2 were significantly improved, and the conductivity of TiO2 was enhanced as well.
Photoelectrochemical (PEC) water splitting is one of the most promising strategies to turn solar energy into chemical fuels. The low efficiency of photo-generated charge separation caused by fast electron-hole recombination is regarded as a challenge that hinders the further improvement of TiO2 photoanode performance in PEC cells. Here, the nitrogen-doped carbon dots (N-CDs) anchored TiO2 photoanodes were fabricated by one-step hydrothermal method. The in-situ transient photovoltage (TPV) technology shows that electron-trap effect is formed in TiO2 photoanode due to the existence of N-CDs. Meanwhile, the enhancement of photo-generated charge separation efficiency was proven as the charge extraction of TiO2 is promoted by similar to 160% after anchoring N-CDs. Besides, N-CDs increase the conductivity of TiO2 photoanode and promote the efficiency of photo-generated charge transfer. In addition, the impedance of TiO2 photoanode and its interface are reduced by similar to 34% and similar to 66%, respectively. Under AM 1.5G light intensity and 1.23 V vs. RHE, the highest photocurrent densities of TiO2/N-CDs (TNCD-15 mg) is 3.09 mA cm(-2) in 1.0 M NaOH, which is similar to 3.22 times as high as that of the primitive TiO2. This work explains the mechanism of anchoring N-CDs to improve PEC performance through in-situ characterization, which provides a new idea for PEC material design to achieve higher PEC performances.

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