2020
DOI: 10.1016/j.carbon.2020.01.097
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Charge transfer mediated photoluminescence enhancement in carbon dots embedded in TiO2 nanotube matrix

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Cited by 22 publications
(6 citation statements)
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“…A variety of oxygen‐containing functional groups exits on the surface of CDs, such as typical ‐OH (≈3424 cm −1 , ≈1073 cm −1 , it can mostly be removed by annealing, i.e., annealed CDs), ─C≐O (≈1708 cm −1 ), and C─O─C (≈1175 cm −1 ) revealed by FTIR (Figure 1e). [ 32,33 ] Corresponding XPS full‐spectrum data also reveals that the percentage of O in the annealed CDs decreases from 20.4% to 12.3% while C increases from 79.6% to 87.7% (Figure 1f); these O reductions are mainly attributed to the decomposition of C─O (from 42.3% to 19.9% at 286.4 eV), [ 34,35 ] C≐O (from 9.5% to 4.8% at 288.2 eV), [ 36,37 ] and O─C≐O (from 8.1% to 0% at 288.8 eV) [ 35,37 ] decomposition of the three oxygen‐containing functional groups (Figure 1g); the same trend is demonstrated in the corresponding O 1s fine spectra, especially C≐O at 530.4 eV [ 38,39 ] and O─C≐O at 531.4 eV (Figure 1h). [ 40,41 ] Some of the oxygen‐containing functional groups containing H are also verified by their corresponding 1 H‐NMR (Figure S2, Supporting Information), including ─COOH at 10.28 ppm, ─CHO at 9.49 ppm, and ─OH at 2.06 ppm.…”
Section: Resultsmentioning
confidence: 98%
“…A variety of oxygen‐containing functional groups exits on the surface of CDs, such as typical ‐OH (≈3424 cm −1 , ≈1073 cm −1 , it can mostly be removed by annealing, i.e., annealed CDs), ─C≐O (≈1708 cm −1 ), and C─O─C (≈1175 cm −1 ) revealed by FTIR (Figure 1e). [ 32,33 ] Corresponding XPS full‐spectrum data also reveals that the percentage of O in the annealed CDs decreases from 20.4% to 12.3% while C increases from 79.6% to 87.7% (Figure 1f); these O reductions are mainly attributed to the decomposition of C─O (from 42.3% to 19.9% at 286.4 eV), [ 34,35 ] C≐O (from 9.5% to 4.8% at 288.2 eV), [ 36,37 ] and O─C≐O (from 8.1% to 0% at 288.8 eV) [ 35,37 ] decomposition of the three oxygen‐containing functional groups (Figure 1g); the same trend is demonstrated in the corresponding O 1s fine spectra, especially C≐O at 530.4 eV [ 38,39 ] and O─C≐O at 531.4 eV (Figure 1h). [ 40,41 ] Some of the oxygen‐containing functional groups containing H are also verified by their corresponding 1 H‐NMR (Figure S2, Supporting Information), including ─COOH at 10.28 ppm, ─CHO at 9.49 ppm, and ─OH at 2.06 ppm.…”
Section: Resultsmentioning
confidence: 98%
“…The valence band edge (VBE) is the point of intersection between the straight-line fits to the valence band and core-level spectra. 35 The VBE of 5BTBNNδ is located at 2.28 eV, which is 0.31 eV greater than the VBE (1.96 eV) of the 5BTBNN sample. This result suggests that there is a shift in the VBE position to higher energy upon cationic vacancy creation in the 5BTBNNδ sample.…”
Section: Optical Propertiesmentioning
confidence: 84%
“…The corresponding plots are shown in Figure a,b. The valence band edge (VBE) is the point of intersection between the straight-line fits to the valence band and core-level spectra . The VBE of 5BTBNNδ is located at 2.28 eV, which is 0.31 eV greater than the VBE (1.96 eV) of the 5BTBNN sample.…”
Section: Resultsmentioning
confidence: 99%
“…The hydrothermal synthesis method also enables CQDs to be directly synthesized onto photoanodes as sole photosensitizers. Other methods have been used to adhere CQDs to photoanodes, such as drop-casting, but yield poor adsorption and stability. , Zhang et al synthesized CQDs directly onto a TiO 2 photoanode via an in situ hydrothermal reaction of CA and ethanediamine with an immersed TiO 2 -coated photoanode . A CQD thin-film coating formed homogeneously on the porous TiO 2 layer, comprising spherical nanostructures with 2–6 nm particles that did not block the TiO 2 pores.…”
Section: Synthesis Methods For Cqdsmentioning
confidence: 99%