Comparative emission characteristics of CQDs synthesized by various research groups.
Synthesis by group | Synthesis technique | % QYa (highest) | Emission characteristics | Emission caused by type (band, surface states, etc.) | Doping/surface passivation | Prepared CQDs employed in application | Ref. |
---|---|---|---|---|---|---|---|
Ya-Ping Sun | Laser ablation | >10% | Blue emission @ 400 nm excitation | Surface states and quantum confinement | Surface passivation | No | 5 |
Excitation-dependent emission: emission intensity decreases and the emission peak red shifts as the incident wavelength increases | |||||||
Ruili Liu | Pyrolysis followed by chemical treatment | 14.70% | Blue emission @ 365 nm excitation | Surface states and quantum confinement | Surface passivation | Bioimaging | 43 |
Excitation-dependent emission: the emission intensity varies and the emission peak red shifts as the excitation wavelength increases from 320−500 nm | |||||||
Hui Peng | Chemical oxidation | 13% | Blue emission @ 360 nm excitation | Surface states and quantum confinement | Surface passivation | No | 50 |
Excitation-dependent emission: the emission intensity varies and the peak red shifts as the excitation wavelength increases beyond 360 nm | |||||||
Xiangyou Li | Laser ablation | — | Blue emission @ 360 nm excitation | Surface states and quantum confinement | Surface passivation | No | 102 |
Excitation-dependent emission: the emission intensity varies and the peak red shifts (from 400–520 nm) as the excitation wavelength is increased from 300–480 nm | |||||||
Dengyu Pan | Pyrolysis | 40.6% | Blue emission @ 365 nm excitation | Large HOMO–LUMO gap of small sp2 clusters | N-Doping | No | 45 |
Excitation-dependent emission: the emission intensity decreases and peak red shifts (from 425–510 nm) as the excitation wavelength is increased from 320–500 nm | |||||||
Emission is also sensitive to pH, solvent and spin | |||||||
Shengliang Hu | Laser ablation | Sample A: 12.2% | Blue emission @ 365 nm excitation (all 3 samples) | Quantum confinement | No | No | 62 |
Sample B: 06.2% | Excitation dependent emission in all the samples: the emission intensity and peak varies with the excitation wavelength | ||||||
Sample C: 01.2% | |||||||
Qi Wang | Microwave irradiation | 14% | Blue emission @ 365 nm excitation | Not mentioned | Not mentioned | A fluorescent probe for sensitive turn-on sensing of glutathione | 37 |
Emission intensity increases with pH | |||||||
Mingbo Wu | Chemical oxidation + hydrothermal (for N-CQD) | CQD: 8.7% | Excitation-dependent emission in both CQDs | Quantum confinement and surface states | N-Doping and surface passivation (N-CQD) | No | 51 |
N-CQD: 15.8% | CQD: yellow emission @ 340 nm excitation. The emission intensity varies and peaks red-shift from 480 to 600 nm as the excitation wavelength increases from 320 to 580 nm | ||||||
N-CQD: blue emission @ 340 nm excitation. The emission peak remains at 475 nm when excitation wavelength increases from 320 nm to 400 nm. As the excitation wavelength further increases to 520 nm, the maximum emission wavelength shows a red-shift from 480 to 540 nm | |||||||
Jianhui Deng | Electrochemical carbonization | CQD(6.0 V): 15.9% | Blue emission @ 365 nm excitation (by all 4-sets of CQDs synthesized under different potentials) | Quantum confinement and surface states | Undoped, surface passivation not required | Bio-imaging of Hela cells | 53 |
CQD(3.0 V): 4.0% | The intensity of emission is very low for CQD (3.0 V), it increases for CQD (4.5 V), and reaches a maximum for CQD (6.0 V) and then decreases for CQD (7.5 V) | ||||||
CQD(4.5 V): 9.1% | Excitation dependent emission: the emission intensity varies and emission peak red shifts as the excitation wavelength increases from 300 nm–500 nm | ||||||
CQD(6.0 V): 15.9% | The PL intensity of the CQDs were independent of pH under acidic conditions, but decreased under basic conditions | ||||||
CQD(7.5 V): 5.0% | |||||||
Hui Ding | Hydrothermal | ∼35% | Blue, green, yellow and red emission @ 365 nm excitation (by selected 4-sets of CQDs having different degrees of oxidation) | Surface states | N-Doping | In vivo bioimaging of mice | 26 |
Excitation-dependent emission: each of the 4 samples have a specific emission centre that does not change with the excitation wavelength but the intensity varies | |||||||
Yubin Song | Hydrothermal | 77.07% (Et-EDA CQD) | Blue emission @ 360 nm excitation (for Et-EDA CQDs) | Molecular states or molecular fluorescence and core states | N-Doping | Bio-application | 108 |
46.36% (Ac-EDA CQD) | Excitation-dependent emission: the emission intensity and peak shifts (from blue to green) as the excitation wavelength is increased from 300–500 nm | ||||||
Xugen Han | Hydrothermal | 84.80% | Blue emission @ 365 nm excitation | Surface states | N-Doping and surface passivation | Silicon-nanowire solar cells | 130 |
Excitation-independent emission: almost no shift in emission peak (peak appears at around 430 nm) but the emission intensity decreases as the excitation wavelength is increased from 300–390 nm | |||||||
Emission intensity is constant for pH values 4–8 but it decreases for too basic or acidic medium | |||||||
Hao Wang | Pyrolysis | ∼36% | Blue emission @ 365 nm excitation | Surface states | N-Doping | QDSC | 47 |
Excitation-dependent emission: the emission intensity varies and peak red shifts (from 425–510 nm) as the excitation wavelength is increased from 300–500 nm | |||||||
Fanglong Yuan | Hydrothermal | ∼75% (blue CQD) | Blue, green, yellow, orange and red emission @365 nm excitation (5 different colors of CQDs were prepared by modification in the synthesis process with the highest QY for blue CQDs) | Quantum confinement (bandgap emission) | N-Doping, surface passivation | LED | 90 |
Excitation independent emission: the emission peak intensity varies but the position remains the same, irrespective of the excitation wavelength for all the CQDs | |||||||
Julian Schneider | Hydrothermal | 53% (ethylenediamine-CQDs) | Blue emission @ 320 nm excitation (by all 3 types of CQDs) | t-CQDs: quantum confinement (core bandgap emission) and surface states e-CQDs | N-Doping | No | 104 |
Excitation dependent emission: the emission peak intensity and peak position changes as the excitation wavelength varies from 300–480 nm | h-CQDs: molecular fluorescence and surface states | ||||||
Gancheng Zuo | Hydrothermal | F-CQD: 31% | Excitation-dependent emission in both CQDs | Surface states | F-CQD: F-doping, N-doping | Red cell imaging and sensitive intracellular Ag + detection | 75 |
Undoped CQD: 28% | F-CQD: yellow emission @ 360 nm excitation | ||||||
Emission varies from 550–600 nm as the excitation varies from 360−580 nm | |||||||
Undoped-CQD: green emission @ 360 nm excitation | |||||||
Emission varies from 480–550 nm as the excitation wavelength varies from 360–500 nm | |||||||
Hinterberger Vanessaa | Microwave irradiation | 5.4% | Blue emission @ 400 nm excitation | Molecular fluorescence | Surface passivation | White LED | 41 |
The emission spectra is also pH sensitive | |||||||
Zexi Liu | Hydrothermal | 79.1% (blue) | Blue to infrared @ 365 nm excitation (by different sets of CQD) | Quantum confinement and surface states | N-Doping | No | 109 |
Out of 25 sets of CQD solutions, some sets exhibited excitation-independent emission and some exhibited excitation-dependent emission | |||||||
Akansha Dager | Pyrolysis | 9.5% | Blue emission @ 365 nm excitation | Surface states | Undoped, surface passivation not required | No | 11 |
Excitation-independent emission: no shift in the PL peak position as the excitation wavelength varies from 240–340 nm only the peak intensity decreases | |||||||
Changing the pH from acidic to basic resulted in a gradual increase in the PL intensity of CQD | |||||||
Yushuang Zhao | Hydrothermal | 16.6% | Blue-green emission @ 365 nm excitation | Surface states and carbon core states | Undoped, non-passivated | Fluorescent Cu2+ nanoprobe | 34 |
Excitation-dependent emission: the emission intensity varies and peak gradually red shift (from 443–489 nm) as the excitation wavelength increases from 320–400 nm. The peak also red shifted (342–379 nm) as the excitation wavelength increased from 400–540 nm. These CQDs exhibited the upconversion emission (anti-Stokes type emission) as the excitation wavelength varied from 760–940 nm | |||||||
Takashi Ogi | Hydrothermal | 39.7% | Blue emission @ 365 nm excitation | Not specified | N-Doping, surface passivation not done | Polyvinyl alcohol (PVA) nanofibers | 33 |
Emission intensity varies with the heating time/temperature and initial precursor concentration | |||||||
Emission is affected the most by the temperature, and the emission intensity first increases and then decreases with the temperature | |||||||
Rabia Riaz | Hydrothermal | 70% | Green emission @ 360 nm and 400 nm | Quantum confinement (bandgap emission) and surface states | N-Doping | DSSC | 131 |
Excitation-independent emission: almost no shift in the emission peak (peak appears at around 520 nm) but the emission intensity decreases as the excitation wavelength increases from 360–400 nm | |||||||
Hang Yang | Hydrothermal | 1.8% | Yellow-green emission @ 360 nm excitation | Surface states | — | No | 35 |
Excitation-dependent emission: the emission intensity varies and the peak shifts as the excitation wavelength varies from 300–450 nm | |||||||
Qiming Yang | Hydrothermal | Not mentioned | Blue emission @ 365 nm excitation | Surface states | N-Doping | DSSC | 140 |
Excitation-dependent emission: the emission intensity varies and peak shifts as the excitation wavelength increases from 310–550 nm | |||||||
Also, as the excitation wavelength changes from 700 to 1000 nm, the PL emission peaks are located in the range from 450 to 540 nm (up-conversion transition or a multi-photon absorption process) | |||||||
Mumtaz Ali | Hydrothermal | 61% (red) | Red emission @ 360 nm excitation | Quantum confinement and surface states | N-Doping | Crystalline silicon solar cells | 133 |
Excitation-independent emission is attributed to the single-transition mode PL of the NR-CQDs, which resulted from the conjugated structure | |||||||
Lili Tong | Hydrothermal | 90.49% (green) | Green emission @ 400–520 nm excitation | Dehalogenation crosslinking and structural reorganization of reactants | N-Doping, surface passivation | Lysosome imaging | 152 |
Excitation-independent emission: no shift in the emission peak (peak appears at around 530 nm) but the emission intensity increases and then decreases as the excitation wavelength increases from 400–520 nm | |||||||
Aysel Başoğlu | Microwave irradiation | 1.8% | Blue emission @ 265 nm excitation | Not specified | Undoped, surface passivation not required | Determination of Fe3+ ions | 42 |
Excitation-dependent emission: the emission intensity varies and peak shifts as the excitation wavelength increases from 300–400 nm | |||||||
Haitao Lin | Microwave irradiation | 85% | Blue emission @ 355 nm excitation | Surface states | Surface functionalization while synthesis | Dopamine fluorescence probe and cellular imaging | 153 |
Excitation-dependent emission: the emission intensity varies and peak red shifts as the excitation wavelength increases from 300–400 nm | |||||||
Lei Tian | Chemical oxidation | 0.43% | Blue emission @ 310 nm excitation | Surface states | Surface functionalization | No | 154 |
QY is irrespective of the excitation wavelength.