Introduction

Key Points
Relative quantum yield can be easily calculated using the [Relative Quantum Yield Calculation] program included as standard with the FP-8050 series.

Quantum yield is one of the key parameters used to evaluate the photophysical properties of luminescent materials. It is defined as the ratio of the number of photons emitted as fluorescence or phosphorescence to the number of excitation photons absorbed by the sample. Two methods are commonly used to determine quantum yield: the relative method and the absolute method.
The absolute method requires an integrating sphere to collect all photons emitted from the sample. In contrast, the relative method enables quantum yield to be determined more easily by comparing the fluorescence intensity of an unknown sample with that of a reference standard of known quantum yield.
In this application note, the fluorescence quantum yields of perylene and rhodamine 6G were measured by the relative method using anthracene as the reference standard.

Overview of Quantum Yield Calculation Using the Relative Method

To determine the relative quantum yield, the following parameters are required:

– The quantum yield of the reference standard.
– The absorbance at the excitation wavelength for both the reference standard and the unknown sample.
– The integrated area of the spectrally corrected emission spectrum for both the reference standard and the unknown sample.

In addition, the following parameters may be required depending on the measurement conditions:

1: The average refractive index of the solvent over the wavelength range used for emission spectrum integration, when the solvents used for the reference standard and the unknown sample are different.
2: The dilution factor, when the sample used for emission spectrum measurement has been diluted relative to the sample used for absorbance measurement.

Table 1    Parameters Required for Relative Quantum Yield Calculation

The following outlines the calculation procedure for determining the quantum yield of an unknown sample using the standard sample as a reference.

Experimental

The literature value¹⁾ of anthracene was used as a reference to calculate the quantum yields of other fluorescent substances.

Sample
Anthracene solution (standard sample, solvent: cyclohexane)
Perylene solution (solvent: cyclohexane)
Rhodamine 6G solution (solvent: ethanol)

System (Fluorescence Spectroscopy)
Instrument:      FP-8550 Spectrofluorometer
Accessories:    ESC-142 Light Source for Spectral Correction (WI)

System (Absorbance Measurement)
Instrument: V-750 UV-Vis Spectrophotometer

*Measurements can also be performed using the FUV-803 absorbance measurement cell block (accessory for the FP-8050 series).

Measurement Conditions (Fluorescence Spectrum)
Measurement Mode: Fluorescence
Excitation bandwidth: 5 nm
Fluorescence bandwidth: 5 nm
Sensitivity: Manual (240 V)
Excitation wavelength: See Table 2
Response: 0.5 s
Scan speed: 500 nm/min

Measurement Conditions (Absorption Spectrum)
UV/Vis bandwidth: 2 nm
Response: 0.24 s
Scan speed: 1000 nm/min
Remarks: Use a U-330 filter for UV-excited samples

Keywords

Quantum yield, relative quantum yield, spectrofluorometer

Results

The measured fluorescence spectra and calculated relative quantum yields are shown below.

Figure 2    Measured Spectra

 Table 2    Quantum Yield Calculation Results Using the Relative Method

*In the relative method, the excitation light absorption area is calculated in reverse from the fluorescence area and quantum yield of the reference substance (in this case, anthracene); therefore, the quantum yield cannot be calculated.

The quantum yields of perylene and rhodamine 6G were calculated using a relative method based on the measurement results for anthracene. Although these three compounds have different excitation wavelengths, appropriate spectral correction allowed us to obtain quantum yields that agree well with literature values, as shown in Table 2.

Conclusion

In the calculation of quantum yields using the relative method, results equivalent to those in the literature were obtained even for samples with different excitation wavelengths or solvents. By selecting appropriate standard samples and setting appropriate measurement conditions, quantum yields can be evaluated with high reliability even using the relative method.

JASCO’s spectrofluorometers come standard with a dedicated program (Fig. 3) that assists in calculating relative quantum yields; by entering the sample’s absorbance data, the quantum yield can be easily calculated.

Figure 3    [Relative Quantum Yield Calculation] Program Screen

 Note
The measurement results in this document are provided for reference only, and we make no guarantees regarding these values.
If the quantum yield varies depending on the reference, the quantum yield calculated using the relative method will vary in proportion to the value in the reference.

References

1. M. Montalti, A. Credi, L. Prodi, M. T. Gandolfi: Handbook of Photochemistry, 3rd ed., CRC Press, Taylor and Francis Group, 2006. DOI:10.1201/9781420015195.
2. A. M. Brouwer: Pure Appl. Chem. 83 , 2213 (2011). DOI: 10.1351/PAC-REP-10-09-31.