Enhancement of up-conversion efficiency by combining rare earth-doped phosphors with PbS quantum dots

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Abstract

This paper aims to enhance the up-conversion phenomena observed in silicon solar cells by combining a rare earth-doped phosphor with PbS quantum dots. Two different ways of adhering the up-converter and the fluorescent material to a bifacial solar cell are implemented: dissolving the powder in a spin-on oxide and by dissolving it in a silicone gel. Characterization is carried out through photocurrent and photoluminescence measurements. The improvement in photocurrent detected by the combination of the up-converter and the PbS quantum dots is 60% better than without them, demonstrating that the absorption and emission characteristics of the quantum dots embedded both in the oxide or the silicone can be tuned to the desired spectral region.

Introduction

Photon converters can enhance the performance of solar cells as they have the ability to condition the solar spectrum, thus suiting the semiconductor bandgap better. In the case of up-conversion (UC), advantage can be taken of the transmitted energy [1]. The implementation and characterization of up-converters (UC) layers on the rear of bifacial silicon solar cells (BSSC) has been reported by several authors [2], [3], [4]. Pan et al. [5] attached some commercial phosphors to the BSSC by dissolving them either in a spin-on oxide or a silicone. The performance was characterized through external quantum efficiency (EQE) measurements, demonstrating a gain in photocurrent in the IR wavelength range. This gain is quite small, firstly because response of the UC process is greatly dependent on light intensity, and also because the wavelength range in which it takes place is very narrow, corresponding to a small absorption range of the rare-earth dopant. The use of photoluminescence materials to enhance the UC phenomena has been suggested a number of times for photovoltaic applications [6], [7], [8]. The idea is to widen the IR light being used through a material that can absorb it in a range of wavelengths where the UC does not respond, and re-emit it in the wavelengths where it does respond.

The UC used in the experiments reported is called PTIR545/F, made by the company Phosphor Technology. PTIR545/F is a very fine pink powder that seems to consist, according to EDX measurements of ZnSO4 doped with ytterbium (Yb) and a small fraction of erbium (Er). This commercial phosphor is typically sold for applications in IR leds, printing inks, credit cards, etc. It can be excited in the 1500 nm range and re-emits it in shorter wavelengths, mainly in the 500 nm range.

PbS quantum dots (QDs) have appropriate absorption and emission properties for combination with the UC and the BSSC [9], and are readily commercially available. There are several requirements of the QDs that have to be fulfilled for this purpose. For instance, Suyver et al. [10] reported that the diameter of the QDs should be below 30 nm to reduce light scattering and for that reason a 5.3 nm diameter PbS QDs made by the company Evident Technology were selected and used in this work. These QDs have large quantum efficiency and high indices of refraction compared to the phosphors, which Si devices can take advantage of [11]. The energy transfer will probably occur through radiative emission from the QDs followed by absorption by the UC phosphor.

Fig. 1 details the normalized EQE as a function of wavelength for the BSSC itself, the BSSC with PTIR545/F-UC, and the absorption and emission of the Evident Technology PbS QDs. While the EQE for the solar cell is significant in the range 350–1100 nm, the UC layer is able to extend it (although with a very low response) in the 1488–1564 nm range. The PbS QDs have absorption precisely in the range where neither the BSSC itself nor the UC take advantage of the light (1200–1500 nm), and the emission takes place in the range where the UC is active, presenting a possible route to improve the UC efficiency.

In this paper we first present the characterization results for the BSSC with UC, discussing the influence of the light power on the UC efficiency. Second, we combine the UC with PbS QDs characterize the approach through measurements of photocurrent and photoluminescence (PL).

Section snippets

Characterization of up-conversion effect under IR LED illumination

As reported in previous deliverables and publications [4] we have manufactured BSSC and attached the UC to the rear using two different methods: either by dissolving it in a spin-on oxide, or by doing so in a silicone gel. Characterization is made through EQE measurements adapted to the IR range, the light source being a quartz–tungsten–halogen (QTH) incandescent lamp (200 W). Fig. 2 shows a comparison of the gain in photocurrent experienced for the two approaches. It demonstrates that the

Enhancement of up-conversion performance by combination with quantum dots

To test the potential enhancement of PTIR545/F-UC performance with the PbS-QDs, they have been dissolved together with the UC, either in the spin-on oxide or in the silicone gel, attached to the BSSC and characterized through measurements of photocurrent and photoluminescence. We can see a schematic structure of the BSSC with UC and QDs in both deposition techniques in Fig. 4.

The increase in photocurrent for the LEDs source detected for a BSSC with UCs and QDs is shown in Fig. 5 for both

Conclusion

This study reports on experimental efforts aimed at using the unique optical properties of high-quality QDs together with UC for solar cells applications.

By increasing the incident light power with an infrared LED lamp as compared to a halogen one, the UC response improves, showing a qualitative relationship between the UCs concentration in the matrix and the increase in photocurrent. The photocurrent extracted from the BSSC is found under excitation from the IR LED (1450–1550 nm), surely

Acknowledgements

This work has been carried out within the framework of the CrystalClear Integrated Project. The E.C. is gratefully acknowledged for financial support under Contract number SES6-CT-2003-502583. It has also been supported by the Brazilian Ministério de Educação e Ciência-CAPES through a scholarship; process BEX1876-03/1.

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