Review: Progress in solar cells from hydrogenated amorphous silicon
Introduction
Thin-film silicon (TF-Si) solar cells are one possible answer to the increasing energy demand of today. Hydrogenated amorphous silicon (a-Si:H) has played a crucial role therein—for decades already as intrinsic absorber layers with doped layers to build PIN junctions, and to an increasingly important extent in combination with crystalline silicon wafers in heterojunction (HIT) solar cells [1]. This article is devoted to single-junction solar cells with a-Si:H absorber layers; however, many findings are relevant to other a-Si:H applications too.
Focusing on device performance, an in-depth discussion of general properties of a-Si:H is beyond the scope of this review and we only introduce the basic concepts that are necessary for the further understanding; the interested reader is referred to the large amount of literature discussed in [2], [3].
Fig. 1 shows the performance of laboratory-scale record solar cells as a function of the bandgap for 1000 W/m2 irradiation with spectrum AM1.5g [4]. The values of open-circuit voltage (Voc), fill factor (FF), short-circuit current density (Jsc), and solar cell conversion efficiency of world-record solar cells are from [5], indicated by markers. The bandgap values are from [6] (crystalline Si, CdTe, GaAs, InP), [7] (perovskite), [8] (CIGS), and from our own measurements of a-Si:H. The lines indicate empirical trends (Voc = Eg/q and Voc =2/3) and physical limits of these parameters. The calculations are compared in appendix A of [9] for the models denoted single-pair [9], Shockley-Queisser [10], Kiess [11], and Green [12], [13], [14].
The performance of a-Si:H solar cells is well below fundamental conversion efficiency limits. Although Jsc and Voc have potential of improvement too, the FF contributes most to the difference between device performance and potential. While high-efficiency a-Si:H solar cells have a FF above 75% and an efficiency above 11% as deposited, the FF and consequently the efficiency drop by typically 10–20% within the first few months of operation. This light-induced degradation (LID) is characteristic for a-Si:H cells and will be discussed at several places in this manuscript. On the module level, LID leads to a significant initial efficiency drop that is accounted for in advertised efficiencies; on long-term, the degradation of a-Si:H solar modules is linear and with about 1%/yr close to other solar technologies [15].
After an overview over the historic development, configurations, and applications of solar cells with an a-Si:H absorber layer in Section 2, we will detail the synthesis of a-Si:H by different methods in Section 3. After an introduction to the specific characteristics of the bandgap of a-Si:H, Section 4 discusses recent improvements in the understanding of the nature and creation of defects in a-Si:H. Section 5 highlights advances in characterization techniques of both single layers and fully operational devices that are particularly useful for a-Si:H solar cells. In Section 6, we present results correlating deposition parameters with absorber layer and solar cell properties. Gathering the puzzle pieces of these subjects together, a consistent picture of the performance of a-Si:H evolves, showing its potential, but also limitations with emphasis on LID.
Whereas LID is to some extent related to the amorphous nature of a-Si:H, other limitations of the a-Si:H solar cell performance are largely caused by interfaces. In Section 7, we will present examples of approaches to overcome both limitations of bulk and interfaces. Finally, we will conclude the manuscript and give an outlook to future applications of a-Si:H solar cells in Section 8.
Part of this manuscript was published in modified form in the PhD theses of M. Stuckelberger [9] and R. Biron [16].
Section snippets
The main players in the past and today
The discovery that a-Si:H as a disordered material could be doped [17] was surprising, and led soon to the first a-Si:H solar cells [18], and to the commercialization of solar cells with monolithic interconnection [19] of single solar cells into small modules for applications such as calculators from Royal, Sharp, Casio, and Teal.
While research on a-Si:H solar cells was driven in early days mainly by the RCA laboratories and the Osaka university, research was lead later by the Colorado School
Different deposition techniques for a-Si:H
Different deposition techniques were evaluated in the past for the growth of a-Si:H for solar cell application: plasma spray [98], reactive chemical vapor deposition [99], ion-beam-assisted evaporation [100], electron cyclotron resonance [101], sputtering [102], high-pressure chemical vapor deposition [103], expanding thermal plasma deposition [104], [105], or hot-wire deposition [106], [107], [108], [109]. However, poor electronic material properties or difficult scaling up prevented the
Defects in a-Si:H
In the following, we distinguish between mid-gap defect states and bandtail states. Mid-gap defect states serve as highly efficient recombination centers; their existence is one of the main limitations of a-Si:H for solar cell and other electronic applications. Although the defect generation is phenomenologically well-described, the mechanisms behind the recombination-induced defect generation—directly through current injection or indirectly through light-induced electron-hole pair
Material characterization
In this section, we focus on the four characterization techniques for a-Si:H that are on one hand standard in several laboratories, and brought on the other hand significant progress to the improvements of a-Si:H solar cells in the last years: spectroscopic ellipsometry, photothermal deflection spectroscopy (PDS), Fourier-transform infrared spectroscopy (FTIR), and Fourier-transform photocurrent spectroscopy (FTPS). Other techniques that were widely used in the past—constant photocurrent method
Absorber layer properties
Although there are techniques to access the quality of a-Si:H directly as highlighted in Section 5.1, these techniques have limitations. First, their resolution is often limited: most important for the high performance of a-Si:H solar cells is the reduction and engineering of defects. While high-defect concentrations can be measured easily, only PDS and FTPS are sensitive enough to quantify small differences in defects concentrations of a-Si:H material as it is used in high-efficiency solar
From bulk to interface limitation
The complexity of interfaces between the thin layers, often not more than a few nanometers thick, governs to a large extent the performance of a-Si:H solar cells. Further complexity is added by bi-phase materials such as microcrystalline/amorphous phases or mixed-compound materials such as silicon-oxides. In both cases, small changes in the deposition conditions or even substrate have a tremendous influence on the film, interface, and device properties. There has been huge effort in the
Conclusions
Despite of the high defect density inherently related to the amorphous nature of this fascinating material, the semiconductor properties of a-Si:H qualify it for the use as absorber layers in solar cells. Although major improvements were achieved in the conversion efficiency of thin-film solar cells and the technologies of PECVD deposition and light-trapping reached a very mature level, the high defect density of a-Si:H fundamentally limits the efficiency of a-Si:H solar cells. In combination
Acknowledgements
We greatly acknowledge Dr. D. T. L. Alexander and Dr. M. Duchamp for their excellent work on TEM, and Dr. E. Johlin, Dr. N. Neykova, and Dr. B. O’Donnell for providing SEM images of the nanohole or nanowire solar cells.
This work was supported in part by the Swiss Federal Office of Energy under Grant SI/500750-01, by the Competence Center Energy and Mobility, and Swisselectric Research (DURSOL project, www.dursol.ch), and by the FP7 Project “Fast Track”, funded by the European Commission under
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2023, Computational Materials ScienceCitation Excerpt :Hydrogenated amorphous silicon (a-Si:H), an important semiconductor material, has been widely used in micro-bolometer, optoelectronic devices, medical instruments and other fields, due to its unique photoelectric properties [1–3], and it has also been studied as an anode of the proton conduction battery due to its reversible absorption and desorption of hydrogen [4]. People tend to think that the a-Si:H structure on short rang is similar to crystalline silicon with tetrahedrally coordinated bonds and is a semiconductor with an indirect bandgap of about 1.7 eV [5,6]. However, the a-Si:H should have different band gaps to meet the application requirements of various devices, such as a narrow-bandgap a-Si:H is applied to the top absorber layer for the micromorph solar cell but a wide-bandgap a-Si:H is applied to the middle absorber layer for the triple-junction solar cell [7–9].