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Register a new userA Silicon-Singlet Fission Parallel Tandem Solar Cell Exceeding 100 % External Quantum Efficiency
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Silicon solar cells dominate the solar cell market with record lab efficiencies reaching almost 26%. However, after 60 years of research, this efficiency saturated close to the theoretical limit for silicon, and radically new approaches are needed to further improve the efficiency. Here we present parallel-connected tandem solar cells based on down-conversion via singlet fission. This design allows raising the theoretical power conversion efficiency limit to 45% with far superior stability under changing sunlight conditions in comparison to traditional series tandems. We experimentally demonstrate a silicon/pentacene parallel tandem solar cell that exceeds 100% external quantum efficiency at the main absorption peak of pentacene, showing efficient photocurrent addition and proving this design as a realistic prospect for real-world applications.
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The spectral response of quantum well solar cells (QWSCs) is well understood. We describe work on QWSC dark current theory which combined with SR theory yields a system efficiency. A methodology published for single quantum well (SQW) systems is extended to MQW systems in the Al(x) Ga(1-x) As and InGa(0.53x) As(x) P systems. The materials considered are dominated by Shockley-Read-Hall (SRH) recombination. The SRH formalism expresses the dark current in terms of carrier recombination through mid-gap traps. The SRH recombination rate depends on the electron and hole densities of states (DOS) in the barriers and wells, which are well known, and of carrier non-radiative lifetimes. These material quality dependent lifetimes are extracted from analysis of suitable bulk control samples. Consistency over a range of AlGaAs controls and QWSCs is examined, and the model is applied to QWSCs in InGaAsP on InP substrates. We find that the dark currents of MQW systems require a reduction of the quasi Fermi level separation between carrier populations in the wells relative to barrier material, in line with previous studies. Consequences for QWSCs are considered suggesting a high efficiency potential.
Singlet fission in tetracene generates two triplet excitons per absorbed photon. If these triplet excitons can be effectively transferred into silicon (Si) then additional photocurrent can be generated from photons above the bandgap of Si. This could alleviate the thermalization loss and increase the efficiency of conventional Si solar cells. Here we show that a change in the polymorphism of tetracene deposited on Si due to air exposure, facilitates triplet transfer from tetracene into Si. Magnetic field-dependent photocurrent measurements confirm that triplet excitons contribute to the photocurrent. The decay of tetracene delayed photoluminescence was used to determine a triplet transfer time of 215 ns and a maximum yield of triplet transfer into Si of ~50 %. Our study suggests that control over the morphology of tetracene during deposition will be of great importance to boost the triplet transfer yield further.
Perovskite-silicon tandem solar cells are currently one of the most investigated concepts to overcome the theoretical limit for the power conversion efficiency of silicon solar cells. For monolithic tandem solar cells the available light must be distributed equally between the two subcells, which is known as current matching. For a planar device design, a global optimization of the layer thicknesses in the perovskite top cell allows current matching to be reached and reflective losses of the solar cell to be minimized at the same time. However, even after this optimization reflection and parasitic absorption losses occur, which add up to 7 mA/cm$^2$. In this contribution we use numerical simulations to study, how well hexagonal sinusoidal nanotextures in the perovskite top-cell can reduce the reflective losses of the combined tandem device. We investigate three configurations. The current density utilization can be increased from 91% for the optimized planar reference to 98% for the best nanotextured device (period 500 nm and peak-to-valley height 500 nm), where 100% refers to the Tiedje-Yablonovitch limit. In a first attempt to experimentally realize such nanophotonically structured perovskite solar cells for monolithic tandems, we investigate the morphology of perovskite layers, which are deposited onto sinusoidally structured substrates.
Following the recent success of monolithically integrated Perovskite/Si tandem solar cells, great interest has been raised in searching for alternative wide bandgap top-cell materials with prospects of a fully earth-abundant, stable and efficient tandem solar cell. Thin film chalcogenides (TFCs) such as the Cu2ZnSnS4 (CZTS) could be suitable top-cell materials. However, TFCs have the disadvantage that generally at least one high temperature step (>500 C) is needed during the synthesis, which could contaminate the Si bottom cell. Here, we systematically investigate the monolithic integration of CZTS on a Si bottom solar cell. A thermally resilient double-sided Tunnel Oxide Passivated Contact (TOPCon) structure is used as bottom cell. A thin (<25 nm) TiN layer between the top and bottom cells, doubles as diffusion barrier and recombination layer. We show that TiN successfully mitigates in-diffusion of CZTS elements into the c-Si bulk during the high temperature sulfurization process, and find no evidence of electrically active deep Si bulk defects in samples protected by just 10 nm TiN. Post-process minority carrier lifetime in Si exceeded 1.5 ,s. i.e., a promising implied open-circuit voltage (i-Voc) of 715 mV after the high temperature sulfurization. Based on these results, we demonstrate a first proof-of-concept two-terminal CZTS/Si tandem device with an efficiency of 1.1% and a Voc of 900 mV. A general implication of this study is that the growth of complex semiconductors on Si using high temperature steps is technically feasible, and can potentially lead to efficient monolithically integrated two-terminal tandem solar cells.
In this study, the optoelectronic properties of a monolithically integrated series-connected tandem solar cell are simulated. Following the large success of hybrid organic-inorganic perovskites, which have recently demonstrated large efficiencies with low production costs, we examine the possibility of using the same perovskites as absorbers in a tandem solar cell. The cell consists in a methylammonium mixed bromide-iodide lead perovskite, CH3NH3PbI3(1-x)Br3x (0 < x < 1), top sub-cell and a single-crystalline silicon bottom sub-cell. A Si-based tunnel junction connects the two sub-cells. Numerical simulations are based on a one-dimensional numerical drift-diffusion model. It is shown that a top cell absorbing material with 20% of bromide and a thickness in the 300-400 nm range affords current matching with the silicon bottom cell. Good interconnection between single cells is ensured by standard n and p doping of the silicon at 5.10^19cm-3 in the tunnel junction. A maximum efficiency of 27% is predicted for the tandem cell, exceeding the efficiencies of stand-alone silicon (17.3%) and perovskite cells (17.9%) taken for our simulations, and more importantly, that of the record crystalline Si cells.
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