Abstract
Multiexciton generation, by which more than a single electron–hole pair is generated on optical excitation, is a promising paradigm for pushing the efficiency of solar cells beyond the Shockley–Queisser limit of 31%. Utilizing this paradigm, however, requires the onset energy of multiexciton generation to be close to twice the band gap energy and the efficiency to increase rapidly above this onset. This challenge remains unattainable even using confined nanocrystals, nanorods or nanowires. Here, we show how both goals can be achieved in a nanorod heterostructure with type-II band offsets. Using pseudopotential atomistic calculation on a model type-II semiconductor heterostructure we predict the optimal conditions for controlling multiexciton generation efficiencies at twice the band gap energy. For a finite band offset, this requires a sharp interface along with a reduction of the exciton cooling and may enable a route for breaking the Shockley–Queisser limit.
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Introduction
Increasing the photovoltaic power conversion efficiencies in solar cells beyond the Shockley–Queisser (SQ) limit1 of 31% remains one of the grand challenges of the field. Several theoretical concepts to overcoming this limit, to as much as 66%, have yet to be realized in state-of-the-art photovoltaic devices2. One promising direction for collecting hot carriers is based on multiexciton generation (MEG)3,4,5 or singlet fission6, in which more than one electron–hole pair is generated on optical excitation, potentially increasing photovoltaic power conversion efficiencies up to 45% (refs 7, 8). To date, solar cells using MEG still show poor performance9, mainly due to the excessively high MEG onset energy (Eon).
The necessary conditions for MEG to be technologically useful are that the onset energy Eon be close to the lower threshold of twice the quasiparticle band gap (2Eg) and that beyond this onset the MEG efficiency (that is, the average number of excitons produced by each absorbed photon) increases rapidly with photon energy7. To push the onset of MEG to 2Eg, the rate of generating multiexcitons needs to exceed the rate of the competing non-radiative exciton cooling channel10. Achieving this goal is very different from older concepts of collecting hot carriers, since the timescales for separating charge carriers are very long compared with the timescales of carrier multiplication by MEG.
In bulk semiconductors, due to conservation of linear momentum and energy and due to the rapid non-radiative relaxation of excitons (exciton cooling), the onset energy is typically Eon≈5Eg (ref. 11). On the other hand, confined semiconductor nanocrystals (NCs) offer improved MEG efficiencies12,13, with an onset energy below Eon≈3Eg (refs 14, 15, 16, 17, 18, 19, 20), rationalized by several theoreti cal treatments10,21,22,23,24,25,26,27,28,29,30,31,32. Among these, perhaps the most intuitively appealing theoretical picture of MEG in NCs is that of impact ionization, describing the decay of an excited charged quaisparticle to an identically charged trion, composed of a quasiparticle and an exciton10,21,22,30. For efficient MEG, the trion formation rate should surpass the combined rate of decay by all other non-radiative exciton cooling channels. Using the impact excitation formalism and a unified Green’s function approach to MEG, we have shown that the interplay of the size scaling of the band gap, Coulomb couplings and density of states (DOS) leads to an overall increase in MEG rates and efficiencies with decreasing NC size31,33. The role of the relative magnitude of the electron and hole effective masses has also been discussed recently34.
Several different approaches have been proposed to further reduce the onset energy of MEG. Gabor et al.35 used a polarized field to decrease Eon in carbon nanotubes photodiodes, a result that was rationalized by a classical description based on field-induced acceleration of the charge carriers36. Sandberg et al.37 studied the role of the shape of nanoparticles on the MEG efficiency and argued for a 60% increase in MEG yields in semiconductor nanorods (NRs) compared with spherical NCs. The role of the diameter and length of the NR on the MEG efficiencies was analysed by considering the scaling of the density of trion states (DOTS) and the Coulomb couplings38. Both show distinct scaling from spherical NCs leading to a surprising result that the MEG efficiencies were roughly independent of the NR length38. This prediction was later verified by experiments39,40.
Two additional handles can be used to control MEG efficiencies. The first is based on suppressing the competing channel of phonon emission. Experimental work along this line by Klimov et al. has shown that MEG onset energy in type-II core-shell NCs can be reduced by partially blocking the non-radiative decay channel5. Theoretically this mechanism has been studied on very small NC sizes41,42. The other, which forms the crux of our approach, is based on controlling the DOTS near 2Eg, thereby reducing the onset energy to Eon≈2Eg and markedly increasing MEG efficiencies near the onset. One way we tried recently to achieve a control of the DOTS was by using seeded NRs heterostructures43. This did not lead to a significant increase of MEG efficiency near 2Eg (ref. 44), but the analysis showed that these efficiencies increase with seed size, contrary to the case of isolated spherical NCs.
In this work, we report on extremely high MEG efficiencies at the onset energy of Eon≈2Eg in type-II NR heterostructures, which can be prepared using cation exchange reactions45. Our work is motivated by the results of MEG in carbon nanotube photodiodes35,36, but uses the internal field in type-II NRs as opposed to applying an external polarized field. We show that by using the internal field energy along with a suppression of the cooling rates, MEG efficiencies can increase to over 150% at 2Eg, significantly above any previously reported result for colloidal nanostructures. The work develops ways for increasing solar cell efficiencies beyond the SQ limit.
Results
Model for a type-II nanorod heterostrucure
To illustrate the core idea and to focus on the effect associated with the role of the internal field, we consider a model system of type-II NR where both building blocks are composed of CdSe with an internal field at the interfacial region of width β and maximal value F≈Δ/β, as depicted in the left panel of Fig. 1 (Δ is defined in the caption of Fig. 1). While more realistic models of type-II nanostructures can be handled within the pseudopotential approach46, the simplified approach we take allows us to delineate the mechanism of generating multiexctions induced by the internal field only, without the complexity of varying the band structure and/or introducing stress and strain across the hetero-junction.
Before we proceed to compute the MEG efficiencies, we first demonstrate that the optical absorption, most importantly the absorption onset energy, does not change with the internal field. We have calculated the absorption cross section using a stochastic approach suitable for thousands of electrons (see ‘Methods’ section for more details) within the pseudopotential model for CdSe47, neglecting the electron–hole interactions which are not important for establishing the dependence of the absorption onset energy on the internal field. In the right panel of Fig. 1 we plot the results for a series of NRs with different internal fields. As can be seen clearly, the absorption onset is independent of the internal field strength within the noise level of the stochastic approach, consistent with the small overlap of the hole and electron wave functions when they are localized on opposite sides of the NR. Moreover, the entire line-shape is very similar for different values of Δ, implying that indeed the band structure of the parent material is preserved with the perturbing internal field, even for rather large potential drops.
MEG efficiencies in a type-II nanorod heterostrucure
We now proceed to compute the MEG efficiencies. This is a complicated many body problem involving singly and doubly excited states and their decay via electron–phonon couplings. Progress can only be made with well-defined, controlled approximations. We have recently shown that the direct24,27,48 or indirect absorption approach15, the coherent reduced density matrix formalism23,26 and the impact excitation10,21,22 all emerge as different limits of a Green’s function formalism33. The impact excitation model proved to be accurate in comparison with a more elaborate Green’s function approach while providing a simple physical picture in which MEG efficiencies become notable if their rates are larger than the competing exciton cooling rates. Furthermore, the MEG process can be described to lowest order in the Coulomb coupling as a decay of an electron/hole to a negative/positive trion state (composed of two electrons and one hole or vice versa), while the other carrier (hole/electron) is a spectator. For these reasons we adopt the impact excitation approach and implement a stochastic method developed in refs 31, 44 to overcome the computational complexity of computing MEG rates in systems with thousands of electrons.
For completeness, we briefly review the approach and the key elements in describing the MEG efficiency nex(ω), the number of excitons per absorbed photon. This can be written as an average over sampled electron–hole pair excitations, S:
where NS is the number of sampled excitons (typically NS=200 is sufficient to converge the results), ES=ħω is the photon and exciton energy, γ is the exciton cooling rate taken to be energy independent, ΓS the MEG rate for exciton S, and is the density of states at energy ɛ),
is the probability of generating exciton S given that a photon of energy ħω was absorbed. In the above, μ0S is the transition dipole from the ground state |0〉 to an excitonic state |S〉. Finally, the MEG rates, ΓS, are given in terms of a sum of negative () and positive () trion formation rates ΓS=+, where
and and are the average screened Coulomb coupling and the density of trion states, respectively. All the required quantities can be obtained within the pseudopotential approach using the stochastic MEG method31,44.
In Fig. 2 we plot the calculated MEG efficiencies for a series of NRs with varying internal fields (left panels) and varying exciton cooling rates (right panels) as a function of the photon energy E=ħω. Consistent with above discussion of the onset of absorption, we scale the photon energy of all NRs with the band gap of the unbiased system, Eg=2.04 eV. The left panel of Fig. 2 illustrates an important result, where the onset energy for MEG, Eon, decreases markedly with the bias potential. Furthermore, comparing the results of the upper and lower left panels of the figure it is clear that a much larger effect is obtained when the length scale for the bias drop is small, namely for a large field. This latter result is consistent with theoretical predictions of the suppression of Auger processes in core-shell nanocrystals, where a sharp interface between the core and shell leads to faster Auger recombination49.
Above a certain threshold value of Δ, the onset energy of MEG can be smaller than 2Eg. This results requires an explanation since the minimal double-exciton energy is twice the energy of the gap, Eg. To explain this seemingly unrealistic result, we sketch two possible relaxation mechanisms for generating multiexcitons in the upper panel of Fig. 3. Consider an electron at high energy delocalized along the entire NR. The electron can either generate a negative trion where all carriers are localized in one building block, or can generate a negative, charge separated, trion. On the basis of energy conservation considerations, in the former the theoretical onset of MEG is Eg−Δ while in the latter it is Eg−2Δ. Thus, due to the potential drop the onset can be pushed below 2Eg. We note that for the charge separated negative trion, the hole orbital must overlap one of the final electron orbitals. The lower panel of Fig. 3 illustrates that this can indeed happen. However, this overlap is rather small and the central contribution comes from the localized trion state. We conclude that the dominant mechanism will push the theoretical onset energy to 2Eg−Δ.
Analysis of the multiexciton generation efficiencies
While a finite value of Δ is required to separate the charge carriers in type-II solar cell junctions, the value of Δ used to increase the MEG efficiency as depicted in the left panels of Fig. 2, will lead to a significant decrease in the photovoltage and as a result, to an overall lower solar cell performance50. As shown in the right panels of Fig. 2, this issue is mitigated when the exciton cooling lifetime is increased above 10 ps (which, in fact, can be induced by an pronounced electron–hole charge separation5), leading to a MEG onset energy below 2Eg, even at moderate values of Δ. It is clear, however, that only by combining a non-negligible internal field and a mechanism to slow down the cooling of excitons by phonon emission, the MEG efficiency can be controlled at the desired onset, while either one of these mechanisms separately will not be sufficient.
The increase of MEG rate near 2Eg is further analysed in Fig. 4, where we plot the DOTS (upper panel) and the average Coulomb coupling for electrons (lower panel). The density of negative and positive trion states ( and , respectively) is plotted along the positive and negative energies, respectively. Each is measured from the bottom/top of the conduction/valence bands of the unbiased CdSe NR. The DOTS is obtained by a triple convolution of the DOS not shown here. For the negative DOTS, the triple convolution involves the DOS of two electrons (that is, the DOS above the Fermi energy) and one hole (that is, the DOS below the Fermi energy) while for the positive DOTS it involves the triple convolution of the DOS of two holes and one electron. Common to both DOTS is the increase in at ɛ=±Eg above/below the conduction/valance band minimum/maximum. Note that we use a semi-logarithmic scale and thus, the magnitude of the effect is rather dramatic with increasing bias. The positive DOTS is typically higher than the negative DOTS at the energies measured from the corresponding band edge, a result that can be explained by the larger DOS of holes44. Furthermore, the negative DOTS shows a stronger dependence on the internal bias potential.
The increase in the DOTS at energies ±Eg above and below the corresponding band extremes is a necessary but not sufficient condition for pushing the onset of MEG to 2Eg. In addition, the coupling of the excited electron–hole pair need not vanish. While the average Coulomb coupling for electrons shown in the lower panel of Fig. 4 is nearly independent of energy at high energies, consistent with the picture emerging for NCs (ref. 31) and NRs (ref. 38), in the important range of ɛ≈Eg there is a notable small increase in as the internal field is increased due to a change in the character of the trion states to which the electron (hole) is coupled. The increase in the DOTS and in small increase in leads to a significant soaring of the trion formation rate above the exciton cooling rate, γ. This interplay of DOSs and Coulomb coupling and the energy dependence is reflected in an increase of MEG efficiencies and a decrease of Eon, as discussed above.
In summary, using MEG in nanostructures for breaking the SQ limit requires a significant increase in the MEG efficiencies at 2Eg. So far, this has been elusive and neither spherical NCs nor core-shell NCs nor NRs push the onset of MEG to 2Eg. Here, we provide the theoretical foundation for the design of materials with large MEG efficiencies near 2Eg. Our predictions are based on an atomistic model for MEG within a fully quantum mechanical description, which has been shown to be accurate in postdicting and predicting MEG in NCs and NRs. The two key elements for pushing down the MEG onset energy are: (a) Using the internal field (Δ/β) in type-II heterostructures with a rather sharp interface between the two building blocks and (b) slowing down the exciton cooling rate by reducing the electron–phonon couplings. Only the two combined effects will lead to a significant increase in the MEG efficiencies at 2Eg. We find that the MEG efficiency at the onset of 2Eg increases with increasing band offsets (Δ), increases with decreasing values of β (that is, sharper interface between the two building block materials) and increases with slower cooling rates, γ. For the current CdSe NR system and for realistic parameters, the MEG efficiency at 2Eg can be as large as 10%−20%. This should be compared with an onset of 3Eg and vanishing carrier multiplications at 2Eg of previously studied colloidal nanostructures.
Further development is required to utilize the current scenario in type-II single cell junctions. For an optimal performance, one requires the design of materials with gaps close to 0.7 eV (ref. 7), a sharp interface between the building blocks and a moderate value of the band offset, Δ, not to reduce significantly the photocurrent voltage. Moreover, an efficient and rapid scheme to collect multiple charge carriers is requires before Auger recombination and/or other relaxation process step in. While some of these targets are already achievable by colloidal chemistry synthesis, the reduction of the cooling rate and the rapid collection of multiple charges requires the development of novel schemes along the lines recently proposed for core/shell nanocrystals5.
Methods
Computational method
All calculations were preformed within the pseudopotential model for CdSe (ref. 47) implemented in a real-space grid of size 96 × 96 × 384 and spacing of 0.8 a.u. sufficient to converge the results. The NR included 3,600 Cd and 3,600 Se atoms and ligand potentials were used to passivate the dangling bonds47. The description of the electronic properties of this system is beyond the current capabilities of deterministic approaches. Therefore, we resort to our recently developed stochastic formalism31. For the MEG efficiency given by equation (1) we have carried the following steps:
First, the DOSs, ρ(ɛ), were obtained using a stochastic trace formula31 with an interpolation polynomial of length NC=16,384 averaged over 50 stochastic iterations. The negative and positive trion DOSs were then generated by a triple convolution of the single-particle DOSs. More details are given in ref. 31. Next, negative and positive trion formation rates in equation (3) were generated using a stochastic procedure31. This involves filtering electron and hole states at a target energy and filtering a resonant negative and positive trion state, respectively, using an interpolation polynomial of length NC=16,384. For each interpolation polynomial filter we have generated 16 electron states and 16 hole states and for each particle a corresponding resonant trion state. The rates were averaged over 10,000 stochastic realizations. In addition, for each electron or hole obtained in the previous step, we have filtered several (10) hole or electron states, respectively, and for each electron–hole pair (20 independent pairs), we calculated the transition dipole μ0S at energy ES and obtained given by equation (2). Since we only sample electron–hole pairs, instead of calculating them all, we have multiplied the result by the density of electrons and holes ρ(ɛe)ρ(ɛh) at the reference energy of the electron (ɛe) and hole (ɛh). For more information see ref. 44. Finally, we have used and to generate the MEG rate for each exciton: ΓS=+ and then obtain nex(ω) by performing the average in equation (1) for NS=50,000.
The absorption cross section, σ(ω)∝ωr(ω) is given in terms of the golden rule absorption rate, , where μ is the dipole operator, is the amplitude of the electromagnetic field, |0〉 is the ground state and |S〉 is an electron–hole pair state. Instead of summing overall electron–hole pairs, an impractical task for the studied NR size, we used the following stochastic formula: , where ζh is a projected random orbital on the occupied space and ζe is a project random orbital on the unoccupied space (see more details about random stochastic orbitals in ref. 51). We used Nζ=10,000 to average the rate of absorption and Nt=105 propagation steps with a time step of 0.025a.u. to propagate the electron–hole stochastic orbitals.
Data availability
The data that support the findings of this study are available from the corresponding authors on request.
Additional information
How to cite this article: Eshet, H. et al. Theory of highly efficient multiexciton generation in type-II nanorods. Nat. Commun. 7, 13178 doi: 10.1038/ncomms13178 (2016).
References
Shockley, W. & Queisser, H. J. Detailed balance limit of efficiency of p-n junction solar cells. J. Appl. Phys. 32, 510 (1961).
Nozik, A. J. Quantum dot solar cells. Physica E-Low-Dimensional Systems & Nanostructures 14, 115–120 (2002).
Nozik, A. J. et al. Semiconductor quantum dots and quantum dot arrays and applications of multiple exciton generation to third-generation photovoltaic solar cells. Chem. Rev. 110, 6873–6890 (2010).
Beard, M. C. Multiple exciton generation in semiconductor quantum dots. J. Chem. Phys. Lett. 2, 1282–1288 (2011).
Klimov, V. I. Multicarrier interactions in semiconductor nanocrystals in relation to the phenomena of auger recombination and carrier multiplication. Ann. Rev. Conden. Mat. Phys 5, 285–316 (2014).
Smith, M. B. & Michl, J. Recent advances in singlet fission. Annu. Rev. Phys. Chem 64, 361–386 (2013).
Beard, M. C. et al. Comparing multiple exciton generation in quantum dots to impact ionization in bulk semiconductors: Implications for enhancement of solar energy conversion. Nano Lett. 10, 3019–3027 (2010).
Klimov, V. I. Detailed-balance power conversion limits of nanocrystal-quantum-dot solar cells in the presence of carrier multiplication. Appl. Phys. Lett. 89, 123118 (2006).
Sambur, J. B., Novet, T. & Parkinson, B. A. Multiple exciton collection in a sensitized photovoltaic system. Science 330, 63–66 (2010).
Rabani, E. & Baer, R. Distribution of multiexciton generation rates in CdSe and InAs nanocrystals. Nano Lett. 8, 4488–4492 (2008).
Christensen, O. Quantum efficiency of internal photoelectric effect in silicon and germanium. J. Appl. Phys. 47, 689–695 (1976).
Padilha, L. A. et al. Carrier multiplication in semiconductor nanocrystals: Influence of size, shape, and composition. Acc. Chem. Res. 46, 1261–1269 (2013).
Shabaev, A., Hellberg, C. S. & Efros, A. L. Efficiency of multiexciton generation in colloidal nanostructures. Acc. Chem. Res. 46, 1242–1251 (2013).
Schaller, R. D. & Klimov, V. I. High efficiency carrier multiplication in PbSe nanocrystals: implications for solar energy conversion. Phys. Rev. Lett. 92, 186601 (2004).
Schaller, R. D., Agranovich, V. M. & Klimov, V. I. High-efficiency carrier multiplication through direct photogeneration of multi-excitons via virtual single-exciton states. Nat. Phys 1, 189–194 (2005).
Ellingson, R. J. et al. Highly efficient multiple exciton generation in colloidal PbSe and PbS quantum dots. Nano Lett. 5, 865–871 (2005).
Beard, M. C. et al. Multiple exciton generation in colloidal silicon nanocrystals. Nano Lett. 7, 2506–2512 (2007).
Schaller, R. D., Pietryga, J. M. & Klimov, V. I. Carrier multiplication in InAs nanocrystal quantum dots with an onset defined by the energy conservation limit. Nano Lett. 7, 3469–3476 (2007).
Trinh, M. T. et al. Anomalous independence of multiple exciton generation on different group IV–VI quantum dot architectures. Nano Lett. 11, 1623–1629 (2011).
Stewart, J. T. et al. Comparison of carrier multiplication yields in PbS and PbSe nanocrystals: the role of competing energy-loss processes. Nano Lett. 12, 622–628 (2012).
Franceschetti, A., An, J. M. & Zunger, A. Impact ionization can explain carrier multiplication in PbSe quantum dots. Nano Lett. 6, 2191–2195 (2006).
Allan, G. & Delerue, C. Role of impact ionization in multiple exciton generation in PbSe nanocrystals. Phys. Rev. B 73, 205423 (2006).
Shabaev, A., Efros, A. L. & Nozik, A. J. Multiexciton generation by a single photon in nanocrystals. Nano Lett. 6, 2856–2863 (2006).
Isborn, C. M., Kilina, S. V., Li, X. S. & Prezhdo, O. V. Generation of multiple excitons in PbSe and CdSe quantum dots by direct photoexcitation: first-principles calculations on small PbSe and CdSe clusters. J. Phys. Chem. C 112, 18291–18294 (2008).
Delerue, C., Allan, G., Pijpers, J. J. H. & Bonn, M. Carrier multiplication in bulk and nanocrystalline semiconductors: mechanism, efficiency, and interest for solar cells. Phys. Rev. B 81, 125306 (2010).
Witzel, W. M., Shabaev, A., Hellberg, C. S., Jacobs, V. L. & Efros, A. L. Quantum simulation of multiple-exciton generation in a nanocrystal by a single photon. Phys. Rev. Lett. 105, 137401 (2010).
Fischer, S. A., Madrid, A. B., Isborn, C. M. & Prezhdo, O. V. Multiple exciton generation in small Si clusters: A high-level, ab initio study. J. Phys. Chem. Lett. 1, 232–237 (2010).
Piryatinski, A. & Velizhanin, K. A. An exciton scattering model for carrier multiplication in semiconductor nanocrystals: theory. J. Chem. Phys. 133, 084508 (2010).
Allan, G. & Delerue, C. Optimization of carrier multiplication for more effcient solar cells: the case of Sn quantum dots. ACS Nano 5, 7318–7323 (2011).
Lin, Z., Franceschetti, A. & Lusk, M. T. Size dependence of the multiple exciton generation rate in CdSe quantum dots. ACS Nano 5, 2503–2511 (2011).
Baer, R. & Rabani, E. Expeditious stochastic calculation of multiexciton generation rates in semiconductor nanocrystals. Nano Lett. 12, 2123–2128 (2012).
Velizhanin, K. A. & Piryatinski, A. Numerical analysis of carrier multiplication mechanisms in nanocrystalline and bulk forms of PbSe and Pbs. Phys. Rev. B 86, 165319 (2012).
Rabani, E. & Baer, R. Theory of multiexciton generation in semiconductor nanocrystals. Chem. Phys. Lett. 496, 227–235 (2010).
Zohar, G., Baer, R. & Rabani, E. Multiexciton generation in IV–VI nanocrystals: the role of carrier effective mass, band mixing, and phonon emission. J. Phys. Chem. Lett. 4, 317–322 (2013).
Gabor, N. M., Zhong, Z. H., Bosnick, K., Park, J. & McEuen, P. L. Extremely efficient multiple electron-hole pair generation in carbon nanotube photodiodes. Science 325, 1367–1371 (2009).
Baer, R. & Rabani, E. Can impact excitation explain efficient carrier multiplication in carbon nanotube photodiodes? Nano Lett. 10, 3277–3282 (2010).
Sandberg, R. L. et al. Multiexciton dynamics in infrared-emitting colloidal nanostructures probed by a superconducting nanowire single-photon detector. ACS Nano 6, 9532–9540 (2012).
Baer, R. & Rabani, E. Communication: biexciton generation rates in CdSe nanorods are length independent. J. Chem. Phys. 138, 051102 (2013).
Padilha, L. A. et al. Aspect ratio dependence of auger recombination and carrier multiplication in PbSe nanorods. Nano Lett. 13, 1092–1099 (2013).
Karki, K. J. et al. Multiple exciton generation in nanocrystals revisited: consistent calculation of the yield based on pump-probe spectroscopy. Sci. Rep. 3, 2287 (2013).
Prezhdo, O. V. Multiple excitons and the electron-phonon bottleneck in semiconductor quantum dots: an ab initio perspective. Chem. Phys. Lett. 460, 1–9 (2008).
Chen, L. L., Bao, H., Tan, T. Z., Prezhdo, O. V. & Ruan, X. L. Shape and temperature dependence of hot carrier relaxation dynamics in spherical and elongated CdSe quantum dots. J. Phys. Chem. C 115, 11400–11406 (2011).
Li, H., Kanaras, A. G. & Manna, L. Colloidal branched semiconductor nanocrystals: state of the art and perspectives. Acc. Chem. Res. 46, 1387–1396 (2013).
Eshet, H., Baer, R., Neuhauser, D. & Rabani, E. Multiexciton generation in seeded nanorods. J. Phys. Chem. Lett. 5, 2580–2585 (2014).
Beberwyck, B. J., Surendranath, Y. & Alivisatos, A. P. Cation exchange: a versatile tool for nanomaterials synthesis. J. Phys. Chem. C 117, 19759–19770 (2013).
Eshet, H., Grunwald, M. & Rabani, E. The electronic structure of CdSe/CdS core/shell seeded nanorods: type-i or quasi-type-II? Nano Lett. 13, 5880–5885 (2013).
Rabani, E., Hetenyi, B., Berne, B. J. & Brus, L. E. Electronic properties of CdSe nanocrystals in the absence and presence of a dielectric medium. J. Chem. Phys. 110, 5355 (1999).
Isborn, C. M. & Prezhdo, O. V. Charging quenches multiple exciton generation in semiconductor nanocrystals: first-principles calculations on small PbSe clusterse. J. Phys. Chem. C 113, 12617–12621 (2009).
Cragg, G. E. & Efros, A. L. Suppression of auger processes in confined structures. Nano Lett. 10, 313–317 (2009).
Hirst, L. C. & Ekins-Daukes, N. J. Fundamental losses in solar cells. Prog. Photovolt: Res. Appl. 19, 286–293 (2011).
Baer, R., Neuhauser, D. & Rabani, E. Self-averaging stochastic Kohn–Sham density-functional theory. Phys. Rev. Lett. 111, 106402 (2013).
Acknowledgements
R.B. gratefully acknowledges support for his sabbatical visit by the Pitzer Center and the Kavli Institute of the University of California, Berkeley and the ISF grant 189/14. E.R. and D.N. acknowledge support from NSF grants CHE-1465064 and CHE-1112500, respectively.
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H.E. performed the calculations and analysed the data, R.B., D.N. and E.R. developed the theoretical framework and analysed the data, all authors co-wrote the paper.
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Eshet, H., Baer, R., Neuhauser, D. et al. Theory of highly efficient multiexciton generation in type-II nanorods. Nat Commun 7, 13178 (2016). https://doi.org/10.1038/ncomms13178
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DOI: https://doi.org/10.1038/ncomms13178
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