Systematic derivation of a surface polarisation model for planar perovskite solar cells
Increasing evidence suggests that the presence of mobile ions in perovskite solar cells (PSCs) can cause a current–voltage curve hysteresis. Steady state and transient current–voltage characteristics of a planar metal halide CH3NH3PbI3 PSC are analysed with a drift-diffusion model that accounts for...
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Published in | European journal of applied mathematics Vol. 30; no. 3; pp. 427 - 457 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge, UK
Cambridge University Press
01.06.2019
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ISSN | 0956-7925 1469-4425 |
DOI | 10.1017/S0956792518000207 |
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Abstract | Increasing evidence suggests that the presence of mobile ions in perovskite solar cells (PSCs) can cause a current–voltage curve hysteresis. Steady state and transient current–voltage characteristics of a planar metal halide CH3NH3PbI3 PSC are analysed with a drift-diffusion model that accounts for both charge transport and ion vacancy motion. The high ion vacancy density within the perovskite layer gives rise to narrow Debye layers (typical width ~2 nm), adjacent to the interfaces with the transport layers, over which large drops in the electric potential occur and in which significant charge is stored. Large disparities between (I) the width of the Debye layers and that of the perovskite layer (~600 nm) and (II) the ion vacancy density and the charge carrier densities motivate an asymptotic approach to solving the model, while the stiffness of the equations renders standard solution methods unreliable. We derive a simplified surface polarisation model in which the slow ion dynamics are replaced by interfacial (non-linear) capacitances at the perovskite interfaces. Favourable comparison is made between the results of the asymptotic approach and numerical solutions for a realistic cell over a wide range of operating conditions of practical interest. |
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AbstractList | Increasing evidence suggests that the presence of mobile ions in perovskite solar cells (PSCs) can cause a current–voltage curve hysteresis. Steady state and transient current–voltage characteristics of a planar metal halide CH3NH3PbI3 PSC are analysed with a drift-diffusion model that accounts for both charge transport and ion vacancy motion. The high ion vacancy density within the perovskite layer gives rise to narrow Debye layers (typical width ~2 nm), adjacent to the interfaces with the transport layers, over which large drops in the electric potential occur and in which significant charge is stored. Large disparities between (I) the width of the Debye layers and that of the perovskite layer (~600 nm) and (II) the ion vacancy density and the charge carrier densities motivate an asymptotic approach to solving the model, while the stiffness of the equations renders standard solution methods unreliable. We derive a simplified surface polarisation model in which the slow ion dynamics are replaced by interfacial (non-linear) capacitances at the perovskite interfaces. Favourable comparison is made between the results of the asymptotic approach and numerical solutions for a realistic cell over a wide range of operating conditions of practical interest. Increasing evidence suggests that the presence of mobile ions in perovskite solar cells (PSCs) can cause a current–voltage curve hysteresis. Steady state and transient current–voltage characteristics of a planar metal halide CH 3 NH 3 PbI 3 PSC are analysed with a drift-diffusion model that accounts for both charge transport and ion vacancy motion. The high ion vacancy density within the perovskite layer gives rise to narrow Debye layers (typical width ~2 nm), adjacent to the interfaces with the transport layers, over which large drops in the electric potential occur and in which significant charge is stored. Large disparities between (I) the width of the Debye layers and that of the perovskite layer (~600 nm) and (II) the ion vacancy density and the charge carrier densities motivate an asymptotic approach to solving the model, while the stiffness of the equations renders standard solution methods unreliable. We derive a simplified surface polarisation model in which the slow ion dynamics are replaced by interfacial (non-linear) capacitances at the perovskite interfaces. Favourable comparison is made between the results of the asymptotic approach and numerical solutions for a realistic cell over a wide range of operating conditions of practical interest. |
Author | COURTIER, N. E. O'KANE, S. E. J. WALKER, A. B. RICHARDSON, G. FOSTER, J. M. |
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CitedBy_id | crossref_primary_10_1039_D0CP04350H crossref_primary_10_1063_5_0136683 crossref_primary_10_1039_D1SE00369K crossref_primary_10_1103_PhysRevApplied_23_014055 crossref_primary_10_1016_j_joule_2019_10_003 crossref_primary_10_1088_2515_7655_acc4e9 crossref_primary_10_1039_C8EE01576G crossref_primary_10_1007_s10825_019_01396_2 crossref_primary_10_1039_D0TA12046D crossref_primary_10_1002_solr_202300742 crossref_primary_10_1002_advs_201901397 crossref_primary_10_1002_aenm_202400955 crossref_primary_10_1103_PhysRevApplied_19_014061 crossref_primary_10_1016_j_chemphys_2021_111422 crossref_primary_10_1063_5_0065983 crossref_primary_10_1103_PhysRevApplied_14_024031 crossref_primary_10_1002_pssa_202100472 crossref_primary_10_1007_s10825_024_02212_2 crossref_primary_10_1017_S0956792519000135 crossref_primary_10_1002_pssa_202200262 crossref_primary_10_1017_S0956792518000293 crossref_primary_10_1103_PhysRevApplied_18_064087 |
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Snippet | Increasing evidence suggests that the presence of mobile ions in perovskite solar cells (PSCs) can cause a current–voltage curve hysteresis. Steady state and... |
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SubjectTerms | Applied mathematics Asymptotic properties Carrier density Charge density Charge transport Current carriers Current voltage characteristics Ion dynamics Metal halides Perovskites Photovoltaic cells Polarization Simplified surfaces Solar cells Stiffness Transient current Vacancies |
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Title | Systematic derivation of a surface polarisation model for planar perovskite solar cells |
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