Double‐Side‐Passivated Perovskite Solar Cells with Ultra‐low Potential Loss

Solar RRL - Tập 3 Số 2 - 2019
Yicheng Zhao1,2, Qi Li2, Wenke Zhou2, Yi Hou1, Yao Zhao2, Rui Fu2, Dapeng Yu3,2, Xin Liu4, Qing Zhao3,2
1Institute of Materials for Electronics and Energy Technology (i‐MEET), Department of Materials Science and Engineering Friedrich‐Alexander‐Universität Erlangen‐Nürnberg Martensstr. 7 91058 Erlangen Germany
2State Key Laboratory for Mesoscopic Physics and Electron Microscopy Laboratory, School of Physics, Peking University, Beijing 100871, China
3Collaborative Innovation Center of Quantum Matter, Beijing 100084, China
4Global Energy Interconnection Research Institute, Beijing, 100871 China

Tóm tắt

An ideal crystal quality in the grain interior of perovskite polycrystalline films is well recognized; therefore, understanding interfacial impact and the ways to limit interfacial recombination is critical to fabricating highly efficient solar cells. In perovskite solar cells, PbI2 has been used to passivate defects at grain boundaries, yet a systematic PbI2 passivation engineering to boost the high‐performance perovskite solar cells has not been fully explored. Here, a novel device structure comprised of double‐side‐passivated perovskite solar cells (DSPC) is devised through intentionally distributing PbI2 to both the front/rear‐side surfaces and grain boundaries of the formamidinium‐lead‐iodide‐based (FAPbI3‐based) perovskite film. The minority carrier lifetime in double‐side‐passivated perovskite is extended to 1.1 μs with single‐exponential decay using time‐resolved photoluminescence. This result indicates a generic passivation effect of PbI2 on perovskite interfaces, resembling SiO2 passivation in silicon solar cells. Correspondingly, the best photovoltaic device with TiO2‐based planar structure presents a stabilized efficiency of 22%. Moreover, DSPC effectively boosts the limits of open circuit voltages toward a record potential loss of 0.38 V for 1.53 eV‐bandgap perovskites. The architecture of double‐side‐passivated perovskite opens up new opportunities to exceed the efficiency of state‐of‐the‐art perovskite solar cells.

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Tài liệu tham khảo

10.1038/nmat4065

10.1126/science.aan2301

10.1126/science.aaa9272

10.1038/nenergy.2016.142

10.1038/natrevmats.2015.7

10.1126/science.aai9081

10.1038/lsa.2016.243

10.1038/nenergy.2016.81

10.1038/nnano.2014.181

10.1126/science.aam6620

10.1021/nl5048779

10.1038/nature14133

10.1039/c3ee43822h

10.1039/C5EE03874J

Saliba M., 2016, Science, 10, 604

10.1126/science.aad5845

10.1021/acs.jpclett.7b01851

10.1039/C5EE03255E

10.1002/aenm.201700677

10.1038/nmat4014

10.1038/lsa.2016.56

10.1038/nenergy.2017.102

10.1038/nenergy.2017.9

10.1002/pip.2978

10.1002/pip.2788

10.1038/s41467-017-00567-8

Dane S. M. V., 2015, Science, 348, 6

10.1126/science.aap9282

10.1126/sciadv.1501170

10.1126/science.aao5561

10.1002/adma.201706275

10.1038/nature25989

10.1039/C7EE03654J

10.1126/science.aaa5760

10.1038/natrevmats.2017.42

10.1126/science.aaa5333

10.1021/nn5036476

10.1021/acsenergylett.6b00060

10.1021/nl501838y

10.1039/C7TA11280G

10.1039/C5EE02555A

10.1002/aenm.201502104

10.1002/adfm.201603968

10.1002/adma.201703852

10.1039/C4EE01138D

10.1038/ncomms10228

10.1021/jacs.5b11076

10.1039/C6EE03182J

10.1021/jacs.6b06320

10.1063/1.4899051

Xiao Z., 2014, Nat. Mater, 14, 8

You J., 2015, Nat. Nanotech, 230, 1

10.1038/nchem.2324

10.1038/ncomms12806

10.1063/1.96799

10.1063/1.101596

10.1063/1.103610

10.1038/s41467-018-04029-7

Chen Q., 2016, Phys. Rev. X, 6, 031042

10.1002/pssb.2221760124

10.1103/PhysRevLett.118.136001

10.1063/1.352225

10.1109/JPHOTOV.2013.2264622

Shao Y., 2014, J. Huang. Nat. Comm, 5, 5874

10.1039/C4CP04479G

10.1021/acs.jpcc.7b04684

10.1021/acs.jpcc.5b11465

10.1063/1.363401

10.1063/1.366686