Abstract

Colloidal quantum dots (CQDs) are promising photovoltaic (PV) materials because of their widely tunable absorption spectrum controlled by nanocrystal size1,2. Their bandgap tunability allows not only the optimization of single-junction cells, but also the fabrication of multijunction cells that complement perovskites and silicon3. Advances in surface passivation2,4,5,6,7, combined with advances in device structures8, have contributed to certified power conversion efficiencies (PCEs) that rose to 11% in 20169. Further gains in performance are available if the thickness of the devices can be increased to maximize the light harvesting at a high fill factor (FF). However, at present the active layer thickness is limited to ~300 nm by the concomitant photocarrier diffusion length. To date, CQD devices thicker than this typically exhibit decreases in short-circuit current (JSC) and open-circuit voltage (VOC), as seen in previous reports3,9,10,11. Here, we report a matrix engineering strategy for CQD solids that significantly enhances the photocarrier diffusion length. We find that a hybrid inorganic–amine coordinating complex enables us to generate a high-quality two-dimensionally (2D) confined inorganic matrix that programmes internanoparticle spacing at the atomic scale. This strategy enables the reduction of structural and energetic disorder in the solid and concurrent improvements in the CQD packing density and uniformity. Consequently, planar devices with a nearly doubled active layer thicknesses (~600 nm) and record values of JSC (32 mA cm−2) are fabricated. The VOC improved as the current was increased. We demonstrate CQD solar cells with a certified record efficiency of 12%.

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Acknowledgements

This publication is based in part on work supported by the Natural Sciences and Engineering Research Council of Canada, by the Ontario Research Fund Research Excellence Program and by Award OSR-2017-CPF-3321-03 made by King Abdullah University of Science and Technology (KAUST). Some of the GIWAXS/GISAXS measurements were performed at the Cornell High Energy Synchrotron Source (CHESS), supported by the NSF Award DMR-1332208. This work also made use of the South Carolina SAXS Collaborative using a SAXSLab Ganesha for the GISAXS/GIWAXS measurements, supported by the NSF Major Research Instrumentation program (award no. DMR-1428620). We thank U. Jeng for the GIWAXS tested at the National Synchrotron Radiation Research Center, Taiwan, China. We thank L. Goncharova for assistance with RBS measurements. We thank D. Kopilovic, E. Palmiano, L. Levina and R. Wolowiec for the technical support.

Author information

Affiliations

  1. Department of Electrical and Computer Engineering, University of Toronto, Toronto, Ontario, Canada

    • Jixian Xu
    • , Oleksandr Voznyy
    • , Mengxia Liu
    • , Grant Walters
    • , Andrew H. Proppe
    • , F. Pelayo García de Arquer
    • , Mingyang Wei
    • , Bin Sun
    • , Min Liu
    • , Olivier Ouellette
    • , Rafael Quintero-Bermudez
    • , Jie Li
    • , James Fan
    • , Lina Quan
    • , Petar Todorovic
    • , Hairen Tan
    • , Sjoerd Hoogland
    •  & Edward H. Sargent
  2. King Abdullah University of Science and Technology (KAUST), KAUST Solar Center (KSC), and Physical Sciences and Engineering Division, Thuwal, Saudi Arabia

    • Ahmad R. Kirmani
    • , Rahim Munir
    • , Maged Abdelsamie
    •  & Aram Amassian
  3. Department of Chemistry, University of Toronto, Toronto, Ontario, Canada

    • Andrew H. Proppe
    •  & Shana O. Kelley
  4. Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, USA

    • Amrita Sarkar
    •  & Morgan Stefik
  5. Institute of Super-microstructure and Ultrafast Process in Advanced Materials, School of Physics and Electronics, Central South University, Changsha, Hunan, China

    • Min Liu
  6. Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada

    • Shana O. Kelley

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Contributions

J.X. conceived the idea and contributed to most experimental work. E.H.S. supervised the project. O.V., A.A. and S.O.K. co-supervised the project. Mengxia Liu assisted in the device fabrication and experiment design. S.H. assisted in the devices certificate and experiment design. A.R.K., M.A. and A.A. performed the in situ measurements of film formation. R.M., M.S., A.S. and R.Q.B. carried out the GISAXS/WAXS measurements. G.W. and M.W. performed the AFM and PL measurements. A.H.P. performed the TA measurements. B.S. carried out the FET measurements. O.V. and O.O. carried out the device simulations. Min Liu carried out microscopic studies. O.V. facilitated the RBS analysis. J.X., O.V. and E.H.S. wrote the manuscript. All the authors assisted in the experiments and provided comments on the text.

Competing interests

The authors declare no competing interests.

Corresponding authors

Correspondence to Aram Amassian or Edward H. Sargent.

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DOI

https://doi.org/10.1038/s41565-018-0117-z