4.8 Article

Stability-limiting heterointerfaces of perovskite photovoltaics

Journal

NATURE
Volume 605, Issue 7909, Pages 268-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-022-04604-5

Keywords

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Funding

  1. US Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under the Solar Energy Technologies Office [DE-EE0008751]
  2. Korea Institute of Energy Technology Evaluation and Planning (KETEP) - Korea government (MOTIE) [20214000000640, 20213030010400]
  3. POSCO Science Fellowship from the POSCO TJ Park Foundation
  4. National Science Foundation (NSF) [DMR-2034738]
  5. National Research Foundation of Korea (NRF) - Korea government (MSIT) [NRF-2022R1C1C1011975, NRF-2021R1A2C2007141]
  6. NRF - MSIT [NRF-2021R1A3B1076723]
  7. National Science Foundation through the UC Irvine Materials Research Science and Engineering Center [DMR-2011967]
  8. Office of Science, Office of Basic Energy Sciences, of the US Department of Energy [DE-AC02-05CH11231]
  9. Korea Institute of Energy Technology Evaluation & Planning (KETEP) [20213030010400, 20214000000640] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Optoelectronic devices rely on heterointerfaces between different semiconducting materials, and the energy-level alignment between them plays a crucial role in device performance. Surface treatments for perovskite solar cells can impact the energetics of the heterointerface, potentially affecting device stability. Balancing the pros and cons of surface treatments is essential for improving PSC stability.
Optoelectronic devices consist of heterointerfaces formed between dissimilar semiconducting materials. The relative energy-level alignment between contacting semiconductors determinately affects the heterointerface charge injection and extraction dynamics. For perovskite solar cells (PSCs), the heterointerface between the top perovskite surface and a charge-transporting material is often treated for defect passivation(1-4) to improve the PSC stability and performance. However, such surface treatments can also affect the heterointerface energetics(1). Here we show that surface treatments may induce a negative work function shift (that is, more n-type), which activates halide migration to aggravate PSC instability. Therefore, despite the beneficial effects of surface passivation, this detrimental side effect limits the maximum stability improvement attainable for PSCs treated in this way. This trade-off between the beneficial and detrimental effects should guide further work on improving PSC stability via surface treatments.

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