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Surface-Activated Corrosion in Tin-Lead Halide Perovskite Solar Cells

Journal Article · · ACS Energy Letters
Mixed tin–lead halide perovskite solar cells have promising power conversion efficiencies, but long-term stability is still a challenge. Herein we examine the stability of a 60:40 tin–lead perovskite to better understand diminished device performance upon thermal treatment, both in ambient and inert atmosphere. Operando X-ray diffraction shows a stable bulk structure of the perovskite absorber, leading to the hypothesis that surface chemistry dominates the degradation mechanism. X-ray photoelectron spectroscopy reveals two new observations post-thermal annealing that accompany previously reported Sn4+ evolution: (i) the formation of I3– intermediates preceding I2 loss at the surface and (ii) evidence of under-coordinated tin and lead surface sites (Snd<2+ and Pbd<2+, respectively) in inert and ambient conditions. These two species indicate an activated corrosion (i.e., both oxidation and reduction) process at the surface as a possible chemical pathway for degradation, which is expected to be accelerated under operando voltage and light biases.
Research Organization:
National Renewable Energy Laboratory (NREL), Golden, CO (United States)
Sponsoring Organization:
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Solar Energy Technologies Office (EE-4S)
DOE Contract Number:
AC36-08GO28308
OSTI ID:
1762455
Report Number(s):
NREL/JA-5900-78853; MainId:32770; UUID:38af78c8-33be-418f-8ad6-e57d02be965e; MainAdminID:19165
Journal Information:
ACS Energy Letters, Journal Name: ACS Energy Letters Journal Issue: 11 Vol. 5
Country of Publication:
United States
Language:
English

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