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Organic solvent free PbI2 recycling from perovskite solar cells using hot water

Abstract:
Perovskite solar cells represent an emerging and highly promising renewable energy technology. However, the most efficient perovskite solar cells critically depend on the use of lead. This represents a possible environmental concern potentially limiting the technologies’ commercialization. Here, we demonstrate a facile recycling process for PbI2, the most common lead-based precursor in perovskite absorber material. The process uses only hot water to effectively extract lead from synthetic precursor mixes, plastic- and glass-based perovskites (92.6 – 100% efficiency after two extractions). When the hot extractant is cooled, crystalline PbI2 in high purity (> 95.9%) precipitated with a high yield: from glass-based perovskites, the first cycle of extraction / precipitation was sufficient to recover 94.4 ± 5.6% of Pb, whereas a second cycle yielded another 10.0 ± 5.2% Pb, making the recovery quantitative. The solid extraction residue remaining is consequently deprived of metals and may thus be disposed as non-hazardous waste. Therefore, exploiting the highly temperature-dependent solubility of PbI2 in water provides a straightforward, easy to implement way to efficiently extract lead from PSC at the end-of-life and deposit the extraction residues in a cost-effective manner, mitigating the potential risk of lead leaching at the perovskites’ end-of-life.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.jhazmat.2023.130829

Authors


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Role:
Author
ORCID:
0000-0002-7061-3596
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Institution:
University of Oxford
Division:
MPLS
Department:
Physics
Sub department:
Condensed Matter Physics
Oxford college:
St Peter's College
Role:
Author
ORCID:
0000-0002-7807-3133


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Funder identifier:
https://ror.org/00k4n6c32
Grant:
763977


Publisher:
Elsevier
Journal:
Journal of Hazardous Materials More from this journal
Volume:
447
Article number:
130829
Place of publication:
Netherlands
Publication date:
2023-01-18
Acceptance date:
2023-01-17
DOI:
EISSN:
1873-3336
ISSN:
0304-3894
Pmid:
36682249


Language:
English
Keywords:
Pubs id:
1327915
Local pid:
pubs:1327915
Deposit date:
2025-01-22

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