2020
DOI: 10.1016/j.nanoen.2020.104483
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Inhibited aggregation of lithium salt in spiro-OMeTAD toward highly efficient perovskite solar cells

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Cited by 70 publications
(71 citation statements)
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“…The PSC using spiro-OMeTAD presents poor stability, and the efficiency is maintained at only 50% after 200 h due to the hygroscopic property of additives in the spiro-OMeTAD. 50 For the PSC based on NiO HTL, because of the hydrophobic property of organics on the surface of NiO nanoparticles, the device exhibits excellent stability, maintaining 91% of the pristine efficiency after 200 h. After treatment with oxygen plasma, the working stability is similar to the control one. By contrast, the device based on hexanethioltreated NiO HTL can only maintain about 10% of the original efficiency after 200 h.…”
Section: Resultsmentioning
confidence: 92%
“…The PSC using spiro-OMeTAD presents poor stability, and the efficiency is maintained at only 50% after 200 h due to the hygroscopic property of additives in the spiro-OMeTAD. 50 For the PSC based on NiO HTL, because of the hydrophobic property of organics on the surface of NiO nanoparticles, the device exhibits excellent stability, maintaining 91% of the pristine efficiency after 200 h. After treatment with oxygen plasma, the working stability is similar to the control one. By contrast, the device based on hexanethioltreated NiO HTL can only maintain about 10% of the original efficiency after 200 h.…”
Section: Resultsmentioning
confidence: 92%
“…One possible reason could be the reduced aggregation of lithium salt, which usually serves as an additive to facilitate more efficient charge transport. 52 Usually, for processing the spiro-OMe-TAD film, another additive of 4-tert-butylpyridine is added into the solution to secure a more homogeneous distribution of the lithium salt. 51 Both 4-tert-butylpyridine and lithium salt could form chemical bonds with spiro-OMeTAD, 53 which provides the possibility of retaining these dopants in the spiro-OMeTAD during the recycling.…”
Section: Resultsmentioning
confidence: 99%
“…Device containing only cobalt salts and t-BP presents PCEs of 17.98% and 15.47% under RS and FS with an HI of 0.140; the decrease of HI could be attributed to the absence of lithium in the device. It has been proven that suppressing the migration of lithium from HTL to ETL could result in the reduced hysteresis of the PSCs [17,31]. In the absence of cobalt salt, devices involving K-FSI/t-BP obtain PCEs of 19.88% and 19.45% under RS and FS, higher than that of 19.16% and 14.57% for the devices using Li-TFSI/t-BP (Table S3).…”
Section: Hysteresis Studymentioning
confidence: 99%
“…For example, lithium bis(trifluoromethanesulfonyl)imide (Li-TFSI) is added to accelerate the oxidation of spiro-OMeTAD [13], and 4-tertbutylpyridine (t-BP) is used to not only enable an effective p-doping through interface interaction between t-BP and the perovskite layer but also increase the solubility of Li-TFSI in the spiro-OMeTAD solution [14,15]. However, these standard bi-dopants of Li-TFSI and t-BP have been identified to conjointly destroy the morphology of hole transport layers (HTLs) and long-term stability due to the hygroscopicity of Li-TFSI and the low boiling point of t-BP [16][17][18]. In the case of exposure to the ambient, the evaporation of t-BP leads to aggregation and hydration of Li-TFSI, which eventually results in the destruction of the PSC devices [15,19].…”
Section: Introductionmentioning
confidence: 99%