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2020
DOI: 10.1016/j.jpowsour.2020.228556
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Toward high-efficiency and thermally-stable perovskite solar cells: A novel metal-organic framework with active pyridyl sites replacing 4-tert-butylpyridine

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Cited by 17 publications
(16 citation statements)
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“…[ 10,18 ] Surprisingly, by adding an optimal amount of Er@C 82 (0.09 mg mL −1 ) into the control Spiro‐Li film, the pinholes in the resultant Spiro‐Li‐Er film are obviously reduced (Figure 2b) and the root‐mean‐square (RMS) roughness of the corresponding film is also decreased to 3.358 nm from 4.926 nm for the Spiro‐Li film. These observations imply that the addition of Er@C 82 has effectively suppressed the aggregation of Li‐TFSI, [ 16,30 ] leading to a uniform distribution of Li‐TFSI in the Spiro‐Li‐Er film. Since the Li‐TFSI dopant is responsible for facilitating the oxidation reaction between Spiro‐OMeTAD and O 2 , according to the following equation [ 12 ] Spiro‐OMeTAD+O2+ Li‐TFSISpiro‐OMeTAD+TFSI+LixnormalOythe more uniformly dispersed Li‐TFSI in the Spiro‐Li‐Er film is believed to come in contact with both Spiro‐OMeTAD and O 2 more easily than that in the Spiro‐Li film, consequently accelerating the oxidation reaction.…”
Section: Resultsmentioning
confidence: 97%
“…[ 10,18 ] Surprisingly, by adding an optimal amount of Er@C 82 (0.09 mg mL −1 ) into the control Spiro‐Li film, the pinholes in the resultant Spiro‐Li‐Er film are obviously reduced (Figure 2b) and the root‐mean‐square (RMS) roughness of the corresponding film is also decreased to 3.358 nm from 4.926 nm for the Spiro‐Li film. These observations imply that the addition of Er@C 82 has effectively suppressed the aggregation of Li‐TFSI, [ 16,30 ] leading to a uniform distribution of Li‐TFSI in the Spiro‐Li‐Er film. Since the Li‐TFSI dopant is responsible for facilitating the oxidation reaction between Spiro‐OMeTAD and O 2 , according to the following equation [ 12 ] Spiro‐OMeTAD+O2+ Li‐TFSISpiro‐OMeTAD+TFSI+LixnormalOythe more uniformly dispersed Li‐TFSI in the Spiro‐Li‐Er film is believed to come in contact with both Spiro‐OMeTAD and O 2 more easily than that in the Spiro‐Li film, consequently accelerating the oxidation reaction.…”
Section: Resultsmentioning
confidence: 97%
“…[ 124 ] Zhou et al . [ 125 ] improved the thermal stability of PSCs by replacing the 4‐ tert ‐butylpyridine ( t ‐BP) with the [In(HPyia)Cl 2 ]CH 3 CN (In‐Pyia) in Figure 11g. Due to their strong coordination effect and robust framework, the In‐Pyia effectively restrained the aggregation, hydration, and ion penetration behaviors of lithium salts.…”
Section: Main Applications Of Mofsmentioning
confidence: 99%
“…Schematic illustration of (a) Li‐TFSI@NH 2 ‐MIL‐101, [ 122 ] (c) POM@MOF‐545, [ 123 ] (e) Zn‐CBOB, [ 124 ] and (g)In‐Pyia. [ 125 ] Long‐term stability for PSCs with (b) Li‐TFSI@NH 2 ‐MIL‐101, (d) POM@MOF‐545, (f) Zn‐CBOB, and (h) In‐Pyia.…”
Section: Main Applications Of Mofsmentioning
confidence: 99%
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“…This result can be promising in terms of highly efficient and long-term stable PSC devices. A further step toward more stable PSCs was made by the same group through the replacement of TBP with a different In-based MOF, namely In(HPyia)Cl 2 ]•CH 3 CN (In-Pyia) [233]. As a matter of fact, TBP, which is highly volatile liquid phase component, caused the aggregation, hydration, and ion penetration of lithium salts into the PSK layer.…”
Section: Rolementioning
confidence: 99%