Abstract:Lead-free PEA
2
SnI
4
-based perovskite
LEDs
are successfully inkjet-printed on rigid and flexible substrates.
Red-emitting devices (λ
max
= 633 nm) exhibit, under
ambient conditions, a maximum external quantum efficiency (EQE
max
) of 1% with a related brightness of 30 cd/m
2
at 10 mA/cm
2
.
“…efficiencies (EQEs) over 20%, [7][8][9][10][11][12][13][14][15][16][17] the device performance of Sn-based PeLEDs is still in an earlier stage with maximum EQEs <6%. [18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33] The performance gap between Sn-based and Pb-based perovskites has been ascribed to the trap-limited nonradiative recombination due to their inherent high-density defect states. [34] These traps are usually induced by the prone oxidation of Sn 2+ to Sn 4+ , and faster crystallization process of Sn-based perovskites than Pb analogs.…”
The performance of tin (Sn)-based perovskite light-emitting diodes (PeLEDs) lags behind their lead analogs due to the challenges of Sn 2+ oxidation, defect passivation, and fast crystallization. Herein, the passivation effects of diphenylphosphine oxide (DPPO) derivatives on the fabrication of PEA 2 SnI 4 films are investigated. The DPPO derivatives with hydroxyl group, or including substituent group with the potential to form hydroxyl group, are unfavorable passivators due to their positive effects in accelerating Sn 2+ oxidation. In comparison, amino-functionalized DPPO molecule is an effective additive to enhance the photoluminescence of PEA 2 SnI 4 films due to the effective defect passivation as well as crystallinity improvement. Based on the optimized films, color-stable pure-red PeLEDs are demonstrated with a full width at half maximum of 23 nm at 630 nm, a maximum luminance of 451 cd m −2 , a maximum external quantum efficiency of 3.51%, and a half-lifetime of 13.7 min at 102 cd m −2 . This work opens new prospects on the selection of effective molecular additives for Sn-based perovskites.
“…efficiencies (EQEs) over 20%, [7][8][9][10][11][12][13][14][15][16][17] the device performance of Sn-based PeLEDs is still in an earlier stage with maximum EQEs <6%. [18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33] The performance gap between Sn-based and Pb-based perovskites has been ascribed to the trap-limited nonradiative recombination due to their inherent high-density defect states. [34] These traps are usually induced by the prone oxidation of Sn 2+ to Sn 4+ , and faster crystallization process of Sn-based perovskites than Pb analogs.…”
The performance of tin (Sn)-based perovskite light-emitting diodes (PeLEDs) lags behind their lead analogs due to the challenges of Sn 2+ oxidation, defect passivation, and fast crystallization. Herein, the passivation effects of diphenylphosphine oxide (DPPO) derivatives on the fabrication of PEA 2 SnI 4 films are investigated. The DPPO derivatives with hydroxyl group, or including substituent group with the potential to form hydroxyl group, are unfavorable passivators due to their positive effects in accelerating Sn 2+ oxidation. In comparison, amino-functionalized DPPO molecule is an effective additive to enhance the photoluminescence of PEA 2 SnI 4 films due to the effective defect passivation as well as crystallinity improvement. Based on the optimized films, color-stable pure-red PeLEDs are demonstrated with a full width at half maximum of 23 nm at 630 nm, a maximum luminance of 451 cd m −2 , a maximum external quantum efficiency of 3.51%, and a half-lifetime of 13.7 min at 102 cd m −2 . This work opens new prospects on the selection of effective molecular additives for Sn-based perovskites.
“…[56,57] To date, (PEA) 2 SnI 4 remains the champion 2D Sn HaP emitter, with record external quantum efficiencies (EQE) in LEDs of 5 % (Figure 4b) [57] and showing promising upscaling prospects. [58] To attain efficient visible emission beyond red, quantum size effects in 2D HaPs must be combined with I À Reproduced with permission from ref. [37].…”
Section: Two-dimensional Sn Hap Emittersmentioning
confidence: 99%
“…[ 56 , 57 ] To date, (PEA) 2 SnI 4 remains the champion 2D Sn HaP emitter, with record external quantum efficiencies (EQE) in LEDs of 5 % (Figure 4b ) [57] and showing promising upscaling prospects. [58] …”
Tin halide perovskites (Sn HaPs) are the top lead-free choice for perovskite optoelectronics, but the oxidation of perovskite Sn 2 + to Sn 4 + remains a key challenge. However, the role of inconspicuous chemical processes remains underexplored. Specifically, the halide component in Sn HaPs (typically iodide) has been shown to play a key role in dictating device performance and stability due to its high reactivity. Here we describe the impact of native halide chemistry on Sn HaPs. Specifically, molecular halogen formation in Sn HaPs and its influence on degradation is reviewed, emphasising the benefits of iodide substitution for improving stability. Next, the ecological impact of halide products of Sn HaP degradation and its mitigation are considered. The development of visible Sn HaP emitters via halide tuning is also summarised. Lastly, halide defect management and interfacial engineering for Sn HaP devices are discussed. These insights will inspire efficient and robust Sn HaP optoelectronics.
“…1 Moreover, 2D materials synthesized by the LPE method can be deposited on any wafer at low temperature (by inkjet printing, screen printing, and spray, among others 4 ) to pattern wires, electrodes, channels, and other complex devices with irregular shapes. 9 This method has been used to fabricate a plethora of solid-state microelectronic devices, including transistors, 10 photodetectors, 11 capacitors, 12 solar cells, 13 and light emitting diodes 14 (among others).…”
Inkjet-printed h-BN memristors exhibit multiple stochastic phenomena that are very attractive for use as entropy sources in electronic circuits for data encryption. The high variability can be exploited to create unique and unpredictable patterns.
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