A series of β‐hydroxy‐vinylimine boron compounds 1–7 have been reported to exhibit unique dual emission, consisting of fluorescence and room temperature phosphorescence (RTP) in solution. This ...finding triggered intensive research of RTP in β‐hydroxy‐vinylimine boron derivatives. Herein, we show clear evidence that the associated dual emission, especially RTP, is caused by the experimental artifact, where bright emission intensity saturates the detection dynamic range of the fluorimeter.
We present evidence that the dual emission of β‐hydroxy‐vinylimine boron compounds consisting of fluorescence and room temperature phosphorescence in solution is caused by the experimental artifact, where bright emission intensity saturates the detection dynamic range of the fluorimeter.
We propose a new concept exploiting thermally activated delayed fluorescence (TADF) molecules as photosensitizers, storage units and signal transducers to harness solar thermal energy. Molecular ...composites based on the TADF core phenoxazine-triphenyltriazine (PXZ-TRZ) anchored with norbornadiene (NBD) were synthesized, yielding compounds PZDN and PZTN with two and four NBD units, respectively. Upon visible-light excitation, energy transfer to the triplet state of NBD occurred, followed by NBD → quadricyclane (QC) conversion, which can be monitored by changes in steady-state or time-resolved spectra. The small S
-T
energy gap was found to be advantageous in optimizing the solar excitation wavelength. Upon tuning the molecule's triplet state energy lower than that of NBD (61 kcal/mol), as achieved by another composite PZQN, the efficiency of the NBD → QC conversion decreased drastically. Upon catalysis, the reverse QC → NBD reaction occurred at room temperature, converting the stored chemical energy back to heat with excellent reversibility.
Four isomeric, homoleptic iridium(III) metal complexes bearing 5‐(trifluoromethyl)imidazo4,5‐bpyridin‐2‐ylidene and 6‐(trifluoromethyl)imidazo4,5‐bpyridin‐2‐ylidene‐based cyclometalating chelates are ...successfully synthesized. The meridional isomers can be converted to facial isomers through acid induced isomerization. The m‐isomers display a relatively broadened and red‐shifted emission, while f‐isomers exhibit narrowed blue emission band, together with higher photoluminescent quantum yields and reduced radiative lifetime relative to the mer‐counterparts. Maximum external quantum efficiencies of 13.5% and 22.8% are achieved for the electrophosphorescent devices based on f‐tpb1 and m‐tpb1 as dopant emitter together with CIE coordinates of (0.15, 0.23) and (0.22, 0.45), respectively. By using f‐tpb1 as the sensitizing phosphor and t‐DABNA as thermally activated delayed fluorescence (TADF) terminal emitter, hyperluminescent OLEDs are successfully fabricated, giving high efficiency of 29.6%, full width at half maximum (FWHM) of 30 nm, and CIE coordinates of (0.13, 0.11), confirming the efficient Förster resonance energy transfer (FRET) process.
Blue emissive Ir(III) emitters with functionalized imidazo4,5‐bpyridin‐2‐ylidene chelates are reported. One such emitter, namely: f‐tpb1, can produce electrophosphorescence with CIEx,y = 0.15, 0.23 and maximum EQE of 13.5% and hyperluminescence with CIEx,y = 0.13, 0.11 and maximum EQE of 29.6%, respectively.
Two-dimensional (2D) Dion–Jacobson (DJ) perovskite solar cells (PSCs), despite their advantage in versatility of n-layer variation, are subject to poor photovoltaic efficiency, particularly in the ...fill factor (FF), compared to their three-dimensional counterparts. To enhance the performance of DJ PSCs, the process of growing crystals and hence the corresponding morphology of DJ perovskites are of prime importance. Herein, we report the fast nonisothermal (NIT) crystallization protocol that is previously unrecognized for 2D perovskites to significantly improve the morphology, orientation, and charge transport of the DJ perovskite films. Comprehensive mechanistic studies reveal that the NIT effect leads to the secondary crystallization stage, forming network-like channels that play a vital role in the FF’s leap-forward improvement and hence the DJ PSC’s performance. As a whole, the NIT crystallized PSCs demonstrate a high power conversion efficiency and an FF of up to 19.87 and 86.16%, respectively. This research thus provides new perspectives to achieve highly efficient DJ PSCs.
A new class of bis-tridentate Ir(III) complexes (Dap-1–4) was synthesized using carbene pincer pro-chelates PC1·H3(PF6)2 or PC2·H3(PF6)2 with either imidazolylidene or ...imidazo4,5-bpyridin-2-ylidene appendages, together with a second cyclometalating 2,6-diaryoxypyridine chelate, L1H2 and L2H2, differed by a NMe2 donor at the central pyridinyl fragment. The respective emission tuning between the ultraviolet and blue region was rationalized using time-dependent density functional theory (TD-DFT) approaches. Next, a highly efficient blue emitter (Dap-5) was synthesized by concomitant addition of two methyl groups and a single CF3 substituent at the central phenyl and peripheral imidazo4,5-bpyridin-2-ylidene entities of the carbene pincer chelate, respectively. The organic light-emitting diode (OLED) device with 15 wt % Dap-5 in DPEPO shows electroluminescence at 468 nm and with CIE (0.14, 0.15) and a max external quantum efficiency (max EQE) of 16.8% with low efficiency roll-off (EQE of 14.4% at 1000 cd m–2); the latter is attributed to the relatively shortened triplet excited-state radiative lifetime. These results highlight the adequateness of bis-tridentate Ir(III) phosphors in fabrication of practical blue-emitting OLEDs.
Aryl transfer between heteroatoms was photochemically available through radical initiation followed by a bimolecular reaction. However, such an excited-state reaction has rarely been reported through ...a photoinduced intramolecular pathway in the π-conjugated systems. Herein, we found, for the first time, a clean photoinduced intramolecular aryl shift for imidazolyl-quinoline derivatives 2NQ (imidazophenanthrene) and 4NQX (imidazophenanthroline), of which the photoproducts are thermally reversible. Upon light irradiation of the studied compounds in solution, an appreciable blue fluorescence along with a gradual change in color appearance was observed, the photoluminescence and photoconversion quantum yields of which were shown to be competitive in the same excited state. We were able to harness the photoconversion quantum yields of the NQ compounds with facile electronic modifications. These, in combination with time-resolved studies on the NQ compounds, gave an oxygen-insensitive aryl transfer rate within 1–100 ns. The anomalously slow intramolecular reaction rates were further proven to be associated with the ∼5.0 kcal/mol transition free energy. The photoproducts NQ_rs were isolated, identified by X-ray analyses, and also shown to demonstrate anti-Vavilov reverse reactions back to the NQ compounds in the higher-lying excited state. The discovery of photoinduced intramolecular aryl transfer paves a new pathway in the synthetic field, which may also be extended and far-reaching to solar–chemical storage under an appropriate design strategy.
The phosphonium-decorated phenanthro-imidazolyl pyridine ligand, LP + Br, readily reacts with zinc(II) and cadmium(II) bromides to give inorganic–organic zero-dimensional compounds LP + ZnBr22ZnBr4 ...(1) and (LP + )2Cd2Br4CdBr4 (2), respectively, upon crystallization. These salts are moderately fluorescent in the solid state under ambient conditions (λem = 458 nm, Φem = 0.11 for 1; λem = 460 nm, Φem = 0.13 for 2). Their emission results from spin-allowed electronic transitions localized on the organic component with the negligible effect of MBr42– and MBr2 units. Contrary to ionic species 1 and 2, lead(II) bromide affords a neutral and water-stable complex (LP + )2Pb3Br8 (3), showing weak room-temperature phosphorescence arising from spin–orbit coupling due to the heavy atom effect. The emission, which is substantially enhanced for the amorphous sample of 3 (λem = 575 nm, Φem = 0.06), is assigned to the intraligand triplet excited state, which is a rare phenomenon among Pb(II) molecular materials.
A series of β‐hydroxy‐vinylimine boron compounds 1–7 have been reported to exhibit unique dual emission, consisting of fluorescence and room temperature phosphorescence (RTP) in solution. This ...finding triggered intensive research of RTP in β‐hydroxy‐vinylimine boron derivatives. Herein, we show clear evidence that the associated dual emission, especially RTP, is caused by the experimental artifact, where bright emission intensity saturates the detection dynamic range of the fluorimeter.
We present evidence that the dual emission of β‐hydroxy‐vinylimine boron compounds consisting of fluorescence and room temperature phosphorescence in solution is caused by the experimental artifact, where bright emission intensity saturates the detection dynamic range of the fluorimeter.
A series of new six (anilido)‐five (thiazole) membered ring boron difluoride dyes, namely BFs, have been synthesized from the corresponding para‐ and meta‐substituted 2‐(2’‐methylaminophenyl) ...benzothiazoles through complexation with boron trifluoride. Depending on the substituent effect, the derivatives can switch the emission properties from fluorescence with 100 % emission yield to slim fluorescence but >90 % triplet state population and peak wavelength tuning from 490 nm to 610 nm. Compared with non‐complexed precursors, the rigid, highly planar structure and significantly red‐shifted absorption and emission for BFs indicate that the boron center facilitates the formation of a bridge leading to increased rigidity, and is also involved in π‐conjugation, increasing the transition dipole and suppressing the non‐radiative internal conversion. Together with optical ∼100 % transparent window around 325–375 nm, BFs may find unique applications, among which the fluorescence up‐conversion via triplet‐triplet annihilation is demonstrated.
Substituent effects: A series of six(anilido)‐five(thiazole) membered ring boron difluoride dyes were designed and synthesized from the corresponding para‐ and meta‐substituted 2‐(2’‐methylaminophenyl) benzothiazoles. Experimentally, following triplet‐triplet energy transfer from one derivative to anthracene, up‐converted anthracene fluorescence via T−T annihilation was demonstrated.
Inverted perovskite solar cells (PSCs) have attracted intense attention because of their insignificant hysteresis and low-temperature fabrication process. However, the efficiencies of inverted PSCs ...are still inferior to those of commercialized silicon solar cells. Also, the poor stability of PSCs is one of the major impedances to commercialization. Herein, we rationally designed and synthesized a new series of electron donor (R,R-diphenylamino) and acceptor (pyridimium-(CH2) n -sulfonates) zwitterions as a boundary modulator and systematically investigated their associated interface properties. Comprehensive physical and optoelectronic studies verify that these zwitterions provide a four-in-one functionality: balancing charge carrier transport, suppressing less-coordinated Pb2+ defects, enhancing moisture resistance, and reducing ion migration. Although each functionality may have been reported by specific passivating molecules, a strategy that simultaneously regulates the charge-transfer balance and three other functionalities has not yet been developed. The results are to make an omnidirectional improvement of PSCs. Among all zwitterions, 4-(4-(4-(di-(4-methoxylphenyl)amino)phenyl)propane-1-ium-1-yl)butane-1-sulfonate (OMeZC3) optimizes the balance hole/electron mobility ratio of perovskite to 0.91, and the corresponding PSCs demonstrate a high power conversion efficiency (PCE) of up to 23.15% free from hysteresis, standing out as one of the champion PSCs with an inverted structure. Importantly, the OMeZC3-modified PSC exhibits excellent long-term stability, maintaining almost its initial PCE after being stored at 80% relative humidity for 35 days.
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