Quantitative Design of Bright Fluorophores and AIEgens by the Accurate Prediction of Twisted Intramolecular Charge Transfer (TICT).

Inhibition of TICT can significantly increase the brightness of fluorescent materials. Accurate prediction of TICT is thus critical for the quantitative design of high-performance fluorophores and AIEgens. TICT of 14 types of popular organic fluorophores were modeled with time-dependent density functional theory (TD-DFT). A reliable and generalizable computational approach for modeling TICT formations was established. To demonstrate the prediction power of our approach, we quantitatively designed a boron dipyrromethene (BODIPY)-based AIEgen which exhibits (almost) barrierless TICT rotations in monomers. Subsequent experiments validated our molecular design and showed that the aggregation of this compound turns on bright emissions with ca. 27-fold fluorescence enhancement, as TICT formation is inhibited in molecular aggregates.

Gene dosage and coexpression with endoplasmic reticulum secretion-associated factors improved the secretory expression of α-galactosidase.

The α-galactosidases, which can catalyze the removal of α-1,6-linked terminal galactose residues from galactooligosaccharide materials, have good potential for industrial applications. The high-level and efficient secretion of the α-galactosidases into the extracellular space has greatly simplified the downstream bioengineering process, facilitating their bioapplications. In this study, the effects of gene dosage and endoplasmic reticulum secretion-associated factors (ERSAs) on the secretory expression of an α-galactosidase gene derived from a Aspergillus oryzae strain were investigated by constructing multicopy expression cassettes and coexpressing the α-galactosidase gene with ERSAs. With the increase in the gene copy-number in the host genome, the expression of GalA was improved. However, the secretory expression level was not linearly related to the copy number. When the number was higher than four copies, the expression level of GalA gene declined. The ERSAs factors HAC1, PDI, and Ero1 improved the secretory expression of α-galactosidase, while Hsp40 inhibited its secretion. After methanol-induced expression in a bench-top bioreactor, Pichia recombinants carrying four copies of GalA genes reached 3520 U/mL in the supernatant of the culture. We further optimized the parameters for α-galactosidase to hydrolyze two types of galactooligosaccharides: raffinose and stachyose. This study has fulfilled the scale-up production of α-galactosidase, thus facilitating its industrial applications.

[Quality control of Dandeng Tongnao Ruanjiaonang based on UPLC fingerprint combined with chemical pattern recognition].

To establish the ultra performance liquid chromatography (UPLC) fingerprint of Dandeng Tongnao Ruanjiaonang and conduct a systemic, comprehensive quality evaluation of the drug by combining with a chemical pattern recognition method. In this study, Waters UPLC ultra-high performance liquid chromatography instrument and ACQUITY UPLCHSS T3 chromatographic colum n were employed to perform the separation with acetonitrile-0.1% formic acid aqueous solution as the mobile phase for gradient elution; and the detection wavelength was set at 256 nm to establish the UPLC fingerprint of 10 batches of Dandeng Tongnao Ruanjiaonang. Then, the further quality assessment of the drug was carried out by similarity evaluation, Cluster Analysis(CA), Principal Component Analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA). Finally, 77 peaks were recognised as common peaks in the fingerprint, and 15 peaks of them were identified using standard references. The similarity value of these 10 batches of drugs was all above 0.960, indicating a relatively stable quality. But minor differences were still discovered between the batches of the drug by CA and PCA. Finally, 6 common peaks were recognised as the quality makers using OPLS-DA method. The analysis method established in this study was scientific, accurate, reliable and simple; fingerprint combined with chemical pattern recognition technique can be used to systematically and comprehensively evaluate the drug quality of Dandeng Tongnao Ruanjiaonang; what's more, it could also provide a reference for the quality control of traditional Chinese medicine and its preparations at the same time.

High-Performance Ternary Organic Solar Cell Enabled by a Thick Active Layer Containing a Liquid Crystalline Small Molecule Donor.

Ternary organic solar cells (OSCs) have attracted much research attention in the past few years, as ternary organic blends can broaden the absorption range of OSCs without the use of complicated tandem cell structures. Despite their broadened absorption range, the light harvesting capability of ternary OSCs is still limited because most ternary OSCs use thin active layers of about 100 nm in thickness, which is not sufficient to absorb all photons in their spectral range and may also cause problems for future roll-to-roll mass production that requires thick active layers. In this paper, we report a highly efficient ternary OSC (11.40%) obtained by incorporating a nematic liquid crystalline small molecule (named benzodithiophene terthiophene rhodanine (BTR)) into a state-of-the-art PTB7-Th:PC71BM binary system. The addition of BTR into PTB7-Th:PC71BM was found to improve the morphology of the blend film with decreased π-π stacking distance, enlarged coherence length, and enhanced domain purity. This resulted in more efficient charge separation, faster charge transport, and less bimolecular recombination, which, when combined, led to better device performance even with thick active layers. Our results show that the introduction of highly crystalline small molecule donors into ternary OSCs is an effective means to enhance the charge transport and thus increase the active layer thickness of ternary OSCs to make them more suitable for roll-to-roll production than previous thinner devices.

n-Type Water/Alcohol-Soluble Naphthalene Diimide-Based Conjugated Polymers for High-Performance Polymer Solar Cells.

With the demonstration of small-area, single-junction polymer solar cells (PSCs) with power conversion efficiencies (PCEs) over the 10% performance milestone, the manufacturing of high-performance large-area PSC modules is becoming the most critical issue for commercial applications. However, materials and processes that are optimized for fabricating small-area devices may not be applicable for the production of high-performance large-area PSC modules. One of the challenges is to develop new conductive interfacial materials that can be easily processed with a wide range of thicknesses without significantly affecting the performance of the PSCs. Toward this goal, we report two novel naphthalene diimide-based, self-doped, n-type water/alcohol-soluble conjugated polymers (WSCPs) that can be processed with a broad thickness range of 5 to 100 nm as efficient electron transporting layers (ETLs) for high-performance PSCs. Space charge limited current and electron spin resonance spectroscopy studies confirm that the presence of amine or ammonium bromide groups on the side chains of the WSCP can n-dope PC71BM at the bulk heterojunction (BHJ)/ETL interface, which improves the electron extraction properties at the cathode. In addition, both amino functional groups can induce self-doping to the WSCPs, although by different doping mechanisms, which leads to highly conductive ETLs with reduced ohmic loss for electron transport and extraction. Ultimately, PSCs based on the self-doped WSCP ETLs exhibit significantly improved device performance, yielding PCEs as high as 9.7% and 10.11% for PTB7-Th/PC71BM and PffBT4T-2OD/PC71BM systems, respectively. More importantly, with PffBT4T-2OD/PC71BM BHJ as an active layer, a prominent PCE of over 8% was achieved even when a thick ETL of 100 nm was used. To the best of our knowledge, this is the highest efficiency demonstrated for PSCs with a thick interlayer and light-harvesting layer, which are important criteria for eventually making organic photovoltaic modules based on roll-to-roll coating processes.

Microfiber-based few-layer black phosphorus saturable absorber for ultra-fast fiber laser.

Few-layer black phosphorus (BP), as the most alluring graphene analogue owing to its similar structure as graphene and thickness dependent direct band-gap, has now triggered a new wave of research on two-dimensional (2D) materials based photonics and optoelectronics. However, a major obstacle of practical applications for few-layer BPs comes from their instabilities of laser-induced optical damage. Herein, we demonstrate that, few-layer BPs, which was fabricated through the liquid exfoliation approach, can be developed as a new and practical saturable absorber (SA) by depositing few-layer BPs with microfiber. The saturable absorption property of few-layer BPs had been verified through an open-aperture z-scan measurement at the telecommunication band. The microfiber-based BP device had been found to show a saturable average power of ~4.5 mW and a modulation depth of 10.9%, which is further confirmed through a balanced twin detection measurement. By integrating this optical SA device into an erbium-doped fiber laser, it was found that it can deliver the mode-locked pulse with duration down to 940 fs with central wavelength tunable from 1532 nm to 1570 nm. The prevention of BP from oxidation through the "lateral interaction scheme" owing to this microfiber-based few-layer BP SA device might partially mitigate the optical damage problem of BP. Our results not only demonstrate that black phosphorus might be another promising SA material for ultrafast photonics, but also provide a practical solution to solve the optical damage problem of black phosphorus by assembling with waveguide structures such as microfiber.

Huge enhancement in two-photon photoluminescence of Au nanoparticle clusters revealed by single-particle spectroscopy.

Aggregated metal nanoparticles have been known to display significantly enhanced two-photon photoluminescence (TPPL) compared to nonaggregated nanoparticles, which could be utilized to develop platforms for two-photon sensing and imaging applications. Here we have conducted single-particle spectroscopic studies on gold (Au) nanoparticle clusters of different sizes to understand the enhancement mechanisms and explore the limit of maximum achievable enhancement. Our studies show that the TPPL intensity of Au nanoparticle clusters significantly increases from monomer to trimer. The averaged intensity of the Au nanosphere dimers and linear trimers is ~7.8 × 10(3) and ~7.0 × 10(4) times that of Au nanosphere monomers, respectively. A highest enhancement of 1.2 × 10(5) folds was obtained for the linear trimer. The TPPL spectra of these single Au nanosphere clusters closely resemble their corresponding scattering spectra, suggesting strong correlation between their TPPL with plasmon resonance. The scattering spectra of dimers and linear trimers displayed cos(2) dependence on the detection polarization, while their TPPL displayed cos(4) dependence on the excitation polarization, which are very similar to Au nanorods. These results suggest that two-photon excitation of dimer and linear trimer is strongly coupled to their longitudinal plasmon resonance modes. These studies help to provide insight on fundamental understanding of the enhancement mechanisms as well as development of biomedical and photonic applications.

Toward Chiral Lasing from All-Solution-Processed Flexible Perovskite-Nanocrystal-Liquid-Crystal Membranes.

Circularly polarized (CP) coherent light sources are of great potential for various advanced optical applications spanning displays/imaging to data processing/encryption and quantum communication. Here, the first demonstration of CP amplified spontaneous emission (ASE)/lasing from a free-standing and flexible membrane device is reported. The membrane device consists of perovskite nanocrystals (PNCs) and cholesteric liquid crystals (CLCs) layers sandwiched within a Fabry-Pérot (F-P) cavity architecture. The chiral liquid crystal cavity enables the generation of CP light from the device. The device is completely solution-processable and displays CP ASE with record dissymmetry factor (glum ) as high as 1.4, which is 3 orders of magnitude higher as compared with glum of CP luminescence of chiral ligand-capped colloidal PNCs. The device exhibits ultraflexibility as the ASE intensity remains unchanged after repeated 100 bending cycles and it is stable for more than 3 months with 80% of its original intensity. Furthermore, the ultraflexibility enables the generation of ASE from various objects of different geometric surfaces covered with the flexible perovskite membrane device. This work not only demonstrates the first CP ASE from a PNCs membrane with extremely high glum but also opens the door toward the fabrication of ultraflexible, extremely stable, and all solution-processable perovskite chiral laser devices.

Designable Layer Edge States in Quasi-2D Perovskites Induced by Femtosecond Pulse Laser.

The low-energy layer edge states (LESs) from quasi 2D hybrid perovskite single crystals have shown great potential because of their nontrivial photoelectrical properties. However, the underlying formation mechanism of the LESs still remains controversial. Also, the presence or creation of the LESs is of high randomness due to the lack of proper techniques to manually generate these LESs. Herein, using a single crystals platform of quasi-2D (BA)2 (MA)n-1 Pbn I3n+1 (n > 1) perovskites, the femtosecond laser ablation approach to design and write the LESs with a high spatial resolution is reported. Fundamentally, these LESs are of smaller bandgap 3D MAPbI3 nanocrystals which are formed by the laser-induced BA escaping from the lattice and thus the lattice shrinkage from quasi-2D to 3D structures. Furthermore, by covering the crystal with tape, an additional high-energy emission state corresponding to the reformation of (BA)2 PbI4 (n = 1) within the irradiation region is generated. This work presents a simple and efficient protocol to manually write LESs on single crystals and thus lays the foundation for utilizing these LESs to further enhance the performance of future photoelectronic devices.

Enhanced Bandwidth Broadening of Infrared Reflector Based on Polymer Stabilized Cholesteric Liquid Crystals with Poly(N-vinylcarbazole) Used as Alignment Layer.

Alignment layer plays a critical role on liquid crystal (LC) conformation for most LC devices. Normally, polyimide (PI) or polyvinyl alcohol (PVA), characterized by their outstanding thermal and electrical properties, have been widely applied as the alignment layer to align LC molecules. Here, we used a semi-conductive material poly(N-vinylcarbazole) (PVK) as the alignment layer to fabricate the cholesteric liquid crystal (CLC) device and the polymer-stabilized cholesteric liquid crystals (PSCLC)-based infrared (IR) reflectors. In the presence of ultraviolet (UV) irradiation, there are hole-electron pairs generated in the PVK layer, which neutralizes the impurity electrons in the LC-PVK junction, resulting in the reduction in the built-in electric field in the LC device. Therefore, the operational voltage of the CLC device switching from cholesteric texture to focal conic texture decreases from 45 V to 30 V. For the PSCLC-based IR reflectors with the PVK alignment layer, at the same applied electric field, the reflection bandwidth is enhanced from 647 to 821 nm, ranging from 685 to 1506 nm in the IR region, which makes it attractive for saving energy as a smart window.

Pitch Gradation by Ion-Dragging Effect in Polymer-Stabilized Cholesteric Liquid Crystal Reflector Device.

An IR reflector based on polymer-stabilized cholesteric liquid crystal (PSCLC) can selectively tune IR light reflection for smart window application. Broadening the reflection bandwidth to block more IR heat radiation requires the expansion of the pitch distribution in the PSCLC. Traditional attempts using ex situ direct current (DC) bias upon an already polymerized PSCLC reflector usually require a sustaining potential difference holding the pitch gradient of the reflector. Removing the DC bias will lead to a reflect bandwidth comeback. Here, we have developed an in situ DC curing strategy to realize an irreversible reflect bandwidth broadening. Briefly, a DC bias was used to drive the redistribution of impurity cations, which can be captured by the ester group of oligomers, during the photopolymerization. During the slow polymerization process, such trapped cations will drag the oligomers towards the cathode and compress the pitch length near the cathode before the oligomers form the long polymer chain. Consequently, a frozen pitch gradient by such an in-situ-electric-field-assisted dynamic ion-dragging effect leads to the formation of a pitch gradient along the electrical field direction. After removing the DC bias, the as-cured polymer is observed to have frozen such a gradient pitch feature without recoverable change. As a result, the PSCLC reflector exhibits steady bandwidth broadening of 480 nm in the IR region, which provides the potential for saving energy as a smart window.

Synthesis of Perovskite Nanocrystals and Their Photon-Emission Application in Conjunction With Liquid Crystals.

Perovskite nanocrystals have attracted worldwide attention due to their outstanding optical versatility, high photoluminescence quantum yields, and facile synthesis. In this review, we firstly revisit the synthetic methods for perovskite nanocrystals (PNCs), including hot injection, anion exchange, solvothermal reaction, etc. In the meantime, we discuss effects of the different synthetic methods on the properties of PNCs, including the crystal size, emission spectral feature, quantum yield, etc., followed by several optimizing strategies. Finally, lasing and display applications of these PNCs in combination with liquid crystal materials are discussed thoroughly. Outlooks on the challenges and opportunities of these nanocrystalline materials in terms of adjunct applications with liquid crystals have been presented at the end, which are highly promising for next-generation light emission applications.

Surface Plasmon-Enhanced Optical Formaldehyde Sensor Based on CdSe@ZnS Quantum Dots.

For the first time, a reproducible surface plasmon-enhanced optical sensor for the detection of gaseous formaldehyde was proposed, which was fabricated by depositing a mixture of CdSe@ZnS quantum dots (QDs), fumed silica (FS), and gold nanoparticles (GNs) on the surface of a silica sphere array to meet the urgent requirement of a rapid, sensitive, and highly convenient formaldehyde detection method. Because of the spectral overlap between QDs and GNs, plasmon-enhanced fluorescence was observed in the film of QDs/FS/GNs. When exposed to formaldehyde molecules, the enhanced fluorescence was quenched linearly with the increase of formaldehyde concentration in the range of 0.5-2.0 ppm. The reason is attributed to the nonradiative electron transfer from QDs to the carbonyl of formaldehyde molecules with the assistance of amino groups. Our results demonstrate that the designed sensors are capable of detecting ultralow concentration gaseous formaldehyde at room temperature with a fast response-recovery time and excellent selectivity, stability, and reproducibility. This work provides a simple and low-cost approach for optical formaldehyde sensor fabrication and shows promising applications in environmental detection.

22% Efficiency Inverted Perovskite Photovoltaic Cell Using Cation-Doped Brookite TiO2 Top Buffer.

Simultaneously achieving high efficiency and high durability in perovskite solar cells is a critical step toward the commercialization of this technology. Inverted perovskite photovoltaic (IP-PV) cells incorporating robust and low levelized-cost-of-energy (LCOE) buffer layers are supposed to be a promising solution to this target. However, insufficient inventory of materials for back-electrode buffers substantially limits the development of IP-PV. Herein, a composite consisting of 1D cation-doped TiO2 brookite nanorod (NR) embedded by 0D fullerene is investigated as a top modification buffer for IP-PV. The cathode buffer is constructed by introducing fullerene to fill the interstitial space of the TiO2 NR matrix. Meanwhile, cations of transition metal Co or Fe are doped into the TiO2 NR to further tune the electronic property. Such a top buffer exhibits multifold advantages, including improved film uniformity, enhanced electron extraction and transfer ability, better energy level matching with perovskite, and stronger moisture resistance. Correspondingly, the resultant IP-PV displays an efficiency exceeding 22% with a 22-fold prolonged working lifetime. The strategy not only provides an essential addition to the material inventory for top electron buffers by introducing the 0D:1D composite concept, but also opens a new avenue to optimize perovskite PVs with desirable properties.

Through-Space Conjugation: An Effective Strategy for Stabilizing Intramolecular Charge-Transfer States.

Intramolecular charge transfer (ICT) has significant impacts on organic optoelectronic materials, photochemistry, biotechnology, and so on. However, it is hard to stabilize the ICT state because of the rapid nonradiative charge recombination process, which often quenches light emission. In this work, we use new foldamers of the protonated pyridine-modified tetraphenylethene derivatives that possess through-space conjugation (TSC) characters as the models to study the impact of TSC on the ICT state. Steady and transient spectroscopies illustrate that the lifetime of the ICT state in the molecule with strong TSC can be much longer than those of molecules without TSC, giving rise to a higher fluorescence quantum yield. By combining the theoretical calculations, we demonstrate that the strong TSC can stabilize the ICT state and slow the charge recombination rate by more efficiently dispersing charges. This is a conceptually new design strategy for functional optoelectronic materials that require more stable ICT states.

Long-lived Photon Upconversion Phosphorescence in RbCaF3:Mn2+,Yb3+ and the Dynamic Color Separation Effect.

The development of luminescence materials with long-lived upconversion (UC) phosphorescence and long luminescence rise edge (LRE) is a great challenge to advance the technology of photonics and materials sciences. The lanthanide ions-doped UC materials normally possess limited UC lifetime and short LRE, restricting direct afterglow viewing in visual images by the naked eye. Here, we show that the RbCaF3:Mn2+,Yb3+ UC luminescence material generates a long UC lifetime of ∼62 ms peaking at 565 nm and an ultralong LRE of ∼5.2 ms. Density functional theory calculations provide a theoretical understanding of the Mn2+-Yb3+ aggregation in the high-symmetry RbCaF3 host lattice that enables the formation of the long-lived UC emission center, superexchange coupled Yb3+-Mn2+ pair. Through screen printing ink containing RbCaF3:Mn2+,Yb3+, the visualized multiple anti-counterfeiting application and information encryption prototype with high-throughput rate of authentication and decryption are demonstrated by the dynamic color separation effect.

Highly stable enhanced near-infrared amplified spontaneous emission in solution-processed perovskite films by employing polymer and gold nanorods.

Solution-processed organo-lead halide perovskites have emerged as promising optical gain media for tunable coherent light sources. The lasing performance is generally determined by the as-synthesized crystal quality. Noble metal nanostructures have been widely utilized to enhance optical responses due to their unique property of localized surface plasmon resonance. Herein, we report a simple method to enhance the near-infrared amplified spontaneous emission (ASE) performance of MAPbI3 polycrystalline films by solution-processing a PMMA spacer layer and an Au NR-doped PMMA top layer on perovskite thin films. As a result, the ASE threshold of the triple-layer perovskite film was significantly reduced by around 36% and the ASE intensity increased by 13.9-fold, compared to the pristine film. The underlying mechanism was attributed to the combined effects of surface passivation by PMMA and plasmon resonance enhancement of Au NRs. The passivation effect results in suppressing the nonradiative recombination and prolonging excited state decay, which have been investigated by transient absorption and pump-probe measurements. The plasmon effect is systematically studied through distance-dependent and spectra-dependent plasmon enhanced emission. The perovskite films with PMMA and Au NR coating showed great stability for 180 min under intense pulse laser continuous irradiation. The improved ASE performance still remained after leaving the film under the atmosphere for more than one month. We have successfully demonstrated a highly stable and sustained ASE output from MAPbI3 films under pulse laser excitation. This study provides a general approach for exploring plasmonic nanostructures in combination with polymers in the development and application of low-cost solution-processed semiconductor lasers.

Therapeutic Nanosystem Consisting of Singlet-Oxygen-Responsive Prodrug and Photosensitizer Excited by Two-Photon Light.

Using light as the sole stimulus and employing the generated singlet oxygen as a therapeutic agent and the trigger to activate chemo-drug release could serve as an elegant way to bring into full play the advantageous features of light and enhance therapeutic efficacy through a combination of chemotherapy and photodynamic therapy. Herein a liposomal drug system has been developed by embedding a fluorescent photosensitizer and a prodrug into phospholipid vesicles. Upon one- or two-photon light irradiation, the photosensitizer generates singlet oxygen, which removes the protecting group of the prodrug and subsequently causes the release of the active drug chlorambucil. With the combined action of O21 and chlorambucil, highly controllable cytotoxicity toward cancer cells was achieved. In addition, the fluorescent photosensitizer gives out fluorescent signal acting as the drug monitoring agent. This strategy may provide an efficient approach for cancer treatment and some useful insights for designing light-stimulated on-demand therapeutic systems.

Magic-Angle Stacking and Strong Intermolecular π-π Interaction in a Perylene Bisimide Crystal: An Approach for Efficient Near-Infrared (NIR) Emission and High Electron Mobility.

A single crystal of N,N'-bis(4-methoxybenzyl)perylene-3,4,9,10-bis(dicarboximide) (mb-PBI) that possesses novel magic-angle stacking (M-type stacking) and strong intermolecular π-π interaction is achieved by physical vapor transport (PVT), which shows attractive optoelectronic functions such as efficient NIR emission and high electron mobility. In this special M-type staking, the strong Frenkel/CT mixing state promotes fluorescence and, importantly, the elimination of long-distance Förster resonance energy transfer enables the minimization of the possible fluorescence quenching, which ensure the highly efficient emission. Moreover, the strong π-π interaction elongates the "supramolecular conjugation" to reduce the energy gap and also benefits the electron mobility of the crystal. The experimental results clearly indicate that M-type staking is a novel approach to optimize the optoelectronic functions of organic semiconducting materials.

Alkali Salt-Doped Highly Transparent and Thickness-Insensitive Electron-Transport Layer for High-Performance Polymer Solar Cell.

Solution-processable highly transparent and thickness-insensitive hybrid electron-transport layer (ETL) with enhanced electron-extraction and electron-transport properties for high-performance polymer solar cell was reported. With the incorporation of Cs2CO3 into the poly[(9,9-bis(6'-((N,N-diethyl)-N-ethylammonium)-hexyl)-2,7-fluorene)-alt-1,4-diphenylsulfide]dibromide (PF6NPSBr) ETL, the power conversion efficiency (PCE) of resulted polymer solar cells (PSCs) was significantly enhanced due to the favorable interfacial contact, energy-level alignment, and thus facile electron transport in the PSC device. These organic-inorganic hybrid ETLs also exhibited high transparency and high electron mobility. All of these combined properties ensured us to design novel thickness-insensitive ETLs that avoid the parasitic absorption of ETL itself simultaneously. With the conventional device structure with poly{4,8-bis[5-(2-ethylhexyl)thiophen-2-yl]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl-alt-3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophene-4,6-diyl} (PTB7-Th) as a donor and [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) as an acceptor, devices with hybrid ETLs exhibited PCE of 8.30-9.45% within a wide range of ETL thickness. A notable PCE of 10.78% was achieved with the thick active layer poly(2,5-thiophene-alt-5,5'-(5,10-bis(4-(2-octyldodecyl)thiophen-2-yl)naphtho[1,2-c:5,6-c']bis([1,2,5]thiadiazole)) (PTNT812):PC71BM. These findings indicated that doping alkali salt into the organic interfacial materials can be a promising strategy to design highly efficient and thickness-insensitive ETL, which may be suitable for large-area PSC modules device fabrication with roll-to-roll printing technique.