Light Stability Research Articles

Anion regulation for surface passivation enables ultrahigh-stability perovskite nanocrystals.

All-inorganic perovskite CsPbBr3 nanocrystals (NCs) display high photoluminescence quantum yield and narrow emission, which show great potential application in optoelectronic devices. However, the poor environment stability of NCs will hinder their practical application. Herein, a series of ionic liquids with different anions (BF4-, Br-, and NO3-) were used as a sole capping ligand to synthesize NCs. Among the three samples, 1-hexadecyl-3-methylimidazolium tetrafluoroborate ([C16MIM]BF4) capped NCs have the highest stability in light, thermal, and water, possibly attributing to the in situ passivation of bromine vacancy via pseudohalogen BF4- and tight binding of ionic liquid ligands and lead atoms. In addition, green-emission [C16MIM]BF4 NCs were used to assemble a white light-emitting diode device, and it possessed a wide National Television System Committee color gamut of 124.5% and a stable emission peak at high driving currents of 380 mA. This work paves the way for resurfacing perovskite NCs with ultrahigh stability, thereby driving the perovskite NC display industry closer to real-world application.

Colloidal Synthesis of Blue-Emitting Cs3TmCl6 Nanocrystals via Localized Excitonic Recombination for Down-Conversion White Light-Emitting Diodes.

Lead-halide perovskite nanocrystals (NCs) have gained significant attention for their promising applications in lighting and display technologies. However, blue-emitting NCs have struggled to match the high efficiency of their red and green counterparts. Moreover, many reported blue-emitting perovskite NCs contain heavy metal lead (Pb), which poses risks to human health and the environment. In this study, we synthesized rare-earth-based Cs3TmCl6 NCs via the hot injection method, which exhibit a broadband blue emission at 440 nm. Combined experimental and theoretical studies indicate that the broadband emission in Cs3TmCl6 arises from self-trapped excitons due to the excited-state structural distortion of the [TmCl6]3- cluster. Furthermore, the ultrafast dynamics of charge carriers were analyzed using time-resolved photoluminescence and transient absorption measurements. Encouraged by the remarkable thermal, light, and water stabilities of Cs3TmCl6 NCs, as evidenced by experimental and theoretical results, a white light-emitting diode was further designed and fabricated using the Cs3TmCl6 NCs as the color converter. The device exhibits outstanding performance, achieving a long half-lifetime of 336 h and a large color-rendering index of 87.0. Combining eco-friendly features and a facile synthesis method, the rare-earth-based Cs3TmCl6 NCs mark a significant breakthrough as a reliable blue emitter, showcasing their future potential in lighting and display applications.

Separation and purification of antimicrobial substances from Paenibacillus polymyxa KH-19 and analysis of its physicochemical characterization.

Soft rot is one of the top ten most dangerous plant pathogens in agricultural production, storage, and transport, and the use of microorganisms and their metabolites to control soft rot is a current research hotspot. In this study, we identified the antimicrobial substance in the metabolite of Paenibacillus polymyxa KH-19, and determined that the antimicrobial substance of this strain was an active protein. The protein was completely precipitated at 40-60% ammonium sulphate saturation and showed good inhibitory effects against seven pathogenic bacteria including Pectobacterium carotovorum BC2 and seven pathogenic fungi including Pyricularia oryzae. The MIC of the protein was 51.563µg/mL, temperature acid-base UV and light stability insensitive to protease, with high-temperature resistance. The antimicrobial protein was isolated and purified by DEAE-anion exchange column and Sephadex G-75 gel filtration chromatography, and the LC-MS/MS assay identified the protein as lysophosphatidyl esterase with a molecular weight of 25.255kDa. The purified antimicrobial protein increased the inhibitory effect against P. carotovorum BC2, with the diameter of the circle of inhibition being 26.50 ± 0.915mm. Bioinformatics analysis showed that the protein has the molecular formula of C1117H1732N316O338S5, encodes 224 amino acids, has an aliphatic index of 88.39, and belongs to the category of hydrophilic unstable proteins. The present study is the first report of an active protein with extreme thermoplastic and resistance to P. carotovorum BC2, which provides a reference for the preparation and application of the antimicrobial substances of P. polymyxa KH-19, as well as a theoretical basis for the study of the function of lysophosphodiesterase protein and its use as a microbial preparation.

Dopant-Free Hole Transport Material Based on Non-Covalent Interaction for Efficient Perovskite Solar Cells.

Hole transport materials (HTMs) have a critical impact on the performance of perovskite solar cells (PSCs). Especially, the dopant-free HTMs could avoid the usage of hygroscopic dopants and reduce costs, which are important for device stability. Most of the current organic dopant-free HTMs are polycyclic aromatic hydrocarbons-based planar conjugated structures. Yet, the synthesis of conjugated fused heterocycles is often complicated. In this work, intramolecular non-covalent interaction is introduced to construct two organic HTMs (DCT and DTC), which can be facilely obtained through simple reactions. Compared to DTC with hexyl chain on the central benzene ring, DCT with hexyloxy chains shows better planarity in the core structure, as a result of the intramolecular non-covalent interactions between oxygen on hexyloxy and sulfur atom on the adjacent thiophene, as reflected from its single crystal structure. Moreover, DCT in a pristine state shows a decent hole mobility comparable to the doped Spiro-OMeTAD. Ultimately, conventional devices using dopant-free DCT as HTM show a high efficiency of 22.50%, with excellent long-term stability, and light and thermal stability. The results show that the noncovalent interaction is a useful and simple design strategy for dopant-free HTMs, that can effectively improve the efficiency and stability of PSCs.

Multidentate Polymer-Stabilized Buried Interface for Efficient Planar Perovskite Solar Cells.

Buried interface engineering is crucial to improve the performance and stability of perovskite solar cells (PSCs). Although coordination materials have been widely used for buried interface modification, they are generally engineered on one surface of the interface through monodentate or bidentate molecules. Here, we propose that a multidentate polymer, sodium alginate (SA), acts with both surfaces via numerous C═O groups to reinforce buried interfaces. SA effectively reduces buried interface defects, adjusts the energy level alignment, and refines carrier dynamics. Notably, it also induces the growth of a perovskite film that is less tensile stressed and free of voids. Consequently, the champion device efficiency after SA treatment increased from 23.05% to 24.98%, along with significant improvements in both light and thermal stability. This work offers insights into efficiency and stability improvement from the perspective of multidentate polymer anchoring.

Multidimensional Exploration of Wood Extractives: A Review of Compositional Analysis, Decay Resistance, Light Stability, and Staining Applications

Extractives, which naturally evolve as fundamental defense mechanisms in wood against environmental stresses, hold an essential place in the field of wood conservation science. Despite their low content in woody substrates, extractives are chemically complex and can be extracted accurately by solvents with different polarities, covering key components such as aliphatic, terpenoid, and phenolic compounds. The application of solvent extraction allows for the effective recovery of these extracts from forestry waste, thereby creating new opportunities for their reuse in wood modification and enhancing the economic value and potential applications of forestry waste. In the wood industry, extractives not only act as efficient preservatives and photo-stabilizers, significantly improving the decay resistance and photodegradation resistance of wood, but also serve as ideal dyes for fast-growing wood due to their abundant natural colors, which lend the product a distinct aesthetic appeal. The aim of this paper is to provide a comprehensive review of the origin and distribution characteristics of wood extractives and to examine the impact of solvent selection on extraction efficiency. At the same time, the mechanism of extractives in enhancing wood decay resistance and slowing down photodegradation is deeply analyzed. In addition, specific examples are presented to illustrate their wide utilization in the wood industry. This is intended to provide references for research and practice in related fields.

Bi2O2.33/Bi4O5I2-heterojunction photocatalysts for adsorption and visible light-driven degradation of pharmaceutical pollutants

This study introduces the innovative Bi4O5I2/Bi2O2.33 heterojunction for diclofenac (DF) degradation. Pharmaceutical pollutants, especially DF, pose significant threats to water sources, necessitating efficient treatment methods. Bi2O2.33, renowned for its unique ferromagnetic properties, emerges as a promising photocatalyst for pollutant degradation. Bi4O5I2, known for strong visible light absorption and stability, holds potential for environmental applications. Interestingly, the inclusion of titanium dioxide (TiO2) in the composite catalysts significantly influences their observed ferromagnetic properties, as revealed by Electron Paramagnetic Resonance (EPR) spectroscopy, by influencing the interactions within the Bi4O5I2/Bi2O2.33 heterojunction and influencing its structure, morphology, and spin behavior. This interaction results in enhanced EPR and Ferromagnetic Resonance (FMR) signals, indicating intriguing spin interactions, polarization effects, charge transfers, surface dynamics, and stabilized magnetic domains. While the enhanced ferromagnetism holds promise for efficient charge separation and potential applications in environmental remediation, the expected boost in visible light-driven activity was not fully realized. This limitation is attributed to TiO2 inherent inability to directly absorb visible light, hindering its utilization for enhanced photocatalysis within the heterojunction. Nevertheless, these findings elucidate the multifaceted role of TiO2 in modulating the magnetic properties of these catalysts, offering valuable insights for future advancements in the design of advanced photocatalysts for effective environmental remediation.

Physico‐chemical characterisation and light stability of dyes and pigments found in cultural heritage objects: Insights from microfading testing for assessing light fastness

AbstractUnderstanding the chemistry of dyes and pigments found in cultural heritage objects and their permanence is central for their preservation. Heritage science research has generally focused on either identification of materials present on actual objects or accelerated and natural ageing of mock‐up samples prepared using historically accurate methods to simulate the materiality of cultural heritage objects. A more recent strategy is the integration of these two research areas, which provides a holistic approach to assess both the chemical composition and stability of materials. Over the last 30 years, microfading testing (MFT) has notably contributed to understanding materials' responsiveness to light, minimising damage to objects from museum lighting and revealing insights into molecular structures of dyes and pigments, when employed in conjunction with other techniques. By combining MFT with diverse analytical methods, including imaging, spectroscopy, microscopy and chromatography, a more comprehensive approach is achieved. This joined‐up strategy contributes to improved decision‐making processes in the conservation and preservation of cultural heritage objects.

Evaluation of the Thermal and Light Stability of β-Carotene Extracted from Mauritia flexuosa Using Ionic Liquid

The growing concern over the adverse effects of synthetic dyes has generated interest in the use of natural pigments by the food industry. β-carotene, a carotenoid found in various plant sources, is recognized for its antioxidant properties and provitamin A activity. The fruit of the buriti palm (Mauritia flexuosa), which is particularly rich in β-carotene, serves as a significant natural source of this pigment. This study aimed to extract β-carotene from buriti fruit using ionic liquids as an alternative to conventional organic solvents like acetone. β-carotene content was determined by HPLC and showed that extraction with [C4mim] [BF4] not only improved β-carotene extraction efficiency compared to acetone (19.21 and 13.13 mg/100 g, respectively) but also provided greater pigment stability during light, thermal and color stability tests. Moreover, ionic liquids are aligned with the principles of green chemistry and offer a sustainable and safe alternative for the food industry. Its favorable characteristics not only reduce environmental impacts associated with conventional solvents, but also ensure an increase in the shelf life of natural dyes, thus promoting the safety and quality of food products.

Defect passivation with spectral shift for improved efficiency and stability of quasi-2D blue perovskite light emitting diodes

Metal halide perovskites are emerging as promising materials for next-generation light-emitting diodes (LEDs), owing to their cost-effectiveness, facile manufacturing, and excellent optoelectronic properties including a narrow emission-line full width at half maximum, high photoluminescence quantum yield, and spectral stability. However, blue-emission perovskite LEDs (PeLEDs) exhibit perovskite phase segregation and halogen ion migration during operation, attributed to crystal defects, halogen vacancies, and phase instability of mixed-halide perovskites. These defects compromise the spectral stability of blue-emitting PeLEDs, resulting in an undesirable color shift toward longer wavelengths. In this study, we introduce a dynamic treatment with phenylphosphonic dichloride (PPOCl2) to address these challenges and achieve blue-emitting PeLEDs. The chloride in PPOCl2 penetrates the quasi-2D sky-blue perovskite, reducing halide defects. Meanwhile, the phosphonic group forms covalent bonds with undercoordinated Pb on the perovskites, effectively passivating defects. PPOCl2-treated perovskite exhibits a spectral blue shift toward a deep-blue wavelength (≤467 nm), enhancing electroluminescence performance. The quasi-2D PPOCl2-treated PeLEDs achieve a maximum external quantum efficiency of 2.31 % with an emission peak at 488 nm. Dynamic treatment with PPOCl2 shows the potential to improve the performance and stability of blue emission perovskite-based LEDs, providing a spectral shift mechanism to achieve deep-blue emission in PeLEDs.

Wet-chemical preparation and physicochemical characterization of nanostructured Zn-Bi2O3/CeO2 composite: A visible-light-driven catalyst for the annihilation of pharmaceutical pollutant

A modified co-precipitation technique assisted with cetyltrimethylammonium bromide (CTAB) surfactant was used to synthesize a nanostructured and zinc-doped mixed metal oxide (Zn-Bi2O3/CeO2) composite. Using X-ray diffraction (XRD), the synthesized nanocomposite was studied in terms of its crystal structure, grain size, percentage crystallinity, and percentage porosity. Energy dispersive X-ray elemental analysis (EDX) was used to ascertain the chemical composition, SEM to confirm the creation of nanostructure material, and Fourier transform infrared spectroscopy (FTIR) to extract the existing functional groups. Investigation of light harvesting properties (UV/Vis) and thermogravimetric analysis (TGA) reveals that the doped composite exhibits a band gap driven by visible light and remarkable thermal stability at high temperatures. The pH value at which a material's net charge is zero, known as pHpzc, is 7.93 for the doped mixed metal oxide composite. The Zn-Bi2O3/CeO2 nanocomposite effectively eliminates 98.4 percent of the quinolone antibiotic (levofloxacin) via a mechanism that integrates sorption and photocatalytic degradation induced by visible light. To determine the optimal circumstances for the efficient operation of a photocatalyst, we experimented with different time intervals, beginning drug concentrations, catalyst dosages, operating temperatures, and pH levels. Reusability tests and post-activity FTIR analysis were used to investigate the long-term usability and structural stability of the newly developed doped composite photocatalyst. The scavenging tests revealed a potential photocatalytic mechanism to explain the annihilation of the levofloxacin drug on the synthesized catalyst. The physicochemical and photocatalytic evaluations recommend that the assembled integrated material has excellent potential for mineralizing medicinal products in pharmaceutical wastes.

Migration of Chemical Compounds from Packaging Materials into Packaged Foods: Interaction, Mechanism, Assessment, and Regulations.

The migration of chemical compounds from packaging polymers to food presents a multifaceted challenge with implications for food safety and public health. This review explores the interaction between packaging materials and food products, focusing on permeation, migration, and sorption processes. The different migration mechanisms of contact migration, gas phase migration, penetration migration, set-off migration, and condensation/distillation migration have been discussed comprehensively. The major migrating compounds are plasticizers, nanoparticles, antioxidants, light stabilizers, thermal stabilizers, monomers, oligomers, printing inks, and adhesives, posing potential health risks due to their association with endocrine disruption and carcinogenic effects. Advanced analytical methods help in the monitoring of migrated compounds, facilitating compliance with regulatory standards. Regulatory agencies enforce guidelines to limit migration, prompting the development of barrier coatings and safer packaging alternatives. Furthermore, there is a need to decipher the migration mechanism for mitigating it along with advancements in analytical techniques for monitoring the migration of compounds.

A Study of the Optical Properties and Stability of Cs0.33WO3 with Different Particle Sizes for Energy-Efficient Window Films in Building Glazing

Cs0.33WO3 (CWO) is a widely used inorganic material in window films and glass coatings, known for its excellent near-infrared radiation (NIR) blocking property and high visible light transmittance (Tvis). However, the stability of NIR blocking and the optical properties of CWO in the process of application is an urgent and important problem, because significant changes in optical results can impact the related products, such as window films, glass coatings, and so on. In this paper, the particle sizes and optical properties of CWO are tested to study the light stability and their relative relations. The results indicate that CWO particle sizes between 130 nm and 100 nm (D90, the point where 90% of the particles have a diameter smaller than the specified value) exhibit high stability in terms of NIR blocking and visible light transmittance (Tvis). CWO particles with D90 < 100 nm experience a greater reduction in NIR blocking, though this ability significantly recovers upon exposure to sunlight, making these coatings particularly suitable for use in tropical and subtropical climates.

Improvement of the Stability of Quantum-Dot Light Emitting Diodes Using Inorganic HfOx Hole Transport Layer.

One of the major challenges in QLED research is improving the stability of the devices. In this study, we fabricated all inorganic quantum-dot light emitting diodes (QLEDs) using hafnium oxide (HfOx) as the hole transport layer (HTL), a material commonly used for insulator. Oxygen vacancies in HfOx create defect states below the Fermi level, providing a pathway for hole injection. The concentration of these oxygen vacancies can be controlled by the annealing temperature. We optimized the all-inorganic QLEDs with HfOx as the HTL by changing the annealing temperature. The optimized QLEDs with HfOx as the HTL showed a maximum luminance and current efficiency of 66,258 cd/m2 and 9.7 cd/A, respectively. The fabricated all-inorganic QLEDs exhibited remarkable stability, particularly when compared to devices using organic materials for the HTL. Under extended storage in ambient conditions, the all-inorganic device demonstrated a significantly enhanced operating lifetime (T50) of 5.5 h, which is 11 times longer than that of QLEDs using an organic HTL. These results indicate that the all-inorganic QLEDs structure, with ITO/MoO3/HfOx/QDs/ZnMgO/Al, exhibits superior stability compared to organic-inorganic hybrid QLEDs.

Tunable electronic and optical properties of a type-II GaP/SiH van der Waals heterostructure as photocatalyst: A first-principles study

In this study, a novel GaP/SiH heterostructure was successfully predicted and constructed. Subsequently, an in-depth and systematic investigation was conducted to explore its structural, electronic, transport and optical properties. The calculated structural performance results revealed that the GaP/SiH heterostructure was a typical type-II van der Waals heterostructure, exhibiting excellent energy stability, mechanical stability and thermodynamic stability. In particular, the formation of the GaP/SiH heterostructure significantly reduced the bandgap of the materials to 2.24eV, and the type-II energy band arrangement effectively suppressed the recombination of photogenerated carriers. Furthermore, the biaxial and vertical strains could finely modulate the electronic structure of the GaP/SiH heterojunction. The electron mobility of the GaP/SiH heterostructure was measured to be 1573.91 cm2 V⁻1 s⁻1, indicating its superior charge carrier transport capabilities. Meanwhile, the GaP/SiH heterostructure also exhibited excellent optical absorption performance in the visible and UV region up to 2.34 × 106 cm−1. Thus, the GaP/SiH heterostructure will be a strong candidate for photocatalytic applications due to its excellent light absorption properties, electrical properties, and stability.

Comparison of free vs. liposomal naringenin in white adipose tissue browning in C57BL/6j mice

Naringenin may play a role in browning by increasing thermogenic gene expression. In this study, we encapsulated naringenin using a liposomal formulation and examined the effects of both free and liposomal naringenin on white adipose tissue browning in C57BL6/J mice. In the first phase of the study, naringenin was encapsulated by the liposome method, which is biocompatible and biodegradable. The physical and chemical properties of liposomal naringenin were tested. In the second phase, a total of 48 six-week-old mice were divided into two main groups: prevention and recovery. Each main group was divided into four subgroups: nano-naringenin, void, free-naringenin, and control. The prevention group received a high-fat diet for 10 weeks along with weekly intravenous injections of 20 µM naringenin. On the other hand, the recovery group was first subjected to a high-fat diet for 10 weeks, followed by an additional 10 weeks of the same diet, along with weekly intravenous injections of 20 µM naringenin. Body weight was measured once per week, and brown adipose tissue, inguinal white adipose tissue, and serum samples were collected from each mouse. The mean particle size, polydispersity index and zeta potential values of liposomal naringenin were ∼207 nm, 0.35, and −27 mV, respectively. The encapsulation and loading efficiencies of liposomal naringenin were 94.6 and 19.2%, respectively. Liposomal naringenin exhibited sustained-release behavior, while free naringenin showed a burst-release profile. Liposomal naringenin showed the best physical stability in light and at 4 °C, while free naringenin was more chemically stable in light and at 4 and 22 °C. Free and liposomal naringenin did not significantly reduce weight gain. In the prevention group, liposomal naringenin increased PRDM16 gene expression in inguinal white adipose tissue 4.29 times more than free naringenin (p = 0.010). However, neither formulation significantly altered the expression levels of other browning or adipogenesis markers in the tissues. The results suggest that free naringenin can be efficiently encapsulated in biocompatible and biodegradable nanoparticles. Further research is needed to better understand the physiological effects of liposomal naringenin.

Egg yolk lecithin delivery system constructed by ovalbumin-fucoidan (OVA-FUC) binary complex: Storage stability, release yield and in vitro digestion characteristics

Unfavorable environmental factors limit the utilization of egg yolk lecithin in functional foods. Therefore, it is necessary to enhance its stability and effectiveness to cater to the diverse food needs of individuals. This study aimed to explore the feasibility of protecting and delivering egg yolk lecithin through O/W emulsions, which were stabilized using ovalbumin-fucoidan (OVA-FUC) binary complexes as emulsifiers. This study investigated the protective effect of OVA-FUC emulsion on egg yolk lecithin and its impact on delivery by examining the storage stability, in vitro release yield, and stability during in vitro digestion of egg yolk lecithin in the emulsion. The results indicate that egg yolk lecithin, when encapsulated in the OVA-FUC emulsion, exhibits a relatively stable behavior during simulated in vitro digestion. Additionally, encapsulation enhanced both the delivery efficiency and drug release of egg yolk lecithin. Furthermore, the thermal and light stability of egg yolk lecithin embedded in OVA-FUC emulsion was improved, significantly improving its storage performance. The emulsion, prepared using the OVA-FUC binary complex, effectively safeguarded and enhanced the delivery efficiency of bioactive substances as an encapsulating material, thus exhibiting immense potential for application in the active protection and delivery of such substances.

Fabrication of Active Z-Scheme Sr2MgSi2O7: Eu2+, Dy3+/COF Photocatalyst for Round-the-Clock Efficient Removal of Total Cr.

Photoreduction is recognized as a desirable treatment method for hexavalent chromium (Cr(VI)). However, it has been limited by the intermittent solar flux and limited light absorption. In this work, a novel Z-scheme photocatalyst combining a covalent organic framework (COF) with Eu2+, Dy3+ co-doped Sr2MgSi2O7 (Sr2MgSi2O7:Eu2+, Dy3+) is synthesized, which shows the high spectral conversion efficiency and works efficiently in both light irradiation and dark for Cr(VI) reduction. Sr2MgSi2O7:Eu2+, Dy3+ serves as both an electron transfer station and active sites for COF molecule activation, thus resulting in 100% photoreduction of Cr(VI) (50 mL, 10 mg/L) with high light stability and over 1 h dark activity. Moreover, the XPS and FT-IR analyses reveal the existence of functional groups (Si-OH on Sr2MgSi2O7:Eu2+, Dy3+, and -NH- on COFTP-TTA) on the composited catalyst as active sites to adsorb the resultant Cr(III) species, demonstrating a synergistic effect for total Cr removal. This work provides an alternative method for the design of a round-the-clock photocatalyst for Cr(VI) reduction, allowing a versatile solid surface activation for establishing a more energy efficient and robust photocatalysis process for Cr pollution cleaning.

Enhancing photovoltaic performance and stability of inverted perovskite solar cells via multifunctional molecular additive

The film quality of perovskite absorber plays a fundamental role in determining the efficiency and stability of perovskite solar cells (PSCs), of which high crystallinity and low defect density are consistently persuaded. Here, a strategy using multifunctional additive of N,N′-Diallyl-L-tartardiamide (NDT) to produce high-quality perovskite film is proposed. The rich coordination and hydrogen bonding between NDT and perovskite effectively passivate trap states, improve film crystallinity, stabilize perovskite crystal structure and confine ions migration, resulting in enhancement of charge transport and suppression of nonradiative recombination. Consequently, compared with the control device (19.07 %), the NDT-modified devices achieve a champion efficiency of 21.71 % with negligible hysteresis as well as excellent air and light stability. This work presents a facile and effective approach via multifunctional molecular additive to achieve high-performance inverted (p-i-n) PSCs.

Dimeric Carbazole Core Based Dopant‐Free Hole Transport Material for n‐i‐p Planar Perovskite Solar Cell

AbstractA profitable approach for improving the stability of n‐i‐p planar perovskite solar cell (PSC) is developing dopant‐free hole transport materials (HTMs) with desirable intrinsic charge transport properties. In this work, by adopting a metal‐free catalytic intramolecular C─C coupling reaction, a carbazole dimer‐based fused‐ring is synthesized, and further developed a small molecular dopant‐free HTM abbreviated as NCz‐DM with appropriate energy level, excellent hole transport and film formation properties. Applied in n‐i‐p planar PSC, an impressive power conversion efficiency (PCE) of 24.0% is achieved, together with enhanced humidity, thermal and light stability, which is among the high level of ever‐reported results for PSCs utilizing small molecular dopant‐free HTM.