N2 Atmosphere Research Articles

Ag Surface Outflow Kinetics in Ag/AlN Nanomultilayers

The heat‐induced microstructure evolution of nanomultilayers (NMLs) with metallic components is widely studied due to its critical importance in ensuring the reliable application of these nanomaterials. The thermal degradation of NMLs is controlled by mass transport of one of the NML components from the NML volume to its surface. The outflow occurs at temperatures well below the melting point of metal, offering new opportunities for the engineering of innovative NML‐based brazing fillers. A combined experimental‐modeling approach for the quantitative analysis of silver (Ag) outflow kinetics in Ag/AlN NMLs is presented. The method is based on in situ monitoring of the X‐ray diffraction intensity evolution of Ag acquired from the near‐surface region of NML (grazing incidence geometry) upon annealing in the temperature range of 230–425 °C (atmosphere of N2). The experimental data are compared to model predictions of Ag diffusion. It is assumed that Ag diffusion is driven by the relaxation of residual stresses in Ag nanolayers. Due to the multilayer geometry, the surface outflow kinetics are mainly defined by the kinetics of Ag diffusion along Ag/AlN interphase boundaries. The parameters defining the Ag surface outflow kinetics, i.e., diffusion coefficients and activation energy for diffusion, are derived.

Colossal permittivity and low dielectric loss of Ta5+ and Al3+ co-doped strontium titanate ceramics sintered in N2 atmosphere

In this work, the ceramics of Sr(Ta1/2Al1/2)xTi1-xO3 (x = 0 %, 0.5 %, 1 %, 2 %, 3 %, 4 %, and 5 %) were produced through the solid-state reaction and sintered under N2 atmosphere. The frequency coefficient of permittivity and dielectric loss for the sample with x = 4 % is blow |24%| and |26%|, respectively, within the frequency of 1 kHz to 1 MHz. This demonstrates favorable frequency stability in the dielectric properties. The sample with x = 4 % exhibits remarkable permittivity (εr ∼ 125,000 @ 1 kHz, εr ∼ 95,000 @ 1 MHz) and low dielectric loss (tanδ ∼ 0.054 @ 1 kHz, tanδ ∼ 0.044 @ 1 MHz) were achieved at room temperature. Through the analysis of HAADF-STEM, XPS, it is concluded that and dielectric relaxation, the colossal permittivity effect is primarily attributed to defect clusters associated with oxygen vacancies such as Ti3+−VO••− Ti3+. The clusters of defect dipoles exert a pinning effect on freedom electrons, constraining their long-range transition and improving the dielectric properties. This study lays the foundation for advancing the electronic components, making a significant milestone in technological advancements.

N-doped graphene quantum dot-decorated MOF-derived yolk-shell ZnO/NiO hybrids to boost lithium and sodium ion battery performance

Surface engineering at the nanoscale to obtain robust interface between metal oxides and quantum dots is essential for improving the performance and stability of battery materials. Herein, we designed and prepared novel N-doped graphene quantum dot-modified ZnO/NiO anode materials with a well-defined yolk-shell structure for lithium and sodium-ion batteries. NG QDs were assembled on the ZnO/NiO microspheres using three different coupling strategies: solvothermal, direct adsorption and annealing under N2 atmosphere. The presence of NG QDs deposited on the ZnO/NiO hybrids promoted enhanced electrical conductivity, lower charge-transfer resistance and provides more active sites. As a result, NG-ZnO/NiO_s anode obtained by solvothermal route exhibited high reversible delithiation capacity of 912 mAh/g at 18.6 mA g−1 and excellent cycling performance with the average delithiation capacity of 525 mAh/g at 372 mA g−1 over 400 cycles. Moreover, application of the NG-ZnO/NiO_s elecrode in Na-ion batteries revealed decent electrochemical behavior with capacity values reaching 235 mAh/g at 18.6 mA g−1. Importantly, surface properties, morphology and electrochemical behavior of obtained NG-ZnO/NiO hybrids were dependent on the combination route of NG QDs with ZnO/NiO microspheres indicating that quality of heterojunction between composite components has significant impact on the electrode performance.

A durable coating constructed by metal-organic framework and polyphosphazene for flame retardant cotton fabric with enhanced mechanical properties

The extremely flammable cellulose macromolecules in cotton fabrics seriously affect their application in the field of flame retardancy. In this paper, the surface of cotton fabric was modified with citric acid, and then metal-organic framework (UiO-66), cationic starch (St) and polyphosphonitrile (PZS) microspheres containing the transition metal element Zr were sequentially deposited to prepare an efficient and economical cotton fabric. St-PZS double-impregnated cotton fabrics have better thermal stability, flame retardancy and mechanical properties. And the coating does not affect the whiteness and stiffness of the cotton fabric. The results of thermogravimetric analysis showed that cotton/UiO-66/2St-PZS had a higher residual char rate (25.34%) under N2 atmosphere, which was 200.1% higher than that of control cotton (8.28%). In addition, cotton/UiO-66/2St-PZS had a 46.6% reduction in peak heat release, a 31.7% reduction in total heat release, and a 35.3% reduction in the peak of CO2 production compared to control cotton. It is worth noting that the average gross calorific value is 63.3% lower than that of the control cotton, indicating that flame retardant cotton fabrics can effectively inhibit the production of flammable gases. In addition, the tensile strength and elongation at break of cotton/UiO-66/2St-PZS are 458.79 N and 11.04%, respectively. After 20 laundering cycles, the mechanical properties remained almost unchanged.

Improving the proton conductivity of HKUST‐1 by hole expansion and ionic liquid introduction

As a new type of proton conductor, metal–organic frameworks (MOFs) have attracted much attention because of their superior properties over conventional materials, such as the modifiability of framework, reversibility of coordination bond, high specific surface area, and porosity. It is predicted that the proton conductivities of MOFs can be improved by hole expansion and ionic liquid introduction. In this work, HKUST‐1 and LP‐HKUST‐1 were prepared, which were filled with different proportions of N‐methylimidazole triflate (MIM‐CF3SO3) to prepare composite materials MIM‐CF3SO3@HKUST‐1‐100% and MIM‐CF3SO3@LP‐HKUST‐1‐x (x = 25%, 50%, 75% and 100%). A total of seven kinds of materials were synthesized. The proton conductivities of all the materials at 75% RH were tested from 303 to 353 K. In this environment, MIM‐CF3SO3@LP‐HKUST‐1‐100% shows excellent proton conductivity (σ = 0.341 S·cm−1 at 353 K, 75% relatively humidity [RH]), being 7060 times that of HKUST‐1, and reaches the peak value of MOF family in recent years. Then, the conductivities of parts of the materials were tested in extreme environments, such as in high‐humidity environment (303–353 K, 100% RH), high‐temperature environment (373–423 K, N2 atmosphere), and low‐temperature environment (253–283 K, 75% RH). The results show that under all conditions above, the proton conductivity of MIM‐CF3SO3@LP‐HKUST‐1‐100% is the best, up to 0.341 S·cm−1 at 353 K and 75% RH, 0.179 S·cm−1 at 353 K and 100% RH, 1.31 × 10−3 S·cm−1 at 283 K and 75% RH, and 2.31 × 10−4 S·cm−1 at 423 K and N2 atmosphere, indicating that proton conductivity of HKUST‐1 is improved by hole expansion and ionic liquid introduction. Finally, the stability test showed that MIM‐CF3SO3@LP‐HKUST‐1‐100% was stable in all environments above. Moreover, the conductive mechanism of HKUST‐1 before and after introduction of ionic liquids was also discussed, providing a theoretical basis for the enhancement of proton conductivities of MOFs using ionic liquid introduction and hole expansion.

Dopants Induce Persistent Room Temperature Phosphorescence in Triarylamine Boronate Esters

AbstractPurely organic materials exhibiting room temperature phosphorescence (RTP) are promising candidates for oxygen sensors and information encryption owing to their cost‐effective and environmentally friendly nature. Herein, we report a bimolecular RTP system where DTBU acts as the guest and TBBU serves as the host. In contrast to previously reported results, we find that both pure DTBU and TBBU do not exhibit RTP in the solid state even under N2 atmosphere. A DTBU/TBBU system with a low doping ratio (0.1 mol %) exhibits persistent yellowish‐green afterglow with a lifetime of 340 ms and is highly sensitive to oxygen. A DTBU/TBBU system with a higher doping ratio (10 mol %) maintains a phosphorescence lifetime of 179 ms under air. Applications of DTBU/TBBU at varied doping ratios in both oxygen sensing and information encryption are demonstrated. We propose that the T1 state of TBBU acts as an energy transfer intermediate between Tn and T1 of DTBU, ultimately leading to the generation of persistent RTP. Overall, this work demonstrates the critical importance of material purity in the design of RTP systems, and how an understanding of host–guest doping enables their photophysical properties to be precisely tuned.

Dopants Induce Persistent Room Temperature Phosphorescence in Triarylamine Boronate Esters.

Purely organic materials exhibiting room temperature phosphorescence (RTP) are promising candidates for oxygen sensors and information encryption owing to their cost-effective and environmentally friendly nature. Herein, we report a bimolecular RTP system where DTBU acts as the guest and TBBU serves as the host. In contrast to previously reported results, we find that both pure DTBU and TBBU do not exhibit RTP in the solid state even under N2 atmosphere. A DTBU/TBBU system with a low doping ratio (0.1 mol %) exhibits persistent yellowish-green afterglow with a lifetime of 340 ms and is highly sensitive to oxygen. A DTBU/TBBU system with a higher doping ratio (10 mol %) maintains a phosphorescence lifetime of 179 ms under air. Applications of DTBU/TBBU at varied doping ratios in both oxygen sensing and information encryption are demonstrated. We propose that the T1 state of TBBU acts as an energy transfer intermediate between Tn and T1 of DTBU, ultimately leading to the generation of persistent RTP. Overall, this work demonstrates the critical importance of material purity in the design of RTP systems, and how an understanding of host-guest doping enables their photophysical properties to be precisely tuned.

A comparative study of the pyrolysis and hydrolysis conversion of tire

In the present study, we pyrolyzed a waste tire at various temperatures under an N2 atmosphere and a water environment in an autoclave reactor to investigate the effect of water on tire degradation. The analysis involved a comparison of product distribution, char properties, oil composition, and the behavior of heteroatom elements (especially oxygen, nitrogen, and sulfur) under different atmospheres. Elemental analysis, functional-group identification, and chemical state analysis of sulfur were performed for chars. In addition, the chemical composition, elemental composition, and molecular weight of the produced oils were evaluated. The heavy fraction of oils, not detectable by gas chromatography-mass spectrometry (GC-MS), was analyzed through Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR MS). The findings revealed that high temperatures promoted oil cracking, resulting in the formation of light oils in both pyrolysis and hydrolysis processes. Compared to pyrolysis, hydrolysis generated a higher yield of low molecular–weight oil. Elevated hydrolysis temperatures promoted aromatization, yielding an oil with a low H/C ratio and a high double bond equivalent number. Consequently, the concentration of aromatics in the light fraction of oils generated from the hydrolysis process exceeded that in oils from the pyrolysis process. Temperature exhibited a limited impact on oil composition during the pyrolysis process. Hydrolysis promoted the release of heteroatom-containing compounds at low temperatures. During pyrolysis, nitrogen was gradually released from the solid phase, whereas nitrogen-containing compounds were released early during hydrolysis, with gas-phase nitrogen accounting for more than 50 wt% at 320 °C. A maximum D-limonene yield of 45.58% was obtained at 360 °C within 0 min of hydrolysis, with the potential conversion of D-limonene into aromatics at higher hydrolysis temperatures. These results contribute to the understanding of tire valorization via hydrolysis.

Pyrolysis of exhausted biochar sorbent: Fates of cadmium and generation of products

Biochar is a promising sorbent for Cd removal from water, while the disposal of the exhausted Cd-enriched biochar remains a challenge. In this study, pyrolysis was employed to treat the exhausted biochar under N2 and CO2 atmospheres at 600–900 °C, and the fate of Cd during pyrolysis and characteristics of high-valued products were determined. The results indicated that higher temperature and CO2 atmosphere favored the volatilization of Cd. Based on the toxicity characteristic leaching procedure (TCLP) results, the pyrolysis treatment under both atmospheres enhanced the stability of Cd, and the leached Cd concentration of regenerated biochar obtained at high temperatures (>800 °C) was lower than 1 mg/L. Compared with the pristine biochar, the regenerated biochar demonstrated higher carbon content and pH, whereas the contents of oxygen and hydrogen declined, and exhibited promising sorption properties (35.79 mg/g). The atmosphere played an important role in modifying biochar properties and syngas composition. The N2 atmosphere facilitated CH4 production, whereas the CO2 atmosphere increased the proportion of CO. These results implied that pyrolysis can be a valuable and environmental-friendly strategy for the treatment and reuse of exhausted biochar sorbent.

Anchoring Charge Selective Self-Assembled Monolayers for Tin-Lead Perovskite Solar Cells.

Self-assembled monolayers (SAMs) have displayed great potential for improving efficiency and stability in p-i-n perovskite solar cells (PSCs). The anchoring of SAMs at the conductiv metal oxide substrates and their interaction with perovskite materials must be rationally tailored to ensure efficient charge carrier extraction and improved quality of the perovskite films. Herein, SAMs molecules with different anchoring groups and spacers to control the interaction with perovskite in the p-i-n mixed Sn-Pb PSCs are selected. It is found that the monolayer with the carboxylate group exhibits appropriate interaction and has a more favorable orientation and arrangement than that of the phosphate group. This results in reduced nonradiative recombination and enhanced crystallinity. In addition, the short chain length leads to an improved energy level alignment of SAMs with perovskite, improving hole extraction. As a result, the narrow bandgap (≈1.25eV) Sn-Pb PSCs show efficiencies of up to 23.1% with an open-circuit voltage of up to 0.89V. Unencapsulated devices retain 93% of their initial efficiency after storage in N2 atmosphere for over 2500 h. Overall, this work highlights the underexplored potential of SAMs for perovskite photovoltaics and provides essential findings on the influence of their structural modification.

Layered carbon nitride films deposited under an oxygen-containing atmosphere and their electronic properties

Layered carbon nitride (g-C3N4) is a novel semiconducting and functional material for optoelectronic applications. The physical and chemical properties of g-C3N4 films differ depending on the preparation atmosphere. Herein, we deposited g-C3N4 films under a mixed oxygen (O2)-nitrogen (N2) gas atmosphere and studied their effects on the carrier transport properties. Although no significant change in the film orientation was observed, the deposition rate decreased as the O2 gas ratio in the mixed N2/O2 atmosphere increased. Despite their thinness, the luminescence intensity of g-C3N4 films deposited under an O2-containing atmosphere increased by 3.5–5.0 times compared to that deposited under an N2 atmosphere. With respect to voltage application, carrier transport owing to the thermionic emission and/or direct tunneling initially followed ohmic conduction, followed by insufficient trap-filled conduction. As the applied voltage increased further, fully trap-filled conduction was confirmed owing to Fowler–Nordheim tunneling. Moreover, the conductivity type could be changed to p-type and n-type using N2 gas and mixed N2/O2 gas atmospheres, respectively, during film deposition. In addition to the intrinsic transport properties, the intentionally formed Schottky barrier also affected the carrier transport; therefore, the diode-like rectifying behavior of the current density was achieved.

A Novel Approach for Post-Mortem Analysis in All-Solid-State Batteries: Isolating Solid Polymer Electrolytes from Lithium Anodes

Polymeric electrolytes are currently at the forefront of research for the next generation of lithium all-solid-state batteries. Polyethylene oxide (PEO), a commonly used polymer for these batteries, operates at elevated temperatures at which it reacts with active metal electrodes (e.g., lithium). Rich surface chemistry is developed at the Li-PEO interfaces, thereby controlling these batteries’ electrochemical behavior. Interfacial studies are essential to comprehend batteries’ stabilization or capacity fading mechanisms. For that, post-mortem analysis with an emphasis on interfaces is a necessary approach to underpinning these mechanisms. While it can be readily done with liquid electrolytes, post-mortem characterization of similar interfaces with solid electrolytes is hampered by the Li-PEO stack firm adhesion, which is impossible to separate. Here, various methods were attempted to separate polymer electrolytes from metallic anodes after Li symmetric cells’ operation, which is a necessary step for solid-state NMR characterization. By a simple method involving exposure to N2(g) atmosphere, PEO-based solid electrolyte samples were successfully isolated from lithium anodes while preserving their morphology and chemical characteristics to enable their direct analysis. This method’s concept was approved by Solid-state NMR spectroscopy. This work opens the door for post-operative analysis of many kinds of solid-state Li batteries.

Mechanical strength changes of combustible municipal solid waste components during their early pyrolysis stage and mechanism analysis.

Implementation of municipal solid waste (MSW) source segregation leads to a more convenient recycle of combustible MSW components. Textiles, plastics and papers are commonly available combustible components in MSW. Their shredding is conducive to resources recovery. But these components usually have high tensile strengths and are difficult to shred. To understand their mechanical strength changes in their early pyrolysis stage will help to address this problem. In this study, a universal electronic testing machine was used to determine the breaking strengths of the materials including cotton towel, polyethylene glycol terephthalate (PET), ivory board (IB), kraft paper (KP) and wool scarf in the temperature range of 30-250°C under N2 atmosphere, and the mechanisms of their strength changes were explored. The reaction force field molecular dynamics (ReaxFF-MD) simulation was used to explain the decomposition behaviours of different sugar groups of hemicellulose in cotton and paper and the change of van der Waals energy of wool during their early pyrolysis stages. The results showed that breaking strengths of all the combustible MSW components reduced as the temperature increased. The breaking strength of PET was found to have the highest descent rate with increasing temperature, then the descent rates of wool and cotton came as the second and third, respectively. Compared with cotton, the breaking strengths of KP and IB decreased more slowly. As the temperature increased, the breaking strength of cotton reduced mainly due to the decomposition of the glucuronic acid in hemicellulose, and the reduction was characterized by CO2 release. The breaking strength reduction of PET was caused by its molecular chain being relaxed. The breaking strength reduction of wool was firstly caused by the decrease in the van der Waals energy between its molecules, and then caused by molecular chain breaking. In addition, in order to understand the influence of material size on the breaking strength change during thermal treatment, the breaking strengths of cotton yarn bundles were correlated with their yarn number and temperature. This study lays the foundation for understanding changes in mechanical strengths of combustible MSW components during their early pyrolysis stage.

Preparation of a three-dimensional bimetallic CoFex/ N-doped carbon nanomaterial used as modified electrode for the efficient electrochemical detection of l-tyrosine

The rapid and sensitive detection of l-tyrosine (L-Tyr) has become a vital issue in the fields of medicine and clinical analysis as lack or overdose of L-Tyr in human body could cause disease. In this paper, a three-dimensional cubic CoFex/N-doped carbon nanocomposite (CoFex-N,C) material was prepared by high-temperature calcination of CoFe-Prussian blue analogues (CoFe-PBA) in N2 atmosphere and then modified on glass carbon electrode (GCE) for L-Tyr detection. The prepared CoFex/N,C nanocomposite not only inherits the uniform morphology, and unique bimetallic active center of CoFe-PBA, but also possesses the high conductivity and large ratio area of nitrogen-doped carbon nanomaterials. Under optimum conditions, the CoFex/N,C nanocomposite electrode presented a broad linear scope of 0.8–354.84 μM, a low detection limit of 0.06 μM (S/N = 3), good anti-interference ability, and very high stability. In addition, the acceptable recoveries were obtained for real sample analysis.

Determination of Effect of Zno Nanoparticles of Invitro Cultrue of Cowpea Beans

The cowpea is a annual herbaceous legume. The root nodules have capacity fo fix the atmosphere N2 that is beneficial for farming.This fixed N2 benefit other crops (intercropping) in various ways. The Zno NPs (Zinx Oxice Nanoparticles) has wide applications in agriculture as a fertilizer to increase the product yield and to limit the onset of fungal and bacterial diseases. The invitro germination of seed followed by the seedling growth needs the intervention of ZnO Np in cowpea beans. This research was developed to study the effect of various doses of ZnO Nps (Zinc Oxide Nanoparticles).

A new model to estimate shallow lake nitrogen removal rate based on satellite derived variables

Lake nitrogen (N) removal, mainly resulting from bacterial denitrification that converts nitrate (NO3 −) to gaseous N (N2), is important for lake water quality and eutrophication control. However, quantifying lake N removal is challenging due to the high background atmosphere N2 concentration and the heavy burden of field surveys, leading to a decoupling of watershed N management and water quality improvement. Here, we developed and validated an innovative nonlinear model for lake N removal rate estimation by linking the N removal rates with remote sensing-derived variables (chlorophyll-a, chromophoric dissolved organic matter, and lake surface water temperature). The model was validated in shallow eutrophic Lake Taihu in the Yangtze River basin and at the global scale. Based on the new N removal model, we estimated that an annual average of 3.21 × 104 t N yr‒1 was removed in Lake Taihu from 2011 to 2020, accounting for 53%–66% of the total lake N loading. The remaining N loading after denitrification removal in Lake Taihu would be approximately 2.37 mg N l‒1, and 0.79 × 104 t N y‒1 of lake N loading still needs to be removed to meet the target of class IV water quality (1.5 mg N l‒1). This is the first study linking lake N removal in sediment microcosm incubations with reach-scale remote sensing derived variables, providing timely-much insights into lake N removal. This approach can be easily applied in other lakes with satellite derived data, to better understand lake N budget, drivers of eutrophication control, and watershed N management.

Role of shielding gas and rolling treatment on mechanical properties of CP-Ti sheet fabricated by selective laser melting

Commercially pure titanium (CP–Ti) took advantages of low stiffness, high corrosion resistance and bio-compatibility, implying an ideal structural material in aerospace, military and medical industries. However, its insufficient mechanical properties have always been the long-standing obstacle for the industrial applications. In this work, we have achieved a superior strong and ductile CP-Ti via active atmosphere-assisted selective laser melting (SLM) and subsequent rolling treatment. By incorporating the active N2 atmosphere during SLM, mechanical properties of CP-Ti were substantially improved, microhardness of the lyaers with 10 at.% and 100 at.% was 63 % and 174.3 % higher than that of CP-Ti with 182.3 HV0.2, the compressive strength of 10 sample was 27.1 % higher than that of 10 L sample when the strain was 52.2 %, and ultimate tensile strength of 10 sample reached 928 MPa with an elongation of 25.6 %, and ultimate tensile strength and elongation of 10 L sample were enhanced simultaneously by 58.3 % and 13.6 % relative to CP-Ti sample. These were attributed to the interstitial strengthening induced by N atoms. After rolling treatment, the mechanical properties of N-doping layers could enhance furtherly. Macroscale cracking along the rolling direction never occur in the 10 L sample during the repeatedly rolling treatment, which could depend to high tolerability of sandwich layers for high-density dislocations. Meanwhile, rolling treatment played an important role for refining grain to enhance the strength further.

Intense O + E + S-band emission from Pr3+-doped ZnF2-based glasses

Pr3+-doped ZnF2-based glasses were prepared by using a melt-quenching method in dry N2 atmosphere. Under the excitation of a 588 nm light emitting diode (LED), ultrabroadband emissions ranging from 1245 to 1640 nm were obtained from the Pr3+-doped ZnF2-based glasses, which originate from the transitions 1D2→1G4 (producing E + S-band emission) and 1G4→3H5 (producing O-band emission) of Pr3+. The shape of the emission spectra could be tailored by varying the concentration of Pr3+. Emission spectra with the maximum full width at half maximum (FWHM) of 215 nm (1289 nm-1504 nm, covering the O + E + S-band) was obtained in the ZnF2-based glass at a doping concentration of 5000 ppm. The effects of the phonon energy of the matrix on O + E + S-band emission were also investigated. Our results showed that Pr3+-doped ZnF2-based glasses with low phonon energy might be used for constructing O + E + S-band lasers and optical amplifiers.

Efficient and Stable Tin‐Lead Mixed Perovskite Solar Cells Using Post‐Treatment Additive with Synergistic Effects

AbstractInhibiting the oxidation of Sn2+ during the crystallization process of Sn−Pb mixed perovskite film is found to be as important as the oxidation resistance of precursor solution to achieve high efficiency, but less investigated. Considering the excellent reduction feature of hydroquinone and the hydrophobicity of tert‐butyl group, an antioxidant 2,5‐di‐tert‐butylhydroquinone (DBHQ) was introduced into Sn−Pb mixed perovskite films using an anti‐solvent approach to solve this problem. Interestingly, we find that DBHQ can act as function alterable additive during its utilization. On the one hand, DBHQ can restrict the oxidation of Sn2+ during the crystallization process, facilitating the fabrication of high‐quality perovskite film; on the other hand, the generated oxidation product 2,5‐di‐tert‐butyl‐1,4‐benzoquinone (DBBQ) can functionalize as defect passivator to inhibit the charge recombination. As a result, this synergetic effect renders the Sn−Pb mixed PSC a power conversion efficiency (PCE) up to 23.0 %, which is significantly higher than the reference device (19.6 %). Furthermore, the unencapsulated DBQH‐modified PSCs exhibited excellent long‐term stability and thermal stability, with the devices maintaining 84.2 % and 78.9 % of the initial PCEs after aging at 25 °C and 60 °C for 800 h and 120 h under N2 atmosphere, respectively. Therefore, the functional alterable strategy provides a novel cornerstone for high‐performance Sn−Pb mixed PSCs.

Efficient and Stable Tin-Lead Mixed Perovskite Solar Cells Using Post-Treatment Additive with Synergistic Effects.

Inhibiting the oxidation of Sn2+ during the crystallization process of Sn-Pb mixed perovskite film is found to be as important as the oxidation resistance of precursor solution to achieve high efficiency, but less investigated. Considering the excellent reduction feature of hydroquinone and the hydrophobicity of tert-butyl group, an antioxidant 2,5-di-tert-butylhydroquinone (DBHQ) was introduced into Sn-Pb mixed perovskite films using an anti-solvent approach to solve this problem. Interestingly, we find that DBHQ can act as function alterable additive during its utilization. On the one hand, DBHQ can restrict the oxidation of Sn2+ during the crystallization process, facilitating the fabrication of high-quality perovskite film; on the other hand, the generated oxidation product 2,5-di-tert-butyl-1,4-benzoquinone (DBBQ) can functionalize as defect passivator to inhibit the charge recombination. As a result, this synergetic effect renders the Sn-Pb mixed PSC a power conversion efficiency (PCE) up to 23.0 %, which is significantly higher than the reference device (19.6 %). Furthermore, the unencapsulated DBQH-modified PSCs exhibited excellent long-term stability and thermal stability, with the devices maintaining 84.2 % and 78.9 % of the initial PCEs after aging at 25 °C and 60 °C for 800 h and 120 h under N2 atmosphere, respectively. Therefore, the functional alterable strategy provides a novel cornerstone for high-performance Sn-Pb mixed PSCs.