Transport Ability Research Articles

Interfacial Engineering‐Assisted Energy Level Modulation Enhances the Photoelectrochemical Water Oxidation Performance of Bismuth Vanadate Photoanodes

AbstractBiVO4 faces significant challenges for widespread application in photoelectrochemical (PEC) water oxidation due to its poor hole transport ability, high surface defect density, and sluggish water oxidation reaction kinetics. Employing interfacial engineering to assist in energy level modulation is an effective strategy to address these challenges. Herein, a CuCrO2 hole transport layer (HTL) is coupled and further grew NiCo‐MOF in situ to prepare a NiCo‐MOF‐CuCrO2‐BiVO4 composite photoanode. The novel composite photoanode not only achieves a photocurrent density of 5.75 mA cm−2 at 1.23 V versus a reversible hydrogen electrode (vs RHE) but also maintains stable operation for over 24 h. Comprehensive physicochemical characterization and density‐functional theory calculations confirm that the built‐in electric field generated by the p–n heterojunction formed between the CuCrO2 HTL and BiVO4 photoanode enhances the hole transport ability. Moreover, the NiCo‐MOF chelated on the photoanode surface not only passivates the surface defect states but also accelerates the kinetics of the water oxidation reaction. Under the synergistic effect of dual modification, the PEC water oxidation performance of the BiVO4 photoanode is dramatically improved. This pioneering work presents a MOF/HTL/BiVO4 configuration that provides a blueprint for the future development of integrated photoanodes for efficient solar energy conversion.

Core-shell upconversion nanoparticles with suitable surface modification to overcome endothelial barrier.

Upconversion nanoparticles (UCNPs), capable of converting near-infrared (NIR) light into high-energy emission, hold significant promise for bioimaging applications. However, the presence of tissue barriers poses a challenge to the effective delivery of nanoparticles (NPs) to target organs. In this study, we demonstrate the core-shell UCNPs modified with cationic biopolymer, i.e., N, N-trimethyl chitosan (TMC), can overcome endothelial barriers. The core-shell UCNP is composed of NaGdF4: Yb3+,Tm3+ (16.7 ± 2.7 nm) as core materials and silica (SiO2) shell. The average particle size of UCNPs@SiO2 is estimated at 26.1 ± 3.7 nm. X-ray diffraction (XRD), transmission electron microscopy (TEM) and element mapping shows the formation of hexagonal crystal structure of β-NaGdF4 and elements doping. The surface of UCNPs@SiO2 has been modified with poly(ethylene glycol) (PEG) to enhance water dispersibility and colloidal stability, and further modified with TMC with the zeta potential increasing from -2.1 ± 0.96 mV to 26.9 ± 12.6 mV. No significant toxic effect is imposed to HUVECs when the cells are treated with core-shell UCNPs with surface modification up to 250 µg/mL. The transport ability of the core-shell UCNPs has been evaluated by using the in vitro endothelial barrier model. Transepithelial electrical resistance (TEER) and immunofluorescence staining of tight junction proteins have been employed to verify the integrity of the in vitro endothelial barrier model. The results indicate that the transport percentage of the UCNPs@SiO2 with PEG and TMC through the model is up to 4.56%, which is twice higher than that of the UCNPs@SiO2 with PEG but without TMC and six times that of the UCNPs@SiO2.

Continuous Electrosynthesis of Pure H2O2 Solution with Medical-Grade Concentration by a Conductive Ni-Phthalocyanine-Based Covalent Organic Framework.

Electrosynthesis of H2O2 provides an environmentally friendly alternative to the traditional anthraquinone method employed in industry, but suffers from impurities and restricted yield rate and concentration of H2O2. Herein, we demonstrated a Ni-phthalocyanine-based covalent-organic framework (COF, denoted as BBL-PcNi) with a higher inherent conductivity of 1.14 × 10-5 S m-1, which exhibited an ultrahigh current density of 530 mA cm-2 with a Faradaic efficiency (H2O2) of ∼100% at a low cell voltage of 3.5 V. Notably, this high level of performance is maintained over a continuous operation of 200 h without noticeable degradation. When integrated into a scale-up membrane electrode assembly electrolyzer and operated at ∼3300 mA at a very low cell voltage of 2 V, BBL-PcNi continuously yielded a pure H2O2 solution with medical-grade concentration (3.5 wt %), which is at least 3.5 times higher than previously reported catalysts and 1.5 times the output of the traditional anthraquinone process. A mechanistic study revealed that enhancing the π-conjugation to reduce the band gap of the molecular catalytic sites integrated into a COF is more effective to enhance its inherent electron transport ability, thereby significantly improving the electrocatalytic performance for H2O2 generation.

Calcium Transport Activity of UV/H2O2-Degraded Fucoidans and Their Structural Characterization

Calcium-chelated polysaccharides have been increasingly considered as promising calcium supplements. In this study, degraded fucoidans (DFs) with different molecular weights (Mws) were prepared after UV/H2O2 treatment; their calcium-chelating capacities and intestinal absorption properties were also investigated. The results showed that the calcium-chelating capacities of DFs were improved with a decrease in Mw. This was mainly ascribed to the increased carboxyl content, which was caused by free-radical-mediated degradation. Meanwhile, the conformation of DF changed from a rod-like chain to a shorter and softer chain. The thermodynamic analysis demonstrated that DF binding to calcium was spontaneously driven by electrostatic interactions. Additionally, DF-Ca chelates with lower Mw showed favorable transport properties across a Caco-2 cell monolayer and could effectively accelerate the calcium influx through intestinal enterocytes. Furthermore, these chelates also exhibited a protective effect on the epithelial barrier by alleviating damage to tight junction proteins. These findings provide an effective free-radical-related approach for the development of polysaccharide-based calcium supplements with improved intestinal calcium transport ability.

P3HT/g-C3N4 composite fiber membranes for high-performance photocatalytic hydrogen evolution

As a superstar semiconducting polymer, poly(3-hexylthiophene) (P3HT) demonstrates high efficiency in carrier transport ability and wide absorption range. However, pristine P3HT exhibits minimal photocatalytic activity as a result of its short carrier transport distance and fast electron-hole recombination. Here, we strategically fabricated P3HT/g-C3N4 composites on polymethyl methacrylate (PMMA) fiber (PTCN) via electrospinning and the physicochemical properties were fully investigated. Raman spectroscopy, ultraviolet–visible (UV–Vis) absorption spectra and X-ray photoelectron spectroscopy (XPS) results demonstrated a well-defined p-n heterojunctions can be formed between P3HT and g-C3N4 molecules through π-π interaction and extended conjugated length of P3HT could be achieved by tuning the ratios of P3HT relative to g-C3N4. The presence of the heterojunctions facilitates the effective disconnection of the electron-hole pairs, resulting in a significantly enhanced photocatalytic hydrogen evolution rate of 7327 μ mol/(h·g) for the PTCN fiber membranes. This value exceeds that of P3HT fibers by 57.7 times and powder g-C3N4 by 6.8 times, respectively. The high photocatalytic hydrogen production activity of P3HT/g-C3N4 fiber membrane expands the application of P3HT. More importantly, these results indicate that the construction of heterojunction fiber materials is a promising approach for improving the photocatalytic ability of conjugated semiconducting polymers.

Effects of asymmetric rough boundaries on turbulent Rayleigh–Bénard convection

We report on an experimental study of turbulent Rayleigh–Bénard convection with asymmetric top and bottom plates. The plates are covered with pyramid-shaped roughness elements whose aspect ratios are $\lambda =1$ or $\lambda =4$ . In the low-Rayleigh-number regime ( $Ra<1.9\times 10^9$ ), the heat transport efficiencies in the asymmetric cells, characterized by the Nusselt number, are smaller than those measured in a symmetric $\lambda = 1$ cell and are greater than those for a symmetric $\lambda = 4$ cell, whereas in the high-Rayleigh-number regime ( $Ra>1.9\times 10^9$ ), the Nusselt numbers of the asymmetric cells are, in turn, greater than those for the symmetric cell with $\lambda = 1$ and smaller than those for the symmetric cell with $\lambda = 4$ . In addition, the heat transports of individual plates are studied based on the temperature drops across both halves of the cell. In the low- $Ra$ regime, the $\lambda =1$ plate shows higher heat transfer than the $\lambda =4$ plate, while for the high- $Ra$ regime, the $\lambda =4$ plate shows a higher heat transport ability. In both regimes, the individual Nusselt number of the plate with lower heat transfer is insensitive to the topology of the other plate. Besides, it is found that the symmetry of the centre temperature distribution is robust to the symmetry breaking of boundary topographies. For the $Ra$ range explored, a weak temperature inversion is observed in the bulk of asymmetric rough cells. Finally, we remark that the temperature fluctuation at the cell centre and the Reynolds number associated with the large-scale circulation show universal power laws in terms of the flux Rayleigh number as $\sigma _{T_{c}}\sim Ra_F^{0.68}$ and $Re_{LSC}\sim Ra_F^{0.36}$ , respectively.

Hydraulic traits exert greater limitations on tree-level maximum sap flux density than photosynthetic ability: Global evidence

Transpiration is a key process that couples the land-atmosphere exchange of water and carbon, and its maximum water transport ability affects plant productivity. Functional traits significantly influence the maximum transpiration rate; however, which factor plays the dominant role remains unknown. SAPFLUXNET dataset, which includes sap flux density of diverse species worldwide, provides fundamental data to test the importance of photosynthetic and hydraulic traits on maximum tree-level sap flux density (Js_max). Here, we investigated variations in Js_max of 2194 trees across 129 species using data from the SAPFLUXNET dataset, and analysed the relationship of Js_max with photosynthetic and hydraulic traits. Our results indicated that Js_max was positively correlated with photosynthetic traits at both leaf and tree level. Regarding hydraulic traits, Js_max was positively related to xylem hydraulic conductivity (Ks), leaf-specific hydraulic conductivity (Kl), xylem pressure inducing 50 % loss of hydraulic conductivity (P50), xylem vessel diameter (Vdia), and leaf-to-sapwood area ratio (AlAs). Random forest model showed that 87 % of the variability in Js_max can be explained by functional traits, and hydraulic traits (e.g., P50 and sapwood area, As) exerted larger effects on Js_max than photosynthetic traits. Moreover, trees with a lower sapwood area or depth could increase their sap flux density to compensate for the reduced whole-tree transpiration. Js_max of the angiosperms was significantly higher than that of the gymnosperms. Mean annual total precipitation (MAP) were positively related to Js_max with a weak correlation coefficient. Furthermore, Js_max showed a significant phylogenetic signal with Blomberg's K below 0.2. Overall, tree species with acquisitive resource economics or more efficient hydraulic systems show higher water transport capacity, and the efficiency of xylem hydraulic system rather than the demand for carbon uptake predominantly determines water transport capacity.

Polymer Based on Asymmetrically Halogenated Benzotriazole Enables High Performance Organic Solar Cells Prepared in Nonhalogenated Solvent.

Halogenation on the A unit of the D-π-A-type polymer donor has been proven as an effective strategy to improve the performance of organic solar cells (OSCs). Compared with fluorination, chlorination usually increases the open-circuit voltage because of the downward shift of energy levels, but decreases the charge transport ability due to the large steric hindrance of the chlorine atom. We reported herein a method to balance the energy loss and charge transport through asymmetric halogenation on the benzotriazole (BTA) unit of the polymer. The designed PE3-FCl based on the BTA unit containing fluorine and chlorine atoms rendered the highest power conversion efficiency (PCE) of 17.83% when eC9-2Cl-γ and o-xylene were used as the electron acceptor and solvent, respectively. The performance is obviously higher than that of the polymer PE3 containing a difluorinated BTA unit (16.65%) and polymer PE3-2Cl with dichlorinated BTA (14.65%) due to the manipulated morphology by preaggregation, improved and more balanced charge carrier transport, and reduced recombination loss. Notably, this PCE is a breakthrough for the BTA-based polymers processed by nonhalogenated solvent. This work gives deep insight into the asymmetric halogenation of polymer donors for high-performance green solvent-processed OSCs.

Green conversion of waste polyester into few-layer graphene for interfacial solar-driven evaporation and hydroelectric electricity generation

The coupling of solar-driven interfacial evaporation with hydrovoltaic technology is emerged as a hopeful approach to alleviate energy crisis and freshwater shortage. However, constructing low-cost evaporators with high-performance freshwater and electricity co-generation and unveiling the co-generation mechanism remain a grand challenge. Herein, we report the green transformation of waste poly(ε-caprolactone) into graphene through a salt-assisted carbonization strategy and build a flexible bi-functional graphene-based evaporator for freshwater and electricity co-generation. The graphene exhibits a typical wrinkled structure with curved edges and is composed of 7–8 discontinuous layers with rich oxygen-containing groups. The graphene-based evaporator exhibits excellent sunlight absorption (98%), photo-to-thermal conversion property, good water transport ability, low water evaporation enthalpy, and low thermal conductivity of 0.06 W m−1 K−1. The evaporator not only exhibits a notable water evaporation rate (2.92 kg m−2 h−1), but also achieves the maximum output voltage of 310 mV, surpassing many previously reported evaporators/generators. The result of molecular dynamics simulation proves the diffusion difference between H+ and OH− in water and graphene, which eventually leads to the voltage generation. Not only will this work help to improve the upcycling of waste plastics and achieve carbon neutrality, but it will also open an avenue for co-generation of freshwater and electricity.

An Easy-to-Handle Route for Bicomponent Porous Tubes Fabrication as Nerve Guide Conduits

Over the past two decades, the development of nerve guide conduits (NGCs) has gained much attention due to the impellent need to find innovative strategies to take care of damaged or degenerated peripheral nerves in clinical surgery. In this view, significant effort has been spent on the development of high-performance NGCs by different materials and manufacturing approaches. Herein, a highly versatile and easy-to-handle route to process 3D porous tubes made of chitosan and gelatin to be used as a nerve guide conduit were investigated. This allowed us to fabricate highly porous substrates with a porosity that ranged from 94.07 ± 1.04% to 97.23 ± 1.15% and average pore sizes—estimated via X-ray computed tomography (XCT) reconstruction and image analysis—of hundreds of microns and an irregular shape with an aspect ratio that ranged from 0.70 ± 0.19 to 0.80 ± 0.15 as a function of the chitosan/gelatin ratio. More interestingly, the addition of gelatin allowed us to modulate the mechanical properties, which gradually reduced the stiffness—max strength from 0.634 ± 0.015 MPa to 0.367 ± 0.021 MPa—and scaffold toughness—from 46.2 kJ/m3 to 14.0 kJ/m3—as the gelatin content increased. All these data fall into the typical ranges of the morphological and mechanical parameters of currently commercialized NGC products. Preliminary in vitro studies proved the ability of 3D porous tubes to support neuroblastoma cell (SH-SY5Y) adhesion and proliferation. In perspective, the proposed approach could also be easily implemented with the integration of other processing techniques (e.g., electrospinning) for the design of innovative bi-layered systems with an improved cell interface and molecular transport abilities.

Construction of Z‐type heterojunction Bi4Ti3O12/g‐C3N4 with pyroelectric effect for enhanced photocatalytic performance

AbstractPhotocatalytic technology has been widely studied, discussed, and tested as a feasible wastewater degradation technology. The present study demonstrated the preparation of g‐C3N4 material using solid‐state sintering method and the construction of Bi4Ti3O12/g‐C3N4 heterostructure via hydrothermal method. This direct contact Z‐type heterojunction improves the wide bandgap of Bi4Ti3O12 monomer, enhances its photoresponsiveness, and thus improves its photocatalytic performance. During the process of photocatalytic experiments, an environment of cold and hot fluctuations were created, and the pyroelectric effect was utilized to induce self‐polarization of the material and formed an internal electric field. It improves the transport ability of electron–hole pairs and suppresses their recombination in the transport path. According to the degradation experiment results, the degradation efficiency of pyroelectric synergistic heterojunction photocatalysis reached 88.7%, which was 2.27 times that of Bi4Ti3O12. It proves that the photocatalysis by pyroelectric synergistic heterojunction has good application prospects.

Molecular Ordering Manipulation in Fused Oligomeric Mixed Conductors for High-Performance n-Type Organic Electrochemical Transistors.

Advanced n-type organic electrochemical transistors (OECTs) play an important part in bioelectronics, facilitating the booming of complementary circuits-based biosensors. This necessitates the utilization of both n-type and p-type organic mixed ionic-electronic conductors (OMIECs) exhibiting a balanced performance. However, the observed subpar electron charge transport ability in most n-type OMIECs presents a significant challenge to the overall functionality of the circuits. In response to this issue, we achieve high-performance OMIECs by leveraging a series of fused electron-deficient monodisperse oligomers with mixed alkyl and glycol chains. Through molecular ordering manipulation by optimizing of their alkyl side chains, we attained a record-breaking OECT electron mobility of 0.62 cm2/(V s) and μC* of 63.2 F/(cm V s) for bgTNR-3DT with symmetrical alkyl chains. Notably, the bgTNR-3DT film also exhibits the highest structural ordering, smallest energetic disorder, and the lowest trap density among the series, potentially explaining its ideal charge transport property. Additionally, we demonstrate an organic inverter incorporating bgTNR-3DT OECTs with a gain above 30, showcasing the material's potential for constructing organic circuits. Our findings underscore the indispensable role of alkyl chain optimization in the evolution of prospective high performance OMIECs for constructing advanced organic complementary circuits.

Step-Scheme SnO₂/Zn₃In₂S₆ Catalysts for Solar Production of Hydrogen Peroxide From Seawater.

Photocatalytic generation of H₂O₂, involving both oxygen reduction and water oxidation without sacrificial agents, necessitates maximized light absorption, suitable band structure, and efficient carrier transport. Leveraging the redox capacity this study designs and constructs a step-scheme heterostructured SnO₂/Zn₃In₂S₆ catalyst for H₂O₂ production from seawater under ambient conditions for the first time. This photocatalyst demonstrates a remarkable H₂O₂ production rate of 43.5µmol g⁻¹ min⁻¹ without sacrificial agents, which can be increased to 80.7µmol g⁻¹ min⁻¹ with additional O₂ injection. Extensive in situ and ex situ characterizations, supported by theoretical calculations, reveal efficient carrier transport and robust redox ability, enabling complete photosynthesis of H₂O₂ at the oxidation and reduction sites in the S-scheme SnO₂/Zn₃In₂S₆ heterojunction. Furthermore, it is hypothesized that substituting SnO₂ with other semiconductors such as TiO₂, WO₃, and BiVO₄ can all form S-scheme and the results confirm the feasibility of such catalyst design. Additionally, it demonstrates the recycling and further utilization of the H₂O₂ produced. These findings offer new insights into the design of heterostructure catalyst architectures and present new opportunities for H₂O₂ production from seawater at ambient conditions without sacrificial agents.

The three-dimensional maneuver control of spinning tether system under a new Lagrangian model

This study explores the modeling and control of the spinning tether system (STS) for maneuvering between arbitrary spinning planes. The spinning tether system garners significant attention for good centrifugal stability and transportation ability. However, conventional STS models face challenges such as singularities and coupling when studying three-dimensional spinning motion. To tackle the aforementioned challenges, a new singularity-adjustable model and a maneuvering control strategy are proposed. Initially, a variable coordinate system is defined, which allows for relocating singularities to unattainable positions during three-dimensional motions. Based on this new coordinate system, the singularity-adjustable Lagrangian model is established. Subsequently, based on the new model, a three-dimensional maneuvering scheme for spatial spinning motions is introduced to define and describe STS maneuvering trajectories in a de-coupled way. Finally, based on the reference maneuvering scheme, a saturated radial basis function network-based controller is designed to attenuate potential disturbances and errors, as electric thrusters used in this work are limited in actuating magnitude. Numerical results demonstrate that, with the new singularity-adjustable Lagrangian model, singularity and coupling phenomena are avoided during the three-dimensional maneuver, and the proposed controller ensures a stable STS three-dimensional maneuvering motion.

Fabrication of visible light responsive BaFe12O19/Ag/AgI composites with enhanced photocatalytic degradation of organic pollutants

A novel visible-light-driven (VLD) BaFe12O19/Ag/AgI photocatalysts were constructed through calcination and hydrothermal methods, in which BaFe12O19 of different mass ratios were introduced. The constructed Z-scheme heterojunction provided BaFe12O19/Ag/AgI composite catalytic with effective space carrier transport and higher redox ability. In particular, the as-prepared BaFe12O19/Ag/AgI degraded nearly 94% of 2- mercaptobenzothiazole within 30minutes of visible-light illumination, which was much superior to that of pure AgI (47%) and BaFe12O19 (3%). Moreover, BaFe12O19/Ag/AgI can be easily magnetically separated, so as to facilitate its efficient separation and recovery in practical application. Photocatalytic activity assays revealed that the as-synthesized BaFe12O19/Ag/AgI also exhibited good photodegradation capability towards Imidacloprid, Tetracycline and Carbamazepine. In particular, the complex had relatively high oxygen activation ability, and its photocatalytic H2O2 production performance was 1.29 times higher than that of the AgI monomer within 120minutes, thus realizing rapid water disinfection. Overall, the constructed efficient Z-scheme BaFe12O19/Ag/AgI photocatalysts provide a novel insight in sewage purification.

Fabrication of gradient band tin oxide electron transport layer using self-separated dual-quantum dots for perovskite solar cells

Constructing a gradient band structure electron transport layer (ETL) and thereby enhancing the performance and stability of perovskite solar cells are an effective approach. Leveraging two types of quantum dots (QDs) with different masses, namely GQDs and Au QDs, along with tin oxide (SnO2) colloidal particles, we successfully prepared an ETL with a gradient band structure. Perovskite solar cells fabricated based on this gradient band ETL achieved a power conversion efficiency (PCE) of 22.2%, whereas those prepared with a conventional SnO2 ETL yielded only 19.6% efficiency. Furthermore, under continuous AM 1.5 G and 45°C temperature illumination for 1000 hours, the cells retained 91% of their initial efficiency. Further investigation revealed that the construction of this gradient band structure effectively compensated for the defects of the SnO2, thereby improving its electrical properties. Additionally, it enhanced the transport and separate ability of charge carriers in the ETL, reducing recombination probabilities. This work provides a simple and effective method for constructing gradient band structures, which not only enhances the performance of perovskite solar cells but also holds promise for other photovoltaic conversion devices.

Retraction: Effect of Photoinduced Size Changes on Protein Refolding and Transport Abilities of Soft Nanotubes.

Retraction: Effect of Photoinduced Size Changes on Protein Refolding and Transport Abilities of Soft Nanotubes.

Iron mediated n → π* electron transitions and mid-gap states formation in CN under low-temperature secondary calcination enhances photodegradation of organic pollutants

Iron modified carbon nitride (CN) materials have attracted widespread attention from researchers in different application fields. In this paper, single atom iron anchored CN (FeCN) with mid-gap states and n → π* electron transition was synthesized through low temperature secondary calcination. The mid-gap states introduce surface states capable of trapping photogenerated electrons, enabling FeCN to absorb photons with energies lower than its intrinsic optical bandgap. 10%FeCN also exhibits distinct optical absorption above 490 nm derived from the n → π* electron transition, which expand the visible light response range of photocatalysts and enhance electron transport ability. Additionally, the Fe-Nx site enhances the separation and transmission efficiency of photoexcited charges. The prepared 10%FeCN exhibits extremely high photocatalysis and photo-Fenton activity. Mercaptobenzothiazole (MBT) degradation rate of 10%FeCN is 3.47 times higher than CN, achieving a mineralization rate of 86.7% in 100 min. Additionally, the oxytetracycline hydrochloride (OTC) degradation rate of 10%FeCN in photo-Fenton reaction is 11.9 times higher than CN. After five cycles, this catalyst still has good reactivity, indicating its good stability.

Biomass-based three-dimensional network porous carbon anodes derived from discontinuous activation for high performance Li-ion batteries

An approach of discontinuous activation and frozon-dry pretreatment toward a three-dimensional network porous carbon was proposed by using apple as the carbon source. The porous carbon, characterized by its high surface area and abundant porosity, was optimized through the manipulation of temperature and activator quantities during the activation process. The sample obtained by first calcining at 500 °C and then at 800 °C shows ultra-high rate electrochemical performance of over 900 mA h g−1 after 100 cycles and over 500 mA h g−1 after 500 cycles under the condition of charging and discharging current density of 0.2 A g−1 due to the high porosity. It is ascribed to the unique porous structure that can make the electrolyte and lithium ion transport and path short on the surface and inside the electrode material, further enhance its fast transport ability. The described approach represents an innovative and potentially impactful method for producing porous carbon electrodes with excellent electrochemical performance, particularly in the context of high-rate capability lithium-ion batteries.

Mutation of rice SM1 enhances solid leaf midrib formation and increases methane emissions.

The leaf midrib system is essential for plant growth and development, facilitating nutrient transport, providing structural support, enabling gas exchange, and enhancing resilience to environmental stresses. However, the molecular mechanism regulating leaf midrib development is still unclear.In this study, we reported a rice solid midrib 1 (sm1) mutant, exhibiting solid leaf aerenchyma and abaxial rolling leaves due to abnormal development of parenchyma and bulliform cells. Map-based cloning revealed that SM1 encodes a litter zipper protein (ZPR). SM1 was mainly expressed in the sheaths and basal midrib and was associated with the nucleus. Further experiments indicated that SM1 can interact with OSHB1, preventing the formation of OSHB:OSHB dimers and subsequently repressing the expression of OSH1 involved in the regulation and maintenance of apical stem meristem formation. The sm1 mutant reduced long-distance oxygen transport ability from shoot to root. The impaired oxygen transport in the sm1 mutant may have contributed to the increase in methanogens and elevated methane emissions. Collectively, our findings revealed that the SM1-OSHB1-OSH1 modules regulate leaf aerenchyma development in rice. These modules not only enhance our understanding of the molecular mechanism of rice leaf aerenchyma development but also offer insights for reducing methane emissions through genetic modification.