Osmotic energy conversion based on bio-inspired layered membranes has garnered significant interest. However, traditional biomass ion-selective membranes suffer from complex preparation, uneconomic nature, poor selectivity, and low power density. Here, we introduce scalable one-step in situ culture for nanofluidic membrane materials (GO/C-BC) composed of graphene oxide (GO), carboxymethyl cellulose sodium salt (CMC), and bacterial cellulose (BC). This preparation method effectively combines 1D and 2D nanochannels, reduces membrane resistance, and increases power density. The GO/C-BC membrane exhibits excellent cation selectivity (0.89), achieving energy conversion efficiency of 31.40 % and delivering a power density of 7.49 W m under a 500-fold concentration gradient. Stability tests under artificial seawater and river water conditions show only a 4.44 % decrease in power density after 20 d, highlighting its excellent stability and durability. Moreover, by connecting 28 power units in series, the membrane can produce a voltage output of -4 V. This scalable and environmentally friendly biomass material presents new avenues for osmotic energy conversion.
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http://dx.doi.org/10.1016/j.ijbiomac.2025.141655 | DOI Listing |
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March 2025
Multidisciplinary Platform of Advanced Engineering, Department of Chemical Engineering, School of Engineering, Monash University Malaysia, Jalan Lagoon Selatan, Bandar Sunway, Selangor, 47500, Malaysia.
The design of highly efficient photocatalysts to photoreduce nitrogen (N) to ammonia (NH) under mild conditions is extremely challenging. In this work, various molar ratio of molybdenum (Mo) is incorporated into BiOCl via a hydrothermal process. The resulting Mo-doped BiOCl exhibits remarkable solar-driven activity for N photo fixation without any scavengers or sacrificial agents.
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March 2025
The Centre of Nanoscale Science and Technology and Key Laboratory of Functional Polymer Materials, State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, China.
Photocatalytic hydrogen production through water splitting represents a promising strategy to store solar energy as chemical energy. Current photocatalysts primarily focus on traditional semiconductor materials, such as metal oxides, sulfides, nitrides, g-CN, etc. However, these materials often suffer from large bandgap and fast charge recombination, which limit sunlight utilization and result in unsatisfactory photon conversion efficiency.
View Article and Find Full Text PDFAdv Mater
March 2025
Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, 430074, China.
Adsorbed natural gas (ANG) storage is emerging as a promising alternative to traditional compressed and liquefied storage methods. However, its onboard application is restricted by low volumetric methane storage capacity. Flexible porous adsorbents offer a potential solution, as their dense structures and unique gate-opening effects are well-suited to enhance volumetric capacity under high pressures.
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March 2025
Xiamen University, College of Chemistry and Chemical Engineering, Xiamen University, 422 Siming Rd., Xiamen 361005, China, 361005, Xiamen, Fujian, China, CHINA.
Renewable energy has made significant strides, with the cost of clean electricity plummeting, making the use of renewable electricity for electrocatalytic CO2 reduction to synthesize high-value chemicals and fuels more economically attractive. Notably, certain non-copper-based electrocatalysts have shown remarkable selectivity for C2+ products at low overpotentials, even enabling the production of multi-carbon molecules that are undetectable on copper-based electrodes. This breakthrough opens up new avenues for research into non-copper catalysts.
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March 2025
School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, P. R. China.
The delicate construction of electrocatalysts with high catalytic activity is a strategic method to enhance the kinetics of lithium-sulfur batteries (LSBs). Adjusting the local structure of the catalyst is always crucial for understanding the structure-activity relationship between atomic structure and catalyst performance. Here, in situ induction of electron-deficient B enables phase engineering MoC, realizing the transition from hexagonal (h-MoC) to cubic phase (c-B-MoC).
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