Rigid-flexible synergistic alginate-based composite membranes reinforced with modified hydrothermal carbon for direct methanol fuel cells

IF 5.8 3区 材料科学 Q1 ELECTROCHEMISTRY
Shuangling Zhong, Lu Kang, Zhixiang Zhao, Lin Liu, Zhuo Tian, Minghui Wang, Xuejun Cui
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引用次数: 0

Abstract

Conventional perfluorinated PEMs hinder sustainable energy transitions due to fossil-fuel dependence and environmental concerns. Herein, we develop rigid-flexible alginate-based crosslinked biomass membranes using sulfonated alginate and acid-base bifunctionalized hydrothermal carbon from corn stalks. l-cysteine grafting creates covalent/amide linkages, Ca²⁺ forms "egg-box" coordination, and thermal treatment reinforces the network. Unlike most biomass-based PEMs that rely on a single crosslinking mode or conventional inorganic fillers, this multilevel crosslinking strategy enhances dimensional stability while providing plentiful proton-hopping sites and channels. The eco-friendly hydrothermal carbon bears functional groups analogous to those of alginate, ensuring its homogeneous dispersion throughout the polymer matrix. Compared with the sulfonated alginate membrane, the optimized membrane containing 6 wt% additive achieves a 68% enhancement in tensile strength (30.87 MPa), a 75% increase in proton conductivity (0.0556 S cm-1), and a threefold improvement in selectivity (16.8 × 104s cm-3). Methanol diffusion is suppressed by 56% to 3.3 × 10–7 cm2 s-1, contributing to a 48% higher maximum power density (59.74 mW cm-2). By employing renewable agricultural waste as an additive precursor and combining it with biodegradable alginate, this membrane avoids toxic and expensive synthetic components, rendering it both eco-friendly and cost-effective. This work demonstrates that functional additives derived from agricultural waste can be used to construct high-performance biomass PEMs, offering a promising alternative to conventional perfluorinated membranes with potential for cost reduction and environmental sustainability.
直接甲醇燃料电池用改性水热炭增强刚柔协同藻酸盐基复合膜
由于对化石燃料的依赖和环境问题,传统的全氟PEMs阻碍了可持续的能源转型。在此,我们利用磺化海藻酸盐和从玉米秸秆中提取的酸碱双功能化水热碳开发了刚柔海藻酸盐基交联生物质膜。l-半胱氨酸接枝产生共价/酰胺键,ca2 +形成“蛋盒”配位,热处理强化了网络。与大多数依赖单一交联模式或传统无机填料的生物质PEMs不同,这种多层交联策略提高了尺寸稳定性,同时提供了丰富的质子跳跃位点和通道。生态友好的水热碳具有类似于海藻酸盐的官能团,确保其均匀分散在整个聚合物基质中。与磺化海藻酸盐膜相比,添加量为6 wt%的优化膜抗拉强度提高68%(30.87 MPa),质子电导率提高75% (0.0556 S cm-1),选择性提高3倍(16.8 × 104s cm-3)。甲醇扩散被抑制了56%,达到3.3 × 10-7 cm2 s-1,最大功率密度提高了48%(59.74 mW cm-2)。通过使用可再生农业废弃物作为添加剂前体,并将其与可生物降解的海藻酸盐结合,这种膜避免了有毒和昂贵的合成成分,使其既环保又具有成本效益。这项工作表明,从农业废弃物中提取的功能性添加剂可用于构建高性能的生物质PEMs,为传统的全氟膜提供了一种有希望的替代品,具有降低成本和环境可持续性的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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