Improving proton conductivity via crystallinity reduction and sulfonate ligand modification based on UiO-66

IF 2.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Xinran Li, Yingying Ma, Xiaotian Zhang, Jiajun Zhong, Wenxuan Yan, Jiefei Bai, Yuxin Li, Xiaofeng Zheng and Zhe Liu
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引用次数: 0

Abstract

As promising candidates for novel proton conductors crucial for electrochemical energy technology, metal–organic frameworks (MOFs) have attracted much attention. The structures of MOFs have been optimized via a crystallinity reduction and sulfonate ligand modification method to improve the proton conductivity. Benzenesulfonic acid (-BSA), p-aminobenzene sulfonic acid (-pASA), and p-sulfobenzoic acid (-pSA) were used for doping in the UiO-66 reaction system. A series of UiO-66-modified target products (UiO-66-X) and the corresponding metal organic gel products (MOG-UiO-66-X; X = -BSA, -pASA or -pSA), were obtained. The proton conductivity was investigated at four different relative humidities (100%, 75%, 50%, and 30%) from 303 K to 353 K. The results showed that MOG-UiO-66-pASA had the maximum σ value of 9.38 × 10−2 S cm−1 at 100% RH and 353 K, 358 times higher than UiO-66, which may be related to the reduced crystallinity and the –SO3H/–NH2 acid–base pairs in the structure from the doped modifying ligand -pASA. The structural attraction and repulsion effects of acids and bases on protons accelerate the transport speeds of protons in the MOG structure, thereby increasing the proton conductivity of the materials. In addition, proton-transfer mechanism studies reveal that the structural responses of the materials to variations in ambient temperature and humidity are reflected in their activation energies, prompting a transition between the Grotthuss (proton hopping) mechanism and the vehicle mechanism. This mechanistic shift ultimately influences the resulting proton conduction performance. This investigation not only proposes a simple crystallinity-reduction strategy and ligand substitution model for MOF modifications to achieve superior proton conductivity but also provides valuable insights into the adaptation mechanism between proton conduction and environmental conditions. It further offers guidance for the performance optimization of proton-conductive materials. The findings lay research foundations for the performance optimization of proton exchange membranes and the enhancement of their environmental durability in proton exchange membrane fuel cells. Compared with the crystal powder material (UiO-66) the modified gel material, MOG-UiO-66-pASA, has more coherent structural channels and –SO3H/–NH2 acid–base pairs, resulting in a 358-fold increase in proton conductivity.

Abstract Image

通过降低结晶度和基于UiO-66的磺酸盐配体修饰提高质子电导率
金属有机骨架(MOFs)作为电化学能源技术中具有重要意义的新型质子导体,受到了广泛的关注。通过降低结晶度和磺酸盐配体修饰等方法优化了mof的结构,提高了质子的导电性。用苯磺酸(-BSA)、对氨基苯磺酸(-pASA)和对巯基苯甲酸(-pSA)掺杂uuo -66反应体系。得到了一系列uio -66修饰的靶产物(UiO-66-X)和相应的金属有机凝胶产物(MOG-UiO-66-X; X = -BSA, -pASA或-pSA)。在303 K ~ 353 K的4种不同相对湿度(100%、75%、50%和30%)下研究了质子电导率。结果表明,MOG-UiO-66-pASA在100% RH和353 K下的最大σ值为9.38 × 10−2 S cm−1,是UiO-66的358倍,这可能与掺杂修饰配体-pASA降低了结晶度和结构中的-SO3H / -NH2酸碱对有关。酸和碱对质子的结构吸引和斥力作用加速了MOG结构中质子的输运速度,从而提高了材料的质子电导率。此外,质子转移机制研究表明,材料对环境温度和湿度变化的结构响应反映在其活化能上,促使质子跳迁机制向载体机制过渡。这种机制的转变最终会影响质子的传导性能。本研究不仅提出了一种简单的晶体还原策略和配体取代模型来修饰MOF以获得优异的质子导电性,而且为质子导电性与环境条件之间的适应机制提供了有价值的见解。进一步为质子导电材料的性能优化提供了指导。研究结果为优化质子交换膜燃料电池的性能和提高其环境耐久性奠定了研究基础。与晶体粉末材料(UiO-66)相比,改性凝胶材料MOG-UiO-66-pASA具有更多的相干结构通道和-SO3H / -NH2酸碱对,使质子电导率提高358倍。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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