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用于光电解应用的阴离子交换膜。

Anionic Exchange Membrane for Photo-Electrolysis Application.

作者信息

Lo Vecchio Carmelo, Carbone Alessandra, Trocino Stefano, Gatto Irene, Patti Assunta, Baglio Vincenzo, Aricò Antonino Salvatore

机构信息

Institute for Advanced Energy Technologies "Nicola Giordano"-CNR-ITAE, Via Salita S. Lucia sopra Contesse 5, 98126 Messina, Italy.

出版信息

Polymers (Basel). 2020 Dec 15;12(12):2991. doi: 10.3390/polym12122991.

Abstract

Tandem photo-electro-chemical cells composed of an assembly of a solid electrolyte membrane and two low-cost photoelectrodes have been developed to generate green solar fuel from water-splitting. In this regard, an anion-exchange polymer-electrolyte membrane, able to separate H evolved at the photocathode from O at the photoanode, was investigated in terms of ionic conductivity, corrosion mitigation, and light transmission for a tandem photo-electro-chemical configuration. The designed anionic membranes, based on polysulfone polymer, contained positive fixed functionalities on the side chains of the polymeric network, particularly quaternary ammonium species counterbalanced by hydroxide anions. The membrane was first investigated in alkaline solution, KOH or NaOH at different concentrations, to optimize the ion-exchange process. Exchange in 1M KOH solution provided high conversion of the groups, a high ion-exchange capacity (IEC) value of 1.59 meq/g and a hydroxide conductivity of 25 mS/cm at 60 °C for anionic membrane. Another important characteristic, verified for hydroxide membrane, was its transparency above 600 nm, thus making it a good candidate for tandem cell applications in which the illuminated photoanode absorbs the highest-energy photons (< 600 nm), and photocathode absorbs the lowest-energy photons. Furthermore, hydrogen crossover tests showed a permeation of H through the membrane of less than 0.1%. Finally, low-cost tandem photo-electro-chemical cells, formed by titanium-doped hematite and ionomer at the photoanode and cupric oxide and ionomer at the photocathode, separated by a solid membrane in OH form, were assembled to optimize the influence of ionomer-loading dispersion. Maximum enthalpy (1.7%), throughput (2.9%), and Gibbs energy efficiencies (1.3%) were reached by using n-propanol/ethanol (1:1 wt.) as solvent for ionomer dispersion and with a 25 µL cm ionomer loading for both the photoanode and the photocathode.

摘要

由固体电解质膜和两个低成本光电极组成的串联光电化学电池已被开发出来,用于通过水分解产生绿色太阳能燃料。在这方面,研究了一种能够将光阴极产生的氢气与光阳极产生的氧气分离的阴离子交换聚合物电解质膜,涉及串联光电化学配置下的离子电导率、缓蚀性能和透光率。基于聚砜聚合物设计的阴离子膜在聚合物网络的侧链上含有正固定官能团,特别是由氢氧根阴离子平衡的季铵类物质。该膜首先在不同浓度的碱性溶液(氢氧化钾或氢氧化钠)中进行研究,以优化离子交换过程。在1M氢氧化钾溶液中进行交换,阴离子膜的基团转化率高,离子交换容量(IEC)值为1.59 meq/g,在60°C时氢氧根电导率为25 mS/cm。氢氧根膜的另一个重要特性是其在600 nm以上的透明度,因此使其成为串联电池应用的良好候选材料,在该应用中,被光照的光阳极吸收最高能量的光子(<600 nm),而光阴极吸收最低能量的光子。此外,氢气渗透测试表明,氢气透过该膜的渗透率小于0.1%。最后,组装了由光阳极处的钛掺杂赤铁矿和离聚物以及光阴极处的氧化铜和离聚物组成的低成本串联光电化学电池,它们由OH形式的固体膜隔开,以优化离聚物负载分散的影响。通过使用正丙醇/乙醇(1:1重量比)作为离聚物分散的溶剂,且光阳极和光阴极的离聚物负载均为25 μL/cm,实现了最大焓效率(1.7%)、通量(2.9%)和吉布斯能量效率(1.3%)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f36/7765393/c9127b0a8fae/polymers-12-02991-g001.jpg

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