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介孔二氧化硅中磷酸的物种形成与质子传导性

Speciation and Proton Conductivity of Phosphoric Acid Confined in Mesoporous Silica.

作者信息

Trevani Liliana N, Lépori Cristian M O, Garro Linck Yamila, Monti Gustavo A, Abuin Graciela C, Vaca Chávez Fabián, Corti Horacio R

机构信息

Faculty of Science, Ontario Tech University, 2000 Simcoe St. North, Oshawa L1H 7K4, Ontario, Canada.

CONICET. Instituto de Física Enrique Gaviola (IFEG), Córdoba 5000, Argentina.

出版信息

ACS Appl Mater Interfaces. 2022 Jul 18. doi: 10.1021/acsami.2c07740.

Abstract

Phosphoric acid (PA) confined in a commercial mesoporous silica (CARIACT G) with porous size in the range of 3 to 10 nm was studied in relation to its coordination with the silanol groups on the silica surface as a function of temperature, up to 180 °C, using P and Si MAS NMR spectroscopy. As the temperature increases, the coordination of Si and P in the mesopores depends on the pore size, that is, on the area/volume ratio of the silica matrix. In the mesoporous silica with the higher pore size (10 nm), a considerable fraction of PA is nonbonded to the silanol groups on the surface, and it seems to be responsible for its higher conductivity at temperatures above 120 °C as compared to the samples with a smaller pore size. The electrical conductivity of the functionalized mesoporous silica was higher than that reported for other silico-phosphoric composites synthesized by sol-gel methods using soft templates, which require high-temperature calcination and high-cost reagents and are close to that of the best PA-doped polybenzimidazole membranes used in high-temperature proton exchange membrane fuel cells (HT-PEMFCs). The rate of PA release from the mesoporous silica matrix when the system is exposed to water has been measured, and it was found to be strongly dependent on the pore size. The low cost and simplicity of the PA-functionalized mesoporous silica preparation method makes this material a promising candidate to be used as an electrolyte in HT-PEMFCs.

摘要

研究了负载于孔径在3至10纳米范围内的商用介孔二氧化硅(CARIACT G)中的磷酸(PA),通过磷和硅的魔角旋转核磁共振光谱法,研究其在高达180°C的温度下与二氧化硅表面硅醇基团的配位情况。随着温度升高,介孔中硅和磷的配位情况取决于孔径,即取决于二氧化硅基质的面积/体积比。在孔径较大(10纳米)的介孔二氧化硅中,相当一部分PA未与表面的硅醇基团键合,这似乎是其在120°C以上温度下比孔径较小的样品具有更高电导率的原因。功能化介孔二氧化硅的电导率高于使用软模板通过溶胶-凝胶法合成的其他硅磷复合材料的报道值,后者需要高温煅烧和高成本试剂,且接近高温质子交换膜燃料电池(HT-PEMFCs)中使用的最佳PA掺杂聚苯并咪唑膜的电导率。已测量了系统暴露于水时PA从介孔二氧化硅基质中的释放速率,发现其强烈依赖于孔径。PA功能化介孔二氧化硅制备方法的低成本和简便性使其成为HT-PEMFCs中用作电解质的有前途的候选材料。

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