Steininger H, Schuster M, Kreuer K D, Kaltbeitzel A, Bingöl B, Meyer W H, Schauff S, Brunklaus G, Maier J, Spiess H W
Max-Planck-Institut für Festkörperforschung, Heisenbergstrasse 1, 70569 Stuttgart, Germany.
Phys Chem Chem Phys. 2007 Apr 21;9(15):1764-73. doi: 10.1039/b618686f. Epub 2007 Feb 27.
The melting behaviour and transport properties of straight chain alkanes mono- and difunctionalized with phosphonic acid groups have been investigated as a function of their length. The increase of melting temperature and decrease of proton conductivity with increasing chain length is suggested to be the consequence of an increasing ordering of the alkane segments which constrains the free aggregation of the phosphonic acid groups. However, the proton mobility is reduced to a greater extent than the proton diffusion coefficient indicating an increasing cooperativity of proton transport with increasing length of the alkane segment. The results clearly indicate that the "spacer concept", which had been proven successful in the optimization of the proton conductivity of heterocycle based systems, fails in the case of phosphonic acid functionalized polymers. Instead, a very high concentration of phosphonic acid functional groups forming "bulky" hydrogen bonded aggregates is suggested to be essential for obtaining very high proton conductivity. Aggregation is also suggested to reduce condensation reactions generally observed in phosphonic acid containing systems. On the basis of this understanding, the proton conductivities of poly(vinyl phosphonic acid) and poly(meta-phenylene phosphonic acid) are discussed. Though both polymers exhibit a substantial concentration of phosphonic acid groups, aggregation seems to be constrained to such an extent that intrinsic proton conductivity is limited to values below sigma = 10(-3) S cm(-1) at T = 150 degrees C. The results suggest that different immobilization concepts have to be developed in order to minimize the conductivity reduction compared to the very high intrinsic proton conductivity of neat phosphonic acid under quasi dry conditions. In the presence of high water activities, however, (as usually present in PEM fuel cells) the very high ion exchange capacities (IEC) possible for phosphonic acid functionalized ionomers (IEC >10 meq g(-1)) may allow for high proton conductivities in the intermediate temperature range (T approximately 120 -160 degrees C).
对带有膦酸基团的直链烷烃单官能和双官能化产物的熔融行为及传输性质随其链长的变化进行了研究。随着链长增加,熔点升高且质子传导率降低,这被认为是烷烃链段有序性增加的结果,而烷烃链段有序性增加会限制膦酸基团的自由聚集。然而,质子迁移率的降低程度大于质子扩散系数,这表明随着烷烃链段长度增加,质子传输的协同性增强。结果清楚地表明,在优化基于杂环体系的质子传导率方面已被证明成功的“间隔基概念”,在膦酸官能化聚合物的情况下并不适用。相反,形成“庞大”氢键聚集体的高浓度膦酸官能团对于获得非常高的质子传导率似乎至关重要。聚集还被认为可以减少在含膦酸体系中普遍观察到的缩合反应。基于这一认识,讨论了聚(乙烯基膦酸)和聚(间苯撑膦酸)的质子传导率。尽管这两种聚合物都含有大量的膦酸基团,但聚集似乎受到很大限制,以至于在T = 150℃时,本征质子传导率被限制在低于σ = 10⁻³ S cm⁻¹的值。结果表明,必须开发不同的固定化概念,以与准干燥条件下纯膦酸非常高的本征质子传导率相比,尽量减少传导率的降低。然而,在高水活度存在的情况下(如通常存在于质子交换膜燃料电池中),膦酸官能化离聚物可能具有的非常高的离子交换容量(IEC >10 meq g⁻¹)可能允许在中间温度范围(T约为120 - 160℃)具有高质子传导率。