Hosseini Ehsan, Zakertabrizi Mohammad, Hosseini Mina, Powell-Palm Matthew J
J. Mike Walker '66 Department of Mechanical Engineering, Texas A&M University, College Station, Texas 77803, United States.
Department of Materials Science and Engineering, Texas A&M University, College Station, Texas 77803, United States.
Nano Lett. 2025 Aug 6;25(31):11986-11992. doi: 10.1021/acs.nanolett.5c02774. Epub 2025 Jul 24.
Achieving stable and sustained power output remains a major challenge in the development of ionic thermoelectric devices (such as thermogalvanic cells and thermoionic capacitors) for low-grade heat harvesting. Many such systems exhibit strong performance in the initial throes of operation but degrade rapidly over time, limiting their utility. Here, we report an aqueous thermogalvanic redox agent ([Ni(bpy)]) with a Seebeck coefficient approximately double that of the canonical [Fe(CN)], which can be utilized continuously for multiple hours under large temperature gradients (Δ ≥ 60 K) without significant change in electrical performance. Molecular dynamics simulations suggest that significant differences in hydration shell behavior between the oxidant and reductant, which in turn provide a significant (here configurational) entropy difference, drive the observed thermopower. This new redox pair demonstrates stability, cyclability, and tunability in both liquid- and gel-based electrolytes, and provides a novel redox platform from which to build next-generation high-thermopower waste-heat recovery cells.
在开发用于低品位热收集的离子热电器件(如热电池和热离子电容器)时,实现稳定且持续的功率输出仍然是一项重大挑战。许多此类系统在运行初期表现出强大的性能,但随着时间的推移会迅速退化,限制了它们的实用性。在此,我们报道了一种水性热电池氧化还原剂([Ni(bpy)]),其塞贝克系数约为标准[Fe(CN)]的两倍,在大温度梯度(Δ≥60 K)下可连续使用数小时,而电性能无显著变化。分子动力学模拟表明,氧化剂和还原剂之间水合壳行为的显著差异,进而提供了显著的(此处为构型)熵差,驱动了所观察到的热功率。这种新的氧化还原对在基于液体和凝胶的电解质中均表现出稳定性、可循环性和可调性,并提供了一个新型的氧化还原平台,可用于构建下一代高热功率废热回收电池。