Atomic Layer Deposition for Surface Area Characterization of Porous Solid Oxide Fuel Cell Electrodes and Beyond

摘要

Conventional surface area determination techniques are inadequate for calculating the surface areas of porous solids with absolute totals less than ～1 m~2, but with nm-scale feature sizes, such as state-of-the-art, lab-scale solid oxide fuel cell electrodes. Meaningful contextualization of their electrochemical performance requires knowing system surface area, but the two predominant classes of techniques, tomography and gas adsorption theory, either lack the resolution or require prohibitive amounts of material. Presented here is a new method for the accurate determination of absolute surface areas on the order of 1-1000 cm~2 with precision ±0.3 cm~2 utilizing atomic layer deposition (ALD) of commonly available trimethylaluminum (TMA) and water vapor to conformally deposit alumina over internal features. The area of alumina can then be quantified using plasma spectroscopy and the known nm-scale thickness of the layer. As a model system, scaffolds of La_(0.8)Sr_(0.2)MnO_(3-δ)/Ce_(0.9)Gd_(0.1)O_(2-δ) (LSM/GDC) of 2.6 m~2/g were measured under the new technique and compared against the B.E.T. method, with remarkably similar results obtained, but with ～1000 times less mass needed for the experiment. Under the modest ALD reactor soak times used (～10 s), and with conservative precursor pulse durations, the penetration depth of the coating was found to be ～50 μm, exceeding the requirement for the electrodes under study. To demonstrate the technique's capabilities further, the LSM/GDC scaffolds were infiltrated with PrO_x nanoparticles of ～50 nm, and the increase in surface area (+ ～25%) and enhanced electrochemical performance were measured. After annealing for 1000 hours at 700°C, both were again measured, and the surface area was found to have reverted to non-infiltrated levels, despite the infiltrated cells maintaining their higher performance. The technique, due to its ease versus other surface area determination methods and its pairing with an established analytical chemistry method, enables a useful combined chemical/morphological approach to the characterization of next-generation solid oxide cell electrodes, and may find other uses among nanostructured yet low absolute surface area systems in the broad field of heterogeneous catalysis.