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Towards First-principles Prediction of Electrocatalytic Activity of ABO3 Perovskites
Başlık:
Towards First-principles Prediction of Electrocatalytic Activity of ABO3 Perovskites
Yazar:
Rong, Xi, author.
Yazar Ek Girişi:
Genel Not:
Source: Dissertation Abstracts International, Volume: 79-11(E), Section: B.
Advisors: Alexie Kolpak.
Özet:
The design of efficient, stable, and inexpensive catalysts such as ABO3 perovskites for the oxygen evolution reaction (OER) and the oxygen reduction reaction (ORR) is crucial for the development of electrochemical energy conversion devices such as water electrolysis, fuel cells, and metal--air batteries. In order to enable high-throughput computation and screening for optimal catalysts, a deeper understanding of composition-structure-activity relationships is required. Currently, this endeavor is hindered by the complexity of the oxide surface structure and challenges in atomic-scale experimental characterization under in operando conditions. In this thesis, we address these issues by employing density functional theory and classical methods, including electrochemical principles and micro-kinetics, for prediction of catalyst surface structure, stability, and reaction mechanism as a function of environment.
We have performed investigations focused on the following thrusts: 1) Predicting the active surface phase under the operation conditions; 2) elucidating possible OER reaction mechanisms and correlating the preferred mechanism to ABO3 stability; 3) identifying electronic structure correlations to surface reactivity; and 4) demonstrating the high efficiency of Ruddlesden-Popper (RP) perovskties. To this end, we have derived a general formalism for incorporating pH- and U-dependent ion exchange at the catalyst surface-solvent interface, and used this approach to determine the surface structure/composition phase diagram of various perovkites, demonstrating that the surface structure of perovskites is highly sensitive to the environment, which in turn alters electrocatalytic activity. These effects are dramatically important for those highly efficient ABO3 compounds, for which we showed that the lattice oxygen becomes an active participant in the OER mechanism. Combining this new mechanism (the lattice oxygen mediated mechanism or LOM) with the conventional adsorbate evolution mechanism (AEM), we developed a new overall activity volcano, and showed that LOM is fundamentally more thermodynamically favorable and thus governs the activity of the most efficient catalysts. Furthermore, we have identified a fundamental descriptor for the binding energy of oxygen surface reaction intermediates based on the shape of the transition metal cation d-projected density of states, as described by its 1st-4th mathematical moments, and provided a strong physical grounding for this descriptor from a tight-binding analysis and use of the moments theorem. This work has led to an essential extension of the widely used d-band theory for metal catalysts to the realm of oxides. With the insights gained from the ABO3 perovskite, we finally extended our study to understand the origin of the high efficiency and stability of some novel types of perovskite.
Together, these efforts have contributed crucial insights into the complete composition-structure-activity relationship, and provided important steps towards the objective of using first-principles computations to predict ABO3 activity for OER and ORR These insights are transferrable to many other catalytic reactions, in which oxide-liquid interfaces play a critical role, and have potential to critically impact our understanding of surface chemistry, corrosion, energy conversion, and electrochemical science.
Keywords Perovskite-based electrocatalysts; oxygen evolution and reduction reactions; density functional theory; surface structure; machine learning (Copies available exclusively from MIT Libraries, libraries.mit.edu/docs - docs mit.edu).
Notlar:
School code: 0753
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Yer Numarası | Demirbaş Numarası | Shelf Location | Lokasyon / Statüsü / İade Tarihi |
---|---|---|---|
XX(696960.1) | 696960-1001 | Proquest E-Tez Koleksiyonu | Arıyor... |
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