虎扑电竞 虎扑电竞

Analyzing the Structure-Performance Relationships of Electrocatalysts

Catalysts are the keys to speeding up sluggish reactions that require large amounts of energy. Therefore, analyzing which types of catalysts speed up reactions the most and what their underlying mechanisms are can help us improve efficiency. A research team at Tohoku University's Advanced Institute for Materials 虎扑电竞 (AIMR) has proposed a strategy to use spinel oxides to improve a reaction called the oxygen evolution reaction (OER). This catalyst overcomes issues typically encountered with previous spinel oxides by involving a rare-earth cerium (Ce) substitution.

Rare-earth induced gradient orbital coupling regime: (a) Qualitative molecular orbital diagram from metal-oxygen interaction in symmetry group of Td and Oh, where the irreducible representations of symmetry refer to canonical Mulliken terms. (b) Band projection view of rare-earth-induced gradient orbital coupling for directing oxygen electrocatalysis contributed by [REO6], [MTO4], and [MOO6]. The whole formation framework is constructed by ionization of metal cations (IRE for rare-earth in Oh, IT for metal in Td, IO for metal in Oh field), electron affinity of anion oxygen Ao, and crystal-field interaction. In crystal-field interaction, the energy term is typically correlated with charge q and Madelung potential VM of chemical species. ?Hao Li et al.

Spinels refer to minerals such as magnesium, nickel, or zinc packed tightly into cubic crystals. Spinel oxides have been explored for their potential as active electrochemical oxygen evolution reaction catalysts. However, the catalytic process for spinel oxides often follows the adsorbate evolution mechanism pathway, which largely inhibits their ability to release O2. This is not helpful for the desired oxygen evolution reaction.

Comparatively, the lattice oxygen mechanism pathway (where the release of O2 is assisted by lattice oxygen from oxides) is much more efficient. In order to best utilize this method, it is important to understand factors such as how to trigger lattice oxygen activation during the oxygen evolution process.

"Even the slightest change can alter how efficient the reaction is," explains Associate Professor Hao Li of AIMR, "Essentially, we want to reliably be able to control which pathway the spinel oxide tends towards, so we can reach the desired outcome every time."

Comprehensive electrochemical performance of oxygen evolution with practical application: Consecutive CV curves for (a) NiCo2O4 and (b) Ce-NiCo2O4 in O2-saturated 0.1 M KOH at a scan rate of 5 mV s-1. (c) LSV curves of catalysts in O2-saturated 0.1 M KOH at a scan rate of 5 mV s-1. Inset shows overpotentials at different current densities. (d) TOF values of Ce-NiCo2O4 and NiCo2O4. (e) Chronoamperometric curves of Ce-NiCo2O4 and NiCo2O4 at 1.5 VRHE. Inset shows current density ratio at different time intervals. (f) LSV curves after accelerated CV cycles. Inset shows the CV curves. (g) LSV curves in AEMWE. Inset shows model of AEMWE. ?Hao Li et al.

The research team used NiCo2O4 as a model with Ce. The catalyst exhibited remarkable OER activity with a low overpotential, satisfactory electrochemical stability, and good practicability in anion-exchange membrane water electrolyzer. Theoretical analyses reveal that OER on the Ce-NiCo2O4 surface follows the more favorable lattice oxygen mechanism (LOM) pathway compared to NiCo2O4, as further verified by pH-dependent behavior and in situ Raman analysis. In order to better characterize the ins-and-outs of the reaction, electrochemical mass spectrometry was used to confirm that the oxygen was specifically originating from the lattice oxygen of Ce-NiCo2O4.

The addition of Ce was successful in promoting the lattice oxygen pathway, which opens new doors for using this and similar catalysts in electrochemical reactions. This work provides a new perspective for designing highly active spinel oxides for OER and offers significant insights into the rare-earth-enhanced LOM mechanism.

In particular, the OER water-splitting process is useful for producing green hydrogen fuels, hence the intense interest in this reaction. In order for things to change so that these environmentally-friendly fuels can start being used more widely, it all starts with a catalyst.

These findings were published in Angewandte Chemie International Edition on October 9, 2024.

LOM mechanism investigation via surface state change and experimental determination: Surface Pourbaix diagrams of (a) *H coverage on NiCo2O4, (b) *H coverage on Ce-NiCo2O4, and (c) various *H2O, *OH, *O, and *H coverages on Ce-NiCo2O4. (d) Schematic models for adsorption of oxygen intermediates on Ce-NiCo2O4. (e) Free energy diagram of the LOM pathway of Ce-NiCo2O4 and NiCo2O4. (f-g) Potential-shifted in situ Raman spectra of NiCo2O4 and Ce-NiCo2O4. (h) The pH-dependence tests with pH values ranging from 14 to 13 for Ce-NiCo2O4. Inset diagrams present the linear relationship between overpotential and pH values for determination of coupling factor TH+e-. (i-j) Detection of 18O-labelled oxygen intermediates for NiCo2O4 and Ce-NiCo2O4. ?Hao Li et al.
Publication Details:

Title: Importing Atomic Rare-Earth Sites to Activate Lattice Oxygen of Spinel Oxides for Electrocatalytic Oxygen Evolution
Authors: Xuan Wang, Jinrui Hu, Tingyu Lu, Huiyu Wang, Dongmei Sun, Yawen Tang, Hao Li, Gengtao Fu
Journal: Angewandte Chemie International Edition
DOI: 10.1002/anie.202415306

虎扑电竞:

Hao Li
Advanced Institute for Materials 虎扑电竞 (WPI-AIMR)
Email: li.hao.b8tohoku.ac.jp
Website: https://www.li-lab-cat-design.com/

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