Various features of NO+CO reaction kinetics on Pt(100) surfaces, including temporal oscillations, are well described by a three‐variable model incorporating only the CO, NO, and O coverages. Here we analyze the corresponding reaction–diffusion equations demonstrating the existence of chemical waves where an ‘‘oscillating phase’’ displaces an unreactive NO/CO phase leaving a spatially periodic structure in its wake; pulses excited via inhomogeneities from an unreactive NO/CO background; and Turing structures for sufficiently unequal NO and CO diffusion rates.

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The choice of coverages ΘO = 0.18(0.05),ΘNO = 0.18(0.45), and ΘCO = 0.04(0.05) for the initial O-rich (-poor) regions is guided by the characteristics of the self-generated structures described above.
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