<div class="section abstract"><div class="htmlview paragraph">The high global warming potential of nitrous oxide (N<sub>2</sub>O) led to its inclusion in the list of regulated greenhouse gas (GHG) pollutants [<span class="xref">1</span>, <span class="xref">2</span>]. The mitigation of N<sub>2</sub>O on aftertreatment catalysts was shown to be ineffective as its formation and decomposition temperatures do not overlap. Therefore, the root causes for N<sub>2</sub>O formation were investigated to enable the catalyst architectures and controls development for minimizing its formation. In a typical heavy-duty diesel exhaust aftertreatment system based on selective catalytic reduction of NOx by ammonia derived from urea (SCR), the main contributors to tailpipe N<sub>2</sub>O are expected to be the undesired reaction between NOx and NH<sub>3</sub> over SCR catalyst and NH<sub>3</sub> slip in to ammonia slip catalyst (ASC), part of which gets oxidized to N<sub>2</sub>O.</div><div class="htmlview paragraph">Based on the empirical measurements and reaction engineering principles it was established that under process conditions, the NOx and NH<sub>3</sub> concentration profiles in the catalyst exponentially decline along the axial direction due to their consumption by SCR reactions. This also entails the decrease in the evolution of N<sub>2</sub>O, an SCR byproduct, along the axial length of the catalyst. In this study, we show that the part of the SCR catalyst facing the exhaust gas where majority of NOx conversion and N<sub>2</sub>O formation occurs, when replaced with a catalyst that makes less N<sub>2</sub>O, for example V-SCR or Fe-SCR, can result in lower tailpipe N<sub>2</sub>O without compromising the NOx conversion. When SCR catalyst facing the exhaust gas has lower NH<sub>3</sub> storage, such architectures also lead to lower NH<sub>3</sub> slip into ASC during low to high temperature transients. Several SCR architectures based on the above principles, i.e., combination of catalysts with inherently low N<sub>2</sub>O formation and low NH<sub>3</sub> storage functions with catalysts having high NOx conversion ability, that have the potential to decrease N<sub>2</sub>O make will be discussed.</div></div>