%AZhang, Xiao%AZhao, Xunhua%AZhu, Peng%AAdler, Zachary%AWu, Zhen-Yu%ALiu, Yuanyue%AWang, Haotian%BJournal Name: Nature Communications; Journal Volume: 13; Journal Issue: 1 %D2022%I %JJournal Name: Nature Communications; Journal Volume: 13; Journal Issue: 1 %K %MOSTI ID: 10352258 %PMedium: X %TElectrochemical oxygen reduction to hydrogen peroxide at practical rates in strong acidic media %XAbstract Electrochemical oxygen reduction to hydrogen peroxide (H 2 O 2 ) in acidic media, especially in proton exchange membrane (PEM) electrode assembly reactors, suffers from low selectivity and the lack of low-cost catalysts. Here we present a cation-regulated interfacial engineering approach to promote the H 2 O 2 selectivity (over 80%) under industrial-relevant generation rates (over 400 mA cm −2 ) in strong acidic media using just carbon black catalyst and a small number of alkali metal cations, representing a 25-fold improvement compared to that without cation additives. Our density functional theory simulation suggests a “shielding effect” of alkali metal cations which squeeze away the catalyst/electrolyte interfacial protons and thus prevent further reduction of generated H 2 O 2 to water. A double-PEM solid electrolyte reactor was further developed to realize a continuous, selective (∼90%) and stable (over 500 hours) generation of H 2 O 2 via implementing this cation effect for practical applications. %0Journal Article