Electric-field-assisted proton coupling enhanced oxygen evolution reaction

Author:

Pan XueleiORCID,Yan Mengyu,Liu Qian,Zhou Xunbiao,Liao XiaobinORCID,Sun Congli,Zhu Jiexin,McAleese Callum,Couture PierreORCID,Sharpe Matthew K.ORCID,Smith Richard,Peng Nianhua,England Jonathan,Tsang Shik Chi EdmanORCID,Zhao YunlongORCID,Mai LiqiangORCID

Abstract

AbstractThe discovery of Mn-Ca complex in photosystem II stimulates research of manganese-based catalysts for oxygen evolution reaction (OER). However, conventional chemical strategies face challenges in regulating the four electron-proton processes of OER. Herein, we investigate alpha-manganese dioxide (α-MnO2) with typical MnIV-O-MnIII-HxO motifs as a model for adjusting proton coupling. We reveal that pre-equilibrium proton-coupled redox transition provides an adjustable energy profile for OER, paving the way for in-situ enhancing proton coupling through a new “reagent”— external electric field. Based on the α-MnO2 single-nanowire device, gate voltage induces a 4-fold increase in OER current density at 1.7 V versus reversible hydrogen electrode. Moreover, the proof-of-principle external electric field-assisted flow cell for water splitting demonstrates a 34% increase in current density and a 44.7 mW/cm² increase in net output power. These findings indicate an in-depth understanding of the role of proton-incorporated redox transition and develop practical approach for high-efficiency electrocatalysis.

Funder

RCUK | Engineering and Physical Sciences Research Council

Publisher

Springer Science and Business Media LLC

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