Enhancing photoelectrochemical performance and stability of Ti-doped hematite photoanode via pentanuclear Co-based MOF modification

Modifying photoanodes with metal-organic frameworks (MOFs) as oxygen evolution reaction (OER) cocatalysts has emerged as a promising approach to enhance the efficiency of photoelectrochemical (PEC) water oxidation. However, designing OER-active MOFs with both high photo- and electrochemical stabilit...

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Published inFrontiers in chemistry Vol. 12; p. 1454524
Main Authors Dong, Guofa, Xie, Fengyan, Kou, Fangxia, Chen, Tingting, Xiao, Caihong, Du, Shaowu, Liang, Jiaqi, Lou, Chenfang, Zhuang, Jiandong
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 30.08.2024
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Summary:Modifying photoanodes with metal-organic frameworks (MOFs) as oxygen evolution reaction (OER) cocatalysts has emerged as a promising approach to enhance the efficiency of photoelectrochemical (PEC) water oxidation. However, designing OER-active MOFs with both high photo- and electrochemical stability remains a challenge, limiting the advancement of this research. Herein, we present a facile method to fabricate a MOF-modified photoanode by directly loading a pentanuclear Co-based MOF (Co-MOF) onto the surface of a Ti-doped hematite photoanode (Ti:Fe O ). The resulting Co-MOF/Ti:Fe O modified photoanode exhibits an enhanced photocurrent density of 1.80 mA∙cm at 1.23 V, surpassing those of the Ti:Fe O (1.53 mA∙cm ) and bare Fe O (0.59 mA∙cm ) counterparts. Additionally, significant enhancements in charge injection and separation efficiencies, applied bias photon-to-current efficiency (ABPE), incident photon to current conversion efficiency (IPCE), and donor density (N ) were observed. Notably, a minimal photocurrent decay of only 5% over 10 h demonstrates the extraordinary stability of the Co-MOF/Ti:Fe O photoanode. This work highlights the efficacy of polynuclear Co-based MOFs as OER cocatalysts in designing efficient and stable photoanodes for PEC water splitting applications.
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ISSN:2296-2646
2296-2646
DOI:10.3389/fchem.2024.1454524