Substituted Ti(IV) in Ce-UiO-66-NH2 Metal-Organic Frameworks Increases H2 and O2 Evolution under Visible Light

Wenqing Hou; Chen Chen; Diya Xie; Yiming Xu

doi:10.1021/acsami.2c18389

Substituted Ti(IV) in Ce-UiO-66-NH₂ Metal-Organic Frameworks Increases H₂ and O₂ Evolution under Visible Light

ACS Appl Mater Interfaces. 2023 Jan 18;15(2):2911-2921. doi: 10.1021/acsami.2c18389. Epub 2023 Jan 7.

Authors

Wenqing Hou¹, Chen Chen¹, Diya Xie¹, Yiming Xu¹

Affiliation

¹ State Key Laboratory of Silicon Materials and Department of Chemistry, Zhejiang University, Hangzhou 310027, P. R. China.

PMID: 36609181
DOI: 10.1021/acsami.2c18389

Abstract

Metal-organic frameworks (MOFs) as photocatalysts have received increasing attention. In this work, a dual metal-substituted UiO-66-NH₂ (Ti/Ce-MOF) containing different Ti/Ce mole ratios (x = 0-2.46) has been prepared via post-synthetic exchange between Ce-UiO-66 and TiCl₄, followed by amination. The solid had a high surface area (828-937 m²/g) and a large pore volume (0.451-0.507 m³/g). Under visible light, Ti/Ce-MOF showed x-dependent activity for H₂O reduction and oxidation on a film electrode, respectively. However, such a change for H₂ evolution in a Na₂S/Na₂SO₃ aqueous solution was observed only after CdS loading. In combination with the photoluminescence and band parameters, we propose that the photoactivity of Ti/Ce-MOF for redox reaction is determined by its ability for electron transfer. Furthermore, there is an interfacial electron transfer from Ti/Ce-MOF to CdS and a hole transfer from CdS to Ti/Ce-MOF, respectively, significantly improving the efficiency of charge separation for redox reactions. This work offers a new insight that Ti substitution benefits the performance of Ce-based MOF.

Keywords: cadmium sulfide; cerium; electrochemistry; metal–organic framework; photocatalysis; substitution; titanium; water splitting.