Two-dimensional (2D) materials have spurred great interest in the field of catalysis due to their fascinating electronic and thermal transport properties. However, adding uniform mesopores to 2D metallic materials has remained a great challenge owing to the inherent high surface energy. Here, we introduce a generic liquid metal interfacial growth and exfoliation strategy to synthesize a library of penetrating mesoporous metallic nanosheets. The formation of liquid-metal/water interface promotes the adsorption of metal ion-encapsulated copolymer micelles, induces the self-limiting galvanic replacement reaction, and enables the exfoliation of products under mechanical agitation. These 2D mesoporous metallic nanosheets with large lateral size, narrow thickness distribution, and uniform perforated structure provide facilitated channels and abundant active sites for catalysis. Typically, the generated mesoporous PtRh nanosheets (mPtRh NSs) exhibit superior electroactivity and durability in hydrogen evolution reaction as well as methanol electrooxidation in alkaline media. Moreover, the constructed symmetric mPtRh NSs cell requires only a relative low electrolysis voltage to achieve methanol-assisted hydrogen production compared with traditional overall water electrolysis. The work reveals a specific growth pattern of noble metals at the liquid-metal/water interface and thus introduces a versatile strategy to form 2D penetrating mesoporous metallic nanomaterials with extensive high-performance applications.
Keywords: Pt-based catalyst; liquid metal; mesoporous structure; methanol reforming; nanosheet.