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Strong Electronic Interaction Enhanced Electrocatalysis of Metal Sulfide Clusters Embedded Metal–Organic Framework Ultrathin Nanosheets toward Highly Efficient Overall Water Splitting

机译:强电子相互作用增强金属硫化物簇的电常分嵌入金属 - 有机框架超薄纳米液朝向高效的整体水分裂

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Unique metal sulfide (MS) clusters embedded ultrathin nanosheets of Fe/Ni metal–organic framework (MOF) are grown on nickel foam (NiFe‐MS/MOF@NF) as a highly efficient bifunctional electrocatalyst for overall water splitting. It exhibits remarkable catalytic activity and stability toward both the oxygen evolution reaction (OER, ? = 230 mV at 50?mA cm?2) and hydrogen evolution reaction (HER, ? = 156 mV at 50?mA cm?2) in alkaline media, and bi‐functionally catalyzes overall alkaline water splitting at a current density of 50?mA cm?2 by 1.74?V cell voltage without iR compensation. The enhancement mechanism is ascribed to the impregnated metal sulfide clusters in the nanosheets, which not only promote the formation of ultrathin nanosheet to greatly enlarge the reaction surface area while offering high electric conductivity, but more importantly, efficiently modulate the electronic structure of the catalytically active atom sites to an electron‐rich state via strong electronic interaction and strengthen the adsorption of oxygenate intermediate to facilitate fast electrochemical reactions. This work reports a highly efficient HER/OER bifunctional electrocatalyst and may shed light on the rational design and synthesis of uniquely structured MOF‐derived catalysts.
机译:独特的金属硫化物(MS)簇嵌入Fe / Ni金属 - 有机框架(MOF)的超薄纳米片以镍泡沫(NiFe-MS / MOF @ NF)生长为整体水分裂的高效双官能电催化剂。它表现出显着的催化活性和朝向氧气进化反应(oer,α= 230mV,α230mV)和碱性介质中的氢进化反应(α= 156mV)并且双功能催化在电流密度为50Ωma = 2的整个碱性水分分裂,达1.74Ω·V电池电压而没有IR补偿。增强机构归因于纳米片中的浸渍金属硫化物簇,其不仅促进超薄纳米片的形成,以极大地扩大反应表面积,同时提供高导电性,但更重要的是,有效地调节催化活性的电子结构通过强电子相互作用和加强含氧化学物质的吸附以促进快速电化学反应的富含电子的原子位点。这项工作报告了一个高效的HER / OER双功能电催化剂,并且可以在合理的设计和合成唯一结构化的MOF衍生的催化剂上脱光。

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