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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Surfactant-Free Approach for Engineering an Ultrathin Ti-Doped Ni(OH)(2) Nanosheet on Carbon Cloth: Experimental and Theoretical Insight into Boosted Alkaline Water Oxidation Activity
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Surfactant-Free Approach for Engineering an Ultrathin Ti-Doped Ni(OH)(2) Nanosheet on Carbon Cloth: Experimental and Theoretical Insight into Boosted Alkaline Water Oxidation Activity

机译:无表面活性剂的工程方法是碳布中的超薄Ti掺杂Ni(OH)(2)纳米液:对增强碱性水氧化活性的实验和理论洞察

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摘要

Ti-based layered double hydroxides (LDHs) have enormous potential in photocatalysis, electrocatalysis, and photoelectrocatalysis. However, Ti-based LDHs are rarely reported because of the difficulties of the preparation process, in which the Ti precursors are more prone to hydrolysis into titanium hydroxide. In this work, toward robust, efficient, and earth-abundant electrocatalysts for water oxidation in alkaline environments, we have engineered Ti-doped Ni(OH)(2) nanosheet arrays on carbon cloth [Ti-Ni(OH)(2)/CC] with a facile solvothermal and surfactant-free method. The experimental tests show that the activity of Ti-Ni(OH)(2)-1/CC (similar to 12.5 atom % Ti substitution) is optimal among these materials. In addition, the activity is correlated with the Ti substitution ratio and reversed with higher Ti doping level (>= 25 atom % Ti substitution). Therein, eta(10) of Ti-Ni(OH)(2)-1/CC is as low as 196 mV, and it is still maintained at 210 mV after a long-term chronopotentiometry (CP) test at a constant current density of 10 mA cm(-2). for 32 h, demonstrating superior activity and long-term durability. Density functional theory calculations further reveal that dilute Ti substitution produces extra active sites and promotes more optimal OH* adsorption to the surface of the electrocatalyst.
机译:基于TI的层状双氢氧化物(LDHs)在光催化,电催化和光电二核分析中具有巨大潜力。然而,由于制备方法的困难,即基于Ti的LDH是很少报道的,其中Ti前体更容易发生成氢氧化钛。在这项工作中,朝向碱性环境中的水氧化的稳健,高效和瓦尔丰富的电催化剂,我们已经设计了Ti-Doped Ni(OH)(2)纳米晶片阵列[Ti-Ni(OH)(2)/ CC]具有容易的溶剂热和无表面活性剂的方法。实验试验表明,Ti-Ni(OH)(2)-1 / Cc(类似于12.5原子%Ti替代)的活性在这些材料中是最佳的。此外,活性与Ti取代率相关,并以更高的Ti掺杂水平(> = 25原子%Ti替代)反转。其中,Ti-Ni(OH)(2)-1 / Cc的ETA(10)低至196mV,并且在恒定电流密度下在长期时间计量(CP)测试之后仍保持在210mV下10 mA cm(-2)。 32小时,展示优异的活动和长期耐久性。密度函数理论计算进一步揭示了稀释Ti取代产生额外的活性位点,并促进更优选OH *对电催化剂表面的吸附。

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