首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >A superior dye adsorbent towards the hydrogen evolution reaction combining active sites and phase-engineering of (1T/2H) MoS2/-MoO3 hybrid heterostructured nanoflowers
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A superior dye adsorbent towards the hydrogen evolution reaction combining active sites and phase-engineering of (1T/2H) MoS2/-MoO3 hybrid heterostructured nanoflowers

机译:朝向氢进化反应的优异染料吸附剂,组合活性位点和(1T / 2H)MOS2 / -MOO3杂交异质结构纳米割草机的活性位点和相工程

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Here, we demonstrate the successful synthesis of (1T/2H) MoS2/-MoO3 heterostructured nanoflowers at a low temperature of 200 degrees C by a one-step hydrothermal method. By tuning the reaction time under the influence of thiourea and hydrazine hydrate, we established a complete phase-engineered MoS2 with 1T and 2H phases on the surface of -MoO3. Active sites associated with the phase-engineered (1T/2H) MoS2/-MoO3 hybrid nanoflowers enable them to exhibit dual roles as a superior dye adsorbent and an electrocatalyst towards the hydrogen evolution reaction. The 2H-rich (1T/2H) MoS2/-MoO3 hybrid heterostructured nanoflowers prepared at 16 h achieved a high surface area of 37.97 m(2) g(-1), and 97% of the RhB dye with an initial concentration of 47.9 mg L-1 was removed within 10 min through the adsorption process, which is the highest known removal efficiency reported in the literature. As a hydrogen evolution reaction (HER) electrocatalyst in acidic solution, the 1T-rich (1T/2H) MoS2/-MoO3 hybrid heterostructured nanoflowers prepared at 12 h exhibited a highly efficient catalytic activity by achieving a low overpotential of 232 mV at a current density of 10 mA cm(-2), which is comparable to those of previously reported HER catalysts based on MoS2. Moreover, this sample reached a low Tafel slope of 81 mV dec(-1) and was stable when operated for more than 1000 cycles.
机译:这里,我们证明(1T / 2H)的MoS 2 / -MoO3异质纳米花的成功合成在由一步法水热法的低温下的200℃。通过硫脲和水合肼的影响下调整反应时间,我们-MoO3的表面上建立了完整的相位设计的二硫化钼与1T和2H阶段。与相工程(1T / 2H)相关联的活性位点的二硫化钼/ -MoO3混合纳米花使它们能够表现出双重角色作为优良染料吸附剂并朝向析氢反应的电催化剂。所述2H富含(1T / 2H)的MoS 2 / -MoO3混合异质结构在16小时制备的纳米花实现37.97米(2)g的高表面积(-1),并用47.9的初始浓度的罗丹明B染料的97%毫克L-1是通过吸附过程,这是最高的已知的去除效率在文献中报道在10分钟内除去。如在酸性溶液中析氢反应(HER)电,富1T-(1T / 2H)的MoS 2 / -MoO3混合异质结构在12小时制备的纳米花通过在当前实现低超电势232毫伏的表现出高效率的催化活性为10mA厘米(-2),这与那些先前报道密度HER基于二硫化钼催化剂。此外,该样品达到81毫伏分解(-1)的低塔菲尔斜率,并且当超过1000次循环操作是稳定的。

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