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Electrochemical maps and movies of the hydrogen evolution reaction on natural crystals of molybdenite (MoS2): basal vs. edge plane activity

机译:辉钼矿(MoS2)天然晶体上氢放出反应的电化学图和影片:基础与边缘平面活性

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摘要

Two dimensional (2D) semiconductor materials, such as molybdenum disulfide (MoS2) have attracted considerable interest in a range of chemical and electrochemical applications, for example, as an abundant and low-cost alternative electrocatalyst to platinum for the hydrogen evolution reaction (HER). While it has been proposed that the edge plane of MoS2 possesses high catalytic activity for the HER relative to the “catalytically inert” basal plane, this conclusion has been drawn mainly from macroscale electrochemical (voltammetric) measurements, which reflect the “average” electrocatalytic behavior of complex electrode ensembles. In this work, we report the first spatially-resolved measurements of HER activity on natural crystals of molybdenite, achieved using voltammetric scanning electrochemical cell microscopy (SECCM), whereby pixel-resolved linear-sweep voltammogram (LSV) measurements have allowed the HER to be visualized at multiple different potentials to construct electrochemical flux movies with nanoscale resolution. Key features of the SECCM technique are that characteristic surface sites can be targeted and analyzed in detail and, further, that the electrocatalyst area is known with good precision (in contrast to many macroscale measurements on supported catalysts). Through correlation of the local voltammetric response with information from scanning electron microscopy (SEM) and atomic force microscopy (AFM) in a multi-microscopy approach, it is demonstrated unequivocally that while the basal plane of bulk MoS2 (2H crystal phase) possesses significant activity, the HER is greatly facilitated at the edge plane (e.g., surface defects such as steps, edges or crevices). Semi-quantitative treatment of the voltammetric data reveals that the HER at the basal plane of MoS2 has a Tafel slope and exchange current density (J 0) of ∼120 mV per decade and 2.5 × 10–6 A cm–2 (comparable to polycrystalline Co, Ni, Cu and Au), respectively, while the edge plane has a comparable Tafel slope and a J 0 that is estimated to be more than an order-of-magnitude larger (∼1 × 10–4 A cm–2). Finally, by tracking the temporal evolution of water contact angle (WCA) after cleavage, it is shown that cathodic polarization has a ‘self-cleaning’ effect on the surface of MoS2, consistent with the time-independent (i.e., time after cleavage) HER voltammetric response.
机译:二维(2D)半导体材料,例如二硫化钼(MoS2)在化学和电化学应用领域中引起了相当大的兴趣,例如,作为用于氢气析出反应(HER)的铂的丰富且低成本的替代电催化剂。虽然有人提出,相对于“催化惰性”的基础平面,MoS2的边缘平面对HER具有较高的催化活性,但该结论主要来自宏观电化学(伏安)测量,反映了“平均”电催化行为复杂的电极组。在这项工作中,我们报告了使用伏安扫描电化学电池显微镜(SECCM)进行的首次空间分辨测量,该测量是对辉钼矿天然晶体进行HER活性的,其中像素分辨线性扫描伏安图(LSV)测量已允许HER在多个不同的电位下可视化以构建具有纳米级分辨率的电化学助焊剂薄膜。 SECCM技术的关键特征是可以针对性地对特征表面进行定位和详细分析,此外,已知电催化剂区域的精度很高(与负载型催化剂的许多宏观测量相反)。通过在多显微镜方法中将局部伏安响应与来自扫描电子显微镜(SEM)和原子力显微镜(AFM)的信息相关联,可以清楚地证明,虽然块状MoS2(2H晶相)的基面具有显着的活性,在边缘平面处大大促进了HER(例如,表面缺陷,例如台阶,边缘或缝隙)。伏安数据的半定量处理表明,MoS2基面上的HER的Tafel斜率和交换电流密度(J 0)为每十倍〜120 mV,2.5×10 –6 A cm –2 (分别相当于多晶Co,Ni,Cu和Au),而边缘平面具有可比的Tafel斜率和J 0,估计大于一个数量级幅度更大(〜1×10 –4 A cm –2 )。最后,通过追踪裂解后水接触角(WCA)的时间演变,表明阴极极化对MoS2表面具有“自清洁”作用,与时间无关(即裂解后的时间)一致HER伏安法反应。

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