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1D Co_4S_3 nanoneedle array with mesoporous carbon derived from double comb copolymer as an efficient solar conversion catalyst

机译:1D CO_4S_3纳尼罩阵列,具有介于高效的太阳能转化催化剂的双梳式共聚物衍生的中孔碳

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摘要

This study investigates the use of a one-dimensional (1D) cobalt sulfide/mesoporous carbon heterogeneous electrocatalyst as counter electrode for high solar energy conversion efficiency in dye-sensitized solar cells (DSSCs). The 1D cobalt oxide (Co4S3) was in situ hydrothermally grown on the fluorine-doped tin oxide glass substrate, followed by sulfurization to form 1D cobalt sulfide (Co4S3) nanoneedle array. The Co4S3 is characterized by a high electrocatalytic activity for reducing/oxidizing the redox couple in the electrolyte. Additionally, the 1D structural feature of the Co4S3 allows fast electron transport through the oriented diffusion pathway. However, the Co4S3 still has relatively low chemical stability and poor electrical conductivity than conventional Pt catalyst. Herein, we incorporated the mesoporous carbon layer derived from the double comb copolymer, i.e., PVDC-g-POEM, which can act as a mesoporous structural template and sufficient carbon source. This strategy increased the electrocatalytic activity and chemical durability of the heterogeneous catalytic materials. The 1D Co4S3/mesoporous carbon heterogeneous catalyst exhibited excellent electrocatalytic activity for the reduction of triiodide, thereby outperforming the conventional Pt counter electrode. The catalytic properties were demonstrated by electrochemical analysis, i.e., cyclic voltammetry and electrochemical impedance spectroscopy. Results suggest that solid-state DSSCs (ssDSSCs) fabricated with the 1D Co4S3/mesoporous carbon counter electrode exhibited a higher solar energy conversion efficiency of 6.2% than the corresponding ssDSSC with conventional Pt (5.7%). The pure 1D Co4S3 or mesoporous carbon showed relatively lower performance than conventional Pt. Accordingly, the 1D Co4S3/mesoporous carbon synergetic approach represents a new strategy for enhancing the catalytic activity and chemical stability for highly efficient ssDSSCs.
机译:本研究研究了一维(1D)钴硫化物/介孔/介孔碳异质电催化剂作为对电极的用于染料敏化太阳能电池(DSSCs)的高太阳能转换效率。将1D钴氧化物(CO 4 S3)原位在氟掺杂的氧化锡玻璃基板上生长,然后硫化以形成1d钴硫化物(CO 4 S3)纳米孔阵列。 Co4S3的特征在于高电催化活性,用于减少/氧化电解质中的氧化还原耦合。另外,CO4S3的1D结构特征允许通过定向的扩散途径快速电子传输。然而,CO 4S3仍具有比常规PT催化剂的化学稳定性较低和差的导电性差。在此,我们掺入源自双梳子共聚物的介孔碳层,即PVDC-G-POEM,其可作为中孔结构模板和足够的碳源。该策略增加了异均相催化材料的电催化活性和化学耐久性。 1D CO 4 S3 /介孔碳异质催化剂表现出优异的电催化活性,用于减少三碘化物,从而优于传统的PT计数器电极。通过电化学分析,即循环伏安法和电化学阻抗光谱证明催化性质。结果表明,用常规Pt(5.7%)表现出与1D CO 4S3 /介孔碳计数器制造的固态DSSCs(SSDSSCs)表现出比相应的SSSSC的更高的太阳能转换效率为6.2%(5.7%)。纯1DCO4S3或中孔碳显示出比常规PT的性能相对较低。因此,1D CO 4S3 /介孔碳协同方法代表了提高高效SSDSSCs的催化活性和化学稳定性的新策略。

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