Zhang Zhen, Liu Bin, Zhou Jian, Sun Zhimei
School of Materials Science and Engineering, Beihang University, Beijing 100191, China.
National Key Laboratory of Spintronics, Hangzhou International Innovation Institute, Beihang University, Hangzhou 311115, China.
Materials (Basel). 2025 Jul 18;18(14):3388. doi: 10.3390/ma18143388.
To investigate the application potential of amorphous transition metal chalcogenides in catalysis, this study successfully synthesized amorphous molybdenum telluride (MoTe) materials and systematically explored their structural characteristics, compositional modulation, and catalytic performance. Experimental results indicate that the synthesized amorphous system consists of particles of approximately 200-300 nm in size. This distinct microstructure facilitates the exposure of abundant active sites and enhances physical adsorption capacity. The amorphous MoTe/MoTe catalysts achieve an approximately 30%/40% degradation of methylene blue (MB) within 90 min, demonstrating significantly enhanced photocatalytic efficiency compared to that of crystalline MoTe (≈20% degradation under identical conditions). Furthermore, when integrated with titanium dioxide (TiO), the composite exhibits exceptional co-catalytic performance, achieving a 90% degradation of MB within 90 min under visible-light irradiation, representing a catalytic efficiency improvement exceeding 160% compared to the results for pristine TiO. Furthermore, through comparative analysis of the catalytic behavior and microstructural variations between amorphous MoTe (a-MoTe) and MoTe (a-MoTe), we observed that the catalytic activity of molybdenum tellurides exhibits a weak correlation with the tellurium content, with co-catalytic efficacy jointly governed by the density of the active sites and the physical adsorption properties. This research provides new methods and insights for the study and improvement of catalytic performance in chalcogenide materials.
为了研究非晶态过渡金属硫族化合物在催化领域的应用潜力,本研究成功合成了非晶态碲化钼(MoTe)材料,并系统地探索了其结构特征、成分调控及催化性能。实验结果表明,合成的非晶态体系由尺寸约为200 - 300 nm的颗粒组成。这种独特的微观结构有利于大量活性位点的暴露,并增强了物理吸附能力。非晶态MoTe/MoTe催化剂在90分钟内可使亚甲基蓝(MB)降解约30%/40%,与结晶态MoTe相比(相同条件下约20%的降解率),光催化效率显著提高。此外,与二氧化钛(TiO)复合时,该复合材料表现出优异的共催化性能,在可见光照射下90分钟内可使MB降解90%,与原始TiO的结果相比,催化效率提高超过160%。此外,通过对非晶态MoTe(a - MoTe)和MoTe(a - MoTe)之间的催化行为和微观结构变化进行对比分析,我们观察到碲化钼的催化活性与碲含量呈弱相关性,共催化效果由活性位点密度和物理吸附性能共同决定。本研究为硫族化合物材料催化性能的研究和改进提供了新方法和新见解。