Mimicking High-Silica Zeolites: Highly Stable Germanium- and Tin-Rich Zeolite-Type Chalcogenides

化学 沸石 吸附 热稳定性 催化作用 化学工程 光催化 离子交换 化学稳定性 无机化学 多孔性 离子 物理化学 有机化学 工程类
作者
Qipu Lin,Xianhui Bu,Chengyu Mao,Xiang Zhao,Koroush Sasan,Pingyun Feng
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:137 (19): 6184-6187 被引量:118
标识
DOI:10.1021/jacs.5b03550
摘要

High-silica zeolites, as exemplified by ZSM-5, with excellent chemical and thermal stability, have generated a revolution in industrial catalysis. In contrast, prior to this work, high-silica-zeolite-like chalcogenides based on germanium/tin remained unknown, even after decades of research. Here six crystalline high-germanium or high-tin zeolite-type sulfides and selenides with four different topologies are reported. Their unprecedented framework compositions give these materials much improved thermal and chemical stability with high surface area (Langmuir surface area of 782 m(2)/g(-1)) comparable to or better than zeolites. Among them, highly stable CPM-120-ZnGeS allows for ion exchange with diverse metal or complex cations, resulting in fine-tuning in porosity, fast ion conductivity, and photoelectric response. Being among the most porous crystalline chalcogenides, CPM-120-ZnGeS (exchanged with Cs(+) ions) also shows reversible adsorption with high capacity and affinity for CO2 (98 and 73 cm(3) g(-1) at 273 and 298 K, respectively, isosteric heat of adsorption = 40.05 kJ mol(-1)). Moreover, CPM-120-ZnGeS could also function as a robust photocatalyst for water reduction to generate H2. The overall activity of H2 production from water, in the presence of Na2S-Na2SO3 as a hole scavenger, was 200 μmol h(-1)/(0.10 g). Such catalytic activity remained undiminished under illumination by UV light for as long as measured (200 h), demonstrating excellent resistance to photocorrosion even under intense UV radiation.
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