Burmeister David, Müller Johannes, Plaickner Julian, Kochovski Zdravko, List-Kratochvil Emil J W, Bojdys Michael J
Department of Chemistry & IRIS Adlershof, Humboldt-Universität zu Berlin, Brook-Taylor-Str. 6, 12489, Berlin, Germany.
Department of Physics & IRIS Adlershof, Humboldt-Universität zu Berlin, Newtonstraße 15, 12489, Berlin, Germany.
Chemistry. 2022 Jun 10;28(33):e202200705. doi: 10.1002/chem.202200705. Epub 2022 May 2.
Semiconducting carbon nitride polymers are used in metal-free photocatalysts and in opto-electronic devices. Conventionally, they are obtained using thermal and ionothermal syntheses in inscrutable, closed systems and therefore, their condensation behavior is poorly understood. Here, the synthetic protocols and properties are compared for two types of carbon nitride materials - 2D layered poly(triazine imide) (PTI) and hydrogen-bonded melem hydrate - obtained from three low-melting salt eutectics taken from the systematic series of the alkali metal halides: LiCl/KCl, LiBr/KBr, and LiI/KI. The size of the anion plays a significant role in the formation process of the condensed carbon nitride polymers, and it suggests a strong templating effect. The smaller anions (chloride and bromide) become incorporated into triazine (C N )-based PTI frameworks. The larger iodide does not stabilize the formation of a triazine-based polymer, but instead it leads to the formation of the heptazine (C N )-based hydrogen-bonded melem hydrate as the main crystalline phase. Melem hydrate, obtained as single-crystalline powders, was compared with PTI in photocatalytic hydrogen evolution from water and in an OLED device. Further, the emergence of each carbon nitride species from its corresponding salt eutectic was rationalized via density functional theory calculations. This study highlights the possibilities to further tailor the properties of eutectic salt melts for ionothermal synthesis of organic functional materials.
半导体氮化碳聚合物用于无金属光催化剂和光电器件中。传统上,它们是在难以捉摸的封闭系统中通过热合成和离子热合成获得的,因此,人们对它们的缩合行为了解甚少。在此,对两种类型的氮化碳材料——二维层状聚(三嗪酰亚胺)(PTI)和氢键连接的蜜勒胺水合物——进行了合成方案和性能比较,这两种材料是由从碱金属卤化物的系统系列中选取的三种低熔点盐共晶体制备得到的:LiCl/KCl、LiBr/KBr和LiI/KI。阴离子的大小在缩合氮化碳聚合物的形成过程中起着重要作用,这表明存在强烈的模板效应。较小的阴离子(氯离子和溴离子)会掺入基于三嗪(C N )的PTI骨架中。较大的碘离子不能稳定基于三嗪的聚合物的形成,而是导致形成以七嗪(C N )为基础的氢键连接的蜜勒胺水合物作为主要晶相。将作为单晶粉末获得的蜜勒胺水合物与PTI在光催化水制氢和OLED器件方面进行了比较。此外,通过密度泛函理论计算解释了每种氮化碳物种从其相应的盐共晶中出现的原因。这项研究突出了进一步调整共晶盐熔体的性质以用于有机功能材料的离子热合成的可能性。