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Direct synthesis of metastable phases of 2D transition metal dichalcogenides

机译:直接合成2D过渡金属二甲基甲基化物的亚稳相

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摘要

The different polymorphic phases of transition metal dichalcogenides (TMDs) have attracted enormous interest in the last decade. The metastable metallic and small band gap phases of group VI TMDs displayed leading performance for electrocatalytic hydrogen evolution, high volumetric capacitance and some of them exhibit large gap quantum spin Hall (QSH) insulating behaviour. Metastable 1T(1T ') phases require higher formation energy, as compared to the thermodynamically stable 2H phase, thus in standard chemical vapour deposition and vapour transport processes the materials normally grow in the 2H phases. Only destabilization of their 2H phaseviaexternal means, such as charge transfer or high electric field, allows the conversion of the crystal structure into the 1T(1T ') phase. Bottom-up synthesis of materials in the 1T(1T ') phases in measurable quantities would broaden their prospective applications and practical utilization. There is an emerging evidence that some of these 1T(1T ') phases can be directly synthesizedviabottom-up vapour- and liquid-phase methods. This review will provide an overview of the synthesis strategies which have been designed to achieve the crystal phase control in TMDs, and the chemical mechanisms that can drive the synthesis of metastable phases. We will provide a critical comparison between growth pathways in vapour- and liquid-phase synthesis techniques. Morphological and chemical characteristics of synthesized materials will be described along with their ability to act as electrocatalysts for the hydrogen evolution reaction from water. Phase stability and reversibility will be discussed and new potential applications will be introduced. This review aims at providing insights into the fundamental understanding of the favourable synthetic conditions for the stabilization of metastable TMD crystals and at stimulating future advancements in the field of large-scale synthesis of materials with crystal phase control.
机译:过渡金属二甲基甲基化物(TMDS)的不同多态性相引起了过去十年的巨大兴趣。 VI TMDS组的亚稳金属和小带隙相显示电催化氢进化,高容量电容和其中一些具有大的间隙量子旋转大厅(QSH)绝缘行为。与热力学稳定的2H相相比,亚稳定的1T(1T')相需要较高的形成能量,因此在标准化学气相沉积和蒸汽转运过程中,材料通常在2H相中生长。只有其2H的普适亚维亚透视或电荷转移或高电场的稳定化允许将晶体结构转化为1T(1T')相。在可衡量的数量中,1T(1T')阶段的自下而上的材料将扩大其前瞻性应用和实际利用。存在新兴的证据表明,这些1T(1T')阶段中的一些可以是直接合成的互相合成VAPOUR和液相方法。该审查将概述已经设计用于在TMDS中实现晶体相控制的合成策略,以及可以驱动亚稳阶段合成的化学机制。我们将在VAPOUR-和液相合成技术中的生长途径之间提供致命的比较。将描述合成材料的形态学和化学特性以及它们作为从水中的氢进化反应的电催化剂的能力。将讨论相位稳定性和可逆性,并介绍新的潜在应用。本综述旨在提供对稳定亚稳态TMD晶体稳定的有利合成条件的基本理解的见解,并在晶体相控件中刺激大规模合成材料领域的未来进展。

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