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基于键能的、低角度晶界或高角度晶界迁移介导的多孔硒碲合成及其在水分解反应中的应用。

Bond-Energy-Driven, Low- or High-Angle-Grain-Boundary-Movement-Mediated Synthesis of Porous Se-Te for Use in Water-Splitting Reactions.

机构信息

Department of Chemistry, Indian Institute of Technology , Kharagpur 721302, India.

Materials Science Centre, Indian Institute of Technology , Kharagpur 721302, India.

出版信息

ACS Appl Mater Interfaces. 2017 Dec 6;9(48):41818-41826. doi: 10.1021/acsami.7b10466. Epub 2017 Nov 27.

DOI:10.1021/acsami.7b10466
PMID:29148703
Abstract

Herein, for the first time, we applied the metal-metal-bond-energy factor to the evolution of a porous Se-Te alloy. The porous Se-Te material has been prepared from the constituents' elemental states, through only a heating-cooling process in silicone oil without the use of any reagent, surfactant, or capping agent. Surprisingly, the reaction occurred at a much lower temperature (240 °C) than the mp (450 °C) of Te. The reaction's nucleation and growth by means of varied bond energy have been clarified for the first time. A difference in the bond energies of a hetero metal-metal bond (Se-Te) and a homo metal-metal bond (Se-Se) directs nucleation and growth toward the fabrication of a porous structure, even from the constituents' elemental states, in which low-angle-grain-boundary (LAGB) and high-angle-grain-boundary (HAGB) movements play governing roles. Proper band-gap alignment of Se and Te makes the alloy composite applicable to water-splitting reactions under Xe-arc-lamp illumination. PEC efficiency of Se-Te was found to be higher than those reported for Se and other composite materials.

摘要

在此,我们首次将金属-金属键能因子应用于多孔硒碲合金的演变。通过仅在硅油中进行加热-冷却过程,从元素状态制备多孔 Se-Te 材料,而无需使用任何试剂、表面活性剂或封端剂。令人惊讶的是,反应发生的温度(240°C)远低于 Te 的熔点(450°C)。首次阐明了通过不同键能进行反应成核和生长的过程。杂金属-金属键(Se-Te)和同金属-金属键(Se-Se)的键能差异指导成核和生长,即使从元素状态的组成部分,也能制备出多孔结构,其中小角度晶界(LAGB)和大角度晶界(HAGB)的运动起着主要作用。Se 和 Te 的适当能带隙排列使合金复合材料适用于 Xe 弧光灯照射下的水分解反应。发现 Se-Te 的 PEC 效率高于报道的 Se 和其他复合材料的效率。

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