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具有高光催化水分解效率的直接Z型PtS/砷烯范德华异质结构

A direct Z-scheme PtS/arsenene van der Waals heterostructure with high photocatalytic water splitting efficiency.

作者信息

Ren Kai, Tang Wencheng, Sun Minglei, Cai Yongqing, Cheng Yuan, Zhang Gang

机构信息

School of Mechanical Engineering, Southeast University, Nanjing, Jiangsu 211189, China.

出版信息

Nanoscale. 2020 Sep 7;12(33):17281-17289. doi: 10.1039/d0nr02286a. Epub 2020 Jul 7.

Abstract

To overcome current serious energy and environmental issues, photocatalytic water splitting holds great promise because it requires only solar energy as an energy input to produce hydrogen. In this work, based on first-principle calculations, we studied the van der Waals heterostructure formed by PtS and arsenene (Are) monolayers that were successfully synthesized on a large scale at high quality. From an analysis of the migration paths of photoinduced electrons and holes, a direct Z-scheme photocatalytic mechanism is demonstrated in this heterostructure. Furthermore, the PtS/Are direct Z-scheme heterostructure has decent band edge positions to promote the redox reaction to decompose water at pH 0. The interfacial charge difference and potential drop are presented, which further support the formation of a direct Z-scheme photocatalyst. More importantly, the PtS/Are heterostructure has quite high solar-to-hydrogen (STH) efficiency (49.32%), significantly enhanced compared with isolated PtS (12.67%) or Are (10.34%) monolayers. This direct Z-scheme PtS/Are heterostructure with excellent STH efficiency suggests its promising application as a photocatalyst for water splitting.

摘要

为了克服当前严峻的能源和环境问题,光催化水分解具有巨大潜力,因为它仅需太阳能作为能量输入来制氢。在这项工作中,基于第一性原理计算,我们研究了由高质量大规模成功合成的PtS和砷烯(Are)单层形成的范德华异质结构。通过对光生电子和空穴迁移路径的分析,证明了该异质结构中存在直接Z型光催化机制。此外,PtS/Are直接Z型异质结构具有合适的能带边缘位置,可促进氧化还原反应在pH值为0时分解水。给出了界面电荷差和电势降,进一步支持了直接Z型光催化剂的形成。更重要的是,PtS/Are异质结构具有相当高的太阳能到氢能(STH)效率(49.32%),与孤立的PtS(12.67%)或Are(10.34%)单层相比有显著提高。这种具有优异STH效率的直接Z型PtS/Are异质结构表明其作为水分解光催化剂具有广阔的应用前景。

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