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用于增强肖特基结压电催化的二硫化钼中的单原子工程与相变优化

Single-Atom Engineering and Phase-Transition Optimization in MoS for Enhanced Schottky Junction Piezocatalysis.

作者信息

Shen Xinjie, Pan Chenglei, Wei Xiuzhen, Liu Jinzhou, Liu Mingyang, Liu Guanyu, Pan Meilan

机构信息

College of Environment, Zhejiang University of Technology, Hangzhou 310014, P. R. China.

Functional Materials Research Laboratory, School of Materials Science and Engineering, Tongji University, Shanghai 201804, China.

出版信息

ACS Nano. 2025 Aug 12;19(31):28257-28267. doi: 10.1021/acsnano.5c05239. Epub 2025 Aug 1.

Abstract

Molybdenum disulfide (MoS) has attracted considerable attention as a piezocatalyst due to its distinctive piezoelectric properties and potential for environmental remediation. However, its practical application is limited by the metastability of the 1T phase and inconsistent doping, which result in nonuniform Schottky barrier heights and inefficient charge transfer, ultimately restricting catalytic performance and long-term stability. In this study, we developed a high-performance piezocatalyst by designing a hybrid-phase MoS Schottky junction, comprising both 1T and 2H phases, and incorporating cobalt single atoms (Co-T/H MoS). The introduction of Co single atoms enhances the piezoelectric properties through local structural distortions induced by Co-S covalent bonding. This incorporation also promotes the formation of the 1T phase in MoS, increasing the density of Schottky junctions, which effectively reduces electron backflow and improves charge separation. Furthermore, the piezoelectric polarization of 2H MoS lowers the Schottky barrier, facilitating electron transfer to the 1T phase. The resulting Co-T/H MoS achieves a reaction rate of 1.08 min for ciprofloxacin (CIP) degradation, which is 15.9 times higher than the 0.068 min rate observed for bare 2H MoS. This superior degradation efficiency is attributed to the high density of Schottky junctions, which enhance oxygen activation and promote the generation of superoxide radicals (•O), crucial for CIP removal. These findings provide valuable insights into piezocatalytic mechanisms and underscore the potential of designing efficient piezocatalysts for practical environmental applications.

摘要

二硫化钼(MoS)因其独特的压电特性和环境修复潜力,作为一种压电催化剂受到了广泛关注。然而,其实际应用受到1T相的亚稳定性和掺杂不一致的限制,这导致肖特基势垒高度不均匀和电荷转移效率低下,最终限制了催化性能和长期稳定性。在本研究中,我们通过设计一种包含1T和2H相的混合相MoS肖特基结,并引入钴单原子(Co-T/H MoS),开发了一种高性能压电催化剂。钴单原子的引入通过Co-S共价键引起的局部结构畸变增强了压电性能。这种引入还促进了MoS中1T相的形成,增加了肖特基结的密度,有效减少了电子回流并改善了电荷分离。此外,2H MoS的压电极化降低了肖特基势垒,促进了电子向1T相的转移。由此得到的Co-T/H MoS对环丙沙星(CIP)降解的反应速率为1.08 min,这比纯2H MoS观察到的0.068 min的速率高15.9倍。这种优异降解效率归因于肖特基结的高密度,其增强了氧活化并促进了超氧自由基(•O)的产生,这对CIP去除至关重要。这些发现为压电催化机制提供了有价值的见解,并强调了设计高效压电催化剂用于实际环境应用的潜力。

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