Advances in plasma-driven solution electrochemistry

化学过程 氧化还原 等离子体 电化学 化学种类 液相 纳米技术 相(物质) 化学反应 血浆药物 化学 材料科学 生化工程 电极 大气压等离子体 有机化学 工程类 物理 量子力学 热力学 物理化学
作者
Peter Bruggeman,Renee R. Frontiera,Uwe Kortshagen,Mark J. Kushner,Suljo Linic,George C. Schatz,Himashi P. Andaraarachchi,Subhajyoti Chaudhuri,Han‐Ting Chen,C. Clay,Tiago Cunha Dias,Scott Doyle,Leighton O. Jones,Mackenzie Meyer,Chelsea M. Mueller,Jae Hyun Nam,Astrid Raisanen,Christopher C. Rich,Tanubhav Srivastava,Chi Xu
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:162 (7)
标识
DOI:10.1063/5.0248579
摘要

Energetic species produced by gas-phase plasmas that impinge on a liquid surface can initiate physicochemical processes at the gas/liquid interface and in the liquid phase. The interaction of these energetic species with the liquid phase can initiate chemical reaction pathways referred to as plasma-driven solution electrochemistry (PDSE). There are several processing opportunities and challenges presented by PDSE. These include the potential use of PDSE to activate chemical pathways that are difficult to activate with other approaches as well as the use of renewable electricity to generate plasmas that could make these liquid-phase chemical conversion processes more sustainable and environmentally friendly. In this review, we focus on PDSE as an approach for controlled and selective chemical conversion including the synthesis of nanoparticles and polymers with desired but currently uncontrollable or unattainable properties as the next step in the use of PDSE. The underpinning redox chemistry and transport processes of PDSE are reviewed as many PDSE-driven processes are transport-limited due to the many short-lived highly reactive species involved.

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