催化作用
生化工程
合理设计
纳米技术
电化学
电化学储能
降级(电信)
离子液体
理论(学习稳定性)
离子键合
计算机科学
设计要素和原则
材料科学
结构稳定性
电化学能量转换
机制(生物学)
金属
工艺工程
燃料电池
化学
数码产品
储能
反应条件
作者
Alexis Hellmer,Mariana Molina-Torres,Rubén Mendoza‐Cruz
标识
DOI:10.1021/acscatal.6c01167
摘要
Single-atom catalysts (SACs) offer significant opportunities for maximizing metal utilization and tailoring active-site structures in electro- and thermocatalytic processes; however, their widespread implementation remains constrained by limited structural stability across synthesis, characterization, and operating conditions. This review critically examines the fundamental origins of SAC instability and systematically analyzes both conventional and emergent stabilization strategies reported in recent literature. The discussion integrates stability challenges arising during catalyst preparation, beam- and environment-induced transformations during characterization, and degradation pathways under electrochemical and high-temperature reaction conditions. Traditional approaches, including spatial confinement, coordination environment engineering, and strong and electronic metal−support interactions, are evaluated alongside emerging strategies such as plasma-based treatments, electrochemical potential control, ligand-assisted stabilization, ionic liquids, and atmosphere-dependent regeneration. By comparing stabilization mechanisms across electrocatalytic and thermocatalytic contexts, this review clarifies how distinct driving forces govern atom migration, dissolution, and aggregation. The major conclusion is that no single strategy universally ensures SAC stability; rather, rational integration of complementary stabilization principles, informed by operando insights, is required to achieve durable single-atom architectures. These insights provide a structured design framework for the development of robust SACs suitable for long-term energy and environmental applications.
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