硝酸盐
电催化剂
环境修复
环境科学
氨生产
水生生态系统
环境化学
生化工程
化学
持续性
水污染
环境工程
电解质
污染
氮气
降级(电信)
营养污染
地下水修复
作者
Tong Zhao,Y. C. Chen,Kang L. Wang,Shih‐Hsin Ho
标识
DOI:10.1021/acs.est.5c14726
摘要
Anthropogenic disruption of the nitrogen cycle has led to pervasive nitrate (NO3–) contamination in aquatic systems, posing risks to environmental integrity and public health. Electrocatalytic nitrate reduction reaction (eNO3–RR) to ammonia (NH3) offers simultaneous remediation and resource recovery under ambient conditions. However, most studies have mainly been conducted in strongly alkaline electrolytes for their high ionic conductivity and suppressed hydrogen evolution reaction, despite inducing corrosive degradation and scaling issues that limit practical deployment. Critically, the neutral pH characteristic of most natural and contaminated waters offers environmentally compatible conditions, spurring growing research interest in neutral media to bridge laboratory-to-field relevance. Given the absence of systematic understanding of neutral eNO3–RR, a timely and comprehensive review is urgently needed. This review provides a comprehensive synthesis of mechanistic understanding, catalyst development, and system-level advances specifically for neutral conditions. We summarize thermodynamic and kinetic insights into NO3–-to-NH3, outline the influence of environmental factors on mechanisms, evaluate strategies including doping, defect, phase control, interfacial engineering, microenvironment tuning, and surface reconstruction, and discuss recent progress in electrolyte optimization and reactor design. Eventually, application scenarios for neutral-pH eNO3–RR are discussed to bridge fundamental understanding with practical implementation, offering perspectives for its role in future sustainable nitrogen management.
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