化学
双金属片
纳米颗粒
吸附
质子化
金属
水溶液
催化作用
表面电荷
零电荷点
静电学
化学工程
脱质子化
无机化学
纳米技术
静电相互作用
航程(航空)
带电粒子
水介质
复合数
初湿浸渍
水溶液中的金属离子
过渡金属
银纳米粒子
作者
John R. Regalbuto,Ismail Paykar,Yanjiao Yi,Nathan Thornburg,Roozbeh Seifollahy Astaraee,Kevin Enyekwe,Chigozie J. Ezeorah,John Meynard M. Tengco
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2026-08-18
卷期号:126 (17): 9987-10043
被引量:1
标识
DOI:10.1021/acs.chemrev.5c01067
摘要
A simple, scientific method to prepare supported metal nanoparticles was proposed almost 50 years ago, which utilizes the protonation-deprotonation chemistry of the nascent hydroxyl groups that populate typical support surfaces. In aqueous solution, these can be protonated and so positively charged in the pH range below the point of zero charge (PZC) of the support, and deprotonated and negatively charged above the support PZC. An oppositely charged metal complex in the impregnating solution will experience a strong electrostatic attraction to the surface and will be firmly anchored during drying. The metal nanoparticles produced after thermochemical conversion of the dried precursor are typically small (<2 nm) and tightly sized. In this review, the past 50 years of literature reporting this method have been summarized and critiqued. Electrostatic adsorption has been applied for 1) the preparation of single metal nanoparticles on a wide variety of supports, including single-atom catalysts, 2) well alloyed bimetallic and dilute limit nanoparticles, and 3) selective metal deposition over composite supports. The method has been extended to 4) incipient wetness impregnation and, most recently, to 5) formed catalyst supports. The limitations, troubleshooting, and future directions of this method are discussed.
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