电催化剂
法拉第效率
催化作用
材料科学
碳纤维
炭黑
纳米颗粒
氧化还原
热解炭
选择性
金属
化学工程
粒径
无机化学
纳米技术
电化学
化学
电极
物理化学
冶金
复合数
复合材料
有机化学
天然橡胶
热解
工程类
作者
Xingyi Deng,Dominic Alfonso,Thuy‐Duong Nguyen‐Phan,Douglas R. Kauffman
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2023-11-10
卷期号:13 (23): 15301-15309
被引量:30
标识
DOI:10.1021/acscatal.3c03446
摘要
We demonstrate that electronic metal–support interactions (EMSIs) between silver and carbon can dramatically improve the CO2 reduction reaction (CO2RR) performance of the small Ag nanoparticles. Ag–C EMSIs were created by ultrahigh vacuum deposition of Ag onto defect-containing (sputtered) highly oriented pyrolytic graphite, and calculations predicted that 1.02 e was transferred from Ag to carbon, which stabilized the *COOH reaction intermediate, lowered the potential-limiting CO2RR step, and improved the predicted CO2-to-CO performance. Experimentally, we identified a scaling relationship between particle size and the relative Ag–C EMSI strength, which improved the CO2-to-CO Faradaic efficiency of sub-2 nm Ag particles from 2 to ∼100% and increased the CO turnover frequency ∼15-fold compared with similarly sized Ag particles grown in the absence of Ag–C EMSIs. We extended this concept to grow sub-2 nm Ag electrocatalysts on commonly used carbon black catalyst supports and showed that the interaction with support defects could sustain CO selectivity comparable to larger particles, suggesting an approach for tailoring CO2RR electrocatalyst performance.
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