对偶(语法数字)
硝酸盐
还原(数学)
化学
Atom(片上系统)
材料科学
组合化学
计算化学
纳米技术
有机化学
数学
计算机科学
几何学
文学类
艺术
嵌入式系统
作者
Yao Hu,Haihui Lan,Junjun He,Wenjing Fang,Wenda Zhang,Shuanglong Lu,Fang Duan,Mingliang Du
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-07-24
卷期号:18 (34): 23168-23180
被引量:6
标识
DOI:10.1021/acsnano.4c05568
摘要
Despite the immense potential of Dual Single-Atom Compounds (DSACs), the challenges in their synthesis process, including complexity, stability, purity, and scalability, remain primary concerns in current research. Here, we present a general strategy, termed "Entropy-Engineered Middle-In Synthesis of Dual Single-Atom Compounds" (EEMIS-DSAC), which is meticulously crafted to produce a diverse range of DSACs, effectively addressing the aforementioned issues. Our strategy integrates the advantages of both bottom-up and top-down paradigms, proposing an insight into optimizing the catalyst structure. The as-fabricated DSACs exhibited excellent activity and stability in the nitrate reduction reaction (NO3RR). In a significant advancement, our prototypical CuNi DSACs demonstrated outstanding performance under conditions reminiscent of industrial wastewater. Specifically, under a NO3– concentration of 2000 ppm, it yielded a Faradaic efficiency (FE) for NH3 of 96.97%, coupled with a mass productivity of 131.47 mg h–1 mg–1 and an area productivity of 10.06 mg h–1 cm–2. Impressively, even under a heightened NO3– concentration of 0.5 M, the FE for NH3 peaked at 90.61%, with a mass productivity reaching 1024.50 mg h–1 mg–1 and an area productivity of 78.41 mg h–1 cm–2. This work underpins the potential of the EEMIS-DSAC approach, signaling a frontier for high-performing DSACs.
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