Mengmeng Du, Tao Sun, Xuyun Guo, Mingzhu Han, Yu Zhang, Wenxuan Chen, Mengxiang Han, Jizhe Ma, Wenfang Yuan, Chunyu Zhou, Valeria Nicolosi, Jian Shang, Ning Zhang, Bocheng Qiu
{"title":"Efficient co-production of ammonia and formic acid from nitrate and polyester <i>via</i> paired electrolysis.","authors":"Mengmeng Du, Tao Sun, Xuyun Guo, Mingzhu Han, Yu Zhang, Wenxuan Chen, Mengxiang Han, Jizhe Ma, Wenfang Yuan, Chunyu Zhou, Valeria Nicolosi, Jian Shang, Ning Zhang, Bocheng Qiu","doi":"10.1039/d5mh00130g","DOIUrl":null,"url":null,"abstract":"<p><p>Paired electrolysis, which integrates a productive cathodic reaction, such as the nitrate reduction reaction (NO<sub>3</sub><sup>-</sup>RR) with selective oxidation at the anode, offers an intriguing way to maximize both atomic and energy efficiency. However, in a conventional design, the NO<sub>3</sub><sup>-</sup>RR is often coupled with the anodic oxygen evolution reaction, leading to substantial energy consumption while yielding low-value oxygen. Here, we report a hybrid electrolysis system that combines cathodic reduction of nitrate to ammonia and anodic oxidation of polyethylene-terephthalate-derived ethylene glycol (EG) to formic acid (FA), utilizing oxygen-vacancy-rich (O<sub>V</sub>) Co<sub>3</sub>O<sub>4</sub> and Cu doped Ni(OH)<sub>2</sub> as the cathode and anode, respectively. Remarkably, this paired electrolysis system demonstrates a faradaic efficiency (FE) of 92% for cathodic ammonia production and a FE of 99% for anodic FA production, while reducing the cell voltage by 0.54 V compared to the conventional NO<sub>3</sub><sup>-</sup>RR system at the same current density of 100 mA cm<sup>-2</sup>. Experimental investigations combined with theoretical calculations reveal that the O<sub>V</sub> introduction effectively addresses the insufficient NO<sub>3</sub><sup>-</sup> adsorption and hydrogenation on bare Co<sub>3</sub>O<sub>4</sub>. Additionally, Cu incorporation increases the Ni-O covalency, resulting in an improved EG adsorption ability. This work presents a promising way for waste management <i>via</i> paired electrolysis.</p>","PeriodicalId":87,"journal":{"name":"Materials Horizons","volume":" ","pages":""},"PeriodicalIF":12.2000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Horizons","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d5mh00130g","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Paired electrolysis, which integrates a productive cathodic reaction, such as the nitrate reduction reaction (NO3-RR) with selective oxidation at the anode, offers an intriguing way to maximize both atomic and energy efficiency. However, in a conventional design, the NO3-RR is often coupled with the anodic oxygen evolution reaction, leading to substantial energy consumption while yielding low-value oxygen. Here, we report a hybrid electrolysis system that combines cathodic reduction of nitrate to ammonia and anodic oxidation of polyethylene-terephthalate-derived ethylene glycol (EG) to formic acid (FA), utilizing oxygen-vacancy-rich (OV) Co3O4 and Cu doped Ni(OH)2 as the cathode and anode, respectively. Remarkably, this paired electrolysis system demonstrates a faradaic efficiency (FE) of 92% for cathodic ammonia production and a FE of 99% for anodic FA production, while reducing the cell voltage by 0.54 V compared to the conventional NO3-RR system at the same current density of 100 mA cm-2. Experimental investigations combined with theoretical calculations reveal that the OV introduction effectively addresses the insufficient NO3- adsorption and hydrogenation on bare Co3O4. Additionally, Cu incorporation increases the Ni-O covalency, resulting in an improved EG adsorption ability. This work presents a promising way for waste management via paired electrolysis.
配对电解,集成了生产阴极反应,如硝酸盐还原反应(NO3-RR)和阳极的选择性氧化,提供了一种有趣的方法来最大化原子和能源效率。然而,在传统的设计中,NO3-RR通常与阳极析氧反应耦合,导致大量的能量消耗,同时产生低价值的氧气。在这里,我们报道了一种混合电解系统,该系统结合了硝酸盐的阴极还原为氨和聚乙烯-对苯二甲酸酯衍生的乙二醇(EG)的阳极氧化生成甲酸(FA),分别利用富氧空位(OV) Co3O4和Cu掺杂Ni(OH)2作为阴极和阳极。值得注意的是,该配对电解系统在相同电流密度为100 mA cm-2的情况下,阴极氨生产的法拉第效率(FE)为92%,阳极FA生产的法拉第效率(FE)为99%,同时电池电压比传统NO3-RR系统降低了0.54 V。实验研究与理论计算相结合表明,OV的引入有效地解决了裸Co3O4上NO3-吸附和加氢不足的问题。此外,Cu的加入增加了Ni-O共价,从而提高了EG的吸附能力。这项工作提出了一种有前途的方法,通过配对电解废物管理。