Zhou Baiqin, Li Zhida, He Xinyue, Zhang Chunyue, Pi Shanshan, Yang Min, Zhang Wei, Li Guifeng, Zhang Ziqi, Lu Lu
State Key Laboratory of Urban Water Resource and Environment, School of Civil and Environmental Engineering, Harbin Institute of Technology, Shenzhen, Shenzhen 518055, China.
iScience. 2024 May 10;27(6):109956. doi: 10.1016/j.isci.2024.109956. eCollection 2024 Jun 21.
Synergetic management of waste activated sludge, heavy metals (HMs) and CO for their valorization and cyclic utilization is rarely reported. Herein, we employed sludge-derived extracellular polymeric substances (EPS) and HMs in wastewater to fabricate a gas diffusion electrode (GDE) for electrochemical CO reduction. This approach atomically dispersed Ni at each nanofiber of the GDE. Abundant N element in the EPS proved to play a key role in the formation of N-Ni (mixture of N-Ni and N-Ni) sites for highly efficient CO to CO conversion. The atomical Ni shows high catalytic activity. Direct gaseous CO reduction in a membrane electrode assembly generated a current density up to 50 mA·cm with CO:H ratio of ∼100 and ∼75% FE under 2.69 cell voltage. This strategy takes advantage of all waste streams generated on site and consolidates traditionally separated treatment processes to save costs, produces value-added products and generates carbon benefits during wastewater treatment.
关于废弃活性污泥、重金属(HMs)和一氧化碳的协同管理以实现其增值和循环利用的报道很少。在此,我们利用污泥衍生的细胞外聚合物(EPS)和废水中的重金属制造了一种用于电化学一氧化碳还原的气体扩散电极(GDE)。这种方法使镍原子分散在GDE的每根纳米纤维上。EPS中丰富的氮元素被证明在形成用于高效一氧化碳到一氧化碳转化的N-Ni(N-Ni和N-Ni的混合物)位点中起关键作用。原子级的镍显示出高催化活性。在膜电极组件中直接进行气态一氧化碳还原,在2.69伏电池电压下,一氧化碳与氢的比例约为100,法拉第效率约为75%时,产生的电流密度高达50毫安·平方厘米。该策略利用了现场产生的所有废物流,整合了传统上分开的处理过程以节省成本,生产增值产品,并在废水处理过程中产生碳效益。