Teng Wei, Fan Jianwei, Zhang Wei-Xian
State Key Laboratory for Pollution Control, School of Environmental Science and Engineering, Shanghai Institute of Pollution Control and Ecological Security, Tongji University, Shanghai 200092, P. R. China.
ACS Appl Mater Interfaces. 2020 Jun 24;12(25):28091-28099. doi: 10.1021/acsami.0c03953. Epub 2020 May 26.
Electrocatalytic denitrification has been considered as one of the most promising technologies to selectively reduce excessive nitrogen oxyanions to benign dinitrogen in polluted water. The development of nonprecious metal catalysts with high performance for the denitrification is imperative but still a great challenge. Herein, we report an iron-based electrocatalyst for high-efficiency and selective denitrification. This nanocatalyst is prepared by template assembly of iron-based metal organic frameworks on surface-functionalized bimodal mesoporous carbon and subsequent pyrolysis under argon atmosphere. It contains well-dispersed FeN sites and Fe nanoparticles (most of them are wrapped by N-doped graphitic carbon), with high surface area (1080 m g) and uniform mesopore and micropore (5.0 and 1.7 nm) for the construction of electrodes. Experimental results confirm that the catalyst can achieve an excellent nitrate removal capacity of 3410 mg N/g Fe, along with a reduction efficiency up to 87% and N selectivity of 81% in neutral electrolyte (100 mg/L NO-N and 0.1 M NaSO) within 24 h. It is proposed that the active FeN sites cooperated with sufficient Fe nanoparticles to be conducive to adsorption of O in NO on the catalyst for the improved performance. The material also presents long-term durability and good adaptability in the range of pH 5-9 and simulated neutral wastewater, mainly contributed by the protection of the mesostructure and graphitic N-doped carbon. These findings open the door to rational design of nonprecious metal iron-based functional electrocatalysts for water purification and environmental remediation.
电催化脱氮被认为是将污染水中过量的氮氧阴离子选择性还原为无害氮气的最具前景的技术之一。开发具有高性能的非贵金属脱氮催化剂势在必行,但仍然是一个巨大的挑战。在此,我们报道了一种用于高效选择性脱氮的铁基电催化剂。这种纳米催化剂是通过在表面功能化的双峰介孔碳上进行铁基金属有机框架的模板组装,并随后在氩气气氛下热解制备而成。它包含分散良好的FeN位点和Fe纳米颗粒(其中大部分被氮掺杂的石墨碳包裹),具有高表面积(1080 m²/g)以及用于构建电极的均匀介孔和微孔(5.0和1.7 nm)。实验结果证实,该催化剂在中性电解质(100 mg/L NO₃-N和0.1 M Na₂SO₄)中24小时内可实现3410 mg N/g Fe的优异硝酸盐去除能力,还原效率高达87%,N选择性为81%。据推测,活性FeN位点与充足的Fe纳米颗粒协同作用,有利于催化剂对NO中的O进行吸附,从而提高性能。该材料在pH值为5 - 9的范围内以及模拟中性废水中还表现出长期耐久性和良好的适应性,这主要得益于介观结构和氮掺杂石墨碳的保护。这些发现为合理设计用于水净化和环境修复的非贵金属铁基功能电催化剂打开了大门。