Zhang Jingsen, Zhang Xiuling, Shi Chuan, Yu Xinyao, Zhou Yitong, Di Lanbo
State Key Laboratory of Fine Chemicals, School of Chemistry, Dalian University of Technology, Dalian, 116024, P. R. China.
College of Physical Science and Technology, Dalian University, Dalian, 116622, P. R. China.
Small. 2024 Dec;20(49):e2406767. doi: 10.1002/smll.202406767. Epub 2024 Sep 9.
Integrating electrochemical upcycling of polyethylene-terephthalate (PET) and the hydrogen evolution reaction (HER) is an energy-saving approach for electrolytic hydrogen (H) production, along with the coproduction of formate. Herein, a novel and rapid strategy of cold plasma phosphating is employed to synthesize CoP-NiP heterointerface decorated on carbon cloth (CoP-NiP/CC) to catalyze H generation and reform PET. Notably, the obtained CoP-NiP/CC exhibits eminent ethylene glycol oxidation reaction (EGOR) and HER activities, effectuating low potentials of merely 1.300 and -0.112 V versus RHE at 100 mA cm for the EGOR and HER, respectively, also attaining an ultralow cell bias of 1.300 V at 10 mA cm for EG oxidation assisted-water splitting. DFT and characterization results validate that the as-formed built-in electric fields in the CoP-NiP heterointerface can accelerate electrons transfer and deepen structural self-reconstruction, thereby boosting effectively water dissociation and ethylene glycol (EG) dehydrogenation. Impressively, coupling HER with PET-derived EG-to-formate in a flow-cell electrolyzer assembled with CoP-NiP/CC pair achieves an intriguing formate Faradaic efficiency of 90.6% and an extraordinary stable operation of over 70 h at 100 mA cm. The work exemplifies a facile and effective strategy for synthesizing metal phosphides electrocatalysts with extraordinary performance toward H generation of water splitting and recycling of PET.
将聚对苯二甲酸乙二酯(PET)的电化学升级循环与析氢反应(HER)相结合,是一种用于电解制氢(H)的节能方法,同时还能联产甲酸盐。在此,采用一种新颖且快速的冷等离子体磷化策略,合成了装饰在碳布上的CoP-NiP异质界面(CoP-NiP/CC),用于催化氢气生成和PET的重整。值得注意的是,所获得的CoP-NiP/CC表现出卓越的乙二醇氧化反应(EGOR)和HER活性,在100 mA cm下,EGOR和HER相对于可逆氢电极(RHE)的低电位分别仅为1.300 V和 -0.112 V,在10 mA cm下,对于乙二醇氧化辅助水分解,其电池偏压也超低,仅为1.300 V。密度泛函理论(DFT)和表征结果证实,CoP-NiP异质界面中形成的内建电场可以加速电子转移并深化结构自重构,从而有效促进水离解和乙二醇(EG)脱氢。令人印象深刻的是,在由CoP-NiP/CC电极对组装的流动池电解槽中,将HER与PET衍生的EG制甲酸盐耦合,实现了90.6%的甲酸盐法拉第效率,并且在100 mA cm下能稳定运行超过70小时。这项工作例证了一种简便有效的策略,用于合成对水分解制氢和PET循环具有优异性能的金属磷化物电催化剂。