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CoNi-NC
Journal of Water Process Engineering · 2026 · IF 6.6

Prussian blue analogue-derived CoNi@NC core-shell microspheres for peroxymonosulfate activation toward tetracycline degradation

Shuqi Su,Jiujiang Guo,Jianxin Li,Lan Liang,Bo Li,Jie Guo,Kai Wang,Cheng Tian,Youkuo Lin,Meiyang Wang,Yongjiang Hou

CoNi@NC core-shell microspheres were synthesized via pyrolysis of Co-Ni PBA. • A temporal knowledge graph model was built to predict dynamic catalytic behavior. • CoNi@NC achieved 73.7% TCH removal efficiency within 3 min and 91.89% within 60 min. • TCH degradation involves radical/non-radical pathways dominated by O 2 •− and 1 O 2 . • The synergistic Co/Ni bimetallic redox cycles accelerate PMS activation. Prussian blue analogue (PBA)-derived carbon catalysts are promising peroxymonosulfate (PMS) activators for antibiotic wastewater purification, yet their time-dependent degradation behavior still requires further evaluation. Herein, a core-shell CoNi@NC catalyst was prepared by pyrolyzing Co Ni PBA, in which Co Ni alloy nanoparticles were confined within an N-doped carbon (NC) matrix. To evaluate the tetracycline hydrochloride (TCH) degradation behavior, a temporal knowledge graph (TKG)-assisted framework was employed as a complementary prediction tool, predicting a shift of the CoNi@NC/PMS system toward high degradation efficiency intervals. In degradation experiments, the CoNi@NC/PMS system exhibited a rapid degradation trend consistent with the prediction, achieving 73.7% TCH removal within 3 min and 91.89% within 60 min. The catalyst retained 86.74% removal efficiency after four degradation cycles, and exhibited good matrix tolerance under different pH conditions and coexisting ions. Mechanistic analysis revealed that TCH degradation proceeded through a radical/non-radical synergistic pathway, in which Co/Ni redox cycles and interfacial electron transfer promoted PMS activation. The reaction products of TCH were identified, and the toxicity assessment indicated reduced phytotoxicity of the treated solution. This work provides a useful reference for developing efficient PBA-derived catalysts for PMS-based antibiotic wastewater purification. Download: Download high-res image (210KB) Download: Download full-size image

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JOURNAL OF MATERIALS RESEARCH · 2023 ·Vol. 38 ·期 9 ·2359-2368 · IF 2.7

The activity of Fe/Co/Ni multi-metal doped electrocatalysts for oxygen reduction reaction

Ma Junjie,Liu Hangcheng,Tao Zeyu,Liu Jianfeng,Yuan Binxia,Pan Weiguo,Shi Zhengrong

In order to reveal the relationship between the structure and the electrochemical oxygen reduction reaction (ORR) activity of different double transition metal decorated catalysts, three different double transition metal and N co-doped carbon material cathode catalyst materials (FeCo–NC, FeNi–NC and CoNi–NC) were prepared in this study. The FeCo–NC catalysts synthesised in this study still showed high ORR activity under alkaline conditions, with a half-wave potential of 0.783 V RHE , a mass activity (MA) of 11.36 A/g (0.77 V RHE ) and an ultimate current density of − 4.46 mA cm −2 ; after 30,000 cycles, the half-wave potential only decreased to 99.3% of the initial potential. Meanwhile, we employ MS to establish three different double transition metal and N co-doped graphene catalysts and to calculate and analyse their desorption properties, leading to the FeCo–NC material being the model with the highest ORR activity, which is consistent with the experimental results. Graphical Abstract

CAS / MDL: 461-58-5 7782-61-8
研究领域: 电化学 · 材料科学 · 催化
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