材料科学
催化作用
氢
化学工程
制氢
化学
化学物理
纳米技术
钯
光化学
物理化学
固体氢
多相催化
联轴节(管道)
产量(工程)
纳米颗粒
作者
Chenkun Zheng,Jianan Li,Dong Zhang,Yi Liu,Yin Wang,X Wang,Yun‐Xiang Pan,Chong Peng
标识
DOI:10.1021/acscatal.6c02430
摘要
Coupling the hydrogen evolution reaction (HER) with PET-derived ethylene glycol oxidation reaction (EGOR) offers an energy-saving route for hydrogen production and plastic upcycling. However, Pt-based bifunctional catalysts are limited by inefficient Pt utilization, nonideal H* adsorption, and anodic oxidation-induced deactivation. Here, we report an oxygen-deficient D-Pt-Ni(OH) 2 /NF catalyst prepared by dielectric barrier discharge plasma treatment and integrated with an alternating-pulse electrolysis strategy. Plasma treatment introduces abundant oxygen vacancies and promotes electron transfer from Ni to Pt, downshifting the Pt d-band center and optimizing H* adsorption. The optimized catalyst requires only 12 mV to reach 10 mA cm –2 for HER and delivers a Pt mass activity of 3.23 A mg –1 Pt at –0.1 V vs RHE, which is 64.6 and 1.68 times higher than those of Pt/C and untreated Pt-Ni(OH) 2 /NF, respectively. In an HER||EGOR electrolyzer, D-Pt-Ni(OH) 2 /NF achieves 100 mA cm –2 at 0.96 V using PET hydrolysate. Alternating-pulse electrolysis suppresses Pt oxidation and enables stable 100 h operation in a membrane-free flow electrolyzer, with >90% Faradaic efficiency for glycolic acid and nearly 100% Faradaic efficiency for H 2 . Techno-economic analysis indicates a net profit of $1080.1 per ton of PET processed. This work demonstrates a catalyst–electrolysis co-engineering strategy that links plasma-induced electronic modulation with durable plastic valorization-assisted hydrogen production.
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