Ce0.25Sr1.75NiO3.75 Assisting with Pd and Co Nanoparticles: Synthesize, Characterization and Catalytic Potentiality for Ethylene Glycol Electrooxidation

Publish Year: 1397
نوع سند: مقاله کنفرانسی
زبان: English
View: 469

متن کامل این Paper منتشر نشده است و فقط به صورت چکیده یا چکیده مبسوط در پایگاه موجود می باشد.
توضیح: معمولا کلیه مقالاتی که کمتر از ۵ صفحه باشند در پایگاه سیویلیکا اصل Paper (فول تکست) محسوب نمی شوند و فقط کاربران عضو بدون کسر اعتبار می توانند فایل آنها را دریافت نمایند.

  • Certificate
  • من نویسنده این مقاله هستم

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

IICC20_136

تاریخ نمایه سازی: 2 تیر 1398

Abstract:

A fuel cell is an electrochemical’ device operating at the different temperatures that convert the chemical energy of a fuel (e.g., alcohol) and an oxidant in the presence of a catalyst to the water, CO2, heat, and electricity [1]. Lately, the metal oxide composites have attracted significant attention as electrocatalysts owing to their low cost, easy preparation, and stable structure [2]. Ethylene glycol can be introduced as a suitable fuel for the fuel cells, due to its low vapor pressure, lower price, easier storage and lower flammability compared to other organic compounds [3]. In this work, the Ce0.25Sr1.75NiO3.75 mixed metal oxide was synthesized in nano-size (⁓ 24 nm) by the co-precipitation method in the presence of oleic acid as surfactant and characterized via spectroscopy and microscopy techniques. Then, Pd and Co nanoparticles were chemically reduced on as-prepared Ce0.25Sr1.75NiO3.75 in chitosan matrix. The physicochemical characteristics and electrochemical behavior were determined for Pd-Co-Ce0.25Sr1.75NiO3.75. The electro-catalytic ability of Ce0.25Sr1.75NiO3.75, Pd, Pd-Co, and Pd-Co-Ce0.25Sr1.75NiO3.75 toward ethylene glycol oxidation was compared via the electrochemical studies in alkaline media. The results showed that the incorporation of as-prepared mixed oxide to Pd-Co was efficient to improve the current density and the transferred charge during the electrooxidation of ethylene glycol

Authors

Safiye Hashemzehi

Department of Chemistry, University of Sistan and Baluchestan, P.O. Box ۹۸۱۳۵-۶۷۴, Zahedan, Iran

Zahra Yavari

Department of Chemistry, University of Sistan and Baluchestan, P.O. Box ۹۸۱۳۵-۶۷۴, Zahedan, Iran

Hamideh Saravani

Department of Chemistry, University of Sistan and Baluchestan, P.O. Box ۹۸۱۳۵-۶۷۴, Zahedan, Iran

Meissam Noroozifar

Department of Chemistry, University of Sistan and Baluchestan, P.O. Box ۹۸۱۳۵-۶۷۴, Zahedan, Iran