Development of non-noble Ni metal-based (Yb1−xCox)2O3−δ catalysts for green H2 production via ammonia decomposition

IF 4.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Yeon-Bin Choi, Tae Wook Kang, Seo Ra Woo, Do yun Kim, Sun Woog Kim and Byungseo Bae
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Abstract

We herein report the preparation of non-noble metal supported Yb2O3–Co3O4 inorganic catalysts for application in H2 production via ammonia (NH3) decomposition. The NH3 decomposition reaction for H2 production was studied using αwt%Ni/(Yb1−xCox)2O3−δ catalysts according to various Co dopant ratios and Ni loadings to evaluate the dependence of oxygen vacancies as active sites. The introduction of Co3O4 into Yb2O3 with a Ni metal support improved the oxygen vacancy density of the catalyst to enhance NH3 decomposition activity for H2 production. The electron-deficient nature of oxygen vacancies enabled the catalysts to act as electron acceptors, facilitating the associative N desorption from NH3 to produce N2 in the NH3 cracking process. The structure–property relationship established in these studies suggests that the oxygen vacancies on the αwt%Ni/(Yb1−xCox)2O3−δ catalysts serve as active sites for NH3 decomposition. The 16wt%Ni/(Yb0.92Co0.08)2O3−δ catalyst showed the highest catalytic activity, which exhibited an NH3 conversion of 100% at temperatures as low as 550 °C and the constant H2 production rate of 6.23 kg per day.

Abstract Image

非贵金属镍基(Yb1−xCox)2O3−δ氨分解绿色制氢催化剂的研制
本文报道了非贵金属负载型Yb2O3-Co3O4无机催化剂的制备及其在氨分解制氢中的应用。采用αwt%Ni/(Yb1−xCox)2O3−δ催化剂,根据不同Co掺杂比和Ni负载对NH3分解制氢反应进行了研究,以评价氧空位作为活性位点的依赖性。在Ni金属载体的Yb2O3中引入Co3O4,提高了催化剂的氧空位密度,提高了NH3分解活性,生成H2。氧空位的缺电子特性使催化剂充当电子受体,促进NH3裂解过程中N的缔合解吸生成N2。这些研究建立的构效关系表明αwt%Ni/(Yb1−xCox)2O3−δ催化剂上的氧空位是NH3分解的活性位点。16wt%Ni/(Yb0.92Co0.08)2O3−δ催化剂表现出最高的催化活性,在低至550℃的温度下NH3转化率为100%,H2产率为6.23 kg / d。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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