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Dissolution-regrowth of hierarchical Fe-Dy oxide modulates the electronic structure of nickel-organic frameworks as highly active and stable water splitting electrocatalysts
Wan, Zixia1; He, Qiuting1; Chen, Jundan1; Isimjan, Tayirjan Taylor3; Wang, Bao2; Yang, Xiulin1
2020-11-01
Source PublicationCHINESE JOURNAL OF CATALYSIS
ISSN0253-9837
Volume41Issue:11Pages:1745-1753
AbstractAs the kinetically sluggish oxygen evolution reaction (OER) is considered to be a bottleneck in overall water splitting, it is necessary to develop a highly active and stable electrocatalyst to overcome this issue. Herein, we successfully fabricated a three-dimensional iron-dysprosium oxide co-regulated in-situ formed MOF-Ni arrays on carbon cloth (FeDy@MOF-Ni/CC) through a facile two-step hydrothermal method. Electrochemical studies demonstrate that the designed FeDy@MOF-Ni/CC catalyst requires an overpotential of only 251 mV to reach 10 mA cm(-2) with a small Tafel slope of 52.1 mV dec(-1). Additionally, the stability declined by only 5.5% after 80 h of continuous testing in 1.0 M KOH. Furthermore, a cell voltage of only 1.57 V in the overall water splitting system is sufficient to achieve 10 mA cm(-2); this value is far better than that of most previously reported catalysts. The excellent catalytic performance originates from the unique 3D rhombus-like structure, as well as coupling synergies of Fe-Dy-Ni species. The combination of lanthanide and transition metal species in the synthesis strategy may open entirely new possibilities with promising potential in the design of highly active OER electrocatalysts. (c) 2020, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
KeywordMetal-organic frameworks Dysprosium oxide Synergistic effect Oxygen evolution Water splitting
DOI10.1016/S1872-2067(20)63606-3
Language英语
WOS KeywordOXYGEN EVOLUTION ; BIFUNCTIONAL ELECTROCATALYST ; EFFICIENT OXYGEN ; QUANTUM DOTS ; HYDROGEN ; NI ; HYDROXIDE ; CORROSION ; ARRAYS ; SITES
Funding ProjectNational Natural Science Foundation of China[21965005] ; Natural Science Foundation of Guangxi Province[2018GXNSFAA294077] ; Project of High-Level Talents of Guangxi[F-KA18015] ; Project of High-Level Talents of Guangxi[2018ZD004] ; Innovation Project of Guangxi Graduate Education[XYCSZ2019056] ; Innovation Project of Guangxi Graduate Education[YCBZ2019031]
WOS Research AreaChemistry ; Engineering
WOS SubjectChemistry, Applied ; Chemistry, Physical ; Engineering, Chemical
Funding OrganizationNational Natural Science Foundation of China ; Natural Science Foundation of Guangxi Province ; Project of High-Level Talents of Guangxi ; Innovation Project of Guangxi Graduate Education
WOS IDWOS:000579729300008
PublisherSCIENCE PRESS
Citation statistics
Document Type期刊论文
Identifierhttp://ir.ipe.ac.cn/handle/122111/42451
Collection中国科学院过程工程研究所
Corresponding AuthorIsimjan, Tayirjan Taylor; Wang, Bao; Yang, Xiulin
Affiliation1.Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, Guangxi Key Lab Low Carbon Energy Mat, Guilin 541004, Guangxi, Peoples R China
2.Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, Beijing 100190, Peoples R China
3.King Abdullah Univ Sci & Technol KAUST, Saudi Arabia Basic Ind Corp SABIC, Thuwal 239556900, Saudi Arabia
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GB/T 7714
Wan, Zixia,He, Qiuting,Chen, Jundan,et al. Dissolution-regrowth of hierarchical Fe-Dy oxide modulates the electronic structure of nickel-organic frameworks as highly active and stable water splitting electrocatalysts[J]. CHINESE JOURNAL OF CATALYSIS,2020,41(11):1745-1753.
APA Wan, Zixia,He, Qiuting,Chen, Jundan,Isimjan, Tayirjan Taylor,Wang, Bao,&Yang, Xiulin.(2020).Dissolution-regrowth of hierarchical Fe-Dy oxide modulates the electronic structure of nickel-organic frameworks as highly active and stable water splitting electrocatalysts.CHINESE JOURNAL OF CATALYSIS,41(11),1745-1753.
MLA Wan, Zixia,et al."Dissolution-regrowth of hierarchical Fe-Dy oxide modulates the electronic structure of nickel-organic frameworks as highly active and stable water splitting electrocatalysts".CHINESE JOURNAL OF CATALYSIS 41.11(2020):1745-1753.
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