001     596487
005     20240110163745.0
024 7 _ |a 10.1002/adma.202305573
|2 doi
024 7 _ |a 0935-9648
|2 ISSN
024 7 _ |a 1521-4095
|2 ISSN
024 7 _ |a altmetric:154498519
|2 altmetric
024 7 _ |a 37734330
|2 pmid
024 7 _ |a WOS:001084218100001
|2 WOS
037 _ _ |a PUBDB-2023-06162
041 _ _ |a English
082 _ _ |a 660
100 1 _ |a Yang, Yuwei
|0 P:(DE-HGF)0
|b 0
245 _ _ |a Defect‐Promoted Ni‐Based Layer Double Hydroxides with Enhanced Deprotonation Capability for Efficient Biomass Electrooxidation
260 _ _ |a Weinheim
|c tbd
|b Wiley-VCH
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1698217136_2148348
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Ni-based hydroxides are promising electrocatalysts for biomass oxidation reactions, supplanting the oxygen evolution reaction (OER) due to lower overpotentials while producing value-added chemicals. The identification and subsequent engineering of their catalytically active sites are essential to facilitate these anodic reactions. Herein, the proportional relationship between catalysts’ deprotonation propensity and Faradic efficiency of 5-hydroxymethylfurfural (5-HMF)-to-2,5 furandicarboxylic acid (FDCA, FE$_{FDCA}$) is revealed by thorough density functional theory (DFT) simulations and atomic-scale characterizations, including in situ synchrotron diffraction and spectroscopy methods. The deprotonation capability of ultrathin layer-double hydroxides (UT-LDHs) is regulated by tuning the covalency of metal (M)-oxygen (O) motifs through defect site engineering and selection of M$^{3+}$ co-chemistry. NiMn UT-LDHs show an ultrahigh FE$_{FDCA}$ of 99% at 1.37 V versus reversible hydrogen electrode (RHE) and retain a high FE$_{FDCA}$ of 92.7% in the OER-operating window at 1.52 V, about 2× that of NiFe UT-LDHs (49.5%) at 1.52 V. Ni–O and Mn–O motifs function as dual active sites for HMF electrooxidation, where the continuous deprotonation of Mn–OH sites plays a dominant role in achieving high selectivity while suppressing OER at high potentials. The results showcase a universal concept of modulating competing anodic reactions in aqueous biomass electrolysis by electronically engineering the deprotonation behavior of metal hydroxides, anticipated to be translatable across various biomass substrates.
536 _ _ |a 6G3 - PETRA III (DESY) (POF4-6G3)
|0 G:(DE-HGF)POF4-6G3
|c POF4-6G3
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, Journals: bib-pubdb1.desy.de
693 _ _ |a PETRA III
|f PETRA Beamline P21.1
|1 EXP:(DE-H253)PETRAIII-20150101
|0 EXP:(DE-H253)P-P21.1-20150101
|6 EXP:(DE-H253)P-P21.1-20150101
|x 0
700 1 _ |a Lie, William Hadinata
|0 P:(DE-HGF)0
|b 1
700 1 _ |a Unocic, Raymond R
|0 P:(DE-HGF)0
|b 2
700 1 _ |a Yuwono, Jodie A
|0 P:(DE-HGF)0
|b 3
700 1 _ |a Klingenhof, Malte
|0 P:(DE-H253)PIP1096056
|b 4
700 1 _ |a Merzdorf, Thomas
|0 P:(DE-H253)PIP1096150
|b 5
700 1 _ |a Buchheister, Paul
|0 P:(DE-H253)PIP1096066
|b 6
700 1 _ |a Kroschel, Matthias
|0 P:(DE-H253)PIP1096517
|b 7
700 1 _ |a Walker, Anne
|0 P:(DE-HGF)0
|b 8
700 1 _ |a Gallington, Leighanne C.
|0 P:(DE-HGF)0
|b 9
700 1 _ |a Thomsen, Lars
|0 P:(DE-HGF)0
|b 10
700 1 _ |a Kumar, Priyank V
|0 P:(DE-HGF)0
|b 11
700 1 _ |a Strasser, Peter
|0 P:(DE-H253)PIP1016552
|b 12
700 1 _ |a Scott, Jason A
|0 P:(DE-HGF)0
|b 13
700 1 _ |a Bedford, Nicholas
|0 P:(DE-H253)PIP1092742
|b 14
|e Corresponding author
773 _ _ |a 10.1002/adma.202305573
|g p. 2305573
|0 PERI:(DE-600)1474949-X
|p 2305573
|t Advanced materials
|v tbd
|y tbd
|x 0935-9648
856 4 _ |u https://bib-pubdb1.desy.de/record/596487/files/Advanced%20Materials%20-%202023%20-%20Yang%20-%20Defect%E2%80%90Promoted%20Ni%E2%80%90Based%20Layer%20Double%20Hydroxides%20with%20Enhanced%20Deprotonation%20Capability.pdf
|y OpenAccess
856 4 _ |u https://bib-pubdb1.desy.de/record/596487/files/Advanced%20Materials%20-%202023%20-%20Yang%20-%20Defect%E2%80%90Promoted%20Ni%E2%80%90Based%20Layer%20Double%20Hydroxides%20with%20Enhanced%20Deprotonation%20Capability.pdf?subformat=pdfa
|x pdfa
|y OpenAccess
909 C O |o oai:bib-pubdb1.desy.de:596487
|p VDB
910 1 _ |a External Institute
|0 I:(DE-HGF)0
|k Extern
|b 4
|6 P:(DE-H253)PIP1096056
910 1 _ |a External Institute
|0 I:(DE-HGF)0
|k Extern
|b 5
|6 P:(DE-H253)PIP1096150
910 1 _ |a External Institute
|0 I:(DE-HGF)0
|k Extern
|b 6
|6 P:(DE-H253)PIP1096066
910 1 _ |a External Institute
|0 I:(DE-HGF)0
|k Extern
|b 7
|6 P:(DE-H253)PIP1096517
910 1 _ |a External Institute
|0 I:(DE-HGF)0
|k Extern
|b 12
|6 P:(DE-H253)PIP1016552
910 1 _ |a External Institute
|0 I:(DE-HGF)0
|k Extern
|b 14
|6 P:(DE-H253)PIP1092742
913 1 _ |a DE-HGF
|b Forschungsbereich Materie
|l Großgeräte: Materie
|1 G:(DE-HGF)POF4-6G0
|0 G:(DE-HGF)POF4-6G3
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-600
|4 G:(DE-HGF)POF
|v PETRA III (DESY)
|x 0
915 _ _ |a Nationallizenz
|0 StatID:(DE-HGF)0420
|2 StatID
|d 2023-08-31
|w ger
915 _ _ |a DEAL Wiley
|0 StatID:(DE-HGF)3001
|2 StatID
|d 2023-08-31
|w ger
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2023-08-31
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2023-08-31
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2023-08-31
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2023-08-31
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2023-08-31
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2023-08-31
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1160
|2 StatID
|b Current Contents - Engineering, Computing and Technology
|d 2023-08-31
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1150
|2 StatID
|b Current Contents - Physical, Chemical and Earth Sciences
|d 2023-08-31
920 1 _ |0 I:(DE-H253)HAS-User-20120731
|k DOOR ; HAS-User
|l DOOR-User
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-H253)HAS-User-20120731
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21