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Search: WFRF:(Zhang Guangzhi) > Increasing Electroc...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003803naa a2200457 4500
001oai:DiVA.org:umu-176883
003SwePub
008201119s2021 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1768832 URI
024a https://doi.org/10.1002/cssc.2020019752 DOI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Zhang, Xin4 aut
2451 0a Increasing Electrocatalytic Oxygen Evolution Efficiency through Cobalt-Induced Intrastructural Enhancement and Electronic Structure Modulation
264 c 2020-11-06
264 1b Wiley-VCH Verlagsgesellschaft,c 2021
338 a electronic2 rdacarrier
520 a Electrolytic water splitting using surplus electricity represents one of the most cost-effective and promising strategies for hydrogen production. The high overpotential of the oxygen-evolution reaction (OER) caused by the multi-electron transfer process with a high chemical energy barrier, however, limits its competitiveness. Here, a highly active and stable OER electrocatalyst was designed through a cobalt-induced intrastructural enhancement strategy combined with suitable electronic structure modulation. A carved carbon nanobox was embedded with tri-metal phosphide from a uniform Ni-Co-Fe Prussian blue analogue (PBA) nanocube by sequential NH3 center dot H2O etching and thermal phosphorization. The sample exhibited an OER activity in an alkaline medium, reaching a current density of 10 mA cm(-2) at an overpotential of 182 mV and displayed a small Tafel slope of 47 mV dec(-1), superior to the most recently reported OER electrocatalysts. Moreover, it showed impressive electrocatalytic durability, increasing by approximately 2.7 % of operating voltage after 24 h of continuous testing. The excellent OER activity and stability are ascribed to a favorable transfer of mass and charge provided by the porous carbon shell, synergistic catalysis between the three-component metal phosphides originating from appropriate electronic structure modulation, more exposed catalytic sites on the hollow structure, and chainmail catalysis resulting from the carbon protective layer. It is foreseen that this successfully demonstrated design concept can be easily extended to other heterogeneous catalyst designs.
650 7a TEKNIK OCH TEKNOLOGIERx Kemiteknikx Annan kemiteknik0 (SwePub)204992 hsv//swe
650 7a ENGINEERING AND TECHNOLOGYx Chemical Engineeringx Other Chemical Engineering0 (SwePub)204992 hsv//eng
653 a carved nanobox
653 a intrastructural enhancement
653 a oxygen evolution reaction
653 a phosphide
653 a prussian blue analogue
700a Zhang, Lei4 aut
700a Zhu, Yuanxin4 aut
700a Li, Ziyao4 aut
700a Wang, Yong4 aut
700a Wågberg, Thomas,d 1971-u Umeå universitet,Institutionen för fysik4 aut0 (Swepub:umu)thwa0002
700a Hu, Guangzhiu Umeå universitet,Institutionen för fysik,Institute for Ecological Research and Pollution Control of Plateau Lakes, School of Ecology and Environmental Science, Yunnan University, China4 aut0 (Swepub:umu)guhu0004
710a Umeå universitetb Institutionen för fysik4 org
773t ChemSusChemd : Wiley-VCH Verlagsgesellschaftg 14:1, s. 467-478q 14:1<467-478x 1864-5631x 1864-564X
856u https://doi.org/10.1002/cssc.202001975y Fulltext
856u https://umu.diva-portal.org/smash/get/diva2:1502098/FULLTEXT02.pdfx primaryx Raw objecty fulltext:print
856u https://doi.org/10.1002/cssc.202001975
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-176883
8564 8u https://doi.org/10.1002/cssc.202001975

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