Search: WFRF:(Zhang Guangzhi) > Increasing Electroc...
Fältnamn | Indikatorer | Metadata |
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000 | 03803naa a2200457 4500 | |
001 | oai:DiVA.org:umu-176883 | |
003 | SwePub | |
008 | 201119s2021 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1768832 URI |
024 | 7 | a https://doi.org/10.1002/cssc.2020019752 DOI |
040 | a (SwePub)umu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Zhang, Xin4 aut |
245 | 1 0 | a Increasing Electrocatalytic Oxygen Evolution Efficiency through Cobalt-Induced Intrastructural Enhancement and Electronic Structure Modulation |
264 | c 2020-11-06 | |
264 | 1 | b 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 | 7 | a TEKNIK OCH TEKNOLOGIERx Kemiteknikx Annan kemiteknik0 (SwePub)204992 hsv//swe |
650 | 7 | a 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 | |
700 | 1 | a Zhang, Lei4 aut |
700 | 1 | a Zhu, Yuanxin4 aut |
700 | 1 | a Li, Ziyao4 aut |
700 | 1 | a Wang, Yong4 aut |
700 | 1 | a Wågberg, Thomas,d 1971-u Umeå universitet,Institutionen för fysik4 aut0 (Swepub:umu)thwa0002 |
700 | 1 | a 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 |
710 | 2 | a Umeå universitetb Institutionen för fysik4 org |
773 | 0 | t ChemSusChemd : Wiley-VCH Verlagsgesellschaftg 14:1, s. 467-478q 14:1<467-478x 1864-5631x 1864-564X |
856 | 4 | u https://doi.org/10.1002/cssc.202001975y Fulltext |
856 | 4 | u https://umu.diva-portal.org/smash/get/diva2:1502098/FULLTEXT02.pdfx primaryx Raw objecty fulltext:print |
856 | 4 | u https://doi.org/10.1002/cssc.202001975 |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-176883 |
856 | 4 8 | u https://doi.org/10.1002/cssc.202001975 |
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