國立虎尾科技大學 |

Electrocatalytic Studies of Group VI Metals.

Record Type:	Language materials, manuscript : Monograph/item
Title/Author:	Electrocatalytic Studies of Group VI Metals./
Author:	Grant, Cameron.
Description:	1 online resource (59 pages)
Notes:	Source: Masters Abstracts International, Volume: 85-11.
Contained By:	Masters Abstracts International85-11.
Subject:	Chemistry. -
Online resource:	click for full text (PQDT)
ISBN:	9798382610955

Electrocatalytic Studies of Group VI Metals.
Grant, Cameron.

Electrocatalytic Studies of Group VI Metals. - 1 online resource (59 pages)

Source: Masters Abstracts International, Volume: 85-11.

Thesis (M.S.)--Indiana University, 2024.

Includes bibliographical references

Formate is one of the only economically viable products from CO2 reduction due to its industrial versatility and excellent compatibility with current liquid-based fuel infrastructure. Here we report group 6 electro catalysts that selectively reduce CO2 to formate with high faradaic efficiencies, 93+-5%. This class of catalysts are based on the structure of M(a-diimine)(CO)4, where M=Cr, Mo, and W. However, their mechanism is not clearly understood. We hypothesize a proton-tautomerization occurs from the ligand to the metal center, generating a metal-hydride with sufficient hydricity to reduce CO2 to formate. Therefore, understanding the effects of metal basicity and ligand conjugation will aid in catalyst design of group 6 metal complexes for optimized proton-coupled reduction processes. NMR and EPR characterization will allow for direct observation of metal-hydride species. Assuming a metal-hydride is observed, further studies with NMR or UV-vis will estimate hydricity values.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2024

Mode of access: World Wide Web

ISBN: 9798382610955Subjects--Topical Terms:

593913
Chemistry.
Subjects--Index Terms:

CatalysisIndex Terms--Genre/Form:

554714
Electronic books.

Electrocatalytic Studies of Group VI Metals.
LDR:02298ntm a22004097 4500 001 1152673
005 20241209114628.5
006 m o d
007 cr mn ---uuuuu
008 250605s2024 xx obm 000 0 eng d
020 $a 9798382610955
035 $a (MiAaPQ)AAI31293888
035 $a AAI31293888
040 $a MiAaPQ $b eng $c MiAaPQ $d NTU
100 1 $a Grant, Cameron. $3 1479737
245 1 0 $a Electrocatalytic Studies of Group VI Metals.
264 0 $c 2024
300 $a 1 online resource (59 pages)
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
500 $a Source: Masters Abstracts International, Volume: 85-11.
500 $a Advisor: Li, Liang-shi.
502 $a Thesis (M.S.)--Indiana University, 2024.
504 $a Includes bibliographical references
520 $a Formate is one of the only economically viable products from CO2 reduction due to its industrial versatility and excellent compatibility with current liquid-based fuel infrastructure. Here we report group 6 electro catalysts that selectively reduce CO2 to formate with high faradaic efficiencies, 93+-5%. This class of catalysts are based on the structure of M(a-diimine)(CO)4, where M=Cr, Mo, and W. However, their mechanism is not clearly understood. We hypothesize a proton-tautomerization occurs from the ligand to the metal center, generating a metal-hydride with sufficient hydricity to reduce CO2 to formate. Therefore, understanding the effects of metal basicity and ligand conjugation will aid in catalyst design of group 6 metal complexes for optimized proton-coupled reduction processes. NMR and EPR characterization will allow for direct observation of metal-hydride species. Assuming a metal-hydride is observed, further studies with NMR or UV-vis will estimate hydricity values.
533 $a Electronic reproduction. $b Ann Arbor, Mich. : $c ProQuest, $d 2024
538 $a Mode of access: World Wide Web
650 4 $a Chemistry. $3 593913
650 4 $a Materials science. $3 557839
650 4 $a Inorganic chemistry. $3 1182077
653 $a Catalysis
653 $a Electrochemistry
653 $a Formate
653 $a Molybdenum
653 $a Pyrazinyl
653 $a Tungsten
655 7 $a Electronic books. $2 local $3 554714
690 $a 0485
690 $a 0794
690 $a 0488
710 2 $a ProQuest Information and Learning Co. $3 1178819
710 2 $a Indiana University. $b Chemistry. $3 1192664
773 0 $t Masters Abstracts International $g 85-11.
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=31293888 $z click for full text (PQDT)