語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
FindBook
Google Book
Amazon
博客來
Insights on Plasmon-Driven Chemical and Photophysical Processes Using Surface Enhanced Raman Spectroscopy : = From the Steady State to the Ultrafast.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Insights on Plasmon-Driven Chemical and Photophysical Processes Using Surface Enhanced Raman Spectroscopy :/
其他題名:
From the Steady State to the Ultrafast.
作者:
Warkentin, Christopher L.
面頁冊數:
1 online resource (169 pages)
附註:
Source: Dissertations Abstracts International, Volume: 84-09, Section: B.
Contained By:
Dissertations Abstracts International84-09B.
標題:
Physical chemistry. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30250159click for full text (PQDT)
ISBN:
9798377643883
Insights on Plasmon-Driven Chemical and Photophysical Processes Using Surface Enhanced Raman Spectroscopy : = From the Steady State to the Ultrafast.
Warkentin, Christopher L.
Insights on Plasmon-Driven Chemical and Photophysical Processes Using Surface Enhanced Raman Spectroscopy :
From the Steady State to the Ultrafast. - 1 online resource (169 pages)
Source: Dissertations Abstracts International, Volume: 84-09, Section: B.
Thesis (Ph.D.)--University of Minnesota, 2023.
Includes bibliographical references
Plasmonic materials can interact with light in unique ways to produce energy-rich nanoscale (i.e. on the scale of nm, 1-100 x 10−9 m) environments. This energy can be harvested by nearby molecules to drive chemical reactions in ways that were previously not possible. However, due to the small size and fast timescale of plasmon decay (10−15 to 10−12s), the processes governing plasmon-driven chemistry are difficult to study and therefore poorly understood. In my thesis work, I have used surface-enhanced Raman spectroscopy (SERS) and other analytical tools to better understand the latent mechanisms involved in these light-driven processes, revealing insights into spatial control, charge transfer, and new applications with these exciting materials.In this thesis, we will first discuss my SERS investigations of plasmon-driven chemistry in the steady state, where we observed a plasmon-mediated methyl rearrangement of N-methylpyridinium to 4-methylpyridine. In this work, we highlight both the ability of plasmonic materials to drive complex/selective reactions and identify potential methods for their simple optical control. In later work, we will explore my application of ultrafast SERS in the first direct observation of plasmon-mediated electron transfer from a molecular perspective. Importantly, by correlating ultrafast SERS with spectroelectrochemical techniques, we were able to quantify the electron transfer from a plasmonic substrate to adsorbed methyl viologen molecules on timescales relevant to plasmon decay. Finally, we examine my investigation of a continuous wave upconversion process with plasmonic copper selenide nanocrystals. Our initial studies suggest that a plasmon-driven thermal mechanism likely plays a role in this unexpected photoluminescence.Lastly, I will describe a number of prospective directions for research on plasmonic systems. We will consider potential routes toward better understanding plasmon-driven chemistries by applying more robust statistical analyses, developing SERS imaging techniques, and investigating the contrasting impacts of pulsed and continuous wave irradiation on plasmon excitation. In conjunction with ultrafast SERS, these characterization techniques have realistic potential to inform the design of future plasmonic photocatalysts.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023
Mode of access: World Wide Web
ISBN: 9798377643883Subjects--Topical Terms:
1981412
Physical chemistry.
Subjects--Index Terms:
PhotocatalysisIndex Terms--Genre/Form:
542853
Electronic books.
Insights on Plasmon-Driven Chemical and Photophysical Processes Using Surface Enhanced Raman Spectroscopy : = From the Steady State to the Ultrafast.
LDR
:03780nmm a2200397K 4500
001
2357740
005
20230725053657.5
006
m o d
007
cr mn ---uuuuu
008
241011s2023 xx obm 000 0 eng d
020
$a
9798377643883
035
$a
(MiAaPQ)AAI30250159
035
$a
AAI30250159
040
$a
MiAaPQ
$b
eng
$c
MiAaPQ
$d
NTU
100
1
$a
Warkentin, Christopher L.
$3
3698270
245
1 0
$a
Insights on Plasmon-Driven Chemical and Photophysical Processes Using Surface Enhanced Raman Spectroscopy :
$b
From the Steady State to the Ultrafast.
264
0
$c
2023
300
$a
1 online resource (169 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: Dissertations Abstracts International, Volume: 84-09, Section: B.
500
$a
Advisor: Frontiera, Renee R.
502
$a
Thesis (Ph.D.)--University of Minnesota, 2023.
504
$a
Includes bibliographical references
520
$a
Plasmonic materials can interact with light in unique ways to produce energy-rich nanoscale (i.e. on the scale of nm, 1-100 x 10−9 m) environments. This energy can be harvested by nearby molecules to drive chemical reactions in ways that were previously not possible. However, due to the small size and fast timescale of plasmon decay (10−15 to 10−12s), the processes governing plasmon-driven chemistry are difficult to study and therefore poorly understood. In my thesis work, I have used surface-enhanced Raman spectroscopy (SERS) and other analytical tools to better understand the latent mechanisms involved in these light-driven processes, revealing insights into spatial control, charge transfer, and new applications with these exciting materials.In this thesis, we will first discuss my SERS investigations of plasmon-driven chemistry in the steady state, where we observed a plasmon-mediated methyl rearrangement of N-methylpyridinium to 4-methylpyridine. In this work, we highlight both the ability of plasmonic materials to drive complex/selective reactions and identify potential methods for their simple optical control. In later work, we will explore my application of ultrafast SERS in the first direct observation of plasmon-mediated electron transfer from a molecular perspective. Importantly, by correlating ultrafast SERS with spectroelectrochemical techniques, we were able to quantify the electron transfer from a plasmonic substrate to adsorbed methyl viologen molecules on timescales relevant to plasmon decay. Finally, we examine my investigation of a continuous wave upconversion process with plasmonic copper selenide nanocrystals. Our initial studies suggest that a plasmon-driven thermal mechanism likely plays a role in this unexpected photoluminescence.Lastly, I will describe a number of prospective directions for research on plasmonic systems. We will consider potential routes toward better understanding plasmon-driven chemistries by applying more robust statistical analyses, developing SERS imaging techniques, and investigating the contrasting impacts of pulsed and continuous wave irradiation on plasmon excitation. In conjunction with ultrafast SERS, these characterization techniques have realistic potential to inform the design of future plasmonic photocatalysts.
533
$a
Electronic reproduction.
$b
Ann Arbor, Mich. :
$c
ProQuest,
$d
2023
538
$a
Mode of access: World Wide Web
650
4
$a
Physical chemistry.
$3
1981412
650
4
$a
Analytical chemistry.
$3
3168300
650
4
$a
Nanoscience.
$3
587832
653
$a
Photocatalysis
653
$a
Plasmon-driven chemsitry
653
$a
Plasmonics
653
$a
Surface-enhanced Raman spectroscopy
653
$a
Ultrafast SERS
655
7
$a
Electronic books.
$2
lcsh
$3
542853
690
$a
0494
690
$a
0486
690
$a
0565
710
2
$a
ProQuest Information and Learning Co.
$3
783688
710
2
$a
University of Minnesota.
$b
Chemistry.
$3
1265998
773
0
$t
Dissertations Abstracts International
$g
84-09B.
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30250159
$z
click for full text (PQDT)
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9480096
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入