東華大學圖書館 |

語系: 繁體中文

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

Studying the Interfacial Structure o...

Hedderick, Konrad Radziszewski.

FindBook

Google Book

Amazon

博客來

Studying the Interfacial Structure of Hydrated Soft Matter Templates via Fluid Cell Atomic Force Microscopy (AFM) Techniques.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Studying the Interfacial Structure of Hydrated Soft Matter Templates via Fluid Cell Atomic Force Microscopy (AFM) Techniques./
作者:	Hedderick, Konrad Radziszewski.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2023,
面頁冊數:	207 p.
附註:	Source: Dissertations Abstracts International, Volume: 85-07, Section: B.
Contained By:	Dissertations Abstracts International85-07B.
標題:	Chemistry. -
電子資源:	https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30814651
ISBN:	9798381414035

Studying the Interfacial Structure of Hydrated Soft Matter Templates via Fluid Cell Atomic Force Microscopy (AFM) Techniques.
Hedderick, Konrad Radziszewski.

Studying the Interfacial Structure of Hydrated Soft Matter Templates via Fluid Cell Atomic Force Microscopy (AFM) Techniques. - Ann Arbor : ProQuest Dissertations & Theses, 2023 - 207 p.

Source: Dissertations Abstracts International, Volume: 85-07, Section: B.

Thesis (Ph.D.)--Cornell University, 2023.

Hydrated soft matter interfaces are ubiquitous in the world around us, underpinning materials in both the natural and man-made world. Nature utilizes these interfaces for biological catalysis, filtration, nucleation control, and more. Similarly, in synthetic systems they are used to develop coatings for healthcare, improve water filtration, direct assembly processes, and many other applications. Looking to the future, promising materials in catalysis, biomedicine and materials templating could be made possible if we can properly leverage these interfaces and their structures. However, despite their widescale importance and use, these interfaces have yet to be fully understood, and the first step towards that understanding is visualization.Towards those ends, in this work both biogenic and synthetic hydrated soft matter interfacial systems are explored. On the biogenic side coccolithophores, a species of single celled marine algae, mineralize amazing calcitic shell architectures (coccoliths) using surprisingly complicated machinery. Part of this process is the accumulation of coacervate particles (complexes of metal ions and polymers) on a coccolithophore baseplate, a fibrous, anisotropic surface on which these shells are created. This work uses established in-situ fluid cell AFM techniques to explore the kinetics and assembly of coacervate attachment to this baseplate - solution interface in the early stages of the coccolith pathway. Tracking this process gives insights into the rates of coacervate attachment and self-limiting growth that could have implications for the coccolith and other biogenic crystallization pathways. This could also help unravel the complicated intermolecular interactions that govern generalized coacervate surface templating.On the synthetic side, highly tunable, amphiphilic block copolymer (BCP) thin films are used to explore how local nanoscale chemistry and topography affect hydrated film and interfacial water structure. First, in situ fluid cell AFM amplitude imaging and force spectroscopy is used to probe these local film-water structures and response to external stimuli. From this we can further learn about how these materials exist and change in aqueous solutions. Next, the BCP-water interfacial structure is investigated and through visualization of this structure, the local energetic landscape might be predicted. To probe these nanometer water-polymer interfaces on mesoscale ordered BCP thin films we use emergent 3D-AFM force mapping techniques to visualize interfacial hydrophilic and hydrophobic regions on representative volumes of interest of the films. These can be visualized not only as an appropriate section of the film surface but to tens of nanometers into solution, giving ordering and distribution of interfacial water at and near the interface. Towards predictive solution nucleation control, we also use force maps to visualize how these regions are polarized, destroyed, or emphasized upon film functionalization with positive and negative click chemistries, heating, salt incorporation, and mixed effects.Overall, using established and emergent fluid cell AFM techniques, this work examines biogenic and synthetic water-polymer interfaces and interfacial structures. This work tracks coacervate attachment and growth on biomaterial templates, probes film evolution in aqueous solutions, and visualizes spatially correlated tiers of hydrophilic and hydrophobic ordering on and above amphiphilic BCP thin films. This helps lay the groundwork towards predictive hydrated soft matter interfacial structure understanding and control.

ISBN: 9798381414035Subjects--Topical Terms:

516420
Chemistry.
Subjects--Index Terms:

Atomic force microscopy

Studying the Interfacial Structure of Hydrated Soft Matter Templates via Fluid Cell Atomic Force Microscopy (AFM) Techniques.
LDR:04843nmm a2200397 4500 001 2403620
005 20241118135851.5
006 m o d
007 cr#unu||||||||
008 251215s2023 ||||||||||||||||| ||eng d
020 $a 9798381414035
035 $a (MiAaPQ)AAI30814651
035 $a AAI30814651
040 $a MiAaPQ $c MiAaPQ
100 1 $a Hedderick, Konrad Radziszewski. $0 (orcid)0000-0002-5730-5628 $3 3773892
245 1 0 $a Studying the Interfacial Structure of Hydrated Soft Matter Templates via Fluid Cell Atomic Force Microscopy (AFM) Techniques.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2023
300 $a 207 p.
500 $a Source: Dissertations Abstracts International, Volume: 85-07, Section: B.
500 $a Advisor: Estroff, Lara.
502 $a Thesis (Ph.D.)--Cornell University, 2023.
520 $a Hydrated soft matter interfaces are ubiquitous in the world around us, underpinning materials in both the natural and man-made world. Nature utilizes these interfaces for biological catalysis, filtration, nucleation control, and more. Similarly, in synthetic systems they are used to develop coatings for healthcare, improve water filtration, direct assembly processes, and many other applications. Looking to the future, promising materials in catalysis, biomedicine and materials templating could be made possible if we can properly leverage these interfaces and their structures. However, despite their widescale importance and use, these interfaces have yet to be fully understood, and the first step towards that understanding is visualization.Towards those ends, in this work both biogenic and synthetic hydrated soft matter interfacial systems are explored. On the biogenic side coccolithophores, a species of single celled marine algae, mineralize amazing calcitic shell architectures (coccoliths) using surprisingly complicated machinery. Part of this process is the accumulation of coacervate particles (complexes of metal ions and polymers) on a coccolithophore baseplate, a fibrous, anisotropic surface on which these shells are created. This work uses established in-situ fluid cell AFM techniques to explore the kinetics and assembly of coacervate attachment to this baseplate - solution interface in the early stages of the coccolith pathway. Tracking this process gives insights into the rates of coacervate attachment and self-limiting growth that could have implications for the coccolith and other biogenic crystallization pathways. This could also help unravel the complicated intermolecular interactions that govern generalized coacervate surface templating.On the synthetic side, highly tunable, amphiphilic block copolymer (BCP) thin films are used to explore how local nanoscale chemistry and topography affect hydrated film and interfacial water structure. First, in situ fluid cell AFM amplitude imaging and force spectroscopy is used to probe these local film-water structures and response to external stimuli. From this we can further learn about how these materials exist and change in aqueous solutions. Next, the BCP-water interfacial structure is investigated and through visualization of this structure, the local energetic landscape might be predicted. To probe these nanometer water-polymer interfaces on mesoscale ordered BCP thin films we use emergent 3D-AFM force mapping techniques to visualize interfacial hydrophilic and hydrophobic regions on representative volumes of interest of the films. These can be visualized not only as an appropriate section of the film surface but to tens of nanometers into solution, giving ordering and distribution of interfacial water at and near the interface. Towards predictive solution nucleation control, we also use force maps to visualize how these regions are polarized, destroyed, or emphasized upon film functionalization with positive and negative click chemistries, heating, salt incorporation, and mixed effects.Overall, using established and emergent fluid cell AFM techniques, this work examines biogenic and synthetic water-polymer interfaces and interfacial structures. This work tracks coacervate attachment and growth on biomaterial templates, probes film evolution in aqueous solutions, and visualizes spatially correlated tiers of hydrophilic and hydrophobic ordering on and above amphiphilic BCP thin films. This helps lay the groundwork towards predictive hydrated soft matter interfacial structure understanding and control.
590 $a School code: 0058.
650 4 $a Chemistry. $3 516420
650 4 $a Biomedical engineering. $3 535387
650 4 $a Materials science. $3 543314
650 4 $a Physical chemistry. $3 1981412
653 $a Atomic force microscopy
653 $a Biomineralization
653 $a Block copolymers
653 $a Crystallization
653 $a Water interfaces
690 $a 0794
690 $a 0485
690 $a 0541
690 $a 0494
710 2 $a Cornell University. $b Materials Science and Engineering. $3 3547480
773 0 $t Dissertations Abstracts International $g 85-07B.
790 $a 0058
791 $a Ph.D.
792 $a 2023
793 $a English
856 4 0 $u https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30814651