Gregory Parsons

Gregory Parsons

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Research Focus & Metrics

Academic Career Length

42Years (1985-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 December 2011 in Journal of Vacuum Science & Technology A
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PPPaul Poodt
Paul Poodt
David CameronDavid Cameron
David Cameron
EDEric Dickey
Eric Dickey
SGSteven George
Steven George
VKVladimir Kuznetsov
Vladimir Kuznetsov
AVAd Vermeer
Ad Vermeer
Atomic layer deposition (ALD) is a technique capable of producing ultrathin conformal films with atomic level control over thickness. A major drawback of ALD is its low deposition rate, making ALD less attractive for applications that require high throughput processing. An approach to overcome this drawback is spatial ALD, i.e., an ALD mode where the half-reactions are separated spatially instead of through the use of purge steps. This allows for high deposition rate and high throughput ALD without compromising the typical ALD assets. This paper gives a perspective of past and current developments in spatial ALD. The technology is discussed and the main players are identified. Furthermore, this overview highlights current as well as new applications for spatial ALD, with a focus on photovoltaics and flexible electronics.

14 May 2020 in Chemistry of Materials
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Journal Article
Closed access
GPGregory Parsons
Gregory Parsons
RCRobert D. Clark
Robert D. Clark

24 March 2021 in Nature Reviews Materials
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Gregory W. PetersonGregory W. Peterson
Gregory W. Peterson
DLDennis T. Lee
Dennis T. Lee
HBHeather F. Barton
Heather F. Barton
TEThomas H. Epps
Thomas H. Epps
GPGregory Parsons
Gregory Parsons

16 October 2013 in Nature Communications
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KAKevin A. Arpin
Kevin A. Arpin
MLMark D. Losego
Mark D. Losego
ACAndrew N. Cloud
Andrew N. Cloud
HNHailong Ning
Hailong Ning
JMJustin Mallek
Justin Mallek
PBPaul V. Braun
Paul V. Braun

22 November 2017 in ACS Applied Materials & Interfaces
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Journal Article
Open access
DLDennis T. Lee
Dennis T. Lee
JZJunjie Zhao
Junjie Zhao
COChristopher J. Oldham
Christopher J. Oldham
Gregory W. PetersonGregory W. Peterson
Gregory W. Peterson
GPGregory Parsons
Gregory Parsons
Metal–organic frameworks (MOFs) chemically bound to polymeric microfibrous textiles show promising performance for many future applications. In particular, Zr-based UiO-66-family MOF-textiles have been shown to catalytically degrade highly toxic chemical warfare agents (CWAs), where favorable MOF/polymer bonding and adhesion are attained by placing a nanoscale metal-oxide layer on the polymer fiber preceding MOF growth. To date, however, the nucleation mechanism of Zr-based MOFs on different metal oxides and how product performance is affected are not well understood. Herein, we provide new insight into how different inorganic nucleation films (i.e., Al2O3, ZnO, or TiO2) conformally coated on polypropylene (PP) nonwoven textiles via atomic layer deposition (ALD) influence the quality, overall surface area, and the fractional yield of UiO-66-NH2 MOF crystals solvothermally grown on fiber substrates. Of the materials explored, we find that TiO2 ALD layers lead to the most effective overall MOF/fiber adhesion, uniformity, and a rapid catalytic degradation rate for a CWA simulant, dimethyl p-nitrophenyl phosphate (DMNP) with t1/2 = 15 min, 580-fold faster than the catalytic performance of untreated PP textiles. Interestingly, compared to ALD TiO2 and Al2O3, ALD ZnO induces a larger MOF yield in solution and mass loading on PP fibrous mats. However, this larger MOF yield is ascribed to chemical instability of the ZnO layer under MOF formation condition, leading to Zn2+ ions that promote further homogeneous MOF growth. Insights presented here improve understanding of compatibility between active MOF materials and substrate surfaces, which we believe will help advanced MOF composite materials for a variety of useful functions.