Manish Tiwari

Prof. Manish Tiwari

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

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

Representative Publications

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10 January 2012 in Nature Communications
Verified
Journal Article
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SJStefan Jung
Stefan Jung
MTManish Tiwari
Manish Tiwari
NDN. Vuong Doan
N. Vuong Doan
DPDimos Poulikakos
Dimos Poulikakos
Understanding ice formation from supercooled water on surfaces is a problem of fundamental importance and general utility. Superhydrophobic surfaces promise to have remarkable 'icephobicity' and low ice adhesion. Here we show that their icephobicity can be rendered ineffective by simple changes in environmental conditions. Through experiments, nucleation theory and heat transfer physics, we establish that humidity and/or the flow of a surrounding gas can fundamentally switch the ice crystallization mechanism, drastically affecting surface icephobicity. Evaporative cooling of the supercooled liquid can engender ice crystallization by homogeneous nucleation at the droplet-free surface as opposed to the expected heterogeneous nucleation at the substrate. The related interplay between droplet roll-off and rapid crystallization is also studied. Overall, we bring a novel perspective to icing and icephobicity, unveiling the strong influence of environmental conditions in addition to the accepted effects of the surface conditions and hydrophobicity.

26 March 2018 in Nature Materials
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CPChaoyi Peng
Chaoyi Peng
ZCZhuyang Chen
Zhuyang Chen
MTManish Tiwari
Manish Tiwari

9 December 2013 in Nano Letters
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Journal Article
Closed access
TMTanmoy Maitra
Tanmoy Maitra
MTManish Tiwari
Manish Tiwari
Carlo AntoniniCarlo Antonini
Carlo Antonini
PSPhilippe Schoch
Philippe Schoch
SJStefan Jung
Stefan Jung
DPDimos Poulikakos
Dimos Poulikakos

21 February 2014 in Nanoscale
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Journal Article
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PEPatric Eberle
Patric Eberle
MTManish Tiwari
Manish Tiwari
TMTanmoy Maitra
Tanmoy Maitra
DPDimos Poulikakos
Dimos Poulikakos
A rational methodology for designing surfaces with extraordinary resistance to ice formation is employed. The so obtained surfaces show robust ice nucleation temperatures and freezing delays of ∼25 hours at −21 °C.

1 July 2012 in Energy
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Journal Article
Closed access
SZSeverin Zimmermann
Severin Zimmermann
IMIngmar Meijer
Ingmar Meijer
MTManish Tiwari
Manish Tiwari
SPStephan Paredes
Stephan Paredes
BMBruno Michel
Bruno Michel
DPDimos Poulikakos
Dimos Poulikakos

7 September 2017 in Advanced Functional Materials
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Journal Article
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FCFaze Chen
Faze Chen
YLYao Lu
Yao Lu
XLXin Liu
Xin Liu
JSJinlong Song
Jinlong Song
Guanjie HeGuanjie He
Guanjie He
IPIvan Parkin
Ivan Parkin
Many advanced materials are designed for separation of immiscible oils/organic solvents and aqueous solutions, including poly(vinylidene fluoride) (PVDF)‐based materials with superwettability. However, due to the limited solubility of PVDF, techniques (e.g., phase inversion and electrospinning) often involve the use of toxic organic solvents. Here a facile organic solvent‐free method is described to prepare a porous PVDF–MWCNT (multiwalled carbon nanotube) foam using table salt as a sacrificial template. The porous PVDF–MWCNT foam is characterized as superhydrophobic–superoleophilic with good elasticity due to its 3D porosity and low surface energy. The foam exhibits high adsorption capacity to a variety of oils/organic solvents and can be easily reused by squeezing, heating, or releasing in other solvents. Moreover, the foam is highly resistant toward UV exposure, corrosive aqueous solutions such as acidic, alkaline, salty solutions, and turbulent environments, and shows effective oils/organic solvents removal in these complex environments. The continuous separation of immiscible oils/organic solvents and corrosive aqueous solutions with vacuum assistance is also presented. The organic solvent‐free and reusable PVDF–MWCNT foam is a promising candidate for large‐scale industrial separation of oils/organic solvents and water in corrosive and turbulent conditions.