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Dive into the research topics where Jeffery W. Baur is active.

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Featured researches published by Jeffery W. Baur.


Journal of Physics D | 2010

Viscoelastic creep of vertically aligned carbon nanotubes

Qiuhong Zhang; Y. C. Lu; Feng Du; Liming Dai; Jeffery W. Baur; D C Foster

The paper reports the viscous creep occurring in vertically aligned carbon nanotubes (VA-CNTs). Nanoindentation experiments are conducted to characterize the creep behaviour of the nanotube materials. By recording the instantaneous control stress and strain rate, the creep strain rate sensitivity of the VA-CNT array is calculated. The creep property is found to depend upon the density of nanotube arrays.


Journal of Intelligent Material Systems and Structures | 2009

Durability Assessment of Styrene- and Epoxy-based Shape-memory Polymer Resins

G. P. Tandon; K. Goecke; K. Cable; Jeffery W. Baur

The present study is a baseline assessment of the durability of styrene- and epoxy-based shape memory polymer resin materials being considered for morphing applications when exposed to service environment. The approach for the experimental evaluation is a measurement of the shape memory properties and elastomeric response before and after separate environmental exposure to (i) water at 49°C for 4 days, (ii) in lube oil at room temperature and at 49°C for 24 h, and (iii) after exposure to xenon arc (63°C, 18 min water and light/102 min light only) and spectral intensity of 0.3—0.4 watts/m2 for 125 cycles (250 h exposure time). Parameters being investigated include modulus in the rubbery and glassy state, stored strain, shape fixity, stress recovery ratio, and linear shape recovery. In addition, we monitor changes in specimen color, weight, and dimensions along with onset of damage due to conditioning and subsequent thermomechanical cycling.


ACS Applied Materials & Interfaces | 2011

In situ SEM Observation of Column-like and Foam-like CNT Array Nanoindentation

Matthew R. Maschmann; Qiuhong Zhang; Robert Wheeler; Feng Du; Liming Dai; Jeffery W. Baur

Quantitative nanoindentation of nominally 7.5 and 600 μm tall vertically aligned carbon nanotube (VACNT) arrays is observed in situ within an SEM chamber. The 7.5 μm array consists of highly aligned and weakly interacting CNTs and deflects similarly to classically defined cylindrical columns, with deformation geometry and critical buckling force well estimated using the Euler-Bernoulli theory. The 600 μm array has a highly entangled foam-like morphology and exhibits sequential buckle formation upon loading, with a buckle first forming near the array bottom at approximately 2% strain, followed by accumulating coordinated buckling at the top surface at strains exceeding 5%.


Journal of Applied Physics | 2012

Photomechanical bending mechanics of polydomain azobenzene liquid crystal polymer network films

Liang Cheng; Yanira Torres; Kyung Min Lee; Amber J. W. McClung; Jeffery W. Baur; Timothy J. White; William S. Oates

Glassy, polydomain azobenzene liquid crystal polymer networks (azo-LCNs) have been synthesized, characterized, and modeled to understand composition dependence on large amplitude, bidirectional bending, and twisting deformation upon irradiation with linearly polarized blue-green (440–514 nm) light. These materials exhibit interesting properties for adaptive structure applications in which the shape of the photoresponsive material can be rapidly reconfigured with light. The basis for the photomechanical output observed in these materials is absorption of actinic light by azobenzene, which upon photoisomerization dictates an internal stress within the local polymer network. The photoinduced evolution of the underlying liquid crystal microstructure is manifested as macroscopic deformation of the glassy polymer film. Accordingly, this work examines the polarization-controlled bidirectional bending of highly concentrated azo-LCN materials and correlates the macroscopic output (observed as bending) to measured ...


Advanced Materials | 2014

Bioinspired carbon nanotube fuzzy fiber hair sensor for air-flow detection.

Matthew R. Maschmann; Gregory J. Ehlert; Benjamin T. Dickinson; David M. Phillips; Cody W. Ray; Greg W. Reich; Jeffery W. Baur

Artificial hair sensors consisting of a piezoresistive carbon-nanotube-coated glass fiber embedded in a microcapillary are assembled and characterized. Individual sensors resemble a hair plug that may be integrated in a wide range of host materials. The sensors demonstrate an air-flow detection threshold of less than 1 m/s with a piezoresistive sensitivity of 1.3% per m/s air-flow change.


Journal of Applied Physics | 2003

Investigation of electrostatic self-assembly as a means to fabricate and interfacially modify polymer-based photovoltaic devices

Michael F. Durstock; Robert J. Spry; Jeffery W. Baur; Barney E. Taylor; Long Y. Chiang

This work focuses on studying a water-based processing method for fabricating and modifying polymer-based photovoltaic devices based on donor–acceptor type complexes. Electrostatic self-assembly is a simple technique that involves immersion of a substrate into dilute aqueous solutions of positively and negatively charged polymers. Extremely thin layers of these polymers are adsorbed onto the surface and their structure can be tailored by manipulating deposition conditions such as the concentration, pH, and salt content. Poly(p-phenylene vinylene) (PPV) containing bilayers were examined as the donor block and water soluble, functionalized C60 molecules were investigated for the acceptor block. By varying the number of bilayers deposited in each individual block (i.e., the block thickness), we have been able to demonstrate a peak in device performance. By controlling the thickness of both the donor and acceptor blocks, we have determined the optimal device architecture for this system. Additionally, we have...


Synthetic Metals | 2001

Electrostatic self-assembly as a means to create organic photovoltaic devices

Michael F. Durstock; Barney E. Taylor; Robert J. Spry; Long Y. Chiang; S. Reulbach; K Heitfeld; Jeffery W. Baur

Abstract Recently, there has been a significant amount of work done on making photovoltaic devices (solar cells) from thin films of conjugated polymers and other organic systems. The advantages over conventional inorganic systems include the potential to create lightweight, flexible, and inexpensive structures. The challenge, however, has been to create more highly efficient devices. To date, the primary photovoltaic device mechanism that has been utilized is that of photoinduced charge transfer between an electron donor and acceptor. In this study, similar photovoltaic devices are fabricated using a water-based electrostatic self-assembly procedure, as opposed to the more conventional spin-coating and/or vacuum evaporation techniques. In this process, layers of oppositely charged species are sequentially adsorbed onto a substrate from an aqueous solution and a film is built up due to the electrostatic attraction between the layers. The technique affords molecular level control over the architecture and gives bilayer thickness values of the order of tens of angstroms. By repeating this process a desired number of times and utilizing different cations and anions, complex architectures can be created with very accurate control over the thickness and the interfaces. We have examined a number of systems built from a variety of components including a cationic PPV precursor, functionalized C 60 , and numerous other polyelectrolytes. We report on the device characteristics of these films and on the overall applicability of this technique to the fabrication of photovoltaic devices.


Synthetic Metals | 2001

Photovoltaic interface modification via electrostatic self-assembly

Jeffery W. Baur; Michael F. Durstock; Barney E. Taylor; Robert J. Spry; S. Reulbach; Long Y. Chiang

The device efficiency of PPV-C 60 based photovoltaic devices has been substantially increased by increasing the interfacial area between the electron donor and acceptor layers. Electrostatic Self-Assembly (ESA) provides a means to deposit thin films of electroactive materials with a very controlled thickness and has shown usefulness in modifying physical and electrical interfaces. In this study, we attempt to control the effective interfacial area by modifying the interface between the PPV electron donor and C 60 -based electron acceptor with molecularly blended ESA bilayers of PPV and derivatized C 60 . It is observed that with only 2 bilayers of (PPV/C 60 - ) a 3-fold increase in device efficiency is obtained. Thus, ESA films offer promise for the nanoscaled modification of interfaces in organic-based photocells.


Smart Materials and Structures | 2015

Detection of flow separation and stagnation points using artificial hair sensors

D M Phillips; C W Ray; B J Hagen; Weihua Su; Jeffery W. Baur; Gregory W. Reich

Recent interest in fly-by-feel approaches for aircraft control has motivated the development of novel sensors for use in aerial systems. Artificial hair sensors (AHSs) are one type of device that promise to fill a unique niche in the sensory suite for aerial systems. In this work, we investigate the capability of an AHS based on structural glass fibers to directly identify flow stagnation and separation points on a cylindrical domain in a steady flow. The glass fibers are functionalized with a radially aligned carbon nanotube (CNT) forest and elicit a piezoresistive response as the CNT forest impinges on electrodes in a micropore when the hair is deflected due to viscous drag forces. Particle image velocimetry is used to measure the flow field allowing for the resulting moment and force acting on the hair to be correlated with the electrical response. It is demonstrated that the AHS provides estimates for the locations of both the stagnation and separation in steady flow. From this, a simulation of a heading estimation is presented to demonstrate a potential application for hair sensors. These results motivate the construction of large arrays of hair sensors for imaging and resolving flow structures in real time.


Smart Materials and Structures | 2012

Force sensitive carbon nanotube arrays for biologically inspired airflow sensing

Matthew R. Maschmann; Ben Dickinson; Gregory J. Ehlert; Jeffery W. Baur

The compressive electromechanical response of aligned carbon nanotube (CNT) arrays is evaluated for use as an artificial hair sensor (AHS) transduction element. CNT arrays with heights of 12, 75, and 225 µm are examined. The quasi-static and dynamic sensitivity to force, response time, and signal drift are examined within the range of applied stresses predicted by a mechanical model applicable to the conceptual CNT array-based AHS (0–1 kPa). Each array is highly sensitive to compressive loading, with a maximum observed gauge factor of 114. The arrays demonstrate a repeatable response to dynamic cycling after a break-in period of approximately 50 cycles. Utilizing a four-wire measurement electrode configuration, the change in contact resistance between the array and the electrodes is observed to dominate the electromechanical response of the arrays. The response time of the CNT arrays is of the order of 10 ms. When the arrays are subjected to constant stress, mechanical creep is observed that results in a signal drift that generally diminishes the responsiveness of the arrays, particularly at stress approaching 1 kPa. The results of this study serve as a preliminary proof of concept for utilizing CNT arrays as a transduction mechanism for a proposed artificial hair sensor. Such a low profile and light-weight flow sensor is expected to have application in a number of applications including navigation and state awareness of small air vehicles, similar in function to natural hair cell receptors utilized by insects and bats.

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G. P. Tandon

University of Dayton Research Institute

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Amber J. W. McClung

Air Force Research Laboratory

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Keith Slinker

Air Force Research Laboratory

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Liming Dai

Case Western Reserve University

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David M. Phillips

Air Force Research Laboratory

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Corey Kondash

Air Force Research Laboratory

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