Augustin J. Hong
IBM
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Publication
Featured researches published by Augustin J. Hong.
ACS Nano | 2011
Augustin J. Hong; Emil B. Song; Hyung Suk Yu; Matthew J. Allen; Ji-Young Kim; Jesse D. Fowler; Jonathan K. Wassei; Youngju Park; Yong Wang; Jin Zou; Richard B. Kaner; Bruce H. Weiller; Kang L. Wang
Graphenes single atomic layer of sp(2) carbon has recently garnered much attention for its potential use in electronic applications. Here, we report a memory application for graphene, which we call graphene flash memory (GFM). GFM has the potential to exceed the performance of current flash memory technology by utilizing the intrinsic properties of graphene, such as high density of states, high work function, and low dimensionality. To this end, we have grown large-area graphene sheets by chemical vapor deposition and integrated them into a floating gate structure. GFM displays a wide memory window of ∼6 V at significantly low program/erase voltages of ±7 V. GFM also shows a long retention time of more than 10 years at room temperature. Additionally, simulations suggest that GFM suffers very little from cell-to-cell interference, potentially enabling scaling down far beyond current state-of-the-art flash memory devices.
symposium on vlsi technology | 2008
Ji-Young Kim; Augustin J. Hong; Masaaki Ogawa; Siguang Ma; Emil B. Song; You-Sheng Lin; Jeong-Hee Han; U-In Chung; Kang L. Wang
A 3-D flash memory cell of VRAT (vertical-recess-array-transistor) has been fabricated using a unique and simple 3-D integration method of PIPE (planarized integration on the same plane), which allows for the successful implementation of ultra high density flash memory. In addition, procedures to increase the memory density further using another advanced structure, Zigzag-VRAT (Z-VRAT), are developed.
Nano Letters | 2010
Augustin J. Hong; Chi-Chun Liu; Yong Wang; Ji-Young Kim; Faxian Xiu; Shengxiang Ji; Jin Zou; Paul F. Nealey; Kang L. Wang
As information technology demands for larger capability in data storage continue, ultrahigh bit density memory devices have been extensively investigated. To produce an ultrahigh bit density memory device, multilevel cell operations that require several states in one cell have been proposed as one solution, which can also alleviate the scaling issues in the current state-of-the-art complementary metal oxide semiconductor technology. Here, we report the first demonstration of metal nanodot memory using a self-assembled block copolymer lift-off. This metal nanodot memory with simple low temperature processes produced an ultrawide memory window of 15 V at the +/-18 V voltage sweep. Such a large window can be adopted for multilevel cell operations. Scanning electron microscopy and transmission electron microscopy studies showed a periodic metal nanodot array with uniform distribution defined by the block copolymer pattern. Consequently, this metal nanodot memory has high potential to reduce the variability issues that metal nanocrystal memories previously had and multilevel cells with ultrawide memory windows can be fabricated with high reliability and manufacturability.
Nature Materials | 2010
Faxian Xiu; Yong Wang; Ji-Young Kim; Augustin J. Hong; Jianshi Tang; Ajey P. Jacob; Jin Zou; Kang L. Wang
Electric-field manipulation of ferromagnetism has the potential for developing a new generation of electric devices to resolve the power consumption and variability issues in todays microelectronics industry. Among various dilute magnetic semiconductors (DMSs), group IV elements such as Si and Ge are the ideal material candidates because of their excellent compatibility with the conventional complementary metal-oxide-semiconductor (MOS) technology. Here we report, for the first time, the successful synthesis of self-assembled dilute magnetic Mn(0.05)Ge(0.95) quantum dots with ferromagnetic order above room temperature, and the demonstration of electric-field control of ferromagnetism in MOS ferromagnetic capacitors up to 100 K. We found that by applying electric fields to a MOS gate structure, the ferromagnetism of the channel layer can be effectively modulated through the change of hole concentration inside the quantum dots. Our results are fundamentally important in the understanding and to the realization of high-efficiency Ge-based spin field-effect transistors.
Nanotechnology | 2011
Ji-Young Kim; Augustin J. Hong; Sung-min Kim; Kyeong-Sik Shin; Emil B. Song; Yongha Hwang; Faxian Xiu; Kosmas Galatsis; Chi On Chui; Rob N. Candler; Si-Young Choi; Joo-Tae Moon; Kang L. Wang
We have demonstrated, for the first time, a novel three-dimensional (3D) memory chip architecture of stacked-memory-devices-on-logic (SMOL) achieving up to 95% of cell-area efficiency by directly building up memory devices on top of front-end CMOS devices. In order to realize the SMOL, a unique 3D Flash memory device and vertical integration structure have been successfully developed. The SMOL architecture has great potential to achieve tera-bit level memory density by stacking memory devices vertically and maximizing cell-area efficiency. Furthermore, various emerging devices could replace the 3D memory device to develop new 3D chip architectures.
ACS Nano | 2012
Jeehwan Kim; Augustin J. Hong; Jae-Woong Nah; Byungha Shin; Frances M. Ross; Devendra K. Sadana
We introduce a cost-effective method of forming size-tunable arrays of nanocones to act as a three-dimensional (3D) substrate for hydrogenated amorphous silicon (a-Si:H) solar cells. The method is based on self-assembled tin nanospheres with sizes in the range of 20 nm to 1.2 μm. By depositing these spheres on glass substrates and using them as an etch mask, we demonstrate the formation of glass nanopillars or nanocones, depending on process conditions. After deposition of 150 nm thick a-Si:H solar cell p-i-n stacks on the glass nanocones, we show an output efficiency of 7.6% with a record fill factor of ~69% for a nanopillar-based 3D solar cell. This represents up to 40% enhanced efficiency compared to planar solar cells and, to the best of our knowledge, is the first demonstration of nanostructured p-i-n a-Si:H solar cells on glass that is textured without optical lithography patterning methods.
Nanotechnology | 2010
Jianshi Tang; Chiu-Yen Wang; Faxian Xiu; Augustin J. Hong; Shengyu Chen; Minsheng Wang; Caifu Zeng; Hong-Jie Yang; Hsing-Yu Tuan; Cho-Jen Tsai; Lih Juann Chen; Kang L. Wang
In this study, we report on the formation of a single-crystalline Ni(2)Ge/Ge/Ni(2)Ge nanowire heterostructure and its field effect characteristics by controlled reaction between a supercritical fluid-liquid-solid (SFLS) synthesized Ge nanowire and Ni metal contacts. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies reveal a wide temperature range to convert the Ge nanowire to single-crystalline Ni(2)Ge by a thermal diffusion process. The maximum current density of the fully germanide Ni(2)Ge nanowires exceeds 3.5 × 10(7) A cm(-2), and the resistivity is about 88 μΩ cm. The in situ reaction examined by TEM shows atomically sharp interfaces for the Ni(2)Ge/Ge/Ni(2)Ge heterostructure. The interface epitaxial relationships are determined to be [Formula: see text] and [Formula: see text]. Back-gate field effect transistors (FETs) were also fabricated using this low resistivity Ni(2)Ge as source/drain contacts. Electrical measurements show a good p-type FET behavior with an on/off ratio over 10(3) and a one order of magnitude improvement in hole mobility from that of SFLS-synthesized Ge nanowire.
Advanced Materials | 2014
Jeehwan Kim; Corsin Battaglia; Mathieu Charrière; Augustin J. Hong; Woo-Shik Jung; Hongsik Park; Christophe Ballif; Devendra K. Sadana
High aspect-ratio three-dimensional (3D) a-Si:H solar cells have been fabricated to enhance a light absorption path while maintaining a short carrier collection length. Substantial efficiency enhancement in 3D solar cells was achieved due to the boost in JSC with no degradation of FF which is comparable to FF obtained from 2D solar cells.
IEEE\/ASME Journal of Microelectromechanical Systems | 2012
Yongha Hwang; Feng Gao; Augustin J. Hong; Rob N. Candler
This paper presents a microscale resonant sensor that has been fabricated with nanoscale pores for enhanced sensitivity to chemical vapors. By building resonators that are made of porous silicon, we take advantage of the increased area for molecular binding and improve the sensitivity of the resonators to the vapor concentration of interest. We present results for resonators whose surfaces are entirely porous silicon. We also examine the use of targeted regions of porosity to keep critical parts of the beam nonporous and mechanically stable while still maximizing surface area. Surface micromachining processes were used to fabricate the silicon resonator mass sensor, allowing nanostructured devices to be fabricated using only standard top-down processing techniques. We have demonstrated an improvement up to 261% and 165% in resonator sensitivity to isopropyl alcohol forfully porous resonators and partially porous resonators, respectively, as compared to nonporous silicon resonators. Combining this increased sensitivity with resonator quality factor suggests an improvement in minimum detectable resolution over the nonporous resonators by 41% and 56% for the fully porous and partially porous resonators, respectively.
Applied Physics Letters | 2011
Jeehwan Kim; Ahmed Abou-Kandil; Augustin J. Hong; Mohamed Saad; Devendra K. Sadana; Tze-Chiang Chen
Carbon (C) incorporation in the p+ hydrogenated amorphous silicon (a-SiC:H) is highly desirable for a-Si:H based solar cells because of the following reasons: (i) it increases the band gap of the p+ layer to ∼2 eV, which allows a majority of the sun light to pass through the thin p+ layer (∼15 nm) and get absorbed in the underlying intrinsic a-Si:H layer, and (ii) it enhances built-in potential of the a-Si:H p-i-n stack, resulting in enhanced short circuit current (JSC) and open circuit voltage (VOC). Hence, it is a desire to incorporate the highest possible C % in the p+ a-Si:H. However, C incorporation results in a Schottky barrier at the p+ a-SiC:H/transparent conducting oxide (TCO) interface, which degrades the fill factor (FF) of the solar cell. In this paper, we present a method that increases the C incorporation in p+ a-SiC:H but without adversely affecting the FF, by adding a thin layer of hydrogenated amorphous germanium (a-Ge:H) buffer at the p+ a-SiC:H/TCO interface. The presence of a-Ge:H can ...