• 한국군사과학기술학회지
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• 제24권6호
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• pp.655-663
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• 2021

In this paper, DFT-Based channel estimation with channel response mirroring is proposed and analyzed. In General, pilot symbols for channel estimation in MIMO(Multi-Input Multi-Output) OFDM(Orthogonal Frequency-Division Multiplexing) Systems have a diamond shape in the time-frequency plane. An interpolation technique to estimate the channel response of sub-carriers between reference symbols is needed. Various interpolation techniques such as linear interpolation, low-pass filtering interpolation, cubic interpolation and DFT interpolation are employed to estimate the non-pilot sub-carriers. In this paper, we investigate the conventional DFT-based channel estimation for noise reduction and channel response interpolation. The conventional method has performance degradation by distortion called "edge effect" or "border effect". In order to mitigate the distortion, we propose an improved DFT-based channel estimation with channel response mirroring. This technique can efficiently mitigate the distortion caused by the DFT of channel response discontinuity. Simulation results show that the proposed method has better performance than the conventional DFT-based channel estimation in terms of MSE.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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• pp.193-193
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• 2013

Perfluorocarbons (PFCs) have been suggested as possible replacements for $SF_6$ and the fluorocarbons used in and emitted during technological plasma treatments because PFCs have significantly low greenhouse warming potentials. Of many PFCs, c-$C_4F_8$ and 2-$C_4F_8$ attract special attention because of their high CF2 radicallevels in commercial plasma treatments. Accordingly, several experimental and theoretical studies of these $C_4F_8$ species have been conducted, although only the geometries at their stationary states and their adiabatic electron affinities (EAs) have been determined. However, this information is not sufficient for a deep understanding of all the possible fates and roles of $C_4F_8$ species and their fragments in plasma phases. Although the performance and reliability ofeach DFT functional have been examined carefully by the development team of each functional form with respect to the training and test data sets of well-known molecular systems, no PFC was included in the data sets. So a careful additional assessment of the reliability of DFT functionals for the study of PFC systems is highly required. In order to find a DFT method appropriate to PFCs, the geometry, energy, and chemical reaction properties of $C_4F_8$ were calculated and compared with reference data.

• 생물환경조절학회지
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• 제8권2호
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• pp.90-98
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• 1999

양액재배시 적합한 배지와 배양액농도를 선발하고자 본 실험을 수행하였으며, 공시작물은 백리향(Thymus vulgaris L.)으로 하였다. 배양액의 농도는 European Vegetable R&D Center에서 개발한 herb 배양액(EC=2.4)을 0.5, 1, 2, 3배로 조제하여 사용하였다. 배지는 고형배지로 펄라이트 단용, 코코피트 단용 그리고 펄라이트와 코코피트 혼용(50:50 v/v)을 사용하였고, 비고형배지로는 DFT를 사용하여 총 4처리로 하였다. 생육은 다른 배지 처리구보다 담액수경에서 가장 좋았다. 펄라이트와 담액수경에서는 배양액농도가 높을수록 생육이 감소하였으나 코코피트는 1배, 혼용 배지는 2배 처리구에서 가장 높은 생체중을 보였다. 엽록소와 비타민 C의 함량 또한 다른 배지 처리구보다 담액수경에서 더 높은 함량을 보였다. 배지의 종류에 따른 무기물 함량은 NO$_{3}$-N과 Mg를 제외하고 모두 코코피트에서 가장 높은 함량을 나타내었다. NO$_{3}$-N의 함량은 담액 수경에서 1000 ppm 내외의 낮은 함량을 보였다. 따라서 본 실험의 결과, 백리향의 생육은 DFT를 사용하여 herb배양액 0.5배(EC =1.2mS/cm)농도로 재배한 처리구에서 가장 좋은 생육을 보였다.

• 한국통신학회논문지
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• 제32권4C호
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• pp.440-446
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• 2007

본 논문은 엘레멘트 인버스 처리에 근거한 재킷 변환을 통한 DFT 행렬의 새로운 표현을 다룬다. DFT 행렬의 역을 단지 재킷 변환의 소행렬 분해에 따라 표현하며 이러한 결과는 DFT 행렬의 역이 단지 이의 희소 행렬과 치환 행렬에만 관련됨을 보여준다. 재킷 행렬을 통한 DFT 행렬의 분해는 블록 변조 특성을 나타내는 강한 기하 구조를 갖는다. 이는 재킷 행렬을 통해 분해된 DFT 행렬은 블록 변조 과정으로 해석할 수 있음을 의미한다.

• 한국통신학회논문지
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• 제32권6C호
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• pp.594-599
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• 2007

본 논문에서는 하이브리드 구조에 의한 DCT/DFT 행렬의 새로운 표현을 제시한다. 엘레멘트 인버스 소행렬 분해 알고리즘에 근거하여 DCT와 DFT가 동일한 반복 연산 패턴을 갖고 있음을 보이며, 몇몇 대각행렬을 이용한 하이브리드 구조를 개발한다.

• 대한전자공학회논문지
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• 제14권6호
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• pp.26-30
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• 1977

DFT 및 FFT의 계산과정에 포함된 redunduncy를 분석하고 이 redundancy를 최대한으로 감소시키는 방장을 제안하였다. 이로서 FFT계산 등을 위한 계산기시간이 대폭감축됨을 실증하였다. T.D.C.F와 T.D.F.T 등을 Discrete한 경우에 확장하여 Digital Signal Processing의 여러 과정에 있어서 더 길은 물리적 뜻을 부여할 수가 있었다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.136-136
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• 2013

High-resolution photoemission spectroscopy (HRPES) measurements were collected and density functional theory (DFT) calculations were conducted to track the coverage dependent variation of the absorption structure of 2-thiophenecarboxaldehyde (C4H3SCHO: TPCA) on the Ge(100) surface at room temperature. In an effort to identify the most probably adsorption structures on the Ge(100) surface, we deposited TPCA molecules at a low coverage and at a high coverage and compared the differences between the electronic features measured using HRPES. The HRPES data provided three possible adsorption structures of TPCA on the Ge(100) surfaces, and DFT calculations were used to determine the plausibility of the structures. HRPES analysis, corroborated by DFT calculations, indicated that an S-dative bonded structure was the most probable adsorption structure at relatively lower coverage levels, the [4+2] cycloaddition structure was the second most probable structure, and the [2+2]-C=O cycloaddition structure was the last probable structure on the Ge(100) surfaces at relatively higher coverage levels.

• Bulletin of the Korean Chemical Society
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• 제35권4호
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• pp.1005-1010
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• 2014

We have performed DFT calculations to devise some possible fullerene dimers (from $C_{60}$ and $C_{80}$) connected through $C_{24}$ and $C_{36}$ bridge cages with the face-to-face linking model. The fullerene dimers with $C_{36}$ bridges have lower binding energies and greater HOMO-LUMO gaps than those of the fullerene dimers with $C_{24}$ bridges. Also, the replacement of $C_{60}$ cages with $C_{80}$ ones always leads to an increase in binding energies and HOMO-LUMO gaps in these systems. Dimerization of $C_{60}$ and $C_{80}$ fullerenes with $C_{24}$ and $C_{36}$ results in a significant decrease in antiaromaticity of the antiaromatic cages $C_{24}$ and $C_{80}$, and an increase in the aromaticity of the aromatic cages $C_{36}$ and $C_{60}$. Therefore, DFT results indicate that those fullerene dimers involving the initially harshly antiaromatic $C_{24}$ or $C_{80}$ cages are more energetically favorable configuration than the fullerene dimers involving the aromatic $C_{36}$ and $C_{60}$ cages.

• 대한화학회지
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• 제50권4호
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• pp.291-297
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• 2006

Cyclopropyl 링과 할로겐 원소가 결합된 붕소원자 사이의 hyperconjugation 효과를 알아보기 위하여 CPDFB와 CPCFB 분자의 여러 conformation과 transition state 구조들에 대해 DFT와 ab initio 방법을 사용하여 다양한 레벨에서 구조최적화 및 NBO 분석을 수행하였다. 그 결과 주요 상호작용 형태는 화합물에 따라 단일결합 오비탈 (C1-C3, C2-C3) n* (B9) 또는 *(B9-Cl11) 오비탈로 전자를 제공하는 것이었고 이때 안정화 에너지는 CPDFB 분자의 경우 6.63 kcal/mol, CPCFB 분자의 경우는 conformation에 따라 6.97(E-form)/6.79(Z-form) kcal/mol 이었다. 또한, BF2와 BFCl 기의 내부회전에 의한 회전장벽의 크기는 각각 5.3~6.7 kcal/mol과 5.7~6.5 kcal/mol로 기존에 보고된 실험값과 잘 일치함을 보였다. 마지막으로 CPCFB 분자의 conformers 중에서 Z-form이 global minimum으로 확인되었고 E-form 보다 0.2 kcal/mol 정도 안정하였다.

• Bulletin of the Korean Chemical Society
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• 제35권3호
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• pp.775-782
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• 2014

The importance of including spin-orbit interactions for the correct description of structures and vibrational frequencies of haloiodomethanes is demonstrated by density functional theory calculations with spin-orbit relativistic effective core potentials (SO-DFT). The vibrational frequencies and the molecular geometries obtained by SO-DFT calculations do not match with the experimental results as well as for other cations without significant relativistic effects. In this sense, the present data can be considered as a guideline in the development of the relativistic quantum chemical methods. The influence of spin-orbit effects on the bending frequency of the cation could well be recognized by comparing the experimental and calculated results for $CH_2BrI$ and $CH_2ClI$ cations. Spin-orbit effects on the geometries and vibrational frequencies of $CH_2XI$ (X=F, Cl, Br, and I) neutral are negligible except that C-I bond lengths of haloiodomethane neutral is slightly increased by the inclusion of spin-orbit effects. The $^2A^{\prime}$ and $^2A^{{\prime}{\prime}}$ states were found in the cations of haloiodomethanes and mix due to the spin-orbit interactions and generate two $^2E_{1/2}$ fine-structure states. The geometries of $CH_2XI^+$ (X=F and Cl) from SO-DFT calculations are roughly in the middle of two cation geometries from DFT calculations since two cation states of $CH_2XI$ (X=F and Cl) from DFT calculations are energetically close enough to mix two cation states. The geometries of $CH_2XI^+$ (X=Br and I) from SO-DFT calculations are close to that of the most stable cation from DFT calculations since two cation states of $CH_2XI$(X=Br and I) from DFT calculations are energetically well separated near the fine-structure state minimum.