• Electrical & Electronic Materials
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• v.8 no.5
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• pp.658-663
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• 1995

전자재료라 총칭하는 재료의 종류는 셀 수 없을 정도로 많다. 대표적인 전자재료로는 반도체재료를 들 수 있으며 다음으로는 전기광학 소자의 재료로 쓰이는 여러가지 광학용 단결정, 그리고 저항이나 축전지 등의 제조에 사용되는 여러가지 재료들도 이에 포함된다. 이러한 전자재료의 특성을 평가하는 방법도 여러가지 있겠으나 여기에서는 그 범위를 임의로 반도체레이저의 제조에 사용되는 화합물반도체에 국한시켜 각 공정별로 이떠한 평가방법이 사용되는지, 그리고 각각의 특성평가 방법에 대하여 간략하게 알아보기로 한다.

• Journal of the Korean Chemical Society
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• v.21 no.2
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• pp.108-120
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• 1977

The approximate rates and stoichiometries of the reaction of lithium borohydride, with fifty two selected organic compounds containing representative functional groups under the standard condition (tetrahydrofuran, $0^{\circ}$), were studied.Among the active hydrogen compounds,primary alcohols and compounds containing an acidic proton liberated hydrogen relatively fast, but secondary and tertiary alcohols very sluggishly. All the carbonyl compounds examined were reduced rapidly within one hour. Especially, among the ${\alpha}{\beta}$-unsaturated carbonyl compounds tested, the aldehydes consumed one hydride cleanly, however the cyclic ketones consumed more than one hydride even at $-20^{\circ}$. Carboxylic acids were reduced very slowly, showing about 60% reduction in 6 days at $25^{\circ}$, however acyl chlorides reduced immediately within 30 minutes. On the other hand, the reductions of cyclic anhydrides proceeded moderately to the hydroxy acid stage, however the further reductions were very slow. Aromatic and aliphatic esters, with exception of the relatively moderate reduction of acetate, were reduced very slowly, however lactones were reduced at a moderate rate. Epoxides reacted slowly, but amides and nitriles as well as the nitro compounds were all inert to this reagent. And cyclohexanone oxime and phenyl isocyanate were reduced very sluggishly. Last of all, all sulfur compounds studied were inert to this hydride.

• Journal of the Korean Electrochemical Society
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• v.19 no.2
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• pp.29-38
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• 2016

Screen printed carbon electrodes (SPCEs) with immobilized osmium-based hydrogel redox polymer, uricase and PEGDGE can be used to apply uric acid electrochemical detecting. The osmium redox complexes were synthesized by the coordinating pyridine group having different functional group at 4-position with osmium compounds. The synthesized poly-osmium hydrogel complexes are described as PAA-PVI-$[Os(dCl-bpy)_2Cl]^{+/2+}$, PAA-PVI-$[Os(dme-bpy)_2Cl]^{+/2+}$, PAA-PVI-$[Os(dmo-bpy)_2Cl]^{+/2+}$. The different concentrations of uric acid were measured by cyclic voltammetry technique using enzyme-immobilized SPCEs. The prepared SPCEs using PAA-PVI-$[Os(dme-bpy)_2Cl]^{+/2+}$ showed no interference from common physiologic interferents such as ascorbic acid (AA) or glucose. The resulting electrical currents at 0.33 V vs. Ag/AgCl displayed a good linear response with uric acid concentrations from 1.0 to 5.0 mM. Therefore, this approach allowed the development of a simple, point of care in the medical field, disposable electrochemical uric acid biosensor.

• Venture DIGEST
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• s.118
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• pp.8-11
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• 2008

국내 반도체 산업이 태동하여 빠르게 발전하던 1990년대, 차세대 반도체 제조용 박막 증착 화합물인 ALD/CVD Precursor 분야는 전적으로 수입에 의존하고 있는 실정이었다. 이 같은 국내 반도체 시장의 한계를 오히려 도전 기회로 삼아 기술개발에 힘쓴 결과, 독자적인 기술로 탄탄한 성장거점을 마련한 유피 케미칼을 만나본다.

• Journal of the Korean Chemical Society
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• v.20 no.1
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• pp.59-72
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• 1976

The addition of one mole of zinc chloride to 2.33 moles of sodium borohydride in tetrahydrofuran at room temperature gave a clear chloride-free supernatant solution of zinc borohydride after stirring three days and standing at room temperature.The approximate rates and stoichiometry of the reaction of zinc borohydride with 54 selected organic compounds were determined in order to test the utility of the reagent as a selective reducing agent. Aldehydes and ketones were reduced rapidly, aromatic ketones being somewhat slowly, and the double bond of cinnamaldehyde was not attacked. Acyl halides were reduced rapidly within one hour, but acid anhydrides were reduced at a moderate rate. Carboxylic acids, both aliphatic and aromatic, were slowly reduced to alcoholic stage. Esters were inert to this reagent but a cyclic ester, γ-butyrolactone, was slowly attacked. Primary amides were reduced slowly with partial evolution of hydrogen, whereas tertiary amides underwent neither reduction nor hydrogen evolution. Epoxides and nitriles were all inert, as well as nitro, azo, and azoxy compounds. Cyclohexanone oxime and phenyl isocyanate were reduced slowly but pyridine was inert. Disulfide, sulfoxide, sulfone and sulfonic acids were stable to this reagent.

• Analytical Science and Technology
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• v.27 no.3
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• pp.167-171
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• 2014

Hydrofluoric acid (HF), a typical inorganic acid, has been used in the industry for its various usage and classified as the toxic compound, because it can cause the pneumonia and pulmonary edema when it was exposed to respiratory organs. The official environmental analytical method for fluorine and its compound in waste has not been developed. For this reason, we have faced some problem to treat the contaminated wastes by the HF leakage from industrial process. In this study, prepared for analytical method for combustible waste (crop, trees, etc.) generated from HF leaking accident and to be applied as the official analytical method for fluorine contaminated waste when the fluorine and its compound will be regulated as a hazardous material by the waste management law later.

• The Korean Journal of Pesticide Science
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• v.7 no.1
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• pp.51-57
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• 2003

For the purpose of a development of new agrochemical fungicides, new compound 4 in which 1,3-thiazoline scaffold as well as urea moiety in the structure was designed through molecular modification of lead compound, 2-imino-1,3-thiazone based on isosterism. The reaction of N-alkylthiourea 5 and bromoacetonitrile in ethanol gave 2,4-diimino-1,3-thiazolidine hydrobromide 6 regioselectively, which was treated with isocyanates gave the corresponding 8 which is tautomer of 4. Antifungal screening (in vivo) of the synthesized compound 8 against typical plant diseases, which include rice blast, rice sheath blight, cucumber gray mold, tomato late blight, wheat leaf rust, and barley powdery mildew, was carried out. Antifungal activities against rice blast of the compound 8 were weaker than those of 2-phenylimino-1,3-thiazoline 1. Some compounds showed weak antifungal activities against wheat leaf rust.

• Proceedings of the Korean Vacuum Society Conference
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• 2000.02a
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• pp.65-65
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• 2000

반도체 소자의 고집적화는 배선에서 많은 문제점을 야기 시킨다. 이러한 문제점들 중에서 대표적인 것이 과도한 전류밀도에 의한 electro-migration(EM)이다. 이는 앞으로 배선의 선폭이 0.25$mu extrm{m}$미만일 경우 더욱 심화될 전망이다. 이에 대안으로 Al-합금에서 Cu로 대체하여 이러한 문제를 해결하려 하고 있다. 그런데, Cu는 Si 및 SiO2와 높은 반응성과 빠른 확산속도를 가지기 때문에 확산방지막이 필요로 되어진다. 현재에는 TiN, TaN 등의 확산방지막이 사용되어지고 있으나, TiN 박막의 경우 표면에 Ti와 oxide와의 결합에 의해 Ti-O 성분이 존재하는데, 이럴 경우 Cu 증착을 하는데 있어 부정적인 요인이 된다. 또한, 이러한 화합물은 Cu와 TiN 계면사이에 밀착성을 나쁘게 하여 고전류 인가시 EM에 있어 높은 저항성을 가질 수가 없다. 따라서, 본 연구는 MOCVD방식으로 Cu 박막을 증착하기에 앞서 수소플라즈마를 이용하여 TiN 표면에 형성된 산소 화합물을 제거한 후 Cu를 증착하여 동일한 조건에서 EM 가속화 실험을 하였다. 그림 1은 Cu/TiN 구조에 있어 수소 전처리를 한 배선의 구조의 MTF(mean time to failure)가 65분이고 전처리를 하지 않은 배선구조는 40분으로 약 50% 긴 MTF를 가지는 것으로 나왔다. 결론적으로 Cu와 TiN 계면에 좋은 밀착성은 EM에 있어 우수한 저항성을 가지는 것으로 나왔다.

• The Korean Journal of Pesticide Science
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• v.10 no.3
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• pp.165-171
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• 2006

A new 3-amino-1,3-thiazoline chemical library was synthesized through parallel synthetic technology and in vivo antifungal activity of the compounds were investigated against the typical 6 plant diseases (100 ppm). The characteristic feature of these derivatives was that both a benzyl moiety in C-2 imino and an amino group in C-3 of 2-imino-1,3-thiazoline scaffold were substituted in the molecule respectively. Some compounds showed antifungal activity with selectivity against tomato late blight and rice blast. The fungitoxicity would be attributed to 3,4-dichlorophenyl moiety of the benzyl group.

• Proceedings of the Materials Research Society of Korea Conference
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• 2009.05a
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• pp.8.2-8.2
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• 2009

구리(Cu)-인듐(In)-갈륨(Ga)-셀레늄(Se)의 4 원소 화합물 반도체인 Cu(InGa)$Se_2$ (CIGS) 태양전지 세계 최고 셀효율은 2008년 현재 19.9% 로서 박막형 태양전지 중 가장 높은 효율을 보이고 있다. 이는 다결정(폴리) 실리콘 태양전지의 20.3%와 대등한 수준이다. 이 CIGS 태양전지는 제조단가를 표준 결정형 실리콘 태양전지 대비 50% 대로 획기적으로 낮출 수 있어 가장 경쟁력이 있는 차세대 재료로 꼽히고 있다. 본 연구에서는 CIGS태양전지를 고진공 물리 증작법으로 제작하였으며 표면과 박막의 순도를 외부오염을 방지하기 위하여 후면전극, 광흡수체 및 전면전극을 동일 진공에서 제작할 수 있는 멀티 챔버 클러스터 증착 시스템을 이용하였다. 기판으로 소다라 임유리, 후면전극으로 Mo, 전면전극으로 I-ZnO/Al:ZnO 및 ITO를 이용하였다. 버퍼층으로 CdS를 chemical bath deposition (CBD)를 이용하였다. 소자는 무반사막을 사용하지 않고 Al/Ni전극 그리드를 이용하였다. 이 소자로부터 0.22 $cm^2$에서 16%의 효율을 얻었다. 각 박막층 간 계면의 분석을 전기적인 특성, ellisometry에 의한 광특성, 표면과 결정성에 대한 SEM 및 XRD의 특성을 보고한다. 또한, 대표적 화합물 반도체 박막 태양전지인 CIGS 태양전지의 기술의 현황, 학문적인 과제 및 실용화의 문제점을 발표하기로 한다.