• 한국표면공학회:학술대회논문집
• /
• 한국표면공학회 2006년도 추계학술발표회 초록집
• /
• pp.89-89
• /
• 2006

• 한국표면공학회지
• /
• 제22권4호
• /
• pp.207-214
• /
• 1989

The surface morphology and the proferred orientation of the Pb-Sn alloy electrodeposite were investated by the change of electrolysis conditions in pulse current electroplating. The preferred orientation of Pb-phase in alloy deposits was changed in the sequence of (110)longrightarrow(100)or(100)+(111)longrightarrow(111) with increasing peak current density, while that of $\beta$-Sn phase changed from (321)+(301)to(301)+(111) mixed orientation. The surface morphology was closely related to the preferred orientation of alloy electrodeposits. The alloy deposits, which had (100)or(111) for pb-phase and (321)or(100)(301)for $\beta$-Sn sespectively, showed the surface structure of granular crystallites. The alloy deposits whih mixed orientations for both phases had microstructure of closely the closely stacked crysrallites, which was inclined to the surface.

• 한국표면공학회지
• /
• 제42권5호
• /
• pp.191-196
• /
• 2009

Nanocrystalline Cu thin films were electrodeposited from sulfate baths and investigated systematically the influences of $Cu^{2+}$ concentration and additives on current efficiency, residual stress, surface morphology, and XRD patterns of electrodeposited Cu film. Current efficiency was nearly 100% at from 0.2M to 1.0 M $Cu^{2+}$ concentration. but it was linearly increased with $Cu^{2+}$ concentration at less than 0.2M. The residual stress was observed in range of 7.9 to 18.4 MPa and tensile stress mode. Dendritic and powdered form was obtained at below 0.1 M. As increased with $Cu^{2+}$ concentration in solution, the main peak in the XRD pattern shifted (111) and (220) from (200). In the other hand, all about 100% current efficiency observed in all additive concentration systems, and residual stress observed in range of 20.4 to 26.3 MPa tensile stress. The condition 5(Ultra make-up - 10 ml/l, Ulta A - 0.5ml/l, Ultr B - 0.5 ml/l) was good surface morphology, and fcc(111) peak in XRD patterns increased with increasing additive concentration.

• 전기화학회지
• /
• 제13권2호
• /
• pp.132-137
• /
• 2010

본 연구는 KOH 전해질에서 전기화학적으로 석출된 망간 산화물이 산소 환원 반응에 미치는 전기화학적 촉매 역할에 대해 고찰하였다. 나노 사이즈 망간 산화물들은 Glassy carbon(GC), Gold(Au) 그리고 Titanium(Ti)로 이루어진 전극에 전해방식으로 석출시켰으며, 각 전극 표면에 나노 사이즈로 균일하게 분포되어 있는 것이 SEM 관찰을 통해서 확인되었다. 망간산화물의 한 종류인 $\gamma$-MnOOH는 산소 환원반응에 수반되는 4-electron 반응에서 촉매 역할을 하는 것을 확인하였다. 망간산화물이 전기화학적으로 석출된 전극들은 전해석출을 하지 않은 전극들에 비해서 양극 전위가 낮아지는 것을 확인할 수 있었다.

• Journal of Electrochemical Science and Technology
• /
• 제2권3호
• /
• pp.168-173
• /
• 2011

The availability, low toxicity, and high degree of technological development make silicon the most likely material to be used in solar cells, the cost of solar cells depends entirely on cost of high purity silicon production. The present work was conducted to electrodeposite of silicon from $K_2SiF_6$, an inexpensive raw material prepared from fluorosilicic acid ($H_2SiF_6$) produced in Iraqi Fertilizer plants, and using inexpensive graphite material as cathode electrode. The preparation of potassium fluorosilicate was performed at ($60^{\circ}C$) in a three necks flask provided with a stirrer, while the electro deposition was performed at $750^{\circ}C$ in a three-electrodes configuration with melt containing in graphite pot. High purity potassium fluorosilicate (99.25%) was obtained at temperature ($60^{\circ}C$), molar ratio-KCl/$H_2SiF_6$(1.4) and agitation (600 rpm). Spongy compact deposits were obtained for silicon with purity not less than (99.97%) at cathode potential (-0.8 V vs. Pt), $K_2SiF_6$ concentration (14% mole percent) with grain size (130 ${\mu}m$) and level of impurities (Cu, Fe and Ni) less than (0.02%).

• 대한금속재료학회지
• /
• 제50권3호
• /
• pp.237-242
• /
• 2012

The objective of this study is to investigate the effect of additives on the mechanical and electrical characteristics of electrodeposited copper foils. Additives A(leveler) and B(brightener) were used in this study and Cl ions were used as an accelerator. In case of using these additives A and B, it showed a disadvantage that decreased the elongation of electrodeposited layer due to decreased grain sizes and increased tensile strength. On the other hand, the Cl ions decreased the specific resistance of the copper layer and increased elongation owing to increasing grain sizes. The highest elongation and lowest resistivity were measured in the group added only Cl ions, whose values were 21.9% and $3.11{\mu}\Omega$-cm, respectively.

• 공업화학
• /
• 제7권2호
• /
• pp.280-288
• /
• 1996

여러 가지 전착 조건에서 티타늄 기판상에 이산화납을 전착시킨 전극을 사용하여 전해질 용액 중에서 오존을 발생시킬 경우 전착된 이산화납의 결정표면 양상이 오존발생 전류효율에 미치는 영향과 이산화납 전극의 표면구조 변화를 고찰하였다. 또한 백금 디스크전극 위에 이산화납을 전착시킨 회전전극을 이용하여 산소전이반응이 오존발생에 미치는 영향과 오존발생용 전극으로 개발하기 위해 이산화납의 내식성과 오존발생 최적 전류밀도도 검토하였다. 전착한 이산화납의 결정표면 입자가 크고 결정성이 좋은 전극일수록 오존발생 전류효율이 높았으며 이러한 오존발생용 이산화납 전극을 전착시키기 위한 최적전류밀도는 $50mA/cm^2$이었으며 전착용액에 글리세린을 소량 첨가하면 오존발생에 유리한 결정구조를 갖는 이산화납이 전착되었다. 또한 $10mA/cm^2$ 이하의 너무 낮거나 $100mA/cm^2$ 이상의 너무 높은 전류밀도에서는 오존발생 성능이 떨어지고 소지금속에 대한 접착성이 좋지 않은 전극이 만들어 졌다. 새로 만들어진 이산화납전극을 오존발생용으로 사용할 때 사용 초기 단계에서 이산화납전극의 표면구조 변화가 일어나며 이는 오존발생에 유리한 효과를 가져왔다. 타원소를 도핑시킨 이산화납 전극에서는 오존발생보다 산소발생 반응이 활발하게 일어나 오존발생은 산소발생의 중간 단계를 거치지 않고 산소발생과는 경쟁적으로 일어나는 것으로 추정되며 $0.7{\sim}0.8A/cm^2$의 전류밀도에서 최대의 오존발생 전류효율을 나타내었다.

• 한국수소및신에너지학회논문집
• /
• 제21권1호
• /
• pp.26-34
• /
• 2010

The electrocatalystic prperties of Pt-Co and Pt-Ni with heteropolyacids (HPAs) entrapped in covalently cross-linked sulfonated poly(ether ether ketone) (CL-SPEEK)/HPA membranes were investigated for water electrolysis. The HP As, including molybdophosphoric acid (MoPA), and tungstophosphoric acid (TPA) were both used as membrane additives and electrocatalysts. The membrane electrode assembly (MEA) was prepared by a nonequilibrium impregnation-reduction (I-R) method. $Pt(NH_3)_4Cl_2$, $NiCl_2$ and $CoCl_2$ as electrocatalytic materials and $NaBH_4$ as reducing agent were used. I order to enhance electrocatalytic activity, the catalyst layer prepared above was electrodeposited (Dep) with HP A. Surface morphologies and physico-chemical properties of MEA were investigated by means of SEM, EDX and XRD. The electrocatalytic properties of composite membranes such as the cell voltage and coulombic charge in CV were in the order of magnitude: CL-SPEEK/MoPA40 (wt%) > CL-SPEEK/TPA30 > Nafion117. In the optimum cell applications for water electrolysis, the cell voltage of Pt/CL-SPEEK-MoPA40/Pt-Co (Dep-MoPA) and Pt/CL-SPEEK-TPA30/Pt-Co (Dep-TPA) was 1.75 Vat $80^{\circ}C$ and $1\;A/cm^2$ and voltage efficiency was 87.1%. Also, the observed activity of Pt-Co (84:16 atomic ratio by EDX) is a little higher than that of Pt-Ni (86: 14). The current density peak of electrodeposited electrodes were better a little than those of unactivated electrodes based on the same membranes.