为了探究在只有阴离子不同的情况下铜颗粒的沉积差异,将第二组硅片平均分为3小堆,每堆4片,分别放入硝酸体系,硫酸体系和氯离子体系中沉积5s,1的英语翻译

为了探究在只有阴离子不同的情况下铜颗粒的沉积差异,将第二组硅片平均分为

为了探究在只有阴离子不同的情况下铜颗粒的沉积差异,将第二组硅片平均分为3小堆,每堆4片,分别放入硝酸体系,硫酸体系和氯离子体系中沉积5s,10s,30s及60s后取出,采用SEM观察铜沉积状态的变化,图2a~d显示了在硝酸铜沉积体系中铜的沉积情况,反应刚开始的10s内,大量铜离子捕获电子形成小铜颗粒沉积在硅表面,使铜铺满整个硅片,随着沉积时间延长,大量铜颗粒沿切割纹聚集形成较大的圆形铜颗粒,对硫酸铜体系,如图2e~h所示,反应刚开始,硅片表面便迅速形成一层致密的铜膜,且铜颗粒尺寸较小,沉积至60s时,铜膜表面出现少量团聚的铜颗粒,说明硫酸铜体系中,铜以分散的,小尺寸的致密铜膜的形态沉积,而不易发生团聚现象;而在氯离子体系中,如图2I~l所示,反应刚开始的形态与硝酸铜类似,沉积10s时便明显出现团聚现象,30s后,硅片表面沿切割纹出现了大量团聚的棒状铜颗粒;图2m~o展示了硅片沉积前以及沉积后硅片的质量变化,可知沉积60s后,硫酸铜,氯化铜体系中沉积前后硅片质量损失在0.002g以内,基本可以认为质量没有变化,而硝酸铜体系中,质量损失达到0.007g,是由硝酸根将硅表面氧化所致,图2p用Q表征铜颗粒的沉积量的相对大小以及铜的沉积速率,其中mCU=m2-m1,可以看出在前30s内,硝酸铜沉积速率最快,而后由于硝酸根的氧化作用,将少量铜颗粒氧化成铜离子,使得铜颗粒的量基本匀速增加,而硫酸铜体系中的铜颗粒则迅速增加,导致60s后铜沉积量超过硝酸铜体系中的铜颗粒,而由于氯化铜溶液中氯离子的极化作用,使得溶液中氯离子和铜离子之间的作用力加强,使得铜离子难以捕获硅片表面电子沉积成铜颗粒,致使铜沉积速率较前两者慢。
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结果 (英语) 1: [复制]
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In order to explore the difference in the deposition of copper particles when only the anions are different, the second group of silicon wafers is divided into 3 small piles, 4 pieces in each pile, and deposited in the nitric acid system, sulfuric acid system and chloride ion system for 5s, 10s. , Take it out after 30s and 60s, and observe the change of copper deposition state by SEM. Figures 2a~d show the copper deposition in the copper nitrate deposition system. In the first 10s of the reaction, a large number of copper ions capture electrons to form small copper particles. On the silicon surface, the copper is spread over the entire silicon wafer. As the deposition time increases, a large number of copper particles gather along the cut lines to form larger round copper particles. For the copper sulfate system, as shown in Figure 2e~h, the reaction just started , A dense copper film is quickly formed on the surface of the silicon wafer, and the size of the copper particles is small. When it is deposited to 60s, a small amount of agglomerated copper particles appear on the surface of the copper film, indicating that in the copper sulfate system, the copper is dispersed and small in size. The morphology of the dense copper film is deposited, and agglomeration is not easy to occur. In the chloride ion system, as shown in Figure 2I~l, the morphology at the beginning of the reaction is similar to copper nitrate, and the agglomeration phenomenon is obvious after 10s of deposition. After 30s, A large number of agglomerated rod-shaped copper particles appeared along the cut lines on the surface of the silicon wafer; Figure 2m~o shows the quality change of the silicon wafer before and after the deposition of the silicon wafer. It can be seen that after 60s of deposition, the copper sulfate and copper chloride systems before and after the deposition of silicon The mass loss of the flakes is within 0.002g, which can basically be considered that the quality has not changed. In the copper nitrate system, the mass loss reaches 0.007g, which is caused by the oxidation of the silicon surface by nitrate. Figure 2p uses Q to characterize the relative deposition of copper particles. Size and copper deposition rate, where mCU=m2-m1, it can be seen that the copper nitrate deposition rate is the fastest in the first 30s, and then due to the oxidation of nitrate, a small amount of copper particles are oxidized into copper ions, which makes the copper particles The amount of copper particles in the copper sulfate system increases rapidly, and the amount of copper deposition exceeds the copper particles in the copper nitrate system after 60s. The polarization of the chloride ions in the copper chloride solution causes the chlorine in the solution to increase. The force between the ions and the copper ions is strengthened, making it difficult for the copper ions to capture the electrons on the surface of the silicon wafer and deposit them into copper particles, resulting in a slower copper deposition rate than the former two
正在翻译中..
结果 (英语) 2:[复制]
复制成功!
In order to explore the sedimentation differences of copper particles with different anions, the second group of silicon wafers was divided into 3 small piles of 4 pieces each, which were deposited in nitric acid systems, sulphuric acid systems and chloride ion systems in 5s, 10s, 30s and 60s. After removal, SEM was used to observe the change of copper deposition status, Figure 2a-d shows the deposition of copper in the copper nitrate deposition system, the reaction began in 10s, a large number of copper ion capture electrons to form small copper particles deposited on the silicon surface, so that copper covered the entire silicon wafer, With the extension of deposition time, a large number of copper particles along the cutting pattern gathered to form a larger round copper particles, copper sulfate system, as shown in Figure 2e to h, the reaction began, the silicon surface will quickly form a dense copper film, and copper particle size is small, deposited to 6 At 0s, a small amount of reunited copper particles appear on the surface of the copper film, indicating that in the copper sulfate system, copper is deposited in the form of a dispersed, small-size dense copper film, and it is not easy to reunite, while in the chloride ion system, as shown in Figure 2I to l, The initial form of the reaction is similar to copper nitrate, the deposition of 10s will obviously appear reunion phenomenon, 30s, the surface of the silicon wafer along the cutting pattern appeared a large number of reuniting rod copper particles; Before and after deposition in the copper chloride system silicon chip quality loss is within 0.002g, it can be basically considered that the quality has not changed, and in the copper nitrate system, the mass loss reached 0.007g, caused by nitric acid root oxidation of the silicon surface, Figure 2p Q shows the relative size of the deposition of copper particles and the deposition rate of copper, wherein mCU is m2-m1, it can be seen that in the first 30s, copper nitrate deposition rate is the fastest, and then due to the oxidation of nitric acid, a small amount of copper particles oxidized into copper ions, The amount of copper particles is increased at a basic uniform rate, while the copper particles in the copper sulfate system increase rapidly, resulting in copper deposits after 60s exceeding the copper particles in the copper nitrate system, and due to the polarization of chloride ions in the copper chloride solution, the force between chlorine and copper ions in the solution is strengthened, making it difficult for copper ions to capture the electronic deposition of silicon wafers into copper particles, resulting in a slower rate of copper deposition than the previous two.
正在翻译中..
结果 (英语) 3:[复制]
复制成功!
In order to explore the deposition difference of copper particles with only different anions, the second group of silicon wafers were divided into three small stacks with four pieces in each pile, which were deposited in nitric acid system, sulfuric acid system and chloride ion system for 5S and 10s respectively, After 30s and 60s, the change of copper deposition state was observed by SEM. Fig. 2A ~ d shows the deposition of copper in the copper nitrate deposition system. In the first 10 seconds of the reaction, a large number of copper ions capture electrons to form small copper particles and deposit on the silicon surface, so that copper covers the whole silicon chip. With the deposition time prolonging, a large number of copper particles gather along the cutting lines to form large round copper particles In copper system, as shown in Fig. 2E ~ h, at the beginning of reaction, a layer of dense copper film is rapidly formed on the surface of silicon wafer, and the size of copper particles is small. When the copper particles are deposited to 60s, a small amount of agglomerated copper particles appear on the surface of the copper film, which indicates that in the copper sulfate system, copper is deposited in the form of dispersed and small-sized dense copper film, which is not easy to agglomerate; in the chloride ion system, as shown in Fig. 2I ~ 1 It is shown that the morphology of the reaction is similar to that of cupric nitrate at the beginning of the reaction. After 10s of deposition, a large number of rod-shaped copper particles appear on the surface of the silicon wafer along the cutting grain after 30s. Figure 2m ~ o shows the quality change of silicon wafer before and after deposition. It can be seen that after 60s of deposition, the mass loss of silicon wafer in copper sulfate and copper chloride system before and after deposition is less than 0.002g, which is basically acceptable It is considered that the mass loss of 0.007g in copper nitrate system is caused by the oxidation of silicon surface by nitrate. In Fig. 2p, q is used to characterize the relative size of copper particles deposition and the deposition rate of copper, where MCU = m2-m1. It can be seen that the deposition rate of copper nitrate is the fastest in the first 30 seconds, and then a small amount of copper particles are oxidized to copper ions due to the oxidation of nitrate The results show that the amount of copper particles increases at a constant rate, while the copper particles in the copper sulfate system increase rapidly, resulting in the copper deposition amount exceeding that in the copper nitrate system after 60 s. due to the polarization of chloride ions in copper chloride solution, the force between chloride ions and copper ions in the solution is strengthened, which makes it difficult for copper ions to capture electrons on the surface of silicon wafer and deposit them into copper particles The deposition rate of copper is slower than the former two<BR>
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