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Effect of dissolution inhibitors on the dissolution characteristics of chemically amplified positive-tone electron beam resist

机译:溶出抑制剂对化学放大正音电子束抗蚀剂溶出特性的影响

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The chemical amplification resist system composed of partially tBOC-protected PVP, a dissolution inhibitor, and an acid generator are investigated as EB resists. As dissolution inhibitors, hydroquinone protected with tert-butoxycarbonyl group (B-HQ) and isophthalic acid protected with tert-butyl group (B-IP) are utilized. It is found that dissolution rate of the resist consisting of B-IP is faster than that of B-HQ in the exposed area. B-HQ and B-IP as dissolution inhibitors convert into HQ and IP as dissolution promoters after exposure, respectively. The pKa of IP is smaller than that of HQ. It is considered that the acidity of IP is higher than that of HQ, so the ability of the dissolution promotion of IP is much larger than that of HQ. IP enhances the solubility of the matrix resin to the alkaline developer larger than HQ. The resist consisting of B-IP has a high dissolution rate ratio between the exposed and unexposed areas, so it is considered that it results in a much improved patten profile. A 0.14 $mu@m lines-and-spaces pattern is successfully fabricated at 17.5 $mu@C/cm$+2$/ using 50 keV. EB.
机译:研究了由部分TBOC保护的PVP,溶解抑制剂和酸产生剂组成的化学扩增抗蚀剂系统作为EB抗蚀剂。作为溶解抑制剂,用叔丁氧基羰基(B-HQ)保护的氢醌和用叔丁基(B-IP)保护的脱苯甲酸(B-IP)。发现由B-IP组成的抗蚀剂的溶出速率比暴露区域中的B-HQ的溶解速率更快。 B-HQ和B-IP作为溶解抑制剂分别在暴露后转化为HQ和IP作为溶解促进剂。 IP的PKA小于HQ的PKA。认为IP的酸度高于HQ的酸度,因此IP的溶解促进的能力远大于HQ。 IP增强基质树脂至大于HQ的碱性显影剂的溶解度。由B-IP组成的抗蚀剂在暴露和未曝光区域之间具有高溶解速率比,因此认为它导致了大大改进的彭定装置轮廓。 014 $ MU @ M行和空间模式以17.5 $ MU @ C / CM $ + 2 $ /使用50 kev成功制作。 EB。

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