JP2014178471A - 感光性樹脂組成物、硬化レリーフパターンの製造方法、半導体装置及び表示体装置 - Google Patents
感光性樹脂組成物、硬化レリーフパターンの製造方法、半導体装置及び表示体装置 Download PDFInfo
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- JP2014178471A JP2014178471A JP2013052116A JP2013052116A JP2014178471A JP 2014178471 A JP2014178471 A JP 2014178471A JP 2013052116 A JP2013052116 A JP 2013052116A JP 2013052116 A JP2013052116 A JP 2013052116A JP 2014178471 A JP2014178471 A JP 2014178471A
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- ASHGTJPOSUFTGB-UHFFFAOYSA-N methyl resorcinol Natural products COC1=CC=CC(O)=C1 ASHGTJPOSUFTGB-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- NFWSQSCIDYBUOU-UHFFFAOYSA-N methylcyclopentadiene Chemical compound CC1=CC=CC1 NFWSQSCIDYBUOU-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- VYKXQOYUCMREIS-UHFFFAOYSA-N methylhexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21C VYKXQOYUCMREIS-UHFFFAOYSA-N 0.000 description 1
- OKQVTLCUHATGDD-UHFFFAOYSA-N n-(benzotriazol-1-ylmethyl)-2-ethyl-n-(2-ethylhexyl)hexan-1-amine Chemical compound C1=CC=C2N(CN(CC(CC)CCCC)CC(CC)CCCC)N=NC2=C1 OKQVTLCUHATGDD-UHFFFAOYSA-N 0.000 description 1
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- 150000004002 naphthaldehydes Chemical class 0.000 description 1
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- XVZMLSWFBPLMEA-UHFFFAOYSA-N trimethoxy(2-pyridin-2-ylethyl)silane Chemical compound CO[Si](OC)(OC)CCC1=CC=CC=N1 XVZMLSWFBPLMEA-UHFFFAOYSA-N 0.000 description 1
- JCGDCINCKDQXDX-UHFFFAOYSA-N trimethoxy(2-trimethoxysilylethyl)silane Chemical compound CO[Si](OC)(OC)CC[Si](OC)(OC)OC JCGDCINCKDQXDX-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- XQEGZYAXBCFSBS-UHFFFAOYSA-N trimethoxy-(4-methylphenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=C(C)C=C1 XQEGZYAXBCFSBS-UHFFFAOYSA-N 0.000 description 1
- QJOOZNCPHALTKK-UHFFFAOYSA-N trimethoxysilylmethanethiol Chemical compound CO[Si](CS)(OC)OC QJOOZNCPHALTKK-UHFFFAOYSA-N 0.000 description 1
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Landscapes
- Exposure And Positioning Against Photoresist Photosensitive Materials (AREA)
- Materials For Photolithography (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)
Abstract
【解決手段】(A)特定構造のフェノール樹脂:100質量部、(B)下記一般式群(1):
で表される化合物からなる群から選択される少なくとも1種のトリアゾール化合物:0.1〜20質量部、及び(C)キノンジアジド基を有する化合物:0.1〜70質量部、を含むポジ型感光性樹脂組成物。
【選択図】なし
Description
しかしながら、前述の特許文献1〜4には、250℃以下で熱硬化した際の硬化膜特性に関しては記載がなく、また特許文献5は用途がフォトレジストであるため、熱硬化した硬化膜(永久膜)としての評価の記載がなかった。
[1] (A)フェノール樹脂:100質量部、
(B)下記一般式群(1):
(C)キノンジアジド基を有する化合物:0.1〜70質量部、
を含むポジ型感光性樹脂組成物であって、
前記(A)フェノール樹脂が、
(a1)下記一般式(2):
(a2)エーテル結合、水酸基、エステル結合、カルボキシル基、チオエーテル結合、チオール基、チオエステル結合、スルホ基、スルホニル基、ウレタン結合、ウレア結合、チオウレタン結合、及びチオ尿素結合からなる群から選択される少なくとも1つの官能基を有する炭素数4〜100の化合物で変性されている、フェノール樹脂、
からなる群から選択される少なくとも1種のフェノール樹脂を含む、ポジ型感光性樹脂組成物。
[2] 前記トリアゾール化合物が、下記一般式群(4):
で表される化合物からなる群から選択される少なくとも1種である、上記[1]に記載のポジ型感光性樹脂組成物。
[3] 前記P3が、下記一般式(5):
[4] 前記一般式(2)中のXが、下記一般式(7):
[5] 前記一般式(2)中のXが、下記式(10):
[6] 前記一般式(2)中のXが、下記式(11):
[7] 前記(A)フェノール樹脂が、下記一般式(12):
[8] 前記(A)フェノール樹脂が前記(a2)フェノール樹脂を含み、かつ前記(a2)フェノール樹脂が、エステル結合及びカルボキシル基からなる群から選択される少なくとも1つの官能基を有する炭素数4〜100の化合物で変性されているフェノール樹脂である、上記[1]〜[7]のいずれかに記載の感光性樹脂組成物。
[9] 前記(A)フェノール樹脂が前記(a2)フェノール樹脂を含み、かつ前記(a2)フェノール樹脂が、炭素数4〜100の不飽和脂肪酸及び炭素数4〜100の不飽和脂肪酸エステルからなる群から選択される少なくとも1つの化合物で変性されているフェノール樹脂である、上記[1]〜[8]のいずれかに記載の感光性樹脂組成物。
[10] 更に(E)架橋剤:0.1〜40質量部を含む、上記[1]〜[9]のいずれかに記載の感光性樹脂組成物。
[11] 以下の工程:
(1)上記[1]〜[10]のいずれかに記載のポジ型感光性樹脂組成物を含むポジ型感光性樹脂層を基板上に形成する工程、
(2)該ポジ型感光性樹脂層を露光する工程、
(3)現像液により露光部を除去して、レリーフパターンを得る工程、及び
(4)該レリーフパターンを加熱処理する工程、
を含む、硬化レリーフパターンの製造方法。
[12] 上記[11]に記載の方法により製造された、硬化レリーフパターン。
[13] 半導体素子と、該半導体素子の上部に設けられた硬化膜とを備える半導体装置であって、該硬化膜は、上記[12]に記載の硬化レリーフパターンである、半導体装置。
[14] 表示体素子と、該表示体素子の上部に設けられた硬化膜とを備える表示体装置であって、該硬化膜は、上記[12]に記載の硬化レリーフパターンである、表示体装置。
本発明の一態様が提供するポジ型感光性樹脂組成物は、
(A)特定構造のフェノール樹脂:100質量部、
(B)特定構造のトリアゾール化合物:0.1〜20質量部、及び
(C)キノンジアジド基を有する化合物:0.1〜70質量部、
を含有する。以下各成分を順に説明する。
本実施形態における(A)フェノール樹脂は、(a1)下記一般式(2):
で表される繰り返し単位を有するフェノール樹脂(以下、(a1)フェノール樹脂ともいう)、並びに、(a2)エーテル結合、水酸基、エステル結合、カルボキシル基、チオエーテル結合、チオール基、チオエステル結合、スルホ基、スルホニル基、ウレタン結合、ウレア結合、チオウレタン結合、及びチオ尿素結合からなる群から選択される少なくとも1つの官能基を有する炭素数4〜100の化合物で変性されているフェノール樹脂(以下、(a2)フェノール樹脂、又は単に変性フェノール樹脂ともいう)からなる群から選択される少なくとも1種のフェノール樹脂を含む。(A)フェノール樹脂は、熱硬化時に、例えばポリイミド前駆体を用いる場合の環化(イミド化)のような構造変化が起こらないため、低温(例えば250℃以下、より典型的には200℃以下)での硬化が可能であるという利点を有する。
本実施形態では、(A)フェノール樹脂は、下記一般式(2):
で表される繰り返し単位を有するフェノール樹脂を含むことが好ましい。上記の繰り返し単位を有するフェノール樹脂は、例えば従来使用されてきたポリイミド樹脂及びポリベンゾオキサゾール樹脂と比べて低温での硬化が可能であり、かつ良好な伸度を有する硬化膜の形成を可能にする。
で表される2価のアルキレンオキシド基、及び下記式群(9):
本実施の形態において、(a2)フェノール樹脂(すなわち変性フェノール樹脂)は、フェノール性水酸基(OH)と水素結合しうる官能基を有する化合物で変性したフェノール樹脂である。変性フェノール樹脂は、より具体的には、エーテル結合、水酸基、エステル結合、カルボキシル基、チオエーテル結合、チオール基、チオエステル結合、スルホ基、スルホニル基、ウレタン結合、ウレア結合、チオウレタン結合、及びチオ尿素結合からなる群から選択される少なくとも1つの官能基を有する炭素数4〜100の化合物で変性されているフェノール樹脂である。コスト、及び硬化膜の引っ張り伸度の観点から、上記官能基はエステル結合又はカルボキシル基であることが好ましい。また該エステル結合又はカルボキシル基を有する化合物の炭素数が4〜100であることは、硬化膜の耐熱性、リフロー処理適用性の観点から好ましい。
好適な不飽和脂肪酸及び不飽和脂肪酸エステルとしては、植物油、クロトン酸、ミリストレイン酸、パルミトレイン酸、オレイン酸、エライジン酸、バクセン酸、ガドレイン酸、エルカ酸、ネルボン酸、リノール酸、α−リノレン酸、エレオステアリン酸、ステアリドン酸、アラキドン酸、エイコサペンタエン酸、イワシ酸及びドコサヘキサエン酸が挙げられる。これらの中でも特に、不飽和脂肪酸エステルである植物油が特に好ましい。
本実施形態では、ポジ型感光性樹脂組成物は、(B)下記一般式群(1):
で表される化合物からなる群から選択される少なくとも1種のトリアゾール化合物(本開示で、(B)トリアゾール化合物ともいう)を含む。ポジ型感光性樹脂組成物が(B)トリアゾール化合物のような特定の含窒素化合物を含むことにより、硬化膜のリフロー処理適用性(硬化レリーフパターン付きウエハーをリフロー処理してもパターン異常が抑えられること)を向上することが出来る。リフロー処理適用性が向上する化学メカニズムは定かではないが、(B)トリアゾール化合物は有機アミンの性質を有し、ブレンステッド塩基であるため、熱硬化時に架橋剤とフェノール化合物(モノマー、オリゴマー等)との架橋を促進し、硬化物の架橋密度が向上しているためと考えられる。
で表される化合物からなる群から選択される少なくとも1種が好ましい。
(C)キノンジアジド基を有する化合物(以下、「(C)キノンジアジド化合物」とも言う)としては、1,2−ベンゾキノンジアジド構造を有する化合物、及び1,2−ナフトキノンジアジド構造を有する化合物を例示でき、米国特許第2,772,972号明細書、米国特許第2,797,213号明細書、及び米国特許第3,669,658号明細書等により公知の物質である。該(C)キノンジアジド化合物は、以降に詳述する特定構造を有するポリヒドロキシ化合物の1,2−ナフトキノンジアジド−4−スルホン酸エステル、及び該ポリヒドロキシ化合物の1,2−ナフトキノンジアジド−5−スルホン酸エステルからなる群から選択される少なくとも一種の化合物(以下、「NQD化合物」ともいう。)であることが好ましい。
で表される3つの2価の有機基から選択されることが好ましい。
で表される1価の有機基であることが好ましい。}
本実施形態におけるポジ型感光性樹脂組成物には、必要に応じて(D)溶剤を含むことができる。
本発明の感光性樹脂組成物には、必要に応じて、(E)架橋剤、熱酸発生剤、シランカップリング剤、染料、溶解促進剤等の各種添加剤を含有させることが可能である。
本実施形態の別の態様は、(1)上述した本発明の感光性樹脂組成物を含む感光性樹脂層を基板に形成する工程、(2)該感光性樹脂層を露光する工程、(3)該露光の後の感光性樹脂層を現像してレリーフパターンを得る工程、及び(4)該レリーフパターンを加熱処理する工程を含む、硬化レリーフパターンの製造方法を提供する。この方法の一例を以下に説明する。
また、本実施形態の感光性樹脂組成物を用いて上述の方法で製造された硬化レリーフパターンを有して成る半導体装置も本実施形態の一態様である。本実施形態の半導体装置は、半導体素子と該半導体素子の上部に設けられた硬化膜とを備え、該硬化膜は上述の硬化レリーフパターンである。ここで当該硬化レリーフパターンは、当該半導体素子に直接接して積層されていてもよく、別の層を間に挟んで積層されていてもよい。例えば、該硬化膜として、表面保護膜、層間絶縁膜、再配線用絶縁膜、フリップチップ装置用保護膜、及びバンプ構造を有する半導体装置の保護膜が挙げられる。本実施形態の半導体装置は、公知の半導体装置の製造方法と上述した本発明の硬化レリーフパターンの製造方法とを組み合わせることで製造することができる。
本実施形態の表示体装置は、表示体素子と該表示体素子の上部に設けられた硬化膜とを備え、該硬化膜は上述の硬化レリーフパターンである。ここで当該硬化レリーフパターンは、当該表示体素子に直接接して積層されていてもよく、別の層を間に挟んで積層されていてもよい。例えば、該硬化膜として、TFT液晶表示素子及びカラーフィルター素子の表面保護膜、絶縁膜、及び平坦化膜、MVA型液晶表示装置用の突起、並びに有機EL素子陰極用の隔壁を挙げることができる。
本実施形態の表示体装置は、本実施形態の半導体装置と同様に、公知の表示体装置の製造方法と上述した本実施形態の硬化レリーフパターンの製造方法とを組み合わせることで製造することができる。
なお、各評価項目の測定条件は以下に示すとおりである。
本実施形態の伸度測定用サンプルを以下の方法で作製した。最表面にアルミ蒸着層を設けた6インチシリコンウエハー基板に、実施例及び比較例で得られた感光性樹脂組成物を、硬化後の膜厚が約10μmとなるように回転塗布し、120℃で180秒間ホットプレートにてプリベークを行い、塗膜を形成した。膜厚は大日本スクリーン製造社製膜厚測定装置(ラムダエース)にて測定した。この塗膜を縦型キュア炉VF200B(光洋サーモシステム社製)にて窒素雰囲気下で200℃で1時間加熱し、膜厚10μmの膜を得た。得られた樹脂硬化膜を、ダイシングソーで3mm幅にカットした後に、希塩酸水溶液によりウエハーから剥離し、得られる20本の試料を温度23℃、相対湿度50%の雰囲気に24時間以上静置後、引っ張り試験機(テンシロン)にて伸度を測定した。測定値として最大値を用い、試料数20点の測定値を数平均した。引っ張り試験機の測定条件は以下の通りであった。結果を表2に示す。
相対湿度:50%
初期試料長さ:50mm
試験速度:40mm/min
ロードセル定格:2kgf
感光性樹脂組成物をシリコンウエハー上にスピンコートし、ホットプレート上において該シリコンウエハー及びスピンコート膜を120℃で180秒間ホットプレートにてプリベークを行い、10μmの膜厚の塗膜を形成した。この塗膜に、テストパターン付きレチクルを通して、i線(365nm)の露光波長を有するステッパNSR2005i8A(ニコン社製)を用いて露光量500mJ/cm2のi線を照射することにより露光した。次に、現像機(D−SPIN)により23℃で2.38%テトラメチルアンモニウムヒドロキシド水溶液AZ−300MIF(AZエレクトロニックマテリアルズ社製)を用いて100秒間現像し、純水でリンスした後、縦型キュア炉VF200B(光洋サーモシステム社製)において、窒素雰囲気下、200℃で1時間に亘って硬化を行い、硬化レリーフパターンを得た。硬化パターンを光学顕微鏡で観察し、下記の基準にて評価した。結果を表2に示す。
○:50μm四方の抜きレリーフパターンが埋まらずに形状を維持している。
×:50μm四方の抜きレリーフパターンが埋まっている。
実施例及び比較例で得られた感光性樹脂組成物を、硬化後の膜厚が約10μmとなるように回転塗布し、120℃で180秒間ホットプレートにてプリベークを行い、塗膜を形成した。膜厚は膜厚測定装置、ラムダエース(大日本スクリーン社製)にて測定した。この塗膜に、テストパターン付きレチクルを通して、i線(365nm)の露光波長を有するステッパーNSR2005i8A(ニコン社製)を用いて露光量500mJ/cm2のi線を照射することにより露光した。次に、現像機D−SPIN(SOKUDO社製)にて23℃で2.38質量%テトラメチルアンモニウムヒドロキシド水溶液AZ−300MIF(AZエレクトロニックマテリアルズ社製)を用いて100秒間現像し、純水でリンスした後、縦型キュア炉VF200B(光洋サーモシステム社製)にて窒素雰囲気下で200℃1時間硬化を行い、硬化レリーフパターンを得た。後述する比較例7は、上述の硬化レリーフパターンの形状評価で、硬化後パターンくずれが発生したため、このリフローテストは実施していない。
○:パターン異常の発生がなく、かつ、膜厚変化が10%未満である。
△:パターン異常の発生、又は、膜厚変化10%以上の膜減り又は膨潤、のいずれかが見られる。
×:パターン異常の発生があり、かつ、膜厚変化10%以上の膜減り又は膨潤が見られる。
−:硬化後パターンくずれが発生し、リフローテストを実施していない
{パターン異常:パターンクラック、又は、パターン表面の荒れ}
<フェノール樹脂(A−1)の合成>
容量0.5リットルのディーン・スターク装置付きセパラブルフラスラスコ中で、フロログルシノール100.9g(0.8mol)、4,4’−ビス(メトキシメチル)ビフェニル(以下「BMMB」ともいう。)121.2g(0.5mol)、ジエチル硫酸3.9g(0.025mol)、ジエチレングリコールジメチルエーテル140gを70℃で混合攪拌し、固形物を溶解させた。
検出器:JASCO RI−930
カラムオーブン:JASCO CO−965 40℃
カラム:Shodex KD−806M 直列に2本
移動相:0.1mol/l LiBr/NMP
流速:1ml/min.
<フェノール樹脂(A−2)の合成>
合成例1のフロログルシノールの代わりに、3,5−ジヒドロキシ安息香酸メチル128.3g(0.76mol)を用いて、合成例1と同様に合成を行い、3,5−ジヒドロキシ安息香酸メチル/BMMBからなる共重合体(フェノール樹脂(A−2))を収率65%で得た。このA−2のGPC法の標準ポリスチレン換算により求めた重量平均分子量は21,000であった。
<フェノール樹脂(A−3)の合成>
容量1.0Lのディーン・スターク装置付きセパラブルフラスコを窒素置換し、その後、該セパラブルフラスコ中で、レゾルシノール81.3g(0.738mol)、BMMB84.8g(0.35mol)、p−トルエンスルホン酸3.81g(0.02mol)、プロピレングリコールモノメチルエーテル(以下、PGMEとも言う)116gを50℃で混合攪拌し、固形物を溶解させた。
<フェノール樹脂(A−5)の合成>
フェノール100質量部、亜麻仁油43質量部及びトリフロオロメタンスルホン酸0.1質量部を混合し、120℃で2時間撹拌し、乾性油変性フェノール誘導体を得た。次いで、上記乾性油変性フェノール誘導体130g、パラホルムアルデヒド16.3g及びシュウ酸1.0gを混合し、90℃で3時間撹拌し反応を行った。次に、120℃に昇温して減圧下で3時間撹拌後、反応液を大気圧下で室温まで冷却し、反応生成物である乾性油変性フェノール樹脂(A−5)を得た。このA−5のGPC法の標準ポリスチレン換算により求めた重量平均分子量は25,000であった。
<フェノール樹脂(A−6)の合成>
上記乾性油変性フェノール誘導体130g、パラホルムアルデヒド16.3g及びシュウ酸1.0gを混合し、90℃で3時間撹拌し反応を行った。次いで、120℃に昇温して減圧下で3時間撹拌した後、反応液に無水コハク酸29g及びトリエチルアミン0.3gを加え、大気圧下、100℃で1時間撹拌した。反応液を室温まで冷却し、反応生成物である乾性油変性フェノール樹脂(A−6)を得た。このA−6のGPC法の標準ポリスチレン換算により求めた重量平均分子量は28,000であった。
表1に示すとおり、フェノール樹脂(A−1)100質量部、トリアゾール化合物(B−1)1質量部、キノンジアジド基を有する化合物(C−1)12質量部、及び架橋剤(E−1)5質量部を、溶剤(D−1)219質量部に溶解させ、0.1μmのフィルターで濾過してポジ型感光性樹脂組成物を調製した。この組成物及びその硬化膜の特性を前記の評価方法に従って測定した。得られた結果を表2に示す。
表1に示した成分からなる組成物を実施例1と同様に調製し、組成物及びその硬化膜の特性を実施例1と同様に測定した。得られた結果を表2に示す。
表1に示した成分からなる組成物を実施例1と同様に調製し、組成物及びその硬化膜の特性を実施例1と同様に測定した。得られた結果を表2に示す。
A−1:フロログルシノール/BMMBからなる共重合体、ポリスチレン換算重量平均分子量(Mw)=15,000
A−2:3,5−ジヒドロキシ安息香酸メチル/BMMBからなる共重合体、ポリスチレン換算重量平均分子量(Mw)=21,000
A−3:レゾルシノール/BMMB/2,6−ビス(ヒドロキシメチル)−p−クレゾールからなる共重合体、ポリスチレン換算重量平均分子量(Mw)=9,900
A−4:フェノール/ビフェニレン樹脂、ポリスチレン換算重量平均分子量(Mw)=2,400(明和化成社製、製品名MEH−7851M)
A−5:炭素数4〜100の不飽和炭化水素基を有する化合物(乾性油)変性フェノール樹脂、ポリスチレン換算重量平均分子量(Mw)=25,000
A−6:炭素数4〜100の不飽和炭化水素基を有する化合物(乾性油)変性フェノール樹脂、ポリスチレン換算重量平均分子量(Mw)=28,000
A−7:ノボラック樹脂、ポリスチレン換算重量平均分子量(Mw)=10,600(旭有機材社製、製品名EP−4080G)
D−1:γ―ブチロラクトン(GBL)
E−1:1,3,4,6−テトラキス(メトキシメチル)グリコールウリル(三和ケミカル製、商品名;ニカラックMX−270)
Claims (14)
- (A)フェノール樹脂:100質量部、
(B)下記一般式群(1):
(C)キノンジアジド基を有する化合物:0.1〜70質量部、
を含むポジ型感光性樹脂組成物であって、
前記(A)フェノール樹脂が、
(a1)下記一般式(2):
(a2)エーテル結合、水酸基、エステル結合、カルボキシル基、チオエーテル結合、チオール基、チオエステル結合、スルホ基、スルホニル基、ウレタン結合、ウレア結合、チオウレタン結合、及びチオ尿素結合からなる群から選択される少なくとも1つの官能基を有する炭素数4〜100の化合物で変性されている、フェノール樹脂、
からなる群から選択される少なくとも1種のフェノール樹脂を含む、ポジ型感光性樹脂組成物。 - 前記トリアゾール化合物が、下記一般式群(4):
で表される化合物からなる群から選択される少なくとも1種である、請求項1に記載のポジ型感光性樹脂組成物。 - 前記P3が、下記一般式(5):
- 前記一般式(2)中のXが、下記一般式(7):
- 前記(A)フェノール樹脂が、下記一般式(12):
- 前記(A)フェノール樹脂が前記(a2)フェノール樹脂を含み、かつ前記(a2)フェノール樹脂が、エステル結合及びカルボキシル基からなる群から選択される少なくとも1つの官能基を有する炭素数4〜100の化合物で変性されているフェノール樹脂である、請求項1〜7のいずれか一項に記載の感光性樹脂組成物。
- 前記(A)フェノール樹脂が前記(a2)フェノール樹脂を含み、かつ前記(a2)フェノール樹脂が、炭素数4〜100の不飽和脂肪酸及び炭素数4〜100の不飽和脂肪酸エステルからなる群から選択される少なくとも1つの化合物で変性されているフェノール樹脂である、請求項1〜8のいずれか一項に記載の感光性樹脂組成物。
- 更に(E)架橋剤:0.1〜40質量部を含む、請求項1〜9のいずれか一項に記載の感光性樹脂組成物。
- 以下の工程:
(1)請求項1〜10のいずれか一項に記載のポジ型感光性樹脂組成物を含むポジ型感光性樹脂層を基板上に形成する工程、
(2)該ポジ型感光性樹脂層を露光する工程、
(3)現像液により露光部を除去して、レリーフパターンを得る工程、及び
(4)該レリーフパターンを加熱処理する工程、
を含む、硬化レリーフパターンの製造方法。 - 請求項11に記載の方法により製造された、硬化レリーフパターン。
- 半導体素子と、該半導体素子の上部に設けられた硬化膜とを備える半導体装置であって、該硬化膜は、請求項12に記載の硬化レリーフパターンである、半導体装置。
- 表示体素子と、該表示体素子の上部に設けられた硬化膜とを備える表示体装置であって、該硬化膜は、請求項12に記載の硬化レリーフパターンである、表示体装置。
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