KR102619325B1 - 환경 광 센서용 광학 필터 - Google Patents
환경 광 센서용 광학 필터 Download PDFInfo
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- KR102619325B1 KR102619325B1 KR1020237011610A KR20237011610A KR102619325B1 KR 102619325 B1 KR102619325 B1 KR 102619325B1 KR 1020237011610 A KR1020237011610 A KR 1020237011610A KR 20237011610 A KR20237011610 A KR 20237011610A KR 102619325 B1 KR102619325 B1 KR 102619325B1
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- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
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- QYBKVVRRGQSGDC-UHFFFAOYSA-N triethyl methyl silicate Chemical compound CCO[Si](OC)(OCC)OCC QYBKVVRRGQSGDC-UHFFFAOYSA-N 0.000 description 1
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- BYMUNNMMXKDFEZ-UHFFFAOYSA-K trifluorolanthanum Chemical compound F[La](F)F BYMUNNMMXKDFEZ-UHFFFAOYSA-K 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
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/22—Absorbing filters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01J—MEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY
- G01J1/00—Photometry, e.g. photographic exposure meter
- G01J1/02—Details
-
- G—PHYSICS
- G01—MEASURING; TESTING
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Abstract
Description
도 2는, 본 발명의 일 실시 형태에 따른 환경 광 센서의 구성을 설명하는 도면이다.
도 3은, 본 발명의 일 실시 형태에 따른 환경 광 센서를 구비하는 전자 기기의 일례를 설명하는 도면이다.
도 4는, 투과 스펙트럼을 수직 방향, 경사 30도의 방향 및 경사 60도의 방향으로 측정하는 구성을 도시한 도면이다.
도 5는, 광학 필터의 수직 방향에 대하여 5°의 각도로 입사한 광의 반사율을 측정하는 방법의 예를 나타내는 개략도이다.
도 6은, 실시예 1에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 7은, 실시예 2에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 8은, 실시예 3에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 9는, 실시예 4에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 10은, 실시예 5에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 11은, 실시예 6에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 12는, 실시예 7에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 13은, 실시예 8에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 14는, 비교예 1에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 15는, 비교예 2에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 16은, 비교예 3에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
도 17은, 비교예 4에서 얻어진 광학 필터의 수직 방향, 수직 방향으로부터 30°의 각도 및 수직 방향으로부터 60°의 각도로 측정한 분광 투과율을 나타내는 그래프이다.
200··· 환경 광 센서
202, 202a, 202b, 202c··· 광전 변환 소자
204··· 하우징
206··· 제1 전극
208··· 광전 변환층
210··· 제2 전극
212a, 212b, 212c··· 컬러 필터
214··· 소자 분리 절연층
216··· 패시베이션막
300··· 전자 기기
302··· 하우징
304··· 표시 패널
306··· 마이크로폰부
308··· 스피커부
310··· 표면 패널
Claims (9)
- 하기 요건 (a)를 충족하는 기재를 가지며, 또한 하기 요건 (b), (c) 및 (d)를 충족하고, 유전체 다층막을 갖지 않는 것을 특징으로 하는 환경 광 센서용 광학 필터이며,
하기 화합물 (B)는 스쿠아릴륨계 화합물, 프탈로시아닌계 화합물, 나프탈로시아닌계 화합물, 크로코늄계 화합물, 시아닌계 화합물, 디이모늄계 화합물, 금속 디티올레이트계 화합물 및 피롤로피롤계 화합물로 이루어지는 군에서 선택되는 적어도 1종의 화합물이며, 금속 산화물을 포함하지 않는 것을 특징으로 하는 환경 광 센서용 광학 필터:
(a) 파장 650nm 이상 800nm 미만의 영역에 흡수 극대를 갖는 화합물 (A), 및 파장 800nm 이상 1850nm 이하의 영역에 흡수 극대를 갖는 화합물 (B)를 포함하는 층을 갖는다;
(b) 파장 800 내지 1000nm의 영역에 있어서, 광학 필터의 한쪽 면에 있어서의 수직 방향에 대하여 5도 경사 방향으로부터 입사하는 광의 반사율의 평균값 Rfa-5와, 다른 쪽 면에 있어서의 수직 방향에 대하여 5도 경사 방향으로부터 입사하는 광의 반사율의 평균값 Rfb-5가, 모두 15% 이하이다;
(c) 파장 430 내지 580nm의 영역에 있어서, 광학 필터의 수직 방향으로부터 입사하는 광의 투과율의 평균값 Ta-0과, 수직 방향에 대하여 30도 경사 방향으로부터 입사하는 광의 투과율의 평균값 Ta-30과, 수직 방향에 대하여 60도 경사 방향으로부터 입사하는 광의 투과율의 평균값 Ta-60이, 모두 20% 이상 75% 미만이다;
(d) 파장 800nm 내지 1200nm의 영역에 있어서, 광학 필터의 수직 방향으로부터 입사하는 광에 대한 광학 농도(OD값)의 평균값 ODa-0과, 수직 방향에 대하여 30도 경사 방향으로부터 입사하는 광에 대한 광학 농도(OD값)의 평균값 ODa-30과, 수직 방향에 대하여 60도 경사 방향으로부터 입사하는 광에 대한 광학 농도(OD값)의 평균값 ODa-60이, 모두 1.5 이상이다. - 제1항에 있어서, 상기 화합물 (A)를 포함하는 층이 투명 수지층인 것을 특징으로 하는 환경 광 센서용 광학 필터.
- 제2항에 있어서, 상기 투명 수지층이 상기 화합물 (B)를 더 포함하는 것을 특징으로 하는 환경 광 센서용 광학 필터.
- 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 화합물 (A)가 스쿠아릴륨계 화합물, 프탈로시아닌계 화합물 및 시아닌계 화합물로 이루어지는 군에서 선택되는 적어도 1종의 화합물인 것을 특징으로 하는 환경 광 센서용 광학 필터.
- 제2항 또는 제3항에 있어서, 상기 투명 수지층을 구성하는 수지가, 환상 폴리올레핀계 수지, 방향족 폴리에테르계 수지, 폴리이미드계 수지, 플루오렌폴리카르보네이트계 수지, 플루오렌폴리에스테르계 수지, 폴리카르보네이트계 수지, 폴리아미드계 수지, 아라미드계 수지, 폴리술폰계 수지, 폴리에테르술폰계 수지, 폴리파라페닐렌계 수지, 폴리아미드이미드계 수지, 폴리에틸렌나프탈레이트계 수지, 불소화 방향족 폴리머계 수지, (변성) 아크릴계 수지, 에폭시계 수지, 실세스퀴옥산계 자외선 경화형 수지, 말레이미드계 수지, 지환 에폭시 열경화형 수지, 폴리에테르에테르케톤계 수지, 폴리아릴레이트계 수지, 알릴에스테르계 경화형 수지, 아크릴계 자외선 경화형 수지, 비닐계 자외선 경화형 수지, 및 졸겔법에 의해 형성된 실리카를 포함하는 수지로 이루어지는 군에서 선택되는 적어도 1종의 수지인 것을 특징으로 하는 환경 광 센서용 광학 필터.
- 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 기재가, 구리 성분을 함유하는 불소인산염계 유리층 또는 인산염계 유리로 이루어지는 기판을 포함하는 것을 특징으로 하는 환경 광 센서용 광학 필터.
- 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 환경 광 센서용 광학 필터에, 수직 방향으로부터 입사한 경우, 수직 방향에 대하여 30°의 방향으로부터 입사한 경우, 및 수직 방향에 대하여 60°의 방향으로부터 입사한 경우에 있어서,
하기 식 (1)로부터 유도되는 R(적색) 투과율의 비의 변화율, 하기 식 (2)로부터 유도되는 G(녹색) 투과율의 비의 변화율, 및 하기 식 (3)으로부터 유도되는 B(청색) 투과율의 비의 변화율이, 모두 0.6 내지 1.1의 범위인 것을 특징으로 하는 환경 광 센서용 광학 필터.
(R 투과율의 비)=(R 투과율)×100/((R 투과율)+(G 투과율)+(B 투과율))··· 식 (1)
(G 투과율의 비)=(G 투과율)×100/((R 투과율)+(G 투과율)+(B 투과율))··· 식 (2)
(B 투과율의 비)=(B 투과율)×100/((R 투과율)+(G 투과율)+(B 투과율))··· 식 (3)
[식 (1) 내지 (3) 중, R 투과율은 파장 580 내지 650nm에 있어서의 평균 투과율, G 투과율은 파장 500 내지 580nm에 있어서의 평균 투과율, B 투과율은 파장 420 내지 500nm에 있어서의 평균 투과율이다.] - 제1항 내지 제3항 중 어느 한 항에 기재된 환경 광 센서용 광학 필터를 구비하는 것을 특징으로 하는 환경 광 센서.
- 제8항에 기재된 환경 광 센서를 갖는 것을 특징으로 하는 전자 기기.
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JP5695356B2 (ja) * | 2010-07-13 | 2015-04-01 | 株式会社カネカ | 近赤外線吸収能を有する硬化性コーティング剤、および近赤外線吸収材 |
CN106405707B (zh) * | 2011-06-06 | 2021-07-20 | Agc株式会社 | 滤光片、固体摄像元件、摄像装置用透镜和摄像装置 |
CN103858028B (zh) * | 2011-10-14 | 2016-12-28 | Jsr株式会社 | 固体摄影装置用滤光器及使用该滤光器的固体摄影装置及照相机模块 |
JP2013155353A (ja) * | 2012-01-31 | 2013-08-15 | Fujifilm Corp | 赤外線吸収性液状組成物、これを用いた赤外線カットフィルタ及びその製造方法、並びに、カメラモジュール及びその製造方法 |
JP6233308B2 (ja) * | 2012-08-23 | 2017-11-22 | 旭硝子株式会社 | 近赤外線カットフィルタおよび固体撮像装置 |
JP5953322B2 (ja) * | 2013-02-14 | 2016-07-20 | 富士フイルム株式会社 | 赤外線吸収組成物ないしは赤外線吸収組成物キット、これを用いた赤外線カットフィルタ及びその製造方法、並びに、カメラモジュール及びその製造方法 |
WO2014192714A1 (ja) * | 2013-05-29 | 2014-12-04 | Jsr株式会社 | 光学フィルターおよび前記フィルターを用いた装置 |
CN104159085A (zh) * | 2014-08-21 | 2014-11-19 | 中南林业科技大学 | 一种基于新型监控镜头和双图像传感器的监控系统 |
KR20180132163A (ko) * | 2015-07-09 | 2018-12-11 | 니혼 이타가라스 가부시키가이샤 | 적외선 컷 필터, 촬상 장치, 및 적외선 컷 필터의 제조 방법 |
US10996105B2 (en) * | 2015-11-30 | 2021-05-04 | Jsr Corporation | Optical filter having low incident angle dependence of incident light, ambient light sensor, sensor module and electronic device |
-
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