CN111285681A - 用于激光照明的全光谱荧光陶瓷及制备方法 - Google Patents

用于激光照明的全光谱荧光陶瓷及制备方法 Download PDF

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CN111285681A
CN111285681A CN201811498016.4A CN201811498016A CN111285681A CN 111285681 A CN111285681 A CN 111285681A CN 201811498016 A CN201811498016 A CN 201811498016A CN 111285681 A CN111285681 A CN 111285681A
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叶勇
王红
张攀德
李东升
冯少尉
李春晖
朱锦超
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Shanghai Aviation Electric Co Ltd
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Abstract

本发明公开用于激光照明的全光谱荧光陶瓷及其制备方法,所述全光谱荧光陶瓷由绿光发光陶瓷组分、黄光发光陶瓷组分及红光发光陶瓷组分组成,使得所述全光谱荧光陶瓷的光谱范围为500‑650nm。本发明的有益效果在于:具有从绿光到红光全部光谱,很有效的解决显色指数差红光和绿光成分缺失的现象。

Description

用于激光照明的全光谱荧光陶瓷及制备方法
技术领域
本发明涉及激光照明用荧光材料领域,特别地是,用于激光照明的全光谱荧光陶瓷及制备方法。
背景技术
随着蓝光LD的技术日趋成熟,激光照明的概念也随之提出,2012年OSRAM公司和BMW公司首先成功将激光照明灯具安装到宝马i8车中。大家对激光照明研究的热度也随之提高。激光照明相对于传统LED照明,其具有发光效率高,结构紧凑,照射距离远等优势。但是,目前激光照明所用的荧光材料光谱多为宽光谱,其显色指数低(55左右),尤其红光成分缺失,R9为负数。
发明内容
人们一直期望解决现有技术中激光照明的色指数低(55左右),尤其红光成分缺失,但始终未能获得成功。本发明提供一种用于激光照明的全光谱荧光陶瓷及其制备方法,能有效地解决上述问题。
本发明的技术方案是这样实现的:用于激光照明的全光谱荧光陶瓷,其特征在于,所述全光谱荧光陶瓷由绿光发光陶瓷组分、黄光发光陶瓷组分及红光发光陶瓷组分组成,使得所述全光谱荧光陶瓷的光谱范围为500-650nm。
作为用于激光照明的全光谱荧光陶瓷的优选方案,所述绿光发光陶瓷组分为Ce3+掺杂LuAG(Lu3Al5O12)和/或Mn2+掺杂的AlON。
作为用于激光照明的全光谱荧光陶瓷的优选方案,所述黄光发光陶瓷组分为Ce3+掺杂的YAG(Y3Al5O12)、GYGAG((Gd,Y)3(Al,Ga)5O12)、GYAG((Gd,Y)3Al5O12)、TYAG((Tb,Y)3Al5O12)、GLuAG((Gd,Lu)3Al5O12)中的一个或多个。
作为用于激光照明的全光谱荧光陶瓷的优选方案,所述红光发光陶瓷组分为Er离子掺杂的YAG或GYGAG或LuAG(Lu3Al5O12),或Eu离子掺杂的SiAlON或M2Si5N8
作为用于激光照明的全光谱荧光陶瓷的优选方案,在蓝光LD激发下,所述全光谱荧光陶瓷发射出的色温在4000-6000K,显色指数为75-90。
用于激光照明的全光谱荧光陶瓷的制备方法,用以制备全光谱荧光陶瓷,包含有以下步骤,
步骤S1,制备陶瓷素坯:选用绿光发光陶瓷组分、黄光发光陶瓷组分及红光发光陶瓷组分;
步骤S2,烧结陶瓷素坯:以及,
步骤S3,加工后处理陶瓷素坯。
作为用于激光照明的全光谱荧光陶瓷的制备方法的优选方案,步骤S11中,包含有,
步骤S111,分别配出绿光发光陶瓷组分、黄光发光陶瓷组分及红光发光陶瓷组分的混合粉体,其中,发光离子掺杂浓度在0.05%到5%;
步骤S112,球磨:球磨5-20小时,球磨转速150r/min-350r/min,球磨介质为氧化铝磨球,氧化铝磨球直径为1-5mm,无水乙醇作为溶剂;
步骤S113,烘干浆料,过筛;以及,
步骤S114,煅烧:烧结温度为500-1000℃,保温1-24小时。
作为用于激光照明的全光谱荧光陶瓷的制备方法的优选方案,步骤S2中,包含有,
步骤S21,素烧,去除有机物:烧结温度为600-1000℃,保温1-24小时;
步骤S22,真空烧结或热压烧结;烧结温度为1400-1850℃,保温时间5-24小时;以及,
步骤S23,退火:退火温度为1400-1550℃,保温时间10-30小时。
作为用于激光照明的全光谱荧光陶瓷的制备方法的优选方案,步骤S3中,包含有,
步骤S31,样品双面抛光,样品厚度为0.1-0.5mm;以及,
步骤S32,样品下表面镀全反膜,样品上表面镀增透膜。
与现有技术相比,本发明的有益效果至少在于:具有从绿光到红光全部光谱,很有效的解决显色指数差红光和绿光成分缺失的现象。
附图说明
图1为本发明的光谱示意图。
具体实施方式
下面通过具体的实施方式结合附图对本发明作进一步详细说明。
实施例1:
本实施例选用发光离子的掺杂浓度为0.5%,绿光成分选用Ce:LuAG,黄光成分选用Ce:YAG,红光成分选用Eu:SiAlON。按照绿光:黄光:红光成分质量比为1:2:2,按照规定的配比进行精确计算配料。将配好的粉体至于球磨罐中球磨6小时,球磨转速300r/min,球磨介质为氧化铝磨球,氧化铝磨球直径为2mm,无水乙醇作为溶剂。球磨后将球磨好的浆料烘干,然后过100目筛,得到混合物粉体,然后称取一定量混合粉体置于模具中成型对模具双向加压,成型压力2MPa。然后通过真空塑封机,将素坯真空包装好。将封好的素坯放入冷等静压机中进行冷等静压,其中压强为200MPa,保压时间为5分钟,然后将素烧后的样品进行热压烧结,压力80MPa,烧结温度为1650℃,保温时间5小时。最后对样品进行退火,退火温度为1400℃,保温时间20小时。对样品进行表面处理,样品双面抛光,样品厚度为0.3mm。对样品底面镀全反膜,对样品上表面镀增透膜,最终制备出所需样品。通过蓝光LD激发,测试发现其色温为4600K,显示指数为87。
实施例2:
本实施例选用发光离子的掺杂浓度为0.8%,绿光成分选用Ce:LuAG,黄光成分选用Ce:GYGAG,红光成分选用Er:YAG。按照绿光:黄光:红光成分质量比为1:3:2,按照规定的配比进行精确计算配料。将配好的粉体至于球磨罐中球磨12小时,球磨转速250r/min,球磨介质为氧化铝磨球,氧化铝磨球直径为2mm,无水乙醇作为溶剂。球磨后将球磨好的浆料烘干,然后过100目筛,得到混合物粉体,然后置于高纯氧化铝坩埚中放入高温马弗炉进行煅烧,烧结温度为1000℃,保温6小时。然后称取一定量混合粉体置于模具中成型对模具双向加压,成型压力2MPa。然后通过真空塑封机,将素坯真空包装好。将封好的素坯放入冷等静压机中进行冷等静压,其中压强为200MPa,保压时间为5分钟,然后将素烧后的样品进行真空烧结,烧结温度为1780℃,保温时间10小时。最后对样品进行退火,退火温度为1400℃,保温时间20小时。对样品进行表面处理,样品双面抛光,样品厚度为0.2mm。对样品底面镀全反膜,对样品上表面镀增透膜,最终制备出所需样品,通过蓝光LD激发,测试发现其色温为4300K,显示指数为83。
实施例3:
本实施例选用发光离子的掺杂浓度为0.3%。绿光成分选用Ce:LuAG,黄光成分选用Ce:GYAG,红光成分选用Eu:SiAlON。按照绿光:黄光:红光成分质量比为2:2:1,按照规定的配比进行精确计算配料。将配好的粉体至于球磨罐中球磨20小时,球磨转速150r/min,球磨介质为氧化铝磨球,氧化铝磨球直径为5mm,无水乙醇作为溶剂。球磨后将球磨好的浆料烘干,然后过100目筛,得到混合物粉体,然后称取一定量混合粉体置于模具中成型对模具双向加压,成型压力2MPa。然后通过真空塑封机,将素坯真空包装好。将封好的素坯放入冷等静压机中进行冷等静压,其中压强为200MPa,保压时间为5分钟,然后将素烧后的样品进行热压烧结,压力60MPa,烧结温度为1700℃,保温时间10小时。最后对样品进行退火,退火温度为1400℃,保温时间20小时。对样品进行表面处理,样品双面抛光,样品厚度为0.2mm。对样品底面镀全反膜,对样品上表面镀增透膜,最终制备出所需样品,通过蓝光LD激发,测试发现其色温为5500K,显示指数为77。
实施例1至3中的光谱范围为500-650nm。以实施例1为例,请参见图1的光谱图。
以上仅表达了本发明的实施方式,其描述较为具体和详细,但且不能因此而理解为对发明专利范围的限制。应当指出的是,对于本领域的普通技术人员来说,在不脱离本发明构思的前提下,还可以做出若干变形和改进,这些都属于本发明的保护范围。因此,本发明专利的保护范围应以所附权利要求为准。

Claims (9)

1.用于激光照明的全光谱荧光陶瓷,其特征在于,所述全光谱荧光陶瓷由绿光发光陶瓷组分、黄光发光陶瓷组分及红光发光陶瓷组分组成,使得所述全光谱荧光陶瓷的光谱范围为500-650nm。
2.根据权利要求1所述的用于激光照明的全光谱荧光陶瓷,其特征在于,所述绿光发光陶瓷组分为Ce3+掺杂LuAG(Lu3Al5O12)和/或Mn2+掺杂的AlON。
3.根据权利要求1所述的用于激光照明的全光谱荧光陶瓷,其特征在于,所述黄光发光陶瓷组分为Ce3+掺杂的YAG(Y3Al5O12)、GYGAG((Gd,Y)3(Al,Ga)5O12)、GYAG((Gd,Y)3Al5O12)、TYAG((Tb,Y)3Al5O12)、GLuAG((Gd,Lu)3Al5O12)中的一个或多个。
4.根据权利要求1所述的用于激光照明的全光谱荧光陶瓷,其特征在于,所述红光发光陶瓷组分为Er离子掺杂的YAG或GYGAG或LuAG(Lu3Al5O12),或Eu离子掺杂的SiAlON或M2Si5N8
5.根据权利要求1至4中任意一项所述的用于激光照明的全光谱荧光陶瓷,其特征在于,在蓝光LD激发下,所述全光谱荧光陶瓷发射出的色温在4000-6000K,显色指数为75-90。
6.用于激光照明的全光谱荧光陶瓷的制备方法,用以制备权利要求1至5中任意一项所述的全光谱荧光陶瓷,其特征在于,包含有以下步骤,
步骤S1,制备陶瓷素坯:选用绿光发光陶瓷组分、黄光发光陶瓷组分及红光发光陶瓷组分;
步骤S2,烧结陶瓷素坯:以及,
步骤S3,加工后处理陶瓷素坯。
7.根据权利要求6所述的用于激光照明的全光谱荧光陶瓷的制备方法,其特征在于,步骤S11中,包含有,
步骤S111,分别配出绿光发光陶瓷组分、黄光发光陶瓷组分及红光发光陶瓷组分的混合粉体,其中,发光离子掺杂浓度在0.05%到5%;
步骤S112,球磨:球磨5-20小时,球磨转速150-350r/min,球磨介质为氧化铝磨球,氧化铝磨球直径为1-5mm,无水乙醇作为溶剂;
步骤S113,烘干浆料,过筛;以及,
步骤S114,煅烧:烧结温度为500-1000℃,保温1-24小时。
8.根据权利要求6所述的用于激光照明的全光谱荧光陶瓷的制备方法,其特征在于,步骤S2中,包含有,
步骤S21,素烧,去除有机物:烧结温度为600-1000℃,保温1-24小时;
步骤S22,真空烧结或热压烧结;烧结温度为1400-1850℃,保温时间5-24小时;以及,
步骤S23,退火:退火温度为1400-1550℃,保温时间10-30小时。
9.根据权利要求6所述的用于激光照明的全光谱荧光陶瓷的制备方法,其特征在于,步骤S3中,包含有,
步骤S31,样品双面抛光,样品厚度为0.1-0.5mm;以及,
步骤S32,样品下表面镀全反膜,样品上表面镀增透膜。
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