High-pressure discharge lamp electrode having a dendritic...

Electric lamp and discharge devices – With gas or vapor – Electrode composition

Reexamination Certificate

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C313S335000, C313S040000, C313S351000

Reexamination Certificate

active

06486602

ABSTRACT:

TECHNICAL FIELD
The invention proceeds from an electrode for a high-pressure discharge lamp in accordance with the preamble of claim 1. At issue, in particular, are mercury short-arc lamps, in particular for the semiconductor industry. There, they are frequently used in photolithographic processes for exposing wafers or other substrates. A further preferred field of application is inert gas high-pressure discharge lamps, in particular xenon high-pressure discharge lamps. Application for metal halide lamps is also possible.
PRIOR ART
Already known from publication EP-A 791 950 is a high-pressure discharge lamp in which the anode is provided outside its tip with a sintered-on layer made from fine-grained tungsten. The surface of the anode is enlarged thereby. The temperature of the anode can thus be lowered during operation, and the bulb blackening can be reduced. The emissivity of such a layer is approximately 0.5.
DE-A 11 82 743 discloses the use of a layer which raises the emissivity and is made from sintered-on tungsten or TaC. The layer is applied to the anode in this case by slurrying a suspension of butyl acetate with cellulose binder and the corresponding metal powder. The sintering process is performed under a vacuum at temperatures above 1800° C. Additional cooling can be achieved by using cooling channels 1-3 mm deep.
SUMMARY OF THE INVENTION
It is the object of the present invention to provide an electrode for a high-pressure discharge lamp in accordance with the preamble of claim 1 which has a very long service life.
This object is achieved by means of the characterizing features of claim 1. Particularly advantageous refinements are to be found in the dependent claims.
The coating according to the invention of the surface of an electrode is suitable as an extremely effective mechanism for cooling the electrode (by thermal radiation). The point is that the higher the emission coefficient the cooler the electrode becomes. Consequently, the tungsten evaporation from the electrode, and thus the bulb blackening can be reduced. Because of the exponential increase in the tungsten evaporation rate with the temperature of the electrode, even a comparatively slight drop in temperature leads to a substantial reduction in the bulb blackening.
In photolithography, in particular, it is required of the lamp that the reduction in the luminous flux should be as slight as possible in the course of the lamp operation. An alternative is the desire for a luminous flux which is as high as possible, so that it is possible to achieve a very short exposure time of the substrate. Consequently, a lengthening of the service life can be achieved, on the one hand. Alternatively, design possibilities are opened up for achieving a higher initial intensity in conjunction with constant maintenance. The dimensions of the electrodes can also possibly be reduced.
The reason for the reduction in the luminous flux is that the electrode material (tungsten being used as a rule) can melt and evaporate in the discharge arc in the case of a high power density. The anode, in particular, is heated up strongly by the impact of the electrons. Tungsten evaporating from the anode is deposited on the bulb and leads to bulb blackening which reduces the luminous flux of the lamp. However, the invention can also be applied in the case of highly loaded cathodes.
The anode temperature depends in this case essentially on the power emitted by it. If the anode is regarded as a Planckian radiator, the emitted power per area (L) is described by the Stefan-Boltzmann law:
L=&egr;×&sgr;×T
4
Here, &sgr;=5.67×10
−8
W m
−2
K
−4
is the Stefan-Boltzmann constant; the emission coefficient &egr; describes the deviation of a thermal radiator (0<&egr;<1) from an ideal blackbody radiator. (&egr;=1). T is the temperature in K.
In the present invention, the coating of the anode with a dendritic metal or a metal compound increases the emission coefficient from approximately 0.3 (pure tungsten) to values above 0.6 (in the case of a temperature of at least 1000° C.) . Values of over 0.8 are even reached for the first time in lamp construction. The dendritic structure is understood here as a multiplicity of needle-shaped, radiation-reflecting outgrowths on the otherwise smooth surface. These outgrowths are located next to one another at a spacing of a few nanometers to more than a hundred micrometers, preferably at a mean spacing of at least 300 nm. A structure in which the depth of the valley between two neighbouring needle-shaped peaks is at least 30% of the spacing of these peaks from one another has proved to be particularly suitable. The dendritic layer can be produced, in principle, from high-melting-point metals. Particularly suitable are rhenium, tungsten, molybdenum and tantalum or their carbides and/or nitrides. Carbides or nitrides of hafnium or zirconium are also suitable. In addition, a normal coating made from a high-melting-point metal can be applied between the core of tungsten and the dendritic layer.
A rhenium layer is particularly suitable, since a dendritic structure can be produced particularly effectively thereby. Its emission coefficient &egr; is approximately 0.9. Consequently, for a prescribed emitted power L it is possible in the case of an anode coated with dendritic rhenium to reduce the temperature by up to 200 K when operating the anode, by comparison with an uncoated anode, or one coated with sintered-on tungsten or TaC. The suitability of the rhenium layer for lamp construction is astonishing to the extent that the vapour pressure of the rhenium is higher by a factor of approximately 75 by comparison with tungsten. This point of view plays no role in the case of a rotary anode operated in a vacuum, since the vapour-deposited material condenses at cold spots. However, in lamp construction the intense deposition would lead to blackening, and thus to reduced service life. Because of the substantial temperature drop, this disadvantageous effect is more than balanced out, however.
This greatly improved anode cooling furthermore greatly reduces the evaporation of the regular electrode material (tungsten) from the deposition surface of the anode facing the discharge. As a consequence thereof, the lamp is distinguished overall in the case of identical light data by a substantially diminished reduction in radiation in the course of the service life.
The front region of the anode is preferably hemispherical or conically tapered. Particularly suitable is a conical frustum with a plane deposition surface for the discharge (called the anode plateau in the following text).
Alternatively, the invention can provide anodes with smaller dimensions in conjunction with an unchanged service life response and the same operating temperature. The smaller dimensioning reduces the shading of the discharge arc by the electrodes, as a result of which the luminous flux of the lamp is increased in conjunction with the same service life response.
For example, it is possible by means of chemical gas phase epitaxy (also known in technical language as CVD (Chemical Vapor Deposition)) to apply to the surface of the anode a metal layer, approximately 10 to 40 &mgr;m thick, with a dendritic surface morphology. It is characterized by needle-shaped crystallites whose mutual spacing is typically approximately 10-30 &mgr;m. The needle-shaped crystallites are positioned approximately perpendicularly on the surface, with the result that incident radiation is virtually completely absorbed by multiple reflection between the lateral surfaces of neighbouring crystals. As a result, such a layer has a high absorptivity and is black. In accordance with the high absorptivity, it has a high emission coefficient of up to &egr;=0.9. The production of such layers is described in U.S. Pat. No. 3,982,148 in connection with an application in rotary anodes for X-ray tubes. Reference is expressly made to this publication. The CVD technique is particularly suitable as a method of production for this

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