Alkali-antimonide photocathodes using co-deposition and an effusion source Md Abdullah A. Mamun Carlos Hernandez-Garcia Matthew Poelker P3 Workshop : Photocathode.

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Alkali-antimonide photocathodes using co-deposition and an effusion source Md Abdullah A. Mamun Carlos Hernandez-Garcia Matthew Poelker P3 Workshop : Photocathode Physics for Photoinjectors, November 3-5, 2014 Lawrence Berkeley National Laboratory, Berkeley, California, USA

Provided an important measure of weak mixing angle and validation of the Standard Model

Too much cesium, some deposited on cathode electrode….

Motivation JLab’s introduction to alkali-antimonide photocathode fabrication… Can an inexpensive effusion source be used to make good alkali-antimonide photocathodes? How does the thickness/amount of Sb dictate the ultimate QE and low voltage lifetime of K x Cs y Sb? To understand the substrate sensitive growth of Sb How does a baked or unbaked system effect on bialkali photocathode and its performance. To understand the role of Sb for the bi-alkali photocathodes

K-Cs Co-deposition using Effusion Source Partial pressure of alkali vapors was monitored using residual gas analyzer (RGA) during deposition, not the usual quartz crystal thickness monitor. Such as, for 387  C at inlet tube, 259  C at dispensing tube, and 184  C at reservoir: Cs PP on RGA:1.35(±0.1)  Torr K PP on RGA:3.15(±0.5)  Torr The duration of deposition, to optimize QE, was also recorded for each case. Evaporation of bi-alkali was controlled by adjusting heater power and gas flow through the effusion source, in the following ranges: Inlet tube:  C Dispensing tube:  C Reservoir tube:  C Substrate temp: Falling from 120  C to  80 C Duration of evaporation varied depending on QE to optimize Monitored QE using a 532 nm green laser with cathode biased at V b =284 V K ampoules (1 gram in argon) from Espimetals, and Cs ampoules (1 gram in argon) from Strehm Chemicals

Role of Sb for Bialkali Photocathode Baked system: Sb PP of 5.5  Torr, T sub = 200  C, 32.7 A from power supply 30 min Sb deposition100 min Sb deposition Same amount of bialkali, No QE on GaAs ? During deposition QE optimized on Ta area Adequate bialkali for Sb on Ta=right stoichiometry Excess bi-alkali for GaAs region with thinner Sb Same amount of bialkali, No QE on Ta ? During deposition QE optimized on GaAs area Adequate bialkali for Sb on GaAs=> right stoichiometry Inadequate bi-alkali for Ta region with thicker Sb Photoemission is sensitive to stoichiometry, Optimum Stoichiometry is essential for good QE Sb thickness variation  variation in amount of bialkali to result the same right stoichiometry Co-deposition of bi-alkali allows optimization of stoichiometry for any thickness of Sb and This is easily achieved using the effusion type evaporation source

Sb growth: Ta vs. GaAs Substrate (Baked System) Sb on TaSb on GaAs Sb on Ta Sb on GaAs Sb PP of 5.5  Torr, 100 min at T sub = 200  C, 32.7 A from power supply Sb PP of 1  Torr, 120 min at T sub = 200  C, 33.6 A from power supply Initially Sb grows more favorably on Ta compared to GaAs. Once the Sb layer is established on GaAs, the Sb structure on both GaAs and Ta substrate observed to be in similar scale. Indicates: Sticking coefficient of Sb on Ta is better than that on GaAs. Time of formation of initial monolayers of Sb on GaAs takes longer than on Ta. The subsequent growth of Sb on Sb monolayers occurs at similar pace on both Ta and GaAs. Max. grain height ~ 600 nm Max. grain height ~ 100 nm FE-SEM images

Sb growth: Baked vs. Unbaked System Sb on TaSb on GaAs Sb on Ta Sb on GaAs Sb PP of 5.5  Torr, 100 min at T sub = 200  C, 32.7 A from power supply Leak-free baked system Post-leak unbaked system Sb growth was enhanced on GaAs in the unbaked system compared to baked system Sb growth was equally favored on both Ta and GaAs substrates in the unbaked system. Indicates : Sticking coefficient of Sb on GaAs is enhanced in the unbaked system and become similar to that on Ta. Monolayers of Sb on both GaAs and Ta grew at the same pace. Sb films on Ta and GaAs are expected to be of similar thickness in the unbaked system. Max. grain height ~ 100 nm Max. grain height ~ 300 nm

QE: Baked vs. Unbaked System Sb PP of 5.5  Torr, T sub = 200  C, 32.7 A from power supply, 532 nm laser 30 min Sb deposition100 min Sb deposition Baked System: QE observed only on one substrate  Dissimilar Sb growth on GaAs and Ta Unbaked System: QE observed on both substrates  Similar Sb growth on both substrates

QE: Baked vs. Unbaked System 5.3% QE on GaAs area No QE on Ta area! ~7% QE on GaAs and Ta area Leak-free baked system Post-leak unbaked system Sb PP of 5.5  Torr, 100 min at T sub = 200  C applying 32.7 A current, 532 nm laser During co-deposition QE was optimized w.r.t GaAs area In the baked system, No QE on Ta ? Same amount of K-Cs => Adequate for thinner Sb on GaAs => But, Inadequate for thicker Sb on Ta GaAs Ta Baked system Unbaked system

Sb Qty. vs. Bialkali Qty. Evaporated amount of both the Cs and K are dependent on Sb amount evaporated. Increasing Sb Thickness => Increasing porosity & Surface roughness=> Larger surface area=> Higher capacity to absorb bi-alkali Granular Amorphous [UBS] Sb/Ta, QE (%) : [UBS] Sb/GaAs, QE (%) : [BS] Sb/Ta, QE (%) : [BS] Sb/GaAs, QE (%) : [UBS]Sb/GaAs, t Sb, nm : >15 > >350 >600 [BS] Sb/GaAs, t Sb, nm : >320 ~600 Inadequate K-Cs Excess K-Cs

Role of Sb for Bialkali Photocathode GranularAmorphous [UBS]Sb/GaAs, t Sb, nm : >15 > >350 >600 [BS] Sb/GaAs, t Sb, nm : >320 ~600 Inadequate K-Cs Excess K-Cs DC voltage: 284 V, = 532 nm, 3.96 mW Sb serves as a sponge

Role of Sb for Bialkali Photocathode Sb is acting as a reservoir to hold the bialkali materials Thicker Sb => Porous crystalline granular film => Rougher topography Thinner Sb => Denser amorphous film => Smoother surface. Porous Sb film => More alkali absorption capacity => Require longer duration of alkali deposition => Delay in showing photo-current during deposition => Longer low voltage lifetime. Denser amorphous Sb film => Lower alkali absorption rate in Sb => Quickly reaches right alkali amount on the surface => Readily show photo-current during deposition => Shorter low voltage lifetime.

Spectral Response With = 425 nm laser and V b =284 V The best QE spot on: Ta:~ 24.2% GaAs:~ 22% With = 532 nm laser and V b =284 V The best QE spot on: Ta:~10% GaAs: ~8% Sb PP of 5.5  Torr, 120 min at T sub = 200  C, 32.7 A from power supply (unbaked system) GaAs Ta

Spectral Response Ref: CHESS seminar 2013 Smedley If we did this measurement earlier when QE was ~10% at 532 nm compared to 9% when this data is taken after 7days of deposition, we could have seen >21.3% (~27 %) QE at 425 nm The best QE spot on Ta = 24.2% and on GaAsa~22% at =425 nm, V b =284 V Sb PP of 5.5  Torr, 120 min at T sub = 200  C, 32.7 A from power supply (unbaked system)

Advantage of Effusion Source Relatively compact Convenient for bi-alkali co-deposition Co-deposition enables achieving optimized stoichiometry for even thicker(>500 nm) Sb Preserves the alkali supply when the rest of the vacuum system is vented Allows alkali replacement without venting the rest of the deposition chamber Very high alkali storage capacity Relatively inexpensive and easy to operate

Backup slides

University of Illinois, ~ 1990CEBAF, ~ 1996

List of Trials Current Supply to Sb furnaceTime of Sb depositionBaked/unbaked system (BS/UBS) 32.7(  0.3) A 30 minBaked & Unbaked 32.7(  0.3) A 70 minBaked & Unbaked 32.7(  0.3) A 100 minBaked & Unbaked 31.0(  0.3) A 120 minUnbaked 33.7(  0.3) A 120 minBaked & Unbaked MGH ~ 100 nm MGH ~ 300 nm MGH ~ 600 nm

Sb Growth on Ta 1  Torr Sb PP, 60 min 1  Torr Sb PP, 120 min 5.5  Torr Sb PP, 100 min Ta Substrate Substrate Temperature, T sub = 200  C With the increase in Sb deposition rate or duration The Sb crystals get bigger The Sb film gets increasingly porous Topography becomes rougher. Sb source: Sb pellet from Alfa Aesar

K-Cs co-deposition on ~50 nm Sb Deposition control parameters Cs PP on RGA:1.35(±0.1)E-10 Torr K PP on RGA:3.15(±0.5)E-11 Torr Substrate temp:Falling from 120 C to 80 C Deposition time: 75 min

Photocurrent from Cs x K y Sb with ~50 nm Sb 7.3 % QE max at 532 nm on GaAs, No QE from Ta

Cs x K y Sb with ~35 nm Sb on GaAs (leakfree baked system) Monitored ~5 % QE max at 532 nm on GaAs, No QE from Ta

Cs x K y Sb with 35 nm Sb on GaAs (post leak unbaked system) Monitored ~6 % QE max at 532 nm on GaAs, ~ 8% on Ta

Sb(~100 nm) on GaAs: Ta vs. GaAs Sb on GaAs Sb on Ta Initially Ta favors growth of Sb film on it, indicating that the relative Sb film thickness differs more as the films get thinner.

Sb(~600 nm) on GaAs: Ta vs. GaAs Sb on GaAs Sb on Ta As Sb grow thicker, the Sb structure on both GaAs and Ta substrate observed to be in similar scale. Which indicates that the relative Sb film thickness difference minimizes as the films get thicker.