Photoelectron Collection Efficiency in Mixtures of Noble Gases with CF4 J. M. D. Escada, P. J. B. M. Rachinhas, T. H. V. T. Dias, J. A. M. Lopes, F. P. Santos, C. A. N. Conde, Member, IEEE, and A. D. Stauffer Abstract--The collection efficiency f for the photoelectrons emitted from a CsI photocathode into CF4 and into Ar-CF4 and Ne-CF4 mixtures is investigated by Monte Carlo simulation. The dependence of f on the reduced electric field E/N in the 0.1-40 Td range, on incident photon energy Eph in the 6.8-9.8 eV (183127 nm) range and on mixture composition is analyzed. Electron drift parameters in CF4, Ar-CF4 and Ne-CF4 are also presented. I. INTRODUCTION models the emission of photoelectrons from a CsI photocathode using the photoelectron energy distributions from [7] for incident monoenergetic VUV photons, and from [8] for the VUV Hg lamp. The emitted photoelectrons are followed along their free paths in the gas taking into account multiple elastic and inelastic collisions, and the probability that a photoelectron is transmitted is the collection efficiency f, obtained as the ratio f = m/m0 between the number m of photoelectrons that are transmitted when m0 are injected into the gas (f =1 in vacuum). ollowing previous Monte Carlo simulation work for Fpure noble gases, noble gas mixtures, and mixtures of Ar - - - CF4 —— 10 sion 2 cm ) sm -16 sm (10 CF4 v4 TEST FIT TUDO sd 1 CF4 MT TEST FIT TUDO CF4 v3 TEST FIT TUDO sion CF4 v indirect FIT TUDO CF4 ATTACH FIT TUDO sexc sn ind s noble gases with CH4 [1]-[5], results are now presented for the collection efficiency f of the photoelectrons emitted from a CsI photocathode into CF4 and into Ar-CF4 and Ne-CF4 mixtures, where f is the fraction of the number of photoelectrons transmitted in the gas compared to vacuum. The addition of CH4 or CF4 to noble gases efficiently increases photoelectron transmission and drift velocity, due to the important role played by the vibrational excitation of the molecules at low electron impact energies. Results are calculated in pure CF4 and in ArCF4 and Ne-CF4 mixtures, for applied electric fields E/N ranging from 0.1 to 40 Td (N is the gas number density and 1 Townsend = 10-17 V cm2) and incident photon energy Eph. We have considered both monoenergetic VUV photons in the 6.89.8 eV (183-127 nm) range and irradiation with a continuous VUV lamp peaked at 6.7 eV (185 nm). Electron drift velocities w are also calculated, and w and f are compared with experimental measurements where available. 100 CF4 ND TEST FIT TUDO CF4 ION TEST FIT TUD Ar MT 10-16cm2 ArgonIon 10-16cm2 ArgonExc 10-16cm2 Dummy for sec.Scale 0.1 sn 4 0.01 0.01 sn 3 0.1 sa 1 10 Electron energy e (eV) 100 100 ↑ Ne - - - CF4 –––– Ne SIGm: SPLINEa 2keV; 10-16*12676 1.7231) até10keV Ne ExcZecca 31.7&1 LN (MC after June2 10 Ne_ION: SPLINE at 10-16*77.35826326* 0.773523838) até10k CF4 MT TEST FIT T sm 2 cm ) II. MONTE CARLO SIMULATION This work was carried out at Centro de Instrumentação do Departamento de Física da Universidade de Coimbra, Portugal (Research Unit 217/94), and received support from FEDER and POCI2010 programs, through FCT (Fundação para a Ciência e Tecnologia) project POCI/FP/63418/2005. J. Escada, P.J.B.M. Rachinhas, T.H.V.T. Dias, J.A.M. Lopes, F.P. Santos, and C.A.N. Conde are with Departamento de Física da Universidade de Coimbra, Portugal (e-mail: fteresa@gian.fis.uc.pt). P.J.B.M. Rachinhas is also with Serviço de Radioterapia, Hospitais da Universidade de Coimbra, Portugal. J.A.M. Lopes is also with Instituto Superior de Engenharia de Coimbra, Portugal. A. D. Stauffer is with Department of Physics and Astronomy, York University, Toronto, Canada. -16 sion (10 CF4 v4 TEST FIT T 2º sd 1 s Detailed descriptions of the simulation model used in the calculations can be found in [1]-[6]. As in our previous studies of electron back-scattering effects [2]-[5], the simulation CF4 v3 TEST FIT TU sion sn ind sm CF4 ATTACH FIT TU CF4 ND TEST FIT T 0.1 CF4 ION TEST FIT T 0.01 0.01 0.1 CF4 v indirect FIT TU sexc sn 3 sn 4 Dummy for Seconda sa 1 Electron energy e 10 100 (eV) Fig. 1. Electron scattering cross-sections in Ar, Ne and CF4 used in the Monte Carlo simulation: elastic momentum transfer (σm), vibrational excitation (σν4, σν3, σνind ), electron attachment (σa), dissociation (σd), excitation (σexc), and ionization (σion). w (106 cm/s This work (Monte Carlo) 10 ekL (eV) M 1 ekT (eV) M w e e kT 0.1 0.01 0.01 0.1 eT Christ. e 1 10 eKL (eV) C LG and Qlth Phys Chem. 100 E/N (Td) Fig. 2. Monte Carlo (continuous curves) and experimental values (symbols) in CF4 for the electron mean energy e , drift velocity w, and characteristic energies εkL=eDL/µ and εkT=eDT/µ, where DL and DT are the longitudinal and transverse diffusion coefficients and µ=w/E is the electron mobility. WHunter et al. 100 □,●, Christophorou et al. 1979 [18], ● 20%CF4 a) ∆,○ Hunter et al. 1985 [19] + Nakamura and Kurachi 1988 [20] * Schmidt and Polenz 1988 [21] W (106cm/s) 90 W (106cm/s) 80 CF4 10 30 20 w (106 cm s-1) B. Collection efficiency : results for monoenergetic VUV incident photons This section describes the Monte Carlo photoelectron collection efficiencies obtained for monoenergetic incident photons with 7 different energies Eph in the range 6.8-9.8 eV. The results for f in CF4 are shown in Fig. 4 as a function of E/N for different Eph, together with the results previously obtained for Ne [2],[5], Ar [2],[3] and CH4 [3]. In Fig. 5, f is presented as a function of Eph and different E/N values for mixtures of Ne and Ar with a 10% concentration of CF4. In Figs. 6 a), b) and c), the f curves obtained for Eph = 6.8, 7.6 and 9.8 eV and different E/N values in Ne-CF4 and Ar-CF4 mixtures are represented as a function of CF4 concentration η. Fig. 4 a) shows that transmission in CF4 is always higher and increases more steeply with E/N than in Ne and Ar, due to the vibrational excitation of the CF4 molecules at low electron energies, similar to previously results for CH4 [3]. While crosssections for vibrational excitation of CF4 (Fig. 1) are in general larger than for CH4 (Fig. 1 in [3]), it is found that transmission in CF4 or mixtures with CF4 is not always higher than in CH4 or equivalent mixtures with CH4. As an example, Fig. 4 b) shows that f in CF4 is only higher than in CH4 for the higher photon energies Eph. On the other hand, while the efficiency f is always higher in Ne than in Ar (see Fig. 4 a), f in a Ne-CF4 mixture may be lower than in the equivalent Ar-CF4 mixture. Emed (eV) e kL RESULTS A. Electron drift parameters The Monte Carlo results for the electron drift velocity w, mean energy e and characteristic energies εkL and εkT in CF4 are shown in Fig. 2 as a function of the density-reduced electric field E/N, and drift velocities in Ar-CF4 and Ne-CF4 mixtures are shown in Fig. 3 at different CF4 concentrations. The agreement between the Monte Carlo results (continuous curves) with data from the literature (symbols) in Fig. 2 and Fig. 3 is a test to our simulation model and of the choice of cross-sections for the scattering of electrons by CF4 molecules. Fig. 3 shows that drift velocity w tends to be higher in CF4 and Ar-CF4 or Ne-CH4 mixtures than in the pure noble gases, a behaviour similar to the observed for CH4 and mixtures of noble gases with CH4. WHunter et A 38 58 (10 CF4 + Christophorou et al. 1996 [16] Christophorou and Olthoff 1999 [17] W_MC (106cm 10 5 2 1 W_MC (106cm 0.5 W_MC (106cm 1 w Ar MCmt Ar Ar-CF4 W 70Ar+30CF4 This work (Monte Carlo) 0,1 0,1 1 10 W 90Ar+10CF4 100 E/N (Td) W 98Ar+2CF4 100 ● Christophorou et al. 1979 [18], ● 10%CF4 b) This work (Monte Carlo) W_MC (106cm Wtab 90Ne-10CF4 w (106 cm/s) 70 (106cm/s) CF4 10 w (106 cm s-1) III. 100 w (106 cm s-1), e (eV), e k (eV) The cross-sections for the scattering of the electrons by Ar and Ne atoms and CF4 molecules used in the present simulation are represented in Fig. 1. In Ar and Ne, they are those previously adopted in [2],[3] for Ar, and in [2],[5] for Ne. A description of the cross-sections in Ar can be found in [2], [3]. In Ne, the cross-sections for elastic momentum transfer follow [9] below 20 eV and [10] above 20 eV, and inelastic scattering cross-sections are based on [11], [12] for excitation, and [13], [14] for ionization. In CF4, the cross-section data recommended in [15], [16], [17] are used, neglecting super-elastic collisions. 5 10 2 W MC (106cm/s) 8 30 W 94.92Ar+5.0 Nakamura W MC (106cm/s) 9 W 99.5Ar+0.5C W MC (106cm/s) 9 2 W MC (106cm/s) 9 W_MC (106cm W MC (106cm/s) 7 1 Ne W_MC (106cm W MC (106cm/s) N Ne-CF4 W (106cm/s) 95 W MC (106cm/s) C W 80Ar+20CF4 Polenz 88 0.1 0.1 1 10 100 E/N (Td) Fig. 3. Monte Carlo (continuous curves) and experimental values (symbols) for the electron drift velocity w: a) in Ar, CF4, and Ar-CF4 mixtures with 0.5%, 1%, 2%, 5%, 10%, 20%, and 30% CF4 concentrations, b) in Ne, CF4, and Ne-CF4 mixtures with 2%, 5%, 10%, 20% and 30% CF4 concentrations. w (106 cm/s) C W 99.505Ar+0. e Nakamura CF4 1 E ph Ne Ar (eV) 1 E ph = 6.8 eV 6.8 eV 6.8 0.8 7.6 eV 0.8 40 Td 7.2 eV 7.2 8.2 eV 7.6 0.6 8.8 eV 0.6 8.8 9.2 0.4 9.2 eV f f 8.2 0.4 9.8 eV 9.8 f_6,8eV CF4 MC f_7,2eV 0.2 CF4 MC f_7,6eV CF4 MC f_8,2eV 0 CF4 MC 0 10 20 30 40 f_8,8eV E/N (Td) CF4 MC f_9,2eV E ph CF4 MC --- CH4 CF4 Series8 1 f_9,8eV (eV) CF4 MC Series9 f_6,8eV 6.8 Ar MC Series10 0.8 f_7,2eV 7.2 Ar MC Series11 f_7,6eV 7.6 Ar MC Series12 0.6 f_8,2eV 8.2 Ar MC Series13 8.8 f_8,8eV 9.2 Ar MC Series14 0.4 f_9,2eV 9.8 Ar MC f_7,2eV f_9,8eV CF4 MC Ar MC f_7,6eV 0.2 CF4 MC f_8,2eV CF4 MC f_8,8eV 0 CF4 MC 0 10 20 30 40 f_9,2eV CF4 MC E/N (Td) f_9,8eV Fig. 4. Monte Carlo collection efficiency f as a function of E/N for CF4 MC photoelectrons emitted from a CsI photocathode into CF4 compared a) with f_6,8eV Ne and Ar b) with CH4 (data from [2],[5] for Ne; [2],[3] for Ar, [3] for CH4). CF4 MC 0.2 a) 1 0.8 a) 0 0 20 40 60 80 Ne-CF4 Ar-CF4 0.8 b) 40 Td 0.6 f 0.4 0.2 0.1 Td E ph = 7.6 eV 0 0 20 40 60 80 90%Ne 40 90%Ar 100 CF4 concentration h (%) 1 c) E ph = 9.8 eV E/N (Td) 100 CF4 concentration h (%) 1 f b) 0.1 Td Ne-CF4 Ar-CF4 0.8 + 10%CF4 3 Ne-CF4 Ar-CF4 f 0.6 0.6 f 0.4 40 Td 0.4 0.2 0.1 0.2 0.1 Td 0 0 0 6.5 7.5 8.5 9.5 E ph (eV) Fig.5. Monte Carlo collection efficiency f for photoelectrons emitted from a CsI photocathode into 90%Ne-10%CF4 and 90%Ar-10%CF4 mixtures, as a function of incident photon energy Eph for the reduced electric fields E/N = 0.1, 3, and 40 Td in CH4. 20 40 60 80 CF4 concentration h (%) 100 0.3 0.5 1 2 3 5 10 15 25 40 0.1 0.1 0.3 0.5 1 2 3 5 10 15 25 40 0.3 0.5 1 2 3 5 10 15 25 40 0.1 0.1 0.3 0.5 1 2 3 5 10 0.3 15 0.5 1 2 3 5 10 15 25 40 0.1 0.1 0.3 0.5 1 2 3 5 10 15 25 40 Fig. 6. Monte Carlo collection efficiency f for photoelectrons emitted from a CsI photocathode into Ne-CF4 and Ar-CF4 mixtures as a function of CF4 concentration η, for E/N = 0.1, 0.3, 0.5, 1, 3, 5, 10, 15, 25, 35 and 40 Td and incident photon energies a) Eph = 6.8 eV, b) Eph = 7.6 eV and c) Eph = 9.8 eV (data from [2], [5] for Ne; and from [2], [3] for Ar). This is shown in Fig. 5 for mixtures with 10%CF4, where f in Ne-CF4 becomes lower than in Ar-CF4 as we move to lower E/N. The calculations in the mixtures are summarized in Fig. 6 where f is seen to increase in general with E/N and decrease with Eph. The dependence of f on CF4 concentration η shows a sharp increase of f at very low η, in some cases going through maxima where f reaches values above pure CF4, and smoothing out at intermediate and higher η. In general, the behaviour of the f curves in CF4, Ne-CF4 or Ar-CF4 and equivalent results involving CH4, can essentially be explained in terms of the ratios ς=nν/nt between the number of vibrational excitation collisions nν and the total number of collisions nt in the gas, where ς is a measure of the competition between vibrational excitation of the molecules and elastic scattering. C. Collection efficiency : results for incident photons from a continuous VUV Hg(Ar) lamp In order to compare with available collection efficiencies f measured when the photocathode is irradiated with a continuous spectrum Hg(Ar) lamp, we used in the simulation the photoelectron energy distribution measured in [8] for this lamp. The Monte Carlo and experimental data in CF4, Ne, Ar and Xe are compared in Fig. 7. The agreement between calculated and measured results is satisfactory, considering that Ne and Ar data are close, and that experimental values are rather scattered and include scintillation feedback above ~4Td for the noble gases. Nevertheless, for Ne, Ar and Xe, the agreement is improved if calculations take into account electron reflection by using a reflection coefficient r~0.3, though r may depend on the electron energy [26]. Also photocathode surface conditions lead to large uncertainties in r and in photoelectron emission energies ε0 [27], and we know that f depends strongly on ε0 for incident photons in the energy range of this lamp [3]. 1 CF4 0,8 0,6 f Ne Ar 0,4 Xe 0,2 0 0 2 4 6 8 10 E/N (Td) Fig. 7. Collection efficiency f in CF4 , Ne, Ar, and Xe for photoelectrons emitted from a CsI photocathode irradiated with a continuous VUV Hg(Ar) lamp with a spectrum peaked at 6.7 eV (185 nm). Curves are our Monte Carlo data (CF4, present; Xe, Ne [5]; Ar [3]). Symbols are experimental results (CF4: [22], [23]; Xe: [23]; Ne: ▲ [23]; Ar: [23], [24], [25]). IV. REFERENCES [1] P. J. B. M. Rachinhas, J. A. M. Lopes, T. H. V. T. Dias, F. P. Santos, C. A. N. Conde and A. D. Stauffer, “Photoelectron Collection Efficiency in Rare Gases: A Monte Carlo Study” in Proc. of MC2000 – International Conference on Advanced Monte Carlo for Radiation Physics, Particle Simulation and Applications, A. Kling, F. Barão, M. Nakagawa, L. Távora and P. Vaz, Eds. Heidelberg: Elsevier, 2001, pp. 535-542. [2] T. H. V. T. Dias, P. J. B. M. Rachinhas, J. A. M. Lopes, F. P. Santos, L. M. N. Távora, C. A. N. Conde and A. D. Stauffer, J. Appl. Phy. vol. 37, pp. 540-549, 2004. [3] J. Escada, P. J. B. M. Rachinhas, T. H. V. T. Dias, J. A. M. Lopes, F. P. Santos, C. A. N. Conde, A. D. Stauffer, “Monte Carlo Study of Backscattering Effects in the Photoelectron Emission into CH4 and ArCH4 Mixtures”, Conf.Record IEEE Nuclear Science Symposium, 16-22 October 2004, Roma, J. A. Seibert ed., vol. 1, pp. 559-563, 2004. [4] P. J. B. M. Rachinhas, J. Escada, T. H. V. T. Dias, F. P. Santos, J. A. M. Lopes, C. A. N. Conde, and A. D. Stauffer, “Photoelectron Collection Efficiency in CH4 and Xe-CH4 Mixtures”, Conf. Record of IEEE Nuclear Science Symposium, 25-29 October2005, Puerto Rico, Bo Yu ed., vol. 3, pp. 1271-1274, 2005. [5] J. Escada, P. J. B. M. Rachinhas, T. H. V. T. Dias, J. A. M. Lopes, F. P. Santos, C. A. N. Conde, and A. D. Stauffer, “Photoelectron Collection Efficiency in Ne-CH4 and Xe-CH4 Mixtures”, presented at ISRP10 - 10th International Symposium on Radiation Physics, 17-22 September, Coimbra, Portugal. [6] T. H. V. T. Dias, F. P. Santos, A. D. Stauffer and C. A. N. Conde, Phys. Rev. A, vol. 48, pp. 2887-2902, 1993. [7] T. H. Di Stefano, W. E. Spicer, Phys. Rev. B, vol.7, pp.1554-1563, 1973. [8] E. Shefer, E. Shefer, A. Breskin, T. Boubol, R. Chechik, H, Cohen, I. Feldman and B. K. Singh, J. Appl. Phys. vol. 92, pp. 4758-4771, 2002. [9] R. P. Mc Eachran and A. D. Stauffer, Physics Letters vol. 107A, pp. 397399, 1985. [10] M. Hayashi, “Recommended Values of Transport Cross Sections for Elastic Collisions and Total Collision Cross Sections for Electrons in Atomic and Molecular Gases”, Technical Report IPPJ-AM-19, Nagoya University,1981. [11] R. S. Brusa, G. P. Karwasz and A. Zecca, Z. Phys. D vol. 38, pp. 279287, 1996. [12] A. Zecca, G. P. Karwasz and R. S. Brusa, J. Phys. B: At. Mol. Opt. Phys. vol. 33, pp. 843-845, 2000. [13] D. Rapp and P. Englander-Golden, J. Chem. Phys. vol. 43, pp. 14641479, 1965. f[14] MC NeE. Krishnakumar and S. K. Srivastava, J. Phys. B: At. Mol. Opt. Phys. vol. 21, pp. 1055-1082, 1988. G.Christophorou, J. K. Olthoff, and M. V. V. S. Rao, J. Phys. Chem. f[15] Ne expL. Coelho et al. 2006 Ref. Data vol. 25, pp. 1341-1388, 1996. [16] L. G.Christophorou and J. K. Olthoff, J. Phys. Chem. Ref. Data vol. 28, f MC Ar pp. 967-982, 1999. [17] M.C. Bordage, P. Ségur, L. G.Christophorou and J. K. Olthoff, J. Appl. 86, pp. 3558-3566, 1999. f Ar expPhys. Coelho vol. et al. 2006 [18] L. G. Christophorou, D. L. McCorkle, D. V. Maxey and J. G. Carter, Nucl. Instrum. Meth. vol. 163, pp. 141-149, 1979. f Ar exp Buzulutskov et al. [19] S. R. Hunter, J. G. Carter and L. G. Christophorou, J. Appl. Phys. vol. 2004 58, pp. 3001-3015, 1985. f[20] Ar expY. Di Mauro et al. 2004 and M. Kurachi, J. Phys. D: Appl. Phys. vol. 21, Nakamura pp. 718-723, 1988. B.Schmidt, Nucl. Instrum. Meth. A vol.273, pp.488-493, 1988. f[21] CF4 exp Breskin et al. S.Polenz, 2002 G3DATA [22] A. Breskin, A. Buzulutskov and R. Chechik, Nucl. Instrum. Meth. A vol. 483, pp. 670-675, 2002. f MC CF4 [23] L. Coelho e t al., to be submitted, 2006. [24] A. Di Mauro, E. Nappi, F. Posa, A. Breskin, A. Buzulutskov, R. f MC XeChechik, S. F. Biagi, G. Paic and F. .Piuz, Nucl. Instrum. Meth. A vol. 371, pp. 137-142, 1996. [25] A. Buzulutskov, R. Chechik, G. Garty, F. Sauli and L. Shekhtman, Nucl. f Xe exp Coelho et al. 2006 Instrum. Meth. A vol. 443, pp. 164-180, 2000. [26] M. Radmilović and Z. Lj. Petrović, Eur. Phys. J. AP vol.11, pp. 35-42, f CF4 exp Coelho et al. 2006 2000. [27] A. V. Phelps and Z. Lj. Petrović, Plasma Sources Sci. Technol. vol.8, pp. R21-R44, 1999.