Correlating Thermionic Emission with Specific Surface Reconstructions in a <100> Hydrogenated Single-Crystal Diamond

被引:8
作者
Dominguez-Andrade, Hugo [1 ]
Anaya, Julian [1 ]
Croot, Alex [1 ]
Cattelan, Mattia [2 ]
Twitchen, Daniel J. [3 ]
Kuball, Martin [4 ]
Fox, Neil A. [1 ]
机构
[1] Univ Bristol, Sch Phys, HH Wills Phys Lab, Bristol BS8 1TL, Avon, England
[2] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[3] Element Six Ltd, Ascot SLS 8BP, Berks, England
[4] Univ Bristol, Ctr Device Thermog, HH Wills Phys Lab, Bristol BS8 1TL, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
thermionic; emission; diamond; hydrogen; surface; NEGATIVE ELECTRON-AFFINITY; CHEMICAL-VAPOR-DEPOSITION; NITROGEN-DOPED DIAMOND; BARIUM OXIDE; DESORPTION; ENERGY; CHEMISORPTION; CONDUCTIVITY; DEPLETION; RESPECT;
D O I
10.1021/acsami.0c01677
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Thermionic emission relies on the low work function and negative electron affinity of the, often functionalized, surface of the emitting material. However, there is little understanding of the interplay between thermionic emission and temperature-driven dynamic surface transformation processes as these are not represented on the traditional Richardson-Dushman equation for thermionic emission. Here, we show a new model for thermionic emission that can reproduce the effect of dynamic surface changes on the electron emission and correlate the components of the thermionic emission with specific surface reconstruction phases on the surface of the emitter. We use hydrogenated <100> single-crystal and polycrystalline diamonds as thermionic emitters to validate our model, which shows excellent agreement with the experimental data and could be applicable to other emitting materials. Furthermore, we find that tailoring the coverage of specific structures of the C(100)-(2 x 1):H surface reconstruction could increase the thermionic emission of diamond by several orders of magnitude.
引用
收藏
页码:26534 / 26542
页数:9
相关论文
共 59 条
[1]   Surface cleaning, electronic states and electron affinity of diamond (100), (111) and (110) surfaces [J].
Baumann, PK ;
Nemanich, RJ .
SURFACE SCIENCE, 1998, 409 (02) :320-335
[2]   Atomic-scale visualization and surface electronic structure of the hydrogenated diamond C(100)-(2x1):H surface -: art. no. 195416 [J].
Bobrov, K ;
Mayne, A ;
Comtet, G ;
Dujardin, G ;
Hellner, L ;
Hoffman, A .
PHYSICAL REVIEW B, 2003, 68 (19)
[3]   Atomic-scale desorption of hydrogen from hydrogenated diamond surfaces using the STM [J].
Bobrov, K ;
Mayne, AJ ;
Hoffman, A ;
Dujardin, G .
SURFACE SCIENCE, 2003, 528 (1-3) :138-143
[4]   Atomic-scale imaging of insulating diamond through resonant electron injection [J].
Bobrov, K ;
Mayne, AJ ;
Dujardin, G .
NATURE, 2001, 413 (6856) :616-619
[5]   EMPIRICAL POTENTIAL FOR HYDROCARBONS FOR USE IN SIMULATING THE CHEMICAL VAPOR-DEPOSITION OF DIAMOND FILMS [J].
BRENNER, DW .
PHYSICAL REVIEW B, 1990, 42 (15) :9458-9471
[6]   First principles methods using CASTEP [J].
Clark, SJ ;
Segall, MD ;
Pickard, CJ ;
Hasnip, PJ ;
Probert, MJ ;
Refson, K ;
Payne, MC .
ZEITSCHRIFT FUR KRISTALLOGRAPHIE, 2005, 220 (5-6) :567-570
[7]   A Model for Barium Oxide Depletion From Hollow Cathode Inserts [J].
Coletti, Michele ;
Gabriel, Stephen B. .
IEEE TRANSACTIONS ON PLASMA SCIENCE, 2009, 37 (01) :58-66
[8]   A powerful rontgen ray tube with a pure electron discharge [J].
Coolidge, WD .
PHYSICAL REVIEW, 1913, 2 (06) :409-430
[9]   TIME-DEPENDENT MONTE-CARLO SIMULATIONS OF H-REACTIONS ON THE DIAMOND (001)(2X1) SURFACE UNDER CHEMICAL-VAPOR-DEPOSITION CONDITIONS [J].
DAWNKASKI, EJ ;
SRIVASTAVA, D ;
GARRISON, BJ .
JOURNAL OF CHEMICAL PHYSICS, 1995, 102 (23) :9401-9411
[10]   Photoelectron emission from nitrogen- and boron-doped diamond (100) surfaces [J].
Diederich, L ;
Kuttel, OM ;
Ruffieux, P ;
Pillo, T ;
Aebi, P ;
Schlapbach, L .
SURFACE SCIENCE, 1998, 417 (01) :41-52