1996
DOI: 10.1016/0925-9635(96)00529-8
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Chemical modification of diamond surfaces using a chlorinated surface as an intermediate state

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Cited by 97 publications
(49 citation statements)
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“…Chlorinated diamond is obtained by thermal reaction of H-terminated diamond with molecular chlorine (Cl 2 ) [45]. This is used as an intermediate to obtain hydroxyl groups (-OH termination) by treatment with water vapor at RT, amino groups by treatment with NH 3 at 425 °C, and -CF groups by treatment with CHF 3 at 600 °C.…”
Section: Reaction Of Halogens To Diamond Surfacesmentioning
confidence: 99%
“…Chlorinated diamond is obtained by thermal reaction of H-terminated diamond with molecular chlorine (Cl 2 ) [45]. This is used as an intermediate to obtain hydroxyl groups (-OH termination) by treatment with water vapor at RT, amino groups by treatment with NH 3 at 425 °C, and -CF groups by treatment with CHF 3 at 600 °C.…”
Section: Reaction Of Halogens To Diamond Surfacesmentioning
confidence: 99%
“…Acid treatments: Hydrogen plasma treatment (Thoms et al 1994;Strother et al 2002;Knickerbocker et al 2003) -Nitric and sulphuric acid (Kong et al 2005a;Huang and Chang 2004;Liu et al 2008;Chao et al 2007;Ushizawa et al 2002) Annealing in hydrogen gas (Härtl et al 2004;Christiaens et al 2006;Saini et al 2008) -Nitric acid Huang et al 2008;Sushchev et al 2008;Mitev et al 2007) Water vapour treatment (Ando et al 1996a) -Hydrochloric acid (Kossovsky et al 1995;Mitev et al 2007) Borane (BH3) (Krüger et al 2006;Neugart et al 2007;Liang et al 2009;Zhang et al 2009b) -Perchloric acid (Xu et al 2005) -Potassium dichromate and sulphuric acid (Mitev et al 2007) -Sulfuric acid and potassium permanganate (Xu et al 2005) Annealing in:…”
Section: Oxidation/carboxylation Reductionmentioning
confidence: 99%
“…-apoobelin ) -aflatoxin B1 (AfB1) ) -DNA (Fu et al 2007) -luciferase Puzyr' et al 2004) -Alpha-bungarotoxin (Liu et al 2008 (Miller and Brown 1996;Knickerbocker et al 2003;Lu et al 2004;Strother et al 2002;Yang et al 2002;Takahashi et al 2003;Yeap et al 2008;Zhang et al 2009b;Zheng et al 2009;Chang et al 2010) (Strother et al 2002;Takahashi et al 2003;Ida et al 2003;Tsubota et al 2003;Härtl et al 2004;Christiaens et al 2006;Chang et al 2010) (Liu et al 2004;Ando et al 1996b;Khabashesku et al 2005;Ando et al 1996a;Ando et al 1993) (Ando et al 1996a;Ikeda et al 1998;Takahashi et al 2003;Miller and Brown 1996) Silanes Aryl Alkyl Amino (Zhang et al 2009b;Liang et al 2009;Krüger et al 2006;Yeap et al 2008 Zheng et al 2009) choice of biological buffer systems or media is also important, since both foetal bovine serum and phosphate buffered saline, two common biological buffer systems, tend to cause re-aggregation (Neugart et al 2007;Vaijayanthimala et al 2009). Despite the challenges involved in preparing and maintaining de-aggregated nanodiamonds, positive results strongly support their use in biological applications.…”
Section: Oxidation/carboxylation Reductionmentioning
confidence: 99%
“…For a high surface loading, it is essential to achieve surface uniformity. Reactions with hydrogen, 59,60 chlorine, 61 and fluorine 62 have been explored to attain surface homogeneity and reactivity enhancement. The surfaces of chlorinated NDs were further modified with hydroxyl, amine, and carbon fluoride groups.…”
Section: Surface Modification Of Ndsmentioning
confidence: 99%
“…Figure 5 summarizes approaches used in the past to introduce various functionalities on the surface of NDs. 48,[59][60][61][62][63][64][65][66] One of the earliest modifications of the ND surface involved the generation of surface radicals, which then acted as substrates for synthesizing carboxylic acid- 59 and dicarboxylic acid- 60 functionalized NDs. For a high surface loading, it is essential to achieve surface uniformity.…”
Section: Surface Modification Of Ndsmentioning
confidence: 99%