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表面转移掺杂可以调节纳米金刚石的胶体稳定性和自组装。

Surface transfer doping can mediate both colloidal stability and self-assembly of nanodiamonds.

机构信息

CEA, LIST, Diamond Sensors Laboratory, F-91191 Gif-sur-Yvette, France.

出版信息

Nanoscale. 2013 Oct 7;5(19):8958-62. doi: 10.1039/c3nr02492j. Epub 2013 Aug 22.

DOI:10.1039/c3nr02492j
PMID:23965659
Abstract

Although undoped diamond is insulating, hydrogenated bulk diamond surfaces exhibit surface conductivity under air and are electrochemically active in aqueous solutions. Due to their large surface/volume ratio, similar surface effects may exhibit a dramatic impact on the properties of nanodiamonds. Here we show that plasma-hydrogenated detonation nanodiamonds (NDs-H) display a positive zeta potential in water due to charge transfer with a redox couple involving oxygen in water. The transfer doping of NDs-H in water can be modulated by pH. Surprisingly, after acid addition, strong Coulomb coupling between NDs-H and adsorbed counterions induces the self-assembly of NDs-H into organized macro-structures reaching millimeter scale.

摘要

虽然未掺杂的金刚石是绝缘的,但氢化的大块金刚石表面在空气中表现出表面导电性,并且在水溶液中具有电化学活性。由于其大的表面积/体积比,类似的表面效应可能对纳米金刚石的性质产生显著影响。在这里,我们表明,由于涉及水中氧的氧化还原对的电荷转移,等离子体氢化爆轰纳米金刚石(NDs-H)在水中显示正的 ζ 电位。NDs-H 在水中的转移掺杂可以通过 pH 值进行调节。令人惊讶的是,在添加酸后,NDs-H 与吸附的抗衡离子之间的强库仑耦合诱导 NDs-H 自组装成达到毫米尺度的有序宏观结构。

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