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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.

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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