Department of Chemistry and Biochemistry, University of California, 1156 High Street, Santa Cruz, CA, 95064, USA.
New Energy Research Center, School of Environment and Energy, South China University of Technology, Guangzhou Higher Education Mega Centre, Guangzhou, 510006, China.
Angew Chem Int Ed Engl. 2016 Jan 22;55(4):1455-9. doi: 10.1002/anie.201508985. Epub 2015 Dec 8.
Two types of platinum nanoparticles (NPs) functionalized with ethynylferrocene were prepared. The subnanometer-sized NPs (Pt10eFc) showed semiconductor-like characteristics with a bandgap of about 1.0 eV, and the other was metal-like with a core size of about 2 nm (Pt314eFc) and no significant bandgap. IR spectroscopic measurements showed a clear red-shift of the C≡C and ferrocenyl ring =C-H vibrational energies with increasing particle core size owing to enhanced intraparticle charge delocalization between the particle-bound ferrocenyl moieties. Electrochemical measurements showed two pairs of voltammetric peaks owing to intervalence charge transfer between the ferrocenyl groups on the nanoparticle surface, which was apparently weaker with Pt10 eFc than with Pt314 eFc. Significantly, the former might be markedly enhanced with UV photoirradiation owing to enhanced nanoparticle electronic conductivity, whereas no apparent effects were observed with the latter.
两种功能化的乙炔基二茂铁铂纳米粒子(NPs)被制备出来。亚纳米尺寸的 NPs(Pt10eFc)表现出半导体特性,带隙约为 1.0eV,另一种 NPs(Pt314eFc)为金属性,核尺寸约为 2nm,且没有明显的带隙。IR 光谱测量表明,随着粒子核尺寸的增加,C≡C 和二茂铁环 =C-H 振动能明显红移,这是由于粒子结合的二茂铁部分之间的粒子内电荷离域增强。电化学测量表明,由于纳米粒子表面的二茂铁基团之间的价间电荷转移,出现了两对伏安峰,这在 Pt10eFc 上明显比在 Pt314eFc 上弱。值得注意的是,前者可能由于纳米粒子电子电导率的增强而在紫外光照射下显著增强,而后者则没有明显的影响。