ABSTRACT
The development of robust and efficient photocatalytic constructs for boosting the water oxidation reaction (WOR) is needed for establishing a sunlight-driven renewable energy infrastructure. Here, we synthesized plasmonic core-shell nanoconstructs consisting of triangular gold nanoprism (AuTNP) core with mixed manganese oxide (MnOx) shell for photoelectrocatalytic WOR. These constructs show electrocatalytic WOR with a low onset overpotential requirement of 270 mV at pH 10. Photoexcitation showed further enhancement of their catalytic activity resulting in â¼15% decrease of the onset overpotential requirement along with the generation of photocurrent density of up to 300 µA/cm2. We showed that such light-driven enhancement of AuTNP@MnOx dyad's catalytic activity toward the WOR process includes contributions from both photocatalytic (hot carriers driven) and photothermal effects with photothermal effect playing the major role for wavelength between 532 and 808 nm. The contribution from the photocatalytic effect is appreciable only for high-energy excitations near the interband region, while the photothermal effect largely dominates for lower energy excitations near the LSPR wavelengths of the dyad.
ABSTRACT
End-to-end dimers of gold nanorods are predicted to be excellent substrates for surface-enhanced spectroscopy. However, the synthesis of solution-stable end-to-end dimers remains challenging. We exploit the pH-dependent configurational change of polyelectrolytes to initiate and terminate the gold nanorod assembly formation to produce end-to-end linked dimers in high yield. The gold nanorods are first overcoated with a polyelectrolyte, and the end-to-end attachment is initiated by adding a thiol linker in acidic medium. The assembly formation is then terminated at the dimer stage by changing the pH of the medium by the addition of an appropriate amount of 1,4-diazabicyclo[2.2.2]octane (DABCO).The nanorod dimers synthesized here are stable in solution for a week without any additional surface encapsulation.
ABSTRACT
End-to-end assemblies of anisotropic plasmonic nanostructures with small nanogaps are of great interest as they create strong hot spots for enhancing weak fluorescence and/or scattering of molecules. Here we report the growth of dithiol-linked end-to-end assemblies of gold nanorods from dimers to large networks containing thousands of individual nanorods, directed by in situ tuning of nanorod's surface charge. Surface charge was lowered to initiate the aggregation process but was subsequently increased to achieve slow tip-specific growth over seven days to form end-to-end networks of nanorods, which were stable in solution for over one month. Furthermore, we showed that these assemblies contained strong plasmonic hot spots which enhanced the fluorescence signal of a weak emitter by 104-fold. This enhancement is approximately 10-fold larger than that obtained using a single gold nanorod and is comparable to the largest enhancement obtained using more expensive lithographically made in-plane antenna arrays.
ABSTRACT
We show that many complex gold nanostructures such as the water chestnut, dog bone, nanobar, and octahedron, which are not easily accessible via a direct seed-growth synthesis approach, can be prepared via overgrowth of the same gold nanorods by varying pH and Ag concentrations in the growth solution. Overgrown nanostructures' shapes were determined by the rate of gold atom deposition, which is faster at higher pH. In the presence of AgNO3, codeposition of gold and silver atoms affects the shapes of overgrown nanostructures, particularly at high pH.
