Environmental impacts
of continued CO2 production have
led to an increased need for new methods of CO2 removal
and energy development. Nanomaterials are of special interest for
these applications, because of their unique chemical and physical
properties that allow for highly active surfaces. Here, we successfully
synthesize AgPd nanodendrite-modified Au nanoprisms in various shapes
(nanoprisms, hexagonal nanoplates, and octahedral nanoparticles) by
selective metal deposition. This strategy involves coupling galvanic
replacement between Ag layers in Au@Ag core–shell nanoprisms
and H2PdCl4 with a coreduction process of silver
and palladium ions. Synthesis of AgPd nanodendrite-tipped (4.14–11.47
wt % Pd) and -edged (25.25–31.01 wt % Pd) Au nanoparticles
can be controlled simply by tuning the concentration of H2PdCl4. More importantly, these multicomponent AgPd nanodendrite-modified
Au nanoparticles show exceptional electrocatalytic performance for
CO2 reduction. AgPd nanodendrite-edged Au nanoprisms show
more favorable potentials (−0.18 V vs RHE) than previously
reported nanocatalysts for the reduction of CO2 to formate,
and exhibit higher faradaic efficiencies (49%) than Au, Au@Ag, and
AgPd nanodendrite-tipped Au nanoprisms in aqueous electrolytes. Moreover,
AgPd nanodendrite-modified Au nanoprisms show much higher selectivity
and faradaic efficiency for CO2 reduction to CO (85–87%)
than Au and Au@Ag nanoprisms (43–64%) in organic electrolytes.
The high performance of these particles for CO2 reduction
is attributed to the unique structure of AgPd nanodendrite-modified
Au nanoprisms and the synergistic effect of Ag having an affinity
for CO2, efficient binding of hydrogen at Pd, and Au as
a stable, conductive support. In addition, AgPd nanodendrite-edged
Au nanoprisms show highly stable catalytic activity during long-term
electrolyses (up to 12 h) and repetitive use. These exciting results
indicate that AgPd nanodendrite-modified Au nanoparticles are promising
for application in CO2 conversion into useful fuels.