Atomically Precise AuPt(thiolate)(dithiolate) Nanoclusters with Excellent Electrocatalytic Hydrogen Evolution Reactivity.

[AuPt(C6)] (C6 = 1-hexanethiolate) is twice as active as commercial Pt nanoparticles in promoting the electrocatalytic hydrogen evolution reaction (HER), thereby attracting attention as new HER catalysts with well-controlled geometric structures. In this study, we succeeded in synthesizing two new Au-Pt alloy nanoclusters, namely, [AuPt(TBBT)(TDT)] (TBBT = 4--butylbenzenethiolate; TDT = thiodithiolate) and [AuPt(TBBT)(PDT)] (PDT = 1,3-propanedithiolate), by exchanging all the ligands of [AuPt(PET)] (PET = 2-phenylethanethiolate) with mono- or dithiolates. Although [AuPt(TBBT)(TDT)] was synthesized serendipitously, a similar cluster, [AuPt(TBBT)(PDT)], was subsequently obtained by selecting the appropriate reaction conditions and optimal combination of thiolate and dithiolate ligands.

Tiara-like Hexanuclear Nickel-Platinum Alloy Nanocluster.

Tiara-like metal nanoclusters (TNCs) have attracted a great deal of attention because of their high stability and easy synthesis under atmospheric conditions as well as their high activity in various catalytic reactions. Alloying is one of the methods that can be used to control the physicochemical properties of nanoclusters, but few studies have reported on alloy TNCs. In this study, we synthesized alloy TNCs [NiPt(PET), where = 1-5 and PET = 2-phenylethanethiolate] consisting of thiolate, nickel (Ni), and platinum (Pt).

Improved activity for the oxygen evolution reaction using a tiara-like thiolate-protected nickel nanocluster.

Practical electrochemical water splitting and carbon-dioxide reduction are desirable for a sustainable energy society. In particular, facilitating the oxygen evolution reaction (OER, the reaction at the anode) will increase the efficiency of these reactions. Nickel (Ni) compounds are excellent OER catalysts under basic conditions, and atomically precise Ni clusters have been actively studied to understand their complex reaction mechanisms.