Aqueous Synthesis of Ultrathin Platinum/Non‐Noble Metal Alloy Nanowires for Enhanced Hydrogen Evolution Activity. Issue 36 (31st July 2018)

• Record Type: Journal Article
• Authors: Liu, Zhaojun; Qi, Jing; Liu, Moxuan; Zhang, Shumeng; Fan, Qikui; Liu, Hongpo; Liu, Kai; Zheng, Haoquan; Yin, Yadong; Gao, Chuanbo
• Is Part Of: Angewandte Chemie international edition. Volume 57:Issue 36(2018)
• Page Start: 11678
• Page End: 11682
• Publication Date: 2018-07-31
• Subjects: aqueous synthesis -- bimetallic alloys -- hydrogen evolution reaction -- platinum -- ultrathin nanowires; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201806194
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Although aqueous synthesis of nanocrystals is advantageous in terms of the cost, convenience, environmental friendliness, and surface cleanness of the product, nanocrystals of Pt and non‐noble metal alloys are difficult to obtain with controlled morphology and composition from this synthesis owing to a huge gap between the reduction potentials of respective metal salts. This huge gap could now be remedied by introducing a sulfite into the aqueous synthesis, which is believed to resemble an electroless plating mechanism, giving rise to a colloid of Pt‐M (M=Ni, Co, Fe) alloy nanowires with an ultrasmall thickness (ca. 2.6 nm) in a high yield. The sulfite also leads to the formation of surface M−S bonds and thus atomic‐level Pt/M–S(OH) interfaces for greatly boosted hydrogen evolution kinetics under alkaline conditions. An activity of 75.3 mA cm −2 has been achieved with 3 μg of Pt in 1 m KOH at an overpotential of 70 mV, which is superior to previously reported catalysts. Abstract : Bridging the gap : Co‐reduction of Pt and a non‐noble metal (Fe, Co, Ni) in a fully aqueous system has been achieved by remedying the huge gap between the reduction potentials of their metal salts by involving a sulfite, which gives rise to ultrathin alloy nanowires with sulfur surface modification. The nanowires show superior hydrogen evolution kinetics reaction in an alkaline electrolyte.