化学
催化作用
成核
碳纤维
电解
铂金
耐久性
化学工程
氢
阳极
电解水
电极
电化学
无机化学
分解水
化学物理
瓶颈
炭黑
过渡金属
纳米技术
爆炸物
多相催化
电催化剂
作者
Maoqiao Xiang,Zhensui Lu,Kuo Liu,Wenjun Ding,Yanyan Li,J ZHU,Puheng Yang,Peng Peng,Yafeng Yang,Huigang Zhang,Qingshan Zhu
摘要
Enhancing the stability of Pt single atoms (SAs) remains a critical bottleneck for practical applications. Herein, we overcome this limitation by developing a ZrCl 3 –CH 4 system that enables an explosive nucleation to directly construct defect-rich ZrC nanoislands (NIs) on carbon cloth as ultrastable anchoring platforms for Pt single atoms (Pt 1 @ZrC NIs). This strategy dramatically enhances the surface number density of ZrC particles by 2 orders of magnitude over conventional methods and eliminates the long-standing issue of free carbon contamination. The Pt 1 @ZrC NI electrode exhibits a strong synergy, where ZrC promotes water adsorption/dissociation and Pt facilitates hydrogen migration/desorption, yielding a mass activity 116- and 132-fold greater than that of the commercial Pt@C catalyst in alkaline and acidic media, respectively. Moreover, owing to the excellent acid- and base-resistance of ZrC and its strong binding to Pt SAs and the substrate, the Pt 1 @ZrC NIs catalyst maintains exceptional stability in both acidic and alkaline media.
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