材料科学
电催化剂
过电位
纳米材料
偶氮苯
纳米技术
催化作用
堆积
化学工程
可逆氢电极
三元运算
电化学
电极
聚合物
有机化学
化学
物理化学
复合材料
参比电极
计算机科学
工程类
程序设计语言
作者
Pengchao Wu,Pengliang Sui,Guiping Peng,Zichao Sun,Fan Liu,Wenqian Yao,Haibao Jin,Shaoliang Lin
标识
DOI:10.1002/adma.202312724
摘要
Abstract The development of high‐reactive single‐atom catalysts (SACs) based on long‐range‐ordered ultrathin organic nanomaterials (UTONMs) (i.e., below 3 nm) provides a significant tactic for the advancement in hydrogen evolution reactions (HER) but remains challenging. Herein, photo‐responsive ultrathin peptoid nanobelts (UTPNBs) with a thickness of ≈2.2 nm and micron‐scaled length are generated using the self‐assembly of azobenzene‐containing amphiphilic ternary alternating peptoids. The pendants hydrophobic conjugate stacking mechanism reveals the formation of 1D ultralong UTPNBs, whose thickness is dictated by the length of side groups that are linked to peptoid backbones. The photo‐responsive feature is demonstrated by a reversible morphological transformation from UTPNBs to nanospheres (21.5 nm) upon alternative irradiation with UV and visible lights. Furthermore, the electrocatalyst performance of these aggregates co‐decorated with nitrogen‐rich ligand of terpyridine (TE) and uniformly‐distributed atomic platinum (Pt) is evaluated toward HER, with a photo‐controllable electrocatalyst activity that highly depended on both the presence of Pt element and structural characteristic of substrates. The Pt‐based SACs using TE‐modified UTPNBs as support exhibit a favorable electrocatalytic capacity with an overpotential of ≈28 mV at a current density of 10 mA cm −2 . This work presents a promising strategy to fabricate stimuli‐responsive UTONMs‐based catalysts with controllable HER catalytic performance.
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