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用于增强全解水的自支撑磷化亚铜纳米线上的半导体异质结构

Heterostructure of Semiconductors on Self-Supported Cuprous Phosphide Nanowires for Enhanced Overall Water Splitting.

作者信息

Xu Xiao, He Ying, Huang Weifeng, Cao Aihui, Kang Longtian, Liu Jingjing

机构信息

Fujian Provincial Key Laboratory of Nanomaterials and Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, P. R. China.

Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China, Fuzhou, Fujian 350108, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2022 Apr 20;14(15):17520-17530. doi: 10.1021/acsami.2c02418. Epub 2022 Apr 8.

Abstract

Rational design, controllable synthesis, and an in-depth mechanism study of Cu-based bifunctional semiconductor heterostructures toward overall water splitting (OWS) are imperative but still face challenges. Herein, n-type iron oxide and p-type nickel phosphide and cobalt phosphide are respectively coupled with p-type cuprous phosphide nanowires on Cu foams via a general growth-phosphorization strategy. These self-supported semiconductor heterojunctions with different built-in potentials () are used as binder-free electrodes for OWS and exhibit significantly improved electrocatalytic activities compared to their counterparts. Among them, the heterostructure with the largest of 1.57 V attains the smallest overpotential of 97 mV at 10 mA cm for the hydrogen evolution reaction and 243 mV at 50 mA cm for the oxygen evolution reaction in 1 M KOH. The corresponding two-electrode electrolyzer requires a cell voltage of 1.685 V at 50 mA cm and shows admirable long-term stability at 100 mA cm with a Faraday efficiency of around 98%. These promoted electrocatalytic performances originate from the enhanced active site, accelerated charge transfer, enlarged electrochemical active surface area, and synergy between different components at the heterointerface. This work represents a promising avenue to construct cost-efficient semiconductor heterostructures as bifunctional electrocatalysts applied to the sustainable energy industry.

摘要

对用于全解水(OWS)的铜基双功能半导体异质结构进行合理设计、可控合成及深入的机理研究势在必行,但仍面临挑战。在此,通过一种通用的生长-磷化策略,分别将n型氧化铁、p型磷化镍和磷化钴与泡沫铜上的p型磷化亚铜纳米线耦合。这些具有不同内建电势()的自支撑半导体异质结用作OWS的无粘结剂电极,与同类电极相比,其电催化活性显著提高。其中,内建电势最大为1.57 V的异质结构在1 M KOH中,析氢反应在10 mA cm时过电位最小为97 mV,析氧反应在50 mA cm时过电位为243 mV。相应的双电极电解槽在50 mA cm时电池电压为1.685 V,在100 mA cm时表现出令人钦佩的长期稳定性,法拉第效率约为98%。这些提升的电催化性能源于活性位点的增强、电荷转移的加速、电化学活性表面积的增大以及异质界面处不同组分之间的协同作用。这项工作为构建具有成本效益的半导体异质结构作为双功能电催化剂应用于可持续能源产业提供了一条有前景的途径。

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