Full-Spectrum Light-Harvesting Solar Thermal Electrocatalyst Boosts Oxygen Evolution

被引:0
|
作者
Xu, Mingxia [1 ,2 ]
Bing, Qiming [2 ]
Tu, Yunchuan [2 ]
Zhang, Yunlong [2 ]
Zhang, Mo [2 ]
Cai, Yafeng [2 ]
Li, Jinlei [3 ]
Meng, Xianguang [2 ]
Zhu, Jia [3 ]
Yu, Liang [2 ,4 ]
Deng, Dehui [2 ,4 ]
机构
[1] Univ Sci & Technol China, Dept Chem Phys, Hefei 230026, Anhui, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Collaborat Innovat Ctr Chem Energy Mat, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Nanjing Univ, Coll Engn & Appl Sci, Natl Lab Solid State Microstruct, Jiangsu Key Lab Artificial Funct Mat, Nanjing 210023, Jiangsu, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Full-spectrum solar thermal conversion; Graphene-encapsulated Metal; Hierarchical Nanocage; Oxygen evolution reaction; CONVERSION; GRAPHENE; GENERATION; CARRIER;
D O I
10.1002/anie.202412049
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enabling high-efficiency solar thermal conversion (STC) at catalytic active site is critical but challenging for harnessing solar energy to boost catalytic reactions. Herein, we report the direct integration of full-spectrum STC and high electrocatalytic oxygen evolution activity by fabricating a hierarchical nanocage architecture composed of graphene-encapsulated CoNi nanoparticle. This catalyst exhibits a near-complete 98 % absorptivity of solar spectrum and a high STC efficiency of 97 %, which is superior than previous solar thermal catalytic materials. It delivers a remarkable potential decrease of over 240 mV at various current densities for electrocatalytic oxygen evolution under solar illumination, which is practically unachievable via traditionally heating the system. The high-efficiency STC is enabled by a synergy between the regulated electronic structure of graphene via CoNi-carbon interaction and the multiple absorption of lights by the light-trapping nanocage. Theoretical calculations suggest that high temperature-induced vibrational free energy gain promotes the potential-limiting *O to *OOH step, which decreases the overpotential for oxygen evolution.
引用
收藏
页数:8
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