Scalable 2D Semiconductor‐Based van der Waals Heterostructure Interface with Built‐in Electric Field for Enhanced Electrochemical Water Splitting

Author:

Eom Jeongha1,Cho Yun Seong1ORCID,Lee Jihun1,Heo Jae Won123,Plutnarová Iva4ORCID,Sofer Zdeněk4ORCID,Kim In Soo123,Rhee Dongjoon15ORCID,Kang Joohoon123ORCID

Affiliation:

1. School of Advanced Materials Science and Engineering Sungkyunkwan University (SKKU) Suwon 16419 Republic of Korea

2. Nanophotonics Research Center Korea Institute of Science and Technology (KIST) Seoul 02792 Republic of Korea

3. KIST‐SKKU Carbon‐Neutral Research Center SKKU Suwon 16419 Republic of Korea

4. Department of Inorganic Chemistry University of Chemistry and Technology Prague Technicka 5 Prague 6 166 28 Czech Republic

5. Department of Electrical and Systems Engineering University of Pennsylvania Philadelphia 19104 PA USA

Abstract

Electrochemical water splitting has received tremendous attention as an eco‐friendly approach to produce hydrogen. Noble metals and their oxides are commonly used as electrocatalysts to reduce activation energy barriers for hydrogen and oxygen evolution reactions in high‐performance electrodes, but their cost, scarcity, and limited stability hinder widespread adoption of electrochemical water splitting. Further advancements are therefore needed to reduce reliance on noble metals and improve the long‐term stability. Herein, solution‐processed 2D van der Waals (vdW) p–n heterostructures as an interfacial layer between catalysts and the electrode are introduced to enhance the catalytic performance. These heterostructures are formed by sequentially assembling electrochemically exfoliated black phosphorus and molybdenum disulfide nanosheets into electronic‐grade p‐ and n‐type semiconductor thin films, with the scalability extending across tens‐of‐centimeter scale areas. Benefiting from the charge distribution and built‐in electric field developed upon heterojunction formation, the vdW heterostructure interfacial layer increases both the catalytic activity and stability of commercial Pt/C and Ir/C catalysts compared to when these catalysts are directly loaded onto electrodes. Additionally, the vdW heterostructure also serves as a template for synthesizing nanostructured Pt and Ir catalysts through electrodeposition, further enhancing the catalytic performance in terms of mass activity and stability.

Funder

National Research Foundation of Korea

Korea Basic Science Institute

Ministry of Education Youth and Sports

Publisher

Wiley

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