Source abstract
Abstract
Thanks to their versatile functionality, metal oxides (MOs) constitute one of the key family materials in a variety of current demands for sensor, catalysis, energy storage and conversion, optical electronics, and piezoelectric mechanics. Much effort has focused on engineering specific nanostructure and macroscopic morphology of MOs that aims to enhance their performances, but the design and controlled synthesis of ultrafine nanostructured MOs in a cost-effective and facile way remains a challenge. In this work, we have exploited the advantages of intrinsic structures of graphene oxide (GO) papers, serving as a sacrificial template, to design and synthesize two-dimensional (2D) layered and free-standing MO papers with ultrafine nanostructures. Physicochemical characterizations showed that these MO materials are nanostructured, porous, flexible, and ultralight. The as-synthesized materials were tested for their potential application in photoelectrochemical (PEC) energy conversion. In terms of PEC water splitting, copper oxide papers were used as an example and exhibited excellent performances with an extremely high photocurrent-to-weight ratio of 3 A cm –2 g –1 . We have also shown that the synthesis method is generally valid for many earth-abundant transition metals including copper, nickel, iron, cobalt, and manganese.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Department of Chemistry, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark
The State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai 201620, China
Funding
Natural Science Foundation of Shanghai · Teknologi og Produktion, Det Frie Forskningsråd · Shanghai Municipal Education Commission · Directorate-General for Research and Innovation · Science and Technology Commission of Shanghai Municipality · China Scholarship Council · National Natural Science Foundation of China · Shanghai Education Development Foundation