Enhanced p–d Orbital Coupling in Unconventional Phase RhSb Alloy Nanoflowers for Efficient Ammonia Electrosynthesis in Neutral Media

Fu Liu (Co-first Author), Jingwen Zhou (Co-first Author), Mingzi Sun (Co-first Author), Zhihang Xu (Co-first Author), Helin Wang, Ning Yao, Yunhao Wang, Fengkun Hao, Yuecheng Xiong, Juan Wang, Liang Guo, Qingbo Wa, Guozhi Wang, Xiang Meng, Mingzheng Shao, Chaohui Wang, Hsiao-Chien Chen*, Hao Ming Chen, Ye Zhu*, Bolong Huang*Zhanxi Fan*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

3 Citations (Scopus)

Abstract

Phase control provides a promising approach for physicochemical property modulation of metal/alloy nanomaterials toward various electrocatalytic applications. However, the controlled synthesis of alloy nanomaterials with unconventional phases remains challenging, especially for those containing both p- and d-block metals. Here, we report the one-pot synthesis of ultrathin RhSb alloy nanoflowers (NFs) with an unconventional 2H phase. Using 2H RhSb NFs as an electrocatalyst for nitrite reduction reaction in neutral media, the optimal NH3 Faradaic efficiency and yield rate can reach up to 96.8% and 47.2 mg h−1 mgcat−1 at −0.3 and −0.6 V (vs. reversible hydrogen electrode), respectively. With 2H RhSb NFs as a bifunctional cathode catalyst, the as-assembled zinc-nitrite/methanol batteries deliver a high energy efficiency of 96.4% and improved rechargeability with 120-h stable running. Ex/in situ characterizations and theoretical calculations have demonstrated that the phase change of RhSb from face-centered cubic (fcc) to 2H has optimized the electronic structure through stronger interactions between Rh and Sb by p–d orbital couplings, which improves the adsorption of key intermediates and reduces the reaction barriers of nitrite reduction to guarantee the efficient electrocatalysis. This work offers a feasible strategy of boosting the electrocatalytic performance of alloy nanostructures by integrating phase control and p–d orbital coupling. © 2025 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.
Original languageEnglish
Article numbere202504641
JournalAngewandte Chemie - International Edition
Online published7 Apr 2025
DOIs
Publication statusOnline published - 7 Apr 2025

Funding

The authors acknowledge the financial support by grants (Project Nos. 22175148 and 52102320) from the National Natural Science Foundation of China, grants (Project Nos. 21309322, 15304023, 15304724, 15307522, N_PolyU502/21, and CRS_PolyU504/22) from the Research Grants Council of Hong Kong, grants (Project Nos. JCYJ20220530140815035 and JCYJ20220531090807017) from the Shenzhen Science and Technology Program, grant (2023A1515012219) from the Natural Science Foundation of Guangdong Province, ITC via the Hong Kong Branch of National Precious Metals Material Engineering Research Center (NPMM), and grants (Project Nos. 9610480, 9610663, 7006007, 7020103, and 9680301) from the City University of Hong Kong. The TEM facility is funded by the Research Grants Council of Hong Kong (Project No. C5029\u201018E).

Research Keywords

  • Alloy nanostructures
  • Ammonia electrosynthesis
  • Electrocatalysis
  • Phase control
  • p–d Orbital coupling

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