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<p>Harvesting hot carriers before they lose energy to the lattice is a critical route toward surpassing the conventional thermodynamic limit in optical-to-electrical (O-E) conversion. However, photocurrent from such hot carriers has remained challenging to directly detect because they equilibrate on picosecond timescales, outpacing conventional electronic measurement. Here, by employing terahertz electronics with sub-picosecond temporal resolution, we directly monitor ultrafast O-E conversion in black phosphorus (BP). Photoexcitation near the metal contact under zero source-drain bias generates an ultrafast photocurrent with a decay time of ~ 400 fs—orders of magnitude faster than the typical sub-nanosecond energy relaxation in BP—demonstrating a measured 3 dB bandwidth of 260 GHz with an intrinsic limit of ~ 600 GHz. Notably, this photocurrent flows via energetic holes toward the contact electrode, regardless of the equilibrium carrier type. We propose super-diffusive hot-carrier transport as the microscopic origin of the ultrafast photocurrent. Furthermore, we show that the ultrafast hot-carrier contribution can coexist with the much slower cold-carrier contribution based on the photovoltaic effect, demonstrating that hot carriers can be harvested without discarding lower-energy carriers. These findings highlight the potential of sub-picosecond hot-carrier extraction to expand the O-E conversion bandwidth without sacrificing efficiency, bridging fundamental hot-carrier physics with ultrahigh-speed technological applications.</p>

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Sub-picosecond extraction of hot carriers in black phosphorus

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年5月13日

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  • Katsumasa Yoshioka,
  • Taro Wakamura,
  • Takuya Okamoto,
  • Norio Kumada

摘要

Harvesting hot carriers before they lose energy to the lattice is a critical route toward surpassing the conventional thermodynamic limit in optical-to-electrical (O-E) conversion. However, photocurrent from such hot carriers has remained challenging to directly detect because they equilibrate on picosecond timescales, outpacing conventional electronic measurement. Here, by employing terahertz electronics with sub-picosecond temporal resolution, we directly monitor ultrafast O-E conversion in black phosphorus (BP). Photoexcitation near the metal contact under zero source-drain bias generates an ultrafast photocurrent with a decay time of ~ 400 fs—orders of magnitude faster than the typical sub-nanosecond energy relaxation in BP—demonstrating a measured 3 dB bandwidth of 260 GHz with an intrinsic limit of ~ 600 GHz. Notably, this photocurrent flows via energetic holes toward the contact electrode, regardless of the equilibrium carrier type. We propose super-diffusive hot-carrier transport as the microscopic origin of the ultrafast photocurrent. Furthermore, we show that the ultrafast hot-carrier contribution can coexist with the much slower cold-carrier contribution based on the photovoltaic effect, demonstrating that hot carriers can be harvested without discarding lower-energy carriers. These findings highlight the potential of sub-picosecond hot-carrier extraction to expand the O-E conversion bandwidth without sacrificing efficiency, bridging fundamental hot-carrier physics with ultrahigh-speed technological applications.